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  • 1.
    Andersson, Jessika
    et al.
    Department of Medicine, Uppsala University Hospital, Uppsala, Sweden.
    Sundström, Johan
    Department of Medicine, Uppsala University Hospital, Uppsala, Sweden.
    Kurland, Lisa
    Department of Medicine, Uppsala University Hospital, Uppsala, Sweden.
    Gustavsson, Thomas
    Department of Signals and Systems, Chalmers University of Technology, Gothenburg, Sweden.
    Hulthe, Johannes
    Wallenberg Laboratory, Sahlgrenska University Hospital, Gothenburg, Sweden; AstraZeneca R&D, Mölndal, Sweden.
    Elmgren, Anders
    AstraZeneca R&D, Mölndal, Sweden.
    Zilmer, Kersti
    Department of Biochemistry, University of Tartu, Tartu, Estonia.
    Zilmer, Mihkel
    Department of Biochemistry, University of Tartu, Tartu, Estonia.
    Lind, Lars
    Department of Medicine, Uppsala University Hospital, Uppsala, Sweden.
    The carotid artery plaque size and echogenicity are related to different cardiovascular risk factors in the elderly: the Prospective Investigation of the Vasculature in Uppsala Seniors (PIVUS) study2009In: Lipids, ISSN 0024-4201, E-ISSN 1558-9307, Vol. 44, no 5, p. 397-403Article in journal (Refereed)
    Abstract [en]

    Carotid plaques can be characterised by ultrasound by size and echogenicity. Both size and echogenicity are predictors of cardiovascular events. The aim of this study was to examine whether traditional risk factors and markers of inflammation and oxidation were associated with plaque size and echogenicity. Computerised analysis of carotid plaque size and echogenicity (grey scale median, GSM) were performed by ultrasound in a population-based health survey in 1,016 subjects aged 70 years (PIVUS study). Information on cardiovascular risk factors was collected, together with markers of inflammation and oxidation. Increased Framingham risk score, systolic blood pressure, higher BMI and decreased HDL, lower glutathione levels were related to echolucent plaques. Previous or present smoking was common with significantly more pack-years related to the echorich plaques. Plaque size was associated with increased Framingham risk score, systolic blood pressure, blood glucose levels, smoking, ApoB/A1 ratio, OxLDL, TNF alpha, HOMA insulin resistance, leucocyte count, decreased BCD-LDL and low levels of l-selectin. Low HDL, increased BMI and decreased glutathione levels were associated with the echolucency of carotid plaques, implying metabolic factors to play a role for plaque composition. Markers of inflammation were related to plaque size alone, implying inflammation to be predominantly associated with the amount of atherosclerosis. These results suggest that plaque size and echogenicity are influenced by different risk factors.

  • 2.
    Andersson, Jonas
    et al.
    Örebro University, School of Medical Sciences. Centre for Clinical Research Sörmland/Uppsala University, Mälarsjukhuset, Eskilstuna, Sweden.
    Nordgren, Lena
    Centre for Clinical Research Sörmland/Uppsala University, Mälarsjukhuset, Eskilstuna, Sweden; Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden.
    Cheng, Ivy
    Örebro University, School of Medical Sciences. Örebro University Hospital. University of Toronto, Sunnybrook Health Sciences Center, Toronto Ontario, Canada.
    Nilsson, Ulrica
    Division of Nursing, Department of Neurobiology, Care Sciences, and Society, Karolinska Institute, Stockholm, Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences.
    Long emergency department length of stay: A concept analysis2020In: International Emergency Nursing, ISSN 1755-599X, E-ISSN 1878-013X, Vol. 53, article id 100930Article in journal (Refereed)
    Abstract [en]

    Introduction: Emergency Department (ED) Length of stay (LOS) has been associated with poor patient outcomes, which has led to the implementation of time targets designed to keep EDLOS below a specific limit. The cut-offs defining long EDLOS varies across settings and seem to be arbitrarily chosen. This study aimed to clarify the meaning of long EDLOS.

    Methods: A concept analysis using the Walker and Avant approach was conducted. It included a literature search aiming to identify all uses of the concept, resulting in a set of defining attributes and a way of measuring the concept empirically.

    Results: Long EDLOS was primarily used as proxy for other phenomena, e.g. boarding or crowding. The definitions had cut-offs ranging between 4 and 48 h. The attributes defining long EDLOS was waiting, a crowded ED environment and an inefficient organization.

    Discussion: Time targets are probably more suitable when directed towards and tailored for specific sub-groups of the ED population.

  • 3.
    Andersson, Åsa
    et al.
    Örebro University, School of Medical Sciences. Department of Geriatrics, School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
    Dahlkvist, Lisabet
    Centre of Clinical Research, Region Värmland, Karlstad, Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Emergency, School of Medical Sciences, Faculty of Medicineand , Health Örebro University, Örebro, Sweden.
    Patient-centered outcomes and outcome measurements for people aged 65 years and older-a scoping review2024In: BMC Geriatrics, E-ISSN 1471-2318, Vol. 24, no 1, article id 528Article, review/survey (Refereed)
    Abstract [en]

    INTRODUCTION: The aging population is a challenge for the healthcare system that must identify strategies that meet their needs. Practicing patient-centered care has been shown beneficial for this patient-group. The effect of patient-centered care is called patient-centered outcomes and can be appraised using outcomes measurements.

    OBJECTIVES: The main aim was to review and map existing knowledge related to patient-centered outcomes and patient-centered outcomes measurements for older people, as well as identify key-concepts and knowledge-gaps. The research questions were: How can patient-centered outcomes for older people be measured, and which patient-centered outcomes matters the most for the older people? STUDY DESIGN: Scoping review.

    METHODS: Search for relevant publications in electronical databases, grey literature databases and websites from year 2000 to 2021. Two reviewers independently screened titles and abstracts, followed by full text review and extraction of data using a data extraction framework.

    RESULTS: Eighteen studies were included, of which six with involvement of patients and/or experts in the process on determine the outcomes. Outcomes that matter the most to older people was interpreted as: access to- and experience of care, autonomy and control, cognition, daily living, emotional health, falls, general health, medications, overall survival, pain, participation in decision making, physical function, physical health, place of death, social role function, symptom burden, and time spent in hospital. The most frequently mentioned/used outcomes measurements tools were the Adult Social Care Outcomes Toolkit (ASCOT), EQ-5D, Gait Speed, Katz- ADL index, Patient Health Questionnaire (PHQ9), SF/RAND-36 and 4-Item Screening Zarit Burden Interview.

    CONCLUSIONS: Few studies have investigated the older people's opinion of what matters the most to them, which forms a knowledge-gap in the field. Future research should focus on providing older people a stronger voice in what they think matters the most to them.

  • 4.
    Aspelund, Amalia Liljequist
    et al.
    Department of Research and Education, Karolinska Institutet, Stockholm, Sweden.
    Patel, Mohamed Quraish
    Department of Surgery, Khayelitsha Hospital, Cape Town, South Africa.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Research and Education, Karolinska Institutet, Stockholm, Sweden.
    McCaul, Michael
    Biostatistics Unit, Division of Epidemiology and Biostatistics, Department of Global Health, Stellenbosch University, South Africa.
    van Hoving, Daniël Jacobus
    Division of Emergency Medicine, Stellenbosch University, Cape Town, South Africa.
    Evaluating trauma scoring systems for patients presenting with gunshot injuries to a district-level urban public hospital in Cape Town, South Africa2019In: African journal of emergency medicine, ISSN 2211-419X, Vol. 9, no 4, p. 193-196Article in journal (Refereed)
    Abstract [en]

    Introduction: Trauma scoring systems are widely used in emergency settings to guide clinical decisions and to predict mortality. It remains unclear which system is most suitable to use for patients with gunshot injuries at district-level hospitals. This study compares the Triage Early Warning Score (TEWS), Injury Severity Score (ISS), Trauma and Injury Severity Score (TRISS), Kampala Trauma Score (KTS) and Revised Trauma Score (RTS) as predictors of mortality among patients with gunshot injuries at a district-level urban public hospital in Cape Town, South Africa.

    Methods: Gunshot-related patients admitted to the resuscitation area of Khayelitsha Hospital between 1 January 2016 and 31 December 2017 were retrospectively analysed. Receiver Operating Characteristic (ROC) analysis were used to determine the accuracy of each score to predict all-cause in-hospital mortality. The odds ratio (with 95% confidence intervals) was used as a measure of association.

    Results: In total, 331 patients were included in analysing the different scores (abstracted from database n = 431, excluded: missing files n = 16, non gunshot injury n = 10, <14 years n = 1, information incomplete to calculate scores n = 73). The mortality rate was 6% (n = 20). The TRISS and KTS had the highest area under the ROC curve (AUC), 0.90 (95% CI 0.83-0.96) and 0.86 (95% CI 0.79-0.94), respectively. The KTS had the highest sensitivity (90%, 95% CI 68-99%), while the TEWS and RTS had the highest specificity (91%, 95% CI 87-94% each).

    Conclusions: None of the different scoring systems performed better in predicting mortality in this high-trauma burden area. The results are limited by the low number of recorded deaths and further studies are needed.

  • 5.
    Becker, Julia
    et al.
    Institute for Disaster and Emergency Management, Berlin, Germany.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Örebro University Hospital, Örebro, Sweden.
    Höglund, Erik
    Örebro University, School of Health Sciences. Örebro University Hospital. Ambulance Department, Örebro Country Council, Örebro, Sweden.
    Hugelius, Karin
    Örebro University, School of Health Sciences. Ambulance Department, Örebro Country Council, Örebro, Sweden.
    Dynamic ambulance relocation: a scoping review2023In: BMJ Open, E-ISSN 2044-6055, Vol. 13, no 12, article id e073394Article, review/survey (Refereed)
    Abstract [en]

    Objectives Dynamic ambulance relocation means that the operators at a dispatch centre place an ambulance in a temporary location, with the goal of optimising coverage and response times in future medical emergencies. This study aimed to scope the current research on dynamic ambulance relocation.

    Design A scoping review was conducted using a structured search in PubMed, Scopus and Web of Science. In total, 21 papers were included.

    Results Most papers described research with experimental designs involving the use of mathematical models to calculate the optimal use and temporary relocations of ambulances. The models relied on several variables, including distances, locations of hospitals, demographic-geological data, estimation of new emergencies, emergency medical services (EMSs) working hours and other data. Some studies used historic ambulance dispatching data to develop models. Only one study reported a prospective, real-time evaluation of the models and the development of technical systems. No study reported on either positive or negative patient outcomes or real-life chain effects from the dynamic relocation of ambulances.

    Conclusions Current knowledge on dynamic relocation of ambulances is dominated by mathematical and technical support data that have calculated optimal locations of ambulance services based on response times and not patient outcomes. Conversely, knowledge of how patient outcomes and the working environment are affected by dynamic ambulance dispatching is lacking. This review has highlighted several gaps in the scientific coverage of the topic. The primary concern is the lack of studies reporting on patient outcomes, and the limited knowledge regarding several key factors, including the optimal use of ambulances in rural areas, turnaround times, domino effects and aspects of working environment for EMS personnel. Therefore, addressing these knowledge gaps is important in future studies.

  • 6.
    Bohm, K.
    et al.
    Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Department of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Emergency Medicine, Örebro University Hospital, Örebro, Sweden.
    The accuracy of medical dispatch: a systematic review2018In: Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine, E-ISSN 1757-7241, Vol. 26, no 1, article id 94Article, review/survey (Refereed)
    Abstract [en]

    BACKGROUND: It is a challenge to dispatch Emergency medical Services (EMS) appropriately with limited resources and maintaining patient safety; this requires accurate dispatching systems. The objective of the current systematic review was to examine the evidence, according to GRADE, for medical dispatching systems to accurately dispatch EMS according to level of acuity and in recognition of specific conditions.

    A systematic search was performed trough PubMed, Web of Science, Embase (free text in all fields), Centre for Reviews and Dissemination (CRD), and Cochrane Central Register of Controlled Trials up to 16th of May, 2017. A combination of keywords and Medical Subject Heading (MeSH) terms relevant to "emergency medical dispatch criteria" were used, to search for articles published between 2012 and 2017. Publications were included according to the inclusion/exclusion criteria using the Systematic Reviews and Meta-Analyses (PRISMA) protocol. Level of evidence was evaluated in accordance with Grading of Recommendations Assessment, Development and Evaluation (GRADE). Articles included were those that provided evidence for at least one of the measures of dispatch system accuracy; i.e. sensitivity, specificity, positive and negative predictive and/or over- and under-triage. The search identified 1445 articles. After the removal of duplicates, 382 titles were reviewed for relevance and an additional 359 articles were excluded based on manuscript title and abstract. An additional five articles were excluded after review of the full text versions of the remaining articles. The current review included 18 publications which all were based on primary research.

    CONCLUSIONS: The 18 articles addressed the identification of cardiac arrest, stroke, medical priority and major trauma using different dispatching systems. The results of the current review show that there is a very low to low overall level of evidence for the accuracy of medical dispatching systems. We suggest that it is necessary to create a consensus on common standards for reporting before consensus can be reached for the level of accuracy in medical dispatching systems.

  • 7.
    Bohm, Katarina
    et al.
    Karolinska Institutet, Institution of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden.
    Kurland, Lisa
    Karolinska Institutet, Institution of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden; Section of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Bartholdson, Sofia
    Karolinska Institutet, Institution of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden.
    Castrèn, Maaret
    Karolinska Institutet, Institution of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden; Section of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Descriptions and presentations of sepsis: A qualitative content analysis of emergency calls2015In: International Emergency Nursing, ISSN 1755-599X, E-ISSN 1878-013X, Vol. 23, no 4, p. 294-298Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Sepsis is a serious condition which requires early treatment. We often fail to recognize sepsis patients in the chain of prehospital care. Knowledge of how sepsis is expressed in calls to the emergency medical communication centre (EMCC) is limited. An increased understanding could lead to earlier identification of patients with sepsis.

    OBJECTIVE: The aim of this study was to describe the descriptions of sepsis used during communication between the caller and the emergency medical dispatcher (EMD).

    METHODS: To achieve the aim of the study, an inductive approach of qualitative content analysis was used. In total, 29 consecutive patients, who arrived at the emergency department by ambulance and received a diagnosis of sepsis according to the International Classification of Diseases (ICD)-10, were included in the study. For each case, the corresponding emergency call recording from the EMCC was transcribed verbatim. Main categories and subcategories from the text were abstracted.

    RESULTS: From fifteen subcategories, three main categories were abstracted: "Deterioration", "Physical signs and symptoms" and "Difficulties establishing satisfactory contact with the patient." The way laymen and professionals expressed themselves seemed to differ.

    CONCLUSIONS: Sepsis was described in terms of the physical symptoms, changes of condition and communication abilities of the patient. This knowledge could lead to the identification of keywords which could be incorporated in the decision tool used by the EMD to increase sepsis identification, but further research is required.

  • 8.
    Brink, Magnus
    et al.
    Infektionskliniken, Sahlgrenska universitetssjukhuset, Göteborg, Sverige.
    Cronqvist, Jonas
    Infektionskliniken, Skånes universitetssjukhus, Malmö, Sverige.
    Fagerberg, Anneli
    Anestesi och intensivvård, Sahlgrenska universitetssjukhuset, Göteborg, Sverige.
    Kurland, Lisa
    Akutkliniken, Universitetssjukhuset Örebro, Örebro, Sverige.
    Lindgren, Pär
    Anestesi och intensivvård, Växjö ­centrallasarett, Växjö, Sverige.
    Lipcsey, Miklos
    Anestesi och intensivvård, Akademiska sjukhuset, Uppsala, Sverige.
    Okas, Mantas
    Akutmedicinkliniken, ­Capio S:t Görans sjukhus AB, Stockholm, Sverige.
    Petersson, Johan
    Funktion perioperativ medicin och intensiv­vård, Karolinska universitetssjukhuset Solna, Stockholm, Sverige.
    Nu gäller Sepsis-3 för definitioner och diagnostiska kriterier [New definition of and diagnostic criteria for sepsis: Swedish use of Sepsis-3]2018In: Läkartidningen, ISSN 0023-7205, E-ISSN 1652-7518, Vol. 115, no 15, p. 660-667, article id E3W9Article in journal (Refereed)
  • 9.
    Brown, Ruth
    et al.
    Emergency Department, Imperial College Healthcare NHS Trust, London, UK.
    Kurland, Lisa
    Örebro University, School of Medical Sciences.
    Lojo Rial, Carlos
    Emergency Department, Carlos Lojo Rial, Guy's and St Thomas' Hospital NHS Foundation Trust, London, UK.
    How should we train emergency physicians for Quality and Safety activities?2023In: European journal of emergency medicine, ISSN 0969-9546, E-ISSN 1473-5695, Vol. 30, no 6, p. 391-392Article in journal (Refereed)
  • 10.
    Castrén, Maaret
    et al.
    Department of Clinical Science and Education at Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Section of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Kurland, Lisa
    Department of Clinical Science and Education at Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Section of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Liljegard, Sofia
    Department of Clinical Science and Education at Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Djärv, Therese
    Department of Clinical Science and Education at Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Emergency Department, Karolinska University Hospital, Solna, Sweden.
    Non-specific complaints in the ambulance; predisposing structural factors2015In: BMC Emergency Medicine, E-ISSN 1471-227X, Vol. 15, article id 8Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: The pre-hospital assessment non-specific complaint (NSC) often applies to patients whose diagnosis does not match any other specific assessment correlating to particular symptoms or diseases, though some previous studies have found them to be related to serious underlying conditions. The aim was to identify whether the structural factors such as urgency according to the dispatch priority of the Emergency Medical Communication Centre (EMCC) or work load in the Emergency Medical Services (EMS) are predisposing factors for the assessment of NSC instead of a specific assessment.

    METHODS: All patients with assessed condition NSCs by the EMS to Södersjukhuset during 2011 (n = 493) were compared with gender- and age-matched controls (n = 493), which were randomly drawn from all patients with specific conditions in the EMS, regarding day of week, time of day and priority set by EMCC with chi-squared tests and multivariate logistic regression models.

    RESULTS: Among patients with NSCs, more were females (58 %) and the median age was 82. Almost all patients were categorized with NSCs during the daytime (8 a.m. to 9 p.m.), i.e. 450 (91 %) as compared to 373 (75 %) of those with specific conditions (p < 0.01). The risk of having an EMS dispatched as low priority by the EMCC was almost doubled among patients with NSCs compared to controls (OR 1.97, 95 % CI 1.38-2.79).

    CONCLUSIONS: Since patients with NSCs appear most frequently during the hours with most transportations for the EMS, i.e. 10 a.m. to 2 p.m., and the risk of having the assessment NSC was doubled if the EMCC dispatched EMS as low priority, structural factors might be predisposing factors for the assessment.

  • 11.
    Celik, Daniel H.
    et al.
    Academic and Community Emergency Specialists, Uniontown Ohio, USA; Summa Health System, Akron Ohio, USA.
    Mencl, Francis R.
    Academic and Community Emergency Specialists, Uniontown Ohio, USA; Summa Health System, Akron Ohio, USA.
    Debacker, Michel
    Research Group on Emergency and Disaster Medicine (ReGEDiM), Vrije Universiteit Brussel, Brussels, Belgium.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Emergency Medicine.
    Wilber, Scott T.
    Summa Health System, Akron Ohio, USA.
    Frey, Jennifer A.
    Summa Health System, Akron Ohio, USA; The Ohio State University, Columbus Ohio, USA.
    Triage Performance of School Personnel Using the SALT System2019In: Prehospital and Disaster Medicine, ISSN 1049-023X, E-ISSN 1945-1938, Vol. 34, no 4, p. 401-406Article in journal (Refereed)
    Abstract [en]

    Introduction: The aim of this study was to determine if school personnel can understand and apply the Sort, Assess, Life-saving interventions, Treat/Transport (SALT) triage methods after a brief training. The investigators predicted that subjects can learn to triage with accuracy similar to that of medically trained personnel, and that subjects can pass an objective-structured clinical exam (OSCE) evaluating hemorrhage control.

    Methods: School personnel were eligible to participate in this prospective observational study. Investigators recorded subject demographic information and prior medical experience. Participants received a 30-minute lecture on SALT triage and a brief lecture and demonstration of hemorrhage control and tourniquet application. A test with brief descriptions of mass-casualty victims was administered immediately after training. Participants independently categorized the victims as dead, expectant, immediate, delayed, or minimal. They also completed an OSCE to evaluate hemorrhage control and tourniquet application using a mannequin arm.

    Results: Subjects from two schools completed the study. Fifty-nine were from a private school that enrolls early childhood through grade eight, and 45 from a public school that enrolls grades seven and eight (n = 104). The average subject age was 45 years and 68% were female. Approximately 81% were teachers and 87% had prior cardiopulmonary resuscitation (CPR) training. Overall triage accuracy was 79.2% (SD = 10.7%). Ninety-six (92.3%) of the subjects passed the hemorrhage control OSCE.

    Conclusions: After two brief lectures and a short demonstration, school personnel were able to triage descriptions of mass-casualty victims with an overall accuracy similar to medically trained personnel, and most were able to apply a tourniquet correctly. Opportunities for future study include integrating high-fidelity simulation and mock disasters, evaluating for knowledge retention, and exploring the study population's baseline knowledge of medical care, among others.

  • 12.
    Cheng, Ivy
    et al.
    Örebro University, School of Medical Sciences. Örebro University Hospital. Division of Emergency Medicine, University of Toronto, Toronto, Ontario, Canada; Sunnybrook Health Sciences Center, Toronto, Ontario, Canada.
    Andersson, Jonas
    Örebro University, School of Medical Sciences. Centre for Clinical Research Sörmland/Uppsala University, Mälarsjukhuset, Eskilstuna, Sweden.
    Lundqvist, Christer
    Health and Medical Care Administration, Örebro County Council, Örebro, Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences.
    An observational pilot study: Prevalence and cost of high frequency emergency department users at Örebro University Hospital, Sweden2022In: PLOS ONE, E-ISSN 1932-6203, Vol. 17, no 9, article id e0274622Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: There is little research on high frequency emergency department users (HEDU) in Sweden. We aim to determine the prevalence and costs of HEDU compared to non-HEDU at Örebro University Hospital (ÖUH). Additionally, we will determine the factors and outcomes associated with being a HEDU.

    METHODS: This was a retrospective, observational cohort study of ED patients presenting to ÖUH, Sweden between 2018-19. Analyses used electronic registry, ambulance, and cost data. The definition for HEDU was ≥4 visits/year. HEDUs were categorized further into Repeat, High and Super HEDU with 4-7, 8-18 and ≥19 visits/year, respectively. We used multivariable logistic regression to determine the adjusted odds ratios for factors and outcomes between HEDU and non-HEDU.

    FINDINGS: Of all ÖUH ED patients, 6.1% were HEDU and accounted for 22.4% of ED visits and associated costs. Compared to the mean cost of non-HEDU, the Repeat, High and Super HEDU were more costly by factors of 4, 8 and 27, respectively. The HEDUs were more likely to be male, self-referred, present with abdominal pain, arrive by ambulance, at night and from the Örebro municipal region. Super HEDU were more likely to be of adult age and assigned lower acuity scores. HEDU were more likely to be directed to the surgical zone, less likely to receive radiologic imaging or achieve a 4-hr time target. In contrast to the Repeat and High HEDU, Super HEDU were less likely to be admitted, but more likely to leave without being seen.

    CONCLUSION: ÖUH has a HEDU population with associated factors and outcomes. They account for a substantial proportion of ED costs compared to non-HEDU.

  • 13.
    Cone, David C
    et al.
    Section of EMS, Department of Emergency Medicine, Yale University School of Medicine, New Haven CT, United States; Yale Emergency Medicine, New Haven CT, United States.
    Serra, John
    Section of EMS, Department of Emergency Medicine, Yale University School of Medicine, New Haven CT, United States.
    Burns, Kevin
    Section of EMS, Department of Emergency Medicine, Yale University School of Medicine, New Haven CT, United States.
    MacMillan, Donald S
    Section of EMS, Department of Emergency Medicine, Yale University School of Medicine, New Haven CT, United States.
    Kurland, Lisa
    Department of Medicine and Emergency Medicine, Uppsala University School of Medicine, Uppsala, Sweden.
    Van Gelder, Carin
    Section of EMS, Department of Emergency Medicine, Yale University School of Medicine, New Haven CT, United States.
    Pilot Test of the SALT Mass Casualty Triage System2019In: Prehospital Emergency Care, ISSN 1090-3127, E-ISSN 1545-0066, Vol. 13, no 4, p. 536-40Article in journal (Refereed)
    Abstract [en]

    INTRODUCTION: No existing mass casualty triage system has been scientifically scrutinized or validated. A recent work group sponsored by the Centers for Disease Control and Prevention, using a combination of expert opinion and the extremely limited research data available, created the SALT (sort-assess-lifesaving interventions-treat/transport) triage system to serve as a national model. An airport crash drill was used to pilot test the SALT system.

    OBJECTIVE: To assess the accuracy and speed with which trained paramedics can triage victims using this new system.

    METHODS: Investigators created 50 patient scenarios with a wide range of injuries and severities, and two additional uninjured victims were added at the time of the drill. Students wearing moulage and coached on how to portray their injuries served as "victims." Assuming proper application of the SALT system, the patient scenarios were designed such that 16 patients would be triaged as T1/red/immediate, 12 as T2/yellow/delayed, 14 as T3/green/minimal, and 10 as T4/black/dead. Paramedics were trained to proficiency in the SALT system one week prior to the drill using a 90-minute didactic/practical session, and were given "flash cards" showing the triage algorithm to be used if needed during the drill. Observers blinded to the study purpose timed and recorded the triage process for each patient during the drill. Simple descriptive statistics were used to analyze the data.

    RESULTS: The two paramedics assigned to the role of triage officers applied the SALT algorithm correctly to 41 of the 52 patients (78.8% accuracy). Seven patients intended to be T2 were triaged as T1, and two patients intended to be T3 were triaged as T2, for an overtriage rate of 13.5%. Two patients intended to be T2 were triaged as T3, for an undertriage rate of 3.8%. Triage times were recorded by the observers for 42 of the 52 patients, with a mean of 15 seconds per patient (range 5-57 seconds).

    CONCLUSIONS: The SALT mass casualty triage system can be applied quickly in the field and appears to be safe, as measured by a low undertriage rate. There was, however, significant overtriage. Further refinement is needed, and effect on patient outcomes needs to be evaluated.

  • 14.
    Cone, David C
    et al.
    Department of Emergency Medicine, Yale University School of Medicine, New Haven CT, USA.
    Serra, John
    Department of Emergency Medicine, University of California, San Diego CA, USA.
    Kurland, Lisa
    Department of Clinical Research and Education, Karolinska Institutet, Stockholm, Sweden.
    Comparison of the SALT and Smart triage systems using a virtual reality simulator with paramedic students2011In: European journal of emergency medicine, ISSN 0969-9546, E-ISSN 1473-5695, Vol. 18, no 6, p. 314-321Article in journal (Refereed)
    Abstract [en]

    OBJECTIVES: Virtual reality systems may allow for organized study of mass casualty triage systems by allowing investigators to replicate the same mass casualty incident, with the same victims, for a large number of rescuers. The study objectives were to develop such a virtual reality system, and use it to assess the ability of trained paramedic students to triage simulated victims using two triage systems.

    METHODS: Investigators created 25 patient scenarios for a highway bus crash in a virtual reality simulation system. Paramedic students were trained to proficiency on the new 'Sort, Assess, Life saving interventions, Treat and Transport (SALT)' triage system, and 22 students ran the simulation, applying the SALT algorithm to each victim. After a 3-month washout period, the students were retrained on the 'Smart' triage system, and each student ran the same crash simulation using the Smart system. Data inputs were recorded by the simulation software and analyzed with the paired t-tests.

    RESULTS: The students had a mean triage accuracy of 70.0% with SALT versus 93.0% with Smart (P=0.0001). Mean overtriage was 6.8% with SALT versus 1.8% with Smart (P=0.0015), and mean undertriage was 23.2% with SALT versus 5.1% with Smart (P=0.0001). The average time for a student to triage the scene was 21 min 3 s for SALT versus 11 min 59 s for Smart (P=0.0001).

    CONCLUSION: The virtual reality platform seems to be a viable research tool for examining mass casualty triage. A small sample of trained paramedic students using the virtual reality system was able to triage simulated patients faster and with greater accuracy with 'Smart' triage than with 'SALT' triage.

  • 15.
    Djalali, Ahmadreza
    et al.
    Center for Research and Education in Emergency and Disaster Medicine, Università Del Piemonte Orientale, Novara, Italy; Department of Clinical Sciences and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Ardalan, Ali
    Department of Disaster and Emergency Health, National Institute of Health Research, Tehran, iran; University of Medical Sciences, Tehran, Iran; Harvard Humanitarian Initiative, Department of Global Health and Population, Harvard School of Public Health, Cambridge MA, United States.
    Ohlen, Gunnar
    Intervention and Technology, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Ingrassia, Pier Luigi
    Center for Research and Education in Emergency and Disaster Medicine, Università Del Piemonte Orientale, Novara, Italy.
    Corte, Francesco Della
    Center for Research and Education in Emergency and Disaster Medicine, Università Del Piemonte Orientale, Novara, Italy.
    Castren, Maaret
    Department of Clinical Sciences and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Section of Emergency Medicine, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Kurland, Lisa
    Department of Clinical Sciences and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Section of Emergency Medicine, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Nonstructural Safety of Hospitals for Disasters: A Comparison Between Two Capital Cities2014In: Disaster Medicine and Public Health Preparedness, ISSN 1935-7893, E-ISSN 1938-744X, Vol. 8, no 2, p. 179-184Article in journal (Refereed)
    Abstract [en]

    OBJECTIVE: Hospitals are expected to function as a safe environment during disasters, but many become unusable because of nonstructural damage. This study compares the nonstructural safety of hospitals to disasters in Tehran and Stockholm.

    METHODS: Hospital safety in Tehran and Stockholm was assessed between September 24, 2012, and April 5, 2013, with use of the nonstructural module of the hospital safety index from the World Health Organization. Hospital safety was categorized as safe, at risk, or inadequate.

    RESULTS: All 4 hospitals in Stockholm were classified as safe, while 2 hospitals in Tehran were at risk and 3 were safe. The mean nonstructural safety index was 90% ± 2.4 SD for the hospitals in Stockholm and 64% ± 17.4 SD for those in Tehran (P = .014).

    CONCLUSIONS: The level of hospital safety, with respect to disasters, was not related to local vulnerability. Future studies on hospital safety should assess other factors such as legal and financial issues. (Disaster Med Public Health Preparedness. 2014;0:1-6).

  • 16.
    Djalali, Ahmadreza
    et al.
    Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Castren, Maaret
    Department of Clinical Sciences and Education and Department of Emergency Medicine, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Hosseinijenab, Vahid
    Department of emergency management, Natural Disaster Research Institute, Tehran, Iran.
    Khatib, Mahmoud
    Tehran social security organization, Tehran, Iran.
    Ohlen, Gunnar
    Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
    Kurland, Lisa
    Department of Clinical Sciences and Education and Department of Emergency Medicine, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Hospital Incident Command System (HICS) performance in Iran; decision making during disasters2012In: Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine, E-ISSN 1757-7241, Vol. 20, article id 14Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Hospitals are cornerstones for health care in a community and must continue to function in the face of a disaster. The Hospital Incident Command System (HICS) is a method by which the hospital operates when an emergency is declared. Hospitals are often ill equipped to evaluate the strengths and vulnerabilities of their own management systems before the occurrence of an actual disaster. The main objective of this study was to measure the decision making performance according to HICS job actions sheets using tabletop exercises.

    METHODS: This observational study was conducted between May 1st 2008 and August 31st 2009. Twenty three Iranian hospitals were included. A tabletop exercise was developed for each hospital which in turn was based on the highest probable risk. The job action sheets of the HICS were used as measurements of performance. Each indicator was considered as 1, 2 or 3 in accordance with the HICS. Fair performance was determined as < 40%; intermediate as 41-70%; high as 71-100% of the maximum score of 192. Descriptive statistics, T-test, and Univariate Analysis of Variance were used.

    RESULTS: None of the participating hospitals had a hospital disaster management plan. The performance according to HICS was intermediate for 83% (n = 19) of the participating hospitals. No hospital had a high level of performance. The performance level for the individual sections was intermediate or fair, except for the logistic and finance sections which demonstrated a higher level of performance. The public hospitals had overall higher performances than university hospitals (P = 0.04).

    CONCLUSIONS: The decision making performance in the Iranian hospitals, as measured during table top exercises and using the indicators proposed by HICS was intermediate to poor. In addition, this study demonstrates that the HICS job action sheets can be used as a template for measuring the hospital response. Simulations can be used to assess preparedness, but the correlation with outcome remains to be studied.

  • 17.
    Djalali, Ahmadreza
    et al.
    Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; RIMEDIM - Center for Research and Education in Emergency and Disaster Medicine, Università del Piemonte Orientale, Novara, Italy.
    Castren, Maaret
    Department of Clinical Sciences and Education and Section of Emergency Medicine, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Khankeh, Hamidreza
    Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Nursing Department, University of Social Welfare and Rehabilitation, Tehran, Iran.
    Gryth, Dan
    Department of Physiology and Pharmacology and Section of Anaesthesiology and Intensive care, Karolinska Institutet, Stockholm, Sweden.
    Radestad, Monica
    Department of Clinical Sciences and Education and Section of Emergency Medicine, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Öhlen, Gunnar
    Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
    Kurland, Lisa
    Department of Clinical Sciences and Education and Section of Emergency Medicine, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Hospital disaster preparedness as measured by functional capacity: a comparison between Iran and Sweden2013In: Prehospital and Disaster Medicine, ISSN 1049-023X, E-ISSN 1945-1938, Vol. 28, no 5, p. 454-461Article in journal (Refereed)
    Abstract [en]

    INTRODUCTION: Hospitals are expected to continue to provide medical care during disasters. However, they often fail to function under these circumstances. Vulnerability to disasters has been shown to be related to the socioeconomic level of a country. This study compares hospital preparedness, as measured by functional capacity, between Iran and Sweden.

    METHODS: Hospital affiliation and size, and type of hazards, were compared between Iran and Sweden. The functional capacity was evaluated and calculated using the Hospital Safety Index (HSI) from the World Health Organization. The level and value of each element was determined, in consensus, by a group of evaluators. The sum of the elements for each sub-module led to a total sum, in turn, categorizing the functional capacity into one of three categories: A) functional; B) at risk; or C) inadequate.

    RESULTS: The Swedish hospitals (n = 4) were all level A, while the Iranian hospitals (n = 5) were all categorized as level B, with respect to functional capacity. A lack of contingency plans and the availability of resources were weaknesses of hospital preparedness. There was no association between the level of hospital preparedness and hospital affiliation or size for either country.

    CONCLUSION: The results suggest that the level of hospital preparedness, as measured by functional capacity, is related to the socioeconomic level of the country. The challenge is therefore to enhance hospital preparedness in countries with a weaker economy, since all hospitals need to be prepared for a disaster. There is also room for improvement in more affluent countries.

  • 18.
    Djalali, Ahmadreza
    et al.
    Department of Clinical Science and Education, Södersjukhuset (KI SÖS), Karolinska Institute, Stockholm, Sweden.
    Khankeh, Hamidreza
    Department of Clinical Science and Education, Södersjukhuset (KI SÖS), Karolinska Institute, Stockholm, Sweden; Nursing Department, University of Social Welfare and Rehabilitation, Tehran, Iran.
    Öhlén, Gunnar
    Department of Clinical Science and Education, Södersjukhuset (KI SÖS), Karolinska Institute, Stockholm, Sweden.
    Castrén, Maaret
    Department of Clinical Science and Education, Södersjukhuset (KI SÖS), Karolinska Institute, Stockholm, Sweden.
    Kurland, Lisa
    Department of Clinical Science and Education, Södersjukhuset (KI SÖS), Karolinska Institute, Stockholm, Sweden.
    Facilitators and obstacles in pre-hospital medical response to earthquakes: a qualitative study2011In: Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine, E-ISSN 1757-7241, Vol. 19, article id 30Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Earthquakes are renowned as being amongst the most dangerous and destructive types of natural disasters. Iran, a developing country in Asia, is prone to earthquakes and is ranked as one of the most vulnerable countries in the world in this respect. The medical response in disasters is accompanied by managerial, logistic, technical, and medical challenges being also the case in the Bam earthquake in Iran. Our objective was to explore the medical response to the Bam earthquake with specific emphasis on pre-hospital medical management during the first days.

    METHODS: The study was performed in 2008; an interview based qualitative study using content analysis. We conducted nineteen interviews with experts and managers responsible for responding to the Bam earthquake, including pre-hospital emergency medical services, the Red Crescent, and Universities of Medical Sciences. The selection of participants was determined by using a purposeful sampling method. Sample size was given by data saturation.

    RESULTS: The pre-hospital medical service was divided into three categories; triage, emergency medical care and transportation, each category in turn was identified into facilitators and obstacles. The obstacles identified were absence of a structured disaster plan, absence of standardized medical teams, and shortage of resources. The army and skilled medical volunteers were identified as facilitators.

    CONCLUSIONS: The most compelling, and at the same time amenable obstacle, was the lack of a disaster management plan. It was evident that implementing a comprehensive plan would not only save lives but decrease suffering and enable an effective praxis of the available resources at pre-hospital and hospital levels.

  • 19.
    Djärv, Therese
    et al.
    Department of Clinical Science and Education, Karolinska Institutet, Stockholm, Sweden.
    Castrén, Maaret
    Department of Clinical Science and Education, Karolinska Institutet, Stockholm, Sweden; Section of Emergency Medicine, Karolinska Institute, Stockholm, Sweden.
    Mårtenson, Linda
    Department of Clinical Science and Education, Karolinska Institutet, Stockholm, Sweden.
    Kurland, Lisa
    Department of Clinical Science and Education, Karolinska Institutet, Stockholm, Sweden; Section of Emergency Medicine, Karolinska Institute, Stockholm, Sweden.
    Decreased general condition in the emergency department: high in-hospital mortality and a broad range of discharge diagnoses2015In: European journal of emergency medicine, ISSN 0969-9546, E-ISSN 1473-5695, Vol. 22, no 4, p. 241-246Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Decreased general condition (DGC) is a frequent presenting complaint within the Adaptive Triage Process. DGC describes a nonspecific decline in health and well-being, and it is common among elderly patients in the emergency department (ED).

    AIM: The aim of this study was to compare the in-hospital mortality among patients presenting with DGC with that among patients in the corresponding triage category presenting with other complaints to an ED. The secondary aim was to describe the discharge diagnoses of patients presenting with DGC.

    METHODS: All patients admitted to Södersjukhuset from the ED in 2008 were included. The difference in the in-hospital mortality rate was stratified for triage category at the ED, between patients with DGC (n=1182) and those with all other presenting complaints (n=20 775), and assessed with sex-adjusted and age-adjusted logistic regression models. Discharge diagnoses were assessed as the primary discharge diagnosis according to International Statistical Classification of Diseases and Related Health Problems 10th revision (ICD-10) in the medical discharge notes.

    RESULTS: A total of 1182 patients with DGC at the ED were admitted for in-hospital care, and they had a four-fold risk of suffering an in-hospital death [odds ratio 4.74 (95% confidence interval 3.88-5.78)] compared with patients presenting with other presenting complaints. The most common discharge diagnoses were diseases of the circulatory system (14%), respiratory system (14%), and genitourinary system (10%).

    INTERPRETATION: Patients presenting with DGC to an ED often receive low triage priority, frequently require admission for in-hospital care, and, because of the three-fold increased risk of in-hospital death compared with others, belong to a high-risk group.

  • 20.
    Druwé, Patrick
    et al.
    Department of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.
    Monsieurs, Koenraad G.
    Department of Emergency Medicine, Antwerp University Hospital, Antwerp, Belgium.
    Piers, Ruth
    Department of Geriatric Medicine, Ghent University Hospital, Ghent, Belgium.
    Gagg, James
    Department of Emergency Medicine, Musgrove Park Hospital, Taunton and Somerset NHS Foundation Trust, Taunton, United Kingdom.
    Nakahara, Shinji
    Teikyo University School of Medicine, Tokyo, Japan.
    Alpert, Evan Avraham
    Emergency Department, Shaare Zedek Medical Center, Jerusalem, Israel.
    van Schuppen, Hans
    Department of Anesthesiology, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.
    Élö, Gabor
    Department of Anaesthesiology and Intensive Therapy, Semmelweis University, Budapest, Hungary.
    Truhlar, Anatolij
    Emergency Medical Services of the Hradec Kralove Region and University Hospital Hradec Kralove, Czech Republic.
    Huybrechts, Sofie A.
    Department of Emergency Medicine, Antwerp University Hospital, Antwerp, Belgium.
    Mpotos, Nicolas
    Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium..
    Joly, Luc-Marie
    Department of Emergency Medicine, Rouen University Hospital, Rouen, France.
    Xanthos, Theodoros
    European University, Nicosia, Cyprus, Hellenic Society of Cardiopulmonary Resuscitation, Athens, Greece.
    Roessler, Markus
    Department of Anaesthesiology, University Medical Centre Göttingen, Göttingen, Germany.
    Paal, Peter
    Department of Anesthesiology and Critical Care Medicine, University Hospital Innsbruck, Austria.
    Cocchi, Michael N.
    Harvard Medical School, Department of Emergency Medicine and Department of Anesthesia, Critical Care and Pain Medicine, Division of Critical Care, Beth Israel Deaconess Medical Center, United States.
    Björshol, Conrad
    Department of Anesthesiology and Intensive Care, Stavanger University Hospital, The Regional Centre for Emergency Medical Research and Development (RAKOS), Department of Clinical Medicine, University of Bergen, Norway.
    Paulikova, Monika
    Department of Anesthesiology and Intensive Care, East Slovak Institute of Oncology, Košice, Slovakia.
    Nurmi, Jouni
    Emergency Medicine and Services, Helsinki University Hospital, Helsinki, Finland.
    Salmeron, Pascual Pinera
    Hospital General Universitario Reina Sofia, Murcia, Spain.
    Owczuk, Radoslaw
    Department of Anaesthesiology and Intensive Therapy, Medical University of Gdansk, Gdansk, Poland.
    Svavarsdottir, Hildigunnur
    Akureyri Hospital and University of Akureyri, Akureyri, Iceland.
    Deasy, Conor
    Department of Emergency Medicine, Cork University Hospital, Cork, Ireland.
    Cimpoesu, Diana
    University of Medicine and Pharmacy Gr.T. Popa and Emergency County Hospital Sf. Spiridon, Iasi, Romania.
    Ioannides, Marios
    Nicosia General Hospital, Nicosia, Cyprus.
    Aguilera Fuenzalida, Pablo
    Pontificia Universidad Católica de Chile, Santiago, Chile.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Clinical Research and Education, Karolinska Institute, Stockholm, Sweden.
    Raffay, Violetta
    Municipal Institute for Emergency Medicine, Novi Sad, Serbia.
    Pachys, Gal
    Emergency Department, Shaare Zedek Medical Center, Jerusalem, Israel.
    Gadeyne, Bram
    Department of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.
    Steen, Johan
    Department of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.
    Vansteelandt, Stijn
    Department of Applied Mathematics, Computer Science and Statistics, Faculty of Sciences, Ghent University, Ghent, Belgium; Department of Medical Statistics, London School of Hygiene and Tropical Medicine, London, United Kingdom.
    De Paepe, Peter
    Department of Emergency Medicine, Ghent University Hospital, Ghent, Belgium.
    Benoit, Dominique D.
    Department of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.
    Perception of inappropriate cardiopulmonary resuscitation by clinicians working in emergency departments and ambulance services: The REAPPROPRIATE international, multi-centre, cross sectional survey2018In: Resuscitation, ISSN 0300-9572, E-ISSN 1873-1570, Vol. 132, p. 112-119Article in journal (Refereed)
    Abstract [en]

    Introduction: Cardiopulmonary resuscitation (CPR) is often started irrespective of comorbidity or cause of arrest. We aimed to determine the prevalence of perception of inappropriate CPR of the last cardiac arrest encountered by clinicians working in emergency departments and out-of-hospital, factors associated with perception, and its relation to patient outcome.

    Methods: A cross-sectional survey was conducted in 288 centres in 24 countries. Factors associated with perception of CPR and outcome were analyzed by Cochran-Mantel-Haenszel tests and conditional logistic models.

    Results: Of the 4018 participating clinicians, 3150 (78.4%) perceived their last CPR attempt as appropriate, 548 (13.6%) were uncertain about its appropriateness and 320 (8.0%) perceived inappropriateness; survival to hospital discharge was 370/2412 (15.3%), 8/481 (1.7%) and 8/294 (2.7%) respectively. After adjusting for country, team and clinician's characteristics, the prevalence of perception of inappropriate CPR was higher for a non-shockable initial rhythm (OR 3.76 [2.13-6.64]; P < .0001), a non-witnessed arrest (2.68 [1.89-3.79]; P < .0001), in older patients (2.94 [2.18-3.96]; P < .0001, for patients > 79 years) and in case of a "poor" first physical impression of the patient (3.45 [2.36-5.05]; P < .0001). In accordance, non-shockable and non-witnessed arrests were both associated with lower survival to hospital discharge (0.33 [0.26 - 0.41]; P < 0.0001 and 0.25 [0.15 - 0.41]; P < 0.0001, respectively), as were older patient age (0.25 [0.14 - 0.44]; P < 0.0001 for patients > 79 years) and a "poor" first physical impression (0.26 [0.19-0.35]; P < 0.0001).

    Conclusions: The perception of inappropriate CPR increased when objective indicators of poor prognosis were present and was associated with a low survival to hospital discharge. Factoring clinical judgment into the decision to (not) attempt CPR may reduce harm inflicted by excessive resuscitation attempts.

  • 21.
    Dryver, Eric T
    et al.
    Emergency Department, Skane's University Hospital, Akutkliniken, Lund, Sweden; Practicum Clinical Skills Centre, Region Skåne, Lund/Malmö, Sweden.
    Eriksson, Anders
    Anesthesiology Department, Ersta Hospital, Stockholm, Sweden.
    Söderberg, Patrik
    Södersjukhus Hospital, Stockholm's County Council, Stockholm, Sweden.
    Kurland, Lisa
    Södersjukhus Hospital, Karolinska Institution, Stockholm, Sweden.
    The Swedish specialist examination in emergency medicine: form and function2017In: European journal of emergency medicine, ISSN 0969-9546, E-ISSN 1473-5695, Vol. 24, no 1, p. 19-24Article in journal (Refereed)
    Abstract [en]

    AIM/BACKGROUND: The purpose of the Swedish specialist examination in Emergency Medicine is not only to determine whether residents have attained the level of competence of specialists, but also to guide and facilitate residency training.

    METHODS: The Swedish Society for Emergency Medicine has developed checklists that delineate criteria of consideration and action items for particular processes. These checklists are freely available and used to assess competence during the examination. They are also intended for use during teaching and clinical care, thus promoting alignment between clinical practice, teaching and assessment. The examination is carried out locally by residency program educators, thereby obviating travel expenses. It consists of a total of 24 stations and over 100 potential scenarios, thereby minimizing case specificity. Each station consists of a scenario based on a real case. The checklists allow for direct feedback to the examinee after each station.

    RESULTS AND CONCLUSION: This model may be of interest to other European countries.

  • 22.
    Ekelund, Ulf
    et al.
    Emergency Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
    Kurland, Lisa
    Department of Clinical Sciences and Education and Section of Emergency Medicine, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Eklund, Fredrik
    Medical Management Centre, Karolinska Institutet, Stockholm, Sweden.
    Torkki, Paulus
    HEMA-Institute, BIT Research Centre, Aalto University, Espoo, Finland.
    Letterstål, Anna
    Emergency Medicine, Karolinska University Hospital, Stockholm, Sweden.
    Lindmarker, Per
    Emergency Medicine, Karolinska University Hospital, Stockholm, Sweden.
    Castrén, Maaret
    Department of Clinical Sciences and Education and Section of Emergency Medicine, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Patient throughput times and inflow patterns in Swedish emergency departments: A basis for ANSWER, A National SWedish Emergency Registry2011In: Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine, E-ISSN 1757-7241, Vol. 19, article id 37Article in journal (Refereed)
    Abstract [en]

    OBJECTIVE: Quality improvement initiatives in emergency medicine (EM) often suffer from a lack of benchmarking data on the quality of care. The objectives of this study were twofold: 1. To assess the feasibility of collecting benchmarking data from different Swedish emergency departments (EDs) and 2. To evaluate patient throughput times and inflow patterns.

    METHOD: We compared patient inflow patterns, total lengths of patient stay (LOS) and times to first physician at six Swedish university hospital EDs in 2009. Study data were retrieved from the hospitals' computerized information systems during single on-site visits to each participating hospital.

    RESULTS: All EDs provided throughput times and patient presentation data without significant problems. In all EDs, Monday was the busiest day and the fewest patients presented on Saturday. All EDs had a large increase in patient inflow before noon with a slow decline over the rest of the 24 h, and this peak and decline was especially pronounced in elderly patients. The average LOS was 4 h of which 2 h was spent waiting for the first physician. These throughput times showed a considerable diurnal variation in all EDs, with the longest times occurring 6-7 am and in the late afternoon.

    CONCLUSION: These results demonstrate the feasibility of collecting benchmarking data on quality of care targets within Swedish EM, and form the basis for ANSWER, A National SWedish Emergency Registry.

  • 23.
    Ekström, Andreas
    et al.
    Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Eng-Larsson, Fredrik
    Stockholm Business School, Stockholm University, Stockholm, Sweden.
    Isaksson, Olov
    Stockholm Business School, Stockholm University, Stockholm, Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Emergency Medicine, Örebro University Hospital, Örebro, Sweden.
    Nordberg, Martin
    Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    The effect of a terrorist attack on emergency department inflow: an observation study using difference-in-differences methodology2019In: Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine, E-ISSN 1757-7241, Vol. 27, no 1, article id 57Article in journal (Refereed)
    Abstract [en]

    STUDY OBJECTIVE: The objective of this study was to investigate how the terrorist attack in Stockholm, Sweden affected patient inflow to the general emergency departments (EDs) in close proximity of the attack. The study analyzed if, and to what extent, the attack impacted ED inflow during the following days and weeks.

    METHODS: In a retrospective observational study, anonymized aggregated data on ED arrivals (inflow of patients) to all seven of the EDs in the Stockholm County was analyzed using the Difference-in-Differences (DiD) estimator. The control groups were the affected hospitals in the years prior to the terrorist attack. The number of ED visits was retrieved from the Stockholm County Council administrative database.

    RESULTS: The study shows a statistically significant reduction in overall ED inflow of 7-9% following the attack. The effect was strongest initially after the attack, and ED inflow regained normal levels within approximately three weeks' time, without any significant rebound effect. The effect on ED inflow also decreased with distance from ground zero, and was not significant further away than 10 km.

    CONCLUSION: The results showed that ED inflow was significantly decreased in the weeks immediately following the Stockholm terrorist attack. The reasons for this cannot be fully explained in this observational study. However, the results suggest that some patients actively choose when, where and if they should go to the ED.

  • 24.
    Ekström, Andreas
    et al.
    Department of Clinical Science and Education, Section of Emergency Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Kurland, Lisa
    Department of Clinical Science and Education, Section of Emergency Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Farrokhnia, Nasim
    Department of Clinical Science and Education, Section of Emergency Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Castrén, Maaret
    Department of Clinical Science and Education, Section of Emergency Medicine, Karolinska Institutet, Stockholm, Sweden.
    Nordberg, Martin
    Department of Clinical Science and Education, Section of Emergency Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Forecasting emergency department visits using internet data2015In: Annals of Emergency Medicine, ISSN 0196-0644, E-ISSN 1097-6760, Vol. 65, no 4, p. 436-442.e1Article in journal (Refereed)
    Abstract [en]

    STUDY OBJECTIVE: Using Internet data to forecast emergency department (ED) visits might enable a model that reflects behavioral trends and thereby be a valid tool for health care providers with which to allocate resources and prevent crowding. The aim of this study is to investigate whether Web site visits to a regional medical Web site, the Stockholm Health Care Guide, a proxy for the general public's concern of their health, could be used to predict the ED attendance for the coming day.

    METHODS: In a retrospective, observational, cross-sectional study, a model for forecasting the daily number of ED visits was derived and validated. The model was derived through regression analysis, using visits to the Stockholm Health Care Guide Web site between 6 pm and midnight and day of the week as independent variables. Web site visits were measured with Google Analytics. The number of visits to the ED within the region was retrieved from the Stockholm County Council administrative database. All types of ED visits (including adult, pediatric, and gynecologic) were included. The period of August 13, 2011, to August 12, 2012, was used as a training set for the model. The hourly variation of visits was analyzed for both Web site and the ED visits to determine the interval of hours to be used for the prediction. The model was validated with mean absolute percentage error for August 13, 2012, to October 31, 2012.

    RESULTS: The correlation between the number of Web site visits between 6 pm and midnight and ED visits the coming day was significant (r=0.77; P<.001). The best forecasting results for ED visits were achieved for the entire county, with a mean absolute percentage error of 4.8%. The result for the individual hospitals ranged between mean absolute percentage error 5.2% and 13.1%.

    CONCLUSION: Web site visits may be used in this fashion to predict attendance to the ED. The model works both for the entire region and for individual hospitals. The possibility of using Internet data to predict ED visits is promising.

  • 25.
    Eriksson, Jan W.
    et al.
    Department of Medicine, Umeå University Hospital, Umeå, Sweden; Department of Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden; AstraZeneca R&D, Mölndal, Sweden.
    Jansson, Per-Anders
    Department of Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden.
    Carlberg, Bo
    Department of Medicine, Umeå University Hospital, Umeå, Sweden.
    Hägg, Anders
    Department of Medicine, Uppsala University Hospital, Uppsala, Sweden.
    Kurland, Lisa
    Department of Medicine, Uppsala University Hospital, Uppsala, Sweden.
    Svensson, Maria K.
    Department of Medicine, Umeå University Hospital, Umeå, Sweden; Department of Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden.
    Ahlström, Håkan
    Department of Radiology, Uppsala University Hospital, Uppsala, Sweden.
    Ström, Conny
    Department of Radiology, Umeå University Hospital, Umeå, Sweden.
    Lönn, Lars
    Department of Radiology, Sahlgrenska University Hospital, Gothenburg, Sweden; Faculty of Health Sciences, Rigshospitalet, Copenhagen, Denmark.
    Öjbrandt, Kristina
    Department of Medicine, Umeå University Hospital, Umeå, Sweden.
    Johansson, Lars
    Department of Radiology, Uppsala University Hospital, Uppsala, Sweden; AstraZeneca R&D, Mölndal, Sweden.
    Lind, Lars
    Department of Medicine, Uppsala University Hospital, Uppsala, Sweden.
    Hydrochlorothiazide, but not Candesartan, aggravates insulin resistance and causes visceral and hepatic fat accumulation: the mechanisms for the diabetes preventing effect of Candesartan (MEDICA) Study2008In: Hypertension, ISSN 0194-911X, E-ISSN 1524-4563, Vol. 52, no 6, p. 1030-1037Article in journal (Refereed)
    Abstract [en]

    Treatment with angiotensin II receptor blockers is associated with lower risk for the development of type 2 diabetes mellitus compared with thiazide diuretics. The Mechanisms for the Diabetes Preventing Effect of Candesartan Study addressed insulin action and secretion and body fat distribution after treatment with candesartan, hydrochlorothiazide, and placebo. Twenty-six nondiabetic, abdominally obese, hypertensive patients were included in a multicenter 3-way crossover trial, and 22 completers (by predefined criteria; 10 men and 12 women) were included in the analyses. They underwent 12-week treatment periods with candesartan (C; 16 to 32 mg), hydrochlorothiazide (H; 25 to 50 mg), and placebo (P), respectively, and the treatment order was randomly assigned and double blinded. Intravenous glucose tolerance tests and euglycemic hyperinsulinemic (56 mU/m(2) per minute) clamps were performed. Intrahepatic and intramyocellular and extramyocellular lipid content and subcutaneous and visceral abdominal adipose tissue were measured using proton magnetic resonance spectroscopy and MRI. Insulin sensitivity (M-value) was reduced following H versus C and P (6.07+/-2.05, 6.63+/-2.04, and 6.90+/-2.10 mg/kg of body weight per minute, mean+/-SD; P<or=0.01). Liver fat content was higher (P<0.05) following H than both P and C. The subcutaneous to visceral abdominal adipose tissue ratio was reduced following H versus C and P (P<0.01). Glycosylated hemoglobin, alanine aminotransferase, aspartate aminotransferase, and high-sensitivity C-reactive protein levels were higher (P<0.05) after H, but not C, versus P. There were no changes in body fat, intramyocellular lipid, extramyocellular lipid, or first-phase insulin secretion. Blood pressure was reduced similarly by C and H versus P. In conclusion, visceral fat redistribution, liver fat accumulation, low-grade inflammation, and aggravated insulin resistance were demonstrated after hydrochlorothiazide but not candesartan treatment. These findings can partly explain the diabetogenic potential of thiazides.

  • 26.
    Garcia-Castrillo, Luis
    et al.
    Emergency Department, Hospital Universitario Marqués de Valdecilla, Santander, Cantabria, Spain.
    Cadamuro, Janne
    Department of Laboratory Medicine, Paracelsus Medical University Salzburg, Salzburg, Austria.
    Dodt, Christoph
    Emergency Department, Universitair Ziekenhuis Brussels, Brussels, Belgium.
    Lauwaert, Door
    München Klinik gGmbH, Clinic for Acute and Emergency Care, Munich, Germany.
    Hachimi-Idrissi, Said
    Universiteit Gent Faculteit Geneeskunde en Gezondheidswetenschappen, Emergency Medicine, Gent, Belgium; Universitair Ziekenhuis Gent, Emergency Medicine, Gent, Belgium.
    Van Der Linden, Christien
    Haaglanden Medical Center, Den Haag, Netherlands.
    Bergs, Jochen
    Faculty of Medicine and Life Sciences, Research Group Healthcare & Ethics, Hasselt University, Limburg, Belgium; Department of Healthcare, PXL University of Applied Sciences and Arts, Hasselt, Netherlands.
    Costelloe, Sean
    Department of Clinical Biochemistry, Cork University Hospital Group, Cork, Ireland.
    Grossmann, Florian
    Emergency Department, University Hospital Basel, Basel, Switzerland.
    Koca, Ayca
    Department of Emergency Medicine, Ankara University School of Medicine, Ankara, Türkiye.
    Palomäki, Ari
    Kanta-Häme Central Hospital, Tampere Universities, Hämeenlinna, Finland.
    Ruiz, Jose Luis
    Emergency Department, Hospital Universitario de La Ribera, Valenciana, Spain.
    Stonys, Ricardas
    Center of Laboratory Medicine, Vilnius University Hospital Santaros Klinikos, Vilnius, Lithuania.
    Thorsteinsdottir, Thordís Katrín
    Faculty of Nursing and Midwifery, University of Iceland Faculty of Nursing and Midwifery, Reykjavik, Island.
    von Meyer, Alexander
    Krankenhaus Barmherzige Brüder München, Munich, Germany.
    Vermeersch, Pieter
    KU Leuven University Hospitals Leuven, Laboratory Medicine, Leuven, Belgium.
    Abellas Alvarez, Maria Concepción
    Hospital do Salnés Xestión Integrada Pontevedra-Salnés, Vilagarcía de Arousa, Spain.
    Eker, Pinar
    Biochemistry and Clinical Biochemistry, Maltepe Universitesi Tip Fakultesi, Istanbul, Türkiye.
    Golea, Adela
    Emergency Department, Cluj-Napoca County Emergency Hospital, Cluj-Napoca, Romania.
    Kurland, Lisa
    Örebro University, School of Medical Sciences.
    Lippi, Giuseppe
    Section of Clinical Biochemistry, Universita degli Studi di Verona, Verona, Italy.
    Zhilenkova, Yulia
    Department of Laboratory Medicine and Genetics, Almazov National Medical Research Centre, Sankt-Peterburg, Russia.
    Sehmi, Kawaldip
    International Alliance of Patients' Organizations, London, UK.
    Recommendations for blood sampling in emergency departments from the European Society for Emergency Medicine (EUSEM), European Society for Emergency Nursing (EuSEN), and European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) Working Group for the Preanalytical Phase. Executive summary2024In: Clinical Chemistry and Laboratory Medicine, ISSN 1434-6621, E-ISSN 1437-4331, Vol. 62, no 8, p. 1538-1547Article in journal (Refereed)
    Abstract [en]

    AIM: Blood Sampling Guidelines have been developed to target European emergency medicine-related professionals involved in the blood sampling process (e.g. physicians, nurses, phlebotomists working in the ED), as well as laboratory physicians and other related professionals. The guidelines population focus on adult patients. The development of these blood sampling guidelines for the ED setting is based on the collaboration of three European scientific societies that have a role to play in the preanalytical phase process: EuSEN, EFLM, and EUSEM. The elaboration of the questions was done using the PICO procedure, literature search and appraisal was based on the GRADE methodology. The final recommendations were reviewed by an international multidisciplinary external review group.

    RESULTS: The document includes the elaborated recommendations for the selected sixteen questions. Three in pre-sampling, eight regarding sampling, three post-sampling, and two focus on quality assurance. In general, the quality of the evidence is very low, and the strength of the recommendation in all the questions has been rated as weak. The working group in four questions elaborate the recommendations, based mainly on group experience, rating as good practice.

    CONCLUSIONS: The multidisciplinary working group was considered one of the major contributors to this guideline. The lack of quality information highlights the need for research in this area of the patient care process. The peculiarities of the emergency medical areas need specific considerations to minimise the possibility of errors in the preanalytical phase.

  • 27.
    Hallberg, P.
    et al.
    Department of Medical Sciences, Uppsala University, Uppsala.
    Karlsson, J.
    Department of Medical Sciences, Uppsala University, Uppsala.
    Lind, L.
    Department of Medical Sciences, Uppsala University, Uppsala.
    Michaëlsson, K.
    Department of Surgical Sciences, Uppsala University, Uppsala.
    Kurland, Lisa
    Department of Medical Sciences, Uppsala University, Uppsala.
    Kahan, T.
    Division of Internal Medicine, Karolinska Institute, Danderyd Hospital, Stockholm.
    Malmqvist, K.
    Division of Internal Medicine, Karolinska Institute, Danderyd Hospital, Stockholm.
    Öhman, K. P.
    Division of Internal Medicine, Karolinska Institute, Danderyd Hospital, Stockholm; Department of Medicine and Care, Faculty of Health Sciences, Linköping.
    Nyström, F.
    Department of Medicine and Care, Faculty of Health Sciences, Linköping; Department of Biomedicine and Surgery, Faculty of Health Sciences, Linköping, Sweden.
    Liljedahl, U.
    Department of Medical Sciences, Uppsala University, Uppsala.
    Syvänen, A. C.
    Department of Medical Sciences, Uppsala University, Uppsala.
    Melhus, H.
    Department of Medical Sciences, Uppsala University, Uppsala.
    Gender-specific association between preproendothelin-1 genotype and reduction of systolic blood pressure during antihypertensive treatment–results from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation versus Atenolol (SILVHIA)2004In: Clinical Cardiology, ISSN 0160-9289, E-ISSN 1932-8737, Vol. 27, no 5, p. 287-90Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Studies suggest that endothelin-1 contributes to the pathogenesis of hypertension. A G5665T gene polymorphism of preproendothelin-1 has been shown to be associated with higher blood pressure in overweight patients. No study has yet determined the effect of this polymorphism on the change in blood pressure during antihypertensive treatment.

    HYPOTHESIS: This study aimed to determine this effect in hypertensive patients with left ventricular (LV) hypertrophy during antihypertensive treatment with either irbesartan or atenolol.

    METHODS: We determined the preproendothelin-1 genotype using minisequencing in 102 patients with essential hypertension and LV hypertrophy verified by echocardiography, randomized in a double-blind fashion to treatment with either the AT1-receptor antagonist irbesartan or the beta1-adrenoceptor antagonist atenolol.

    RESULTS: The change in systolic blood pressure (SBP) after 12 weeks of treatment was related to the preproendothelin-1 genotype in men; after adjustment for potential covariates (age, blood pressure, and LV mass index at study entry, dose of irbesartan/atenolol, and type of treatment), those carrying the T-allele responded on average with a more than two-fold greater reduction than those with the G/G genotype (-21.9 mmHg 13.9] vs. -8.9 [2.3], p = 0.007). No significant differences in blood pressure change between G/G and carriers of the T-allele were seen among women.

    CONCLUSIONS: Our finding suggests a gender-specific relationship between the G5665T preproendothelin-1 polymorphism and change in SBP in response to antihypertensive treatment with irbesartan or atenolol, suggesting the endothelin pathway to be a common mechanism included in the hypertensive action of the drugs.

  • 28.
    Hallberg, Pär
    et al.
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Karlsson, Julia
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Kurland, Lisa
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Lind, Lars
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden; AstraZeneca Research & Development, Mölndal, Sweden.
    Kahan, Thomas
    Division of Internal Medicine, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
    Malmqvist, Karin
    Division of Internal Medicine, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
    Öhman, K. Peter
    AstraZeneca Research & Development, Mölndal, Sweden; Department of Medicine and Care, Faculty of Health Sciences, Linköping, Sweden.
    Nyström, Fredrik
    Department of Medicine and Care, Faculty of Health Sciences, Linköping, Sweden; Department of Biomedicine and Surgery, Faculty of Health Sciences, Linköping, Sweden.
    Melhus, Håkan
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    The CYP2C9 genotype predicts the blood pressure response to irbesartan: results from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation vs Atenolol (SILVHIA) trial2002In: Journal of Hypertension, ISSN 0263-6352, E-ISSN 1473-5598, Vol. 20, no 10, p. 2089-2093Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: The cytochrome P450 CYP2C9 enzyme (CYP2C9) metabolizes many clinically important drugs, for example, phenytoin, warfarin and the angiotensin II type 1 (AT(1)) receptor antagonists, losartan and irbesartan. Single nucleotide polymorphisms in the CYP2C9 gene result in the expression of three important variants, CYP2C9*1(wild-type), CYP2C9*2 and CYP2C9*3, the last two exhibiting reduced catalytic activity compared with the wild-type. The CYP2C9 genotype is known to determine sensitivity to and dose requirements for both warfarin and phenytoin, and also the rate of metabolism of losartan. However, its influence on clinical response to treatment with the AT(1) receptor antagonist, irbesartan, has not been investigated.

    OBJECTIVE: To determine whether the CYP2C9genotype influences the blood pressure-decreasing response to antihypertensive treatment with irbesartan.

    DESIGN AND METHODS: One hundred and two patients with essential hypertension and left ventricular hypertrophy were allocated randomly to groups to receive double-blind treatment with either irbesartan (n = 49) or the beta(1)-adrenergic receptor blocker, atenolol ( n= 53). Blood pressure was measured before and after 12 weeks of treatment. genotyping was performed using solid-phase minisequencing.

    RESULTS: The diastolic blood pressure (DBP) response differed in relation to the CYP2C9 genotype in patients given irbesartan: the reduction in patients with genotype CYP2C9*1/CYP2C9*1 (n = 33) was 7.5% and that with CYP2C9*1/CYP2C9*2 (n = 12) was 14.4% ( P= 0.036). A similar trend was seen for systolic blood pressure. In contrast, no relation was seen between the CYP2C9 genotype and blood pressure response to atenolol, a drug not metabolized via CYP2C9.

    CONCLUSIONS: The CYP2C9 genotype seems to predict the DBP response to irbesartan, but not to atenolol, in patients with essential hypertension.

  • 29.
    Hallberg, Pär
    et al.
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Lind, Lars
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden; AstraZeneca Research & Development, Mölndal, Sweden.
    Billberger, Katarina
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Michaelsson, Karl
    Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
    Karlsson, Julia
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Kurland, Lisa
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Kahan, Thomas
    Division of Internal Medicine, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
    Malmqvist, Karin
    Division of Internal Medicine, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
    Öhman, K. Peter
    AstraZeneca Research & Development, Mölndal, Sweden; Department of Medicine and Care, Faculty of Health Sciences, Linköping, Sweden.
    Nyström, Fredrik
    Department of Medicine and Care, Faculty of Health Sciences, Linköping, Sweden; Department of Biomedicine and Surgery, Faculty of Health Sciences, Linköping, Sweden.
    Liljedahl, Ulrika
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Syvänen, Ann-Christine
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Melhus, Håkan
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Transforming growth factor beta1 genotype and change in left ventricular mass during antihypertensive treatment–results from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation versus Atenolol (SILVHIA)2004In: Clinical Cardiology, ISSN 0160-9289, E-ISSN 1932-8737, Vol. 27, no 3, p. 169-173Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Angiotensin II, via the angiotensin II type 1 (AT1) receptor, may mediate myocardial fibrosis and myocyte hypertrophy seen in hypertensive left ventricular (LV) hypertrophy through production of transforming growth factor beta1 (TGF-beta1); AT1-receptor antagonists reverse these changes. The TGF-beta1 G + 915C polymorphism is associated with interindividual variation in TGF-beta1 production. No study has yet determined the impact of this polymorphism on the response to antihypertensive treatment.

    HYPOTHESIS: We aimed to determine whether the TGF-beta1 G + 915C polymorphism was related to change in LV mass during antihypertensive treatment with either an AT1-receptor antagonists or a beta1-adrenoceptor blocker. The polymorphism was hypothesized to have an impact mainly on the irbesartan group.

    METHODS: We determined the association between the TGF-beta1 genotype and regression of LV mass in 90 patients with essential hypertension and echocardiographically diagnosed LV hypertrophy, randomized in a double-blind study to receive treatment for 48 weeks with either the AT1-receptor antagonist irbesartan or the beta1-adrenoceptor blocker atenolol.

    RESULTS: Irbesartan-treated patients who were carriers of the C-allele, which is associated with low expression of TGF-beta1, responded with a markedly greater decrease in LV mass index (LVMI) than subjects with the G/G genotype (adjusted mean change in LVMI -44.7 g/m2 vs. -22.2 g/m2, p = 0.007), independent of blood pressure reduction. No association between genotype and change in LVMI was observed in the atenolol group.

    CONCLUSIONS: The TGF-beta1 G + 915C polymorphism is related to the change in LVMI in response to antihypertensive treatment with the AT1-receptor antagonist irbesartan.

  • 30. Hallberg, Pär
    et al.
    Lind, Lars
    Michaëlsson, Karl
    Karlsson, Julia
    Kurland, Lisa
    Kahan, Thomas
    Malmqvist, Karin
    Öhman, K. Peter
    Nyström, Fredrik
    Melhus, Håkan
    B2 bradykinin receptor (B2BKR) polymorphism and change in left ventricular mass in response to antihypertensive treatment: results from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation versus Atenolol (SILVHIA) trial2003In: Journal of Hypertension, ISSN 0263-6352, E-ISSN 1473-5598, Vol. 21, no 3, p. 621-624Article in journal (Refereed)
    Abstract [en]

    OBJECTIVE: Hypertension is associated with a number of adverse morphologic and functional changes in the cardiovascular system, including left ventricular (LV) hypertrophy. Studies have demonstrated that bradykinin, through the B2 bradykinin receptor (B2BKR), mediates important cardiovascular effects that may protect against LV hypertrophy. Recently, a +9/-9 exon 1 polymorphism of the B2BKR was shown to be strongly associated with LV growth response among normotensive males undergoing physical training. We aimed to clarify whether the processes found in exercise-induced LV growth in normotensive people also occur in pathological LV hypertrophy.

    DESIGN AND METHODS: We determined the B2BKR genotype of 90 patients with essential hypertension and echocardiographically diagnosed LV hypertrophy, included in a double-blind study to receive treatment for 48 weeks with either the angiotensin II type 1 (AT1) receptor antagonist irbesartan or the beta1-adrenoceptor antagonist atenolol.

    RESULTS: B2BKR +9/+9 genotypes responded poorly in LV mass regression, independent of blood pressure reduction or treatment, as compared to the other genotypes (adjusted mean change in LV mass index = -10.0 +/- 4.6 versus -21.6 +/- 2.2 g/m2, P = 0.03).

    CONCLUSIONS: Our results suggest an impact of the B2BKR polymorphism on LV mass regression during antihypertensive treatment.

  • 31.
    Hallberg, Pär
    et al.
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Lind, Lars
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden; AstraZeneca Research & Development, Mölndal, Sweden.
    Michaëlsson, Karl
    Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
    Kurland, Lisa
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Kahan, Thomas
    Division of Internal Medicine, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
    Malmqvist, Karin
    Division of Internal Medicine, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
    Öhman, Karl Peter
    AstraZeneca Research & Development, Mölndal, Sweden; Department of Medicine and Care, Faculty of Health Sciences, Linköping, Sweden.
    Nyström, Fredrik
    Department of Medicine and Care, Faculty of Health Sciences, Linköping, Sweden; Department of Biomedicine and Surgery, Faculty of Health Sciences, Linköping, Sweden.
    Liljedahl, Ulrika
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Syvänen, Ann-Christine
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Melhus, Håkan
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Adipocyte-derived leucine aminopeptidase genotype and response to antihypertensive therapy2003In: BMC Cardiovascular Disorders, ISSN 1471-2261, E-ISSN 1471-2261, Vol. 3, article id 11Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Adipocyte-derived leucine aminopeptidase (ALAP) is a recently identified member of the M1 family of zinc-metallopeptidases and is thought to play a role in blood pressure control through inactivation of angiotensin II and/or generation of bradykinin. The enzyme seems to be particularly abundant in the heart. Recently, the Arg528-encoding allele of the ALAP gene was shown to be associated with essential hypertension.

    METHODS: We evaluated the influence of this polymorphism on the change in left ventricular mass index in 90 patients with essential hypertension and echocardiographically diagnosed left ventricular hypertrophy, randomised in a double-blind study to receive treatment with either the angiotensin II type I receptor antagonist irbesartan or the beta1-adrenoceptor blocker atenolol for 48 weeks. Genyotyping was performed using minisequencing.

    RESULTS: After adjustment for potential covariates (blood pressure and left ventricular mass index at baseline, blood pressure change, age, sex, dose and added antihypertensive treatment), there was a marked difference between the Arg/Arg and Lys/Arg genotypes in patients treated with irbesartan; those with the Arg/Arg genotype responded on average with an almost two-fold greater regression of left ventricular mass index than patients with the Lys/Arg genotype (-30.1 g/m2 [3.6] vs -16.7 [4.5], p = 0.03).

    CONCLUSIONS: The ALAP genotype seems to determine the degree of regression of left ventricular hypertrophy during antihypertensive treatment with the angiotensin II type I receptor antagonist irbesartan in patients with essential hypertension and left ventricular hypertrophy. This is the first report of a role for ALAP/aminopeptidases in left ventricular mass regulation, and suggests a new potential target for antihypertensive drugs.

  • 32.
    Hansen, Kim
    et al.
    Emergency Department, Prince Charles Hospital, Chermside, Queensland, Australia; Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia.
    Boyle, Adrian
    Emergency Department, Addenbrooke's Hospital, Cambridge, Cambridgeshire, UK.
    Holroyd, Brian
    Department of Emergency Medicine, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada; Emergency Strategic Clinical Network, Alberta Health Services, Edmonton, Alberta, Canada.
    Phillips, Georgina
    Emergency Department, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia; Department of Epidemiology and Preventive Medicine, Monash University, Clayton, Victoria, Australia.
    Benger, Jonathan
    Academic Department of Emergency Care, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
    Chartier, Lucas B.
    Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Emergency Department, University Health Network, Toronto, Ontario, Canada.
    Lecky, Fiona
    Health Services Research, University of Sheffield, Sheffield, UK; Emergency Department /TARN, Salford Royal Hospitals NHS Foundation Trust, Salford, UK.
    Vaillancourt, Samuel
    Emergency Department, St Michael's Hospital, Toronto, Ontario, Canada.
    Cameron, Peter
    Department of Epidemiology and Preventive Medicine, Monash University, Clayton, Victoria, Australia; Emergency Department, Alfred Hospital, Melbourne, Victoria, Australia.
    Waligora, Grzegorz
    Emergency Department, Wroclaw Medical University, Wroclaw, Dolnoslaskie, Poland.
    Kurland, Lisa
    Örebro University, School of Medical Sciences.
    Truesdale, Melinda
    Emergency Department, Royal Melbourne Hospital, Melbourne, Victoria, Australia; Emergency Department, Royal Women's Hospital, Parkville, Victoria, Australia.
    Updated framework on quality and safety in emergency medicine2020In: Emergency Medicine Journal, ISSN 1472-0205, E-ISSN 1472-0213, Vol. 37, no 7, p. 437-442Article in journal (Refereed)
    Abstract [en]

    OBJECTIVES: Quality and safety of emergency care is critical. Patients rely on emergency medicine (EM) for accessible, timely and high-quality care in addition to providing a 'safety-net' function. Demand is increasing, creating resource challenges in all settings. Where EM is well established, this is recognised through the implementation of quality standards and staff training for patient safety. In settings where EM is developing, immense system and patient pressures exist, thereby necessitating the availability of tiered standards appropriate to the local context.

    METHODS: The original quality framework arose from expert consensus at the International Federation of Emergency Medicine (IFEM) Symposium for Quality and Safety in Emergency Care (UK, 2011). The IFEM Quality and Safety Special Interest Group members have subsequently refined it to achieve a consensus in 2018.

    RESULTS: Patients should expect EDs to provide effective acute care. To do this, trained emergency personnel should make patient-centred, timely and expert decisions to provide care, supported by systems, processes, diagnostics, appropriate equipment and facilities. Enablers to high-quality care include appropriate staff, access to care (including financial), coordinated emergency care through the whole patient journey and monitoring of outcomes. Crowding directly impacts on patient quality of care, morbidity and mortality. Quality indicators should be pragmatic, measurable and prioritised as components of an improvement strategy which should be developed, tailored and implemented in each setting.

    CONCLUSION: EDs globally have a remit to deliver the best care possible. IFEM has defined and updated an international consensus framework for quality and safety.

  • 33.
    Henricson, Joakim
    et al.
    Department of Biomedical and Clinical Sciences, Faculty of Health Sciences, Linköping University, Linköping, Sweden; Department of Emergency Medicine, Local Health Care Services in Central Östergötland, Region Östergötland, Linköping, Sweden.
    Ekelund, Ulf
    Department of Emergency Medicine, Skåne University Hospital, Lund University, Lund, Sweden.
    Hartman, Jens
    Department of Biomedical and Clinical Sciences, Faculty of Health Sciences, Linköping University, Linköping, Sweden.
    Ziegler, Bruno
    Department of Emergency Medicine Örebro University Hospital, Örebro, Sweden; Örebro University, Örebro, Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Emergency Medicine Örebro University Hospital, Örebro, Sweden.
    Björk Wilhelms, Daniel
    Department of Emergency Medicine, Local Health Care Services in Central Östergötland, Region Östergötland, Linköping, Sweden; Division of Drug Research, Department of Biomedical and Clinical Sciences, Faculty of Health Sciences, Linköping University, Linköping, Sweden.
    Pathways to the emergency department: a national, cross-sectional study in Sweden2022In: BMC Emergency Medicine, E-ISSN 1471-227X, Vol. 22, no 1, article id 58Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Swedish Emergency Departments (EDs) see 2.6 million visits annually. Sweden has a strong tradition of health care databases, but information on patients' pathways to the ED is not documented in any registry. The aim of this study was to provide a national overview of pathways, degree of medical acuteness according to triage, chief complaints, and hospital admission rates for adult patients (≥18 years) visiting Swedish EDs during 24 h.

    METHODS: A national cross-sectional study including all patients at 43 of Sweden's 72 EDs during 24 h on April 25th, 2018. Pathway to the ED, medical acuteness at triage, admission and basic demographics were registered by dedicated assessors present at every ED for the duration of the study. Descriptive data are reported.

    RESULTS: A total of 3875 adult patients (median age 59; range 18 to 107; 50% men) were included in the study. Complete data for pathway to the ED was reported for 3693 patients (98%). The most common pathway was self-referred walk-in (n = 1310; 34%), followed by ambulance (n = 920; 24%), referral from a general practitioner (n = 497; 1 3%), and telephone referral by the national medical helpline "1177" (n = 409; 10%). In patients 18 to 64 years, self-referred walk-in was most common, whereas transport by ambulance dominated in patients > 64 years. Of the 3365 patients who received a medical acuteness level at triage, 4% were classified as Red (Immediate), 18% as Orange (very urgent), 47% as Yellow (Urgent), 26% as Green (Standard), and 5% as Blue (Non-Urgent). Abdominal or chest pain were the most common chief complaints representing approximately 1/3 of all presentations. Overall, the admission rate was 27%. Arrival by ambulance was associated with the highest rate of admission (53%), whereas walk-in patients and telephone referrals were less often admitted.

    CONCLUSION: Self-referred walk-in was the overall most common pathway followed by ambulance. Patients arriving by ambulance were often elderly, critically ill and often admitted to in-patient care, whereas arrival by self-referred walk-in was more common in younger patients.

  • 34.
    Holroyd, Brian R.
    et al.
    Department of Emergency, Medicine University of Alberta, Edmonton, Alberta, Canada.
    Beeson, Michael S.
    Department of Emergency, Medicine Northeast Ohio Medical University, Akron, OH, USA.
    Hughes, Thomas
    John Radcliffe Hospital, Oxford, UK.
    Kurland, Lisa
    Örebro University, School of Medical Sciences.
    Sherbino, Jonathan
    Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
    Truesdale, Melinda
    Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia.
    Hersh, William
    Department of Medical Informatics & Clinical Epidemiology ,Oregon Health & Science University, Portland, OR, USA.
    Clinical Informatics Competencies in the Emergency Medicine Specialist Training Standards of Five International Jurisdictions2018In: AEM education and training, ISSN 2472-5390, Vol. 2, no 4, p. 293-300Article in journal (Refereed)
    Abstract [en]

    Background: The field of clinical informatics (CI), and specifically the electronic health record, has been identified as a key facilitator to achieve a sustainable evidence-based health care system for the future. International graduate medical education (GME) programs have been challenged to ensure that their trainees are provided with appropriate skills to deliver effective and efficient health care in an evolving environment.

    Objectives: This study explored how international emergency medicine (EM) specialist training standards address competencies and training in relevant areas of CI.

    Methods: A list of categories of CI competencies relative to EM was developed following a thematic review of published references documenting CI curriculum and competencies. Publicly available documents outlining core content, curriculum, and competencies from international organizations responsible for specialty GME and/or credentialing in EM for Australasia, Canada, Europe, the United Kingdom, and the United States were identified. These EM training standards were reviewed to identify inclusion of topics related to the relevant categories of CI competencies.

    Results: A total of 23 EM curriculum documents were included in the review. Curricula content related to critical appraisal/evidence-based medicine, leadership, quality improvement, and privacy/security were included in all EM curricula. The CI topics related to fundamental computer skills, computerized provider order entry, and patient-centered informatics were only included in the EM curricula documents for the United States and were absent for the other jurisdictions.

    Conclusion: There is variation in the CI-related content of the international EM specialty training standards reviewed. Given the increasing importance of CI in the future delivery of health care, organizations responsible for training and credentialing specialist emergency physicians must ensure that their training standards incorporate relevant CI content, thus ensuring that their trainees gain competence in essential aspects of CI.

  • 35.
    Hruska, Katrin
    et al.
    Emergency Department, Karolinska University Hospital, Huddinge, Sweden.
    Castrén, Maaret
    Department of Emergency Medicine and Services, Helsinki University Hospital, Helsinki, Finland.
    Banerjee, JAY
    University Hospitals of Leicester NHS Trust, Leicester, UK.
    Behringer, Wilhelm
    Department of Emergency Medicine, Jena University, Jena, Germany.
    Bjørnsen, Lars P.
    Department of Emergency Medicine and Pre-hospital Services, St Olav’s Hospital HF, Trondheim University Hospital, Trondheim, Norway; Department of Circulation and Medical Imaging, Norwegian University of Science and Technology, Trondheim, Norway.
    Cameron, Peter
    Department of Emergency Medicine and Pre-hospital Services, St Olav’s Hospital HF, Trondheim University Hospital, Trondheim, Norway.
    Einav, Sharon
    S´haare Zedek Medical Centre and Hebrew University Faculty of Medicine, Jerusalem, Israel.
    Holroyd, Brian R.
    Emergency Strategic Clinical Network, Alberta Health Services, University of Alberta, Alberta, Canada; Department of Emergency Medicine, Faculty of Medicine and Dentistry, University of Alberta, Alberta, Canada.
    Jones, Peter
    Department of Surgery, Universtiy of Auckland, Auckland, New Zealand; Department of Emergency Medicine Research, Auckland City Hospital, Auckland, New Zealand.
    Lassen, Annmarie
    Department of Emergency Medicine, Odense University Hospital, Odense, Denmark.
    Truesdal, Melinda
    The Royal Melbourne Hospital, Parkville, Melbourne, Australia.
    Kurland, Lisa
    Örebro University, School of Medical Sciences.
    Template for uniform reporting of emergency department measures, consensus according to the Utstein method2019In: European journal of emergency medicine, ISSN 0969-9546, E-ISSN 1473-5695, Vol. 26, no 6, p. 417-422Article in journal (Refereed)
    Abstract [en]

    Objective: To develop a template for uniform reporting of standardized measuring and describing of care provided in the emergency department (ED).

    Methods: An international group of experts in emergency medicine, with broad experience from different clinical settings, met in Utstein, Norway. Through a consensus process, a limited number of measures that would accurately describe an ED were chosen and a template was developed.

    Results: The final measures to be reported and their definitions were grouped into six categories: Structure, Staffing and governance, Population, Process times, Hospital and healthcare system and Outcomes. The template for Utstein-style uniform reporting is presented.

    Conclusion: The suggested template is intended for use in studies carried out in EDs to improve comparability and knowledge translation.

  • 36.
    Hugelius, Karin
    et al.
    Örebro University, School of Health Sciences.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Emergency Medicine, Örebro University Hospital, Örebro, Sweden.
    Medical Experiences from a Consular Repatriation and Evacuation Operation from Afghanistan in August 2021: A Field Report2022In: Prehospital and Disaster Medicine, ISSN 1049-023X, E-ISSN 1945-1938, Vol. 37, no 1, p. 139-141Article in journal (Refereed)
    Abstract [en]

    Following the Taliban influx in August 2021, several Western countries repatriated nationals and evacuated others from Kabul Airport in Afghanistan. This report aimed to describe medical experiences from the consular repatriation and evacuation operation.Memos from personal conversations with seven professionals involved in these operations formed the basis for this report.Minor trauma, gastrointestinal symptoms, dehydration, fever, and mental distress were common. Bandages, oral rehydration solution, and the administration of paracetamol were needed, in addition to medical evaluation of acuity. In consular repatriation and humanitarian evacuations, medical attendance should be prioritized to manage medical needs of individuals being evacuated, but also from a public health perspective. The medical needs covered a broad specter of infection disease symptoms, trauma, and mental health problems among patients of all ages. Since the nature of consular repatriations and evacuations can be challenging from safety and infrastructural aspects, general medical emergency awareness with an ability to effectively evaluate and manage both somatic and mental health emergencies on the ground and in the air, among both children and adults, is needed.

  • 37.
    Hugelius, Karin
    et al.
    Örebro University, School of Health Sciences.
    Kurland, Lisa
    Örebro University, School of Medical Sciences.
    Passningsuppdrag i Region Örebro län: en analys av befolkningstäckning med fokus på tidskritiska tillstånd2022Conference paper (Other academic)
  • 38.
    Hugelius, Karin
    et al.
    Örebro University, School of Health Sciences.
    Rådestad, M.
    Department of Clinical Science and Education, Karolinska Institutet, SödersjukhusetStockholm, Sweden; Capio St. Görans Hospital, Stockholm, Sweden.
    Al-Dhahir, H.
    Department of Emergency Medicine, Örebro University Hospital, Örebro, Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Medical Sciences.
    Decision-making by medical officer in charge during major incidents: a qualitative study2021In: Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine, E-ISSN 1757-7241, Vol. 29, no 1, article id 120Article in journal (Refereed)
    Abstract [en]

    Background: An incident command structure is commonly used to manage responses to major incidents. In the hospital incident command structure, the medical officer in charge (MOC) is in a key position. The decision-making process is essential to effective management, but little is known about which factors influence the process. Therefore, the current study aimed to describe factors influencing decision-making of MOCs.

    Methods: A conventional content analysis was conducted based on 16 individual interviews with medical doctors who had been deployed as MOCs at Swedish hospitals during major incidents.

    Results: The results showed that the decision-making and re-evaluation process was a comprehensive analysis influenced by three categories of factors: event factors, including consequences from the type of event, levels of uncertainty and the circumstances; organizational factors, including the doctor's role, information management and the response to the event; and personal factors, such as competence, personality and mental preparedness.

    Conclusions: Reliable and timely information management structure enabling the gathering and analysis of essential information, a clear command structure and appropriate personal qualities were essential and contributed to successful MOCs decision making in major incidents.

  • 39.
    Ivic, R.
    et al.
    Karolinska Institutet, Department of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden; Academic Emergency Medical Service, Region Stockholm, Stockholm, Sweden.
    Vicente, V.
    Karolinska Institutet, Department of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Region Stockholm, Health and Medical Care Administration, Stockholm, Sweden; Karolinska Institutet, Department of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden.
    Svensson, J.
    Falck Ambulans AB, Stockholm, Sweden.
    Sahdev Klintemård, R.
    Falck Ambulans AB, Stockholm, Sweden.
    Castrén, M.
    Karolinska Institutet, Department of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden; Emergency Medicine, Helsinki University and Department of Emergency Medicine and Services, Helsinki University Hospital, Helsinki, Finland.
    Bohm, K.
    Karolinska Institutet, Department of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden; Department of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Pre-hospital emergency nurse specialist's experiences in caring for patients with non-specific chief complaints in the ambulance: A qualitative interview study2022In: International Emergency Nursing, ISSN 1755-599X, E-ISSN 1878-013X, Vol. 63, article id 101178Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Pre-hospital emergency nurse (PEN) specialists are faced with patients presenting with non-specific chief complaints (NSC) to the emergency medical service (EMS) on a daily basis. These patients are often elderly and one in three has a serious condition and their acuity is not recognized.

    OBJECTIVE: The aim of the current study was to explore PEN specialists' experiences in caring for patients presenting with non-specific chief complaints.

    DESIGN: A qualitative study design with eleven individual interviews of PENs, between 2018 and 2020. Qualitative content analysis was used.

    RESULTS: The analyses generated three categories including subcategories. The categories were "Unexplained suffering". "Systematic approach and experience enhances medical safety". "Organizational processes can be optimized". The relation between the categories compiled as ́In-depth systematic assessment is perceived to reduce suffering and increases patient safetý.

    CONCLUSION: The PENs experiences in caring for patients presenting with non-specific chief complaints show that an in-depth systematic assessment may lead to a meaningful caring encounter which enables the identification of the cause of the chief complaint. Experience and a systematic approach were considered as essential to enhance medical safety. This could be strengthened through feedback on the nurse's care provided by care managers and employers. To optimize organizational processes, the development of the opportunity to convey the patient to different levels of care can be an important component.

  • 40.
    Ivic, Robert
    et al.
    Karolinska Institute, Department of Clinical Science and Education,Södersjukhuset, Stockholm, Sweden; Academic Emergency Medical Service, Region Stockholm, Stockholm,Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Karolinska Institute, Department of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden.
    Vicente, Veronica
    Karolinska Institute, Department of Clinical Science and Education,Södersjukhuset, Stockholm, Sweden; Academic Emergency Medical Service, Region Stockholm, Stockholm,Sweden.
    Castrén, Maaret
    Karolinska Institute, Department of Clinical Science and Education,Södersjukhuset, Stockholm, Sweden; Emergency Medicine, Helsinki University and Department of EmergencyMedicine and Services, Helsinki University Hospital, Helsinki, Finland.
    Bohm, Katarina
    Karolinska Institute, Department of Clinical Science and Education,Södersjukhuset, Stockholm, Sweden; Academic Emergency Medical Service, Region Stockholm, Stockholm,Sweden; Department of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Serious conditions among patients with non-specific chief complaints in the pre-hospital setting: a retrospective cohort study2020In: Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine, E-ISSN 1757-7241, Vol. 28, no 1, article id 74Article in journal (Refereed)
    Abstract [en]

    Background: Emergency Medical Services (EMS) are faced daily with patients presenting with a non-specific chief complaints (NSC); i.e. decreased general condition, general malaise, sense of illness, or just being unable to cope with usual daily activities. Patients presenting with NSCs often have normal vital signs. It has previously been established that however, NSCs may have a serious underlying condition that has yet to be identified. The primary outcome of this study was to determine the prevalence of serious conditions in patients presenting with NSCs to the EMS.

    Method: A retrospective cohort study of patients >= 18 years of age who were reported as presenting with chief complaints compatible with NSCs to the EMS in Stockholm Region and transported to an emergency department between January 1st, 2013 and December 31st, 2013. Patients were identified via the EMS electronic health care record and followed via records from the National Patient Registry and Causes of Death Registry at Sweden's National Board for Health and Welfare. The definition of serious condition was defined by expert consensus. Descriptive statistics as well as regression analyses were used.

    Results: A total of 3780 patients were included, with a median age of 77 years. A serious condition was present in 35.3% of the patients. The in-hospital mortality rate for the group with serious conditions was 10.1% (OR 6.8, CI 95%, 4.1-11.3), and the 30-day mortality rate was 20.2% (OR 3.1, CI 95%, 2.3-4.0). In the group with no serious conditions the rates were 1.0 and 4.2%, respectively. The total hospitalization rate was 67.6%. The presence of serious conditions as well as increased mortality rates were associated with Rapid Emergency Triage and Treatment system (RETTS) as well as National Early Warning Score (NEWS) irrespective of triage score.

    Conclusion: More than one-third of the patients presenting with NSCs to EMS had a serious underlying condition which was associated with increased mortality and hospitalization rates.

  • 41.
    Ivic, Robert
    et al.
    Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Academic Emergency Medical Service, Region Stockholm, Stockholm, Sweden.
    Nurmi, Jouni
    Emergency Medicine, Helsinki University and Department of Emergency Medicine and Services, Helsinki University Hospital, Helsinki, Finland.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Vicente, Veronica
    Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
    Lindström, Veronica
    Karolinska Institutet, Department of Neurobiology, Care Sciences and Society, division of nursing, Stockholm, Sweden; Samariten Ambulance Stockholm, Stockholm, Sweden.
    Djärv, Therese
    Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
    Kaartinen, Johanna
    Emergency Medicine, Helsinki University and Department of Emergency Medicine and Services, Helsinki University Hospital, Helsinki, Finland.
    Castrén, Maaret
    Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Emergency Medicine, Helsinki University and Department of Emergency Medicine and Services, Helsinki University Hospital, Helsinki, Finland.
    Bohm, Katarina
    Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Department of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Soluble urokinase plasminogen activator receptor and lactate as prognostic biomarkers in patients presenting with non-specific chief complaints in the pre-hospital setting - the PRIUS-study2021In: Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine, E-ISSN 1757-7241, Vol. 29, no 1, article id 116Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Emergency Medical Services (EMS) are faced daily with patients presenting with non-specific chief complaints (NSC). Patients presenting with NSCs often have normal vital signs. It has previously been established that NSCs may have a serious underlying condition that has yet to be identified. The aim of the current study was to determine if soluble urokinase plasminogen activator receptor (suPAR) and lactate could be used to identify serious conditions among patients presenting with NSCs to the EMS. The secondary aim was to describe the prognostic value for mortality in the group.

    METHOD: A blinded prospective observational cohort study was conducted of patients brought to the ED by ambulance after calling the national emergency number 112 and who were assessed as having NSC by the EMS. Biomarkers were measured during index EMS assessment before transportation to the ED. Patients were followed via EMS and hospital electronic health records. Descriptive and logistic regression analyses were used.

    RESULTS: A total of 414 patients were included, with a median age of 82 years. A serious condition was present in 15.2% of the patients. Elevated suPAR above 3 ng/ml had a positive likelihood ratio (LR+) of 1.17 and a positive predictive value (PPV) of 17.3% as being predictive of a prevalent serious condition. Elevated suPAR above 9 ng/ml had LR+ 4.67 and a PPV of 16.7% as being predictive of 30-day mortality. Lactate was not significantly predictive.

    CONCLUSION: Pre-hospital suPAR and lactate cannot differentiate serious conditions in need of urgent treatment and assessment in the ED among patients presenting with non-specific chief complaints. suPAR has shown to be predictive of 30-day mortality, which could add some value to the clinical assessment.

    TRIAL REGISTRATION: NCT03089359. Registered 20 March 2017, retrospectively registered, https://clinicaltrials.gov/ct2/show/NCT03089359 .

  • 42.
    Jacobsson, Andreas
    et al.
    Department of Emergency Care, Örebro University Hospital, Örebro, Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Emergency Care, Örebro University Hospital, Örebro, Sweden.
    Höglund, Erik
    Örebro University, School of Health Sciences. Department of Emergency Care, Örebro University Hospital, Örebro, Sweden; University Health Care Research Center, Örebro University, Örebro, Sweden.
    Direct in-hospital admission via ambulance (DIVA): A retrospective observational study2020In: International Emergency Nursing, ISSN 1755-599X, E-ISSN 1878-013X, Vol. 52, article id 100906Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Prolonged stays in emergency departments increase the risk of adverse events in elderly patients. To optimize care for nonurgent patients who need in-hospital admission, a patient-focused improvement project named Direct In-hospital admission Via Ambulance (DIVA) was launched at Örebro University Hospital.

    PURPOSE: This study describes the effects of DIVA. The primary outcome was time to in-hospital admission. Secondary outcomes were the in-hospital admission rate, the in-hospital length of stay and patient characteristics.

    METHOD: This was a retrospective observational study. Descriptive and comparative statistics were used. All patients identified by the ambulance nurse as nonurgent but with an apparent need for in-hospital admission were candidates for direct in-hospital admission. The results were compared with those of a reference group.

    RESULT: In total, 127 patients were included, with 45 patients in the DIVA group and 82 patients in the reference group. In the DIVA group, 24 patients were directly admitted. The median time to in-hospital admisson was 49.5 min for direct admitted patients and 278.5 min for the reference group. There was a statistical significant difference between the groups (p < 0.01).

    CONCLUSION: The current study indicates that time to in-hospital admission could be reduced by DIVA.

  • 43.
    Karlsson, Adam
    et al.
    Department of Medical Sciences, Örebro University, Örebro, Sweden.
    Stassen, Willem
    Division of emergency Medicine, University of Cape Town, Cape Town, South Africa.
    Loutfi, Amy
    Örebro University, School of Science and Technology.
    Wallgren, Ulrika M.
    Örebro University, School of Medical Sciences. Örebro University Hospital. Department of Clinical Science and Education, Karolinska Institutet, Söderssjukhuset, Stockholm, Sweden; Department of Emergency Medicine, Örebro University Hospital and School of Medicine, Örebro University, Örebro, Sweden.
    Larsson, Eric
    Department of Infectious Diseases, Centralsjukhuset, Karlstad, Sweden.
    Kurland, Lisa
    Örebro University, School of Medical Sciences. Department of Emergency Medicine.
    Predicting mortality among septic patients presenting to the emergency department-a cross sectional analysis using machine learning2021In: BMC Emergency Medicine, E-ISSN 1471-227X, Vol. 21, no 1, article id 84Article in journal (Refereed)
    Abstract [en]

    Background: Sepsis is a life-threatening condition, causing almost one fifth of all deaths worldwide. The aim of the current study was to identify variables predictive of 7- and 30-day mortality among variables reflective of the presentation of septic patients arriving to the emergency department (ED) using machine learning.

    Methods: Retrospective cross-sectional design, including all patients arriving to the ED at Sodersjukhuset in Sweden during 2013 and discharged with an International Classification of Diseases (ICD)-10 code corresponding to sepsis. All predictions were made using a Balanced Random Forest Classifier and 91 variables reflecting ED presentation. An exhaustive search was used to remove unnecessary variables in the final model. A 10-fold cross validation was performed and the accuracy was described using the mean value of the following: AUC, sensitivity, specificity, PPV, NPV, positive LR and negative LR.

    Results: The study population included 445 septic patients, randomised to a training (n = 356, 80%) and a validation set (n = 89, 20%). The six most important variables for predicting 7-day mortality were: "fever", "abnormal verbal response", "low saturation", "arrival by emergency medical services (EMS)", "abnormal behaviour or level of consciousness" and "chills". The model including these variables had an AUC of 0.83 (95% CI: 0.80-0.86). The final model predicting 30-day mortality used similar six variables, however, including "breathing difficulties" instead of "abnormal behaviour or level of consciousness". This model achieved an AUC = 0.80 (CI 95%, 0.78-0.82).

    Conclusions: The results suggest that six specific variables were predictive of 7- and 30-day mortality with good accuracy which suggests that these symptoms, observations and mode of arrival may be important components to include along with vital signs in a future prediction tool of mortality among septic patients presenting to the ED. In addition, the Random Forests appears to be a suitable machine learning method on which to build future studies.

  • 44.
    Karlsson, J.
    et al.
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Lind, L.
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden; AstraZeneca Research and Development, Mölndal, Sweden.
    Hallberg, P.
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Michaëlsson, K.
    Department of Surgical Sciences, Uppsala University, Uppsala.
    Kurland, Lisa
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Kahan, T.
    Division of Internal Medicine, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
    Malmqvist, K.
    Division of Internal Medicine, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
    Öhman, K. P.
    AstraZeneca Research and Development, Mölndal, Sweden; Department of Medicine and Care, Faculty of Health Sciences, Linköping, Sweden.
    Nyström, F.
    Department of Medicine and Care, Faculty of Health Sciences, Linköping, Sweden; Department of Biomedicine and Surgery, Faculty of Health Sciences, Linköping, Sweden.
    Melhus, H.
    Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
    Beta1-adrenergic receptor gene polymorphisms and response to beta1-adrenergic receptor blockade in patients with essential hypertension2004In: Clinical Cardiology, ISSN 0160-9289, E-ISSN 1932-8737, Vol. 27, no 6, p. 347-350Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Studies suggest that the Ser49Gly and Arg389Gly polymorphisms in the beta1-adrenergic receptor might be of functional importance for the cardiovascular system. Both have been associated with altered receptor activity in vitro, and with hypertension and cardiac failure in vivo.

    HYPOTHESIS: The aim of this study was to test whether these polymorphisms were associated with the change in heart rate or blood pressure in patients with essential hypertension and left ventricular (LV) hypertrophy treated with the beta1-adrenergic receptor blocker atenolol.

    METHODS: Blood pressure and heart rate were measured in 101 hypertensive patients with echocardiographically verified LV hypertrophy, randomized in a double-blind study to treatment with either the beta1-adrenergic receptor blocker atenolol or the angiotensin II type I receptor antagonist irbesartan. Changes in blood pressure and heart rate were evaluated after 12 weeks. Beta1-adrenergic receptor genotyping was performed using polymerase chain reaction and restriction fragment length polymorphism.

    RESULTS: We found no significant associations between the changes in the measured variables and either of the two polymorphisms. However, carriers of the 49Gly allele showed a tendency toward a greater reduction in heart rate compared with patients with the Ser/Ser49 genotype (p = 0.06).

    CONCLUSIONS: The Ser49Gly and Arg389Gly beta1-adrenergic receptor polymorphisms do not seem to exert a major effect on the changes in heart rate and blood pressure during 12 weeks of treatment with atenolol in patients with essential hypertension and LV hypertrophy.

  • 45.
    Khankeh, Hamidreza
    et al.
    University of Social Welfare & Rehabilitation Sciences, Tehran, Iran; Department of Clinical Science and Education, Karolinska Institute, Stockholm, Sweden.
    Nakhaei, Maryam
    University of Social Welfare & Rehabilitation Sciences, Tehran, Iran.
    Masoumi, Gholamreza
    Iran University of Medical Sciences, Teheran, Iran.
    Hosseini, Mohammadali
    University of Social Welfare & Rehabilitation Sciences, Tehran, Iran.
    Parsa-Yekta, Zohreh
    Tehran University of Medical Sciences, Teheran, Iran.
    Kurland, Lisa
    Department of Clinical Science and Education, Karolinska Institute, Stockholm, Sweden.
    Castren, Maaret
    Department of Clinical Science and Education, Karolinska Institute, Stockholm, Sweden.
    Life recovery after disasters: a qualitative study in the Iranian context2013In: Prehospital and Disaster Medicine, ISSN 1049-023X, E-ISSN 1945-1938, Vol. 28, no 6, p. 573-9Article in journal (Refereed)
    Abstract [en]

    INTRODUCTION: Planned and organized long-term rehabilitation services should be provided to victims of a disaster for social integration, economic self-sufficiency, and psychological health. There are few studies on recovery and rehabilitation issues in disaster situations. This study explores the disaster-related rehabilitation process.

    METHOD: This study was based on qualitative analysis. Participants included 18 individuals (eight male and ten female) with experience providing or receiving disaster health care or services. Participants were selected using purposeful sampling. Data were collected through in-depth and semi-structured interviews. All interviews were transcribed and content analysis was performed based on qualitative content analysis.

    RESULTS: The study explored three main concepts of recovery and rehabilitation after a disaster: 1) needs for health recovery; 2) intent to delegate responsibility; and 3) desire for a wide scope of social support. The participants of this study indicated that to provide comprehensive recovery services, important basic needs should be considered, including the need for physical rehabilitation, social rehabilitation, and livelihood health; the need for continuity of mental health care; and the need for family re-unification services. Providing social activation can help reintegrate affected people into the community.

    CONCLUSION: Effective rehabilitation care for disaster victims requires a clear definition of the rehabilitation process at different levels of the community. Involving a wide set of those most likely to be affected by the process provides a comprehensive, continuous, culturally sensitive, and family-centered plan.

  • 46.
    Kurland, Lisa
    Örebro University, School of Medical Sciences.
    Sverige: akutsjukvård i nästan 20 år2017In: Finska Läkaresällskapets Handlingar, ISSN 0015-2501, no 2, p. 10-14Article in journal (Refereed)
  • 47.
    Kurland, Lisa
    et al.
    Swedish Society for Emergency Medicine, Stockholm, Sweden; Department of Clinical Research and Education, Karolinska Institutet, Stockholm, Sweden; Department of Emergency Medicine, Södersjukhuset, Stockholm, Sweden.
    Graham, Colin A
    Department of Emergency Medicine, Chinese University, Hong Kong, China.
    Emergency medicine development in the Nordic countries2014In: European journal of emergency medicine, ISSN 0969-9546, E-ISSN 1473-5695, Vol. 21, no 3, p. 163-163Article in journal (Refereed)
  • 48.
    Kurland, Lisa
    et al.
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Hallberg, Pär
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Melhus, Håkan
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Liljedahl, Ulrika
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Hashemi, Nashmil
    Division of Cardiovascular Medicine, Department of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
    Syvänen, Ann-Christine
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Lind, Lars
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Kahan, Thomas
    Division of Cardiovascular Medicine, Department of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
    The relationship between the plasma concentration of irbesartan and the antihypertensive response is disclosed by an angiotensin II type 1 receptor polymorphism: results from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation vs. Atenolol (SILVHIA) Trial.2008In: American Journal of Hypertension, ISSN 0895-7061, E-ISSN 1941-7225, Vol. 21, no 7, p. 836-839Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: The aim of this study was to investigate the effect of the plasma concentration of irbesartan, a specific angiotensin II type 1 receptor (AT1R) antagonist, and the blood pressure response in relation to AT1R gene polymorphisms.

    METHODS: Plasma irbesartan was analyzed in 42 patients with mild-to-moderate hypertension and left ventricular hypertrophy from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation vs. Atenolol (SILVHIA) trial, who were treated with irbesartan as monotherapy for 12 weeks. Blood pressure and irbesartan concentration were measured at trough, i.e., 24 +/- 3 h after the last dose. Five AT1R gene polymorphisms were analyzed by minisequencing.

    RESULTS: Neither the plasma concentration of irbesartan, nor any of the AT1R polymorphisms were associated with the blood pressure response to irbesartan treatment. However, the interaction term between the plasma concentration of irbesartan and the AT1R C5245T polymorphism was related to the reduction in systolic blood pressure after 12 weeks of treatment (P = 0.025). Furthermore, the plasma concentration of irbesartan was related to the change in systolic blood pressure in individuals homozygous for the AT1R 5245 T allele (r = -0.56, P = 0.030), but not for other genotypes.

    CONCLUSIONS: There was an association between plasma concentrations of irbesartan and the blood pressure response for hypertensive patients with AT1R 5245 TT. Because of the small sample size, this study needs to be viewed as hypothesis generating. This is the first study, to our knowledge, indicating that the concentration-response relationship of an antihypertensive drug may be genotype dependent.

  • 49.
    Kurland, Lisa
    et al.
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Liljedahl, Ulrika
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Karlsson, Julia
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Kahan, Thomas
    Division of Medicine, Karolinska Institute Danderyd Hospital, Stockholm, Sweden.
    Malmqvist, Karin
    Division of Medicine, Karolinska Institute Danderyd Hospital, Stockholm, Sweden.
    Melhus, Håkan
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Syvänen, Ann Christine
    Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
    Lind, Lars
    AstraZeneca R&D, Mölndal, Sweden.
    Angiotensinogen gene polymorphisms: relationship to blood pressure response to antihypertensive treatment. Results from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation vs Atenolol (SILVHIA) trial.2004In: American Journal of Hypertension, ISSN 0895-7061, E-ISSN 1941-7225, Vol. 17, no 1, p. 8-13Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: The renin-angiotensin-aldosterone system (RAAS) is important for the development of hypertension, and several antihypertensive drugs target this system. Our aim was to determine whether specific single nucleotide polymorphisms (SNPs) in RAAS genes were related to the blood pressure (BP) lowering effect of antihypertensive treatment.

    METHODS: Patients with mild to moderate primary hypertension and left ventricular hypertrophy were randomized in a double-blind fashion to treatment with either the angiotensin II type 1 receptor antagonist irbesartan (n = 48) or the beta(1)-adrenergic receptor blocker atenolol (n = 49) as monotherapy. A microarray-based minisequencing system was used to genotype 30 SNPs in seven genes in the RAAS. These polymorphisms were related to the antihypertensive response after 12 weeks treatment.

    RESULTS: The BP reductions were similar in the atenolol and the irbesartan groups. Presence of the angiotensinogen (AGT) -6A allele or the AGT 235T allele were both associated with the most pronounced systolic BP response to atenolol treatment (P =.001 when -6 AA+AG was compared with GG and P =.008 for presence of the 235T variant compared with 235 MM).

    CONCLUSIONS: We found that SNPs in the angiotensinogen gene were associated with the BP lowering response to atenolol. This study is limited by a relatively small sample size, and the results should therefore be viewed as preliminary. Despite this limitation, these results illustrate the potential of using SNP genotyping as a pharmacogenetic tool in antihypertensive treatment.

  • 50.
    Kurland, Lisa
    et al.
    Department of Medical Sciences, Uppsala University Hospital, Sweden; Department of Medicine, University Hospital, Uppsala, Sweden.
    Melhus, H
    Department of Medical Sciences, Uppsala University Hospital, Sweden.
    Sarabi, M
    Department of Medical Sciences, Uppsala University Hospital, Sweden.
    Millgård, J
    Department of Medical Sciences, Uppsala University Hospital, Sweden.
    Ljunghall, S
    Department of Medical Sciences, Uppsala University Hospital, Sweden.
    Lind, L
    Department of Medical Sciences, Uppsala University Hospital, Sweden.
    Polymorphisms in the renin-angiotensin system and endothelium-dependent vasodilation in normotensive subjects2001In: Clinical Physiology, ISSN 0144-5979, E-ISSN 1365-2281, Vol. 21, no 3, p. 343-349Article in journal (Refereed)
    Abstract [en]

    BACKGROUND: Our aim was to test the hypothesis that genes encoding components in the renin-angiotensin system influence endothelial vasodilatory function.

    METHODS: In 59 apparently healthy, normotensive individuals, endothelium-dependent vasodilation (EDV) and endothelial-independent vasodilation (EIDV) was evaluated by infusing metacholine and sodium nitroprusside into the brachial artery. Forearm blood flow was measured by venous occlusion plethysmography. The ACE insertion (I)/deletion (D) polymorphism, the T174M and M235T angiotensinogen restriction fragments length polymorphisms, the angiotensin II receptor type 1 (AT1R) A1166C, and the aldosterone synthase gene (CYP11B2) C-344T polymorphisms were analysed.

    RESULTS: When analysing the ACE, the two angiotensinogen and the aldosterone synthase CYP11B2 genotypes independently, no significant association with endothelial vasodilatory function was found. However, a significant reduction in endothelium-dependent vasodilation was observed in the subjects (n=9) with the ACE D allele and the angiotensinogen T174M genotype (P<0.05). Subjects with the AT1R genotype AC showed a reduction in both EDV (P=0.05) and EIDV (P=0.04) when compared with those with the AA genotype.

    CONCLUSIONS: The subjects with the ACE D allele in combination with the angiotensinogen T174M genotype are associated with a reduced EDV. This together with the observation that the AC AT1R genotype is associated with a reduction in both EDV and EIDV, supports the hypothesis that endothelial vasodilatory function is influenced by genes in the renin-angiotensinogen system.

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