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Control of hypercapnia and mortality in home mechanical ventilation: the population-based DISCOVERY study
Department of Medical Sciences, Respiratory, Allergy and Sleep Research, Uppsala University, Uppsala, Sweden.
Department of Clinical Sciences, Respiratory Medicine, Allergology and Palliative Medicine, Faculty of Medicine, Lund University, Lund, Sweden.
Department of Medical Sciences, Respiratory, Allergy and Sleep Research, Uppsala University, Uppsala, Sweden.
Department of Medical Sciences, Clinical Physiology, Uppsala University, Uppsala, Sweden; Department of Women's and Children's Health, Physiotherapy, Uppsala University, Uppsala, Sweden.
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2024 (English)In: ERJ Open Research, E-ISSN 2312-0541, Vol. 10, no 6, article id 00461-2024Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Studies on the survival of patients with home mechanical ventilation (HMV) are sparse. We aimed to analyse the impact of controlled hypercapnia on survival over 27 years among patients with HMV in Sweden.

STUDY DESIGN AND METHODS: Population-based cohort study of adult patients starting HMV in the Swedish Registry for Respiratory Failure (Swedevox) during 1996-2022 cross-linked with the National Cause of Death registry. Mortality risk factors were analysed using crude and multivariable Cox regression models, including adjustments for anthropometrics, comorbidities, the underlying diagnosis causing chronic hypercapnic respiratory failure (CRF) and the control of hypercapnia (P aCO2 ≤6.0 kPa) at follow-up.

RESULTS: We included 10 190 patients (50.1% women, age 62.9±14.5 years). Control of hypercapnia at follow-up after 1.3±0.9 years was associated with lower mortality, hazard ratio (HR) 0.74 (95% CI 0.68-0.80) and the association was strongest in those with pulmonary disease, restrictive thoracal disease (RTD), obesity hypoventilation syndrome (OHS) and amyotrophic lateral sclerosis (ALS). Predictors for increased mortality included age, Charlson Comorbidity Index, supplemental oxygen therapy and acute start of HMV therapy. Median survival varied between 0.8 years (95% CI 0.8-0.9 (n=1401)) for ALS and 7.6 years (95% CI 6.9-8.6 (n=1061)) for neuromuscular disease. Three-year survival decreased from 76% (95% CI 71-80) between 1996 and 1998 to 52% (95% CI 50-55) between 2017 and 2019. When adjusting for underlying diagnosis and age, the association between start year and decreased survival disappeared, HR 1.00 (95% CI 0.99-1.01).

CONCLUSION: Controlling P aCO2 is a key treatment goal for survival in HMV therapy. Survival differed markedly between diagnosis and age groups, and survival rates have declined as the patient group has aged.

Place, publisher, year, edition, pages
European Respiratory Society, 2024. Vol. 10, no 6, article id 00461-2024
National Category
Respiratory Medicine and Allergy
Identifiers
URN: urn:nbn:se:oru:diva-117739DOI: 10.1183/23120541.00461-2024ISI: 001414601200007PubMedID: 39655175Scopus ID: 2-s2.0-85216205971OAI: oai:DiVA.org:oru-117739DiVA, id: diva2:1920361
Funder
Swedish Heart Lung Foundation, 20230392Swedish Heart Lung Foundation, 20180567Swedish Heart Lung Foundation, 20210529Swedish Heart Lung Foundation, 20220686Region Örebro County, OLL-939092Swedish Research Council, 2019-02081
Note

Funding Agencies:

A. Palm was supported by the Swedish Heart and Lung Foundation (20230392), ALF (the agreement concerning the research and education of doctors) (ALF-979044) and by the Swedish Respiratory society. L. Grote was supported by the Swedish Heart and Lung Foundation (20180567 and 20210529) and ALF (GBG725601 and GBG966283). M. Ljunggren was supported by the Swedish Heart and Lung Foundation (20220686) and ALF (ALF-979044). J. Sundh was supported by ALF funding in Region Örebro County (OLL-939092). M. Ekström was supported by an unrestricted grant from the Swedish Research Council (2019-02081). 

Available from: 2024-12-11 Created: 2024-12-11 Last updated: 2025-02-19Bibliographically approved

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