Validating microscopic colitis (MC) in Swedish pathology registersShow others and affiliations
2018 (English)In: Scandinavian Journal of Gastroenterology, ISSN 0036-5521, E-ISSN 1502-7708Article in journal (Refereed) Published
Abstract [en]
OBJECTIVE: Microscopic colitis (MC), encompassing collagenous colitis (CC) and lymphocytic colitis (LC), is a diagnosis which relies on histopathologic criteria. This report examines the validity of having a diagnosis of MC in Swedish pathology registers.
METHODS: We reviewed patient charts from 215 randomly selected individuals from 15 pathology departments in five healthcare regions in Sweden with a relevant histopathology code for MC on colon biopsies. Information on clinical symptoms and laboratory data were obtained from medical chart review. We obtained sufficient data on 211 individuals for calculating positive predictive values (PPVs) for MC.
RESULTS: In total, 200/211 patients with a histopathology diagnosis of MC were confirmed as also having a clinical diagnosis of MC after chart review, yielding a PPV of 95% (95%CI =91-97%). The PPV for CC was 95% (95%CI =87-98%) and 85% for LC (95%CI =78-90%). The median age at biopsy was 67 years (range 17-90 years), and 72% (n = 154) were women. The most common symptoms in patients with MC histopathology were diarrhea (96% of patients), weight loss (24%) and abdominal pain (13%). Four percent (4/111) of patients with available data on stool culture were positive for gastrointestinal pathogens (none had Clostridium difficile). In 81 patients with available celiac serology, five (6%) were positive. Twenty-six percent of all patients had at least one other autoimmune disease, the most frequent being hypothyroidism (8%) and celiac disease (6%).
CONCLUSIONS: This study found a high validity for MC as recorded in Swedish pathology registers.
Place, publisher, year, edition, pages
Taylor & Francis, 2018.
Keywords [en]
Microscopic colitis, collagenous colitis, histopathology, lymphocytic colitis, validation
National Category
Gastroenterology and Hepatology
Identifiers
URN: urn:nbn:se:oru:diva-71183DOI: 10.1080/00365521.2018.1543446ISI: 000456881600008PubMedID: 30600733Scopus ID: 2-s2.0-85059556123OAI: oai:DiVA.org:oru-71183DiVA, id: diva2:1277233
2019-01-092019-01-092023-12-08Bibliographically approved