Elisabeth Schorling, Sebastian Knorr, Sonja Lick, Pablo Steinberg, Dagmar Adeline Brüggemann
{"title":"Probability of sequelae following Campylobacter spp. infections: Update of systematic reviews and meta‐analyses","authors":"Elisabeth Schorling, Sebastian Knorr, Sonja Lick, Pablo Steinberg, Dagmar Adeline Brüggemann","doi":"10.1002/puh2.145","DOIUrl":null,"url":null,"abstract":"Reactive arthritis (REA) and Guillain–Barré syndrome (GBS) are postinfectious complications of Campylobacter enteritis (CE); associations with inflammatory bowel diseases and irritable bowel syndrome (IBS) are also discussed. The objective of this study was to summarize existing evidence on the probability of sequelae following confirmed CE.All studies included in previous reviews and meta‐analyses on this topic were retrieved and assessed for eligibility; a systematic literature search was conducted to collect more recent reports. For each sequela, random effects meta‐analyses were performed; the risk of bias and the quality of evidence were evaluated.In total, 50 reports of observational studies were included; between 110,765 and 175,839 CE cases were considered for each sequela. The pooled proportion of CE cases that developed a sequela was 1.72% (95% CI 0.81–3.61; prediction interval [PI]: 0.03–47.65) for REA, 0.07% (0.03–0.16; PI: 0.003–1.59) for GBS, 0.22% (0.06–0.73; PI: 0.002–20.69) for Crohn's disease (CD), 0.35% (0.11–1.15; PI: 0.003–28.16) for ulcerative colitis (UC), and 4.48% (1.92–10.08; PI: 0.09–70.62) for IBS. The high between‐study heterogeneity could partially be explained by study size and design, the method of assessing sequelae, and the period between CE and sequelae onset. The quality of evidence was rated as moderate for GBS and UC, and low for REA, CD, and IBS.Updated estimates of the probability to develop sequelae after CE are provided, for CD and UC for the first time. However, uncertainty regarding the true probabilities remains, which is reflected in the broad PIs.","PeriodicalId":74613,"journal":{"name":"Public health challenges","volume":"3 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Public health challenges","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/puh2.145","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Reactive arthritis (REA) and Guillain–Barré syndrome (GBS) are postinfectious complications of Campylobacter enteritis (CE); associations with inflammatory bowel diseases and irritable bowel syndrome (IBS) are also discussed. The objective of this study was to summarize existing evidence on the probability of sequelae following confirmed CE.All studies included in previous reviews and meta‐analyses on this topic were retrieved and assessed for eligibility; a systematic literature search was conducted to collect more recent reports. For each sequela, random effects meta‐analyses were performed; the risk of bias and the quality of evidence were evaluated.In total, 50 reports of observational studies were included; between 110,765 and 175,839 CE cases were considered for each sequela. The pooled proportion of CE cases that developed a sequela was 1.72% (95% CI 0.81–3.61; prediction interval [PI]: 0.03–47.65) for REA, 0.07% (0.03–0.16; PI: 0.003–1.59) for GBS, 0.22% (0.06–0.73; PI: 0.002–20.69) for Crohn's disease (CD), 0.35% (0.11–1.15; PI: 0.003–28.16) for ulcerative colitis (UC), and 4.48% (1.92–10.08; PI: 0.09–70.62) for IBS. The high between‐study heterogeneity could partially be explained by study size and design, the method of assessing sequelae, and the period between CE and sequelae onset. The quality of evidence was rated as moderate for GBS and UC, and low for REA, CD, and IBS.Updated estimates of the probability to develop sequelae after CE are provided, for CD and UC for the first time. However, uncertainty regarding the true probabilities remains, which is reflected in the broad PIs.
反应性关节炎(REA)和吉兰-巴雷综合征(GBS)是弯曲杆菌肠炎(CE)的感染后并发症;本研究还讨论了它们与炎症性肠病和肠易激综合征(IBS)的关系。本研究的目的是总结有关确诊 CE 后遗症发生概率的现有证据。研究人员检索了以往有关该主题的综述和荟萃分析中包含的所有研究,并对其资格进行了评估;还进行了系统性文献检索,以收集更多最新报告。针对每种后遗症进行了随机效应荟萃分析,并对偏倚风险和证据质量进行了评估。共纳入了 50 份观察性研究报告;每种后遗症的 CE 病例数在 110,765 到 175,839 之间。出现后遗症的 CE 病例的汇总比例为:REA:1.72%(95% CI 0.81-3.61;预测区间 [PI]:0.03-47.65);GBS:0.07%(0.03-0.16;PI:0.003-1.59);REA:0.22%(0.06-0.73;PI:0.002-20.69),溃疡性结肠炎(UC)为 0.35%(0.11-1.15;PI:0.003-28.16),IBS 为 4.48%(1.92-10.08;PI:0.09-70.62)。研究间的高度异质性可部分归因于研究规模和设计、评估后遗症的方法以及 CE 与后遗症发生之间的时间间隔。GBS和UC的证据质量被评为中等,REA、CD和IBS的证据质量被评为低。然而,真实概率仍存在不确定性,这反映在广泛的 PIs 中。