Postinfectious irritable bowel syndrome - A meta-analysis

被引:240
作者
Halvorson, Heather A.
Schlett, Carey D.
Riddle, Mark S.
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Prevent Med & Biometr, Bethesda, MD 20814 USA
[2] USN, Med Res Unit 3, Cairo, Egypt
关键词
D O I
10.1111/j.1572-0241.2006.00654.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: Irritable bowel syndrome (IBS) is a heterogeneous disorder affecting :12% of the population worldwide. Several studies identify IBS as a sequela of infectious gastroenteritis (IGE) with reported prevalence ranging from 4% to 31% and relative risk from 2.5 to 11.9. This meta-analysis was conducted to explore the differences between reported rates and provide a pooled estimate of risk for postinfectious irritable bowel syndrome (PI-IBS). DATA SOURCES: Electronic databases (MEDLINE, OLDMEDLINE, EMBASE, Cochrane database of clinical trials) and pertinent reference lists (including other review articles). REVIEW Data were abstracted from included studies by two independent investigators; study quality. METHODS: heterogeneity, and publication bias were assessed; sensitivity analysis was performed; and a summative effect estimate was calculated for risk of PI-IBS. RESULTS: Eight studies were included for analysis and all reported elevated risk of IBS following IGE. Median prevalence of IBS in the IGE groups was 9.8% (IQR 4.0-13.3) and 1.2% in control groups (IQR 0.4-1.8) (sign-rank test, p = 0.01). The pooled odds ratio was 7.3 (95% CI, 4.7-11.1) without significant heterogeneity (chi(2) heterogeneity statistic, p = 0.41). Subgroup analysis revealed an association between PI-IBS risk and IGE definition used. CONCLUSIONS: This study provides supporting evidence for PI-IBS as a sequela of IGE and a pooled risk estimate revealing a sevenfold increase in the odds of developing IBS following IGE. The results suggest that the long-term benefit of reduced PI-IBS may be gained from primary prevention of IGE.
引用
收藏
页码:1894 / 1899
页数:6
相关论文
共 29 条
[11]   Post-infectious irritable bowel syndrome in patients with Shigella infection [J].
Ji, S ;
Park, H ;
Lee, D ;
Song, YK ;
Choi, JP ;
Lee, SI .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2005, 20 (03) :381-386
[12]   THE EPIDEMIOLOGY OF IRRITABLE-BOWEL-SYNDROME IN A RANDOM-POPULATION - PREVALENCE, INCIDENCE, NATURAL-HISTORY AND RISK-FACTORS [J].
KAY, L ;
JORGENSEN, T ;
JENSEN, KH .
JOURNAL OF INTERNAL MEDICINE, 1994, 236 (01) :23-30
[13]  
MANTEL N, 1959, J NATL CANCER I, V22, P719
[14]   Dyspepsia and irritable bowel syndrome after a Salmonella gastroenteritis outbreak:: One-year follow-up cohort study [J].
Mearin, F ;
Pérez-Oliveras, M ;
Perelló, A ;
Vinyet, J ;
Ibañez, A ;
Coderch, J ;
Perona, M .
GASTROENTEROLOGY, 2005, 129 (01) :98-104
[15]   Drug therapy: Irritable bowel syndrome [J].
Mertz, HR .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (22) :2136-2146
[16]   Post-diarrhea chronic intestinal symptoms and irritable bowel syndrome in North American travelers to Mexico [J].
Okhuysen, PC ;
Jiang, ZD ;
Carlin, L ;
Forbes, C ;
DuPont, HL .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2004, 99 (09) :1774-1778
[17]   Intestinal infection and irritable bowel syndrome [J].
Parry, S ;
Forgacs, I .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2005, 17 (01) :5-9
[18]   Factors associated with the development of post-infectious functional gastrointestinal diseases: does smoking play a role? [J].
Parry, SD ;
Barton, JR ;
Welfare, MR .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2005, 17 (10) :1071-1075
[19]   Does bacterial gastroenteritis predispose people to functional gastrointestinal disorders? A prospective, community-based, case-control study [J].
Parry, SD ;
Stansfield, R ;
Jelley, D ;
Gregory, W ;
Phillips, E ;
Barton, JR ;
Welfare, MR .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2003, 98 (09) :1970-1975
[20]  
Quigley Eamonn M M, 2005, Chin J Dig Dis, V6, P122, DOI 10.1111/j.1443-9573.2005.00202.x