Benefit of antibiotic therapy on pouchitis after ileal pouch anal anastomosis: a systematic
review and meta-analysis of clinical trials
Elahi B, Nikfar S, Derakhshani S, Vafaie M, Abdollahi M
CRD summary
The authors concluded that antibiotics improved pouchitis symptoms following ileal pouch anal anastomosis, but the
results should be interpreted with caution given the small number of trials and patients. Potential for error and bias in
the review, the unclear quality and small number of included studies and absence of data from most eligible studies
made the authors' caution warranted.
Authors' objectives
To assess the efficacy of antibiotics in the management of pouchitis following ileal pouch anal anastomosis (IPAA).
Searching
PubMed, EMBASE, Web of Science, Scopus and Cochrane Central Register of Controlled Trials (CENTRAL) were
searched between 1966 and July 2008 for articles in any language. Search terms were reported. References of retrieved
articles were handsearched.
Study selection
Randomised controlled trials that compared antibiotic therapy to placebo or other active therapies in patients with
pouchitis were eligible for inclusion if they assessed clinical improvement and/or remission of pouchitis. Uncontrolled
studies of antibiotic therapy for pouchitis also appeared to be eligible for inclusion. Only published studies were eligible
for inclusion.
Included studies evaluated metronidazole, riflaxin or ciprofloxacin monotherapy or combination therapy of
ciprofloxacin and tinidazole, ciprofloxacin and rifaximin, and ciprofloxacin and metronidazole in varying doses in
patients with acute or chronic pouchitis. Duration of therapy ranged from seven days to three months. Concomitant
mesalamine therapy was administered in one study. Outcomes reported were remission, stool frequency, pouchitis
disease activity scores and quality of life scores.
Two reviewers assessed the studies for review.
Assessment of study quality
The authors did not state that they assessed the methodological quality of the included studies
Data extraction
Data were extracted for three studies included in the meta-analysis. Data were not extracted for the other six studies
that met inclusion criteria. Number of patients in each group with clinical improvement or remission was extracted and
used to calculate odds ratios (OR) with 95% confidence intervals (CI). The outcome of clinical improvement was not
defined.
The authors did not state how many reviewers performed data extraction.
Methods of synthesis
A pooled odds ration with 95% CI was calculated using a fixed-effects model. Statistical heterogeneity was assessed
using the Breslow-Day test and visual inspection of L'Abbe plot.
Results of the review
Nine studies met the inclusion criteria. Results were reported for three RCTs (n=69). No results were reported for the
other six studies.
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