Trial sequential analyses of meta-analyses of complications in laparoscopic vs. small-incision cholecystectomy: more randomized patients are needed
Abstract
Objective
Conclusions based on meta-analyses of randomized trials carry a status of “truth.” Methodological components may identify trials with systematic errors (“bias”). Trial sequential analysis (TSA) evaluates random errors in meta-analysis. We analyzed meta-analyses on laparoscopic vs. small-incision cholecystectomy regarding different outcome measures for the occurrence of type I errors.
Study Design and Setting
Using TSA, we calculated the required information size (IS) and the trial sequential monitoring boundaries regarding complications in our Cochrane review with meta-analyses of cholecystectomy. For each outcome, we calculated a low risk of bias heterogeneity-adjusted IS. As a sensitivity analysis, we calculated an a priori heterogeneity-adjusted IS.
Results
According to the trial sequential analyses based on a low risk of bias heterogeneity-adjusted IS definitive evidence may be reached by conducting one more randomized trial. Information may be required on 582 and 119 additional randomized patients to evaluate the effect on severe complications and serious adverse events (SAEs), respectively.
Conclusion
Our results provide incentives to conduct a new trial with a low risk of bias focusing on a new composite outcome measure of SAEs to obtain conclusive evidence on which operative method to recommend.
Keywords: Cumulative meta-analysis, Trial sequential analysis, Meta-analysis, Random error, Cholecystectomy, Trial sequential monitoring boundaries
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Funding: No funding was obtained for this study. All researchers were dependent on funding.
Conflict of interest: All authors declare that there are no personal interests, no competing interests, and no funding interests. Therefore, the authors have nothing to declare.
Guarantor of the article: F. Keus and J. Wetterslev had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
PII: S0895-4356(09)00278-9
doi:10.1016/j.jclinepi.2009.08.023
© 2010 Elsevier Inc. All rights reserved.
