2011
DOI: 10.1016/j.jclinepi.2011.01.012
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GRADE guidelines 6. Rating the quality of evidence—imprecision

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Cited by 2,093 publications
(1,230 citation statements)
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References 26 publications
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“…The same research group designed and conducted all three studies on seroma, and the studies were methodologically homogeneous. The quality of evidence was downgraded to moderate because of missing methodological information resulting in moderate risk of bias, and because of the few studies, with small sample sizes41, 44.…”
Section: Resultsmentioning
confidence: 99%
“…The same research group designed and conducted all three studies on seroma, and the studies were methodologically homogeneous. The quality of evidence was downgraded to moderate because of missing methodological information resulting in moderate risk of bias, and because of the few studies, with small sample sizes41, 44.…”
Section: Resultsmentioning
confidence: 99%
“…We defined treatment effect estimates as precise when pooled estimates had narrow 95 % CIs or the pooled sample had >300 events (using 25 % relative effect difference for calculation of optimal information size). 70 We did not quantify publication biases or selective outcome reporting biases because of the questionable statistical validity of the available tests. 71 We defined a high level of evidence on the basis of consistent findings from low risk-of-bias RCTs.…”
Section: Methodsmentioning
confidence: 99%
“…The quality of the overall evidence (confidence in the estimates) was moderate to high for efficacy vs. placebo, low to moderate for side effects (limited by imprecision) and likely low for the ranking suggesting superiority of escitalopram (limited by indirectness of comparative data). 42,43 In conclusion, given the promising positive effects of SSRIs on hot flashes and the likely favorable side effect profile, their use seems to be an acceptable option for treating menopausal women with hot flashes and is a good alternative to HRT. Future trials should investigate different SSRIs over a long time period (e.g., 6-12 months) and should not use placebo for comparison in order to provide high-quality comparative effectiveness evidence.…”
Section: Implications For Practice and Researchmentioning
confidence: 99%