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Published 19 October 2009, doi:10.1136/bmj.b4012
Cite this as: BMJ 2009;339:b4012
Lisa Hartling, assistant professor, Maria Ospina, project manager, Yuanyuan Liang, research scientist and biostatistician, Donna M Dryden, assistant professor, Nicola Hooton, project coordinator, Jennifer Krebs Seida, project coordinator, Terry P Klassen, professor
1 Alberta Research Centre for Health Evidence, Department of Pediatrics, University of Alberta, Aberhart Centre One, Edmonton, AB, Canada T6G 2J3
Correspondence to: L Hartling hartling{at}ualberta.ca
Design Cross sectional study.
Study sample 163 trials in children.
Main outcome measures Inter-rater agreement between reviewers assessing trials using the risk of bias tool (weighted
), time to apply the risk of bias tool compared with other approaches to quality assessment (paired t test), degree of correlation for overall risk compared with overall quality scores (Kendalls
statistic), and magnitude of effect estimates for studies classified as being at high, unclear, or low risk of bias (metaregression).
Results Inter-rater agreement on individual domains of the risk of bias tool ranged from slight (
=0.13) to substantial (
=0.74). The mean time to complete the risk of bias tool was significantly longer than for the Jadad scale and Schulz approach, individually or combined (8.8 minutes (SD 2.2) per study v 2.0 (SD 0.8), P<0.001). There was low correlation between risk of bias overall compared with the Jadad scores (P=0.395) and Schulz approach (P=0.064). Effect sizes differed between studies assessed as being at high or unclear risk of bias (0.52) compared with those at low risk (0.23).
Conclusions Inter-rater agreement varied across domains of the risk of bias tool. Generally, agreement was poorer for those items that required more judgment. There was low correlation between assessments of overall risk of bias and two common approaches to quality assessment: the Jadad scale and Schulz approach to allocation concealment. Overall risk of bias as assessed by the risk of bias tool differentiated effect estimates, with more conservative estimates for studies at low risk.
This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
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