Objective The modest effect sizes of most pain treatments make it essential that randomized controlled trials (RCTs) use methods that clearly define treatment effects of interest and consider the role of concurrent treatments. This study aims to determine how frequently concurrent analgesic use is reported in interventional pain RCTs and how accounting for analgesic use can affect pain intensity outcomes.
Design Meta-epidemiologic study.
Methods We conducted a study of concurrent analgesic use among RCTs from a recent systematic review of non-surgical interventional pain treatments (n= 37). We calculated the prevalence of different methods used to report concurrent analgesic use. We performed meta-analyses to compare treatment effects on pain intensity with vs. without accounting for concurrent analgesic use via a novel quantitative composite outcome, the “QPAC1.5.”
Results About half of interventional pain RCTs reported concurrent analgesic use, but only one RCT directly accounted for concurrent analgesic use in their pain intensity outcome. Analyses accounting for concurrent analgesic use using the QPAC1.5 substantially increased the estimated treatment effect of interventions on pain intensity by an average of −0.45 numeric rating scale points (95% CI −0.76 to −0.14; p<0.001), as compared to analyses that did not adjust for analgesic use.
Conclusion Concurrent analgesic use is sometimes reported in interventional pain RCTs, but rarely accounted for when examining treatment effects on pain intensity. Accounting for concurrent analgesic use changes the treatment effect of interest to remove differential analgesic rates and has the potential to significantly affect estimates of effect sizes on pain treatments.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis work was supported by the CLEAR Center and grant P30AR072572 from the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) of the National Institutes of Health.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data reported in the present work are already publicly available in previously published research articles or contained in the manuscript.
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