Introduction and Objectives: Many studies have reported putative factors for the development of chronic pain after surgery. However, advances in knowledge about the etiology and prognosis of chronic postsurgical pain (CPSP) could be gained by improving methodology within studies of surgical pain. The purpose of this study was to review predictive factors and to propose core risk factor and outcome domains for inclusion in future epidemiological studies investigating CPSP.
Methods: Using the Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials as a framework we reviewed risk factor and outcome domains, methodological issues and standardized measurement tools based on findings from narrative and systematic reviews, primary clinical and epidemiological studies and published guidelines for chronic pain clinical trials.
Results: Five “core” risk factor domains (demographic, pain, clinical, surgery-related, and psychological) and 4 outcome domains (pain, physical functioning, psychological functioning, and global ratings of outcome) were identified. Important methodological issues, related to the definition and timing of follow-up to assess transition from acute to chronic pain are discussed. We also propose the use of validated, standardized measurement tools to capture risk factor and outcome domains at multiple time points.
Discussion: There is potential to advance the field of CPSP research by striving for consensus among pain experts; this would advance current evidence by improving our ability to compare findings from different studies and would facilitate the aggregation of surgical cohort datasets to allow international comparisons. We propose these findings as a starting point to build a comprehensive framework for epidemiological studies investigating chronic pain after surgery.
*Department of Anesthesiology and Perioperative Medicine, School of Nursing, Queen’s University, Kingston, ON, Canada
†Department of Experimental Health Psychology, Clinical Psychological Science, Maastricht University, Maastricht, The Netherlands
‡Warwick Clinical Trials Unit, University of Warwick, Coventry, UK
Supported by the Ontario Ministry of Research and Innovation International Strategic Opportunities Program and the Collaborative Research Grant (2011) from the International Association for the Study of Pain (IASP). Additional funding for investigator travel and meetings was provided by the Principal’s Development Fund and the School of Nursing Research Development Fund, Queen’s University and by the University of Aberdeen and Maastricht University. The authors declare no conflict of interest.
Reprints: Elizabeth G. VanDenKerkhof, DrPH, Department of Anesthesiology and Perioperative Medicine, School of Nursing, Queen’s University, Kingston, ON, Canada K7L 2V7 (e-mail: email@example.com).
Received August 15, 2011
Accepted December 17, 2011