Pain Registries

Research Articles on Pain Registries

• Accuracy of Self-reported Prescribed Analgesic Medication Use Linkage Between the Quebec Pain Registry and the Quebec Administrative Prescription Claims Database
  Lacasse A, Ware M, Bourgault P, et al Clin J Pain Volume 32, Number 2, February 2016
• As if one pain problem was not enough: prevalence and patterns of coexisting chronic pain conditions and their impact on treatment outcomes
  Page M, Fortier M, Ware M, Choiniere M Journal of Pain Research 2018:11
• Development and Implementation of a Registry of Patients Attending Multidisciplinary Pain Treatment Clinics: The Quebec Pain Registry
  Choinière M, Ware MA, Pagé MG, et al Pain Research and Management Volume 2017
• Effectiveness of long-term opioid therapy among chronic non-cancer pain patients attending multidisciplinary pain treatment clinics: A Quebec Pain Registry Study
  Saidi H, Page M, Boulanger A, et al Canadian Journal of Pain, 2:1, 113-124
• Establishment of the Australasian electronic Persistent Pain Outcomes Collaboration
  Tardif H, Arnold C, Hayes C, Eagar K Pain Medicine, Volume 18, Issue 6, June 2017, Pages 1007–1018
• Expectations predict chronic pain treatment outcome
  Cormiera S, Lavigneb G, Choiniere M, et al PAIN. February 2016 Volume 157 Number 2
• Implementation of Patient‐Reported Outcomes (PROMs) from specialist pain clinics in England and Wales: Experience from a nationwide study
  Price CM, C. de C. Williams A, Smith BH, Bottle A Eur J Pain. 2019; 23: 1368– 1377
• Is the Quebec provincial administrative database a valid source for research on chronic non-cancer pain?
  Lacasse A, Ware M, Dorais M, et al pharmacoepidemiology and drug safety 2015; 24: 980–990
• Normative data for common pain measures in chronic pain clinic populations: closing a gap for clinicians and researchers
  Nicholas MK, Costa DS, Blanchard M, Tardif H, Asghari A, Blyth FM PAIN. 2019 May;160(5):1156-1165
• Pain registries and similar data collections: A systematic review
  Freytag A, Scriba B, Kaiser U, Meissner W Schmerz. 2016 Dec;30(6):568-575
• Pain-related functional interference in patients with chronic neuropathic postsurgical pain: an analysis of registry data
  Stamer UM, Ehrler M, Lehmann T, Meissner W, Fletcher D PAIN 160(8):p 1856-1865, August 2019
• Predicting treatment outcomes of pain patients attending tertiary multidisciplinary pain treatment centers: A pain trajectory approach
  Page M, Escobar M, Ware M, et al Canadian Journal of Pain, 1:1, 61-74
• Pregabalin for chronic pain: does one medication fit all?
  Giladi H, Choinière M, Fitzcharles M, et al Current Medical Research and Opinion, 31:7, 1403-1411
• Risk of Opioid Abuse and Biopsychosocial Characteristics Associated With This Risk Among Chronic Pain Patients Attending a Multidisciplinary Pain Treatment Facility
  Page M, Saidi H, Ware M, et al Clin J Pain Volume 32, Number 10, October 2016
• The Paediatric electronic Persistent Pain Outcomes Collaboration (PaedePPOC): establishment of a binational system for benchmarking children's persistent pain services
  Lord SM, Tardif HP, Kepreotes EA, Blanchard M, Eagar K Pain. 2019 Jul;160(7):1572-1585
• Finding the vulnerable postoperative population: A two‐step cluster analysis of the PAIN‐OUT registry
  Polanco-García M, Granero R, Gallart L, García-Lopez J, Montes A European Journal of Pain, 26, 1732– 1745

Other Articles of Relevance

• Australian Commission on Safety and Quality in Health Care: Framework for Australian clinical quality registries
  ACSQHC, March 2014
• Impact of clinical registries on quality of patient care and clinical outcomes: A systematic review
  Hoque DME, Kumari V, Hoque M, Ruseckaite R, Romero L, Evans SM PLoS One. 2017 Sep 8;12(9):e0183667