4.6 Article

Post-operative pain following cardiac implantable electronic device implantation: insights from the BRUISE CONTROL trials

Journal

EUROPACE
Volume 23, Issue 5, Pages 748-756

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/europace/euaa349

Keywords

Cardiac implantable electronic device implantation; Pacemaker; Implantable cardioverter-defibrillator; Predictors of post-operative pain; Pain prediction score; BRUISE CONTROL trials

Funding

  1. Canadian Institutes of Health Research (CIHR)
  2. CIHR Clinician Scientist Award
  3. University of Ottawa Heart Institute Academic Medical Organization Alternate Funding Program (Ministry of Health of Ontario)
  4. Heart and Stroke Foundation of Canada [G-14-0005725]
  5. Fonds de recherche du Quebec-Sante (FRQS) Clinical Research Scholar Award
  6. Bayer HealthCare AG, Leverkusen, Germany
  7. Pfizer
  8. Bristol-Myers Squibb, New York, NY, USA
  9. Boehringer Ingelheim, Germany

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The study identified multiple predictors of post-operative pain after CIED insertion and developed a prediction score for post-operative pain that can help identify individuals at risk for significant post-operative pain.
Aims Post-operative pain following cardiac implantable electronic device (CIED) insertion is associated with patient dissatisfaction, emotional distress, and emergency department visits. We sought to identify factors associated with post-operative pain and develop a prediction score for post-operative pain. Methods and results All patients from the BRUISE CONTROL-1 and 2 trials were included in this analysis. A validated Visual Analogue Scale (VAS) was used to assess the severity of pain related to CIED implant procedures. Patients were asked to grade the most severe post-operative pain, average post-operative pain, and pain on the day of the first post-operative clinic. Multivariable regression analyses were performed to identify predictors of significant post-operative pain and to develop a pain-prediction score. A total of 1308 patients were included. Multivariable regression analysis found that the presence of post-operative clinically significant haematoma {CSH; P value < 0.001; odds ratio (OR) 3.82 [95% confidence interval (CI): 2.37-6.16]}, de novo CIED implantation [P value < 0.001; OR 1.90 (95% CI: 1.47-2.46)], female sex [P value < 0.001; OR 1.61 (95% CI: 1.22-2.12)], younger age [<65 years; P value < 0.001; OR 1.54 (95% CI: 1.14-2.10)], and lower body mass index [<20 kg/m(2); P value < 0.05; OR 2.05 (95% CI: 0.98-4.28)] demonstrated strong and independent associations with increased post-operative pain. An 11-point post-operative pain prediction score was developed using the data. Conclusion Our study has identified multiple predictors of post-operative pain after CIED insertion. We have developed a prediction score for post-operative pain that can be used to identify individuals at risk of experiencing significant post-operative pain.

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