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Remifentanil versus fentanyl during cardiac surgery on the incidence of chronic thoracic pain (REFLECT): study protocol for a randomized controlled trial

Overview of attention for article published in Trials, November 2014
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Title
Remifentanil versus fentanyl during cardiac surgery on the incidence of chronic thoracic pain (REFLECT): study protocol for a randomized controlled trial
Published in
Trials, November 2014
DOI 10.1186/1745-6215-15-466
Pubmed ID
Authors

Sjoerd de Hoogd, Sabine JGM Ahlers, Eric PA van Dongen, Dick Tibboel, Albert Dahan, Catherijne AJ Knibbe

Abstract

Chronic thoracic pain after cardiac surgery is prevalent (11 to 56%) and may affect patients' physical and mental health status. Despite its favorable pharmacokinetic and pharmacodynamic properties, high doses of remifentanil administered during surgery are reported to cause acute postoperative pain and increased requirements for analgesics. Recently, an association between remifentanil use and the incidence of chronic thoracic pain in the long term was also reported. Our objective is to investigate the influence of the intraoperative remifentanil on chronic postoperative pain in a prospective randomized controlled trial.Methods/design: In this prospective, randomized, single-blind clinical trial, all patients (N =126) between 18 and 85 years undergoing cardiac surgery via sternotomy receive a continuous infusion of propofol together with intermittent intravenous fentanyl at predetermined times perioperatively. Patients are randomized to receive either an additional continuous infusion of remifentanil (0.15 mug-1kgIBW-1 min-1) or additional fentanyl (200 to 500 mug) as needed during surgery.The primary end point is the prevalence of chronic thoracic pain 12 months after surgery. Secondary end points include acute postoperative pain; postoperative analgesic use; chronic thoracic pain 3 and 6 months after surgery; quality of life (SF-12) at 3, 6 and 12 months after surgery; work productivity; and use of health care. In addition, thermal detection and pain thresholds are measured preoperatively, 3 days after surgery and 12 months after surgery using quantitative sensory testing (QST). Finally, the influence of several genetic variances on the different outcomes will be measured.

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Mendeley readers

The data shown below were compiled from readership statistics for 77 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 77 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 12 16%
Student > Postgraduate 9 12%
Researcher 7 9%
Student > Bachelor 6 8%
Other 5 6%
Other 14 18%
Unknown 24 31%
Readers by discipline Count As %
Medicine and Dentistry 29 38%
Nursing and Health Professions 5 6%
Pharmacology, Toxicology and Pharmaceutical Science 5 6%
Psychology 5 6%
Economics, Econometrics and Finance 2 3%
Other 5 6%
Unknown 26 34%