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Tramadol-paracetamol for postoperative pain after spine surgery - A randomized, double-blind, placebo-controlled study.
Lappalainen, Emma; Huttunen, Jukka; Kokki, Hannu; Toroi, Petri; Kokki, Merja.
Affiliation
  • Lappalainen E; Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.
  • Huttunen J; Department of Neurosurgery, Neuro Centre, Kuopio University Hospital, Kuopio, Finland.
  • Kokki H; Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.
  • Toroi P; Department of Anaesthesiology and Intensive care, Kuopio University Hospital, PO Box 100, FI-70029 KYS, Kuopio, Finland.
  • Kokki M; Department of Anaesthesiology and Intensive care, Kuopio University Hospital, PO Box 100, FI-70029 KYS, Kuopio, Finland.
Scand J Pain ; 24(1)2024 Jan 01.
Article in En | MEDLINE | ID: mdl-38708610
ABSTRACT

OBJECTIVES:

Multimodal pain management is one component in enhanced recovery after surgery protocol. Here we evaluate the efficacy of tramadol-paracetamol in acute postoperative pain and pain outcome at 12 months after spine surgery in randomized, double-blind, placebo-controlled trial.

METHODS:

We randomized 120 patients undergoing spine surgery to receive, for add-on pain management, two tramadol-paracetamol 37.5 mg/325 mg (n = 61) or placebo tablets (n = 59) twice a day for 5 postoperative days. In the hospital, multimodal pain management consisted of dexketoprofen and oxycodone. After discharge, patients were prescribed ibuprofen 200 mg, maximum 1,200 mg/day. Pain, analgesic use, and satisfaction with pain medication were followed up with the Brief Pain Inventory questionnaire before surgery and at 1 and 52 weeks after surgery. The primary outcome was patients' satisfaction with pain medication 1 week after surgery.

RESULTS:

At 1 week after surgery, patients' satisfaction with pain medication was similarly high in the two groups, 75% [interquartile range, 30%] in the placebo group and 70% [40%] in the tramadol-paracetamol group (p = 0.949) on a scale 0% = not satisfied, 100% = totally satisfied. At 1 week, ibuprofen dose was lower in the placebo group 200 mg [1,000] compared to the tramadol-paracetamol group, 800 mg [1,600] (p = 0.016). There was no difference in the need for rescue oxycodone. Patients in the tramadol-paracetamol group had more adverse events associated with analgesics during the first postoperative week (relative risk = 1.8, 95% confidence interval, 1.2-2.6).

CONCLUSION:

Add-on pain treatment with tramadol-paracetamol did not enhance patients' satisfaction with early pain management after back surgery.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pain, Postoperative / Tramadol / Analgesics, Opioid / Acetaminophen Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Scand J Pain Year: 2024 Document type: Article Affiliation country: Publication country: ALEMANHA / ALEMANIA / DE / DEUSTCHLAND / GERMANY

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pain, Postoperative / Tramadol / Analgesics, Opioid / Acetaminophen Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Scand J Pain Year: 2024 Document type: Article Affiliation country: Publication country: ALEMANHA / ALEMANIA / DE / DEUSTCHLAND / GERMANY