Literature DB >> 16856101

Tramadol for osteoarthritis.

M S Cepeda1, F Camargo, C Zea, L Valencia.   

Abstract

BACKGROUND: Tramadol is increasingly used for the treatment of osteoarthritis because, in contrast to nonsteroidal anti-inflammatory drugs (NSAIDs), tramadol does not produce gastrointestinal bleeding or renal problems, and does not affect articular cartilage.
OBJECTIVES: We sought to determine the analgesic effectiveness, the effect on physical function, the duration of benefit and the safety of oral tramadol in people with osteoarthritis. SEARCH STRATEGY: We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, EMBASE and LILACS databases up to August 2005. SELECTION CRITERIA: We included randomized controlled trials (RCTs) that evaluated the effect of tramadol or tramadol plus paracetamol on pain levels and/or physical function in people with osteoarthritis. No language restriction was applied. DATA COLLECTION AND ANALYSIS: We analyzed separately placebo-controlled and active-controlled studies. We used fixed-effect models for the meta-analyses as the results across studies were similar. MAIN
RESULTS: We included eleven RCTs with a total of 1019 participants who received tramadol or tramadol/paracetamol and 920 participants who received placebo or active-control. The placebo-controlled studies indicated that participants who received tramadol had less pain (-8.5 units on a 0 to 100 scale; 95% confidence interval (CI) -12.0 to -5.0) than patients who received placebo. This represents a 12% relative decrease in pain intensity from baseline. Participants who received tramadol had a 37% increase (95% CI 1.2 to 1.5) in the likelihood of reporting moderate improvement (number needed to treat to benefit = 6; 95% CI 4 to 9). Participants who received tramadol had 2.27 times the risk of developing minor adverse events and 2.6 times the risk of developing major adverse events, compared to participants who received placebo. Of every eight people who receive tramadol or tramadol/paracetamol, one will stop taking the medication because of adverse events, number needed to treat to harm (NNTH)= 8 (95% CI 7 to 12) for major adverse events. No conclusion could be drawn on how tramadol or tramadol/paracetamol compared with available pharmacological treatments because of the limited number of studies that evaluated such therapies. AUTHORS'
CONCLUSIONS: Tramadol or tramadol/paracetamol decreases pain intensity, produces symptom relief and improves function, but these benefits are small. Adverse events, although reversible and not life threatening, often cause participants to stop taking the medication and could limit tramadol or tramadol plus paracetamol usefulness.

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Year:  2006        PMID: 16856101     DOI: 10.1002/14651858.CD005522.pub2

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  37 in total

1.  Tramadol for osteoarthritis.

Authors:  Karine Toupin April; Jacinthe Bisaillon; Vivian Welch; Lara J Maxwell; Peter Jüni; Anne Ws Rutjes; M Elaine Husni; Jennifer Vincent; Tania El Hindi; George A Wells; Peter Tugwell
Journal:  Cochrane Database Syst Rev       Date:  2019-05-27

2.  Tramadol extended-release tablets in moderate to moderately severe chronic pain in adults: profile report.

Authors:  Philip I Hair; Monique P Curran; Susan J Keam
Journal:  CNS Drugs       Date:  2007       Impact factor: 5.749

Review 3.  Adverse events associated with medium- and long-term use of opioids for chronic non-cancer pain: an overview of Cochrane Reviews.

Authors:  Charl Els; Tanya D Jackson; Diane Kunyk; Vernon G Lappi; Barend Sonnenberg; Reidar Hagtvedt; Sangita Sharma; Fariba Kolahdooz; Sebastian Straube
Journal:  Cochrane Database Syst Rev       Date:  2017-10-30

Review 4.  Tramadol for neuropathic pain in adults.

Authors:  Rudolf Martin Duehmke; Sheena Derry; Philip J Wiffen; Rae F Bell; Dominic Aldington; R Andrew Moore
Journal:  Cochrane Database Syst Rev       Date:  2017-06-15

Review 5.  Viscosupplementation for osteoarthritis: a primer for primary care physicians.

Authors:  M Carrington Reid
Journal:  Adv Ther       Date:  2013-11-08       Impact factor: 3.845

6.  PEER umbrella systematic review of systematic reviews: Management of osteoarthritis in primary care.

Authors:  Joey Ton; Danielle Perry; Betsy Thomas; G Michael Allan; Adrienne J Lindblad; James McCormack; Michael R Kolber; Scott Garrison; Samantha Moe; Rodger Craig; Nicolas Dugré; Karenn Chan; Caitlin R Finley; Rhonda Ting; Christina S Korownyk
Journal:  Can Fam Physician       Date:  2020-03       Impact factor: 3.275

7.  Opioids for chronic noncancer pain in the elderly: an osteoarthritis case.

Authors:  Beverley Karras; Nora McKee; Loren Regier; Shannon Stone
Journal:  Can Fam Physician       Date:  2011-08       Impact factor: 3.275

8.  Opioids for osteoarthritis pain: benefits and risks.

Authors:  Noah Ivers; Irfan A Dhalla; G Michael Allan
Journal:  Can Fam Physician       Date:  2012-12       Impact factor: 3.275

Review 9.  Clinical pharmacology of analgesics assessed with human experimental pain models: bridging basic and clinical research.

Authors:  Bruno Georg Oertel; Jörn Lötsch
Journal:  Br J Pharmacol       Date:  2013-02       Impact factor: 8.739

Review 10.  Tramadol with or without paracetamol (acetaminophen) for cancer pain.

Authors:  Philip J Wiffen; Sheena Derry; R Andrew Moore
Journal:  Cochrane Database Syst Rev       Date:  2017-05-16
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