Association de Formation Médicale Continue - Formation et Informations Médicales - ---------au service des professionnels de santé et de la santé ------------ depuis 1974

Lombalgie aiguë et manipulation vertébrale (MV).

Lombalgie aiguë et manipulation vertébrale (MV).

Résultats d'une étude incluant 104 patients traités par les médicaments classiques,
 dont 52 ont bénéficié en outre de MV.

 La diminution de la douleur et la consommation d'antalgiques ont été identiques dans les 2 groupes.

Jüni & Coll., Annals of the Rheumatic Diseases, 5 septembre 2008 ; prépublication en ligne

Objective: To determine whether treatment with spinal manipulative therapy (SMT) administered in addition to standard care is associated with clinically relevant early reductions in pain and analgesic consumption.

Methods: We randomised 104 patients with acute low back pain to SMT in addition to standard care (n=52) or standard care alone (n=52). Standard care consisted of general advice and paracetamol, diclofenac or dihydrocodein as required. Other analgesic drugs or non-pharmacological treatments were not allowed. Primary outcomes were pain intensity assessed on the 11 point box scale (BS-11) and analgesic use based on diclofenac equivalence doses during days 1 to 14. An extended follow-up was performed at 6 months.

Results: Pain reductions were similar in experimental and control groups, with the lower limit of the 95% confidence interval (95%-CI) excluding a relevant benefit of SMT (difference 0.5 on the BS-11, 95%-CI -0.2 to 1.2, p=0.13). Analgesic consumptions were also similar (difference -18 mg diclofenac equivalents, 95%-CI -43 mg to 7 mg, p=0.17), with small initial differences diminishing over time. There were no differences between groups in any of the secondary outcomes and stratified analyses provided no evidence for potential benefits of SMT in specific patient groups. The extended follow-up showed similar patterns.

: SMT is unlikely to result in relevant early pain reduction in patients with acute low back pain. [ Identifier: NCT00294229]
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