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Intravenous immunoglobulin treatment of the complex regional pain syndrome: a randomized trial.
Goebel, Andreas; Baranowski, Andrew; Maurer, Konrad; Ghiai, Artemis; McCabe, Candy; Ambler, Gareth.
Afiliação
  • Goebel A; University of Liverpool, Clinical Sciences Building, University Hospital Aintree, Liverpool L9 7AL, United Kingdom.
Ann Intern Med ; 152(3): 152-8, 2010 Feb 02.
Article em En | MEDLINE | ID: mdl-20124231
ABSTRACT

BACKGROUND:

Treatment of long-standing complex regional pain syndrome (CRPS) is empirical and often of limited efficacy. Preliminary data suggest that the immune system is involved in sustaining this condition and that treatment with low-dose intravenous immunoglobulin (IVIG) may substantially reduce pain in some patients.

OBJECTIVE:

To evaluate the efficacy of IVIG in patients with longstanding CRPS under randomized, controlled conditions.

DESIGN:

A randomized, double-blind, placebo-controlled crossover trial. (National Research Registry number N0263177713; International Standard Randomised Controlled Trial Number Registry 63918259)

SETTING:

University College London Hospitals Pain Management Centre. PATIENTS Persons who had pain intensity greater than 4 on an 11-point (0 to 10) numerical rating scale and had CRPS for 6 to 30 months that was refractory to standard treatment. INTERVENTION IVIG, 0.5 g/kg, and normal saline in separate treatments, divided by a washout period of at least 28 days. MEASUREMENTS The primary outcome was pain intensity 6 to 19 days after the initial treatment and the crossover treatment.

RESULTS:

13 eligible participants were randomly assigned between November 2005 and May 2008; 12 completed the trial. The average pain intensity was 1.55 units lower after IVIG treatment than after saline (95% CI, 1.29 to 1.82; P < 0.001). In 3 patients, pain intensity after IVIG was less than after saline by 50% or more. No serious adverse reactions were reported.

LIMITATION:

The trial was small, and recruitment bias and chance variation could have influenced results and their interpretation.

CONCLUSION:

IVIG, 0.5 g/kg, can reduce pain in refractory CRPS. Studies are required to determine the best immunoglobulin dose, the duration of effect, and when repeated treatments are needed. PRIMARY FUNDING SOURCE Association of Anaesthetists of Great Britain and Ireland, University College London Hospitals Charity, and CSL-Behring.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunoglobulinas Intravenosas / Síndromes da Dor Regional Complexa / Fatores Imunológicos Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male Idioma: En Revista: Ann Intern Med Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunoglobulinas Intravenosas / Síndromes da Dor Regional Complexa / Fatores Imunológicos Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male Idioma: En Revista: Ann Intern Med Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Reino Unido