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Targeting the Opioid Pathway for Uremic Pruritus: A Systematic Review and Meta-analysis

BACKGROUND: Patients undergoing hemodialysis or peritoneal dialysis often experience pruritus which is associated with morbidity and mortality. One proposed treatment approach is to target the opioid pathway using either µ-opioid antagonists or κ-opioid agonists. OBJECTIVE: To review the efficacy of...

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Detalles Bibliográficos
Autores principales: Jaiswal, Deep, Uzans, Drea, Hayden, Jill, Kiberd, Bryce A., Tennankore, Karthik K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332085/
https://www.ncbi.nlm.nih.gov/pubmed/28270926
http://dx.doi.org/10.1177/2054358116675345
Descripción
Sumario:BACKGROUND: Patients undergoing hemodialysis or peritoneal dialysis often experience pruritus which is associated with morbidity and mortality. One proposed treatment approach is to target the opioid pathway using either µ-opioid antagonists or κ-opioid agonists. OBJECTIVE: To review the efficacy of targeting the opioid pathway for pruritus among dialysis patients (uremic pruritus). DESIGN: Systematic review and meta-analysis. SETTING/METHODS: The systematic review included randomized controlled and randomized crossover trials identified in the MEDLINE, EMBASE, and Cochrane databases (1990 to June 2014) evaluating the efficacy of µ-opioid antagonists or κ-opioid agonists in the treatment of uremic pruritus. PATIENTS: Adult (≥18 years) chronic dialysis patients. MEASUREMENTS: The primary outcome being evaluated was reduction in itch severity measured on a patient-reported visual analog scale (VAS). RESULTS: Five studies out of 3587 screened articles met the inclusion criteria. Three studies evaluated the efficacy of naltrexone, a µ-opioid antagonist, and 2 studies evaluated the efficacy of nalfurafine, a κ-opioid agonist. Duration of included studies was short, ranging from 2 to 9 weeks. LIMITATIONS: Due to the heterogeneity in reporting of outcomes, data from the studies evaluating naltrexone could not be pooled. Pooled analysis, using a random effects model, found that use of nalfurafine resulted in a 9.50 mm (95% confidence interval [CI], 6.27-12.74, P < .001) greater reduction of itch severity (measured on a 100-mm VAS) than placebo in the treatment of uremic pruritus. CONCLUSIONS: Nalfurafine holds some promise with respect to the treatment of uremic pruritus among dialysis patients. However, more long-term randomized controlled trials evaluating the efficacy of therapies targeting the opioid pathway for uremic pruritus are required.