Efficacy of Pharmacological Therapies for the Treatment of Opioid-Induced Constipation: Systematic Review and Meta-Analysis

被引:82
作者
Ford, Alexander C. [1 ,2 ]
Brenner, Darren M. [3 ]
Schoenfeld, Philip S. [4 ]
机构
[1] St James Univ Hosp, Leeds Gastroenterol Inst, Leeds LS9 7TF, W Yorkshire, England
[2] Univ Leeds, Leeds Inst Biomed & Clin Sci, Leeds, W Yorkshire, England
[3] NW Mem Hosp, Chicago, IL 60611 USA
[4] Univ Michigan, Sch Med, Div Gastroenterol, Ann Arbor, MI USA
关键词
INDUCED BOWEL DYSFUNCTION; CHRONIC IDIOPATHIC CONSTIPATION; PROLONGED-RELEASE OXYCODONE; CHLORIDE CHANNEL ACTIVATOR; CONTROLLED PHASE-3 TRIAL; DOUBLE-BLIND; SUBCUTANEOUS METHYLNALTREXONE; NONMALIGNANT PAIN; RISK-FACTORS; LUBIPROSTONE;
D O I
10.1038/ajg.2013.169
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: There has been no definitive synthesis of the evidence for any benefit of available pharmacological therapies in opioid-induced constipation (OIC). We conducted a systematic review and meta-analysis to address this deficit. METHODS: We searched MEDLINE, EMBASE, EMBASE Classic, and the Cochrane central register of controlled trials through to December 2012 to identify placebo-controlled trials of mu-opioid receptor antagonists, prucalopride, lubiprostone, and linaclotide in the treatment of adults with OIC. No minimum duration of therapy was required. Trials had to report a dichotomous assessment of overall response to therapy, and data were pooled using a random effects model. Effect of pharmacological therapies was reported as relative risk (RR) of failure to respond to therapy, with 95% confidence intervals (CIs). RESULTS: Fourteen eligible randomized controlled trials (RCTs) of mu-opioid receptor antagonists, containing 4,101 patients, were identified. These were superior to placebo for the treatment of OIC (RR of failure to respond to therapy =0.69; 95% CI 0.63-0.75). Methylnaltrexone (six RCTs, 1,610 patients, RR=0.66; 95 % CI 0.54-0.84), naloxone (four trials, 798 patients, RR=0.64; 95 % CI 0.56-0.72), and alvimopan (four RCTs, 1,693 patients, RR=0.71; 95 % CI 0.65-0.78) were all superior to placebo. Total numbers of adverse events, diarrhea, and abdominal pain were significantly commoner when data from all RCTs were pooled. Reversal of analgesia did not occur more frequently with active therapy. Only one trial of prucalopride was identified, with a nonsignificant trend toward higher responder rates with active therapy. Two RCTs of lubiprostone were found, with significantly higher responder rates with lubiprostone in both, but reporting of data precluded meta-analysis. CONCLUSIONS: mu-Opioid receptor antagonists are safe and effective for the treatment of OIC. More data are required before the role of prucalopride or lubiprostone in the treatment of OIC are clear.
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页码:1566 / 1574
页数:9
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