Holder Renee M, Rhee Diane
Department of Medicine Section of Palliative Care, MedStar Washington Hospital Center, Washington, District of Columbia.
College of Pharmacy, Roseman University of Health Sciences, Henderson, Nevada.
Pharmacotherapy. 2016 Mar;36(3):287-99. doi: 10.1002/phar.1711. Epub 2016 Mar 6.
Opioid analgesics are frequently prescribed and play an important role in chronic pain management. Opioid-induced bowel dysfunction, which includes constipation, hardened stool, incomplete evacuation, gas, and nausea and vomiting, is the most common adverse event associated with opioid use. Mu-opioid receptors are specifically responsible for opioid-induced bowel dysfunction, resulting in reduced peristaltic and secretory actions. Agents that reverse these actions in the bowel without reversing pain control in the central nervous system may be preferred over traditional laxatives. The efficacy and safety of these agents in chronic noncancer pain were assessed from publications identified through Ovid and PubMed database searches. Trials that evaluated the safety and efficacy of oral agents for opioid-induced constipation or opioid-induced bowel dysfunction, excluding laxatives, were reviewed. Lubiprostone and naloxegol are approved in the United States by the Food and Drug Administration for use in opioid-induced constipation. Axelopran (TD-1211) and sustained-release naloxone have undergone phase 2 and phase 1 studies, respectively, for the same indication. Naloxegol and axelopran are peripherally acting μ-opioid receptor antagonists. Naloxone essentially functions as a peripherally acting μ-opioid receptor antagonist when administered orally in a sustained-release formulation. Lubiprostone is a locally acting chloride channel (CIC-2) activator that increases secretions and peristalsis. All agents increase spontaneous bowel movements and reduce other bowel symptoms compared with placebo in patients with noncancer pain who are chronic opioid users. The most common adverse events were gastrointestinal in nature, and none of the drugs were associated with severe adverse or cardiovascular events. Investigations comparing these agents to regimens using standard laxative and combination therapy and trials in special populations and patients with active cancer are needed to further define their role in therapy.
阿片类镇痛药经常被处方使用,在慢性疼痛管理中发挥着重要作用。阿片类药物引起的肠道功能障碍,包括便秘、大便干结、排便不畅、腹胀以及恶心和呕吐,是与使用阿片类药物相关的最常见不良事件。μ-阿片受体是阿片类药物引起肠道功能障碍的具体原因,会导致蠕动和分泌作用减弱。与传统泻药相比,能逆转肠道这些作用而不逆转中枢神经系统疼痛控制的药物可能更受青睐。通过检索Ovid和PubMed数据库确定的出版物评估了这些药物在慢性非癌性疼痛中的疗效和安全性。对评估口服药物治疗阿片类药物引起的便秘或阿片类药物引起的肠道功能障碍(不包括泻药)的安全性和疗效的试验进行了综述。鲁比前列酮和纳洛西醇在美国已获美国食品药品监督管理局批准用于治疗阿片类药物引起的便秘。阿克洛普仑(TD-1211)和缓释纳洛酮分别针对相同适应症进行了2期和1期研究。纳洛西醇和阿克洛普仑是外周作用的μ-阿片受体拮抗剂。纳洛酮口服缓释制剂时基本上起外周作用的μ-阿片受体拮抗剂的作用。鲁比前列酮是一种局部作用的氯离子通道(CIC-2)激活剂,可增加分泌和蠕动。与安慰剂相比,所有药物均可增加慢性阿片类药物使用者的非癌性疼痛患者的自发排便次数,并减轻其他肠道症状。最常见的不良事件本质上是胃肠道方面的,且没有一种药物与严重不良事件或心血管事件相关。需要将这些药物与使用标准泻药和联合疗法的方案进行比较的研究,以及在特殊人群和患有活动性癌症的患者中进行试验,以进一步明确它们在治疗中的作用。