Velázquez Rivera Ignacio, Velázquez Clavarana Lourdes, García Velasco Pilar, Melero Ramos Carmen
Pain Unit, Hospital Alta Resolución de Guadix, Granada, Spain.
Nurse, Hospital Materno Infantil de Málaga, Málaga, Spain.
J Opioid Manag. 2019 Jan/Feb;15(1):69-76. doi: 10.5055/jom.2019.0487.
Opioid-induced constipation (OIC) is a common adverse effect of opioid analgesic therapy that significantly affects the patient's quality of life and may lead to poor adherence and treatment failure. Tapentadol, oxycodone/naloxone, and some transcutaneous opioids were associated with less frequent OIC than morphine or oxycodone in controlled clinical trials. However, few studies compare these newer opioids with each other in terms of OIC.
We performed a cross-sectional observational study that evaluated the degree of OIC and risk factors in patients receiving long-term treatment (>1 year) at a tertiary care pain unit with tapentadol, oxycodone/naloxone, hydromorphone, fentanyl, or buprenorphine. The degree of constipation was evaluated using the Bowel Function Index (BFI).
Out of 180 enrolled patients (median age: 61.5 years, 66.7 percent women, mean treatment duration: 3 years), 57.2 percent suffered from nociceptive pain, 33.9 percent from mixed pain, and 8.9 percent from neuropathic pain. The most commonly prescribed opioids were oxycodone/naloxone (44.4 percent) and tapentadol (37.8 percent). At the time of the study, 73.9 percent of patients had constipation (BFI > 29), and 21.7 percent had severe constipation (BFI > 69). In a multiple linear regression analysis, previous constipation, morphine equivalent dose, treatment with fentanyl and interaction between morphine equivalent dose and hydromorphone were associated with more severe constipation.
Most patients receiving long-term treatment with opioids present symptoms of constipation. The bowel function profile was more favorable for tapentadol and oxycodone, with no differences between them, even though morphine equivalent doses were on average higher in the tapentadol group.
阿片类药物引起的便秘(OIC)是阿片类镇痛治疗常见的不良反应,严重影响患者生活质量,可能导致依从性差及治疗失败。在对照临床试验中,曲马多、羟考酮/纳洛酮及一些经皮阿片类药物相比吗啡或羟考酮,引起OIC的频率更低。然而,很少有研究在OIC方面对这些新型阿片类药物进行相互比较。
我们进行了一项横断面观察性研究,评估在三级护理疼痛科接受曲马多、羟考酮/纳洛酮、氢吗啡酮、芬太尼或丁丙诺啡长期治疗(>1年)的患者的OIC程度及危险因素。使用肠道功能指数(BFI)评估便秘程度。
180名入组患者(中位年龄:61.5岁,66.7%为女性,平均治疗时长:3年)中,57.2%患有伤害性疼痛,33.9%患有混合性疼痛,8.9%患有神经性疼痛。最常开具的阿片类药物为羟考酮/纳洛酮(44.4%)和曲马多(37.8%)。在研究时,73.9%的患者有便秘(BFI>29),21.7%的患者有严重便秘(BFI>69)。在多元线性回归分析中,既往便秘、吗啡等效剂量、芬太尼治疗以及吗啡等效剂量与氢吗啡酮之间的相互作用与更严重的便秘相关。
大多数接受阿片类药物长期治疗的患者出现便秘症状。曲马多和羟考酮的肠道功能状况更佳,二者之间无差异,尽管曲马多组的吗啡等效剂量平均更高。