Belay Birlie Yimer, Mehreen Soomro, John McBeth, Carlos Raul Ramirez Medina, Mark Lunt, William G Dixon, Meghna Jani
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引用次数: 0
Abstract
Background: Constipation is a frequent adverse event associated with opioid medications that can have a considerable impact on patients' quality of life. In patients who require opioids for pain relief, less is known about the risk conferred by specific opioids given their diverse pharmacology and the effect of daily dose and potency. The aim of the study was to evaluate the comparative risk of severe constipation by opioid type and dose in patients with non-cancer pain admitted to hospital.
Methods: We conducted a retrospective cohort study using hospital electronic health records in Northwest England between December 1, 2009, and December 31, 2020. Patients who were ≥ 18 years and without a history of cancer were included. Opioid exposure was measured using administered drug information in hospital. The outcome was a severe constipation event defined as administration of an enema or suppository. Incidence rates by opioid use status, type of opioid class and morphine milligram equivalent (MME) per day were calculated, and a Cox regression model was used to determine associations with incident constipation after adjusting for confounders.
Results: The study included 80,475 eligible patients who were administered an opioid in hospital. Compared to codeine, morphine (HR 1.59, 95% CI 1.45-1.74), oxycodone (HR 1.46, 95% CI 1.32-1.63), fentanyl (HR 1.37, 95% CI 1.14-1.64) and combination opioids (HR 1.85, 95% CI 1.66-2.06) were associated with a higher risk of constipation in the fully adjusted models. Tramadol demonstrated a significantly lower risk compared to codeine (HR 0.80, 95% CI 0.64-1.00). Higher opioid doses of more than ≥ 50 MME/day in comparison to < 50 MME/day were associated with an increased risk of constipation (compared to < 50 MME/day, 50 to < 120 MME/day: HR 1.95, 95% CI 1.78-2.15; ≥ 120 MME/day: HR 1.45, 95% CI 1.32-1.60).
Conclusions: Morphine, oxycodone, fentanyl and combination opioids administration were associated with a significantly higher risk of severe constipation compared to codeine. Tramadol was associated with the lowest risk of the outcome compared to codeine. Patients on ≥ 50 MME/day experienced a higher risk of severe constipation compared to those on < 50 MME/day. These results can be used to guide better shared decisions with patients to balance benefit and harms of specific opioid types and doses.
背景:便秘是与阿片类药物相关的常见不良事件,对患者的生活质量有相当大的影响。对于需要阿片类药物缓解疼痛的患者,由于其不同的药理学以及日剂量和效价的影响,对特定阿片类药物所带来的风险知之甚少。该研究的目的是评估入院的非癌性疼痛患者阿片类药物类型和剂量的严重便秘的比较风险。方法:我们在2009年12月1日至2020年12月31日期间使用英格兰西北部的医院电子健康记录进行了一项回顾性队列研究。年龄≥18岁且无癌症病史的患者纳入研究。使用医院给药信息测量阿片类药物暴露。结果是严重便秘事件定义为灌肠或栓剂的管理。计算阿片类药物使用状况、阿片类药物类型和每天吗啡毫克当量(MME)的发病率,并使用Cox回归模型在调整混杂因素后确定与发生率便秘的关系。结果:该研究包括80,475名在医院接受阿片类药物治疗的合格患者。与可待因相比,吗啡(HR 1.59, 95% CI 1.45-1.74)、羟考酮(HR 1.46, 95% CI 1.32-1.63)、芬太尼(HR 1.37, 95% CI 1.14-1.64)和复方阿片类药物(HR 1.85, 95% CI 1.66-2.06)与便秘风险较高相关。曲马多的风险明显低于可待因(HR 0.80, 95% CI 0.64-1.00)。结论:与可待因相比,吗啡、羟考酮、芬太尼和阿片类药物联合给药与严重便秘的风险显著增加相关。与可待因相比,曲马多的预后风险最低。服用≥50 MME/天的患者发生严重便秘的风险高于服用该药的患者
期刊介绍:
BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.