门诊使用加巴喷丁类药物治疗疼痛的特征分析。

Characterization of Outpatient Gabapentinoid Prescribing for Pain.

机构信息

Callan Banks, PharmD, Lindsay A. Bowman, PharmD, BCPS, Jessica Merrey, PharmD, MBA, BCPS, BCACP, BCGP, and Julie M. Waldfogel, PharmD, BCGP, Department of Pharmacy, The Johns Hopkins Hospital, Baltimore, Maryland, USA.

出版信息

J Pain Palliat Care Pharmacother. 2023 Jun;37(2):143-147. doi: 10.1080/15360288.2023.2174635. Epub 2023 Feb 10.

Abstract

Two statements from national organizations outline recommended minimum effective doses of gabapentin and pregabalin for the treatment of diabetic peripheral neuropathy (DPN). However, studies of real-world gabapentinoid dosing demonstrate that the recommended dose targets are frequently not met and do not consider renal insufficiency. This study aimed to characterize gabapentinoid prescribing patterns in patients receiving primary care at two internal medicine clinics within an academic medical center. This retrospective chart review included adult outpatients who were newly initiated on gabapentin or pregabalin between October 1, 2017 and October 1, 2020 and reviewed for 12 months. A total of 1,221 patients were included in the study with 1,079 (88.4%) prescribed gabapentin and 142 (11.6%) prescribed pregabalin. Only 22.4% of patients prescribed gabapentin and 33.3% of patients prescribed pregabalin with adequate renal function met the minimum effective dosing of gabapentin 1800 mg per day and pregabalin 300 mg per day provided by the American Diabetes Association (ADA) and American Academy of Neurology (AAN). This study supports the need for optimization of gabapentinoid dosing to ensure an adequate trial at the minimum effective dose is completed.

摘要

两个国家组织的声明概述了推荐的加巴喷丁和普瑞巴林的最小有效剂量,用于治疗糖尿病周围神经病变 (DPN)。然而,对现实世界中加巴喷丁类药物剂量的研究表明,推荐的剂量目标经常无法达到,且没有考虑到肾功能不全。本研究旨在描述在学术医疗中心的两个内科诊所接受初级保健的患者中加巴喷丁类药物的开方模式。这是一项回顾性图表审查,包括在 2017 年 10 月 1 日至 2020 年 10 月 1 日期间新开始使用加巴喷丁或普瑞巴林的成年门诊患者,并进行了 12 个月的随访。共有 1221 名患者纳入研究,其中 1079 名(88.4%)患者开了加巴喷丁,142 名(11.6%)患者开了普瑞巴林。仅 22.4%的服用加巴喷丁的患者和 33.3%的肾功能正常的服用普瑞巴林的患者符合美国糖尿病协会 (ADA) 和美国神经病学学会 (AAN) 提供的最小有效剂量 1800mg/天的加巴喷丁和 300mg/天的普瑞巴林。这项研究支持优化加巴喷丁类药物剂量,以确保完成最低有效剂量的充分试验。

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