Shinger Gavindeep, Haymond Jennifer, Young Flora, Leung Timothy S
, BSc, PharmD, ACPR, is a Clinical Pharmacist with the Royal Columbian Hospital, Lower Mainland Pharmacy Services, New Westminster, British Columbia.
, BSc(Pharm), ACPR, PharmD, is the Supervisor of Clinical Pharmacy Services and a Clinical Pharmacy Specialist - Critical Care Medicine with the Royal Columbian Hospital, Lower Mainland Pharmacy Services, New Westminster, British Columbia. She is also a Clinical Instructor with the Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, British Columbia.
Can J Hosp Pharm. 2025 Apr 9;78(2):e3663. doi: 10.4212/cjhp.3663. eCollection 2025.
Guidelines recommend nimodipine as the standard of care for patients with aneurysmal subarachnoid hemorrhage (aSAH). Compared with placebo, this agent has been shown to reduce death and dependency on others for activities of daily living. However, retrospective data suggest that patients may not receive full treatment with nimodipine.
The primary objective was to determine the proportion of patients with aSAH admitted to an intensive care unit (ICU) or high-acuity unit (HAU) at a tertiary referral hospital who received the guideline-recommended dose and duration of nimodipine. A secondary objective was to describe barriers to receiving full treatment.
This retrospective chart review involved a convenience sample of 100 patients with aSAH who were admitted to the ICU or HAU of a tertiary referral hospital between January 1, 2012, and August 31, 2022. The analysis was based on descriptive statistics.
Of the 100 patients with aSAH admitted to the ICU or HAU, 1 (1%) received the guideline-recommended dose and duration of nimodipine. Ninety-five (95%) of the patients experienced a delay to initiation, mainly due to transfer from another hospital ( = 45, 47%) and/or lack of a safe enteral route ( = 62, 65%). Sixty-six (66%) of the patients received alternative dosing, most because their blood pressure was below target ( = 16, 24%) or because of vasospasm requiring a higher blood pressure target ( = 22, 33%). A total of 99 patients (99%) had early discontinuation and/or treatment interruption of nimodipine; reasons included vasospasm requiring a higher blood pressure target ( = 12, 12%) and nimodipine not being continued on transfer or discharge ( = 14, 14%).
Most of the patients in this study did not receive the full course of nimodipine therapy due to multiple barriers. Pharmacists can play a role in optimizing treatment by educating staff at transferring sites about timely initiation of therapy, reconciling medications on transfer or discharge, and mitigating interactions with concomitant medications.
指南推荐尼莫地平作为动脉瘤性蛛网膜下腔出血(aSAH)患者的标准治疗药物。与安慰剂相比,该药物已被证明可降低死亡率以及减少日常生活活动对他人的依赖。然而,回顾性数据表明患者可能未接受尼莫地平的全程治疗。
主要目的是确定在一家三级转诊医院的重症监护病房(ICU)或高 acuity 病房(HAU)收治的 aSAH 患者中,接受指南推荐剂量和疗程尼莫地平治疗的患者比例。次要目的是描述接受全程治疗的障碍。
这项回顾性病历审查涉及一个便利样本,即 2012 年 1 月 1 日至 2022 年 8 月 31 日期间在一家三级转诊医院的 ICU 或 HAU 收治的 100 例 aSAH 患者。分析基于描述性统计。
在收治到 ICU 或 HAU 的 100 例 aSAH 患者中,1 例(1%)接受了指南推荐剂量和疗程的尼莫地平治疗。95 例(95%)患者开始治疗出现延迟,主要原因是从另一家医院转来(n = 45,47%)和/或缺乏安全的肠内给药途径(n = 62,65%)。66 例(66%)患者接受了替代给药方案,大多数原因是其血压低于目标值(n = 16,24%)或因血管痉挛需要更高的血压目标值(n = 22,33%)。共有 99 例患者(99%)出现尼莫地平早期停药和/或治疗中断;原因包括因血管痉挛需要更高的血压目标值(n = 12,12%)以及在转院或出院时未继续使用尼莫地平(n = 14,14%)。
由于多种障碍,本研究中的大多数患者未接受尼莫地平的全程治疗。药剂师可以通过对转诊机构的工作人员进行关于及时开始治疗、在转院或出院时协调用药以及减轻与伴随用药的相互作用等方面的教育,在优化治疗中发挥作用。