Causes of Noncompliance With Nimodipine and Its Impact on 90-day Outcome After Aneurysmal Subarachnoid Hemorrhage.

IF 2
Mina Seo, Venkatesh Aiyagari, Jorge Moreno, DaiWai M Olson, Moez M I Bashir, Josephine Tenii
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Abstract

Background: Guidelines recommend the use of enteral nimodipine for 21 days after aneurysmal subarachnoid hemorrhage (aSAH). The recommended duration (21 d) and frequency of administration (every 4 h) may lead to noncompliance. Nurses play a critical role in medication administration, monitoring adverse reactions, and ensuring patient compliance with prescribed regimens. The aim of this study is to assess the degree of compliance with nimodipine use, causes of noncompliance and explore if adherence to nimodipine in clinical practice correlates with improved neurological outcomes as indicated by modified Rankin Scale (mRS) scores.

Methods: A retrospective study of consecutive aSAH admissions to a comprehensive stroke center over a 67-month period. Compliance was defined as receiving at least 80% of the recommended doses of nimodipine over 21 days. A chart review was performed to explore the reasons for noncompliance. We examined hospital disposition at discharge and 90-day mRS, adjusted for severity of aSAH. Compliance rates before and after a pharmacist-guided intervention were also examined.

Results: Among 141 patients, the overall compliance rate was just 30%. The leading reasons for missed doses included hypotension (68.1%) and patients being off the unit (56%). Compliance was not associated with improvement in 90-day mRS scores for low-grade aSAH (P=0.3638) and high-grade aSAH (P=0.227). After pharmacist-guided intervention, compliance improved from 18.2% to 43.8%.

Conclusion: There is a high rate of noncompliance with nimodipine use in aSAH, but it did not significantly impact patient outcomes. Although pharmacist interventions improved compliance, full compliance remains challenging.

尼莫地平对动脉瘤性蛛网膜下腔出血术后90天预后的影响
背景:指南推荐动脉瘤性蛛网膜下腔出血(aSAH)后21天内应用尼莫地平。推荐的持续时间(21天)和给药频率(每4小时)可能导致不合规。护士在药物管理、监测不良反应和确保患者遵守处方方案方面发挥着关键作用。本研究的目的是评估尼莫地平使用的依从性程度,不依从性的原因,并探讨临床实践中尼莫地平的依从性是否与改进的兰金量表(mRS)评分所显示的神经预后相关。方法:回顾性研究在67个月期间连续aSAH入院的综合卒中中心。依从性定义为在21天内接受至少80%的尼莫地平推荐剂量。进行图表审查以探讨不符合的原因。我们检查了出院时的医院情况和90天mRS,并根据aSAH的严重程度进行了调整。还检查了药剂师指导干预前后的依从率。结果:141例患者的总体依从率仅为30%。漏给剂量的主要原因包括低血压(68.1%)和患者离开单位(56%)。依从性与低级别aSAH (P=0.3638)和高级别aSAH (P=0.227)的90天mRS评分改善无关。经药师指导干预后,依从性从18.2%提高到43.8%。结论:尼莫地平在aSAH中的不依从性很高,但对患者的预后没有显著影响。尽管药剂师的干预措施改善了依从性,但完全依从性仍然具有挑战性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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