Department of Pharmacy, Rhode Island Hospital, Providence, Rhode Island, USA.
Department of Pharmacy, Rhode Island Hospital, Providence, Rhode Island, USA; Department of Health Services, Policy, and Practice, Brown University School of Public Health, Providence, Rhode Island, USA.
World Neurosurg. 2022 Feb;158:e501-e508. doi: 10.1016/j.wneu.2021.11.016. Epub 2021 Nov 11.
Nimodipine improves outcomes in patients with aneurysmal subarachnoid hemorrhage (aSAH). However, the impact of alternative dosing strategies on outcome remains unclear.
We performed a retrospective cohort study of consecutive patients admitted with aSAH to an academic referral center from 2016 to 2019. Patients with a confirmed aneurysm cause who received nimodipine were included; patients who died or had withdrawal of life-sustaining treatment within 24 hours of admission were excluded. Univariable and multivariable modified Poisson regression models were used to identify predictors of using modified nimodipine dosing (30 mg every 2 hours) versus standard dosing (60 mg every 4 hours). Inverse probability weighted and modified Poisson regression models were used to estimate adjusted risk ratios (RRs) for outcome measures, with poor outcome defined as modified Rankin Scale score 4-6 at 3 months.
We identified 175 patients with aSAH who met eligibility criteria (mean [SD] age = 57 [13.2] years, 62% female, 73% White); 49% (n = 86) received modified nimodipine dosing. A modified dose was used more frequently in women (RR 2.08, 95% confidence interval [CI] 1.11-3.89, P = 0.02), patients with vasospasm (RR 3.47, 95% CI 1.84-6.51, P < 0.001), and patients who required vasopressors (RR 1.73, 95% CI 1.3-2.32, P < 0.001). Modified dosing was not associated with poor functional outcome (inverse probability weighted RR 1.1, 95% CI 0.8-1.4, P = 0.65).
Modified dosing of nimodipine is well tolerated and may not be associated with worse functional outcome. Prospective studies are needed to better assess the relationship between nimodipine dosing and outcomes in patients with aSAH.
尼莫地平可改善蛛网膜下腔出血(aSAH)患者的预后。然而,替代剂量策略对预后的影响尚不清楚。
我们对 2016 年至 2019 年期间在一家学术转诊中心因 aSAH 入院的连续患者进行了回顾性队列研究。纳入接受尼莫地平治疗且有明确动脉瘤病因的患者;排除入院后 24 小时内死亡或停止维持生命治疗的患者。使用单变量和多变量修正泊松回归模型确定使用改良尼莫地平剂量(每 2 小时 30 毫克)与标准剂量(每 4 小时 60 毫克)的预测因素。使用逆概率加权和修正泊松回归模型估计结局指标的校正风险比(RR),3 个月时改良 Rankin 量表评分为 4-6 定义为预后不良。
我们确定了 175 名符合入选标准的 aSAH 患者(平均[标准差]年龄 57[13.2]岁,62%为女性,73%为白人);49%(n=86)接受了改良尼莫地平剂量。女性更常使用改良剂量(RR 2.08,95%置信区间 [CI] 1.11-3.89,P=0.02),有血管痉挛(RR 3.47,95%CI 1.84-6.51,P<0.001)和需要血管加压药(RR 1.73,95%CI 1.3-2.32,P<0.001)的患者。改良剂量与不良功能结局无关(逆概率加权 RR 1.1,95%CI 0.8-1.4,P=0.65)。
改良尼莫地平剂量耐受良好,与不良功能结局无关。需要前瞻性研究来更好地评估 aSAH 患者尼莫地平剂量与结局之间的关系。