Duman Enes, Karakoç Fatma, Pinar H Ulas, Dogan Rafi, Fırat Ali, Yıldırım Erkan
1 63994 Baskent University School of Medicine , Konya Research Center, Department of Radiology, Konya, Turkey.
2 63994 Baskent University School of Medicine , Konya Research Center, Department of Anesthesiology, Konya, Turkey.
Interv Neuroradiol. 2017 Dec;23(6):636-643. doi: 10.1177/1591019917732288. Epub 2017 Sep 28.
Background Cerebral vasospasm (CV) is a major cause of delayed morbidity and mortality in patients with subarachnoid hemorrhage (SAH). Various cerebral protectants have been tested in patients with aneurysmal SAH. We aimed to research the success rate of treatment of CV via intra-arterial milrinone injection and aggressive pharmacological therapy for refractory CV. Methods A total of 25 consecutive patients who received intra-arterial milrinone and nimodipine treatment for CV following SAH between 2014 and 2017 were included in the study. Patients who underwent surgical clipping were excluded. Refractory vasospasm was defined as patients with CV refractory to therapies requiring ≥3 endovascular interventions. Overall, six patients had refractory CV. Long-term neurological outcome was assessed 6-18 months after SAH using a modified Rankin score and Barthel index. Results The median modified Rankin scores were 1 (min: 0, max: 3) and Barthel index scores were 85 (min: 70, max: 100) From each vasospastic territory maximal 10-16 mg milrinone was given to patients; a maximum of 24 mg milrinone was given to each patient in a session and a maximum of 42 mg milrinone was given to a patient in a day. Both milrinone and nimodipine were given to three patients. There was a large vessel diameter increase after milrinone and nimodipine injections. No patient died due to CV; only one patient had motor dysfunction on the right lower extremity. Conclusion Higher doses of milrinone can be used effectively to control refractory CV. For exceptional patients with refractory CV, high dose intra-arterial nimodipine and milrinone infusion can be used as a rescue therapy.
脑血管痉挛(CV)是蛛网膜下腔出血(SAH)患者延迟发病和死亡的主要原因。各种脑保护剂已在动脉瘤性SAH患者中进行了测试。我们旨在研究通过动脉内注射米力农和积极的药物治疗难治性CV来治疗CV的成功率。方法:本研究纳入了2014年至2017年间25例连续接受动脉内米力农和尼莫地平治疗SAH后CV的患者。排除接受手术夹闭的患者。难治性血管痉挛定义为对需要≥3次血管内干预的治疗难治的CV患者。总体而言,6例患者患有难治性CV。使用改良Rankin量表和Barthel指数在SAH后6-18个月评估长期神经功能结局。结果:改良Rankin量表的中位数为1(最小值:0,最大值:3),Barthel指数评分中位数为85(最小值:70,最大值:100)。向每个血管痉挛区域的患者给予最大10-16mg米力农;每次给予患者的米力农最大剂量为24mg,每天给予患者的米力农最大剂量为42mg。3例患者同时接受了米力农和尼莫地平治疗。注射米力农和尼莫地平后大血管直径增加。无患者因CV死亡;仅1例患者右下肢有运动功能障碍。结论:更高剂量的米力农可有效用于控制难治性CV。对于难治性CV的特殊患者,高剂量动脉内尼莫地平和米力农输注可作为挽救治疗。