Stuart Daniel, Christian Robin, Uschmann Hartmut, Palokas Michelle
School of Nursing, Department of Neurology, University of Mississippi Medical Center, Jackson, USA.
Mississippi Centre of Evidence-Based Practice: a Joanna Briggs Institute Centre of Excellence.
JBI Database System Rev Implement Rep. 2018 Oct;16(10):2013-2026. doi: 10.11124/JBISRIR-2017-003493.
The objective of this review was to determine the effectiveness of intrathecal nicardipine compared to usual care on cerebral vasospasm and its impact on the following outcome measures: mean flow velocities, angiographic and/or clinical vasospasm, and infection rates.
The results of non-traumatic (aneurysmal) subarachnoid hemorrhage can have devastating effects on patients in terms of functional outcomes. Although other medications have been and continue to be used, Nimodipine is the only Food and Drug Administration-approved medication for treating and improving outcomes following non-traumatic subarachnoid hemorrhage, which may be caused by aneurysmal rupture or arteriovenous malformation. Cerebral vasospasm after non-traumatic subarachnoid hemorrhage is a major concern; cerebral vasospasm refers to the narrowing of the cerebral vessels, which can lead to stroke. Delayed ischemic neurological deficit, as a result of cerebral vasospasm, is the number one reason for death and disability following subarachnoid hemorrhage. This review will determine the effects that intrathecal nicardipine has on cerebral vasospam following non-traumatic subarachnoid hemorrhage.
The participants of this review included adult patients (18 years and over) in intensive care units. The patients must have had a subarachnoid hemorrhage without history of trauma as cause of subarachnoid hemorrhage, along with the presence of an external ventricular drain. The intervention was administration of intrathecal nicardipine in patients with cerebral vasospasm as a result of non-traumatic subarachnoid hemorrhage. The comparator was usual care, which does not include use of intrathecal nicardipine as part of the treatment regimen. The current review considered both experimental and quasi-experimental study designs. The primary outcomes measured included presence of cerebral vasospasm (identified by mean flow velocities measured by transcranial Doppler and the presence of angiographic vasospasm identified on angiogram) and clinical/symptomatic vasospasm. Secondarily, infection rates as a result of intrathecal nicardipine administration were evaluated.
The search strategy aimed to find both published and unpublished studies. Seven databases were searched with no date limitations due to the limited amount of research on this topic.Two independent reviewers assessed the methodological validity of the papers prior to inclusion in the review using the standardized critical appraisal instruments from Joanna Briggs Institute System for the Unified Management, Assessment and Review of Information (JBI SUMARI).Quantitative data was extracted from included studies using the standardized data extraction tool from JBI SUMARI.Statistical pooling was not possible; therefore findings were presented in a narrative form.
Two studies examined the effect that intrathecal nicardipine has on cerebral vasospasm, clinical/symptomatic vasospasm and safety concerns (i.e. infection). The studies indicate that intrathecal nicardipine has shown potential benefits and safety in the treatment of cerebral vasospasm.
Although intrathecal nicardipine has shown potential to be effective in treating cerebral vasospasm, variance existed among those who received intrathecal nicardipine. In terms of safety, one study had no occurrences of associated bacterial meningitis and the other study had two reported cases of bacterial meningitis out of 50 among those who received intrathecal nicardipine. Limited studies on the use of intrathecal nicardipine following non-traumatic subarachnoid hemorrhage and lack of pooling of results for this review demonstrate the need for more research in this field.
本综述的目的是确定鞘内注射尼卡地平与常规治疗相比对脑血管痉挛的有效性及其对以下结局指标的影响:平均血流速度、血管造影和/或临床血管痉挛以及感染率。
非创伤性(动脉瘤性)蛛网膜下腔出血的结果在功能结局方面可能对患者产生毁灭性影响。尽管其他药物已经并仍在使用,但尼莫地平是美国食品药品监督管理局批准的唯一用于治疗和改善非创伤性蛛网膜下腔出血(可能由动脉瘤破裂或动静脉畸形引起)后结局的药物。非创伤性蛛网膜下腔出血后的脑血管痉挛是一个主要问题;脑血管痉挛是指脑血管变窄,可导致中风。由于脑血管痉挛导致的迟发性缺血性神经功能缺损是蛛网膜下腔出血后死亡和残疾的首要原因。本综述将确定鞘内注射尼卡地平对非创伤性蛛网膜下腔出血后脑血管痉挛的影响。
本综述的参与者包括重症监护病房的成年患者(18岁及以上)。患者必须有蛛网膜下腔出血且无创伤史作为蛛网膜下腔出血的原因,同时要有外置脑室引流管。干预措施是对因非创伤性蛛网膜下腔出血导致脑血管痉挛的患者鞘内注射尼卡地平。对照为常规治疗,不包括将鞘内注射尼卡地平作为治疗方案的一部分。本综述考虑了实验性和半实验性研究设计。测量的主要结局包括脑血管痉挛的存在(通过经颅多普勒测量的平均血流速度和血管造影上确定的血管造影性血管痉挛来确定)以及临床/症状性血管痉挛。其次,评估鞘内注射尼卡地平导致的感染率。
检索策略旨在查找已发表和未发表的研究。由于关于该主题的研究数量有限,对七个数据库进行了检索,无日期限制。两名独立评审员在将论文纳入综述之前,使用乔安娜·布里格斯研究所统一管理、评估和审查信息系统(JBI SUMARI)的标准化批判性评估工具评估论文的方法学有效性。使用JBI SUMARI的标准化数据提取工具从纳入研究中提取定量数据。无法进行统计合并;因此,研究结果以叙述形式呈现。
两项研究探讨了鞘内注射尼卡地平对脑血管痉挛、临床/症状性血管痉挛和安全性问题(即感染)的影响。研究表明,鞘内注射尼卡地平在治疗脑血管痉挛方面显示出潜在益处和安全性。
尽管鞘内注射尼卡地平在治疗脑血管痉挛方面显示出潜在效果,但接受鞘内注射尼卡地平的患者之间存在差异。在安全性方面,一项研究未发生相关细菌性脑膜炎,另一项研究在接受鞘内注射尼卡地平的50名患者中有两例报告的细菌性脑膜炎病例。关于非创伤性蛛网膜下腔出血后使用鞘内注射尼卡地平的研究有限,且本综述缺乏结果合并,这表明该领域需要更多研究。