Reversible cerebral vasoconstriction syndrome: Transcranial doppler findings in a case series of 90 patients

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY Journal of Clinical Neuroscience Pub Date : 2025-02-28 DOI:10.1016/j.jocn.2025.111157
Srinath Ramaswamy , Samuel D. Jacobson , Cyrus X. Colah , Jackson Roberts , Minghua Liu , Randolph S. Marshall
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Abstract

Background

Transcranial Doppler (TCD) can be used in the diagnosis and monitoring of reversible cerebral vasoconstriction syndrome (RCVS). Whether TCD abnormalities can extend beyond 8–12 weeks has not been studied. We performed a single-center, retrospective analysis of TCD abnormalities in RCVS, specifically, whether elevated mean flow velocities (MFV) can persist beyond 90 days of symptom onset.

Methods

Consecutive patients were identified retrospectively using our hospital coding and billing data, and EMR search (2012–2023). Inclusion criteria were diagnosis of RCVS, any age, and available Spectral TCD (non-imaging) (TCD-S). Exclusion criteria were RCVS patients without TCD-S studies, or patients deemed to have other vasculopathies upon adjudication. We recorded demographics, RCVS triggers, and clinical and imaging features. Presence of elevated MFV on TCD-S above the upper reference range was considered abnormal.

Results

Ninety patients with RCVS had TCD-S performed (mean age 39.8 ± 11.8 years, 91% female). Six patients (6.7%) were pregnant and 25 (27.8%) were postpartum. Vasoconstriction was seen on imaging in 56 (62.2%). Median RCVS2 score was 9 (7–10). Complications of RCVS included subarachnoid hemorrhage in 25 (27.8%), intracerebral hemorrhage in 19 (21.1%), and cerebral infarction in 11 (12.2%). TCD-S was abnormal (elevated MFV) in seventy-nine (87.8%). Among those with serial (≥2) TCD-S (n = 67), twenty-two (32.8%) had normalization in MFV at a median time of 73 days (50–132) from symptom onset. Forty-five (67.2%) did not show normalization as per their last available TCD-S at a median of 41 days (16–177). Twenty-six (31.9%) patients had available TCD-S results beyond 90 days, of which 21 (81%) had elevated MFV.

Conclusions

Patients with RCVS can have elevated TCD-S mean flow velocities beyond 90 days. TCD-S may have utility in the diagnosis of RCVS in the early or mild cases, where CTA or MRA may not capture the vasospasm. Prospective studies of the duration of TCD-S abnormalities are necessary to confirm these findings, and to inform clinical management, such as the duration of follow-up and the effects of calcium channel blocker treatment.
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可逆性脑血管收缩综合征:90例患者的经颅多普勒表现
背景经颅多普勒(transcranial Doppler, TCD)可用于可逆性脑血管收缩综合征(RCVS)的诊断和监测。TCD异常是否会持续超过8-12周还没有研究。我们对RCVS的TCD异常进行了单中心回顾性分析,特别是平均血流速度升高(MFV)是否会持续超过症状出现90天。方法回顾性分析我院编码、计费数据和EMR检索(2012-2023年)的连续患者。纳入标准为RCVS诊断、任何年龄、可用的TCD谱(非成像)(TCD- s)。排除标准是没有TCD-S研究的RCVS患者,或经裁定认为有其他血管病变的患者。我们记录了人口统计学、RCVS触发因素以及临床和影像学特征。TCD-S上MFV高于上参考范围被认为是异常的。结果90例RCVS患者行TCD-S手术(平均年龄39.8±11.8岁,女性占91%)。妊娠6例(6.7%),产后25例(27.8%)。影像学上血管收缩56例(62.2%)。RCVS2评分中位数为9分(7-10分)。RCVS的并发症包括蛛网膜下腔出血25例(27.8%),脑出血19例(21.1%),脑梗死11例(12.2%)。79例(87.8%)TCD-S异常(MFV升高)。在连续(≥2)TCD-S患者中(n = 67), 22例(32.8%)在症状出现后73天(50-132天)MFV恢复正常。45名(67.2%)患者在最后一次可用的TCD-S中位数为41天(16-177天)时未显示出正常化。26例(31.9%)患者的TCD-S结果超过90天,其中21例(81%)患者MFV升高。结论RCVS患者在90天后TCD-S平均血流速度升高。在CTA或MRA不能捕捉到血管痉挛的早期或轻度RCVS病例中,TCD-S可能有诊断价值。有必要对TCD-S异常持续时间进行前瞻性研究,以证实这些发现,并为临床管理提供信息,例如随访时间和钙通道阻滞剂治疗的效果。
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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来源期刊
Journal of Clinical Neuroscience
Journal of Clinical Neuroscience 医学-临床神经学
CiteScore
4.50
自引率
0.00%
发文量
402
审稿时长
40 days
期刊介绍: This International journal, Journal of Clinical Neuroscience, publishes articles on clinical neurosurgery and neurology and the related neurosciences such as neuro-pathology, neuro-radiology, neuro-ophthalmology and neuro-physiology. The journal has a broad International perspective, and emphasises the advances occurring in Asia, the Pacific Rim region, Europe and North America. The Journal acts as a focus for publication of major clinical and laboratory research, as well as publishing solicited manuscripts on specific subjects from experts, case reports and other information of interest to clinicians working in the clinical neurosciences.
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