Analysis of Characteristics in Patients with Non-Hemorrhagic Reversible Cerebral Vasoconstriction syndrome NH-RCVS

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Analysis of Characteristics in Patients with Non-Hemorrhagic Reversible Cerebral Vasoconstriction syndrome NH-RCVS Owais Mufti, MBBS Aaron McMurtray, MD, PhD and Bijal K. Mehta, MD, MPH, MA Department of Neurology, SUNY Buffalo, The Jacobs Neurology Institute, Buffalo, NY. Department of Neurology, David Geffen School of Medicine at UCLA, Harbor-UCLA Medical Center, Torrance, CA.

Analysis of Reversible Cerebrovascular Vasoconstriction Syndrome WITHOUT Subarachnoid or Intracerebral Hemorrhage Owais Mufti, Ghulam Mustafa*, Aman Dabir*, Haris Kamal*, Ping Li*, Mohammed Shafie**, and Han Lee**, Aaron McMurtray**, and Bijal K. Mehta** * Department of Neurology, SUNY Buffalo, Buffalo, NY 14204 **Department of Neurology, UCLA, Harbor-UCLA Medical Center, Torrance, CA 90509 Background: Reversible vasoconstriction syndrome is a phenomenon where the vasculature of the brain begins to spasm. Although initially thought to be only associated with intracranial and subarachnoid hemorrhage, recently, this has expanded to include non-hemorrhagic states. The etiology and physiology of this type of reversible vasoconstriction syndrome remains to be worked out. Methods: Our meta-analysis will discuss the demographic, past medical and concurrent medical history, and imaging characteristics, including CT and conventional angiograms of non-hemorrhagic cases in the literature. This includes prior studies and cases/case series where data of non-hemorrhagic cases where vasospasm was noted. A review of treatments, including endovascular approaches, will also be discussed. Results: Similarities and differences from reversible vasoconstriction syndrome associated with hemorrhage will be noted. A discussion of how patients with nonhemorrhagic reversible vasoconstriction syndrome are managed. Conclusion: Reversible vasoconstriction syndrome may present differently in patients without associated subarachnoid or intracranial hemorrhage.

WHAT IS NH-RCVS? Reversible Cerebral Vasoconstriction syndrome (RCVS) has been proposed as a unifying term for variety of previously named similar syndromes, including Call-Fleming syndrome. In literature many sporadic case reports or small analysis of collection of cases of nonhemorrhagic RCVS.

Pathophysiology RCVS is possibly caused by a transient dysregulation of cerebral vascular tone, leading to multi-focal arterial constriction and dilation.

AIMS OF THIS ANALYTIC STUDY RCVS is associated with hemorrhage but no distinguishing data or guidelines exist for diagnosis or predicting the RCVS patients without associated hemorrhage (NH-RCVS) Establish NH-RCVS as a distinct clinical phenomenon as no ideal set of common presenting symptoms have been assembled in order to help predict or diagnose NH-RCVS Establish potential causal relationships, triggers and associations from sporadic case reports as it has not been so far attempted.

Methods Analysis on selected case reports on NH-RCVS published from 2004-2011. A total of 66 case reports were included in this Analysis out of a total 335 case reports on Cerebral Vasoconstriction.

METHODS Analysis of symptomatology Analysis of diagnostic investigations Analysis of potential triggers/etiology of NH-RCVS Analysis of potential clinical outcome for NH-RCVS being a rare etiologic agent itself.

Methods INCLUSION CRITERIA: Sudden thunderclap headache with/without focal signs. Evidence of beading pattern on CTA, MRA or Cerebral Angiogram without any evidence of IC bleeding or vessel rupture. Established evidence of negative vasculitis work up if ordered. Positive response to Calcium Channel blockers on f/u imaging. No prior history of steroid exposure.

METHODS: EXCLUSION CRITERIA Cases with patients having evidence of: Sub-arachnoid hemorrhage Intracerebral hemorrhage Prior Intracerebral Neurosurgical intervention

Results: Clinical Features Mean age of 40. All of them presented with acute onset of severe thunderclap headache In the patients with localized headaches 20 had occipital headaches, 11 had diffuse bilateral headaches, 4 had frontal while 2 patients complained of headaches localized to the vertex. 26 patients were found to present with hypertensive crisis while 5 were merely hypertensive.

MALE : FEMALE RATIO (18:48) 60 50 40 30 20 10 0 No of patient Male Female Column1

RESULTS: Features AURA WAS GENERALLY REPORTED TO BE MISSING.HOWEVER WAS PRESENT IN PATIENTS WITH HX OF MIGRAINES. HEADACHE WAS REPORTED AS NON-THROBBING.

Motor Symptoms 7 6 6 5 4 3 3 2 1 1 0 Monoparesis Hemiparesis Quadriparetic

SYMPTOMS 14 12 13 10 8 9 6 4 2 0 5 3 3 2 1 1 No of patients Imparied vision Homonymous heminopia Amaurosis Cortical Blindness Photophobia Dysarthria Phonophobia Hyperacusis Linear (Imparied vision)

RESULTS: Symptoms 3.5 3 3 Axis Title 2.5 2 1.5 2 1 1 1 0.5 0 Monoparesis Hemisensory loss Dysphasia Neglect

Other Symptoms 40 35 30 25 20 15 10 5 0 Seizures Myoclonous GI symptoms Vomiting GaitDisturbance Breathing difficulty

Vitals HYPERTENSIVE CRISES : 26 HTN: 5 OTHERS :NORMOTENSIVE

Results: 35 Positive finding on Imaging 12-4-29 30 25 20 15 10 5 0 No of Patient with positive findings MRI CTA Conventional Angiogram

RESULTS: Investigations CSF/LABS Out of 42 patients who underwent a spinal tap, 38 had normal CSF, while 4 had abnormal results with elevated proteins but no xanthochromia. A vasculitis workup done in 22 of these patients was normal, with ESR, CRP being normal in almost all these cases.

RESULTS: Treatment/Response Removal of inciting medication/factors, calcium channel blocker. Oral calcium channel blockers can be considered as a preliminary treatment option after removal of the offending agents, with other options including oral steroids or IA Calcium Channel blockers.

Conclusion Certain common clinical features may be identified for rapid diagnosis and better treatment of NH-RCVS patients. Do not delay imaging studies to lead to diagnosis of Non-Hemorrhagic RCVS Certain associations if identified are strongly related to NH-RCVS onset and can be potential etiologic agents in various settings.

CONCLUSION MRA appears to show vasoconstriction more often than CTA in our review and should be obtained as a preliminary step for patients with a high suspicion; but if negative for any vascular abnormalities, a conventional angiogram is the modality of choice for diagnosis If identified early can be rapidly treated with oral or intraarterial CCB with excellent response.

CONCLUSION-Summary NH-RCVS can be an uncommon cause of headaches with distinct clinical/radiologic features with excellent response to CCB NH-RCVS can be an uncommon cause of ischemic stroke NH-RCVS can be an uncommon cause of seizures

CONCLUSION Large scale clinical trials are needed to study this increasingly common group of disorders.

TAKE HOME MESSAGE Thunderclap headaches with no bleed seen on imaging, or negative CSF, accompanied with nausea and vomiting with/without focal signs should alert the Physician to the possibility of NH-RCVS especially if a history of recent childbirth, use of vasoactive drugs, OCPs, SSRIs or other severe emotional stressors are obtained. Imaging should not be delayed.

Reference: 1. Ahsan Sattar, Georgios Manousakis, and Matthew B Jensen :Systematic Review of Reversible Cerebral Vasoconstriction: Expert Rev Cardiovasc Ther. 2010 October; 8(10): 1417 1421. 2. Case reports on RCVS on pubmed. 3. Call GK, Fleming MC, Sealfon S, Levine H, Kistler JP, Fisher CM. Reversible cerebral segmental vasoconstriction. Stroke. 1988;19(9):1159 1170 4. Noskin O, Jafarimojarrad E, Libman RB, Nelson JL. Diffuse cerebral vasoconstriction (Call Fleming syndrome) and stroke associated with antidepressants. Neurology. 2006;67(1):159 160 5. Gerretsen P, Kern RZ. Reversible cerebral vasoconstriction syndrome: a thunderclap headache-associated condition. Curr Neurol Neurosci Rep. 2009;9(2):108 114 6. Singhal AB. Cerebral vasoconstriction syndromes. Top Stroke Rehabil. 2004;11(2):1 6. 7. Reversible Segmental Cerebral Arterial Vasospasm and Cerebral Infarction: Possible Association With Excessive Use of Sumatriptan and Midrin:James F. Meschia, MD; Marc D. Malkoff, MD; José Biller, MD 8. Arch Neurol. 1998;55(5):712-714. doi:10.1001/archneur.55.5.712.