Literature DB >> 7915439

Dynamic transcranial Doppler assessment of positional vertebrobasilar ischemia.

M Sturzenegger1, D W Newell, C Douville, S Byrd, K Schoonover.   

Abstract

BACKGROUND AND
PURPOSE: A hemodynamic as opposed to an embolic origin of vertebrobasilar ischemia may be suspected when symptoms are brief and triggered by changes in the position of the head or neck. It may be difficult, and not without risk, to reproduce the symptoms and to prove the short-lived hemodynamic changes during angiography. If transcranial Doppler sonography (TCD) could detect these changes, it would be useful as a noninvasive screening method to select patients for further diagnostic evaluation.
METHODS: TCD monitoring of the P1 segments of both posterior cerebral arteries was performed during different head movements in 14 patients referred for evaluation of suspected hemodynamic vertebrobasilar ischemia and in 10 healthy control subjects with a two-channel, 2-MHz, computerized Doppler system. Patients' symptoms were correlated with the Doppler findings.
RESULTS: Four patients with stereotypical symptoms had a severe drop in posterior cerebral artery blood flow velocities (BFVs) to 20% of baseline (mean; SD, 14.3; range, 0% to 48%) and subsequent reactive hyperemia with an increase in BFV to 149% (mean; SD, 20.6; range, 110% to 186%) dependent on head rotation to one side (group 1). Compared with the values found in group 2 patients and in control subjects, these drops were significant (P = .0001 for both). Symptoms together with BFV changes could be reproduced several times. Angiography confirmed severe vertebral artery obstruction during head rotation and the presence of anomalies in the posterior circulation. In 10 patients (group 2), symptoms were not short-lived, stereotyped, or clearly dependent on head movements and could not be reproduced during TCD testing. Their BFVs dropped to 88% (mean; SD, 9.0; range, 64% to 102%) of baseline values during maximal head rotation, to 86% (mean; SD, 10.3; range, 64% to 100%) during flexion, and to 88% (mean; SD, 6.7; range, 75% to 103%) during extension. In the 10 control subjects, BFVs dropped to 86% (mean; SD, 8.8; range, 61% to 98%) of baseline values during rotation, to 90% (mean; SD, 10.3; range, 74% to 107%) during flexion, and to 76% (mean; SD, 17.1; range, 54% to 104%) during extension.
CONCLUSIONS: Monitoring posterior cerebral artery BFV during head movements is a simple, noninvasive method to document a hemodynamic etiology of symptoms in patients with suspected positional vertebrobasilar ischemia. The correlation of symptoms to the hemodynamic findings proved a useful screening method to identify those patients with true position-evoked hemodynamic insufficiency in the posterior circulation. These patients should be selected for angiographic evaluation to identify the source and site of arterial compression.

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Year:  1994        PMID: 7915439     DOI: 10.1161/01.str.25.9.1776

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  5 in total

1.  Magnetic resonance angiographic analysis of atlanto-axial rotation: anatomic bases of compression of the vertebral arteries.

Authors:  J L Dumas; J Salama; P Dreyfus; P Thoreux; D Goldlust; J P Chevrel
Journal:  Surg Radiol Anat       Date:  1996       Impact factor: 1.246

2.  DynaCT angiography for the diagnosis of bilateral bow hunter's syndrome.

Authors:  Tony Lu; Ponraj Chinnadurai; Javier E Anaya-Ayala; Orlando M Diaz
Journal:  Interv Neuroradiol       Date:  2016-10-27       Impact factor: 1.610

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Authors:  Sarah Marti; Stefan Hegemann; Hans-Christian von Büdingen; Ralf W Baumgartner; Dominik Straumann
Journal:  J Neurol       Date:  2008-02-18       Impact factor: 4.849

4.  [Syncope from the viewpoint of a neurologist].

Authors:  A Bickel; J Röther
Journal:  Herz       Date:  2014-06       Impact factor: 1.443

5.  Transitional nystagmus in a Bow Hunter's Syndrome case report.

Authors:  Yasuyuki Nomura; Teruo Toi; Yasuo Ogawa; Takeshi Oshima; Yuichiro Saito
Journal:  BMC Neurol       Date:  2020-11-30       Impact factor: 2.474

  5 in total

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