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Cerebral Haemodynamics following Acute Ischaemic Stroke: Effects of Stroke Severity and Stroke Subtype.

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journal contribution
posted on 2018-08-15, 15:06 authored by Osian Llwyd, Angela S. M. Salinet, Ronney B. Panerai, Man Y. Lam, Nazia P. Saeed, Fiona Brodie, Edson Bor-Seng-Shu, Thompson G. Robinson, Ricardo C. Nogueira
BACKGROUND: Acute ischaemic stroke (AIS) patients often show impaired cerebral autoregulation (CA). We tested the hypothesis that CA impairment and other alterations in cerebral haemodynamics are associated with stroke subtype and severity. METHODS: AIS patients (n = 143) were amalgamated from similar studies. Data from baseline (< 48 h stroke onset) physiological recordings (beat-to-beat blood pressure [BP], cerebral blood flow velocity (CBFV) from bilateral insonation of the middle cerebral arteries) were calculated for mean values and autoregulation index (ARI). Differences were assessed between stroke subtype (Oxfordshire Community Stroke Project [OCSP] classification) and severity (National Institutes of Health Stroke Scale [NIHSS] score < 5 and 5-25). Correlation coefficients assessed associations between NIHSS and physiological measurements. RESULTS: Thirty-two percent of AIS patients had impaired CA (ARI < 4) in affected hemisphere (AH) that was similar between stroke subtypes and severity. CBFV in AH was comparable between stroke subtype and severity. In unaffected hemisphere (UH), differences existed in mean CBFV between lacunar and total anterior circulation OCSP subtypes (42 vs. 56 cm•s-1, p < 0.01), and mild and moderate-to-severe stroke severity (45 vs. 51 cm•s-1, p = 0.04). NIHSS was associated with peripheral (diastolic and mean arterial BP) and cerebral haemodynamic parameters (CBFV and ARI) in the UH. CONCLUSIONS: AIS patients with different OCSP subtypes and severity have homogeneity in CA capability. Cerebral haemodynamic measurements in the UH were distinguishable between stroke subtype and severity, including the association between deteriorating ARI in UH with stroke severity. More studies are needed to determine their clinical significance and to understand the determinants of CA impairment in AIS patients.

Funding

This study was supported by UK Engineering and Physical Sciences Research Council (grant No. EP/K041207/1) and São Paulo Research Foundation (FAPESP – N. 2014/04955-8 & 2013/25953-0).

History

Citation

Cerebrovascular Diseases Extra, 2018, 8 (2), pp. 80-89

Author affiliation

/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine/Department of Cardiovascular Sciences

Version

  • VoR (Version of Record)

Published in

Cerebrovascular Diseases Extra

Publisher

Karger Publishers Open Access

eissn

1664-5456

Acceptance date

2018-02-07

Copyright date

2018

Available date

2018-08-15

Publisher version

https://www.karger.com/Article/FullText/487514

Language

en

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