Relationship of White Matter Lesions with Intracerebral Hemorrhage Expansion and Functional Outcome : MISTIE II and CLEAR III

التفاصيل البيبلوغرافية
العنوان: Relationship of White Matter Lesions with Intracerebral Hemorrhage Expansion and Functional Outcome : MISTIE II and CLEAR III
المؤلفون: Hansen, Björn M., Ullman, Natalie, Muschelli, John, Norrving, Bo, Dlugash, Rachel, Avadhani, Radhika, Awad, Issam, Zuccarello, Mario, Ziai, Wendy C., Hanley, Daniel F., Thompson, Richard E., Lindgren, Arne
المصدر: Neurocritical Care EpiHealth: Epidemiology for Health. 33(2):516-524
مصطلحات موضوعية: Cerebral hemorrhage, Cerebral small vessel diseases, Leukoaraiosis, Leukoencephalopathies, Prognosis, Stroke, Medicin och hälsovetenskap, Klinisk medicin, Neurologi, Medical and Health Sciences, Clinical Medicine, Neurology
الوصف: Background/Objective: Intracerebral hemorrhage (ICH) patients commonly have concomitant white matter lesions (WML) which may be associated with poor outcome. We studied if WML affects hematoma expansion (HE) and post-stroke functional outcome in a post hoc analysis of patients from randomized controlled trials. Methods: In ICH patients from the clinical trials MISTIE II and CLEAR III, WML grade on diagnostic computed tomography (dCT) scan (dCT, < 24 h after ictus) was assessed using the van Swieten scale (vSS, range 0–4). The primary outcome for HE was > 33% or > 6 mL ICH volume increase from dCT to the last pre-randomization CT (< 72 h of dCT). Secondary HE outcomes were: absolute ICH expansion, > 10.4 mL total clot volume increase, and a subgroup analysis including patients with dCT < 6 h after ictus using the primary HE definition of > 33% or > 6 mL ICH volume increase. Poor functional outcome was assessed at 180 days and defined as modified Rankin Scale (mRS) ≥ 4, with ordinal mRS as a secondary endpoint. Results: Of 635 patients, 55% had WML grade 1–4 at dCT (median 2.2 h from ictus) and 13% had subsequent HE. WML at dCT did not increase the odds for primary or secondary HE endpoints (P ≥ 0.05) after adjustment for ICH volume, intraventricular hemorrhage volume, warfarin/INR > 1.5, ictus to dCT time in hours, age, diabetes mellitus, and thalamic ICH location. WML increased the odds for having poor functional outcome (mRS ≥ 4) in univariate analyses (vSS 4; OR 4.16; 95% CI 2.54–6.83; P < 0.001) which persisted in multivariable analyses after adjustment for HE and other outcome risk factors. Conclusions: Concomitant WML does not increase the odds for HE in patients with ICH but increases the odds for poor functional outcome. Clinical Trial Registration: http://www.clinicaltrials.govTest trial-identifers: NCT00224770 and NCT00784134.
الوصول الحر: https://lup.lub.lu.se/record/dc691817-3afd-43a5-91b7-c917958852b4Test
http://dx.doi.org/10.1007/s12028-020-00916-4Test
قاعدة البيانات: SwePub
الوصف
تدمد:15416933
DOI:10.1007/s12028-020-00916-4