Association of asymptomatic hemorrhage after endovascular stroke treatment with outcomes.


Journal

Journal of neurointerventional surgery
ISSN: 1759-8486
Titre abrégé: J Neurointerv Surg
Pays: England
ID NLM: 101517079

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 15 11 2020
revised: 11 01 2021
accepted: 14 01 2021
pubmed: 10 2 2021
medline: 23 11 2021
entrez: 9 2 2021
Statut: ppublish

Résumé

Intracerebral hemorrhage (ICH) occurs in ~20%-30% of stroke patients undergoing endovascular therapy (EVT). However, there is conflicting evidence regarding the effect of asymptomatic ICH (aICH) on post-EVT outcomes. We sought to evaluate the effect of aICH on immediate and 90-day post-EVT neurological outcomes. In this post-hoc analysis of the multicenter, prospective Blood Pressure after Endovascular Therapy (BEST) study we identified subjects with ICH following EVT. This population was divided into no ICH, aICH, and symptomatic ICH (sICH). Associations with 90-day modified Rankin Scale (mRS) dichotomized by functional independence (0-2 vs 3-6) and early neurological recovery (ENR) were determined using univariate/multivariate logistic regression models. Of 485 patients enrolled in BEST, 446 had 90-day follow-up data available. 92 (20.6%) developed aICH, and 18 (4%) developed sICH. Compared with those without ICH, aICH was not associated with worse 90-day outcome or lower ENR (OR 0.84 [0.53-1.35], P=0.55, aOR 0.84 [0.48-1.44], P=0.53 for 90-day mRS 0-2; OR 0.77 [0.48-1.23], P=0.34, aOR 0.72 [0.43-1.22] for ENR). aICH was not associated with 90-day outcome or ENR in patients with mTICI ≥2 b (OR 0.78 [0.48-1.26], P=0.33 for 90-day mRS 0-2; OR 0.89 [0.69-1.12], P=0.15 for ENR). A higher proportion of patients with aICH had mTICI ≥2 b than those without ICH (97%vs 87%, P=0.01). aICH was not associated with worse outcomes in patients with large-vessel stroke treated with EVT. aICH was more frequent in patients with successful recanalization. Further validation of our findings in large cohort studies of EVT-treated patients is warranted.

Sections du résumé

BACKGROUND BACKGROUND
Intracerebral hemorrhage (ICH) occurs in ~20%-30% of stroke patients undergoing endovascular therapy (EVT). However, there is conflicting evidence regarding the effect of asymptomatic ICH (aICH) on post-EVT outcomes. We sought to evaluate the effect of aICH on immediate and 90-day post-EVT neurological outcomes.
METHODS METHODS
In this post-hoc analysis of the multicenter, prospective Blood Pressure after Endovascular Therapy (BEST) study we identified subjects with ICH following EVT. This population was divided into no ICH, aICH, and symptomatic ICH (sICH). Associations with 90-day modified Rankin Scale (mRS) dichotomized by functional independence (0-2 vs 3-6) and early neurological recovery (ENR) were determined using univariate/multivariate logistic regression models.
RESULTS RESULTS
Of 485 patients enrolled in BEST, 446 had 90-day follow-up data available. 92 (20.6%) developed aICH, and 18 (4%) developed sICH. Compared with those without ICH, aICH was not associated with worse 90-day outcome or lower ENR (OR 0.84 [0.53-1.35], P=0.55, aOR 0.84 [0.48-1.44], P=0.53 for 90-day mRS 0-2; OR 0.77 [0.48-1.23], P=0.34, aOR 0.72 [0.43-1.22] for ENR). aICH was not associated with 90-day outcome or ENR in patients with mTICI ≥2 b (OR 0.78 [0.48-1.26], P=0.33 for 90-day mRS 0-2; OR 0.89 [0.69-1.12], P=0.15 for ENR). A higher proportion of patients with aICH had mTICI ≥2 b than those without ICH (97%vs 87%, P=0.01).
CONCLUSIONS CONCLUSIONS
aICH was not associated with worse outcomes in patients with large-vessel stroke treated with EVT. aICH was more frequent in patients with successful recanalization. Further validation of our findings in large cohort studies of EVT-treated patients is warranted.

Identifiants

pubmed: 33558440
pii: neurintsurg-2020-017123
doi: 10.1136/neurintsurg-2020-017123
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1095-1098

Informations de copyright

© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: RVC receives research grants from Medtronic and Cerenovus. PK receives research grant support from Cerenovus. EAM reports grant support from NIH/NINDS (K23NS113858). Remaining authors have no disclosures.

Auteurs

Michael J Feldman (MJ)

Department of Neurosurgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA michael.j.feldman@vumc.org eva.a.mistry@vumc.org.

Steven Roth (S)

Department of Neurosurgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Matthew R Fusco (MR)

Department of Neurosurgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Tapan Mehta (T)

Interventional Neuroradiology and Neurology, Hartford Hospital, Hartford, Connecticut, USA.

Niraj Arora (N)

Neurology, University of Missouri, Columbia, Missouri, USA.

James E Siegler (JE)

Cooper Neurologic Institute, Cooper University Health Care, Camden, New Jersey, USA.

Matthew Schrag (M)

Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Shilpi Mittal (S)

Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Howard Kirshner (H)

Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Akshitkumar M Mistry (AM)

Department of Neurosurgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Shadi Yaghi (S)

Neurology, New York University Medical Center, New York, New York, USA.

Rohan V Chitale (RV)

Department of Neurosurgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Pooja Khatri (P)

Neurology, University of Cincinnati, Cincinnati, Ohio, USA.

Eva A Mistry (EA)

Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA michael.j.feldman@vumc.org eva.a.mistry@vumc.org.

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