Tirofiban Protocol Protects Against Delayed Cerebral Ischemia: A Case-Series Study.


Journal

Neurosurgery
ISSN: 1524-4040
Titre abrégé: Neurosurgery
Pays: United States
ID NLM: 7802914

Informations de publication

Date de publication:
15 10 2020
Historique:
received: 27 09 2019
accepted: 17 03 2020
pubmed: 18 5 2020
medline: 2 3 2021
entrez: 17 5 2020
Statut: ppublish

Résumé

There has not been any effective prophylaxis for delayed cerebral ischemia delayed cerebral ischemia (DCI) since the introduction of nimodipine. Platelet inhibition may reduce the risk by preventing the formation of microthrombi. Tirofiban has been used as a single monotherapy bridge given its safety profile and controlled platelet inhibition. To assess the risk of DCI in aneurysmal subarachnoid hemorrhages (aSAH) patients treated with the tirofiban protocol. aSAH patients between December 2010 and March 2019 who were treated with stent assisted coiling or flow-diverting device were started on a continuous tirofiban infusion protocol and were compared with patients who underwent coil embolization without antiplatelet therapy. Safety analysis was performed to assess DCI, hemorrhagic, and ischemic events. A total of 21 patients were included in the tirofiban series and 81 in the control group. There was no statistical difference in age, gender, Hunt-Hess grade, and Fisher scale between the 2 groups except for a higher Fisher grade II in the tirofiban group. Multivariate analysis revealed tirofiban to reduce the risk of vasospasm by 72 percent (OR .28, P = .03), without affecting the risk of hemorrhagic complications (OR = 0.50, P = .26). Tirofiban reduced the risk of symptomatic stroke endovascular procedure but it did not reach significance (P = .06). DCI, older age, and postprocedural symptomatic stroke were significant predictors of mortality. Tirofiban reduced the mortality risk, but this association was not statistically significant. The tirofiban protocol in aSAH patients reduces the risk of DCI without conferring additional risks. This supports previous findings were antiplatelet therapy reduced DCI in human and animal models.

Sections du résumé

BACKGROUND
There has not been any effective prophylaxis for delayed cerebral ischemia delayed cerebral ischemia (DCI) since the introduction of nimodipine. Platelet inhibition may reduce the risk by preventing the formation of microthrombi. Tirofiban has been used as a single monotherapy bridge given its safety profile and controlled platelet inhibition.
OBJECTIVE
To assess the risk of DCI in aneurysmal subarachnoid hemorrhages (aSAH) patients treated with the tirofiban protocol.
METHODS
aSAH patients between December 2010 and March 2019 who were treated with stent assisted coiling or flow-diverting device were started on a continuous tirofiban infusion protocol and were compared with patients who underwent coil embolization without antiplatelet therapy. Safety analysis was performed to assess DCI, hemorrhagic, and ischemic events.
RESULTS
A total of 21 patients were included in the tirofiban series and 81 in the control group. There was no statistical difference in age, gender, Hunt-Hess grade, and Fisher scale between the 2 groups except for a higher Fisher grade II in the tirofiban group. Multivariate analysis revealed tirofiban to reduce the risk of vasospasm by 72 percent (OR .28, P = .03), without affecting the risk of hemorrhagic complications (OR = 0.50, P = .26). Tirofiban reduced the risk of symptomatic stroke endovascular procedure but it did not reach significance (P = .06). DCI, older age, and postprocedural symptomatic stroke were significant predictors of mortality. Tirofiban reduced the mortality risk, but this association was not statistically significant.
CONCLUSION
The tirofiban protocol in aSAH patients reduces the risk of DCI without conferring additional risks. This supports previous findings were antiplatelet therapy reduced DCI in human and animal models.

Identifiants

pubmed: 32415850
pii: 5838033
doi: 10.1093/neuros/nyaa170
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0
Tirofiban GGX234SI5H

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

E552-E556

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 by the Congress of Neurological Surgeons.

Auteurs

Mario Zanaty (M)

Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Carlos Osorno-Cruz (C)

Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Stefano Byer (S)

Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Jorge A Roa (JA)

Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa.
Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Kaustubh Limaye (K)

Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Daizo Ishii (D)

Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Daichi Nakagawa (D)

Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa.
Department of Neurosurgery, University of Tokyo, Tokyo, Japan.

James Torner (J)

Department of Epidemiology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Lu Yongjun (L)

Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Santiago Ortega-Gutiérrez (S)

Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Edgar A Samaniego (EA)

Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Lauren Allan (L)

Department of Surgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

David Hasan (D)

Department of Neurosurgery, University of Tokyo, Tokyo, Japan.

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