Predictors of Hemorrhagic Transformation After IV Continuous Cangrelor Infusion Initiated During Mechanical Thrombectomy
BACKGROUND: Cangrelor, a fast-acting intravenous P2Y12 receptor inhibitor, is increasingly used during mechanical thrombectomy for acute ischemic stroke to treat or prevent thrombotic complications. While effective, its use may increase the risk of hemorrhagic transformation (HT). We investigated clinical, imaging, and procedural predictors of HT in this specific patient population. METHODS: We performed a retrospective post hoc single-center study including 101 patients with acute ischemic stroke treated with intravenous cangrelor initiated directly after mechanical thrombectomy and continued for 12 hours between January 2021 and June 2024. Univariate and multivariable logistic regression models were used to assess associations between HT and clinical, radiological, and procedural factors. RESULTS: Among the 101 patients included, 25 (24.7%) developed HT, and 9 (8.9%) experienced symptomatic intracerebral hemorrhage. In multivariable analysis, baseline blood glucose (adjusted odds ratio, 6.51 [95% CI, 1.35–31.4]; P =0.02), leukocytosis (adjusted odds ratio, 1.18 [95% CI, 1.00–1.38]; P =0.047), and subarachnoid hemorrhage on postmechanical thrombectomy cone-beam computed tomography (adjusted odds ratio, 16.60 [95% CI, 2.97–92.8]; P =0.0014) were independent predictors of HT. Contrast enhancement was associated with HT in univariate analysis but did not remain significant after adjustment. CONCLUSIONS: Baseline blood glucose, leukocytosis, and isolated subarachnoid hemorrhage on postmechanical thrombectomy cone-beam computed tomography emerged as independent predictors of HT. Identifying high-risk patients using readily available clinical and imaging markers may support individualized antiplatelet strategies and help reduce hemorrhagic complications during cangrelor treatment. REGISTRATION URL: https://www.clinicaltrials.gov ; Unique identifier: NCT03776877
Authors
- Pierre Seners (ORCID: https://orcid.org/0000-0002-2134-0691)
- Simon Escalard (ORCID: https://orcid.org/0000-0003-1306-1008)
- William Boisseau (ORCID: https://orcid.org/0000-0001-8120-5128)
- Erwan Robichon
- Simon Clariot (ORCID: https://orcid.org/0000-0003-3162-2155)
- Humain Baharvahdat (ORCID: https://orcid.org/0000-0002-1154-8843)
- Hocine Redjem (ORCID: https://orcid.org/0000-0002-6943-9922)
- Alexandre Bani‐Sadr (ORCID: https://orcid.org/0000-0002-1808-2484)
- Jean‐Philippe Désilles (ORCID: https://orcid.org/0000-0001-8395-6312)
- Benjamin Maïer (ORCID: https://orcid.org/0000-0003-3993-1024)
- François Delvoye (ORCID: https://orcid.org/0000-0002-0697-2156)
- Mikaël Mazighi (ORCID: https://orcid.org/0000-0003-0911-8999)
- Michel Piotin (ORCID: https://orcid.org/0000-0002-1354-4328)
- Aurélien Freiherr von Seckendorff (ORCID: https://orcid.org/0000-0003-4051-5351)
- Andrea Gambino (ORCID: https://orcid.org/0000-0002-9142-1331)
- Jean‐Marc Olivot (ORCID: https://orcid.org/0000-0003-2027-2276)
- Marie Ernst (ORCID: https://orcid.org/0000-0002-9002-5783)
- Raphaël Blanc (ORCID: https://orcid.org/0000-0002-3975-3865)
- Nicolas Engrand (ORCID: https://orcid.org/0000-0002-6051-5474)
- Manar Abomulay
- Amira Al Raaisi
- Stanislas Smajda
- David Weisenburger-Lile
- Benoit Ho-Tin-Noé (ORCID: https://orcid.org/0000-0002-7428-1760)
Institutions
- Université Claude Bernard Lyon 1 (FR)
- Inserm (FR)
- University of Liège (BE)
- Délégation Paris 7 (FR)
- Université Fédérale de Toulouse Midi-Pyrénées (FR)
- Université Paris Cité (FR)
- Statistics Belgium (BE)
- Hôpital Pierre Wertheimer (FR)
- Fondation de Rothschild (FR)
- Centre Hospitalier Universitaire de Liège (BE)
- Centre de Recherche en Acquisition et Traitement de l'Image pour la Santé (FR)
- Hôpital Foch (FR)
- French Clinical Research Infrastructure Network (FR)
Publication Details
- Journal
- Stroke Vascular and Interventional Neurology
- Published
- 2026-09-17
- DOI
- https://doi.org/10.1161/svin.126.002475
- Primary Topic
- Acute Ischemic Stroke Management
- Type
- article
- Field-Weighted Citation Impact
- 0.00