[Cerebrolysin and the optimal timing of anticoagulation resumption in stroke: combined post hoc survival analysis of the CEREHETIS trial].
Kalinin MN, Khasanova DR · 2025 · Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova; 2025
Study findings
The analysis modeled hemorrhagic-transformation risk over time and reported lower hazards with Cerebrolysin in selected risk groups.
- Population and setting
- CEREHETIS post hoc analysis plus observational validation cohort
- Evidence type
- Human comparative study
- Preparation
- See the original report; formulation details require verification.
- Source language
- rus
- Title source
- Title as recorded in the linked source or index. A separate original-language title has not been transcribed unless shown above.
Study limitations
- Model-derived anticoagulation timing is not validated prescribing guidance.
- Reuses CEREHETIS participants; separate publication does not mean independent confirmation.
- Full methods and risk of bias have not been independently assessed.
Publication counts are not counts of independent trials. Reviews, translations and reports sharing participants may overlap. Findings apply to the studied preparation, population and endpoints.
Related-report group: CEREHETIS. Reports in this group are not assumed to be independent trials.
Source access and review scope
Indexed record and available abstract checked; full text not reviewed.
Recorded source-check date: 2026-10-07. This date does not imply a completed systematic review.
Citation and original source
Original source: Kalinin MN, Khasanova DR. [Cerebrolysin and the optimal timing of anticoagulation resumption in stroke: combined post hoc survival analysis of the CEREHETIS trial]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova; 2025 2025.
Molekul research summary: https://molekul.io/research/cbl-update-40123141. Cite the original publication for its findings and this page when referring to Molekul’s summary or evidence appraisal.
Bibliography entry