American Society of Hirudotherapy

Safety and efficacy of argatroban combined with antiplatelet therapy for acute mild-to-moderate ischemic stroke with large artery atherosclerosis

Research article published in Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association (2025)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportDrug DevelopmentYan et al. · Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 2025

Abstract

BACKGROUND AND PURPOSE: Patients with stroke due to large artery atherosclerosis are at risk of early progression and recurrence. The efficacy and safety of argatroban in stroke patients who did not receive reperfusion therapy, and which patients may benefit from it, are uncertain. METHODS: We conducted a cohort study to assess whether argatroban given within 72 hours of symptom onset, combined with antiplatelet therapy, improved neurological outcomes of patients with acute mild to moderate ischemic stroke in China. Patients were divided into the combined treatment group and the control group. Inverse probability of treatment weighting was used to balance baseline covariates. The primary efficacy outcome is the proportion of mRS score 0-2 at 90 days. The secondary efficacy outcomes included END proportion, change in NIHSS score from the baseline to day 7, recurrent cardiovascular events, and cardiovascular death. The safety outcomes were hemorrhagic transformation (HT) of infarction and organ hemorrhage at 7 days. RESULTS: Compared with the control group, a higher proportion of mRS (0-2) at 90 days was found in patients in the combined treatment group (85.3% vs 74.5%, p=0.042). There was no significant difference in the safety outcomes between the two groups. Exploratory subgroup analysis showed positive associations with argatroban combined therapy and good prognosis in NIHSS score ≥5 and age ≥70 subgroups. CONCLUSIONS: Our study suggested that argatroban can improve neurological outcomes for mild to moderate LAA patients but not increase the risk of bleeding.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal Article
Indexed MeSH termsHumansPipecolic AcidsArginineMaleFemaleSulfonamidesAgedMiddle AgedTreatment OutcomeIschemic StrokePlatelet Aggregation InhibitorsDrug Therapy, Combination

Summary

Peer-reviewed pharmacology and drug-development research relevant to anticoagulants and leech-derived compounds. Indexed in PubMed and verified against the NCBI record.

Why This Matters for Hirudotherapy

This cohort study assessed whether argatroban, a synthetic direct thrombin inhibitor, given within 72 hours of onset and combined with antiplatelet therapy, improved outcomes in acute mild-to-moderate ischemic stroke due to large-artery atherosclerosis; using inverse-probability weighting, the combined-treatment group had a higher proportion of mRS 0-2 at 90 days (85.3% vs 74.5%, p=0.042) with no significant difference in bleeding or other safety outcomes, and the authors concluded argatroban can improve neurological outcomes without raising bleeding risk. For hirudotherapy, the relevance is mechanistic rather than direct: argatroban inhibits thrombin, the same coagulation enzyme targeted by the leech peptide hirudin, so the study illustrates the clinical reach of the direct-thrombin-inhibitor class that hirudin pioneered. Caveat: this is an observational cohort (not a randomized trial) of a synthetic drug in stroke patients in China — it does not evaluate medicinal-leech therapy, and the weighted associations require confirmation in prospective randomized studies.

Citation

Safety and efficacy of argatroban combined with antiplatelet therapy for acute mild-to-moderate ischemic stroke with large artery atherosclerosis.

Yan et al. · Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 2025

Added to ASH library: May 29, 2026 · Site last updated: June 18, 2026

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