Key result
Clopidogrel loading dose linked to ~85% lower risk of early neurological deterioration in branch atheromatous disease.
Why the study?
Many patients with branch atheromatous disease-type cerebral infarction experience neurological deterioration despite acute phase therapeutic interventions, and the efficacy of clopidogrel loading dose is unclear.
Does a clopidogrel loading dose reduce early neurological deterioration in patients with branch atheromatous disease-type cerebral infarction?
Cohort (n=95)
No
Does a clopidogrel loading dose reduce early neurological deterioration in patients with branch atheromatous disease-type cerebral infarction?
A 300 mg clopidogrel loading dose significantly reduces early neurological deterioration in patients with branch atheromatous disease-type cerebral infarction receiving combination antithrombotic therapy.
Clopidogrel loading was associated with reduced early deterioration in BAD; hypothesis-generating, warranting randomized confirmation before practice change.
Objective Despite aggressive therapeutic interventions during the acute phase of branch atheromatous disease (BAD)-type cerebral infarction, many patients, even those with a mild condition at the onset, experience neurological deterioration after hospitalization and develop serious deficits. We compared the therapeutic efficacy of multiple antithrombotic therapies for BAD between patients who received a clopidogrel loading dose (loading group; LG) and those without loading (non-loading group; NLG). Patients Between January 2019 and May 2022, patients with BAD-type cerebral infarction in the lenticulostriate artery admitted within 24 h of the onset were recruited. This study included 95 consecutive patients who received combination argatroban and dual antiplatelet therapy (aspirin and clopidogrel). Methods Patients were classified into the LG and NLG according to whether or not a loading dose of clopidogrel (300 mg) had been administered on admission. Changes in neurological severity [National Institutes of Health Stroke Scale (NIHSS) score] during the acute phase were retrospectively evaluated. Results There were 34 (36%) and 61 (64%) patients in the LG and NLG, respectively. On admission, the median NIHSS score was similar between the groups [LG: 2.5 (2-4) vs. NLG: 3 (2-4), p=0.771]. At 48 h following admission, the median NIHSS scores were 1 (0.25-4), and 2 (1-5) in the LG and NLG, respectively (p=0.045). Early neurological deterioration (END; defined as worsening of the NIHSS score by ≥4 points at 48 h after admission) occurred in 3% of LG and 20% of NLG patients (p=0.028). Conclusion Administration of a clopidogrel loading dose with combination antithrombotic therapy for BAD reduced END.
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Deguchi et al. (2023) conducted a cohort in Branch atheromatous disease (BAD)-type cerebral infarction (n=95). Clopidogrel loading dose vs. No clopidogrel loading dose was evaluated on Early neurological deterioration (worsening of NIHSS score by ≥4 points at 48 h after admission) (p=0.028). Administration of a 300 mg clopidogrel loading dose significantly reduced early neurological deterioration from 20% to 3% compared to no loading dose in patients with branch atheromatous disease.
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