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Meta-analysis of Shuxuening injection for vascular cognitive impairment reports improved cognitive scores in Chinese patients.

Meta-analysis of Shuxuening injection for vascular cognitive impairment reports improved cognitive s…
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Key Takeaway
Note limited certainty for Shuxuening injection in vascular cognitive impairment due to methodological weaknesses.

This systematic review and meta-analysis evaluates the efficacy and safety of Shuxuening injection (SXNI), a standardized injectable formulation of Ginkgo biloba leaf extract, in patients with vascular cognitive impairment. Data from 2,375 participants in China compared SXNI plus conventional treatment against conventional treatment alone. The primary outcome assessed was the Mini-Mental State Examination, with secondary outcomes including the Hasegawa Dementia Scale, Barthel Index, overall response rate, National Institutes of Health Stroke Scale, and adverse event incidence.

Patients receiving SXNI showed higher Mini-Mental State Examination scores with a mean difference of 3.61 (95% CI 3.06–4.17). Improvements were observed for the Hasegawa Dementia Scale (MD 1.30, 95% CI 0.21–2.39) and Barthel Index (MD 9.06, 95% CI 4.66–13.45). Overall response rate was higher (RR 1.27, 95% CI 1.21–1.33), while National Institutes of Health Stroke Scale scores were lower (MD -6.17, 95% CI -7.90 to -4.45).

Seven studies reported adverse events, showing no significant difference in incidence between groups (RR 0.72, 95% CI 0.36–1.44). Serious adverse events and discontinuations were not reported. The authors note significant limitations, including methodological weaknesses and uncertainty regarding the comparability of preparations from different manufacturers. The certainty of evidence is limited.

High-quality studies are needed to confirm these findings. Clinicians should interpret these results cautiously given the noted methodological constraints. The association between SXNI and improved outcomes may provide benefit, but causality remains unconfirmed.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
BackgroundShuxuening injection (SXNI), a standardized injectable formulation of Ginkgo biloba leaf extract, is widely used in China for vascular cognitive impairment (VCI), However, evidence-based evaluation remains limited.MethodsRandomized controlled trials published before 1 September 2025, were searched in eight databases. Patients had vascular cognitive impairment (VCI), with the control group receiving conventional treatment and the treatment group receiving additional SXNI therapy. The primary outcome was the Mini-Mental State Examination (MMSE), while secondary outcomes included the Hasegawa Dementia Scale (HDS), Barthel Index (BI), overall response rate, National Institutes of Health Stroke Scale (NIHSS), and adverse event incidence. Risk of bias was assessed using the revised Cochrane Risk of Bias tool. Risk ratios (RR) were used for binary variables; mean differences (MD) with 95% confidence intervals (CI) were used for continuous variables.ResultsTwenty-two trials (n = 2,375) were included. All trials were conducted in China between 2005 and 2025. Compared with the control group, SXNI was associated with higher MMSE (MD 3.61, 95% CI 3.06–4.17), HDS (MD 1.30, 95% CI 0.21–2.39), and BI (MD 9.06, 95% CI 4.66–13.45), a higher overall response rate (RR 1.27, 95% CI 1.21–1.33), and lower NIHSS (MD −6.17, 95% CI −7.90 to −4.45). Seven studies reported adverse events; and there was no significant difference in the incidence of adverse events (RR 0.72, 95% CI 0.36–1.44).ConclusionThe addition of SXNI to conventional treatment may provide additional benefits in cognition, neurological function, and activities of daily living with no significant increase in reported adverse events compared with conventional treatment. However, the certainty of evidence is limited by methodological weaknesses and uncertainty regarding the comparability of preparations from different manufacturers. Therefore, high-quality studies are needed to confirm these findings.Systematic Review Registrationhttps://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=557472, identifier CRD42024557472.
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