Observational studyNeuroradiology2025
Dose-response and infusion duration of intra-arterial nimodipine in cerebral vasospasm after aneurysmal subarachnoid hemorrhage: a single-center case series.
Observational study in Neuroradiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05276934 (Prospective Assessment of Brain Imaging After Aneurysmal of AVM-related Intracranial Hemorrhage), which is not on this map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Prospective Assessment of Brain Imaging After Aneurysmal of AVM-related Intracranial Hemorrhage
Who cites it
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
12 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThis single-center case series evaluates the effects on arterial diameter, perfusion imaging, and safety of intra-arterial (IA) nimodipine administration for CV following aSAH.
methodsIn this prospective single-center observational study (SAVEBRAIN PWI; NCT05276934), 14 patients with CV refractory to medical treatment were treated with IA nimodipine. We assessed changes in vessel diameter and perfusion parameters pre- and post-treatment. Associations between nimodipine dose, infusion duration, and outcomes were analyzed using regression models.
resultsThe median age of patients was 48 years; 50% were male. The median nimodipine dose was 2.00 mg with a median infusion duration of 10 minutes. Post-treatment, the median artery diameter increased from 1.50 mm to 1.90 mm (25% change), TMAX decreased from 2.58 to 2.11 seconds, and TTD decreased from 4.58 to 4.09 seconds. Higher nimodipine doses (> 2 mg) were associated with increased odds of hypotension requiring injection breaks (OR 3.6, 95% CI 2.1 to 5.6, p < 0.001). Retreatment was necessary in 69% of cases, with a median time to retreatment of 2 days.
conclusionsIA nimodipine administration appears to improve vascular diameters and perfusion parameters in CV following aSAH but carries a significant risk of hypotension, especially at doses > 2 mg. Longer infusion durations may reduce hypotension risk. These findings emphasize the need for careful dose management and further research to standardize treatment protocols.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.