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Updated: Jun 23, 2025

Pre-Chiasmatic, Single Injection of Autologous Blood to Induce Experimental Subarachnoid Hemorrhage in a Rat Model
Published on: June 18, 2021
Cerebrospinal Fluid Pharmacokinetics of Nicardipine Following Intrathecal Administration in Subarachnoid Hemorrhage
Ofer Sadan1, Yoo-Seong Jeong2, Shany Cohen-Sadan1
1Department of Neurology and Neurosurgery, Division of Neurocritical Care, Emory University School of Medicine, Atlanta, GA, USA.
Insights
This study characterizes the population pharmacokinetics of intrathecal nicardipine in subarachnoid hemorrhage patients, finding intracranial pressure affects drug clearance and volume. Dosing every 6 or 8 hours showed similar outcomes.
Area of Science:
- Neuroscience
- Pharmacology
- Clinical Pharmacy
Background:
- Subarachnoid hemorrhage (SAH) is a severe stroke with high mortality.
- Cerebral vasospasm and delayed cerebral ischemia (DCI) are major complications impacting SAH patient outcomes.
- Intrathecal (IT) nicardipine is an off-label intervention showing promise in reducing DCI and improving outcomes.
Purpose of the Study:
- To characterize the population pharmacokinetic (popPK) properties of intermittent IT nicardipine in SAH patients.
- To develop a popPK model describing nicardipine disposition in cerebrospinal fluid (CSF).
- To investigate the influence of patient factors on IT nicardipine pharmacokinetics.
Main Methods:
- Serial CSF samples were collected from 16 SAH patients receiving IT nicardipine (q6h or q8h).
- High-performance liquid chromatography quantified CSF nicardipine concentrations.
- A two-compartment popPK model with lag time was developed and validated.
Main Results:
- The popPK model adequately described IT nicardipine CSF pharmacokinetics.
- Intracranial pressure significantly influenced nicardipine total clearance and central volume (negative correlation).
- Pharmacokinetic parameters were comparable between q6h and q8h dosing regimens.
Conclusions:
- A reliable popPK model for IT nicardipine in SAH patients was successfully developed.
- Intracranial pressure is a key factor influencing IT nicardipine disposition.
- Findings may guide future clinical trials for optimizing IT nicardipine dosing strategies.
Abstract:
Subarachnoid hemorrhage (SAH) is a devastating type of stroke, leading to high mortality and morbidity rates. Cerebral vasospasm and delayed cerebral ischemia (DCI) are common complications following SAH that contribute significantly to the poor outcomes observed in these patients. Intrathecal (IT) nicardipine delivered via an existing external ventricular drain is an off-label intervention that has been shown to be correlated with reduced DCI and improved patient outcomes. The current study aims to characterize the population pharmacokinetic (popPK) properties of intermittent IT nicardipine. Following informed consent, serial cerebrospinal fluid (CSF) samples were obtained from 16 SAH patients (50.4 ± 9.3 years old; 13 females) treated with IT nicardipine every 6 h (q6h, n = 8) or every 8 h (q8h, n = 8) for an average of 72 ± 21 doses. High-performance liquid chromatography was used to quantify CSF concentration from each sample. Our popPK analysis showed that the CSF pharmacokinetics of IT nicardipine in the cohort was adequately described by a two-compartment model with a lag time. Model parameter estimates were reliable (relative standard error <50%). Intracranial pressure influenced both the total clearance and the central volume of nicardipine (i.e., negative correlation, P <-.001). Calculated PK parameters were similar between q6h and q8h dosing regimens. Despite a small cohort of SAH patients, we successfully developed a popPK model to describe the nicardipine disposition kinetics in the CSF following IT administration. These findings may help inform future clinical trials designed to examine the optimal dosing of IT nicardipine.
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