J Neurol Surg A Cent Eur Neurosurg 2012; 73(03): 153-159
DOI: 10.1055/s-0032-1313724
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Prophylactic Intravenous Nimodipine Treatment in Skull Base Surgery: Pharmacokinetic Aspects[*]

C. Scheller
1   University of Halle-Wittenberg, Department of Neurosurgery, Halle (Saale), Germany
,
A.-S. Vogel
1   University of Halle-Wittenberg, Department of Neurosurgery, Halle (Saale), Germany
,
S. Simmermacher
1   University of Halle-Wittenberg, Department of Neurosurgery, Halle (Saale), Germany
,
J. C. Rachinger
1   University of Halle-Wittenberg, Department of Neurosurgery, Halle (Saale), Germany
,
J. Prell
1   University of Halle-Wittenberg, Department of Neurosurgery, Halle (Saale), Germany
,
C. Strauss
1   University of Halle-Wittenberg, Department of Neurosurgery, Halle (Saale), Germany
,
M. Reinsch
1   University of Halle-Wittenberg, Department of Neurosurgery, Halle (Saale), Germany
,
U. Kunter
2   Analytisches Zentrum Biopharm GmbH Berlin, Bioanalytics, Berlin, Germany
,
A. Wienke
3   University of Halle-Wittenberg, Institue for Medical Epidemilogy, Halle, Germany
,
J. Neumann
5   Institute of Pharmacology and Toxicology, University of Halle-Wittenberg, Halle, Germany
,
K. Scheller
4   University Halle-Wittenberg, Oral and Maxillofacial Plastic Surgery, Halle, Germany
› Author Affiliations
Further Information

Publication History

Publication Date:
03 May 2012 (online)

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Abstract

Background Nimodipine is primarily used in subarachnoid hemorrhage (SAH). Clinical trials revealed also a beneficial effect of prophylactic nimodipine treatment on cranial nerve functions following vestibular schwannoma surgery.

Objective The unknown pharmacokinetics of prophylactically administered nimodipine were investigated.

Methods Samples were taken from 27 patients with skull base lesions. Prophylactic intravenous nimodipine infusion was started 5.8–25.8 h (mean 17.9 h) before surgery. Nimodipine concentrations were determined in serum (intra- and postoperatively), cerebrospinal fluid (CSF) (intraoperatively), and tissue samples.

Results Wide interindividual differences were observed. Mean concentrations for nimodipine were 46.9 ng/ml (SD: 6.4; min. 4.1 and max. 92.7 ng/ml) in intraoperative serum, 73.2 ng/ml (SD: 16.7; min. 6.6 and max. 253 ng/ml) in postoperative serum and 8.3 ng/ml (SD: 1.5; min. 1.0 und max. 29.7 ng/ml) in intraoperative CSF. The correlation between intra- and postoperative serum (p=0.004, r=0.560) and between intra­operative serum and CSF concentration (p=0.003, r=0.567) were statistically significant. Furthermore the correlation between intraoperative serum concentration and concentrations collected from vestibular nerves was high (r=0.711), but not statistically significant (p=0.178).

Conclusions Interindividually, continously administered intravenous nimodipine produces considerably variable serum levels. Controls of nimodipine serum concentrations may be useful to optimize nimodipine medication in skull base surgery and in the management of SAH. The serum nimodipine level is a useful marker for CSF and intracranial nerve tissue concentrations of nimodipine.

* This article was originally published online in Central European Neurosurgery on January 12, 2012 (DOI: 10.1055/s-0031-1291207)