J Neurol Surg A Cent Eur Neurosurg 2014; 75(01): 002-006
DOI: 10.1055/s-0033-1345686
Original Article
Georg Thieme Verlag KG Stuttgart · New York

Therapeutic Anticoagulation After Craniotomies: Is the Risk for Secondary Hemorrhage Overestimated?

Christian Scheller
1   Department of Neurosurgery, University of Halle-Wittenberg, Halle, Germany
,
Jens Rachinger
1   Department of Neurosurgery, University of Halle-Wittenberg, Halle, Germany
,
Christian Strauss
1   Department of Neurosurgery, University of Halle-Wittenberg, Halle, Germany
,
Alex Alfieri
1   Department of Neurosurgery, University of Halle-Wittenberg, Halle, Germany
,
Julian Prell
1   Department of Neurosurgery, University of Halle-Wittenberg, Halle, Germany
,
Gershom Koman
1   Department of Neurosurgery, University of Halle-Wittenberg, Halle, Germany
› Author Affiliations
Further Information

Publication History

12 July 2012

14 January 2013

Publication Date:
19 August 2013 (online)

Abstract

Objective Deep venous thrombosis (DVT) and pulmonary embolism (PE) are major causes of postoperative morbidity and mortality in surgery. However, there is neither a standardized protocol for perioperative prevention of DVT or PE in neurosurgery nor a consensus concerning the management of postoperative DVT or PE after craniotomy in the early postoperative course.

Methods We retrospectively analyzed management and complications in a group of patients with postoperative DVT or PE after craniotomy between 2006 and 2011 to estimate the risk of secondary hemorrhage under therapeutic anticoagulation. The interval between time of craniotomy and diagnosis of PE or DVT, administered anticoagulation, and the appearance of a clinically relevant secondary hemorrhage were analyzed.

Results Forty-two patients met the given criteria. Indications for surgery were intracranial tumors (n = 33), aneurysms (n = 5), and hematomas (n = 4). PE or DVT was observed between the first and the 28th postoperative day (median, fifth postoperative day). Therapeutic anticoagulation was performed with enoxaparin or heparin (according to partial thromboplastin time levels). Full heparinization was applied in 30 patients between the second and the 30th postoperative day (median, 12th postoperative day). None of these patients developed a secondary hemorrhage.

Conclusion The documented differences in the anticoagulative drug used, the drug's dosage, and the start of medication reflect the lack of a standardized protocol concerning the treatment of postoperative PE or DVT after craniotomy. A more aggressive management regarding the application of anticoagulative drugs after craniotomy may be justified considering the absence of clinically relevant hemorrhages in this study and the life-threatening potential of perioperative DVT or PE.

 
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