LETTER TO EDITOR
|Year : 2013 | Volume
| Issue : 5 | Page : 531--532
A case of post varicella cortical venous thrombosis successfully treated with dabigatran
Thomas Mathew, Alexander Manuel Lobo, Gosala Raja Kukkuta Sarma, Raghunandan Nadig
Department of Neurology, St. John's Medical College Hospital, Bangalore, Karnataka, India
Department of Neurology, St. John«SQ»s Medical College Hospital, Bangalore, Karnataka
|How to cite this article:|
Mathew T, Lobo AM, Kukkuta Sarma GR, Nadig R. A case of post varicella cortical venous thrombosis successfully treated with dabigatran.Neurol India 2013;61:531-532
|How to cite this URL:|
Mathew T, Lobo AM, Kukkuta Sarma GR, Nadig R. A case of post varicella cortical venous thrombosis successfully treated with dabigatran. Neurol India [serial online] 2013 [cited 2022 Aug 18 ];61:531-532
Available from: https://www.neurologyindia.com/text.asp?2013/61/5/531/121939
Dabigatran is a novel reversible direct thrombin inhibitor and does not need monitoring.  It has been recently approved by the Food and Drug Administration for use in stroke prevention in nonvalvular atrial fibrillation , and has been proven to be noninferior to warfarin in the prevention of recurrent venous thromboembolism in two recent double-blinded randomized controlled studies.  Here, we describe a patient with cortical venous sinus thrombosis, following varicella infection treated successfully with dabigatran.
A 33-year-old married lady with no previous comorbidities presented with vesiculopapular rash over the body and head of 10 days duration which has been diagnosed as varicella zoster infection and was treated with acyclovir. Six days later, she developed severe right hemicranial headache associated with vomiting. Clinical examination revealed bilateral papilledema. Magnetic resonance imaging and venography revealed thrombosis of right transverse, sigmoid, and straight sinuses without venous infarcts or hemorrhages. She had no history of recent pregnancy, abortions, or oral contraceptive use. There was no family history of thrombotic episodes. As she had extensive skin lesions over the body precluding the use of subcutaneous heparin and follow-up for coagulation monitoring was doubtful as she resided in a remote area, it was decided to use dabigatran for anticoagulation. After obtaining an informed consent, the patient was started on 150 mg twice a day of dabigatran along with antiedema measures. Patient reported relief of headache within 2 days of treatment and was discharged on the 4 th day of admission. She has followed-up with us with complete relief of headache and resolution of papilledema.
Dabigatran is finding favor among clinicians because its rapid onset of action and favorable safety profile.  It has a predictable anticoagulation effect that precludes frequent coagulation monitoring and has minimal food and drug interactions. Due to its rapid onset of action, it does not require bridging therapy with heparin and its analogues thereby cutting hospital stay and costs.
Current therapeutic options for cortical venous sinus thrombosis include dose-adjusted intravenous heparin or body weight adjusted subcutaneous low molecular weight heparin, followed by oral anticoagulation ranging from 3 months to lifelong anticoagulation depending on risk factors. If proven efficacious, dabigatran could substitute traditional oral and intravenous/subcutaneous anticoagulants as a treatment option for cortical venous sinus thrombosis, thereby bringing down the need of intravenous/subcutaneous therapy, cost of treatment, and cumbersome monitoring of coagulation parameters.
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