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Successful Spinal Cord Stimulator Trial Placement in a Patient with Presumed Heparin-Induced Thrombocytopenia Treated with Argatroban: A Case Report
Author(s) -
Ravneet Bhullar
Publication year - 2020
Publication title -
interventional pain management reports
Language(s) - English
Resource type - Journals
ISSN - 2575-9841
DOI - 10.36076/pmcr.2020/4/61
Subject(s) - medicine , argatroban , spinal cord stimulator , anesthesia , discontinuation , surgery , dabigatran , spinal cord , warfarin , spinal cord stimulation , platelet , psychiatry , thrombin , atrial fibrillation
Background: Interventional pain procedures such as spinal cord stimulator placement are safely performed whenanticoagulation medications are discontinued beforehand in accordance with published recommendations.However, current guidelines for direct thrombin inhibitors are limited to dabigatran, rivaroxaban,apixaban, and edoxaban. One recommendation is to allow a 5-half-life interval between discontinuationof these medications and a high-risk interventional spine procedure to avoid complications such as spinalhematoma.Case Report: We report a case of a 53-year-old woman with multiple comorbidities who was placed on a heparin infusionafter presenting with acute radial artery occlusion and right hand ischemia. The patient underwentvascular bypass of the right arm and then developed compartment syndrome postoperatively, which wastreated via fasciotomy. The patient subsequently developed heparin-induced thrombocytopenia and beganargatroban for anticoagulation. The patient developed severe right upper extremity ischemic pain, but bothmedical management and treatment via peripheral nerve catheters failed to control her pain. A cervicalspinal cord stimulator trial was placed. The patient did not report significant pain relief after 7 days, sothe spinal cord stimulator was removed. Five half-lives were used for discontinuation of argatroban beforeboth spinal cord stimulator trial lead placement and removal. Five half-lives were also used for restartingargatroban following these procedures. No complications were seen with the placement or removal ofspinal cord stimulator leads.Conclusion: This case report demonstrates that discontinuing argatroban 5 half-lives before cervical spinal cord stimulatortrial placement can be done safely in this patient population and reveals the need for larger casestudies to provide additional evidence for guideline recommendations.Key words: Anticoagulation guidelines, direct thrombin inhibitors, interventional pain, interventional spine, ischemicpain, neuromodulation

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