Furman Michael B, Bernstein Jesse, Gilhool Lelia, Bednarek Christopher, Caplan Holden, Kurup Ajay, Schneider Byron J
Department of Physical Medicine and Rehabilitation, OSS Health, 1855 Powder Mill Rd, York, PA, 17402, USA.
Department of Physical Medicine and Rehabilitation, Monterey Spine and Joint, 12 Upper Ragsdale Drive, Monterey, CA, 93940, USA.
Interv Pain Med. 2023 Sep 13;2(3):100277. doi: 10.1016/j.inpm.2023.100277. eCollection 2023 Sep.
There is a lack of substantiated evidence to support or refute the risks of ceasing vs maintaining anticoagulant and/or antiplatelet medications (ACAP) prior to cervical and thoracic interlaminar epidural steroid injections. The ACAP medication is frequently stopped pre-procedure due to concerns for potential bleeding complications, particularly epidural hematomas (EH). This article provides evidence regarding EH incidence in this population.
Data for this study was collected retrospectively on all patients from September 19, 2009-Jun 16, 2017 who were scheduled for an Interlaminar Cervical and/or Thoracic Epidural Steroid Injections (IL-CTESI) and were on an ACAP medication at the time a procedure was scheduled. All possible adverse outcomes were then retrospectively analyzed via extensive data mining of the electronic medical record system with special emphasis on EHs.
591 IL-CTESI were performed on patients taking ACAP medications. In total, 351 patients ceased their ACAP medication prior to the procedure and 240 maintained ACAP medication. Our findings demonstrate that there were no clinically relevant incidents of EHs in either cohort.
This data gives critical insight into the post-procedural EH risk for patients who had continued or stopped taking their ACAP medications prior to their IL-CTESI. The results from this study suggest re-evaluating the potential post-procedural EH risks associated with continuing vs ceasing these medications.
对于在颈椎和胸椎椎间孔硬膜外类固醇注射之前停用或继续使用抗凝和/或抗血小板药物(ACAP)的风险,缺乏确凿的证据来支持或反驳。由于担心潜在的出血并发症,尤其是硬膜外血肿(EH),ACAP药物在术前经常被停用。本文提供了关于该人群中EH发生率的证据。
本研究的数据是回顾性收集的,对象为2009年9月19日至2017年6月16日期间所有计划进行颈椎和/或胸椎椎间孔硬膜外类固醇注射(IL-CTESI)且在安排手术时正在服用ACAP药物的患者。然后通过电子病历系统的广泛数据挖掘对所有可能的不良结局进行回顾性分析,特别关注EHs。
对服用ACAP药物的患者进行了591次IL-CTESI。总共有351名患者在手术前停用了ACAP药物,240名患者继续使用ACAP药物。我们的研究结果表明,两组中均未发生具有临床意义的EH事件。
这些数据为在进行IL-CTESI之前继续或停止服用ACAP药物的患者术后EH风险提供了重要见解。本研究结果表明,需要重新评估与继续或停用这些药物相关的术后EH潜在风险。