An Evaluation of the Safety of Half-Dose Direct Oral Anticoagulants Following Total Joint Arthroplasty: A Pilot Study.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL Cureus Pub Date : 2024-10-24 eCollection Date: 2024-10-01 DOI:10.7759/cureus.72283
Harrison A Patrizio, Rex W Lutz, Stephanie A Kwan, Adam Lencer, Gregory K Deirmengian
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Abstract

Background Total joint arthroplasty (TJA) patients on preoperative anticoagulation therapy present a challenge for adult reconstruction surgeons. The goal in managing such patients is to limit bleeding complications associated with administering the medications while preventing medical complications from withholding them. At our institution, we began a protocol in 2017 that utilizes a half-dose direct oral anticoagulant (DOAC) regimen for one week followed by resuming of the full-dose regimen in select patients who underwent TJA. This study investigated the 90-day safety profile associated with this protocol compared to previous literature. Methodology A retrospective review of 898 patients from a single institution was conducted including all patients receiving a half-dose DOAC protocol for one week followed by resuming of the full-dose regimen after total knee and total hip arthroplasty between 2017 and 2022. Data were collected on patient demographics, type of surgery, and DOAC dosage. Ninety-day complications were collected and separated into reduced dose complications of DOAC (such as cerebrovascular accidents (CVAs) or venothrombotic events (VTEe)) and DOAC therapy-related complications (including wound and bleeding complications). Results In the total hip arthroplasty (THA) subgroup (n = 396, 44.10%), there were four major VTE occurrences, aligning with the range seen in historical protocols. Deep vein thrombosis (DVT) and pulmonary embolism (PE) incidents were three and one, respectively, both within the historical range. In the total knee arthroplasty (TKA) subgroup of 502 (55.90%) patients, there were seven major VTE events, with five DVTs and two PEs, also aligning with historical ranges. Medical complications in the THA group included no CVA events and one myocardial infarction, with the latter slightly higher than the historical range. In the TKA group, there were two medical complications, both being CVAs. Regarding bleeding complications, THA patients showed four major bleeding incidents, two blood transfusions, and two hemorrhages, with these numbers comparable to or lower than historical ranges. There were seven minor bleeding events. For TKA, there were two major bleeding events, two blood transfusions, no hemorrhages, and five minor bleeding events. Wound complications in THA included five surgery-related complications, two cases of wound dehiscence, and three infections. TKA patients experienced 17 surgery-related complications, six cases of wound dehiscence, and 11 infections. Conclusions This study suggests that the half-dose DOAC protocol in patients undergoing TJA is non-inferior to historical full-dose DOAC protocols warranting further investigation to generalize across broader populations.

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评估全关节成形术后半剂量直接口服抗凝药的安全性:试点研究。
背景 接受术前抗凝治疗的全关节成形术(TJA)患者给成人重建外科医生带来了挑战。管理这类患者的目标是限制因用药而引起的出血并发症,同时防止因停药而出现医疗并发症。我院于 2017 年开始实施一项方案,在接受 TJA 的特定患者中使用半剂量直接口服抗凝剂 (DOAC) 方案一周,然后恢复全剂量方案。本研究调查了与以往文献相比,该方案的 90 天安全性概况。方法 对一家医疗机构的 898 例患者进行回顾性研究,包括 2017 年至 2022 年间所有接受半剂量 DOAC 方案一周后恢复全剂量方案的全膝关节和全髋关节置换术患者。收集的数据包括患者人口统计学、手术类型和 DOAC 剂量。收集的九十天并发症分为DOAC减量并发症(如脑血管意外(CVA)或静脉血栓事件(VTEe))和DOAC治疗相关并发症(包括伤口和出血并发症)。结果 在全髋关节置换术(THA)亚组(n = 396,44.10%)中,发生了四次主要的 VTE 事件,与历史方案中的范围一致。深静脉血栓(DVT)和肺栓塞(PE)分别为3例和1例,均在历史范围内。在由 502 名(55.90%)患者组成的全膝关节置换术(TKA)亚组中,共发生了 7 起重大 VTE 事件,其中 5 起为深静脉血栓,2 起为肺栓塞,也符合历史记录范围。THA组的医疗并发症包括无CVA事件和1例心肌梗死,后者略高于历史范围。TKA组有两例医疗并发症,均为CVA。在出血并发症方面,THA 患者发生了四次大出血、两次输血和两次出血,这些数字与历史范围相当或更低。有七次轻微出血事件。在全膝关节置换术中,有两例大出血、两例输血、无出血和五例轻微出血。THA的伤口并发症包括五例手术相关并发症、两例伤口开裂和三例感染。TKA患者出现17例手术相关并发症、6例伤口裂开和11例感染。结论 本研究表明,在接受 TJA 手术的患者中,半剂量 DOAC 方案不劣于以往的全剂量 DOAC 方案,值得进一步研究,以便在更广泛的人群中推广。
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