Pharmacy Department at CoxHealth South National Avenue, Springfield, MO, USA.
CoxHealth Emergency Department, Springfield, MO, USA.
J Pharm Pract. 2023 Apr;36(2):221-226. doi: 10.1177/08971900211026839. Epub 2021 Jul 7.
The use of factor Xa inhibitors has grown in popularity; however, the risk of major bleeding events requires for the appropriate reversal agent. The recent approved agent for factor Xa inhibitor reversal, andexanet alfa, has limited clinical efficacy and safety data, and it can be a financial burden on healthcare systems due to its high cost. Four-factor prothrombin complex concentrate (4F-PCC) has been utilized off label in patients with factor Xa inhibitor-related bleedings. The aim of this study was to assess the safety and efficacy of 4F-PCC in managing factor Xa inhibitor-related bleedings.
This is an observational, retrospective review of 4F-PCC usage in treating factor Xa inhibitor-related bleeds from May 2014 to December 2018 at a single health system. Efficacy was evaluated using the assessment criteria described by Sarode et al. Secondary outcomes analyzed included thromboembolic events, length of stay, mortality, and discharge disposition.
Fifty-nine patient charts were reviewed, and 48 patients were included in the study analysis. The administration of 4F-PCC achieved effective hemostasis in 33 patients (68%), and effective hemostasis was achieved in 12 patients (86%) who had intracranial hemorrhage and did not receive any surgical intervention. Thromboembolic events occurred in 4 patients within 30 days from 4F-PCC use. A majority of patients (85.4%) were discharged from the hospital to home or long-term care; 7 patients (14.6%) expired in the hospital.
Efficacy was achieved in over half of the patient population in this cohort who received 4F-PCC for factor Xa inhibitor-related bleeding events.
Xa 因子抑制剂的应用日益普及;然而,大出血事件的风险需要使用适当的逆转剂。最近批准的 Xa 因子抑制剂逆转剂andexanet alfa 具有有限的临床疗效和安全性数据,并且由于其高成本,可能给医疗保健系统带来经济负担。四因子凝血酶原复合物浓缩物(4F-PCC)已被超适应证用于接受 Xa 因子抑制剂相关出血的患者。本研究旨在评估 4F-PCC 在管理 Xa 因子抑制剂相关出血中的安全性和疗效。
这是对 2014 年 5 月至 2018 年 12 月在单一医疗系统中使用 4F-PCC 治疗 Xa 因子抑制剂相关出血的观察性、回顾性研究。采用 Sarode 等人描述的评估标准评估疗效。分析的次要结局包括血栓栓塞事件、住院时间、死亡率和出院去向。
共回顾了 59 份患者病历,其中 48 份患者纳入研究分析。4F-PCC 的给药在 33 例患者(68%)中实现了有效的止血,在未接受任何手术干预的 12 例(86%)颅内出血患者中也实现了有效的止血。在使用 4F-PCC 后的 30 天内,有 4 例患者发生血栓栓塞事件。大多数患者(85.4%)从医院出院回家或长期护理;7 例(14.6%)在医院死亡。
在接受 4F-PCC 治疗 Xa 因子抑制剂相关出血的患者中,该队列的一半以上患者达到了疗效。