Ghaziri Dania, Bou Fakhreddine Hisham, Sawaya Fadi, Jaber Farah, Bou Akl Imad
Department of Pharmacy American University of Beirut Medical Center, Beirut, Lebanon.
Department of Internal Medicine American University of Beirut Medical Center, Beirut, Lebanon.
Case Rep Crit Care. 2024 Aug 21;2024:3839630. doi: 10.1155/2024/3839630. eCollection 2024.
In pulmonary embolism (PE), when used for catheter-directed thrombolysis (CDT), low-dose alteplase is associated with good outcomes. Tenecteplase has been only used as intravenous for this indication. In the context of our national economic crisis where alteplase was unavailable, we describe our experience with tenecteplase CDT. A 73-year-old male, hypertensive and smoker with COPD, presented to the ED with intermediate high-risk PE.(ED) with intermediate high-risk PE. Heparin infusion was initiated. A few hours later, the patient developed atrial fibrillation (AF) for which amiodarone infusion was started. Also, a left femoral and popliteal vein thrombosis was also confirmed by the lower extremity duplex. As the patient remained dyspneic with unstable vital signs, the decision was to perform a CDT. In the absence of alteplase, tenecteplase was used at 0.5 mg/h over 30 h, for a total of 15 mg. Twenty-four hours after tenecteplase initiation, dyspnea and vital signs had significantly improved. Oxygen support was gradually dropping to finally stop. Being on concomitant heparin infusion, the patient had a mild blood oozing at the femoral vein site of entry; however, this did not require any transfusion or discontinuation of heparin. The patient regained his baseline physical and mental functions and was discharged on enoxaparin and amiodarone tablet. This is the first experience describing the use of tenecteplase as part of CDT in a patient with acute intermediate high-risk PE. The combination to therapeutic heparin infusion, already described in different clinical scenarios with intravenous tenecteplase, was safe and well tolerated CDT with tenecteplase was, for the first time, safely and effectively used in an intermediate high-risk PE patient. However, more studies are needed to confirm and establish these findings.
在肺栓塞(PE)中,低剂量阿替普酶用于导管直接溶栓(CDT)时,疗效良好。替奈普酶仅用于该适应证的静脉给药。在我国经济危机且无阿替普酶可用的情况下,我们描述了使用替奈普酶进行CDT的经验。一名73岁男性,患有高血压、吸烟且患有慢性阻塞性肺疾病(COPD),因中度高危PE就诊于急诊科。开始静脉输注肝素。数小时后,患者发生心房颤动(AF),开始静脉输注胺碘酮。此外,下肢双功超声检查证实左股静脉和腘静脉血栓形成。由于患者仍有呼吸困难且生命体征不稳定,决定进行CDT。因无阿替普酶,使用替奈普酶以0.5mg/h的速度持续输注30小时,总量为15mg。替奈普酶开始输注24小时后,呼吸困难和生命体征明显改善。氧支持逐渐减少直至最终停止。在同时静脉输注肝素的情况下,患者股静脉穿刺部位有轻度渗血;然而,这并不需要任何输血或停用肝素。患者恢复了基线身心功能,出院时使用依诺肝素和胺碘酮片。这是首次描述在急性中度高危PE患者中使用替奈普酶作为CDT一部分的经验。在不同临床场景中已描述过的与静脉注射替奈普酶联合使用治疗性肝素输注的方法,是安全且耐受性良好的。替奈普酶CDT首次在中度高危PE患者中安全有效地使用。然而,需要更多研究来证实和确立这些发现。