Waxman Aaron B, McElderry Hugh T, Gomberg-Maitland Mardi, Burke Martin C, Ross Edgar L, Bersohn Malcolm M, Pangarkar Sanjog S, Tarver James H, Zwicke Diane L, Feldman Jeremy P, Chakinala Murali M, Frantz Robert P, Thompson Geoffrey B, Torres Fernando, Rauck Richard L, Clagg Kathy, Durst Louise, Li Pei, Morris Marty, Southall Kara L, Peterson Leigh, Bourge Robert C
Brigham & Women's Hospital, Boston, MA.
University of Alabama at Birmingham, Birmingham, AL.
Chest. 2017 Dec;152(6):1128-1134. doi: 10.1016/j.chest.2017.04.188. Epub 2017 Jun 3.
Prostacyclins improve symptoms and survival in pulmonary arterial hypertension (PAH). In response to risks associated with external delivery systems, an implantable IV infusion system was developed. A multicenter, prospective, single-arm, clinical trial (DelIVery for PAH) was conducted to evaluate this system for treprostinil in PAH. This analysis describes the findings related to the implant procedure.
Patients (N = 64) with PAH (World Health Organization group 1) receiving stable IV treprostinil were enrolled. Patients were transitioned to a temporary peripheral IV infusion catheter prior to the procedure. System implantation was performed at 10 centers under general anesthesia or deep IV sedation by clinicians from various specialties. Central venous access was via the cephalic, subclavian, jugular, or axillary vein. Using an introducer and fluoroscopic guidance, the distal tip of the infusion catheter was placed at the superior caval-atrial junction. The catheter was tunneled from the venous access site to an abdominal subcutaneous pocket, where the pump was placed.
Of the 64 patients enrolled, four exited prior to implantation. All 60 implant procedures were successful. At baseline, all patients were receiving treprostinil via an external pump at a mean dose of 71.4 ± 27.8 ng/kg/min (range: 22-142 ng/kg/min). The implant averaged 102 ± 32 min (range: 47-184 min). Clinically significant implant procedure-related complications included one pneumothorax, two infections, and one episode of atrial fibrillation. There were three postimplantation catheter dislocations in two patients. Common implant-related events that were not complications included implant site pain (83%) and bruising (17%).
The procedure for inserting a fully implantable system for treprostinil was successfully performed, with few complications.
ClinicalTrials.gov; No.: NCT01321073; URL: www.clinicaltrials.gov.
前列环素可改善肺动脉高压(PAH)患者的症状并提高其生存率。鉴于外部输送系统存在相关风险,研发了一种植入式静脉输液系统。开展了一项多中心、前瞻性、单臂临床试验(PAH的DelIVery试验),以评估该系统用于PAH患者曲前列尼尔治疗的效果。本分析描述了与植入手术相关的研究结果。
纳入64例接受稳定静脉注射曲前列尼尔治疗的PAH患者(世界卫生组织1组)。术前患者改用临时外周静脉输液导管。10个中心的临床医生在全身麻醉或深度静脉镇静下为患者进行系统植入,涉及多个专业。中心静脉通路通过头静脉、锁骨下静脉、颈静脉或腋静脉建立。在导丝引导和透视引导下,将输液导管的远端置于上腔静脉与心房交界处。导管从静脉通路部位经皮下隧道引至腹部皮下囊袋,在此处放置泵。
64例纳入患者中,4例在植入前退出。所有60例植入手术均成功。基线时,所有患者均通过外部泵接受曲前列尼尔治疗,平均剂量为71.4±27.8 ng/kg/min(范围:22 - 142 ng/kg/min)。植入手术平均用时102±32分钟(范围:47 - 184分钟)。与植入手术相关的具有临床意义的并发症包括1例气胸、2例感染和1例房颤发作。2例患者出现3次植入后导管移位。与植入相关的常见非并发症事件包括植入部位疼痛(83%)和瘀斑(17%)。
成功实施了用于曲前列尼尔的完全植入式系统的插入手术,并发症较少。
ClinicalTrials.gov;编号:NCT01321073;网址:www.clinicaltrials.gov。