Department of Surgery, Plastic and Reconstructive Surgery Service, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, Mailbox 24, New York, NY 10065, United States.
Department of Anesthesiology and Critical Care, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
J Plast Reconstr Aesthet Surg. 2021 Sep;74(9):2227-2236. doi: 10.1016/j.bjps.2021.01.017. Epub 2021 Feb 4.
Aggressive or restricted perioperative fluid management has been shown to increase complications in patients undergoing microsurgery. Goal-directed fluid therapy (GDFT) aims to administer fluid, vasoactive agents, and inotropes according to each patient's hemodynamic indices. This study assesses GDFT impact on perioperative outcomes of autologous breast reconstruction (ABR) patients, as there remains a gap in management understanding. We hypothesize that GDFT will have lower fluid administration and equivocal outcomes compared to patients not on GDFT.
A single-center retrospective review was conducted on ABR patients from January 2010-April 2017. An enhanced recovery after surgery (ERAS) using GDFT was implemented in April 2015. With GDFT, patients were administered intraoperative fluids and vasoactive agents according to hemodynamic indices. Patients prior to April 2015 were included in the pre-ERAS cohort. Primary outcomes included the amount and rate of fluid delivery, urine output (UOP), vasopressor administration, major (i.e., flap failure) and minor (i.e., seroma) complications, and length of stay (LOS).
Overall, 777 patients underwent ABR (ERAS: 312 and pre-ERAS: 465). ERAS patients received significantly less total fluid volume (ERAS median: 3750 mL [IQR: 3000-4500 mL]; pre-ERAS median: 5000 mL [IQR 4000-6400 mL]; and p<0.001), had lower UOP, were more likely to receive vasopressor agents (47% vs 35% and p<0.001), and had lower LOS (ERAS: 4 days [4-5]; pre-ERAS: 5 [4-6]; and p<0.001) as compared to pre-ERAS patients. Complications did not differ between cohorts.
GDFT, as part of ERAS, and the prudent use of vasopressors were found to be safe and did not increase morbidity in ABR patients. GDFT provides individualized perioperative care to the ABR patient.
已证明,在接受显微手术的患者中,积极或限制围手术期液体管理会增加并发症。目标导向液体治疗(GDFT)旨在根据每个患者的血流动力学指标给予液体、血管活性药物和正性肌力药物。本研究评估了 GDFT 对自体乳房重建(ABR)患者围手术期结局的影响,因为在管理理解方面仍存在差距。我们假设 GDFT 的液体给药量较低,与未接受 GDFT 的患者相比,结果相似。
对 2010 年 1 月至 2017 年 4 月期间接受 ABR 的患者进行了单中心回顾性研究。2015 年 4 月实施了术后加速康复(ERAS)并使用 GDFT。使用 GDFT 时,根据血流动力学指标给予患者术中液体和血管活性药物。2015 年 4 月前的患者被纳入 ERAS 前队列。主要结局包括液体输送量和速率、尿量(UOP)、血管加压剂给药、主要(即皮瓣失败)和次要(即血清肿)并发症以及住院时间(LOS)。
总体而言,有 777 名患者接受了 ABR(ERAS:312 例,ERAS 前:465 例)。ERAS 患者接受的总液体量明显较少(ERAS 中位数:3750ml[IQR:3000-4500ml];ERAS 前中位数:5000ml[IQR:4000-6400ml];p<0.001),UOP 较低,更可能使用血管加压剂(47%比 35%,p<0.001),LOS 较短(ERAS:4 天[4-5];ERAS 前:5[4-6];p<0.001)与 ERAS 前患者相比。两组并发症无差异。
作为 ERAS 的一部分,GDFT 和谨慎使用血管加压剂被发现是安全的,并且不会增加 ABR 患者的发病率。GDFT 为 ABR 患者提供个体化围手术期护理。