Division of Head and Neck Oncology and Surgery, Department of Otolaryngology-Head and Neck Surgery, University of Arkansas for Medical Sciences, Little Rock.
Department of Anesthesiology, University of Arkansas for Medical Sciences, Little Rock.
JAMA Otolaryngol Head Neck Surg. 2021 Dec 1;147(12):1059-1064. doi: 10.1001/jamaoto.2021.1841.
Continuous vasopressor use in free-flap reconstruction is a point of contention among microvascular surgeons despite data demonstrating safety.
To investigate the association between continuous vasopressor use and the incidence of reoperation in the early postoperative period.
DESIGN, SETTING, AND PARTICIPANTS: In this cohort study, a retrospective medical record review was conducted of patients who underwent head and neck free-flap reconstructions between May 1, 2014, and October 31, 2019, in an academic tertiary care center. All patients undergoing free-flap reconstruction for head and neck defects were included.
Continuous intraoperative vasopressors.
Patient medical records were queried for demographic variables; intraoperative use of vasopressors; vasopressor type, duration, and infusion rate; reoperation within the first 5 postoperative days; and reason for reoperation.
Four hundred forty-nine consecutive free-flap reconstructions were performed on 426 patients. The mean age was 62 years (IQR, 55.7-71.1); 293 patients were men (65.3%), 380 were White (84.6%), 55 were Black (12.2%), and 14 were of other race or ethnicity (3.1%). A total of 174 patients received a continuous vasopressor during their reconstruction. Twenty-three reoperations occurred within 5 days postoperatively, 8 of which included vasopressors during initial intervention. Vasopressor type had no association with reoperation (4.5% vs 5.5% [8/174 vs 15/275, respectively] for patients who received vasopressors vs those who did not) (dobutamine odds ratio [OR], 1.02 [95% CI, 0.21-2.91]; dopamine OR, 1.48 [95% CI, 0.33-4.26]). No difference was seen in the duration (dobutamine OR, 1.50 [95% CI, 0.78-2.90]; dopamine OR, 0.87 [95% CI, 0.59-1.28]) or infusion rate (dobutamine OR, 1.50 [95% CI, 0.99-1.02]; dopamine OR, 1.00 [95% CI, 0.99-1.01]) of vasopressors between patients who underwent reoperation and those who did not. Analysis after the exclusion of reasons for reoperation that did not represent possible microvascular anastomosis failure (eg, Doppler malfunction, donor site complications) showed no increased propensity for reoperation (OR, 1.18; 95% CI, 0.27-3.9).
In this cohort study, use of vasopressors for extensive periods intraoperatively during free-tissue transfer appeared to have no association with the rate of reoperation within 5 days of intervention, regardless of agent used, simultaneous use of agents, type of free-flap operation performed, or reason for reoperation. This study adds to the body of literature supporting the judicious use of vasopressors in patients requiring intraoperative pharmacological pressure support during free-flap reconstruction.
尽管有数据表明其安全性,但连续使用血管加压素在游离皮瓣重建中仍是微血管外科医生争论的焦点。
研究连续使用血管加压素与早期术后再次手术的发生率之间的关联。
设计、地点和参与者:在这项队列研究中,对 2014 年 5 月 1 日至 2019 年 10 月 31 日期间在学术性三级护理中心接受头颈部游离皮瓣重建的患者进行了回顾性病历审查。所有接受头颈部缺损游离皮瓣重建的患者均包括在内。
术中连续使用血管加压素。
查询患者病历中的人口统计学变量;术中使用血管加压素;血管加压素的类型、持续时间和输注率;术后 5 天内再次手术;以及再次手术的原因。
在 426 名患者中进行了 449 例连续游离皮瓣重建。平均年龄为 62 岁(IQR,55.7-71.1);293 名男性(65.3%),380 名白人(84.6%),55 名黑人(12.2%),14 名其他种族或民族(3.1%)。共有 174 名患者在重建过程中接受了连续血管加压素治疗。23 例患者在术后 5 天内再次手术,其中 8 例在初次干预时使用了血管加压素。血管加压素的类型与再次手术无关(接受血管加压素的患者为 4.5%(8/174),未接受血管加压素的患者为 5.5%(15/275))(多巴酚丁胺比值比[OR],1.02[95%CI,0.21-2.91];多巴胺 OR,1.48[95%CI,0.33-4.26])。血管加压素的持续时间(多巴酚丁胺 OR,1.50[95%CI,0.78-2.90];多巴胺 OR,0.87[95%CI,0.59-1.28])或输注率(多巴酚丁胺 OR,1.50[95%CI,0.99-1.02];多巴胺 OR,1.00[95%CI,0.99-1.01])在再次手术和未再次手术的患者之间没有差异。排除了代表可能的微血管吻合失败的再次手术原因(例如,多普勒功能障碍、供区并发症)后进行的分析显示,再次手术的可能性没有增加(OR,1.18;95%CI,0.27-3.9)。
在这项队列研究中,游离组织转移术中长时间连续使用血管加压素似乎与干预后 5 天内再次手术的发生率无关,无论使用的药物、同时使用的药物、进行的游离皮瓣手术类型或再次手术的原因如何。这项研究增加了支持在需要游离皮瓣重建术中进行药理学压力支持的患者中合理使用血管加压素的文献证据。