From the Division of Plastic and Reconstructive Surgery, Stanford Hospital and Clinics.
SUNY Upstate Medical University.
Plast Reconstr Surg. 2024 Dec 1;154(6):1309-1315. doi: 10.1097/PRS.0000000000011437. Epub 2024 Apr 2.
BACKGROUND: Conflicting data exist regarding increased perioperative venous thromboembolism (VTE) risk with feminizing hormone therapy. The effect has been poorly studied within the transgender population. Acute perioperative cessation of feminizing hormone therapy often leads to unpleasant side effects and exacerbates gender dysphoria in the perioperative period. The authors sought to identify VTE incidence in patients undergoing facial feminization surgery while continuing hormone replacement therapy throughout the time of surgery. METHODS: A 38-year retrospective cohort study within a 2-surgeon practice (D.K.O. and J.C.D.-B.) was designed to evaluate postoperative VTE in patients continuing hormone therapy. The primary outcome variable was postoperative VTE. RESULTS: A total of 1715 patients underwent facial feminization surgery within our search window. A total of 953 patients met final inclusion criteria. One patient (0.10%) was diagnosed with a VTE postoperatively, comparable to reported literature rates for similar cosmetic and orthognathic procedures. The average Caprini score of all patients was 3.1 ± 1.0 and the average case length was 491.9 ± 111.0 minutes. Subgroup analysis of patients before and after internal practice changes identified 714 patients (77.7%) continuing full-dose hormonal therapy perioperatively, 197 (20.7%) undergoing hormonal dose reduction to 25% to 50% perioperatively, and 8 who were either not taking hormonal therapy or stopped in the perioperative period. There was no significant difference in VTE incidence among the 3 subgroups ( P > 0.99). CONCLUSIONS: Perioperative use of feminizing hormonal therapy does not increase risk for perioperative VTE in patients undergoing facial feminization surgery. Therefore, it is reasonable to continue these medications through the time of surgery. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, III.
背景:关于女性激素治疗增加围手术期静脉血栓栓塞症(VTE)风险,存在相互矛盾的数据。在跨性别群体中,这一影响尚未得到充分研究。急性围手术期停止女性激素治疗往往会导致不愉快的副作用,并在围手术期加重性别焦虑。作者试图确定在继续激素替代治疗的情况下,接受面部女性化手术的患者的 VTE 发生率。
方法:设计了一项由两位外科医生(D.K.O.和 J.C.D.-B.)进行的 38 年回顾性队列研究,以评估继续激素治疗的患者术后 VTE。主要观察变量是术后 VTE。
结果:在我们的搜索窗口内,共有 1715 名患者接受了面部女性化手术。共有 953 名患者符合最终纳入标准。1 名患者(0.10%)术后诊断为 VTE,与类似美容和正颌手术的报告文献发生率相当。所有患者的平均 Caprini 评分均为 3.1±1.0,平均手术时间为 491.9±111.0 分钟。对术前和术后内部实践变化的患者进行亚组分析,发现 714 名患者(77.7%)在围手术期继续全剂量激素治疗,197 名患者(20.7%)在围手术期减少激素剂量至 25%至 50%,8 名患者未接受激素治疗或在围手术期停止治疗。这 3 个亚组之间的 VTE 发生率无显著差异(P>0.99)。
结论:在接受面部女性化手术的患者中,围手术期使用女性化激素治疗不会增加围手术期 VTE 的风险。因此,在手术期间继续使用这些药物是合理的。
临床问题/证据水平:治疗性,III 级。
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