Liu Chenyu, Shahid Mohammed, Yu Qian, Orra Susan, Ranganath Bharat, Chao Jerry W
From the George Washington University School of Medicine and Health Sciences.
George Washington University Hospital.
Plast Reconstr Surg. 2024 Jun 1;153(6):1240-1251. doi: 10.1097/PRS.0000000000010691. Epub 2023 May 16.
BACKGROUND: Breast augmentation is the most commonly performed procedure for gender affirmation in transfeminine individuals. Although adverse events among breast augmentation in cisgender women are well described, their relative incidence in transfeminine patients is less elucidated. This study aims to compare complication rates after breast augmentation between cisgender women and transfeminine patients and to evaluate the safety and efficacy of breast augmentation in transfeminine individuals. METHODS: PubMed, the Cochrane Library, and other resources were queried for studies published up to January of 2022. A total of 1864 transfeminine patients from 14 studies were included in this project. Primary outcomes including complications (capsular contracture, hematoma or seroma, infection, implant asymmetry/malposition, hemorrhage, skin or systemic complications), patient satisfaction, and reoperation rates were pooled. A direct comparison of these rates was performed against historical rates in cisgender women. RESULTS: Within the transfeminine group, the pooled rate of capsular contracture was 3.62% (95% CI, 0.0038 to 0.0908); the hematoma/seroma rate was 0.63% (95% CI, 0.0014 to 0.0134); the infection incidence was 0.08% (95% CI, 0.0000 to 0.0054); and implant asymmetry rate was 3.89% (95% CI, 0.0149 to 0.0714). There was no statistical difference between rates of capsular contracture ( P = 0.41) and infection ( P = 0.71) between the transfeminine versus cisgender groups, whereas there were higher rates of hematoma/seroma ( P = 0.0095) and implant asymmetry/malposition ( P < 0.00001) in the transfeminine group. CONCLUSION: Breast augmentation is an important procedure for gender affirmation and, in transfeminine individuals, carries relatively higher rates of postoperative hematoma and implant malposition relative to cisgender women.
背景:隆胸是跨性别女性进行性别确认时最常实施的手术。虽然顺性别女性隆胸后的不良事件已有详尽描述,但跨性别患者中这些不良事件的相对发生率尚不清楚。本研究旨在比较顺性别女性与跨性别患者隆胸后的并发症发生率,并评估跨性别个体隆胸的安全性和有效性。 方法:检索了截至2022年1月发表的研究的PubMed、Cochrane图书馆及其他资源。本项目纳入了14项研究中的1864名跨性别患者。汇总了包括并发症(包膜挛缩、血肿或血清肿、感染、植入物不对称/位置异常、出血、皮肤或全身并发症)、患者满意度和再次手术率等主要结局指标。将这些发生率与顺性别女性的历史发生率进行直接比较。 结果:在跨性别组中,包膜挛缩的汇总发生率为3.62%(95%CI,0.0038至0.0908);血肿/血清肿发生率为0.63 %(95%CI,0.0014至0.0134);感染发生率为0.08%(95%CI,0.0000至0.0054);植入物不对称率为3.89%(95%CI,0.0149至0.0714)。跨性别组与顺性别组之间包膜挛缩发生率(P = 0.41)和感染发生率(P = 0.71)无统计学差异,而跨性别组的血肿/血清肿发生率(P = 0.0095)和植入物不对称/位置异常发生率(P < 0.00001)较高。 结论:隆胸是性别确认的一项重要手术,对于跨性别个体而言,相对于顺性别女性,术后血肿和植入物位置异常的发生率相对较高。
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