Aesthet Surg J. 2024 Oct 15;44(11):NP749-NP761. doi: 10.1093/asj/sjae156.
Rhytidectomy poses a significant risk of bleeding. Several studies have reported the safety profile and efficacy of tranexamic acid (TXA), an antifibrinolytic agent, in minimizing perioperative sequelae, particularly hematoma and bleeding.
The aim of this systematic review was to analyze the effect of TXA administration in facelift surgery, its effect with different routes of administration, and to compare different administration routes in reducing intraoperative blood loss, postoperative edema, and ecchymosis in rhytidectomy.
A systematic literature search was conducted to identify studies that reported on TXA in facelift surgery. The primary outcomes of interest were intraoperative blood loss, time to achieve hemostasis, operation duration, and postoperative hematoma, edema, ecchymosis, drain output, and major and minor complications. Meta-analyses of hematoma, operation duration, drain output, and major and minor complications were performed, and the risk of bias was assessed with ROBINS-I for nonrandomized studies, and Cochrane's RoB 2.0, a tool for randomized controlled trials.
In total, 104 articles were included in the initial screening. Out of 388 participants 170 patients were administered TXA, predominantly female (over 91%), with ages from the late 50s to mid-60s. TXA administration varied, with subcutaneous injection being the most common method. The meta-analysis revealed that the pooled prevalence of minor and major hematoma in TXA recipients was remarkably low, with a significant reduction in the risk of minor hematoma (odds ratio [OR] = 0.18, 95% CI 0.05-0.62, P < .001) and no significant difference in major hematoma risk. Interestingly, TXA significantly reduced postoperative drainage compared to the controls (mean difference = -25.59, 95% CI, -30.4--20.77, P < .01). Additionally, neither minor nor major complications were significantly different between the TXA recipients and controls. Specifically, the pooled odds for the incidence of major complications were not significantly different (OR = 1.47, 95% CI, 0.23-9.19, P = .68), and similar results were found for minor complications (OR = 0.59, 95% CI, 0.23-1.48, P = .26).
TXA significantly reduces postoperative drain output and minor hematomas in facelift surgery without increasing major complications. It also reduces edema, ecchymosis, and intraoperative blood loss. However, further studies are required to explore the efficacy of TXA with different dosages and administration routes.
除皱术存在较大的出血风险。多项研究报告了氨甲环酸(TXA)这种抗纤维蛋白溶解剂在减少围手术期并发症(尤其是血肿和出血)方面的安全性和疗效。
本系统评价旨在分析 TXA 在面部提升术中的应用效果,不同给药途径的效果,并比较不同给药途径在减少术中失血量、术后水肿和瘀斑方面的效果。
系统检索了报告 TXA 在面部提升术中应用的研究。主要结局指标为术中失血量、达到止血时间、手术时间以及术后血肿、水肿、瘀斑、引流液排出量和主要及次要并发症。对血肿、手术时间、引流液排出量和主要及次要并发症进行了荟萃分析,并使用 ROBINS-I 评估非随机研究的偏倚风险,以及 Cochrane 的 RoB 2.0 评估随机对照试验的偏倚风险。
共纳入 104 篇初始筛选文章,388 名参与者中 170 名患者接受了 TXA 治疗,主要为女性(超过 91%),年龄在 50 多岁到 60 多岁之间。TXA 的给药方式多种多样,其中最常见的是皮下注射。荟萃分析显示,TXA 组患者的轻微和严重血肿发生率明显较低,且轻微血肿的风险显著降低(比值比 [OR] = 0.18,95%置信区间 [CI] 0.05-0.62,P <.001),而严重血肿的风险无显著差异。有趣的是,与对照组相比,TXA 显著减少了术后引流液排出量(平均差 = -25.59,95%CI,-30.4--20.77,P <.01)。此外,TXA 组与对照组的轻微和严重并发症发生率均无显著差异。具体来说,严重并发症的总发生率差异无统计学意义(OR = 1.47,95%CI,0.23-9.19,P =.68),轻微并发症也有类似的结果(OR = 0.59,95%CI,0.23-1.48,P =.26)。
TXA 可显著减少面部提升术中的术后引流液排出量和轻微血肿,且不增加严重并发症。它还可以减少水肿、瘀斑和术中失血量。然而,需要进一步研究来探讨不同剂量和给药途径的 TXA 的疗效。