Systemic vs. in-irrigation tranexamic acid in percutaneous nephrolithotomy

被引:0
|
作者
Hinojosa-Gonzalez, David E. [1 ]
Somani, Bhaskar [2 ]
Olvera-Posada, Daniel [3 ]
Segall, Michal [4 ]
Villanueva-Congote, Juliana [5 ]
Eisner, Brian H. [5 ]
机构
[1] Baylor Coll Med, Scott Dept Urol, Houston, TX USA
[2] Univ Hosp Southampton NHS Fdn Trust, Southampton, England
[3] Hosp Zambrano Hellion, Nuevo Leon, Mexico
[4] Albert Einstein Coll Med, Bronx, NY USA
[5] Harvard Med Sch, Massachusetts Gen Hosp, Dept Urol, Boston, MA 02115 USA
来源
CUAJ-CANADIAN UROLOGICAL ASSOCIATION JOURNAL | 2024年 / 18卷 / 09期
关键词
MANAGEMENT; PREVENTION;
D O I
10.5489/cuaj.8721
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
INTRODUCTION: Percutaneous nephrolithotomy (PCNL) is the gold-standard treatment for large renal stones. One potentially significant complication of PCNL is blood loss, which can result in transfusion requirement and poorer stone-free outcomes. Tranexamic acid (TXA) has emerged as a promising intervention, administered systemically (TXA-S) or as part of irrigation fluid (TXA-I) in endourology. This study aimed to comprehensively analyze existing evidence regarding the applications of TXA in PCNL through a Bayesian network meta-analysis, offering insights into its efficacy and comparative effectiveness. METHODS: In February 2022, a PRISMA-compliant systematic review (PROSPERO registration number CRD42021270593) was performed to identify randomized controlled clinical trials (RCT) on TXA as either systemic therapy or in irrigation fluid. Studies in languages other than English and Spanish were not considered. A Bayesian network was built using results from identified studies to create models that were later run through Markov Chain Monte Carlo sampling through 200 000 iterations. RESULTS: Eight RCTs compared TXA-S vs. placebo, one TXA-I vs. placebo, and one TXA-I vs. TXA-S. TXA-I had lower risk of transfusion (relative risk [RR] 0.63 [0.47,0.84], SUCRA 0.950) than TXA-S (RR 0.79 [0.65,0.95], SUCRA 0.545). TXA-I had a lower risk of complications (RR 0.38 [0.21,0.67], SUCRA=0.957) compared to TXA-S (RR 0.55 [0.39, 0.78], SUCRA 0.539). TXA-I had a lower postoperative decrease in hemoglobin (mean difference [MD]-1.2 [1.3, 1.0], SUCRA 0.849) compared to TXA-S (MD-0.97 [-1.0,-0.93], SUCRA 0.646]). CONCLUSIONS: TXA, regardless of the route of administration, is an effective intervention in decreasing bleeding, postoperative complications, and risk of transfusion when compared with placebo. Further studies directly comparing TXA-S to TXA-I would be useful to determine the optimal route of delivery.
引用
收藏
页码:E285 / E290
页数:6
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