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标准经皮肾镜取石术与无管经皮肾镜取石术在儿科人群中的安全性和有效性:一项更新的系统评价和荟萃分析。

Safety and efficacy of standard vs. tubeless percutaneous nephrolithotomy in pediatric populations: an updated systematic review and meta-analysis.

作者信息

Fang Honggang, Wang Zihan, Wei Kuan, Liu Xing, Wu Shengde, Hua Yi, Lin Tao, He Dawei, Wei Guanghui, Zhang Deying

机构信息

Department of Urology, Children's Hospital of Chongqing Medical University, Chongqing, 400014, China.

National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Structural Birth Defect and Reconstruction, Chongqing, China.

出版信息

BMC Urol. 2025 May 2;25(1):110. doi: 10.1186/s12894-025-01798-4.

Abstract

OBJECTIVE

This study aims to compare the safety and efficacy of standard versus tubeless percutaneous nephrolithotomy (PCNL) in pediatric populations.

METHODS

A systematic search was conducted in the Web of Science, Cochrane Library, PubMed, and Embase databases to identify studies that met the inclusion criteria. Two authors independently screened the literature and extracted data. A meta-analysis was performed using RevMan 5.4 software. This study has been prospectively registered with PROSPERO (ID: CRD42024622238). Sensitivity analysis was performed using Stata 17.0 to assess the impact of low-quality studies, and publication bias was evaluated using funnel plots.

RESULTS

A total of 3 randomized controlled trials and 10 case-control studies were included, comprising 661 cases. The meta-analysis revealed that, in pediatric populations, the tubeless PCNL group had significantly shorter hospital stays compared to the standard PCNL group (WMD = -1.60, 95% CI: -2.27 to -0.92, P < 0.01), as well as shorter operative times (WMD = -2.06, 95% CI: -4.02 to -0.10, P = 0.04). The stone clearance rate was higher in the tubeless PCNL group than in the standard group (OR = 2.18, 95% CI: 1.09 to 4.34, P = 0.03). Additionally, the tubeless PCNL group had lower rates of postoperative fever (OR = 0.46, 95% CI: 0.27 to 0.78, P < 0.01) and postoperative urine leakage (OR = 0.20, 95% CI: 0.08 to 0.50, P < 0.01) compared to the standard group. The tubeless PCNL group also had shorter pain management times (WMD = -2.00, 95% CI: -2.44 to -1.56, P < 0.01) and lower visual analog scale (VAS) scores (WMD = -2.52, 95% CI: -2.81 to -2.22, P < 0.01). However, no significant differences were observed between the two groups in terms of hemoglobin decline, overall complications (including perinephric fluid collections, urinary tract infections, and blood transfusion requirements), and reoperation rates.

CONCLUSION

In children with kidney stones and low stone burden or an uneventful procedure, tubeless PCNL offers clear clinical advantages, including shorter hospital stays, higher stone clearance rates, and lower postoperative fever. Additionally, it improves surgical efficiency, reduces postoperative complications, and decreases the need for analgesia. These benefits suggest that tubeless PCNL can be safely applied in pediatric patients, yielding outcomes comparable to standard PCNL, provided that indications are properly managed".

CLINICAL TRIAL NUMBER

Not applicable.

摘要

目的

本研究旨在比较标准经皮肾镜取石术(PCNL)与无管PCNL在儿科患者中的安全性和有效性。

方法

在Web of Science、Cochrane图书馆、PubMed和Embase数据库中进行系统检索,以确定符合纳入标准的研究。两位作者独立筛选文献并提取数据。使用RevMan 5.4软件进行荟萃分析。本研究已在PROSPERO(ID:CRD42024622238)上进行前瞻性注册。使用Stata 17.0进行敏感性分析,以评估低质量研究的影响,并使用漏斗图评估发表偏倚。

结果

共纳入3项随机对照试验和10项病例对照研究,共661例病例。荟萃分析显示,在儿科患者中,无管PCNL组的住院时间明显短于标准PCNL组(加权均数差[WMD]= -1.60,95%置信区间[CI]:-2.27至-0.92,P<0.01),手术时间也较短(WMD = -2.06,95% CI:-4.02至-0.10,P = 0.04)。无管PCNL组的结石清除率高于标准组(比值比[OR]= 2.18,95% CI:1.09至4.34,P = 0.03)。此外,与标准组相比,无管PCNL组的术后发热率(OR = 0.46,95% CI:0.27至0.78,P<0.01)和术后尿漏率(OR = 0.20,95% CI:0.08至0.50,P<0.01)较低。无管PCNL组的疼痛管理时间也较短(WMD = -2.00,95% CI:-2.44至-1.56,P<0.01),视觉模拟评分(VAS)较低(WMD = -2.52,95% CI:-2.81至-2.22,P<0.01)。然而,两组在血红蛋白下降、总体并发症(包括肾周积液、尿路感染和输血需求)和再次手术率方面未观察到显著差异。

结论

对于肾结石且结石负荷低或手术过程顺利的儿童,无管PCNL具有明显的临床优势,包括住院时间短、结石清除率高和术后发热率低。此外,它提高了手术效率,减少了术后并发症,并减少了镇痛需求。这些益处表明,只要适应证得到妥善管理,无管PCNL可以安全地应用于儿科患者,其结果与标准PCNL相当。

临床试验编号

不适用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12049033/25c0a073fdf0/12894_2025_1798_Fig1_HTML.jpg

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