Transitioning From Blind to Real-Time Ultrasound-Guided Kidney Biopsy in Children: Diagnostic Yield and Bleeding Outcomes in a Vietnamese Tertiary Referral Hospital, a Retrospective Cohort Study.

IF 1.9 Q3 UROLOGY & NEPHROLOGY
International Journal of Nephrology Pub Date : 2026-07-30 eCollection Date: 2026-01-01 DOI:10.1155/ijne/7390086
Binh Thanh Le, Tien Quoc Nguyen, Anh Xuan Nguyen, Cam Thao Nguyen, Tru Huy Vu, Dinh Quang Truong, Tien Minh Nguyen, Quang Duc Nguyen, Linh Ngoc Huynh, Khanh Ngoc Minh Nguyen, Tam Ngoc Minh Bui, Siyu Chen, Binbin Ji, Jackson Tan, Minh Cuong Duong
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引用次数: 0

Abstract

Background: Kidney biopsy is the gold standard for diagnosing renal parenchymal diseases, guiding treatment and assessing prognosis. Real-time ultrasound-guided biopsy is widely regarded as the preferred technique. However, the implementation may be affected by equipment availability, trained personnel and workflow constraints in resource-limited settings worldwide.

Objective: This study compared the safety and effectiveness of real-time ultrasound-guided and blind kidney biopsy techniques in a paediatric tertiary referral hospital in Vietnam and examined the practical implications of transitioning to real-time ultrasound guidance.

Methods: A retrospective cohort study was conducted at the Nephro-Endocrinology Department, City Children's Hospital, Ho Chi Minh City, Vietnam, from May 2018 to April 2025. All native kidney biopsies performed during the study period were included. A standardised questionnaire was used to extract data from medical records, including demographics, biopsy techniques, glomerular yield, samples containing ≥ 10 and ≥ 25 glomeruli, and inadequate yield and complications, including macroscopic haematuria and major complications.

Results: Among 221 participants (median age: 11 [IQR 7-13] years), 173 underwent real-time ultrasound-guided biopsy and 48 used the blind technique. The ultrasound-guided group had a significantly higher median glomerular count (p = 0.01) and greater proportion of samples with ≥ 10 (p < 0.001) and ≥ 25 glomeruli (p = 0.04). There were no significant differences in inadequate sample rates (p = 0.06), macroscopic haematuria (p = 0.63) or major complications (p = 0.60). Lower eGFR was independently associated with post-biopsy bleeding events, mainly macroscopic haematuria (AOR = 0.809 per 10 mL/min/1.73 m2 increase, 95% CI 0.671-0.975, p = 0.03).

Conclusion: In this Vietnamese paediatric tertiary referral setting, real-time ultrasound-guided biopsy provided superior tissue adequacy compared with the blind technique, without a detectable increase in macroscopic haematuria or major complications. Lower estimated glomerular filtration rate was associated with post-biopsy bleeding events in this cohort, mostly macroscopic haematuria rather than major bleeding.

从盲转向实时超声引导下的儿童肾活检:越南三级转诊医院的诊断率和出血结局,一项回顾性队列研究。
背景:肾活检是诊断肾实质疾病、指导治疗和评估预后的金标准。实时超声引导活检被广泛认为是首选技术。然而,在全球资源有限的情况下,实施可能会受到设备可用性、受过培训的人员和工作流程限制的影响。目的:本研究比较了实时超声引导和盲肾活检技术在越南一家儿科三级转诊医院的安全性和有效性,并研究了过渡到实时超声引导的实际意义。方法:回顾性队列研究于2018年5月至2025年4月在越南胡志明市市儿童医院肾内分泌科进行。所有在研究期间进行的肾脏活检都被纳入研究范围。采用标准化问卷从医疗记录中提取数据,包括人口统计学、活检技术、肾小球量、肾小球≥10和≥25个样本、肾小球量不足和并发症,包括宏观血尿和主要并发症。结果:221名参与者(中位年龄:11 [IQR 7-13]岁)中,173名接受了实时超声引导活检,48名采用盲法。超声引导组肾小球中位数显著高于对照组(p = 0.01),肾小球≥10个(p < 0.001)和≥25个(p = 0.04)的比例较高。两组在样本不足率(p = 0.06)、肉眼血尿(p = 0.63)和主要并发症(p = 0.60)方面无显著差异。较低的eGFR与活检后出血事件独立相关,主要是肉眼可见的血尿(AOR = 0.809 / 10 mL/min/1.73 m2增加,95% CI 0.671-0.975, p = 0.03)。结论:在这个越南儿科三级转诊设置中,与盲法相比,实时超声引导活检提供了更好的组织充分性,没有可检测到的肉眼血尿增加或主要并发症。在这个队列中,较低的肾小球滤过率与活检后出血事件有关,主要是肉眼可见的血尿,而不是大出血。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Nephrology
International Journal of Nephrology UROLOGY & NEPHROLOGY-
CiteScore
3.40
自引率
4.80%
发文量
44
审稿时长
17 weeks
期刊介绍: International Journal of Nephrology is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies focusing on the prevention, diagnosis, and management of kidney diseases and associated disorders. The journal welcomes submissions related to cell biology, developmental biology, genetics, immunology, pathology, pathophysiology of renal disease and progression, clinical nephrology, dialysis, and transplantation.
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