儿童心内血栓:三级医院十年的经验。

IF 1.2 4区 医学 Q4 HEMATOLOGY
Pediatric Hematology and Oncology Pub Date : 2025-09-01 Epub Date: 2025-07-31 DOI:10.1080/08880018.2025.2531011
Tzofnat Farbstein-Aljanati, Tal Tirosh-Wagner, Ivan Budnik, Uriel Katz, Sharon Borik, Assaf A Barg, Gili Kenet, Sarina Levy-Mendelovich
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引用次数: 0

摘要

儿童心内血栓(ICT)是一种严重且可能危及生命的疾病,特别是在住院患者中。关于信息和通信技术的儿科专用数据仍然很少,这对以证据为基础的最佳管理提出了挑战。本研究旨在分析十年来的儿童ICT病例,以确定临床特征、管理策略和结果。这项回顾性研究在一家三级转诊中心进行,纳入了2012年至2023年间诊断为ICT的所有儿科患者(年龄0-18岁)。临床和人口统计数据从电子病历中提取,经IRB批准。23名儿童被确定(中位年龄:39个月;52%的女性)。主要危险因素包括中心静脉置管(60.9%)、先天性或获得性心脏病(52.2%)和恶性肿瘤(34.8%)。大多数血栓(78.3%)位于右侧。56.5%的病例被偶然诊断为ICT;在其他情况下,症状导致通过超声心动图、CT或心导管显像。87%的患者开始了抗凝治疗。由于持续性血栓或持续的危险因素,8名患者需要无限期治疗,而其他患者接受的中位治疗时间为4个月。3例患者因临床原因未接受抗凝治疗。手术取栓4例(17.4%),1例行导管溶栓。无大出血事件。60.9%的患者血栓完全溶解,26.1%的患者血栓部分改善。儿童ICT与可识别的危险因素相关,通常采用抗凝治疗。在某些情况下可能需要手术或介入治疗。早期识别高危患者对于改善预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intracardiac thrombi in children: A decade of experience at a tertiary care hospital.

Intracardiac thrombus (ICT) in children is a serious and potentially life-threatening condition, particularly among hospitalized patients. Pediatric-specific data on ICT remain scarce, posing challenges for optimal, evidence-based management. This study aimed to analyze pediatric ICT cases over a decade to identify clinical characteristics, management strategies, and outcomes.

This retrospective study was conducted at a tertiary referral center and included all pediatric patients (ages 0-18) diagnosed with ICT between 2012 and 2023. Clinical and demographic data were extracted from electronic medical records, following IRB approval.

Twenty-three children were identified (median age: 39 months; 52% female). Major risk factors included central venous catheters (60.9%), congenital or acquired heart disease (52.2%), and malignancy (34.8%). Most thrombi (78.3%) were right-sided. ICT was incidentally diagnosed in 56.5% of cases; in others, symptoms led to imaging via echocardiography, CT, or cardiac catheterization.

Anticoagulation therapy was initiated in 87% of patients. Eight required indefinite treatment due to persistent thrombi or ongoing risk factors, while others received a median therapy duration of four months. Three patients did not receive anticoagulation due to clinical considerations. Surgical thrombectomy was performed in four cases (17.4%), and one patient underwent catheter-based thrombolysis. There were no major bleeding events. Complete thrombus resolution was achieved in 60.9% of cases, with partial improvement in 26.1%.

ICT in children is associated with identifiable risk factors and is commonly managed with anticoagulation. Surgical or interventional procedures may be needed in select cases. Early identification of high-risk patients is essential to improve outcomes.

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来源期刊
CiteScore
2.60
自引率
5.90%
发文量
71
审稿时长
6-12 weeks
期刊介绍: PHO: Pediatric Hematology and Oncology covers all aspects of research and patient management within the area of blood disorders and malignant diseases of childhood. Our goal is to make PHO: Pediatric Hematology and Oncology the premier journal for the international community of clinicians and scientists who together aim to define optimal therapeutic strategies for children and young adults with cancer and blood disorders. The journal supports articles that address research in diverse clinical settings, exceptional case studies/series that add novel insights into pathogenesis and/or clinical care, and reviews highlighting discoveries and challenges emerging from consortia and conferences. Clinical studies as well as basic and translational research reports regarding cancer pathogenesis, genetics, molecular diagnostics, pharmacology, stem cells, molecular targeting, cellular and immune therapies and transplantation are of interest. Papers with a focus on supportive care, late effects and on related ethical, legal, psychological, social, cultural, or historical aspects of these fields are also appreciated. Reviews on important developments in the field are welcome. Articles from scientists and clinicians across the international community of Pediatric Hematology and Oncology are considered for publication. The journal is not dependent on or connected with any organization or society. All submissions undergo rigorous peer review prior to publication. Our Editorial Board includes experts in Pediatric Hematology and Oncology representing a wide range of academic and geographic diversity.
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