儿童急性早幼粒细胞白血病的特征和并发症:全国数据库分析。

IF 1.2 4区 医学 Q4 HEMATOLOGY
Pediatric Hematology and Oncology Pub Date : 2024-09-01 Epub Date: 2024-07-08 DOI:10.1080/08880018.2024.2352727
Ariella Barhen, Paul A Martinez, Prithvi Sendi, Balagangadhar R Totapally
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引用次数: 0

摘要

急性早幼粒细胞白血病(APL)是急性髓性白血病(AML)中一种不常见的亚型,曾是急性白血病中最致命的形式之一。随着诊断和治疗的进步,APL 已成为最容易治愈的髓系白血病之一。APL 治疗失败的主要原因是患者在开始治疗后过早死亡。我们对医疗成本与利用项目 2016 年和 2019 年儿童住院病人数据库进行了回顾性横断面分析,诊断结果为 APL 或未缓解的 AML(根据 ICD-10-CM 编码定义)。我们比较了美国住院儿童 APL 和 AML(不包括 APL)的相关并发症和结果,并描述了每年的全国发病率。APL的全国发病率为每年每百万儿童中有2.2例。患 APL 的儿童更有可能出现心肺并发症(OR 1.79;CI 1.20-2.67;P = 0.004)、凝血异常或 DIC(OR 7.75;CI 5.81-10.34;P P P P = 0.13),而死于 APL 的儿童的中位住院时间比死于 AML 的儿童短(2(IQR:1-7)天对 25(IQR:5-66)天;P = 0.004)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics and complications of acute promyelocytic leukemia in children: an analysis of a national database.

Acute promyelocytic leukemia (APL) is an uncommon subtype of acute myelogenous leukemia (AML) that was previously one of the most fatal forms of acute leukemia. With advances in diagnosis and treatment, APL has become one of the most curable myeloid leukemias. The major reason for treatment failure in APL is early death after initiation of treatment. We performed a retrospective cross-sectional analysis of the Healthcare Cost and Utilization Project 2016 and 2019 Kids' Inpatient Database, with the diagnosis of APL or AML not in remission as defined by ICD-10-CM codes. We compared complications and outcomes associated with APL and AML (exclusive of APL) in hospitalized children in the U.S. and described yearly national incidence. The national incidence of APL was 2.2 cases per million children per year. Children with APL were more likely to have cardiopulmonary complications (OR 1.79; CI 1.20-2.67; p = 0.004), coagulation abnormalities or DIC (OR 7.75; CI 5.81-10.34; p < 0.001), pulmonary hemorrhage (OR 2.18; CI 1.49-3.17; p < 0.001), and intracranial hemorrhage (OR 10.82; CI 5.90-19.85; p < 0.001) and less likely to have infectious complications (OR 0.48; CI 0.34-0.67; p < 0.001) compared to children with AML. In-hospital mortality rates were similar in children with APL and AML (4.2% vs 2.6%; OR 1.62; CI 0.86-3.06; p = 0.13), while the median length of stay for children who died from APL was shorter compared to AML (2 (IQR: 1-7) versus 25 (IQR: 5-66) days; p < 0.05). Hemorrhagic complications occur more often, and infectious complications occur less often in hospitalized children with APL compared to AML.

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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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