诊断和治疗实体瘤患儿急性心力衰竭的管理和经验。

IF 3.4 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiovascular Toxicology Pub Date : 2025-02-28 DOI:10.1007/s12012-025-09981-7
Zizheng Yi, Xuandi Li, Xiufang He, Juncheng Liu, Jia Zhu, Shujuan Li
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引用次数: 0

摘要

急性心力衰竭是儿童实体瘤治疗过程中出现的一种危及生命的严重并发症。它的死亡率很高,给治疗带来了挑战,也影响了肿瘤治疗的整体预后。目前,这方面的临床诊断和治疗数据有限。为了解实体瘤患儿急性心力衰竭在治疗过程中的特点和结局,分享治疗经验,提供监测、治疗和预防的管理策略。选取5例具有代表性的实体瘤患儿,总结急性心力衰竭发生过程中的临床特征、辅助检查数据、个体化治疗方案及治疗效果。分析了实体瘤患儿急性心力衰竭的可能诱因、发病时间点、治疗反应及影响因素。5例实体瘤患儿均在化疗后出现急性心力衰竭症状,心功能分级为II级至IV级。大多数病例发生在化疗后的骨髓抑制期,心衰早期心率明显增快。使用蒽环类药物的患儿未达到国际推荐的最大累积剂量。两名心功能Ⅳ级的患儿在完成肿瘤治疗后改变了治疗计划,一名心功能Ⅳ级并同时患有肾功能障碍的患儿中断了化疗。所有患儿都接受了口服抗心衰治疗和营养心肌治疗。两名心功能II级的患儿在口服药物后恢复正常;三名心功能IV级的患儿在心衰急性期接受了静脉血管活性药物治疗,并在后期定期加强治疗。三个病例(心功能 IV 级)的心功能均有所改善,其中一个病例恢复正常,一个病例的非压迫性心肌病恢复缓慢,逐渐接近正常,还有一个病例虽然同时存在肾功能障碍,但心功能仅有轻度改善。患实体瘤的儿童在骨髓抑制期容易出现急性心力衰竭,心率增快是一个早期预警信号。积极的抗心衰治疗是有效的。对于严重病例,在维持期定期静脉注射血管活性药物可促进心功能恢复,肾功能障碍是影响心功能恢复不良的重要因素。
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Management and Experiences in Diagnosing and Treating Acute Heart Failure in Children with Solid Tumors.

Acute heart failure is a critical and life-threatening complication that occurs during the treatment of solid tumors in children. It has a high mortality rate, poses treatment challenges, and also affects the overall prognosis of tumor treatment. Currently, there are limited clinical diagnostic and treatment data in this area. To understand the characteristics and outcomes of acute heart failure in children with solid tumors during the treatment process, share treatment experiences, and provide management strategies for monitoring, treatment, and prevention. Five representative cases of children with solid tumors were selected to summarize the clinical features, auxiliary examination data, individualized treatment plans, and treatment effects during the occurrence of acute heart failure. The possible triggers and time points for the onset of acute heart failure in children with solid tumors were analyzed, along with treatment responses and influencing factors. All five cases of children with solid tumors exhibited symptoms of acute heart failure after chemotherapy, with heart functions staging from class II to class IV. Most cases occurred during the bone marrow suppression period after chemotherapy, with a noticeable increase in heart rate during the early stages of heart failure. Those using anthracycline drugs did not reach the internationally recommended maximum cumulative dose. Two children with heart function class IV altered their tumor treatment plans to completion, and one child with heart function class IV and concurrent renal dysfunction had chemotherapy interrupted. All children received oral anti-heart failure treatment and nutritional myocardial therapy. Two children with heart function class II returned to normal after oral medication; three children with heart function class IV received intravenous vasoactive agents during the acute phase of heart failure, followed by regular reinforcement in the later stage. The heart function improved in all three cases (heart function class IV), with one case returning to normal, one case with slow recovery in non-compaction cardiomyopathy gradually approaching normalcy, and one case with only mild improvement in heart function despite concurrent renal dysfunction. Children with solid tumors are susceptible to acute heart failure during the bone marrow suppression period and an increased heart rate serves as an early warning signal. Active anti-heart failure treatment is effective. For severe cases, regular intravenous administration of vasoactive agents during the maintenance period can promote the recovery of heart function, with renal dysfunction emerging as a significant factor influencing poor recovery of heart function.

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来源期刊
Cardiovascular Toxicology
Cardiovascular Toxicology 医学-毒理学
CiteScore
6.60
自引率
3.10%
发文量
61
审稿时长
>12 weeks
期刊介绍: Cardiovascular Toxicology is the only journal dedicated to publishing contemporary issues, timely reviews, and experimental and clinical data on toxicological aspects of cardiovascular disease. CT publishes papers that will elucidate the effects, molecular mechanisms, and signaling pathways of environmental toxicants on the cardiovascular system. Also covered are the detrimental effects of new cardiovascular drugs, and cardiovascular effects of non-cardiovascular drugs, anti-cancer chemotherapy, and gene therapy. In addition, Cardiovascular Toxicology reports safety and toxicological data on new cardiovascular and non-cardiovascular drugs.
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