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儿科溶血尿毒综合征的心脏受累。

Cardiac involvement in pediatric hemolytic uremic syndrome.

机构信息

Department of Pediatric Nephrology, Hopital Femme-Mere-Enfant, Lyon, France.

Service de Pédiatrie Et Néonatalogie, Hôpitaux du Pays du Mont Blanc, Sallanches, France.

出版信息

Pediatr Nephrol. 2022 Dec;37(12):3215-3221. doi: 10.1007/s00467-022-05427-2. Epub 2022 Mar 14.

DOI:10.1007/s00467-022-05427-2
PMID:35286451
Abstract

BACKGROUND

Cardiac involvement is a known but rare complication of pediatric hemolytic uremic syndrome (HUS). We conducted a nationwide observational, retrospective case-control study describing factors associated with the occurrence of myocarditis among HUS patients.

METHODS

Cases were defined as hospitalized children affected by any form of HUS with co-existent myocarditis in 8 French Pediatric Intensive Care Units (PICU) between January 2007 and December 2018. Control subjects were children, consecutively admitted with any form of HUS without coexistent myocarditis, at a single PICU in Lyon, France, during the same time period.

RESULTS

A total of 20 cases of myocarditis were reported among 8 PICUs, with a mean age of 34.3 ± 31.9 months; 66 controls were identified. There were no differences between the two groups concerning the season and the typical, Shiga toxin-producing Escherichia coli (STEC-HUS), or atypical HUS (aHUS). Maximal leukocyte count was higher in the myocarditis group (29.1 ± 16.3G/L versus 21.0 ± 9.9G/L, p = 0.04). The median time between admission and first cardiac symptoms was of 3 days (range 0-19 days), and 4 patients displayed myocarditis at admission. The fatality rate in the myocarditis group was higher than in the control group (40.0% versus 1.5%, p < 0.001). Thirteen (65%) children from the myocarditis group received platelet transfusion compared to 19 (29%) in the control group (p = 0.03).

CONCLUSION

Our study confirms that myocarditis is potentially lethal and identifies higher leukocyte count and platelet transfusion as possible risk factors of myocarditis. A higher resolution version of the Graphical abstract is available as Supplementary information.

摘要

背景

心脏受累是小儿溶血尿毒综合征(HUS)已知但罕见的并发症。我们进行了一项全国性的观察性、回顾性病例对照研究,描述了与 HUS 患者心肌炎发生相关的因素。

方法

病例定义为在 2007 年 1 月至 2018 年 12 月期间,法国 8 个儿科重症监护病房(PICU)中任何形式的 HUS 合并心肌炎的住院患儿。对照组为同期法国里昂的单个 PICU 中任何形式的 HUS 无合并心肌炎的连续入院患儿。

结果

在 8 个 PICU 中报告了 20 例心肌炎病例,平均年龄为 34.3±31.9 个月;共确定了 66 名对照。两组在季节、产志贺毒素大肠杆菌(STEC-HUS)或非典型 HUS(aHUS)方面无差异。心肌炎组白细胞计数最高(29.1±16.3G/L 与 21.0±9.9G/L,p=0.04)。从入院到首次出现心脏症状的中位时间为 3 天(范围 0-19 天),4 例患者在入院时即出现心肌炎。心肌炎组的死亡率高于对照组(40.0%比 1.5%,p<0.001)。与对照组(29%)相比,心肌炎组中有 13 名(65%)患儿接受了血小板输注,而对照组中有 19 名(29%)(p=0.03)。

结论

我们的研究证实心肌炎是潜在致命的,并确定了更高的白细胞计数和血小板输注可能是心肌炎的危险因素。更清晰的图表摘要版本可在补充信息中查看。

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本文引用的文献

1
Cardiac Manifestation among Children with Hemolytic Uremic Syndrome.溶血尿毒综合征患儿的心脏表现。
J Pediatr. 2021 Aug;235:144-148.e4. doi: 10.1016/j.jpeds.2021.03.067. Epub 2021 Apr 2.
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Myocarditis. A histopathologic definition and classification.心肌炎。组织病理学定义与分类。
Am J Cardiovasc Pathol. 1987 Jan;1(1):3-14.
非典型溶血性尿毒症综合征:补体失调、遗传易感性及多器官受累综述
J Clin Med. 2025 Apr 7;14(7):2527. doi: 10.3390/jcm14072527.
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Haemolytic uremic syndrome as a cause of chronic kidney disease stage 5 in children is in retreat: results from the Polish Registry of Kidney Replacement Therapy in children (2000-2023).溶血性尿毒症综合征作为儿童慢性肾脏病5期的病因正在减少:来自波兰儿童肾脏替代治疗登记处(2000 - 2023年)的结果。
Pediatr Nephrol. 2025 Apr;40(4):1069-1079. doi: 10.1007/s00467-024-06584-2. Epub 2024 Nov 16.