Hemolytic uremic syndrome in children: Clinical characteristics and predictors of outcome

IF 2.3 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Clinical Epidemiology and Global Health Pub Date : 2024-07-14 DOI:10.1016/j.cegh.2024.101715
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Abstract

Background

Hemolytic uremic syndrome (HUS) is the most common thrombotic microangiopathy (TMA) occurring in children.

Objectives

To study the clinico-laboratory profile and identify the potential outcome predictors in children with hemolytic uremic syndrome.

Methodology

A retrospective observational study was conducted at a tertiary center in South India. Children diagnosed with HUS during the study period of 10 years were included. The demographic, clinical, and laboratory details, complications, and outcomes were recorded. Predictors of mortality were analyzed.

Results

Among 44 children with HUS, 14 (31.8 %) children were diagnosed with D + HUS while 30 had D-HUS. The median age at diagnosis was 6.3 years. Male preponderance (55.9 %) was observed. Presenting symptoms included oliguria in 36 (86.4 %), followed by fever, observed in 34 (77.3 %). 12 (27.2 %) children had anuria. Seizures and altered sensorium were present in 12 (27.35) and 16 (36.4 %) children respectively. Hypertension was observed in 33 (75 %) children. Plasmapheresis was performed in 18 (13.6 %) children. 17 (38.6 %) children underwent hemodialysis, and 7 (15.9 %) underwent peritoneal dialysis. The median duration of hospital stay was 18 (9.7, 27.7) days. Complications observed during the study were CNS involvement was seen in 16 (36.4 %) children, while coagulopathy was observed in 3 (6.8 %) children. Mortality was observed in 16 children (36.4 %). Anuria at admission was more prevalent in non-survivors (10 out of 16 children; p 0.003). The median albumin and C3 levels were significantly low in non-survivors (p-value <0.001 and 0.008 respectively). A total leucocyte count >15,000 X 109 cells/L was independently associated with mortality even after adjustment with duration of symptoms before diagnosis >10 days and low C3 levels (adjusted OR [95 % CI]: 1.12 [1.02, 1.92] (p-value 0.03).

Conclusion

Hypoalbuminemia and hypocomplementemia were observed in higher proportions among non-survivors. Elevated leucocyte count at admission was an independent predictor of mortality.

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儿童溶血性尿毒症综合征:临床特征和预后因素
背景溶血性尿毒症综合征(HUS)是发生在儿童身上最常见的血栓性微血管病变(TMA)。研究纳入了 10 年间诊断为 HUS 的儿童。研究记录了人口统计学、临床和实验室细节、并发症和结果。结果在44名HUS患儿中,14名(31.8%)患儿被诊断为D+HUS,30名患儿为D-HUS。确诊时的中位年龄为 6.3 岁。男性占多数(55.9%)。36名患儿(86.4%)出现少尿症状,34名患儿(77.3%)出现发热症状。12名患儿(27.2%)出现无尿。分别有 12 名(27.35%)和 16 名(36.4%)儿童出现癫痫发作和感觉改变。33名(75%)患儿出现高血压。18名(13.6%)患儿接受了血浆置换术。17名儿童(38.6%)接受了血液透析,7名儿童(15.9%)接受了腹膜透析。住院时间中位数为 18(9.7,27.7)天。研究期间观察到的并发症有:16 名儿童(36.4%)出现中枢神经系统受累,3 名儿童(6.8%)出现凝血功能障碍。16名患儿(36.4%)死亡。入院时无尿症在非幸存者中更为常见(16 名儿童中有 10 名;P 0.003)。非存活者的白蛋白和 C3 水平中位数明显偏低(p 值分别为 0.001 和 0.008)。即使对诊断前症状持续时间为 10 天和 C3 水平低进行调整后,白细胞总数仍与死亡率独立相关(调整后 OR [95 % CI]:结论低白蛋白血症和低补体血症在非幸存者中的比例较高。入院时白细胞计数升高是预测死亡率的一个独立因素。
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来源期刊
Clinical Epidemiology and Global Health
Clinical Epidemiology and Global Health PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
4.60
自引率
7.70%
发文量
218
审稿时长
66 days
期刊介绍: Clinical Epidemiology and Global Health (CEGH) is a multidisciplinary journal and it is published four times (March, June, September, December) a year. The mandate of CEGH is to promote articles on clinical epidemiology with focus on developing countries in the context of global health. We also accept articles from other countries. It publishes original research work across all disciplines of medicine and allied sciences, related to clinical epidemiology and global health. The journal publishes Original articles, Review articles, Evidence Summaries, Letters to the Editor. All articles published in CEGH are peer-reviewed and published online for immediate access and citation.
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