伊拉克巴士拉儿童血红蛋白病患者的COVID-19感染情况

IF 0.1 Q4 HEMATOLOGY
Nael Sameer Faisal, Meaad Kadhum Hassan
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引用次数: 0

摘要

背景:血红蛋白病患者被认为是免疫功能低下;然而,尚不清楚他们是否更容易感染COVID-19并经历更严重的病程。研究目的:本研究的目的是评估患有血红蛋白病的儿童患者中COVID-19的临床表现和严重程度,评估研究患者的危险因素和结局。患者和方法:从2021年5月1日至2022年9月,对患有血红蛋白病的儿童和青少年进行了一项分析性横断面研究。除了患者的资料和全面的体格检查外,还对患者的病程、并发症和疾病结局进行了随访。调查包括全血细胞计数、炎症标志物、肝肾功能检查。结果:42例合并血红蛋白病和COVID-19的患者中,35例(83.3%)患者有COVID-19暴露史,暴露时间中位数为5天,23例(54.8%)患者需要住院治疗。所有患者均有发热,其次是咳嗽36例(85.7%)和呼吸短促(42.9%)。研究患者中无死亡报告。与地中海贫血患者相比,镰状细胞病(SCD)合并COVID-19患者淋巴细胞计数显著降低,c反应蛋白和d -二聚体水平显著升高。0.05. 轻度22例(52.4%),中度12例(28.6%),重度8例(19%)。回归分析显示,急性胸综合征(ACS)作为COVID-19感染的表现,白细胞计数高,血清总胆红素升高是与COVID-19严重感染相关的显著变量,P <0.05. 结论:新型冠状病毒感染的血红蛋白病患者的临床病程与普通人群相似,无死亡病例报告。然而,治疗SCD患者的临床医生在诊断ACS时需要注意COVID-19感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COVID-19 infection among pediatric patients with hemoglobinopathies in Basrah, Iraq
Abstract: BACKGROUND: Patients with hemoglobinopathies are considered as immunocompromised; however, it is unclear if they are more susceptible to COVID-19 infection and experience a more severe illness course. AIMS OF STUDY: The aims of this study were to evaluate the clinical presentation and severity of COVID-19 among pediatric patients with hemoglobinopathies, assess risk factors, and outcome among studied patients. PATIENTS AND METHODS: An analytical, cross-sectional study has been carried out on children and adolescents with hemoglobinopathies, for the period from the first of May 2021 to September 2022. In addition to patient’s data and thorough physical examination, patients were followed concerning the course, complications, and disease outcome. Investigations included complete blood count, inflammatory markers, liver, and renal function tests. RESULTS: Out of 42 patients with hemoglobinopathies and COVID-19, the majority of patients 35 (83.3%) gave a history of COVID-19 exposure, with a median of 5 days for the presentation since exposure and 23 (54.8%) needed hospitalization. All studied patients had fever, followed by cough in 36 (85.7%) and shortness of breath (42.9%). No death was reported in studied patients. The lymphocyte count was significantly lower and C-reactive protein and D-dimer levels were significantly higher in sickle cell disease (SCD) patients with COVID-19 as compared to thalassemia patients, P < 0.05. Twenty-two patients (52.4%) had mild COVID-19 disease, 12 (28.6%) moderate, and 8 (19%) with severe disease. Regression analysis revealed that acute chest syndrome (ACS) as COVID-19 infection presentation, high white blood cells count, and elevated total serum bilirubin were significant variables associated with severe COVID-19 infection, P < 0.05. CONCLUSION: The clinical course of hemoglobinopathy patients with COVID-19 infection is similar to that in the general population and no death was reported among studied patients. However, clinicians treating patients with SCD need to be aware of COVID-19 infection when diagnosing ACS.
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