Children with sickle cell disease: are they protected from serious COVID-19?

IF 2.1 3区 医学 Q2 PEDIATRICS
Frontiers in Pediatrics Pub Date : 2024-10-07 eCollection Date: 2024-01-01 DOI:10.3389/fped.2024.1337377
Walaa Aboulkasem Shahin, Hayam Aldeeb, Majed Alsulami, Abdullah Tammas, Fatma Albatniji, Aljawhara Almanea, Abdalla Mohamed Zayed, Fahad Alabbas, Azzah Alzahrani, Tahani Bin Ali, Ghaleb Elyamany, Rana Hassan Almaghrabi, Huda Elfaraidi
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引用次数: 0

Abstract

Background: COVID-19, the pandemic that hit the world in 2020, resulted in millions of deaths, with the elderly and adults succumbing to the disease more often than children. However, the presence of underlying morbidities increased the risk of death. Sickle cell disease (SCD) was previously classified as a major risk factor for severe COVID-19 disease. However, presently, there are only a limited number of studies that identify the clinical course of children with SCD and COVID-19.

Methods: We conducted a retrospective observational study on children with SCD admitted due to COVID-19 at three different institutions in Saudi Arabia between March 2020 and March 2022. We studied the demographic and clinical characteristics of patients admitted to the hospital.

Results: Seventy-six patients with SCD had PCR-confirmed SARS-CoV-2 during the study period; 50.0% of our patient population were children (6-12 years old). Gender was evenly distributed, with 53.9% girls and 46.1% boys. Symptoms more commonly related to the COVID-19 infection included fever, cough, malaise, and vomiting. Chest x-ray findings revealed mild and non-specific symptoms only in approximately one-third (28) of the included children. The most common symptoms associated with SCD were vaso-occlusive crisis (47.4%) and abdominal pain (11.8%). The overall general appearance of most of the patients was reassuring. The median length of hospital stay was 4.2 ± 2.7 days. The mean white blood cell count was 11.4 ± 5.2 × 109/L, and the mean hemoglobin level was 8.3 ± 1.5 g/dl. Despite the fact that higher levels of mean D-dimer, lactate dehydrogenase, and ferritin were reported in these patients, the clinical outcome was not affected. All recruited patients received hydroxyurea as maintenance therapy. The outcome of our study was reassuring, with no significant morbidity or mortality observed among the recruited patients.

Conclusion: Despite SCD being a chronic disease with known specific complications, there has been a claim that COVID-19 infection adds further risk. The results of this study suggest that the overall outcome of COVID-19 was favorable, with no reported mortality. Further research is needed to understand the factors that contributed to this favorable outcome. In children with SCD, it is still questionable whether hydroxyurea is one of the protective factors against severe COVID-19. Validation through large-scale research is recommended.

患有镰状细胞病的儿童:他们会受到严重 COVID-19 的保护吗?
背景:COVID-19 是 2020 年袭击全球的大流行病,导致数百万人死亡,其中老年人和成年人比儿童更容易感染该疾病。然而,潜在疾病的存在会增加死亡风险。镰状细胞病(SCD)曾被列为严重 COVID-19 疾病的主要风险因素。然而,目前只有少数研究能确定 SCD 和 COVID-19 儿童的临床病程:我们对 2020 年 3 月至 2022 年 3 月期间沙特阿拉伯三个不同机构收治的 COVID-19 SCD 患儿进行了一项回顾性观察研究。我们研究了入院患者的人口统计学和临床特征:研究期间,76 名 SCD 患者经 PCR 证实感染了 SARS-CoV-2;50.0% 的患者为儿童(6-12 岁)。性别分布均匀,女孩占 53.9%,男孩占 46.1%。更常见的与 COVID-19 感染有关的症状包括发烧、咳嗽、乏力和呕吐。胸部X光检查结果显示,只有约三分之一(28名)的患儿有轻微的非特异性症状。与 SCD 相关的最常见症状是血管闭塞性危象(47.4%)和腹痛(11.8%)。大多数患者的总体外观令人欣慰。住院时间中位数为 4.2 ± 2.7 天。平均白细胞计数为 11.4 ± 5.2 × 109/L,平均血红蛋白水平为 8.3 ± 1.5 g/dl。尽管这些患者的平均 D-二聚体、乳酸脱氢酶和铁蛋白水平较高,但临床结果未受影响。所有招募的患者都接受了羟基脲作为维持治疗。我们的研究结果令人欣慰,在招募的患者中未观察到明显的发病率或死亡率:结论:尽管 SCD 是一种慢性疾病,有已知的特殊并发症,但有人认为 COVID-19 感染会增加更多风险。本研究结果表明,COVID-19 的总体疗效良好,无死亡报告。需要进一步研究以了解导致这一良好结果的因素。在 SCD 患儿中,羟基脲是否是预防严重 COVID-19 的保护因素之一仍存在疑问。建议通过大规模研究进行验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Pediatrics
Frontiers in Pediatrics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
3.60
自引率
7.70%
发文量
2132
审稿时长
14 weeks
期刊介绍: Frontiers in Pediatrics (Impact Factor 2.33) publishes rigorously peer-reviewed research broadly across the field, from basic to clinical research that meets ongoing challenges in pediatric patient care and child health. Field Chief Editors Arjan Te Pas at Leiden University and Michael L. Moritz at the Children''s Hospital of Pittsburgh are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Pediatrics also features Research Topics, Frontiers special theme-focused issues managed by Guest Associate Editors, addressing important areas in pediatrics. In this fashion, Frontiers serves as an outlet to publish the broadest aspects of pediatrics in both basic and clinical research, including high-quality reviews, case reports, editorials and commentaries related to all aspects of pediatrics.
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