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3
Immunocompromised Seroprevalence and Course of Illness of SARS-CoV-2 in One Pediatric Quaternary Care Center.免疫功能低下患者血清 SARS-CoV-2 阳性率和疾病进程:一家儿科四级保健中心的研究
J Pediatric Infect Dis Soc. 2021 Apr 30;10(4):426-431. doi: 10.1093/jpids/piaa123.
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单中心报告:COVID-19 疾病过程及肝移植儿科患者的管理。

A single-center report of COVID-19 disease course and management in liver transplanted pediatric patients.

机构信息

Pediatric Gastroenterology-Hepatology, Liver Transplantation Center, Koç University Hospital, Istanbul, Turkey.

Koç University Research Center for Translational Medicine (KUTTAM)-Liver Immunology Lab, Istanbul, Turkey.

出版信息

Pediatr Transplant. 2021 Nov;25(7):e14061. doi: 10.1111/petr.14061. Epub 2021 Jun 2.

DOI:10.1111/petr.14061
PMID:34076953
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8237072/
Abstract

BACKGROUND

In 2019, SARS-CoV-2 causing COVID-19 emerged. Severe COVID-19 symptoms may evolve by virtue of hyperactivation of the immune system. Equally, immunocompromised patients may be at increased risk to develop COVID-19. However, treatment guidelines for children following liver transplantation are elusive.

METHODS

As a liver transplantation center, we diagnosed and followed up 10 children (male/female: 8/2) with a median age of 8.5 years (IQR: 5.2-11.0), with COVID-19 post-liver transplant between March 2019 and December 2020. COVID-19 diagnosis was based on PCR test and or florid X-ray findings compatible with COVID-19 in the absence of other cause. We retrospectively collected clinical and laboratory data from electronic patient records following written consent from patients/parents.

RESULTS

Nine patients were diagnosed as definitive (PCR positive) with one patient being diagnosed as probable COVID-19. Seven patients recovered without any support whereas three were admitted for non-invasive oxygenation. Lymphopenia and/or high levels of serum IL-6 were detected in four patients. Six patients mounted anti-SARS-CoV-2 antibodies at median 30 days (IQR: 26.5-119.0) following COVID-19 diagnosis. Antibiotic therapy, favipiravir, anakinra, and IVIG were used as treatment in 4,1,1 and 2 patients, respectively. Furthermore, we kept the tacrolimus with or without everolimus but stopped MMF in 2 patients. Importantly, liver allograft function was retained in all patients.

CONCLUSIONS

We found that being immunocompromised did not affect disease severity nor survival. Stopping MMF yet continuing with tacrolimus was an apt treatment modality in these patients.

摘要

背景

2019 年,SARS-CoV-2 引起了 COVID-19。严重的 COVID-19 症状可能是由于免疫系统的过度激活而演变而来。同样,免疫功能低下的患者可能面临更高的 COVID-19 发病风险。然而,肝移植后儿童的治疗指南尚不清楚。

方法

作为一家肝移植中心,我们诊断并随访了 10 名(男/女:8/2)肝移植后儿童 COVID-19 患者,中位年龄为 8.5 岁(IQR:5.2-11.0),诊断时间为 2019 年 3 月至 2020 年 12 月。COVID-19 的诊断基于 PCR 检测和/或无其他原因的符合 COVID-19 的典型 X 光表现。我们从电子病历中回顾性收集了临床和实验室数据,并获得了患者/父母的书面同意。

结果

9 例患者被诊断为确诊(PCR 阳性),1 例患者被诊断为可能 COVID-19。7 例患者在未接受任何支持的情况下康复,而 3 例患者因非侵入性吸氧而入院。4 例患者出现淋巴细胞减少和/或血清 IL-6 水平升高。6 例患者在 COVID-19 诊断后中位 30 天(IQR:26.5-119.0)时产生了抗 SARS-CoV-2 抗体。4 例患者分别接受了抗生素治疗、法匹拉韦、阿那白滞素和 IVIG,1 例患者接受了阿那白滞素治疗,1 例患者接受了 IVIG 治疗。此外,我们保留了他克莫司,或停用他克莫司但保留依维莫司,在 2 例患者中停用了霉酚酸酯。重要的是,所有患者的肝移植功能均得以保留。

结论

我们发现免疫功能低下并不影响疾病的严重程度或存活率。在这些患者中,停用霉酚酸酯但保留他克莫司是一种合适的治疗方法。