[Clinical characteristics of children with severe SARS-CoV-2 infection in Yunnan].

Y. Li, X. Z. Hu, C. Y. Liu, X. Tao, R. Wang, R. Lu, Y. Pu, C. R. Mu, J. H. Xu, H. Fu
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引用次数: 0

Abstract

Objective: To investigate the clinical characteristics of 130 children with severe SARS-CoV-2 infection in Yunnan province after the relaxation of non-pharmaceutical interventions, and analyze the risk factors for mortality. Methods: This study is a retrospective case summary that analyzed the demographic data, underlying diseases, clinical diagnoses, disease outcomes, and laboratory results of 130 children with severe COVID-19 infections admitted to nine top-tier hospitals in Yunnan Province from December 2022 to March 2023. According to the prognosis, the patients were divided into survival group and death group. The clinical and laboratory data between the two groups were compared, and the risk factors of death were evaluated. The χ2 test and Mann-Whitney U test were employed to compare between groups, while Spearman correlation test and multiple Logistic regression were used to analyze the risk factors for death. The predictive value of independent risk factors was evaluated by receiver operating characteristic curve. Results: The 130 severe patients included 80 males and 50 females with an onset age of 28.0 (4.5, 79.5) months. There were 97 cases in the survival group and 33 cases in the death group with no significant differences in gender and age between the two groups (P>0.05). Twenty-five cases (19.2%) out of the 130 patients had underlying diseases, and the number with underlying diseases was significantly higher in death group than in survival group (36.4% (12/33) vs. 13.4%(13/97), χ2=8.36, P=0.004). The vaccination rate in the survival group was significantly higher than that in the death group (86.1% (31/36) vs. 7/17, χ2=9.38, P=0.002). A total of 42 cases (32.3%) of the 130 patients were detected to be infected with other pathogens, but there was no significant difference in the incidence of co-infection between the death group and the survival group (39.3%(13/33) vs. 29% (29/97), χ2=1.02, P>0.05). Among the 130 cases, severe respiratory cases were the most common 66 cases (50.8%), followed by neurological severe illnesses 34 cases (26.2%) and circulatory severe cases 13 cases (10%). Compared to the survival group, patients in the death group had a significantly higher levels of neutrophil, ferritin, procalcitonin, alanine aminotransferase, lactate dehydrogenase, creatine kinase isoenzyme, B-type natriuretic peptide, interleukin-6 and 10 (6.7 (4.0, 14.0) vs. 3.0 (1.6, 7.0)×109/L, 479 (298, 594) vs. 268 (124, 424) μg/L, 4.8 (1.7, 10.6) vs. 2.0 (1.1, 3.1) μg/L, 66 (20, 258) vs. 23 (15, 49) U/L, 464 (311, 815) vs. 304 (252, 388) g/L, 71(52, 110) vs. 24(15, 48) U/L, 484 (160, 804) vs. 154 (26, 440) ng/L, 43 (23, 102) vs. 19 (13, 27) ng/L, 216 (114, 318) vs. 86 (45, 128) ng/L, Z=-4.21, -3.67, -3.76, -3.31, -3.75, -5.74, -3.55, -4.65, -5.86, all P<0.05). The correlated indexes were performed by multivariate Logistic regression and the results showed that vaccination was a protective factor from death in severe cases (OR=0.01, 95%CI 0-0.97, P=0.049) while pediatric sequential organ failure assessment (PSOFA) (OR=3.31, 95%CI 1.47-7.47, P=0.004), neutrophil-to-lymphocyte ratio (NLR) (OR=1.56, 95%CI 1.05-2.32, P=0.029) and D dimer (OR=1.49, 95%CI 1.00-1.02, P=0.033) were independent risk factors for death (all P<0.05). The area under the curve of the three independent risk factors for predicting death were 0.86 (95%CI 0.79-0.94), 0.89 (95%CI 0.84-0.95) and 0.87 (95%CI 0.80-0.94), all P<0.001, and the cut-off values were 4.50, 3.66 and 4.69 mg/L, respectively. Conclusions: Severe SARS-CoV-2 infection can occur in children of all ages, primarily affecting the respiratory system, but can also infect the nervous system, circulatory system or other systems. Children who died had more severe inflammation, tissue damage and coagulation disorders. The elevations of PSOFA, NLR and D dimer were independent risk factors for death in severe children.
[云南重症 SARS-CoV-2 感染儿童的临床特征]。
目的调查云南省 130 名重症 SARS-CoV-2 感染儿童在放宽非药物干预后的临床特征,并分析死亡的危险因素。研究方法本研究为回顾性病例总结,分析了2022年12月至2023年3月云南省9家三甲医院收治的130例重症COVID-19感染患儿的人口学资料、基础疾病、临床诊断、疾病结局和实验室结果。根据预后将患者分为生存组和死亡组。比较两组患者的临床和实验室数据,并评估死亡的危险因素。组间比较采用χ2检验和Mann-Whitney U检验,死亡危险因素分析采用Spearman相关检验和多元Logistic回归。通过接收者操作特征曲线评估独立风险因素的预测价值。结果130 例重症患者中,男性 80 例,女性 50 例,发病年龄为 28.0(4.5,79.5)个月。存活组 97 例,死亡组 33 例,两组在性别和年龄上无明显差异(P>0.05)。130 例患者中有 25 例(19.2%)患有基础疾病,死亡组患有基础疾病的人数明显高于存活组(36.4% (12/33) vs. 13.4%(13/97), χ2=8.36, P=0.004)。存活组的疫苗接种率明显高于死亡组(86.1% (31/36) vs. 7/17,χ2=9.38,P=0.002)。130 例患者中共有 42 例(32.3%)被检测出感染了其他病原体,但死亡组与存活组的合并感染率无明显差异(39.3%(13/33) vs. 29%(29/97),χ2=1.02,P>0.05)。在 130 例重症病例中,呼吸系统重症病例最多,为 66 例(50.8%),其次是神经系统重症病例 34 例(26.2%)和循环系统重症病例 13 例(10%)。与存活组相比,死亡组患者的中性粒细胞、铁蛋白、降钙素原、丙氨酸氨基转移酶、乳酸脱氢酶、肌酸激酶同工酶、B 型钠尿肽、白细胞介素-6 和白细胞介素-10 的水平明显更高(6.7 (4.0, 14.0) vs. 3.0 (1.6, 7.0)×109/L, 479 (298, 594) vs. 268 (124, 424) μg/L, 4.8 (1.7, 10.6) vs. 2.0 (1.1, 3.1) μg/L,66 (20, 258) vs. 23 (15, 49) U/L, 464 (311, 815) vs. 304 (252, 388) g/L,71(52, 110) vs. 24(15, 48) U/L, 484 (160, 804) vs. 154 (26, 440) μg/L。154(26,440)纳克/升,43(23,102)纳克/升 vs. 19(13,27)纳克/升,216(114,318)纳克/升 vs. 86(45,128)纳克/升,Z=-4.21,-3.67,-3.76,-3.31,-3.75,-5.74,-3.55,-4.65,-5.86,所有P<0.05)。通过多变量 Logistic 回归对相关指标进行分析,结果显示接种疫苗是重症病例死亡的保护因素(OR=0.01,95%CI 0-0.97,P=0.049),而小儿序贯器官衰竭评估(PSOFA)(OR=3.31,95%CI 1.47-7.47,P=0.004)、中性粒细胞与淋巴细胞比值(NLR)(OR=1.56,95%CI 1.05-2.32,P=0.029)和D二聚体(OR=1.49,95%CI 1.00-1.02,P=0.033)是死亡的独立危险因素(均P<0.05)。预测死亡的三个独立风险因素的曲线下面积分别为 0.86(95%CI 0.79-0.94)、0.89(95%CI 0.84-0.95)和 0.87(95%CI 0.80-0.94),均 P<0.001,临界值分别为 4.50、3.66 和 4.69 mg/L。结论严重的 SARS-CoV-2 感染可发生在所有年龄段的儿童中,主要影响呼吸系统,但也可感染神经系统、循环系统或其他系统。死亡儿童的炎症、组织损伤和凝血功能障碍更为严重。PSOFA、NLR和D二聚体的升高是导致重症儿童死亡的独立风险因素。
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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