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免疫功能低下状态患者罹患新型冠状病毒感染的临床分析

Clinical characteristics of immunocompromised patients infected with COVID-19

摘要目的:分析免疫功能低下状态患者罹患新型冠状病毒感染(coronavirus disease 2019,COVID-19)的临床特征,并与免疫功能正常患者进行比较。方法:采取单中心回顾性观察性研究方法,纳入于2022年12月至2023年10月在北京大学人民医院确诊为COVID-19的213例住院患者,分为免疫功能低下组(102例,47.9%)和免疫功能正常组(111例,52.1%),比较两组间的临床资料。将免疫功能低下组分为死亡组(18例,17.6%)和非死亡组(84例,82.4%),对两组的实验室检查指标进行比较,进一步对其中数据完整的死亡组(10例,9.8%)和非死亡组(36例,35.3%)的淋巴细胞亚群进行差异分析。结果:免疫功能低下组重型、危重型比例以及病死率均高于免疫功能正常组(47.1% vs. 40.5%、18.6% vs. 9.0%、17.6% vs. 9.0%, P<0.05)。与免疫功能正常组相比,免疫功能低下组接种疫苗比例偏低(26.5% vs. 44.1%, P<0.05),多合并高血压、肾脏疾病及感染(63.7% vs. 48.6%、30.4% vs. 9.0%、49.0% vs. 19.8%,均 P<0.05),影像学表现实变影比例、接受抗病毒治疗比例和核酸阳性持续时间均偏高[40.2% vs. 18.9%、48.0% vs. 30.6%、14(7.0,19.3)d vs. 9(7.0,18.0)d,均 P<0.05],乳酸脱氢酶、降钙素原、白细胞介素-6和铁蛋白水平显著高于免疫功能正常组(均 P<0.05)。死亡组的中性粒细胞、C反应蛋白、PCT、IL-6、铁蛋白和D-二聚体水平均显著高于非死亡组(均 P<0.05),但淋巴细胞、CD4 +T细胞、CD8 +T细胞、B细胞计数和血红蛋白均显著低于非死亡组(均 P<0.05)。 结论:免疫功能低下状态患者重型和危重型超过60%,病死率较高,机体清除新冠病毒能力下降。淋巴细胞总数、CD4 +T细胞、CD8 +T细胞和B细胞减少,降钙素原、铁蛋白和D-二聚体升高提示患者预后不良。

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abstractsObjective:To analyze the clinical features of COVID-19 infection in hospitalized immunocompromised patients in comparison with immunocompetent patients.Methods:A single-center retrospective observational study was conducted on 213 inpatients diagnosed with COVID-19 in the Peking University People′s Hospital between December 2022 and October 2023. They were divided into an immunocompromised group (102 patients, 47.9%) and an immunocompetent group(111 patients, 52.1%), and clinical data were compared between the two groups. The immunocompromised group was further divided into death group (18 cases, 17.6%) and non-death group (84 cases, 82.4%). The differences in laboratory examination findings were compared. Further analysis was performed on the lymphocyte subset differences between the death group(10 patients, 9.8%) and the non-death group (36 patients, 35.3%) with complete data.Results:The proportion of severe and critical cases and the mortality rate, were significantly higher in the immunocompromised group than the immunocompetent group (47.1% vs. 40.5%, 18.6% vs. 9.0%, 17.6% vs. 9.0%, P<0.05). The immunocompromised group had lower vaccination rate (26.5% vs. 44.1%, P<0.05). Hypertension, kidney disease and infections were more common in the immunocompromised group (63.7% vs. 48.6%, 30.4% vs. 9.0%, 49.0% vs. 19.8%, all P<0.05). CT findings of consolidation (40.2% vs. 18.9%), rate of antiviral treatment (48.0% vs. 30.6%) and the positive duration of viral nucleic acid [median 14(7.0, 19.3) days vs. 9(7.0, 18.0) days] were higher in the immunocomprised group (all P<0.05). Lactate dehydrogenase (LDH), procalcitonin (PCT), interleukin-6 (IL-6) and ferritin were higher in the immunocompromised group than those in the immunocompetent group (all P<0.05). In the death group, neutrophils (NEU), C-reactive protein (CRP), PCT, IL-6, ferritin and D-dimer were higher, while lymphocytes (LY), CD4 +T-cells, CD8 +T-cells, B-cell counts and hemoglobin (HGB) were significantly lower than those in the non-death group (all P<0.05). Conclusions:More than 60% of patients in the immunocompromised group were classified as severe or critical type, with a higher mortality rate and decreased ability to clear severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Decreases in total lymphocytes, CD4 +T lymphocytes, CD8 +T lymphocytes, and B lymphocytes, along with elevated levels of procalcitonin, ferritin, and D-dimer, indicated poor prognosis.

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