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The mNCP-SPI Score Predicting Risk of Severe COVID-19 among Mild-Pneumonia Patients on Admission

机译:MNCP-SPI评分预测严重肺炎患者严重Covid-19的风险

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Purpose: To predict the risk of developing severe pneumonia among mild novel coronavirus pneumonia (mNCP) patients on admission. Methods: A retrospective cohort study was conducted at three hospitals in Shanghai and Wuhan from January 2020 to February 2020. Real-time polymerasechain–reaction assays were used to detect COVID-19. A total of 529 patients diagnosed with NCP were recruited from three hospitals and classified by four severity types during hospitalization following the standards of the Chinese Diagnosis and Treatment of Pneumonia Caused by New Coronavirus Infection (eighth version). Patients were excluded if admitted by ICU on admission (n=92, on a general ward while meeting the condition of severe or critical type on admission (n=25), or there was insufficient clinical information (n=64). In sum, 348 patients with mNCP were finally included, and 68 developed severe pneumonia. Results: mNCP severity prognostic index values were calculated based on multivariate logistic regression: history of diabetes (OR 2.064, 95% CI 1.010– 4.683; p =0.043), time from symptom onset to admission ≥ 7 days (OR 1.945, 95% CI 1.054– 3.587; p =0.033), lymphocyte count ≤ 0.8 (OR 1.816, 95% CI 1.008– 3.274; p =0.047), myoglobin ≥ 90 mg/L (OR 2.496, 95% CI 1.235– 5.047; p =0.011), and D-dimer ≥ 0.5 mg/L (OR 2.740, 95% CI 1.395– 5.380; p =0.003). This model showed a c -statistics of 0.747, with sensitivity and specificity 0.764 and 0.644, respectively, under cutoff of 165. Conclusion: We designed a clinical predictive tool for risk of severe pneumonia among mNCP patients to provided guidance for medicines. Further studies are required for external validation.
机译:目的:预测入院患者轻度新型冠状病毒肺炎(MNCP)患者中发育严重肺炎的风险。方法:从2020年1月到2020年2月在上海和武汉的三家医院进行了回顾性队列研究。使用实时聚合物 - 反应测定检测Covid-19。招募了529例患有NCP的患者,从三家医院招募并在住院期间在患有新的冠状病毒感染引起的肺炎和治疗肺炎的标准期间,在住院期间分类为四种严重程度类型(第八版)。如果ICU在入场(N = 92)上录取(N = 92,在普通病房的情况下达成严重或临界类型的临时类型(n = 25)的情况,则被排除在外,或者临床信息不足(n = 64)。总和,最终包括348例MNCP患者,68例发育严重的肺炎。结果:MNCP严重程度基于多变量逻辑回归计算:糖尿病史(或2.064,95%CI 1.010-4.683; P = 0.043)。入学症状≥7天(或1.945,95%CI 1.054- 3.587; P = 0.033),淋巴细胞计数≤0.8(或1.816,95%CI 1.008- 3.274; P = 0.047),肌蛋白≥90mg/ l(或2.496,95%CI 1.235- 5.047; p = 0.011),D-二聚体≥0.5mg/ l(或2.740,95%CI 1.395- 5.380; p = 0.003)。该模型显示出0.747的AC类,与截止值为165的敏感性和特异性0.764和0.644。结论:我们设计了一种临床预测工具,用于MNCP患者中严重肺炎的风险,以提供Guidan CE用于药物。外部验证需要进一步的研究。

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