Research on risk factors for mortality and a predictive model for severe fever with thrombocytopenia syndrome
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摘要:
目的 研究重症发热伴血小板减少综合征(SFTS)患者死亡的危险因素,建立风险预测模型,以期为重症SFTS的预后判断提供依据。 方法 回顾分析2023年1—12月中国科学技术大学附属第一医院(安徽省立医院)感染科收治的30例重症SFTS患者,根据预后分为存活组(15例)和死亡组(15例),对2组的临床资料进行分析。 结果 选择热程≥7 d(a)、是否昏迷(b)、活化部分凝血活酶时间(APTT, c)、天冬氨酸转氨酶(AST,d)、肌酸激酶(CK, e)、白细胞介素-6(IL-6, f)、单核细胞(MONO,g),通过Fisher判别分析建立预测死亡(X)函数为:X=-23.731+2.632a+18.146b+0.425c-0.009d+0.002f+0.650g;预测存活(Y)函数为:Y=-16.245-4.594a-0.416b+0.491c-0.015d-0.001e+0.002f+16.057g;得到判别函数值,预测死亡(X)风险模型判别正确率为93.3%,预测存活(Y)概率模型正确率为100.0%,整体预测准确率为96.7%。 结论 重症SFTS患者多数为老年人,具有较高的死亡率,基于热程≥7 d、昏迷、APTT、AST、CK、IL-6、MONO建立的死亡预测模型准确率高,有预测价值。 -
关键词:
- 发热伴血小板减少综合征 /
- 死亡危险因素 /
- 预测模型
Abstract:Objective To investigate risk factors associated with mortality in patients with severe fever with thrombocytopenia syndrome (SFTS) and to establish a mortality risk prediction model, with the aim of providing evidence for therapeutic decision-making and prognosis judgement of SFTS. Methods A retrospective analysis was conducted on 30 patients with severe SFTS admitted to the Department of Infectious Disease of the First Affiliated Hospital of USTC (Anhui Provincial Hospital) from January to December 2023. The patients were divided into a survival group (n=15) and the death group (n=15) based on their outcomes. Clinical characteristics and laboratory indicators from the two groups were compared. Results Seven variables were selected for further analysis: fever duration ≥ 7 days (a), coma (b), activated partial thromboplastin time (APTT, c), aspartate aminotransferase (AST, d), creatine kinase (CK, e), interleukin-6 (IL-6, f), and monocyte count (MONO, g). The Fisher discriminant analysis was used to establish a predictive death (X) function as follows: X=-23.731+2.66a+18.146b+0.425c-0.009d+0.002f+0.650g, and a predicted survival (Y) function: Y=-16.245-4.594a-0.416b+0.491c-0.015d-0.001e+0.002f+16.057g. The discriminant function values showed that the mortality (X) prediction model had an accuracy of 93.3%, the survival (Y) probability model had an accuracy of 100.0%, and the overall prediction accuracy was 96.7%. Conclusion Severe SFTS is associated with high mortality. The mortality prediction model based on fever duration≥7 days, coma, APTT, AST, CK, IL-6, and MONO demonstrates high accuracy and possesses significant predictive value. -
表 1 2组SFTS患者基线特征比较
Table 1. Comparison of baseline characteristics between the two groups of SFTS patients
组别 例数 年龄(x±s,岁) 性别(男性/女性,例) 发病到确诊时间[M(P25, P75),d] 发病到入住ICU时间(x±s,d) 总住院时间[M(P25, P75),d] ≥2个基础疾病[例(%)] 高血压[例(%)] 糖尿病[例(%)] 脑卒中[例(%)] 存活组 15 64.93±13.80 11/4 7(4, 9) 8.13±2.62 16(13, 20) 5(33.33) 7(46.67) 1(6.67) 3(20.00) 死亡组 15 72.40±7.12 9/6 6(4, 8) 8.20±2.21 5(2, 7) 5(33.33) 6(40.00) 3(20.00) 4(26.67) 统计量 1.863a -0.912c 0.075a -4.455c P值 0.077 0.700b 0.362 0.940 <0.001 0.999b 0.598b 0.999b 0.999b 注:a为t值,b为采用Fisher精确检验,c为Z值。 表 2 2组SFTS患者临床症状比较[例(%)]
Table 2. Comparison of clinical manifestations between the two groups of SFTS patients
项目 例数 存活组(n=15) 死亡组(n=15) P值a 发热≥7 d 16 4(26.67) 12(80.00) 0.001 呼吸系统症状 19 6(40.00) 13(86.67) 0.002 神经系统症状 25 10(66.67) 15(100.00) 0.100 昏迷 16 1(6.67) 15(100.00) <0.001 皮肤黏膜出血 19 4(26.67) 15(100.00) <0.001 胃肠道出血 8 4(26.67) 4(26.67) 0.450 心律失常 26 13(86.67) 13(86.67) 0.999 休克 10 2(13.33) 8(53.33) 0.050 心功能不全 15 6(40.00) 9(60.00) 0.466 注:a为采用Fisher精确检验。 表 3 2组SFTS患者治疗方式比较[例(%)]
Table 3. Comparison of treatments between the two groups of SFTS patients [cases (%)]
组别 例数 皮质类固醇 丙球蛋白 升压剂 需要呼吸支持 CRRT 存活组 15 14(93.33) 14(93.33) 2(13.33) 4(26.67) 1(6.67) 死亡组 15 13(86.67) 15(100.00) 10(66.67) 15(100.00) 6(40.00) P值a 0.999 0.999 0.008 <0.001 0.080 注:a为采用Fisher精确检验。 表 4 2组SFTS患者实验室检查指标比较
Table 4. Comparison of laboratory examinations between the two groups of SFTS patients
项目 存活组(n=15) 死亡组(n=15) 统计量 P值 WBC[M(P25, P75), ×109/L] 1.80(1.17, 6.20) 2.0(1.55, 3.33) -0.228a 0.820 NE[M(P25, P75), ×109/L] 3.28(1.10, 6.32) 1.43(0.80, 2.56) -0.933a 0.351 L(x±s, ×109/L) 0.65±0.28 0.62±0.32 0.266b 0.792 N/L[M(P25, P75)] 5.64(2.52, 8.87) 3.18(1.46, 4.32) 0.850a 0.395 MONO[M(P25, P75), ×109/L] 0.57(0.28, 0.88) 0.08(0.05,0.20) -3.342a 0.001 PLT[M(P25, P75), ×109/L] 22(11, 28) 24(12, 28) -0.312a 0.755 AST[M(P25, P75), U/L] 217(96, 406) 576(356, 1104) -2.821a 0.005 LDH[M(P25, P75), U/L] 1 249(569, 1 899) 2 507(1 299, 3192) -2.883a 0.004 CK[M(P25, P75), U/L] 565(290, 1 243) 3 537(1 210, 5 181) -3.443a < 0.001 APTT[M(P25, P75), s] 53.00(44.40, 66.90) 74.00(64.00, 80.00) -2.884a 0.004 CRP[M(P25, P75), mg/L] 23.68(10.30, 49.65) 28.32(8.37, 65.00) -0.311a 0.756 SF[M(P25, P75), μg/mL] 2 944(2 109, 3 124) 2 201(1 636, 2 837) -1.421a 0.155 IL-6 [M(P25, P75), pg/mL] 18.6(6.5, 34.1) 124.0(69.0, 304.0) -3.878a < 0.001 核酸阳性[例(%)] 15(50.00) 14(46.67) 0.999c 核酸Ct值(x±s) 23.90±2.94 21.36±4.84 1.720b 0.097 注:a为Z值,b为t值,c为采用Fisher精确检验。 表 5 Fisher判别分析预测SFTS患者临床结局
Table 5. Fisher discriminate analysis predict the accuracy of SFTS patient outcomes
结局指标 好转[例(%)] 死亡[例(%)] 总计(例) 好转 14(93.30) 1(6.70) 15 死亡 0 15(100.00) 15 -
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