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吲哚菁绿清除试验联合总胆红素留存率对人工肝治疗HBV相关慢加急性肝衰竭患者短期预后的评估价值

都泓莲 李烨 王波 马琳坤 胡甜甜 盛云建 陈文 吴刚 邓存良

引用本文:
Citation:

吲哚菁绿清除试验联合总胆红素留存率对人工肝治疗HBV相关慢加急性肝衰竭患者短期预后的评估价值

DOI: 10.3969/j.issn.1001-5256.2023.02.009
基金项目: 

四川省卫生健康委员会医学科技项目 (21PJ098)

伦理学声明:本研究方案于2022年1月7日经由西南医科大学附属医院伦理委员会审批,批号:KY2022003。
利益冲突声明:本研究不存在研究者、伦理委员会成员、受试者监护人以及与公开研究成果有关的利益冲突。
作者贡献声明:都泓莲、李烨、盛云建负责课题设计,资料分析,撰写论文;都泓莲、王波、马琳坤、胡甜甜参与收集数据,修改论文;陈文、吴刚、邓存良负责拟定写作思路,指导撰写文章。
详细信息
    通信作者:

    邓存良,dengcunl64@vip.sina.com (ORCID: 0000-0002-9120-8661)

Value of indocyanine green clearance test combined with total bilirubin actual resident rate in evaluating the short-term prognosis of patients with hepatitis B virus-related acute-on-chronic liver failure after artificial liver support system therapy

Research funding: 

Medical Science and Technology Project of the Health Commission of Sichuan Province (21PJ098)

More Information
  • 摘要:   目的  联合吲哚菁绿清除试验(ICG)和总胆红素留存率(TBARR)建立预测经人工肝治疗的HBV相关慢加急性肝衰竭(HBV-ACLF)患者短期预后的新模型。  方法  回顾性收集2017年6月—2021年7月西南医科大学附属医院感染科收治的136例经人工肝治疗的HBV-ACLF患者的临床资料,据随访3个月时的转归情况分为存活组(n=92)和死亡组(n=44),检测确诊ACLF时的生化、凝血、吲哚菁绿15分钟滞留率(ICG R15)及肝有效血流量(EHBF)等指标,计算终末期肝病模型(MELD)评分、MELD差值(ΔMELD)、Child-Turcotte-Pugh(CTP)评分、总胆红素清除率(TBCR)、总胆红素反弹率(TBRR)和TBARR。偏态分布的计量资料两组间比较采用Mann-Whitney U检验;计数资料两组间比较则采用χ2检验。应用二分类Logistic回归分析法,构建人工肝治疗HBV-ACLF短期预后的联合预测模型。应用受试者工作特征曲线下面积(AUC)评估各种模型对人工肝治疗HBV-ACLF短期预后判断的准确性,AUC的比较采用Z检验。  结果  死亡组与存活组两组间比较,MELD评分、ΔMELD、CTP评分、ICG R15、EHBF、TBRR、TBARR、中性粒细胞计数、中性粒细胞百分比、淋巴细胞计数、PLT、ALP、GGT、Alb、PT、INR、PTA、总胆红素、前白蛋白、纤维蛋白原、血清Na、年龄及肝性脑病发生率差异均有统计学意义(P值均<0.05)。多因素Logistic回归分析显示,年龄(OR=1.096,95%CI:1.056~1.137,P<0.001)、中性粒细胞计数(OR=1.214,95%CI:1.044~1.411,P=0.012)、TBRR(OR=0.989,95%CI:0.982~0.996,P=0.001)、TBARR(OR=1.073,95%CI:1.049~1.098,P<0.001)、ΔMELD(OR=1.480,95%CI:1.288~1.701,P<0.001)、CTP评分(OR=2.081,95%CI:1.585~2.732,P<0.001)以及ICG R15(OR=1.116,95%CI:1.067~1.168,P<0.001)是经人工肝治疗HBV-ACLF患者短期死亡的独立影响因素。应用二分类Logistic回归分析,构建了4种人工肝治疗HBV-ACLF短期预后的联合预测模型,分别为TBRR-ICG R15、TBARR-ICG R15、TBARR-ICG R15-ΔMELD和TBARR-ICG R15-ΔMELD-年龄,AUC分别为0.830、0.867、0.900、0.917,联合预测模型的AUC高于单一指标(年龄、中性粒细胞计数、TBRR、TBARR、ΔMELD、MELD评分、CTP评分、ICG R15),其中TBARR-ICG R15-ΔMELD-年龄模型的AUC最大。联合模型TBARR-ICG R15-ΔMELD和TBARR-ICG R15-ΔMELD-年龄的敏感度和特异度均在80%以上。  结论  ICG R15联合TBARR构建的联合预测模型对人工肝治疗HBV-ACLF患者的短期预后有较好的预测价值,联合模型对预后判断的准确性优于单一模型。

     

  • 图  1  部分单项指标和联合预测模型的ROC曲线

    Figure  1.  ROC curves of partial single indicators and combined predictive models

    表  1  存活组和死亡组各项指标比较

    Table  1.   Comparison of various indicators between survival and non-survival group

    项目 总数(n=136) 存活组(n=92) 死亡组(n=44) 统计值 P
    男/女(例) 117/19 80/12 37/7 χ2=0.203 0.652
    年龄(岁) 50(42~56) 47(38~54) 54(45~60) Z=-5.625 <0.001
    肝硬化[例(%)] 70(51.47) 42(45.65) 28(63.64) χ2=3.854 0.050
    HBeAg阳性[例(%)] 48(35.29) 34(36.96) 14(31.82) χ2=0.344 0.557
    HBV DNA载量(log10) 6.62(4.80~7.39) 6.59(4.74~7.38) 6.66(4.95~7.41) Z=-0.293 0.770
    腹膜炎[例(%)] 115(84.56) 75(81.52) 40(90.91) χ2=1.354 0.245
    肝性脑病[例(%)] 30(22.06) 7(7.61) 23(52.27) χ2=34.536 <0.001
    人工肝次数 3(3~4) 3(3~4) 3(3~5) Z=-1.913 0.056
    WBC(×109/L) 6.88(5.40~8.56) 6.81(5.24~8.56) 7.05(5.51~8.27) Z=-1.215 0.224
    中性粒细胞百分比(%) 73.60(67.70~79.60) 71.65(65.95~75.68) 78.50(72.85~82.80) Z=-6.721 <0.001
    中性粒细胞计数(×109/L) 4.97(3.71~6.40) 4.79(3.44~6.40) 5.16(4.14~6.81) Z=-2.743 0.006
    淋巴细胞计数(×109/L) 1.02(0.79~1.42) 1.10(0.85~1.51) 0.84(0.63~1.15) Z=-6.639 <0.001
    Hb(g/L) 133(120~148) 134(122~148) 132(120~147) Z=-0.729 0.466
    PLT(×109/L) 108(81~138) 115(92~148) 91(71~115) Z=-5.713 <0.001
    ALT(U/L) 848.7(308.0~1 513.8) 924.1(303.2~1 580.4) 648.3(345.9~1 346.0) Z=-1.723 0.085
    AST(U/L) 558.3(234.6~1 298.5) 598.3(235.9~1 304.4) 557.5(222.05~1 170.6) Z=-0.207 0.836
    ALP(U/L) 154.0(123.6~187.2) 146.0(118.3~187.2) 164.8(133.5~190.8) Z=-1.970 0.049
    GGT(U/L) 116.5(70.9~176.3) 118.9(80.1~188.5) 104.8(64.3~160.3) Z=-2.615 0.009
    pAlb(g/L) 44.4(29.6~62.9) 45.8(31.6~63.4) 41.2(21.6~61.2) Z=-2.400 0.016
    Alb(g/L) 32.3(29.0~35.2) 32.6(29.0~36.3) 31.0(28.5~33.8) Z=-2.819 0.005
    TBil(μmol/L) 300.3(226.3~381.1) 286.1(194.7~366.1) 341.9(252.3~461.0) Z=-4.424 <0.001
    PT(s) 23.4(20.6~26.6) 21.7(19.8~25.6) 25.5(23.9~31.8) Z=-9.192 <0.001
    INR 2.09(1.78~2.42) 1.90(1.69~2.26) 2.29(2.12~2.99) Z=-9.425 <0.001
    PTA(%) 37(32~45) 41(35~47) 34(25~37) Z=-9.312 <0.001
    Fib(g/L) 1.67(1.43~1.92) 1.74(1.52~2.03) 1.57(1.39~1.82) Z=-4.286 <0.001
    肌酐(μmol/L) 65.6(58.2~75.8) 66.3(57.8~75.2) 65.6(58.2~76.9) Z=-0.139 0.889
    K(mmol/L) 3.94(3.64~4.30) 3.93(3.65~4.27) 4.04(3.61~4.41) Z=-0.670 0.503
    Na(mmol/L) 137.4(135.6~139.6) 138.0(135.8~139.7) 136.6(134.2~139.3) Z=-2.369 0.018
    AFP(ng/mL) 47.37(15.05~138.32) 59.14(15.05~169.96) 40.00(14.46~123.5) Z=-1.587 0.112
    TBCR(%) 48.86(31.99~61.17) 46.45(33.09~61.74) 52.67(31.19~60.31) Z=-0.646 0.518
    TBRR(%) 63.19(26.21~113.26) 57.07(19.43~99.95) 72.64(42.22~149.55) Z=-4.335 <0.001
    TBARR(%) 87.32(71.92~97.40) 78.54(70.65~90.96) 96.12(88.77~102.78) Z=-8.587 <0.001
    MELD评分 22.19(19.93~25.22) 21.46(18.32~23.62) 24.62(21.92~28.22) Z=-7.495 <0.001
    △MELD(分) 5.62(3.48~8.15) 4.64(3.04~6.74) 8.00(5.36~10.05) Z=-7.736 <0.001
    CTP评分 11(10~12) 10(9~11) 12(11~13) Z=-9.977 <0.001
    ICG R15(%) 52.5(45.8~58.3) 50.9(42.5~54.9) 56.6(50.9~63.8) Z=-8.236 <0.001
    EHBF(L/min) 0.18(0.14~0.22) 0.20(0.16~0.25) 0.15(0.12~0.18) Z=-8.276 <0.001
    注:pAlb,前白蛋白;Fib,纤维蛋白原。
    下载: 导出CSV

    表  2  单项指标和联合预测模型的AUC、敏感度、特异度及临界值

    Table  2.   AUC, sensitivity, specificity and cut-off values of single indicators and combined predictive models

    项目 AUC 敏感度(%) 特异度(%) 临界值
    年龄(岁) 0.667 70.45 55.43 49
    中性粒细胞计数(×109/L) 0.601 47.73 69.57 5.57
    TBRR(%) 0.671 52.27 76.09 94.36
    TBARR(%) 0.788 81.82 69.57 85.46
    △MELD(分) 0.760 63.64 79.35 7.03
    MELD评分 0.751 65.91 78.26 23.75
    CTP评分 0.781 93.18 51.09 10
    ICG R15(%) 0.773 50.00 89.13 58.3
    TBRR-ICG R15 0.830 61.36 90.22 -0.1
    TBARR-ICG R15 0.867 84.09 79.35 -0.8
    TBARR-ICG R15-△MELD 0.900 86.36 80.43 -0.76
    TBARR-ICG R15-△MELD-年龄 0.917 88.64 85.87 -0.6
    下载: 导出CSV
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    覃婷, 李前龙. 总胆红素反弹率对血浆置换治疗乙肝相关慢加急性肝衰竭的短期预测价值[J]. 临床消化病杂志, 2021, 33(5): 351-355. DOI: 10.3870/lcxh.j.issn.1005-541X.2021.05.11.
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  • 收稿日期:  2022-07-19
  • 录用日期:  2022-08-25
  • 出版日期:  2023-02-20
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