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张明周,吴学玲,王长征,唐婷.277例弥漫性实质性肺疾病住院患者死亡危险因素分析[J].陆军军医大学学报(原第三军医大学学报),2016,38(06):642-646.
Zhang Mingzhou,Wu Xueling,Wang Changzheng,Tang Ting.Death risk factors of hospitalized patients with diffuse parenchymal lung disease: a retrospective case control study[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(06):642-646.
张明周,吴学玲,王长征,唐婷.277例弥漫性实质性肺疾病住院患者死亡危险因素分析[J].陆军军医大学学报(原第三军医大学学报),2016,38(06):642-646. DOI:
Zhang Mingzhou,Wu Xueling,Wang Changzheng,Tang Ting.Death risk factors of hospitalized patients with diffuse parenchymal lung disease: a retrospective case control study[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(06):642-646. DOI:
目的 探讨277例弥漫性实质性肺疾病住院患者死亡的影响因素。 方法 本院呼吸内科弥漫性实质性肺疾病(DPLD)的病例依据病因分为结缔组织疾病相关DPLD组(CTD-IP)、其他已知病因DPLD组和特发性间质性肺炎(IIPS)组,每组按预后情况分又为非死亡组和死亡组两个亚组,采用病例对照的研究方法进行风险因素回顾性分析。 结果 IIPS组死亡亚组年龄平均、基础疾病患病率及CRP、ALT、AST指标高于非死亡组,CTD-IP组死亡亚组的CRP、WBC、AST指标高于非死亡组,其他病因组两亚组的病因构成提示有统计学差异,其死亡亚组CRP、PT、APTT、ALT、AST高于非死亡组。将上述各组指标进行曲线分析,AUC大于0.7指标作为死亡风险预测指标,并计算出其截断点作为最佳诊断阈值纳入多因素logistics回归分析。结果显示IIPS组中CRP40(mg/L)和年龄70(岁)、CTD-IP中CRP40(mg/L)、其他组中CRP50(mg/L) 为独立死亡危险因素。 结论 CRP升高、高龄及药物继发性DPLD是弥漫性实质性肺疾病患者住院死亡的危险因素,其中前者是DPLD患者的共同危险因素,而后两者分别是IIPS组和其他病因组的独立危险因素。上述因素在用于预测不同类型DPLD患者死亡风险中需区别分析。
Objective To explore the death risk factors of 277 cases of diffuse parenchymal lung disease (DPLD) in the hospital. Methods According to the etiology
the patients with interstitial lung disease were divided into 4 groups: connective tissue disease associated DPLD group (CTD-IP group)
idiopathic interstitial pneumonia (IIPS) group and other known cause associated DPLD group. And each group was further divided into non-death subgroup and death subgroup. All cases were analyzed retrospectively with a case-control study method. Results In the IIPS group
the average age
basic disease prevalence rate
C-reactive protein (CRP)
alanine aminotransferase (ALT)
and aspartate aminotransferase (AST) in the death subgroup were higher than those in the non-death subgroup. In the CTD-IP group
the CRP
white blood cell (WBC) and AST in the death subgroup were higher than those in the non-death subgroup. In the other known cause associated DPLD group
the CRP
prothrombin time (PT)
activated partial thromboplastin time (APTT)
ALT and AST in the death subgroup were higher than those in the non-death subgroup
and the difference of etiologies between two subgroups was significant. The above indexes with AUC higher than 0.7 in curve analysis were taken as death risk forecast indexes
and the calculated cutoff points were taken as the best diagnostic thresholds. Multiple logistic regression analysis showed that independent risk factors were CRP40 mg/L and age70 years old in the IIPS group
CRP40 mg/L in the CTD-IP group
and CRP50 mg/L in the other known cause associated DPLD group. Conclusion Elevated CRP
advanced age and drug-induced DPLD are death risk factors of DPLD patients in the hospital. The elevated CRP is common death risk factor for DPLD patients
and the advanced age and drug-induced DPLD are independent risk factors for the IIPS group and the other known cause-associated DPLD group
respectively. When the factors are used to predict the death risk of the patients with DPLD
the difference of various types of DPLD needs to be considered.
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