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中国防痨杂志 ›› 2011, Vol. 33 ›› Issue (9): 570-574.

• 论著 • 上一篇    下一篇

结核性毁损肺发生的相关因素分析

蔡宝云 张金福 初乃惠 康万里 郑素华 梁清涛 李琦   

  1. 首都医科大学附属北京胸科医院
  • 收稿日期:2011-05-23 出版日期:2011-09-10 发布日期:2012-01-29
  • 通信作者: 张金福 E-mail:zjinfu1960@sina.com

Analysis on correlative factors of tuberculous destroyed lung

CAI Bao-yun,ZHANG Jin-fu,CHU Nai-hui,KANG Wan-li,ZHENG Su-hua,LIANG Qing-tao,LI Qi   

  1. Beijing Chest Hospital, Capital Medical University
  • Received:2011-05-23 Online:2011-09-10 Published:2012-01-29
  • Contact: ZHANG Jin-fu E-mail:zjinfu1960@sina.com

摘要: 目的  分析结核性毁损肺发生的相关因素,为避免毁损肺发生提供依据。 方法  对2005年5月至2010年5月住院的结核性毁损肺患者100例和同期非毁损肺的肺结核患者100例进行比较。对患者的一般资料、病程、用药是否规律、耐药情况、肺内感染情况、肺病变数量、合并症、咯血、脓胸及是否有呼吸衰竭等相关因素做统计分析。结果  在单因素中,结核病病程(χ2=84.040,P<0.001)、耐药(χ2=53.107,P<0.001)、是否发生呼吸衰竭(χ2=11.753,P=0.001)、血红蛋白计数(Hg)(χ2=12.106,P=0.001)、是否有肺内感染(χ2=8.036,P=0.005)、咯血(χ2=11.293,P=0.001)、是否排菌(χ2=8.413, P=0.035)、有无脓胸发生(χ2=13.211,P<0.001),以及病变数量(χ2=22.917,P<0.001)是结核性毁损肺发生的危险因素,两组患者相比差异有统计学意义。 不规律治疗(χ2=25.149,P<0.001)、有无慢性阻塞性肺疾病(COPD)(χ2=5.647, P=0.017)、血清白蛋白(ALB)(χ2=6.650,P=0.010)亦是结核性损毁肺的危险因素,两组患者相比差异有统计学意义。在多因素分析中:病程长短[Wald χ2=24.47,P<0.01,OR=3.81(95%CI:2.24~6.64)]、耐药[Waldχ2=20.09,P<0.01,OR=27.11 (95%CI:6.40~114.79)]、合并症[Wald χ2=9.76,P<0.01, OR=4.88 (95%CI:1.81~13.20)]是结核性毁损肺发生的危险因素,两组患者相比差异有统计学意义;Hg[Wald χ2=3.95,P=0.050,OR=0.38(95%CI:0.14~0.99)]、是否排菌[Wald χ2=4.68,P=0.030,OR=0.61(95%CI:0.39~0.95)]、肺病变数量[Wald χ2=5.08,P=0.020,OR=26.53 (95%CI:1.54~458.52)]也是结核性毁损肺的危险因素,两组患者相比差异有统计学意义(P≤005)。结论  结核性毁损肺发生的原因是多方面的,为避免结核性毁损肺的发生要进行早期整体综合治疗。

关键词: 结核, 肺/并发症, 肺疾病, 危险因素

Abstract: Objective To analyze correlative factors of tuberculous destroyed lung in order to reduce occurrence of the disease.  Methods The data from 100 pulmonary tuberculosis patients with destroyed lung and 100 pulmonary tuberculosis patients without destroyed lung, who were admitted from May, 2005 to May, 2010,were investigated. Several factors including demographic data, duration of the disease, regular therapy, drug resistance, lung infection, the number of lesions, complications, hemoptysis, empyema, respiratory failure were analyzed. Results By using single factor analysis, several factors had a significant difference between two groups, including duration of the disease(χ2=84.040,P<0.001), drug resistance(χ2=53.107,P<0.001), respiratory failure(χ2=11.753, P=0.001), concentration of hemoglobin(χ2=12.106, P=0.001), lung infection(χ2=8.036,P=0.005)、hemoptysis(χ2=11.293, P=0.001), positive sputum AFB (χ2=8.413, P=0.035), empyema(χ2=13.211,P<0.001) and the number of lesions(χ2=22.917,P<0.001). In addition, factors such as regular therapy(χ2=25.149,P<0.001), complicated with COPD(χ2=5.647, P=0.017) and concentration of albumin(χ2=6.650,P=0.010) showed significant difference between two groups. By using multivariate analysis, factors such as duration of disease[Wald χ2=24.47, P<0.01, OR=3.81(2.24-6.64)], drug resistance[Wald χ2=20.09, P<0.01, OR=27.11 (6.40-114.79)], complications [Wald χ2=9.76,P<0.01, OR=4.88 (1.81-13.20)], concentration of hemoglobin[Wald χ2=3.95,P=0.050, OR=0.38 (0.14-0.99)], positive sputum AFB [Wald χ2=4.68, P=0.030, OR=0.61(0.39-0.95)] and the number of lesions [Wald χ2=5.08, P=0.020,OR=26.53 (1.54-458.52)]were risk factors for the occurrence of destroyed lung. Conclusion Various factors contribute to the occurrence of tuberculous destroyed lung. Early and comprehensive therapy can reduce the occurrence of tuberculous destroyed lung.

Key words: Tuberculosis,pulmonary/complications, Lung diseases, Risk factors