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中国防痨杂志 ›› 2014, Vol. 36 ›› Issue (1): 9-13.doi: 10.3969/j.issn.1000-6621.2014.01.003

• 论著 • 上一篇    下一篇

肝脏基础疾病对抗结核药物性肝损伤的影响及防治措施评价

雷建平 邓国防 刘   

  1. 330008 南昌,江西省胸科医院结核科(雷建平、刘);深圳市第三人民医院肺二科(邓国防)
  • 收稿日期:2013-09-13 出版日期:2014-01-10 发布日期:2014-01-05
  • 通信作者: 雷建平 E-mail:Lei-jianping@vip.sina.com

Impact of other liver diseases against TB drugs-induced liver injury and its prevention

LEI Jian-ping, DENG Guo-fang, LIU Zhou   

  1. Department of Tuberculosis Medicine, the Chest Hospital of Jiangxi Province,Nanchang 330008,China
  • Received:2013-09-13 Online:2014-01-10 Published:2014-01-05
  • Contact: LEI Jian-ping E-mail:Lei-jianping@vip.sina.com

摘要: 目的 探讨肝脏基础疾病对抗结核药物性肝损伤的影响及评价若干肝损伤防治措施的临床效果。方法 对2011年1月至2012年12月收治的全部1337例患者(A组)实施肝损伤防治措施(其中有肝脏基础疾病患者287例),肝损伤患者245例为B组;B组又分为肝损伤前未接受防治措施211例为B1组和接受防治措施后发生肝损伤34例为B2组。分析肝脏基础疾病对抗结核药物性肝损伤的影响并评价防治效果。计数资料采用χ2检验,计量资料采用t检验,P<0.05为差异有统计学意义。结果 有肝脏基础疾病患者肝损伤发生率40.4%(116/287),高于无基础疾病患者(12.3%,129/1050);合并乙型肝炎患者肝损伤发生率58.5%(83/142),高于全部患者(18.3%,245/1337),差异均有统计学意义(χ2值分别为16.2320、119.7547,P值均<0.01)。B1组丙氨酸转氨酶(ALT)≥8倍正常值上限(ULN)(41/211)或(和)总胆红素(TBIL)≥4倍 ULN者(44/211)高于B2组(0/34和2/34),差异均有统计学意义(χ2值分别为7.9344、4.3033, P<0.01或P<0.05)。B2组ALT、天门冬氨酸转氨酶(AST)、谷氨酰转肽酶(GGT)、TBIL、直接胆红素(DBIL)和间接胆红素(IBIL)[(173.8±197.0)IU/L、(113.3±208.6)IU/L、(74.5±73.4)IU/L、(22.3±84.9)μmol/L、(11.3±36.9)μmol/L、(10.7±25.4)μmol/L]均低于B1组[(343.4±235.4)IU/L、(270.7±246.6)IU/L、(115.5±83.5)IU/L、(84.6±102.6)μmol/L、(34.7±42.8)μmol/L、(30.5±30.7)μmol/L],而白蛋白(Alb)[(35.5±3.8)g/L]高于B1组[(32.5±3.7)g/L],差异均有统计学意义(t值分别为3.9805、3.5226、2.6990、3.2093、2.8648、3.4089和t′=4.0968, P值<0.01或<0.05)。B2组治疗中断率低于B1组(2/34,211/211),差异有统计学意义(χ2=220.2098, P<0.01)。结论 肝脏基础疾病可增加抗结核药物性肝损伤发生,抗结核治疗中执行肝损伤防治措施可减少肝损伤的发生并减少治疗中断率。

关键词: 抗结核药, 肝炎, 中毒性, 肝疾病

Abstract: Objective  Study on the relationship between some foundation diseases in liver and antituberculosis drug-induced liver injury to approach the controlling and preventing measures.   Methods  For patients with other liver disease before anti-TB treatment, records the patient’s medical history and laboratory test results, development of appropriate anti-TB treatment regime to take measures to protect the liver. Assess effect of these measures in the treatment process of 1337 cases from January 2011 to December 2012. The data uses the card side examination; the measurement uses the t-test, carries on statistics analysis. P<0.05 means significance differences.   Results  Incidence of liver injury in patients with underlying disease of the liver (40.4%,116/287), was higher than patients without underlying disease (12.3%,129/1050);Merged incidence of liver injury in patients with hepatitis b (58.5%,83/142), above all of the cases (18.3%,245/1337), the differences were statistically significant respectively (χ2=16.2320, and 119.7547,P<0.01).The liver harm group B1 group alanine aminotransferase (ALT) ≥8 times the upper limit of normal value (ULN) or (and) total bilirubin (TBIL) ≥ 4 times ULN is higher than the B2 Group, the differences are statistically significant (χ2=7.9344, χ2=4.3033, P<0.01 or P<0.05).Group B2 ALT, aspartate aminotransferase (AST), transformation of l-glutamine peptide enzyme (GGT), TBIL, direct bilirubin (DBIL) and indirect bilirubin (IBIL) ((173.8±197.0) IU/L,(113.3±208.6) IU/L,(74.5±73.4) IU/L,(22.3±84.9) μmol/L,(11.3±36.9) μmol/L,(10.7±25.4) μmol/L) are below B1 ((343.4±235.4) IU/L,(270.7±246.6) IU/L,(115.5±83.5) IU/L,(84.6±102.6) μmol/L,(34.7±42.8) μmol/L,(30.5±30.7) μmol/L), and albumin (Alb) ((35.5±3.8) g/L) is higher than the B1 Group ((32.5±3.7) g/L), the differences are statistically significant (t=3.9805,3.5226,2.6990,3.2093,3.8648,3.4089 and t′=4.0968, P-value <0.01 or <0.05).Treatment of group B2 group interrupt rate is lower than B1 (2/34,211/211) and the difference was statistically significant (χ2=220.2098, P<0.01).  Conclusion  The study suggests the some liver diseases can significantly increase the liver injury induced by anti-tuberculosis drugs, implementation of anti-TB treatment liver damage control measures can reduce the incidence of liver damage and reduce the rates of treatment interruption.

Key words: Antitubercular agents, Hepatitis, toxic, Liver diseases