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Mdrtb: Current Status

机译:Mdrtb:当前状态

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Drug resistant tuberculosis has been reported since the early days of the introduction of chemotherapy, but recently multi-drug resistant tuberculosis (MDR-TB) has been an area of growing concern and is posing a threat to control of tuberculosis. A review of 63 surveys conducted between 1985 and 1994 suggested that primary and acquired MDR-TB was between 0-10.8% and 0-48% respectively. However, the qualities of these studies were variable due to the lack of proper representativeness and size of population sampled, as well as lack of standardized laboratory methods in some of them. In 1994, WHO-IUATLD carried out a surveillance which concluded that the problem is global; the median prevalence of primary and acquired multi drug resistance was 1.4% (0-14.4%) and 13% (0-54.4%) respectively. A second WHO-IUATLD global project on drug surveillance carried out in 1996-1999 in 58 countries, found that the median prevalence of primary and acquired multi-drug resistance was 1% (0-14%) and 9% (0 - 48%) respectively. Current estimates report, the prevalence of primary and acquired multidrug resistance in India as 3.4% and 25% respectively.. It must be emphasized that optimal treatment of MDR-TB alone will not curb the epidemic. Efforts must be focused on the effective use of first line drugs in every new patient so as to prevent the ultimate emergence of multidrug resistance. The use of reserve drugs to cure multi-drug resistant tuberculosis and to reduce further transmission should be considered, but only as part of well structured programmes of tuberculosis control.
机译:自从化疗开始以来就已经报告了耐药性结核病,但是最近耐多药结核病(MDR-TB)成为人们日益关注的领域,并且对控制结核病构成威胁。 1985年至1994年进行的63项调查的回顾表明,原发性和获得性耐多药结核分别在0-10.8%和0-48%之间。然而,由于缺乏适当的代表性和抽样人群的规模,以及其中一些缺乏标准化的实验室方法,这些研究的质量是可变的。 1994年,WHO-IUATLD进行了监测,得出的结论是该问题是全球性的。原发性和获得性多重耐药的中位患病率分别为1.4%(0-14.4%)和13%(0-54.4%)。 WHO-IUATLD的第二个全球药物监控项目于1996-1999年在58个国家实施,发现原发性和获得性多药耐药性的中位数患病率分别为1%(0-14%)和9%(0-48% ) 分别。目前的估计报告指出,印度原发性和获得性多药耐药性的患病率分别为3.4%和25%。必须强调的是,仅对耐多药结核病进行最佳治疗并不能遏制这一流行病。必须将努力集中在每个新患者中有效使用一线药物,以防止最终出现多药耐药性。应该考虑使用储备药物治疗耐多药结核病并减少进一步的传播,但这仅是结核病控制结构良好计划的一部分。

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