Abe C
Research Institute of Tuberculosis, Japan Anti-Tuberculosis Association, Tokyo, Japan.
Kekkaku. 1998 Nov;73(11):649-55.
Drug susceptibility testing is one of the most difficult procedures to standardize in mycobacteriology laboratories. International standardization of the test is needed for comparative evaluation of controlled chemotherapeutic trials, for epidemiological surveys on the prevalence of drug resistance, and for guidance in the treatment of tuberculosis patients. In 1996, a new procedure for drug susceptibility testing was proposed by an ad hoc committee of the Japanese Society for Tuberculosis. The proposal is for a test with the proportion method using an Ogawa egg medium similar to those recommended by the WHO. Resistance is expressed as the percentage of colonies that grow on critical concentrations of the drugs, i.e. 0.2 microgram/ml for isoniazid, 40 micrograms/ml for rifampicin, 10 micrograms/ml for streptomycin and 2.5 micrograms/ml for ethambutol. Strains of tubercle bacilli which are grown on drug-containing media represents more than 1% of the number of colonies that develop on drug-free media are considered to be clinically resistant to that agent. The results are recorded as susceptible (S) or resistant (R) on the laboratory forms. The proportion method using agar- and liquid-based media is used worldwide. In the near future a test with agar- or liquid-based media will be discussed for standardization of the test in Japan, as described by the National Committee for Clinical Laboratory Standards of the United States.
药物敏感性试验是分枝杆菌学实验室中最难标准化的程序之一。为了对对照化疗试验进行比较评估、开展耐药性流行情况的流行病学调查以及指导结核病患者的治疗,需要对该试验进行国际标准化。1996年,日本结核病协会特设委员会提出了一种新的药物敏感性试验程序。该提议是采用比例法,使用与世界卫生组织推荐的类似的小川鸡蛋培养基进行试验。耐药性以在临界药物浓度下生长的菌落百分比表示,即异烟肼为0.2微克/毫升、利福平为40微克/毫升、链霉素为10微克/毫升、乙胺丁醇为2.5微克/毫升。在含药培养基上生长的结核杆菌菌株数量超过在不含药培养基上生长的菌落数量的1%,则被认为对该药物临床耐药。结果在实验室表格上记录为敏感(S)或耐药(R)。使用基于琼脂和液体培养基的比例法在全球范围内使用。正如美国国家临床实验室标准委员会所描述的那样,在不久的将来,将讨论使用基于琼脂或液体培养基的试验,以实现日本该试验的标准化。