Wexler H M
Research Service, Veterans Administration Medical Center, West Los Angeles, California 90073.
Clin Microbiol Rev. 1991 Oct;4(4):470-84. doi: 10.1128/CMR.4.4.470.
The demand for susceptibility testing of anaerobes has increased, yet consensus as to procedure and interpretation in this area has not been achieved. While routine testing of anaerobic isolates is not needed, certain isolates in specific clinical settings should be tested. Also, laboratories may monitor their local antibiograms by doing periodic surveillance batch testing. The National Committee for Clinical Laboratory Standards has published a protocol of methods approved for susceptibility testing of anaerobic bacteria. Both agar and broth microdilution are included; however, the broth disk elution method is no longer approved by the National Committee for Clinical Laboratory Standards because of method-related interpretive errors. A number of newer methods are undergoing evaluation and seem promising. Clinicians and microbiologists reviewing susceptibility reports should be aware of sources of variability in the test results. Variables in susceptibility testing of anaerobes include the media and methods used, organisms chosen for testing, breakpoints chosen for interpretation, antibiotic, and determination of endpoint. Clustering of MICs around the breakpoint may lead to significant variability in test results. Adherence of testing laboratories to approved methods and careful descriptions of the method and the breakpoints used for interpretation would facilitate interlaboratory comparisons and allow problems of emerging resistance to be noted. A variety of resistance mechanisms occurs in anaerobic bacteria, including the production of beta-lactamase and other drug-inactivating enzymes, alteration of target proteins, and inability of the drug to penetrate the bacterial wall. Antimicrobial resistance patterns in the United States and abroad are described.
对厌氧菌药敏试验的需求有所增加,但在该领域的操作程序和结果解读方面尚未达成共识。虽然不需要对所有厌氧分离株进行常规检测,但在特定临床环境中的某些分离株应该进行检测。此外,实验室可以通过定期进行监测批量检测来监测当地的抗菌谱。美国国家临床实验室标准委员会已经发布了一份用于厌氧菌药敏试验的批准方法协议。琼脂稀释法和肉汤稀释法都包括在内;然而,由于方法相关的解读错误,肉汤纸片洗脱法已不再被美国国家临床实验室标准委员会批准。一些更新的方法正在接受评估,看起来很有前景。审查药敏报告的临床医生和微生物学家应该了解检测结果变异性的来源。厌氧菌药敏试验中的变量包括所使用的培养基和方法、用于检测的菌株、用于解读的折点、抗生素以及终点的判定。最低抑菌浓度(MIC)在折点附近聚集可能导致检测结果出现显著差异。检测实验室坚持使用批准的方法,并仔细描述所使用的方法和用于解读的折点,将有助于实验室间的比较,并能够发现新出现的耐药问题。厌氧菌中存在多种耐药机制,包括β-内酰胺酶和其他药物灭活酶的产生、靶蛋白的改变以及药物无法穿透细菌细胞壁。文中描述了美国国内外的抗菌药物耐药模式。