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The World Health Organization's External Quality Assurance System Proficiency Testing Program Has Improved the Accuracy of Antimicrobial Susceptibility Testing and Reporting among Participating Laboratories Using NCCLS Methods

机译:世界卫生组织的外部质量保证体系能力验证计划使用NCCLS方法提高了参与实验室中抗菌药物敏感性测试和报告的准确性

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摘要

A total of 150 laboratories in 33 countries that followed the NCCLS testing procedures participated in the World Health Organization's External Quality Assurance System for Antimicrobial Susceptibility Testing (EQAS-AST) from January 1998 through March 2001. Laboratories tested seven bacterial isolates for antimicrobial resistance and reported the results to the Centers for Disease Control and Prevention (CDC) in Atlanta, Ga. The results were compared to the results generated at the CDC with the NCCLS broth microdilution and disk diffusion reference methods. Although there were few testing errors with Salmonella enterica subsp. enterica serovar Enteritidis, drugs that are not appropriate for therapy of Salmonella infections were tested and reported by 136 (91%) of 150 laboratories. In addition, 29 (20%) of 150 laboratories used the Staphylococcus aureus breakpoints to report oxacillin results for Staphylococcus saprophyticus. For a vanB-containing Enterococcus faecalis strain, 124 (83%) of 150 laboratories correctly reported vancomycin results that were ±1 doubling dilution from the reference MIC or ±3 mm from the reference disk diffusion result. Of the laboratories that tested Streptococcus agalactiae by disk diffusion, 17% reported nonsusceptible results for penicillin in error. While 110 laboratories (73%) tested the S. pneumoniae challenge isolate against a fluoroquinolone, 83% tested it against ciprofloxacin, for which there are no NCCLS interpretive criteria. Ten of 12 laboratories testing levofloxacin and 4 of 4 laboratories testing ofloxacin by an MIC method correctly reported resistant results for the isolate. Feedback letters sent to participating laboratories highlighted areas of susceptibility testing in individual laboratories that needed improvement. The positive impact of the feedback letters and the overall effectiveness of the EQAS program were documented in repeat testing challenges with pneumococci and staphylococci. The 31 and 19% increases in the numbers of laboratories using appropriate testing methods for pneumococci and staphylococci, respectively, in 2000 versus 1998 indicate that laboratory performance is improving.
机译:1998年1月至2001年3月,在33个国家/地区中共有150个遵循NCCLS测试程序的实验室参加了世界卫生组织的抗菌素敏感性测试外部质量保证体系(EQAS-AST)。实验室测试了7种细菌分离株的抗菌素耐药性并报告了将该结果提供给佐治亚州亚特兰大疾病控制与预防中心(CDC)。将结果与使用NCCLS肉汤微稀释法和圆盘扩散参考法在CDC上产生的结果进行比较。尽管沙门氏菌肠亚种几乎没有测试错误。 150个实验室中的136个(占91%)对不适合治疗沙门氏菌感染的药物进行了测试。此外,在150个实验室中,有29个实验室(占20%)使用金黄色葡萄球菌断点报告了腐生葡萄球菌的奥沙西林结果。对于含vanB的粪肠球菌菌株,在150个实验室中,有124个(83%)正确报告了万古霉素结果,其稀释度是参考MIC的±1倍稀释度或参考圆盘扩散结果的±3 mm。在通过圆盘扩散法检测无乳链球菌的实验室中,有17%的实验室报告了对青霉素错误的不敏感结果。虽然有110个实验室(73%)对肺炎链球菌挑战菌株进行了氟喹诺酮类药物的测试,但83%的实验室对环丙沙星进行了测试,目前尚无NCLLS解释标准。通过MIC方法测试左氧氟沙星的12个实验室中的10个以及通过MIC方法测试氧氟沙星的4个实验室中的4个正确报告了该菌株的耐药结果。发送给参与实验室的反馈信强调了各个实验室中药敏测试的领域,这些领域需要改进。反馈信的积极影响和EQAS计划的整体有效性已在肺炎球菌和葡萄球菌的重复测试中得到证明。使用适当的肺炎球菌和葡萄球菌检测方法,实验室数量分别比2000年和1998年分别增加了31%和19%,这表明实验室的性能正在提高。

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