Weinstein Melvin P, Klugman Keith P, Jones Ronald N
Department of Medicine, University of Medicine and Dentistry, New Jersey-Robert Wood Johnson Medical School, New Brunswick, NJ 08901-1109, USA.
Clin Infect Dis. 2009 Jun 1;48(11):1596-600. doi: 10.1086/598975.
In January 2008, the Clinical and Laboratory Standards Institute published revised susceptibility breakpoints for penicillin and Streptococcus pneumoniae, and shortly thereafter, the United States Food and Drug Administration similarly revised its breakpoints via changes in the package insert for penicillin. The revised susceptibility breakpoint is < or =2 microg/mL for nonmeningeal infections treated with parenteral penicillin at a dosage of 12 million units-24 million units per day. The susceptibility breakpoint of < or =0.06 microg/mL remains unchanged for pneumococcal meningitis treated with parenteral penicillin at a dosage of > or =18 million units per day. Herein, we review the scientific basis for the revisions to the breakpoints, which were supported by microbiologic, pharmacokinetic and/or pharmacodynamic, and clinical data. Clinicians, once again, should feel comfortable prescribing penicillin for pneumococcal pneumonia and other pneumococcal infections outside the central nervous system.
2008年1月,临床和实验室标准协会公布了青霉素与肺炎链球菌药敏折点的修订版,此后不久,美国食品药品监督管理局也通过修改青霉素包装说明书中的折点进行了类似修订。对于每日剂量为1200万单位至2400万单位的非脑膜炎性感染,采用静脉注射青霉素治疗时,修订后的药敏折点为≤2微克/毫升。对于每日剂量≥1800万单位的静脉注射青霉素治疗的肺炎球菌性脑膜炎,≤0.06微克/毫升的药敏折点保持不变。在此,我们回顾了折点修订的科学依据,这些依据得到了微生物学、药代动力学和/或药效学以及临床数据的支持。临床医生在为中枢神经系统以外的肺炎球菌性肺炎和其他肺炎球菌感染开具青霉素处方时,应再次感到安心。