Hellinger W C, Brewer N S
Division of Infectious Diseases and Internal Medicine, Mayo Clinic Jacksonville, Florida, USA.
Mayo Clin Proc. 1999 Apr;74(4):420-34. doi: 10.4065/74.4.420.
Imipenem and meropenem, members of the carbapenem class of beta-lactam antibiotics, are among the most broadly active antibiotics available for systemic use in humans. They are active against streptococci, methicillin-sensitive staphylococci, Neisseria, Haemophilus, anaerobes, and the common aerobic gram-negative nosocomial pathogens including Pseudomonas. Resistance to imipenem and meropenem may emerge during treatment of P. aeruginosa infections, as has occurred with other beta-lactam agents; Stenotrophomonas maltophilia is typically resistant to both imipenem and meropenem. Like the penicillins, the carbapenems have inhibitory activity against enterococci. In general, the in vitro activity of imipenem against aerobic gram-positive cocci is somewhat greater than that of meropenem, whereas the in vitro activity of meropenem against aerobic gram-negative bacilli is somewhat greater than that of imipenem. Daily dosages may range from 0.5 to 1 g every 6 to 8 hours in patients with normal renal function; the daily dose of meropenem, however, can be safely increased to 6 g. Infusion-related nausea and vomiting, as well as seizures, which have been the main toxic effects of imipenem, occur no more frequently during treatment with meropenem than during treatment with other beta-lactam antibiotics. The carbapenems should be considered for treatment of mixed bacterial infections and aerobic gram-negative bacteria that are not susceptible to other beta-lactam agents. Indiscriminate use of these drugs will promote resistance to them. Aztreonam, the first marketed monobactam, has activity against most aerobic gram-negative bacilli including P. aeruginosa. The drug is not nephrotoxic, is weakly immunogenic, and has not been associated with disorders of coagulation. Aztreonam may be administered intramuscularly or intravenously; the primary route of elimination is urinary excretion. In patients with normal renal function, the recommended dosing interval is every 8 hours. Patients with renal impairment require dosage adjustment. Aztreonam is used primarily as an alternative to aminoglycosides and for the treatment of aerobic gram-negative infections. It is often used in combination therapy for mixed aerobic and anaerobic infections. Approved indications for its use include infections of the urinary tract or lower respiratory tract, intra-abdominal and gynecologic infections, septicemia, and cutaneous infections caused by susceptible organisms. Concurrent initial therapy with other antimicrobial agents is recommended before the causative organism has been determined in patients who are seriously ill or at risk for gram-positive or anaerobic infection.
亚胺培南和美罗培南属于β-内酰胺类抗生素中的碳青霉烯类,是可用于人类全身治疗的活性最广泛的抗生素之一。它们对链球菌、甲氧西林敏感葡萄球菌、奈瑟菌、嗜血杆菌、厌氧菌以及包括铜绿假单胞菌在内的常见需氧革兰氏阴性医院病原体具有活性。在铜绿假单胞菌感染治疗期间,可能会出现对亚胺培南和美罗培南的耐药性,就像其他β-内酰胺类药物那样;嗜麦芽窄食单胞菌通常对亚胺培南和美罗培南均耐药。与青霉素类一样,碳青霉烯类对肠球菌具有抑制活性。一般而言,亚胺培南对需氧革兰氏阳性球菌的体外活性略强于美罗培南,而美罗培南对需氧革兰氏阴性杆菌的体外活性略强于亚胺培南。肾功能正常的患者,每日剂量范围为每6至8小时0.5至1克;然而,美罗培南的每日剂量可安全增至6克。与输注相关的恶心和呕吐以及癫痫发作是亚胺培南的主要毒性作用,在使用美罗培南治疗期间出现的频率并不高于使用其他β-内酰胺类抗生素治疗期间。对于混合细菌感染以及对其他β-内酰胺类药物不敏感的需氧革兰氏阴性菌感染,应考虑使用碳青霉烯类药物治疗。滥用这些药物会导致对它们产生耐药性。氨曲南是首个上市的单环β-内酰胺类抗生素,对包括铜绿假单胞菌在内的大多数需氧革兰氏阴性杆菌具有活性。该药物无肾毒性,免疫原性弱,且与凝血功能障碍无关。氨曲南可通过肌内注射或静脉注射给药;主要排泄途径是经尿液排泄。肾功能正常的患者,推荐的给药间隔为每8小时一次。肾功能损害患者需要调整剂量。氨曲南主要用作氨基糖苷类药物的替代品,用于治疗需氧革兰氏阴性菌感染。它常用于混合需氧菌和厌氧菌感染的联合治疗。其批准的适应证包括由易感菌引起的尿路感染或下呼吸道感染、腹腔内和妇科感染、败血症以及皮肤感染。对于病情严重或有革兰氏阳性菌或厌氧菌感染风险的患者,在确定病原体之前,建议同时使用其他抗菌药物进行初始治疗。