Eggimann P, Glauser M P, Aoun M, Meunier F, Calandra T
Department of Internal Medicine, Centre Hospitalier Universitaire, Vaudois, Lausanne, Switzerland.
J Antimicrob Chemother. 1993 Nov;32 Suppl B:151-63. doi: 10.1093/jac/32.suppl_b.151.
In a pilot study, we evaluated the efficacy and the safety of cefepime, a new cephalosporin with extended-spectrum activity against both Gram-positive and Gram-negative bacteria, as empirical monotherapy for 108 febrile episodes in 84 granulocytopenic cancer patients. Cefepime (2 g tds) was given for a minimum of 7 days or until resolution of infection. Of the 108 episodes, 91 were evaluable. Microbiologically documented infections occurred in 25 patients (27%) (18 Gram-positive, 7 Gram-negative), of whom 18 had bacteraemia. Infection was clinically documented in 47 patients (52%) and fever was unexplained in 19 (21%). Overall, 71% (65/91) of the infections resolved. Response rates were 86% (6/7) for Gram-negative infections, 44% (8/18) for Gram-positive infections (57% for cefepime-susceptible Gram-positive bacteria), 77% (36/47) for clinically documented infections and 79% (15/19) for unexplained fevers. Of the 26 patients (29%) whose primary infections did not improve with cefepime monotherapy, 23 responded after the addition of other antibiotics. Sixteen patients (18%) developed secondary infections of which 13 were microbiologically documented; Gram-positive bacteria were isolated from seven patients, Gram-negative bacteria from two, fungi from three and a virus from one. Adverse effects were mild and did not require premature discontinuation of therapy except for one patient who developed an immediate allergic reaction after the first dose of cefepime from which he recovered fully. The survival rate after resolution of granulocytopenia was 96%; three patients died of primary bacterial infection and one from secondary disseminated candidiasis. In this pilot study, cefepime monotherapy appeared safe and effective as empirical therapy for fever in cancer patients with granulocytopenia. Whether cefepime is superior to other advanced-generation cephalosporins for the treatment of Gram-positive infections will require evaluation in a larger comparative study.
在一项初步研究中,我们评估了头孢吡肟(一种对革兰氏阳性菌和革兰氏阴性菌均有广谱活性的新型头孢菌素)作为84例粒细胞减少性癌症患者108次发热发作的经验性单药治疗的疗效和安全性。给予头孢吡肟(2克,每日三次)至少7天或直至感染消退。在108次发作中,91次可评估。25例患者(27%)发生了微生物学证实的感染(18例革兰氏阳性菌感染,7例革兰氏阴性菌感染),其中18例有菌血症。47例患者(52%)有临床记录的感染,19例(21%)发热原因不明。总体而言,71%(65/91)的感染得到缓解。革兰氏阴性菌感染的缓解率为86%(6/7),革兰氏阳性菌感染的缓解率为44%(8/18)(对头孢吡肟敏感的革兰氏阳性菌为57%),临床记录感染的缓解率为77%(36/47),不明原因发热的缓解率为79%(15/19)。在26例(29%)原发性感染采用头孢吡肟单药治疗无改善的患者中,23例在加用其他抗生素后有反应。16例患者(18%)发生了继发性感染,其中13例有微生物学记录;7例患者分离出革兰氏阳性菌,2例分离出革兰氏阴性菌,3例分离出真菌,1例分离出病毒。不良反应轻微,除1例患者在首次使用头孢吡肟后立即发生过敏反应,但已完全康复外,均无需过早停药。粒细胞减少症缓解后的生存率为96%;3例患者死于原发性细菌感染,1例死于继发性播散性念珠菌病。在这项初步研究中,头孢吡肟单药治疗作为粒细胞减少性癌症患者发热的经验性治疗似乎是安全有效的。头孢吡肟在治疗革兰氏阳性菌感染方面是否优于其他新一代头孢菌素,需要在更大规模的比较研究中进行评估。