Bow E J, Mandell L A, Louie T J, Feld R, Palmer M, Zee B, Pater J
Health Sciences Centre, Winnipeg, Manitoba, Canada.
Ann Intern Med. 1996 Aug 1;125(3):183-90. doi: 10.7326/0003-4819-125-3-199608010-00004.
To determine whether augmented quinolone-based antibacterial prophylaxis in neutropenic patients with cancer reduces infections caused by gram-positive cocci and preserves the protective effect against aerobic gram-negative bacilli.
Open, randomized, controlled, multicenter clinical trial.
Centers participating in the National Cancer Institute of Canada Clinical Trials Group.
111 eligible and evaluable patients hospitalized for severe neutropenia (neutrophil count < 0.5 x 10(9)/L lasting at least 14 days) who were receiving cytotoxic therapy for acute leukemia or bone marrow autografting.
One of three oral antibacterial prophylactic regimens (norfloxacin, 400 mg every 12 hours; ofloxacin, 400 mg every 12 hours; or ofloxacin, 400 mg, plus rifampin, 300 mg every 12 hours) beginning with cytotoxic therapy.
Incidence and cause of suspected or proven infection.
Microbiologically documented overall infection rates for norfloxacin, ofloxacin, and ofloxacin plus rifampin were 47%, 24%, and 9%, respectively (P < 0.001). Corresponding rates were 24%, 13%, and 3%, respectively for staphylococcal bacteremia (P = 0.03) and, 21%, 3%, and 3%, respectively for streptococcal bacteremia (P < 0.01). The pattern of bacteremia suggested that rifampin played a role in suppressing staphylococcal infection. Both ofloxacin alone and ofloxacin plus rifampin had a clinically significant antistreptococcal effect. Aerobic gram-negative rods were cleared from rectal surveillance cultures in all patients after a median of 5.5 days and caused infection in only one patient (0.9%). The reductions in the number of microbiologically documented infections among ofloxacin recipients and ofloxacin plus rifampin recipients were offset by concomitant increases in the number of unexplained fevers (24% of norfloxacin recipients, 53% of ofloxacin recipients, and 49% of ofloxacin plus rifampin recipients; P = 0.02). No statistically significant difference was found among the treatment arms with respect to the overall incidence of febrile neutropenic episodes as defined for this trial (79% for the norfloxacin group, 82% for the ofloxacin group, and 77% for the ofloxacin plus rifampin group).
Quinolone-based antibacterial chemoprophylaxis protected patients from aerobic gram-negative bacillary infections. Augmentation of the gram-positive activity reduced the incidence of gram-positive infections but did not influence the overall incidence of febrile neutropenic episodes.
确定在癌症中性粒细胞减少患者中强化喹诺酮类抗菌药物预防措施是否能降低革兰氏阳性球菌引起的感染,并维持对需氧革兰氏阴性杆菌的保护作用。
开放、随机、对照、多中心临床试验。
参与加拿大国家癌症研究所临床试验组的中心。
111例符合条件且可评估的患者,因严重中性粒细胞减少(中性粒细胞计数<0.5×10⁹/L持续至少14天)住院,正在接受急性白血病细胞毒性治疗或骨髓自体移植。
三种口服抗菌预防方案之一(诺氟沙星,每12小时400毫克;氧氟沙星,每12小时400毫克;或氧氟沙星400毫克加利福平300毫克,每12小时一次),从细胞毒性治疗开始。
疑似或确诊感染的发生率及病因。
诺氟沙星、氧氟沙星以及氧氟沙星加利福平的微生物学确诊总体感染率分别为47%、24%和9%(P<0.001)。葡萄球菌血症的相应发生率分别为24%、13%和3%(P = 0.03),链球菌血症的相应发生率分别为21%、3%和3%(P<0.01)。菌血症模式表明利福平在抑制葡萄球菌感染中起作用。单独使用氧氟沙星和氧氟沙星加利福平均有显著的抗链球菌作用。所有患者直肠监测培养物中的需氧革兰氏阴性杆菌在中位时间5.5天后清除,仅1例患者(0.9%)发生感染。氧氟沙星组和氧氟沙星加利福平组微生物学确诊感染数量的减少被不明原因发热数量的相应增加所抵消(诺氟沙星组24%、氧氟沙星组53%、氧氟沙星加利福平组49%;P = 0.02)。就本试验定义的发热性中性粒细胞减少发作的总体发生率而言,各治疗组之间未发现统计学显著差异(诺氟沙星组79%、氧氟沙星组82%、氧氟沙星加利福平组77%)。
喹诺酮类抗菌药物化学预防可保护患者免受需氧革兰氏阴性杆菌感染。增强革兰氏阳性菌活性可降低革兰氏阳性菌感染的发生率,但不影响发热性中性粒细胞减少发作的总体发生率。