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Imipenem versus gentamicin combined with either cefuroxime or cephalothin as initial therapy for febrile neutropenic patients.

机译:亚胺培南与庆大霉素联合头孢呋辛或头孢噻吩作为发热性中性粒细胞减少患者的初始治疗。

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摘要

A prospective randomized study was conducted to determine the efficacy of imipenem-cilastatin (hereafter referred to as imipenem) (500 mg four times daily) versus combination therapy for febrile neutropenic patients receiving either no prophylaxis or ciprofloxacin for prevention of infections. Combination therapy consisted of gentamicin (80 mg every 8 h) plus either cefuroxime (1,500 mg every 8 h) or cephalothin (1,000 mg every 4 h) for suspected catheter-related infections. Ninety-four neutropenic fever episodes in 87 patients were evaluable for efficacy. The overall clinical rate of response to imipenem was significantly higher than that to combination therapy (91 versus 74%; P = 0.05). The difference in efficacy was most pronounced in patients with microbiologically documented infections (89 versus 53%; P = 0.025), which were predominantly caused by gram-positive bacteria. Differences in susceptibility may have caused the better rate of response to imipenem. Two of 29 gram-positive bacteria were imipenem resistant, whereas 10 were resistant to cephalothin and cefuroxime and 12 were resistant to gentamicin. No causative gram-negative bacterium and 24 gram-positive bacteria were isolated in 61 fever episodes with ciprofloxacin prophylaxis (oral). In contrast, nine causative gram-negative and five gram-positive bacteria were isolated in 33 episodes without prophylaxis. The difference in distribution proved to be statistically significant for gram-negative (P = 0.0001) as well as gram-positive (P = 0.025) bacteria, indicating that ciprofloxacin effectively prevented the occurrence of gram-negative bacteria and may have contributed to the relatively large number of gram-positive bacteria isolated. Empirical initial therapy with imipenem may be a valuable alternative to combination therapy for neutropenic fever episodes.
机译:进行了一项前瞻性随机研究,以确定亚胺培南-西司他丁(以下简称亚胺培南)(500 mg每天四次)与联合治疗对未接受预防或环丙沙星预防感染的发热性中性粒细胞减少患者的疗效。组合疗法由庆大霉素(每8小时80毫克)加头孢呋辛(每8小时1,500毫克)或头孢菌素(每4小时1,000毫克)组成,用于可疑的导管相关感染。在87例患者中有94例中性粒细胞减少症发作,可评估疗效。亚胺培南的总体临床反应率显着高于联合治疗(91比74%; P = 0.05)。在微生物学记载的感染(主要由革兰氏阳性细菌引起)的患者中,疗效差异最为明显(89对53%; P = 0.025)。敏感性的差异可能导致对亚胺培南的较好反应率。 29株革兰氏阳性细菌中有2株对亚胺培南具有抗药性,而10株对头孢菌素和头孢呋辛有抗药性,而12株对庆大霉素有抗药性。在预防环丙沙星(口服)的61例发烧发作中,未分离到革兰氏阴性菌和24克革兰氏阳性菌。相反,在33例发作中未分离到9株革兰氏阴性菌和5株革兰氏阳性菌。事实证明,革兰氏阴性菌(P = 0.0001)和革兰氏阳性菌(P = 0.025)的分布差异具有统计学意义,表明环丙沙星有效地预防了革兰氏阴性菌的发生,并且可能对分离出大量革兰氏阳性细菌。亚胺培南的经验性初始治疗可能是中性粒细胞减少症发作的联合治疗的有价值的替代方法。

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