首页> 美国卫生研究院文献>Journal of the National Medical Association >Clinical experience with linezolid in the treatment of resistant gram-positive infections.
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Clinical experience with linezolid in the treatment of resistant gram-positive infections.

机译:利奈唑胺治疗耐药革兰氏阳性感染的临床经验。

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摘要

This study presents our clinical experience with linezolid in 19 patients with serious resistant gram-positive infections enrolled as part of the compassionate study. In this prospective, non-randomized, noncomparative study, 19 patients were enrolled as part of the National Compassionate Study Protocol conducted by Pharmacia-Upjohn. At the time of this writing, these patients had not been published in the literature. All of the patients had to have documented evidence of serious gram-positive infections in normally sterile sites and should have been unable to tolerate available antimicrobial therapy or be unresponsive to available drugs. Clinical characteristics, laboratory values, and pharmacokinetic and pharmacodynamic parameters were obtained. Patients were followed both short-term and long-term after completion of therapy. Nineteen patients were enrolled: 13 females and 6 males. The average age was 63 years. The average length of therapy with linezolid was 22 days. Methicillin-resistant Staphylococcus aureus (MRSA) was treated in eight patients, methicillin-resistant Staphylococcus epidermidis (MRSE) in two patients, vancomycin-resistant Enterococcus faecium (VREF) in eight patients, and coagulase-negative Staphylococcus in two patients. Co-infecting organisms include Enterococcus species colonization in six patients, Pseudomonas species in one patient, Serratia marcenens in one patient, and Candida albicans in one patient. Sterile sites that were infected included bone and joint (wounds and septic joints) in six patients, gastrointestinal system (hepatobiliary, liver abscess, Crohn's) in five patients, genitourinary (kidney and urine) in two patients, blood in five patients, respiratory in one patient, and aortic valve in 1 patient. Linezolid was given at 600 mg IV every 12 hours with a mean length of therapy of 22 days. Surgical drainage was used in combination with linezolid in 11 of the patients. Seventy nine percent of these patients achieved clinical and microbiologic cure, and none of the deaths reported in this series were related to the drug. Adverse events included skin rash in one patient, mild bone marrow suppression in two patients, and mild elevation in liver function tests in two patients. No life-threatening adverse events were noted. It appears that linezolid, along with surgical intervention (when necessary), appears to be an effective treatment option for resistant gram-positive infections. Long-term studies evaluating the possible resistance rates are necessary.
机译:这项研究介绍了我们对利奈唑胺治疗19例具有严重抵抗力的革兰氏阳性感染的患者的临床经验,这是同情研究的一部分。在这项前瞻性,非随机,非对照研究中,有19名患者入选了Pharmacia-Upjohn进行的“国家同情研究计划”。在撰写本文时,这些患者尚未在文献中发表。所有患者都必须在正常无菌部位记录有严重的革兰氏阳性感染的证据,并且不能耐受现有的抗微生物治疗或对现有药物无反应。获得临床特征,实验室值以及药代动力学和药效学参数。治疗结束后,对患者进行短期和长期随访。招募了19位患者:13位女性和6位男性。平均年龄为63岁。利奈唑胺的平均治疗时间为22天。耐甲氧西林金黄色葡萄球菌(MRSA)接受治疗8例,耐甲氧西林表皮葡萄球菌(MRSE)接​​受治疗2例,耐万古霉素粪便肠球菌(VREF)接受治疗,两名患者接受凝固酶阴性葡萄球菌治疗。合并感染的生物包括6名患者的肠球菌菌落定植,1名患者的假单胞菌菌种,1名患者的粘质沙雷氏菌和1名患者的白色念珠菌。感染的不育部位包括6例患者的骨骼和关节(伤口和化脓性关节),5例患者的肠胃系统(肝胆,肝脓肿,克罗恩氏病),2例患者的泌尿生殖系统(肾脏和尿液),5例患者的血液,5例患者的呼吸道1位患者,主动脉瓣1位。每12小时静脉注射利奈唑胺600 mg,平均治疗时间为22天。手术引流结合利奈唑胺用于11例患者。这些患者中有79%获得了临床和微生物学治愈,该系列报道的死亡均与该药物无关。不良事件包括一名患者的皮疹,两名患者的轻度骨髓抑制以及两名患者的肝功能检查轻度升高。没有发现威胁生命的不良事件。利奈唑胺与外科手术(必要时)一起似乎是抗药性革兰氏阳性感染的有效治疗选择。评估可能的耐药率的长期研究是必要的。

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