Berg Melody L, Crank Christopher W, Philbrick Alexander H, Hayden Mary K
Midwestern University Chicago College of Pharmacy, Downers Grove, IL, USA.
Ann Pharmacother. 2008 Feb;42(2):207-12. doi: 10.1345/aph.1K365. Epub 2008 Jan 29.
Infections caused by extended-spectrum beta-lactamase (ESBL)-producing gram-negative organisms are becoming increasingly common and present significant challenges in terms of treatment. Carbapenems is the antibiotic class of choice for treatment of these types of infections. Ertapenem is the newest carbapenem, capable of being dosed once daily, and has some in vitro but little in vivo evidence supporting its use for the treatment of these resistant infections.
To examine the clinical and microbiologic outcomes associated with ertapenem therapy of ESBL-producing Escherichia coli, Klebsiella pneumoniae, and Proteus mirabilis infections.
This was a retrospective case series that examined the clinical and microbiologic outcomes of 22 patients who received ertapenem for treatment of an ESBL infection at Rush University Medical Center in Chicago, IL, during 2003-2005.
The majority (16/22) of patients received ertapenem for consolidation rather than initial therapy. Different antibiotics most commonly used were other carbapenems, piperacillin/tazobactam, and aminoglycosides. The most common infections treated were lower urinary tract infections and osteomyelitis. Clinical efficacy was determined in all 22 patients, with 20 (91%) patients having a positive outcome, defined as either clinical improvement or clinical cure. The best clinical cure rate was seen with wound infections, where all 3 patients examined were found to be clinically cured. Microbiologic efficacy was determined in 7 patients, with 6 (85.7%) defined as microbiologic cure. One patient was found to be both a clinical and microbiologic failure and was also found to have developed an ertapenem-resistant strain of E. coli.
These results demonstrate potential microbiologic and clinical efficacy of ertapenem for treatment of ESBL-producing infections and the need for a prospective, randomized study examining its efficacy versus that of other carbapenems.
由产超广谱β-内酰胺酶(ESBL)的革兰氏阴性菌引起的感染日益常见,在治疗方面带来了重大挑战。碳青霉烯类是治疗这类感染的首选抗生素类别。厄他培南是最新的碳青霉烯类药物,能够每日给药一次,并且有一些体外但体内证据很少支持其用于治疗这些耐药感染。
研究厄他培南治疗产ESBL的大肠埃希菌、肺炎克雷伯菌和奇异变形杆菌感染的临床和微生物学结果。
这是一项回顾性病例系列研究,考察了2003年至2005年期间在伊利诺伊州芝加哥市拉什大学医学中心接受厄他培南治疗ESBL感染的22例患者的临床和微生物学结果。
大多数(16/22)患者接受厄他培南进行巩固治疗而非初始治疗。最常用的其他抗生素是其他碳青霉烯类、哌拉西林/他唑巴坦和氨基糖苷类。治疗的最常见感染是下尿路感染和骨髓炎。对所有22例患者确定了临床疗效,其中20例(91%)患者有阳性结果,定义为临床改善或临床治愈。伤口感染的临床治愈率最高,所有3例接受检查的患者均临床治愈。对7例患者确定了微生物学疗效,其中6例(85.7%)定义为微生物学治愈。1例患者在临床和微生物学方面均治疗失败,并且还发现产生了对厄他培南耐药的大肠埃希菌菌株。
这些结果证明了厄他培南治疗产ESBL感染的潜在微生物学和临床疗效,以及需要进行一项前瞻性、随机研究来考察其与其他碳青霉烯类药物相比的疗效。