Ataturk Education and Research Hospital, Ankara, Turkey.
Infection. 2011 Dec;39(6):515-8. doi: 10.1007/s15010-011-0161-1. Epub 2011 Jul 26.
Acinetobacter baumannii is a non-fermenting aerobic gram-negative bacteria and one of the important nosocomial pathogens, especially in intensive care units (ICUs). In recent years, multidrug-resistant (MDR) isolates have been an emerging problem, with limited therapeutic options. Tigecycline is a novel antimicrobial, with its in vitro activity against most gram-positive and gram-negative pathogens.
This is a retrospective study that was conducted in a tertiary care hospital with 550 beds in Ankara, Turkey, from January 2009 to July 2010. Thirty-three patients who had carbapenem-resistant Acinetobacter spp. infections and received tigecycline alone or in combination with other antibiotics for at least 3 days were included.
The median age of the patients was 62 (18-87) years. All of the patients were diagnosed and treated in the ICU. Clinical responses were observed in 23 patients (69.7%). Ten patients (30%) had clinical failure. There was no significant difference between ventilator-associated pneumonia (VAP) and bloodstream infection (BSI) in terms of clinical or microbiological outcome (p > 0.05). The microbiological response rate was 50%. Superinfection was detected in 13 patients (43.3%) and Pseudomonas aeruginosa was the most frequently isolated pathogen. The 30-day overall mortality rate and attributable mortality rates were 57.6 and 24.2%, respectively. The attributable mortality rate was higher in the group in which microbiological eradication was not provided.
Although it is approved by the Food and Drug Administration (FDA) for the treatment of complicated intra-abdominal infections, complicated skin and soft tissue infections, and community-acquired bacterial pneumonia, emerged resistance of Acinetobacter spp. and limited therapeutic options left physicians no choice but to use tigecycline for off-label indications.
鲍曼不动杆菌是非发酵需氧革兰阴性菌,是重要的医院获得性病原体之一,尤其在重症监护病房(ICU)中。近年来,多药耐药(MDR)分离株已成为一个新出现的问题,治疗选择有限。替加环素是一种新型抗菌药物,对大多数革兰阳性和革兰阴性病原体具有体外活性。
这是一项在土耳其安卡拉一家拥有 550 张床位的三级保健医院进行的回顾性研究,研究时间为 2009 年 1 月至 2010 年 7 月。33 例碳青霉烯类耐药鲍曼不动杆菌感染患者单独或联合其他抗生素至少使用 3 天接受替加环素治疗,将其纳入研究。
患者的中位年龄为 62(18-87)岁。所有患者均在 ICU 确诊和治疗。23 例患者(69.7%)观察到临床应答。10 例患者(30%)临床治疗失败。呼吸机相关性肺炎(VAP)和血流感染(BSI)在临床或微生物学结局方面无显著差异(p>0.05)。微生物学应答率为 50%。13 例患者(43.3%)发生二重感染,最常分离到的病原体是铜绿假单胞菌。30 天总死亡率和归因死亡率分别为 57.6%和 24.2%。未提供微生物学清除的患者组归因死亡率更高。
尽管替加环素已获美国食品药品监督管理局(FDA)批准用于治疗复杂性腹腔内感染、复杂性皮肤和软组织感染以及社区获得性细菌性肺炎,但鲍曼不动杆菌的出现耐药和有限的治疗选择使得医生不得不将替加环素用于超适应证治疗。