Kirkegaard-Biosca Cristina, Del Barrio-Tofiño Ester, Villamarín Miguel, Larrosa Nieves, Campany David, González-López Juan José, Ferrer Ricard, Viñado Belén, Doménech Laura, Sellarès-Nadal Julia, Escolà-Vergé Laura, Fernández-Hidalgo Nuria, Los-Arcos Ibai
Infectious Diseases Department, Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.
Department of Medicine, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.
Antibiotics (Basel). 2024 Sep 12;13(9):874. doi: 10.3390/antibiotics13090874.
VIM-type-producing Gram-negative bacteria (GNB) infections are difficult to treat. This is a retrospective single-center study of 34 patients who received cefiderocol for the treatment of VIM-type-producing GNB infections, including 25 spp., 7 , and 5 sp. Primary outcomes were clinical failure (defined as death, lack of clinical improvement, or a switch to another drug) at day 14 and 30-day all-cause mortality. The median age was 59 years (IQR 53.7-73.4), and the median Charlson comorbidity index was 3.5 (IQR 2-5). The main infections were respiratory tract infections ( = 9, 27%) and skin and soft tissue infections ( = 9, 27%). Eight patients exhibited bacteremia. In 9/17 patients with a drainable focus, drainage was performed. The median cefiderocol treatment duration was 13 days (IQR 8-24). Five patients (15%) experienced clinical failure on day 14, and the thirty-day mortality rate was 9/34 (27%); two cases occurred because of an uncontrolled infection source, and one was due to a new infection caused by the same bacteria. The other six deaths were unrelated to the index infection. Five patients experienced microbiological recurrence within three months. Susceptibility testing revealed the development of cefiderocol resistance in 1/7 cases with persistent or recurrent positive cultures. Cefiderocol, even in monotherapy, could be considered for the treatment of VIM-type-producing GNB infections.
产VIM型革兰氏阴性菌(GNB)感染难以治疗。这是一项回顾性单中心研究,纳入了34例接受头孢地尔治疗产VIM型GNB感染的患者,其中包括25种菌株、7种[未提及具体菌名]和5种[未提及具体菌名]。主要结局为第14天的临床失败(定义为死亡、缺乏临床改善或改用另一种药物)和30天全因死亡率。中位年龄为59岁(四分位间距53.7 - 73.4),中位查尔森合并症指数为3.5(四分位间距2 - 5)。主要感染为呼吸道感染(n = 9,27%)和皮肤及软组织感染(n = 9,27%)。8例患者出现菌血症。17例有可引流病灶的患者中,9例进行了引流。头孢地尔的中位治疗持续时间为13天(四分位间距8 - 24)。5例患者(15%)在第14天出现临床失败,30天死亡率为9/34(27%);2例死亡是由于感染源未得到控制,1例是由于同一细菌引起的新感染。其他6例死亡与索引感染无关。5例患者在三个月内出现微生物学复发。药敏试验显示,在7例持续或反复培养阳性的病例中,有1例出现了对头孢地尔的耐药。即使是单药治疗,头孢地尔也可考虑用于治疗产VIM型GNB感染。