Pellicé Martina, Rodríguez-Núñez Olga, Rico Verónica, Agüero Daiana, Morata Laura, Cardozo Celia, Puerta-Alcalde Pedro, Garcia-Vidal Carolina, Rubio Elisa, Fernandez-Pittol Mariana J, Vergara Andrea, Pitart Cristina, Marco Francesc, Santana Gemina, Rodríguez-Serna Laura, Vilella Ana, López Ester, Soriano Alex, Martínez Jose Antonio, Del Rio Ana
Service of Infectious Diseases, Hospital Clínic de Barcelona, Barcelona, Spain.
Service of Microbiology, Hospital Clínic de Barcelona, Barcelona, Spain.
Front Microbiol. 2021 Feb 1;12:630826. doi: 10.3389/fmicb.2021.630826. eCollection 2021.
KPC-producing (KPCKP) is a threat for patients admitted to healthcare institutions. To assess the efficacy of several decolonization strategies for KPCKP rectal carriage. Observational study performed in a 750-bed university center from July to October 2018 on the efficacy of a 10-day non-absorbable oral antibiotic (NAA) regimen (colistin 10 mg/ml, amikacin 8 mg/ml, and nystatin 30 mg/ml, 10 ml/6 h) vs. the same regimen followed by a probiotic (Vivomixx®) for 20 days in adult patients with KPCKP rectal colonization acquired during an outbreak. Seventy-three patients colonized by KPCKP were included, of which 21 (29%) did not receive any treatment and 52 (71.2%) received NAA either alone ( = 26, 35.6%) or followed by a probiotic ( = 26, 35.6%). Eradication was observed in 56 (76.7%) patients and the only variable significantly associated with it was not receiving systemic antibiotics after diagnosis of rectal carriage [22/24 (91.6%) vs. 34/49 (69.3%), = 0.04]. Eradication in patients receiving NAA plus probiotic was numerically but not significantly higher than that of controls [23/26 (88.4%) vs. 15/21 (71.4%), = 0.14] and of those receiving only NAA (OR = 3.4, 95% CI = 0.78-14.7, = 0.09). In an outbreak setting, rectal carriage of KPCKP persisted after a mean of 36 days in about one quarter of patients. The only factor associated with eradication was not receiving systemic antibiotic after diagnosis. A 10-day course of NAA had no impact on eradication. Probiotics after NAA may increase the decolonization rate, hence deserving further study.
产KPC酶(KPCKP)对入住医疗机构的患者构成威胁。为评估几种去定植策略对KPCKP直肠定植的疗效。2018年7月至10月在一家拥有750张床位的大学中心进行了一项观察性研究,比较了为期10天的不可吸收口服抗生素(NAA)方案(黏菌素10mg/ml、阿米卡星8mg/ml和制霉菌素30mg/ml,10ml/每6小时)与在爆发期间获得KPCKP直肠定植的成年患者中,同样方案后加用益生菌(Vivomixx®)20天的疗效。纳入了73例KPCKP定植患者,其中21例(29%)未接受任何治疗,52例(71.2%)接受了NAA,单独使用NAA的有26例(35.6%),使用NAA后加用益生菌的有26例(35.6%)。56例(76.7%)患者实现了根除,与之显著相关的唯一变量是在诊断直肠定植后未接受全身抗生素治疗[22/24(91.6%)对34/49(69.3%),P = 0.04]。接受NAA加益生菌治疗的患者根除率在数值上高于对照组,但无显著差异[23/26(88.4%)对15/21(71.4%),P = 0.14],与仅接受NAA治疗的患者相比(OR = 3.4,95%CI = 0.78 - 14.7,P = 0.09)。在爆发情况下,约四分之一的患者在平均36天后KPCKP直肠定植仍持续存在。与根除相关的唯一因素是诊断后未接受全身抗生素治疗。为期10天的NAA疗程对根除无影响。NAA后使用益生菌可能会提高去定植率,因此值得进一步研究。