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Impact of single-room contact precautions on acquisition and transmission of vancomycin-resistant enterococci on haematological and oncological wards, multicentre cohort-study, Germany, January−December 2016

BACKGROUND: Evidence supporting the effectiveness of single-room contact precautions (SCP) in preventing in-hospital acquisition of vancomycin-resistant enterococci (haVRE) is limited. AIM: We assessed the impact of SCP on haVRE and their transmission. METHODS: We conducted a prospective, multicentr...

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Detalles Bibliográficos
Autores principales: Biehl, Lena M., Higgins, Paul G., Stemler, Jannik, Gilles, Meyke, Peter, Silke, Dörfel, Daniela, Vogel, Wichard, Kern, Winfried V., Gölz, Hanna, Bertz, Hartmut, Rohde, Holger, Klupp, Eva-Maria, Schafhausen, Philippe, Salmanton-García, Jon, Stecher, Melanie, Wille, Julia, Liss, Blasius, Xanthopoulou, Kyriaki, Zweigner, Janine, Seifert, Harald, Vehreschild, Maria J.G.T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Centre for Disease Prevention and Control (ECDC) 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759111/
https://www.ncbi.nlm.nih.gov/pubmed/35027104
http://dx.doi.org/10.2807/1560-7917.ES.2022.27.2.2001876
Descripción
Sumario:BACKGROUND: Evidence supporting the effectiveness of single-room contact precautions (SCP) in preventing in-hospital acquisition of vancomycin-resistant enterococci (haVRE) is limited. AIM: We assessed the impact of SCP on haVRE and their transmission. METHODS: We conducted a prospective, multicentre cohort study in German haematological/oncological departments during 2016. Two sites performed SCP for VRE patients and two did not (NCP). We defined a 5% haVRE-risk difference as non-inferiority margin, screened patients for VRE, and characterised isolates by whole genome sequencing and core genome MLST (cgMLST). Potential confounders were assessed by competing risk regression analysis. RESULTS: We included 1,397 patients at NCP and 1,531 patients at SCP sites. Not performing SCP was associated with a significantly higher proportion of haVRE; 12.2% (170/1,397) patients at NCP and 7.4% (113/1,531) patients at SCP sites (relative risk (RR) 1.74; 95% confidence interval (CI): 1.35–2.23). The difference (4.8%) was below the non-inferiority margin. Competing risk regression analysis indicated a stronger impact of antimicrobial exposure (subdistribution hazard ratio (SHR) 7.46; 95% CI: 4.59–12.12) and underlying disease (SHR for acute leukaemia 2.34; 95% CI: 1.46–3.75) on haVRE than NCP (SHR 1.60; 95% CI: 1.14–2.25). Based on cgMLST and patient movement data, we observed 131 patient-to-patient VRE transmissions at NCP and 85 at SCP sites (RR 1.76; 95% CI: 1.33–2.34). CONCLUSIONS: We show a positive impact of SCP on haVRE in a high-risk population, although the observed difference was below the pre-specified non-inferiority margin. Importantly, other factors including antimicrobial exposure seem to be more influential.