Abstract

Background

Carbapenem-resistant Enterobacterales (CRE) are a substantial problem in Cape Town. CRE epidemiology is largely unknown and mortality remains high.

Objectives

To describe and characterize the clinical and microbiological epidemiology of CRE within Cape Town hospitals to better inform therapy with regard to current and novel antibiotics, as well as improve antimicrobial stewardship (AMS), and infection prevention and control (IPC).

Methods

This prospective, multicentre study performed between 1 November 2020 and 30 November 2022, across three public and three private hospitals included hospitalized participants with CRE from clinical cultures. Participant demographics, clinical information and microbiology results were collected and analysed.

Results

Ninety percent of participants were from public hospitals. The age distribution ranged from 7 days to 88 years. Notable risk factors for CRE infection included recent exposure to antibiotics, medical devices and surgery. The most prevalent species was Klebsiella pneumoniae. However, a higher proportion of Serratia marcescens compared with previous reports was identified. The detected carbapenemases were blaOXA-48-like (80%) and blaNDM (11%). With the exception of amikacin (63%), tigecycline (65%), colistin (95%) and ceftazidime/avibactam (87%), susceptibility to antibiotics was low.

Conclusions

This study identified common risk factors for CRE infection and generated a description of carbapenemase enzymes, species distribution and antibiograms, enabling a better understanding of CRE epidemiology. This provides insights into transmission patterns and resistance determinants of CREs, beneficial to informing data-driven regional patient management, AMS and IPC strategies.

Details

Title
Carbapenem-resistant Enterobacterales among hospitalized patients in Cape Town, South Africa: clinical and microbiological epidemiology
Author
Hafsah Deepa Tootla 1   VIAFID ORCID Logo  ; Prentice, Elizabeth 2   VIAFID ORCID Logo  ; Moodley, Clinton 2   VIAFID ORCID Logo  ; Marais, Gert 2   VIAFID ORCID Logo  ; Nyakutira, Nyasha 3 ; Reddy, Kessendri 4 ; Bamford, Colleen 3 ; Niehaus, Abraham 5   VIAFID ORCID Logo  ; Whitelaw, Andrew 4 ; Brink, Adrian 2   VIAFID ORCID Logo  ; Page, Claudine; Schoeman, Elizabeth; Elizma de Klerk; Lategan, Karin; Pienaar, Karlien; Henning, Liezl; Mandy Du Plessis; Maseko, Nomfundo; Nel, Salome; Narainsamy, Melenie; Vermeulen, Michelle; Narissa du Toit; Teresa van Heerden; Sitharam, Liza; Barendse, Asa; Nagel, Dane; Prince, Jacqueline; Vass, Letitia; Strauss, Rileen; Fakier, Rushana; Samuel, Catherine; Marelieze van Zyl; Isaacs, Leigh-Ann; Hendricks, Shareefa; Dodd, Amy; Daniels, Reecka; Zemanay, Widaad; Judi Van Heerden; Hapeela, Nchimunya; Brown, Parveen; Daniels, Zubayr; Claassen, Shantelle; Patel, Fadheela; Vasuthevan, Sharon; Scott, Enid; Ricks, Esmeralda; Curle, Patricia; Wojno, Justyna

 Division of Medical Microbiology, National Health Laboratory Service, Red Cross War Memorial Children’s Hospital , Cape Town , South Africa 
 Division of Medical Microbiology, National Health Laboratory Service, Groote Schuur Hospital , Cape Town , South Africa 
 Division of Medical Microbiology, Faculty of Health Sciences, University of Cape Town , Cape Town , South Africa 
 Division of Medical Microbiology, National Health Laboratory Service, Tygerberg Hospital , Cape Town , South Africa 
 Division of Medical Microbiology, Ampath , Cape Town , South Africa 
Publication year
2024
Publication date
Apr 2024
Publisher
Oxford University Press
e-ISSN
26321823
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3170563445
Copyright
© The Author(s) 2024. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.