Notes from the Field: Candida auris and Carbapenemase-Producing Organism Prevalence in a Pediatric Hospital Providing Long-Term Transitional Care — Chicago, Illinois, 2019
Weekly / August 28, 2020 / 69(34);1180–1181
Tristan D. McPherson, MD1,2; Kelly A. Walblay, MPH2; Elissa Roop, MSN3; David Soglin, MD3; Ann Valley4; Latania K. Logan, MD5; Snigdha Vallabhaneni, MD6; Stephanie R. Black, MD2; Massimo Pacilli, MS, MPH2 (View author affiliations)
View suggested citationCandida auris is an emerging fungal pathogen that is frequently drug-resistant; C. auris can be difficult to identify, and it has been associated with outbreaks in health care settings.* The first case of C. auris in Chicago, Illinois, was identified in May 2016 (1). Additional cases continue to be reported, particularly in high-acuity, postacute–care facilities (1), and spread of C. auris within this type of facility has been documented nationwide (2). To monitor local trends in the prevalence of C. auris, point prevalence surveys (PPSs) have been conducted in Chicago since August 2016 (1). In addition to C. auris, a high prevalence of carbapenemase-producing organisms (CPOs) has also been described in Chicago long-term acute-care hospitals since 2010 (3). C. auris and CPOs can colonize persons over prolonged periods and, because of antimicrobial resistance, cause invasive infections with limited treatment options (2,3). Co-colonization with these organisms has been identified (4). Adults in long-term acute-care hospitals are at increased risk for acquiring C. auris and CPOs because of serious underlying medical conditions, extended lengths of stay, presence of indwelling medical devices, and frequent health care worker contact (3,4). As of June 2019, among residents of Chicago’s four long-term acute-care hospitals, the median prevalences of colonization with C. auris and CPO were 31% and 24%, respectively (Chicago Department of Public Health, personal communication, January 3, 2020). Although prevalence among adults is well characterized, prevalence of C. auris colonization has not been described among pediatric populations in Chicago, and limited data exist on CPO colonization among children outside of intensive care units (5).
To assess C. auris and CPO colonization among children, in August 2019, the Chicago Department of Public Health conducted a PPS in a 49-bed pediatric hospital providing long-term transitional care for patients leaving pediatric intensive care units. All hospitalized patients were included unless parental consent could not be obtained. Presence and type of medical devices (i.e., gastrostomy tubes, tracheostomies, mechanical ventilators, and central venous catheters) and lengths of stay were documented for all hospitalized patients. Specimens collected for testing consisted of composite bilateral axillary and inguinal swabs for C. auris and rectal swabs for CPO testing. The Wisconsin State Laboratory of Hygiene tested all specimens. Real-time polymerase chain reaction (PCR) assays were used to detect C. auris DNA and the carbapenemase genes blaKPC, blaNDM, blaVIM, blaOXA-48, and blaIMP (Xpert Carba-R Assay, Cepheid). All axillary and inguinal swabs were processed by real-time PCR and culture to identify C. auris. For CPOs, culture was attempted on real-time PCR-positive specimens. Among all 29 hospitalized patients, 25 (86%) were screened for C. auris and CPOs. Two rectal specimens were unsatisfactory and produced invalid CPO test results. Patient census was matched to the Illinois extensively drug resistant organism (XDRO) registry to identify previous reports of C. auris and CPO colonization or infection. Facility prevalence of C. auris and CPOs was calculated as the number of patients with a PPS-related specimen that was positive or a previous report of these organisms in the XDRO registry divided by the facility census count provided by the facility on the day of PPS.
Among the 29 hospitalized patients, median age was 1.2 years (range = 26 days–17.4 years; interquartile range [IQR] = 289 days–2.6 years), 26 (90%) had a gastrostomy tube, 24 (83%) had a tracheostomy, 20 (69%) required mechanical ventilation, and three (10%) had a central venous catheter. Median length of stay was 35 days (IQR = 13–71 days). No patient had a previous report of C. auris or CPO. No patient specimens were positive for C. auris, and a specimen from one patient was positive for blaOXA-48, yielding a facility prevalence for CPOs of 3.4%. No organism was recovered from the specimen that tested positive for blaOXA-48.
This PPS is the first documented screening for C. auris colonization in a transitional care pediatric hospital in the United States. Despite a high prevalence of C. auris and CPOs among patients in adult health care settings of similar acuity in the region, C. auris was not identified and CPOs were rare at this pediatric hospital. Biannual assessment of this facility is planned. Because this PPS includes only one facility in a region, additional evaluations in similar pediatric health care settings need to be conducted to improve understanding of C. auris and CPO prevalence in this population.
Corresponding author: Tristan D. McPherson, tmcpherson@cdc.gov, 312-473-0414.
1Epidemic Intelligence Service, CDC; 2Communicable Disease Program, Chicago Department of Public Health, Illinois; 3La Rabida Children’s Hospital, Chicago, Illinois; 4Wisconsin State Laboratory of Hygiene; 5Rush University Medical Center, Chicago, Illinois; 6Division of Healthcare Quality Promotion, National Center for Emerging and Zoonotic Infectious Diseases, CDC.
All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. No potential conflicts of interest were disclosed.
References
- Kerins JL, Tang AS, Forsberg K, et al. 923. Rapid emergence of Candida auris in the Chicago region. Open Forum Infect Dis 2018;5(Suppl 1):S28. CrossRef
- Tsay S, Welsh RM, Adams EH, et al. Notes from the field: ongoing transmission of Candida auris in health care facilities—United States, June 2016–May 2017. MMWR Morb Mortal Wkly Rep 2017;66:514–5. CrossRef PubMed
- Lin MY, Lyles-Banks RD, Lolans K, et al. The importance of long-term acute care hospitals in the regional epidemiology of Klebsiella pneumoniae carbapenemase-producing Enterobacteriaceae. Clin Infect Dis 2013;57:1246–52. CrossRef PubMed
- Pacilli M, Kerins JL, Clegg WJ, et al. Regional emergence of Candida auris in Chicago and lessons learned from intensive follow-up at 1 ventilator-capable skilled nursing facility. Clin Infect Dis 2020. Epub April 14, 2020. CrossRef PubMed
- Viau RA, Hujer AM, Marshall SH, et al. “Silent” dissemination of Klebsiella pneumoniae isolates bearing K. pneumoniae carbapenemase in a long-term care facility for children and young adults in Northeast Ohio. Clin Infect Dis 2012;54:1314–21. CrossRef PubMed
Suggested citation for this article: McPherson TD, Walblay KA, Roop E, et al. Notes from the Field: Candida auris and Carbapenemase-Producing Organism Prevalence in a Pediatric Hospital Providing Long-Term Transitional Care — Chicago, Illinois, 2019. MMWR Morb Mortal Wkly Rep 2020;69:1180–1181. DOI: http://dx.doi.org/10.15585/mmwr.mm6934a5.
MMWR and Morbidity and Mortality Weekly Report are service marks of the U.S. Department of Health and Human Services.
Use of trade names and commercial sources is for identification only and does not imply endorsement by the U.S. Department of
Health and Human Services.
References to non-CDC sites on the Internet are
provided as a service to MMWR readers and do not constitute or imply
endorsement of these organizations or their programs by CDC or the U.S.
Department of Health and Human Services. CDC is not responsible for the content
of pages found at these sites. URL addresses listed in MMWR were current as of
the date of publication.
All HTML versions of MMWR articles are generated from final proofs through an automated process. This conversion might result in character translation or format errors in the HTML version. Users are referred to the electronic PDF version (https://www.cdc.gov/mmwr) and/or the original MMWR paper copy for printable versions of official text, figures, and tables.
Questions or messages regarding errors in formatting should be addressed to mmwrq@cdc.gov.