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Outbreak or pseudo-outbreak? Integrating SARS-CoV-2 sequencing to validate infection control practices in a dialysis facility - 24/09/21

Doi : 10.1016/j.ajic.2021.08.001 
Bridget L. Pfaff, MS a, Craig S. Richmond, PhD b, Arick P. Sabin, DO c, Deena M. Athas, MD a, Jessica C. Adams, BSN d, Megan E. Meller, MS, MPH a, Kumari Usha, MD e, Sarah A. Schmitz, RN f, Brian J. Simmons, CIC a, Andrew J. Borgert, PhD g, Paraic A. Kenny, PhD b,
a Departments of Infection Control, Gundersen Health System, La Crosse, WI 
b Kabara Cancer Research Institute, Gundersen Medical Foundation, La Crosse, WI 
c Infectious Disease, Gundersen Health System, La Crosse, WI 
d Renal Dialysis, Gundersen Health System, La Crosse, WI 
e Nephrology, Gundersen Health System, La Crosse, WI 
f Employee Health, Gundersen Health System, La Crosse, WI 
g Medical Research Department, Gundersen Medical Foundation, La Crosse, WI 

Address correspondence to Paraic A. Kenny, PhD, Kabara Cancer Research Institute, Gundersen Medical Foundation, 1300 Badger St, La Crosse, WI, 54601.Kabara Cancer Research InstituteGundersen Medical Foundation1300 Badger StLa CrosseWI,54601USA

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Abstract

Background

The COVID-19 pandemic poses a particularly high risk for End Stage Renal Disease (ESRD) patients so rapid identification of case clusters in ESRD facilities is essential. Nevertheless, with high community prevalence, a series of ESRD patients may test positive contemporaneously for reasons unrelated to their shared ESRD facility. Here we describe a series of 5 cases detected within 11 days in November 2020 in a hospital-based 32-station ESRD facility in Southwest Wisconsin, the subsequent facility-wide testing, and the use of genetic sequence analysis to evaluate links between cases.

Methods

Four patient cases and one staff case were identified in symptomatic individuals by RT-PCR. Facility-wide screening was conducted using rapid SARS-CoV-2 antigen tests. SARS-CoV-2 genome sequences were obtained from residual diagnostic specimens.

Results

Facility-wide screening of 47 staff and 107 patients identified no additional cases. Residual specimens from 4 of 5 cases were available for genetic sequencing. Clear genetic differences proved that these contemporaneous cases were not linked.

Conclusions

With high community prevalence, epidemiological data alone is insufficient to deem a case cluster an outbreak. Cluster evaluation with genomic data, when available with a short turn-around time, can play an important role in infection prevention and control response programs.

El texto completo de este artículo está disponible en PDF.

Highlights

Dialysis patient care poses infection control challenges due to high COVID19 risk.
High community case loads can create “pseudo-outbreaks” of unlinked cases.
Rapid sequencing can refute presumed COVID19 outbreaks in congregate settings.

El texto completo de este artículo está disponible en PDF.

Key Words : COVID-19, End stage renal disease, Infection prevention, Genome sequencing, Epidemiology


Esquema


 Funding: This work was supported by the Gundersen Medical Foundation and by a grant from Fast Grants (#2243) to PAK. The funders had no role in the study design.
 Conflict of interest: The authors declare that they have no conflicts of interest.
 Author contributions: Conception and Design: PAK, CSR, BLP, APS. Acquisition and analysis of data: DMA, JCA, MEM, KU, SAS, BJS, AJB, CSR, BLP, PAK. Drafting and revision of manuscript: BLP, APS, PAK. Approval of final manuscript: All authors.


© 2021  Association for Professionals in Infection Control and Epidemiology, Inc.. Publicado por Elsevier Masson SAS. Todos los derechos reservados.
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Vol 49 - N° 10

P. 1232-1236 - octobre 2021 Regresar al número
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