Household Transmission of Carbapenemase-producing Enterobacterales in Ontario, Canada

Author:

Jamal Alainna J12ORCID,Faheem Amna2,Farooqi Lubna2,Zhong Xi Zoe2,Armstrong Irene13,Boyd David A4,Borgundvaag Emily2,Coleman Brenda L12,Green Karen2,Jayasinghe Kithsiri2,Johnstone Jennie12,Katz Kevin5,Kohler Philipp2,Li Angel X2,Mataseje Laura4,Melano Roberto6,Muller Matthew P17,Mulvey Michael R4,Nayani Sarah2,Patel Samir N6,Paterson Aimee2,Poutanen Susan2,Rebbapragada Anu8,Richardson David9,Sarabia Alicia10,Shafinaz Shumona2,Simor Andrew E11,Willey Barbara M2,Wisely Laura2,McGeer Allison J12

Affiliation:

1. Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada

2. Department of Microbiology, Sinai Health System, Toronto, Ontario, Canada

3. Communicable Disease Control, Toronto Public Health, Toronto, Ontario, Canada

4. Antimicrobial Resistance and Nosocomial Infections, National Microbiology Laboratory, Winnipeg, Manitoba, Canada

5. Department of Infection Prevention and Control, North York General Hospital, Toronto, Ontario, Canada

6. Bacteriology, Public Health Ontario Laboratory, Toronto, Ontario, Canada

7. Department of Infection Prevention and Control, St. Michael’s Hospital, Toronto, Ontario, Canada

8. Scientific Affairs and Market Access, Hologic Inc., Toronto, Ontario, Canada

9. Department of Infection Prevention and Control, William Osler Health System, Brampton, Ontario, Canada

10. Department of Infection Prevention and Control, Trillium Health Partners, Mississauga, Ontario, Canada

11. Department of Infection Prevention and Control, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada

Abstract

Abstract Background Data on household transmission of carbapenemase-producing Enterobacterales (CPE) remain limited. We studied risk of CPE household co-colonization and transmission in Ontario, Canada. Methods We enrolled CPE index cases (identified via population-based surveillance from January 2015 to October 2018) and their household contacts. At months 0, 3, 6, 9, and 12, participants provided rectal and groin swabs. Swabs were cultured for CPE until September 2017, when direct polymerase chain reaction (PCR; with culture of specimens if a carbapenemase gene was detected) replaced culture. CPE risk factor data were collected by interview and combined with isolate whole-genome sequencing to determine likelihood of household transmission. Risk factors for household contact colonization were explored using a multivariable logistic regression model with generalized estimating equations. Results Ninety-five households with 177 household contacts participated. Sixteen (9%) household contacts in 16 (17%) households were CPE-colonized. Household transmission was confirmed in 3/177 (2%) cases, probable in 2/177 (1%), possible in 9/177 (5%), and unlikely in 2/177 (1%). Household contacts were more likely to be colonized if they were the index case’s spouse (odds ratio [OR], 6.17; 95% confidence interval [CI], 1.05–36.35), if their index case remained CPE-colonized at household enrollment (OR, 7.00; 95% CI, 1.92–25.49), or if they had at least 1 set of specimens processed after direct PCR was introduced (OR, 6.46; 95% CI, 1.52–27.40). Conclusions Nine percent of household contacts were CPE-colonized; 3% were a result of household transmission. Hospitals may consider admission screening for patients known to have CPE-colonized household contacts.

Funder

Canadian Institutes of Health Research

Government of Canada Vanier Canada Graduate Scholarship

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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