Evidence map›Paper›PMID 32869855›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2021

Household Transmission of Carbapenemase-producing Enterobacterales in Ontario, Canada.

Alainna J Jamal, Amna Faheem, Lubna Farooqi, Xi Zoe Zhong, Irene Armstrong, David A Boyd, Emily Borgundvaag, Brenda L Coleman, Karen Green, Kithsiri Jayasinghe and 20 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 44% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 14 citations in OpenAlex.

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  11. Genomic Epidemiology of Carbapenemase-ProducingAntimicrobial agents and chemotherapy · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors at 9 institutions in 1 country.

Alainna J JamalDalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0001-7082-3027
Amna FaheemDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Lubna FarooqiDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Xi Zoe ZhongDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Irene ArmstrongDalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
David A BoydAntimicrobial Resistance and Nosocomial Infections, National Microbiology Laboratory, Winnipeg, Manitoba, Canada.
Emily BorgundvaagDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Brenda L ColemanDalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Karen GreenDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Kithsiri JayasingheDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Jennie JohnstoneDalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Kevin KatzDepartment of Infection Prevention and Control, North York General Hospital, Toronto, Ontario, Canada.
Philipp KohlerDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Angel X LiDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Laura MatasejeAntimicrobial Resistance and Nosocomial Infections, National Microbiology Laboratory, Winnipeg, Manitoba, Canada.
Roberto MelanoBacteriology, Public Health Ontario Laboratory, Toronto, Ontario, Canada.
Matthew P MullerDalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Michael R MulveyAntimicrobial Resistance and Nosocomial Infections, National Microbiology Laboratory, Winnipeg, Manitoba, Canada.
Sarah NayaniDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Samir N PatelBacteriology, Public Health Ontario Laboratory, Toronto, Ontario, Canada.
Aimee PatersonDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Susan PoutanenDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Anu RebbapragadaScientific Affairs and Market Access, Hologic Inc., Toronto, Ontario, Canada.
David RichardsonDepartment of Infection Prevention and Control, William Osler Health System, Brampton, Ontario, Canada.
Alicia SarabiaDepartment of Infection Prevention and Control, Trillium Health Partners, Mississauga, Ontario, Canada.
Shumona ShafinazDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Andrew E SimorDepartment of Infection Prevention and Control, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Barbara M WilleyDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Laura WiselyDepartment of Microbiology, Sinai Health System, Toronto, Ontario, Canada.
Allison J McGeerDalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Sinai Health System · CAUniversity of Toronto · CAPublic Health Ontario · CANorth York General Hospital · CASt. Michael's Hospital · CASunnybrook Health Science Centre · CAToronto Public Health · CATrillium Health Centre · CAWilliam Osler Health System · CA

Funding

CIHR 313039Government of Canada Vanier Canada Graduate Scholarship
6 · The paper itself

Abstract

backgroundData on household transmission of carbapenemase-producing Enterobacterales (CPE) remain limited. We studied risk of CPE household co-colonization and transmission in Ontario, Canada.

methodsWe 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.

resultsNinety-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).

conclusionsNine 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.

Indexed as

Enterobacteriaceae InfectionsBacterial Proteinsbeta-LactamasesHumansOntarioBacterial Proteinsbeta-Lactamasescarbapenemasecarbapenem-resistant Enterobacteriaceaedisease transmissionepidemiologypublic healthβ-lactamases

Identifiers

PMID32869855
PMCPMC8662791
OpenAlexW3082942988

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.