Development of a tool to assess evidence for causality in studies implicating sink drains as a reservoir for hospital-acquired gammaproteobacterial infection.


Journal

The Journal of hospital infection
ISSN: 1532-2939
Titre abrégé: J Hosp Infect
Pays: England
ID NLM: 8007166

Informations de publication

Date de publication:
11 2020
Historique:
received: 26 04 2020
accepted: 26 08 2020
pubmed: 9 9 2020
medline: 2 7 2021
entrez: 8 9 2020
Statut: ppublish

Résumé

Decades of studies document an association between Gammaproteobacteria in sink drains and hospital-acquired infections, but the evidence for causality is unclear. We aimed to develop a tool to assess the quality of evidence for causality in research studies that implicate sink drains as reservoirs for hospital-acquired Gammaproteobacterial infections. We used a modified Delphi process with recruited experts in hospital epidemiology to develop this tool from a pre-existing causal assessment application. Through four rounds of feedback and revision we developed the 'Modified CADDIS Tool for Causality Assessment of Sink Drains as a Reservoir for Hospital-Acquired Gammaproteobacterial Infection or Colonization'. In tests of tool application to published literature during development, mean percent agreement ranged from 46.7% to 87.5%, and the Gwet's AC1 statistic (adjusting for chance agreement) ranged from 0.13 to 1.0 (median 68.1). Areas of disagreement were felt to result from lack of a priori knowledge of causal pathways from sink drains to patients and uncertain influence of co-interventions to prevent organism acquisition. Modifications were made until consensus was achieved that further iterations would not improve the tool. When the tool was applied to 44 articles by two independent reviewers in an ongoing systematic review, percent agreement ranged from 93% to 98%, and the Gwet's AC1 statistic was 0.91-0.97. The modified causality tool was useful for evaluating studies that implicate sink drains as reservoirs for hospital-acquired infections and may help guide the conduct and reporting of future research.

Sections du résumé

BACKGROUND
Decades of studies document an association between Gammaproteobacteria in sink drains and hospital-acquired infections, but the evidence for causality is unclear.
AIM
We aimed to develop a tool to assess the quality of evidence for causality in research studies that implicate sink drains as reservoirs for hospital-acquired Gammaproteobacterial infections.
METHODS
We used a modified Delphi process with recruited experts in hospital epidemiology to develop this tool from a pre-existing causal assessment application.
FINDINGS
Through four rounds of feedback and revision we developed the 'Modified CADDIS Tool for Causality Assessment of Sink Drains as a Reservoir for Hospital-Acquired Gammaproteobacterial Infection or Colonization'. In tests of tool application to published literature during development, mean percent agreement ranged from 46.7% to 87.5%, and the Gwet's AC1 statistic (adjusting for chance agreement) ranged from 0.13 to 1.0 (median 68.1). Areas of disagreement were felt to result from lack of a priori knowledge of causal pathways from sink drains to patients and uncertain influence of co-interventions to prevent organism acquisition. Modifications were made until consensus was achieved that further iterations would not improve the tool. When the tool was applied to 44 articles by two independent reviewers in an ongoing systematic review, percent agreement ranged from 93% to 98%, and the Gwet's AC1 statistic was 0.91-0.97.
CONCLUSION
The modified causality tool was useful for evaluating studies that implicate sink drains as reservoirs for hospital-acquired infections and may help guide the conduct and reporting of future research.

Identifiants

pubmed: 32898614
pii: S0195-6701(20)30412-6
doi: 10.1016/j.jhin.2020.08.024
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

454-464

Informations de copyright

Copyright © 2020 The Healthcare Infection Society. Published by Elsevier Ltd. All rights reserved.

Auteurs

C Volling (C)

Mount Sinai Hospital, Toronto, ON, Canada; University of Toronto, Toronto, ON, Canada. Electronic address: cheryl.volling@mail.utoronto.ca.

S Thomas (S)

Mount Sinai Hospital, Toronto, ON, Canada.

J Johnstone (J)

Mount Sinai Hospital, Toronto, ON, Canada; University of Toronto, Toronto, ON, Canada.

H C Maltezou (HC)

National Public Health Organization, Athens, Greece.

D Mertz (D)

Hamilton Health Sciences, Hamilton, ON, Canada; McMaster University, Hamilton, ON, Canada.

R Stuart (R)

Monash Health, Clayton, Victoria, Australia; Monash University, Clayton, Victoria, Australia.

Alainna J Jamal (AJ)

Mount Sinai Hospital, Toronto, ON, Canada; University of Toronto, Toronto, ON, Canada.

C Kandel (C)

Mount Sinai Hospital, Toronto, ON, Canada; University of Toronto, Toronto, ON, Canada.

N Ahangari (N)

Mount Sinai Hospital, Toronto, ON, Canada.

B L Coleman (BL)

Mount Sinai Hospital, Toronto, ON, Canada; University of Toronto, Toronto, ON, Canada.

A McGeer (A)

Mount Sinai Hospital, Toronto, ON, Canada; University of Toronto, Toronto, ON, Canada.

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Classifications MeSH