Sustained reduction of catheter-associated bloodstream infections with enhancement of catheter bundle by chlorhexidine dressings over 11 years.


Journal

Intensive care medicine
ISSN: 1432-1238
Titre abrégé: Intensive Care Med
Pays: United States
ID NLM: 7704851

Informations de publication

Date de publication:
06 2019
Historique:
received: 12 11 2018
accepted: 06 04 2019
pubmed: 19 4 2019
medline: 25 2 2020
entrez: 19 4 2019
Statut: ppublish

Résumé

Prospective randomized controlled studies have demonstrated that addition of chlorhexidine (CHG) dressings reduces the rate of catheter (central venous and arterial)-associated bloodstream infections (CABSIs). However, studies confirming their impact in a real-world setting are lacking. We conducted a real-world data study evaluating the impact of incrementally introducing chlorhexidine dressings (sponge or gel) in addition to an ongoing catheter bundle on the rates of CABSI, expressed as incidence density rates per 1000 catheter-days measured as part of a surveillance program. Poisson regression models were used to compare infection rates over time. Both dressings were used simultaneously during one of the five study periods. From 2006 to 2014, 18,286 patients were admitted (91,292 ICU-days and 155,242 catheter-days). We recorded 111 CABSIs. We observed a progressive but significant decrease of CABSI rates from 1.48 (95% CI 1.09-2.01) without CHG dressings to 0.69 (95% CI 0.43-1.09) and 0.23 (95% CI 0.11-0.48) episodes per 1000 catheter-days when CHG sponge and CHG gel dressings were used (p = 0.0007; p < 0.001). A non-significant lower rate of infections occurred with CHG gel compared with CHG sponge dressings. An identical low rate of allergic skin reactions (0.3/1000 device-days) was observed with both types of CHX dressings. Post-study data until 2018 confirmed a sustained decrease of infection rates over 11 years. The addition of chlorhexidine dressings to all CVC and arterial lines to an ongoing catheter bundle was associated with a sustained 11-year reduction of all catheter-associated bloodstream infections. This large real-world data study further supports the current recommendations for the systematic use of CHG dressings on all catheters of ICU patients.

Sections du résumé

BACKGROUND
Prospective randomized controlled studies have demonstrated that addition of chlorhexidine (CHG) dressings reduces the rate of catheter (central venous and arterial)-associated bloodstream infections (CABSIs). However, studies confirming their impact in a real-world setting are lacking.
METHODS
We conducted a real-world data study evaluating the impact of incrementally introducing chlorhexidine dressings (sponge or gel) in addition to an ongoing catheter bundle on the rates of CABSI, expressed as incidence density rates per 1000 catheter-days measured as part of a surveillance program. Poisson regression models were used to compare infection rates over time. Both dressings were used simultaneously during one of the five study periods.
RESULTS
From 2006 to 2014, 18,286 patients were admitted (91,292 ICU-days and 155,242 catheter-days). We recorded 111 CABSIs. We observed a progressive but significant decrease of CABSI rates from 1.48 (95% CI 1.09-2.01) without CHG dressings to 0.69 (95% CI 0.43-1.09) and 0.23 (95% CI 0.11-0.48) episodes per 1000 catheter-days when CHG sponge and CHG gel dressings were used (p = 0.0007; p < 0.001). A non-significant lower rate of infections occurred with CHG gel compared with CHG sponge dressings. An identical low rate of allergic skin reactions (0.3/1000 device-days) was observed with both types of CHX dressings. Post-study data until 2018 confirmed a sustained decrease of infection rates over 11 years.
CONCLUSIONS
The addition of chlorhexidine dressings to all CVC and arterial lines to an ongoing catheter bundle was associated with a sustained 11-year reduction of all catheter-associated bloodstream infections. This large real-world data study further supports the current recommendations for the systematic use of CHG dressings on all catheters of ICU patients.

Identifiants

pubmed: 30997542
doi: 10.1007/s00134-019-05617-x
pii: 10.1007/s00134-019-05617-x
pmc: PMC6534662
doi:

Substances chimiques

Anti-Infective Agents, Local 0
Chlorhexidine R4KO0DY52L

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

823-833

Commentaires et corrections

Type : CommentIn

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Auteurs

Philippe Eggimann (P)

Service of Adult Intensive Care Medicine, University Hospital of Lausanne, University of Lausanne, Lausanne, Switzerland. Philippe.eggimann@chuv.ch.
Department of Locomotor Apparatus, Centre Hospitalier Universitaire Vaudois (CHUV), Bugnon 46, BH 14-309, 1211, Lausanne, Switzerland. Philippe.eggimann@chuv.ch.

Jean-Luc Pagani (JL)

Service of Adult Intensive Care Medicine, University Hospital of Lausanne, University of Lausanne, Lausanne, Switzerland.

Elise Dupuis-Lozeron (E)

Unit of Population Epidemiology, Department of Community Medicine, Primary Care and Emergency Medicine, Geneva University Hospitals, Geneva, Switzerland.

Bruce Ekholm Ms (BE)

3M Health Care Business, 3M Center, St. Paul, MN, USA.

Marie-Josèphe Thévenin (MJ)

Service of Hospital Preventive Medicine, University Hospital of Lausanne, University of Lausanne, Lausanne, Switzerland.

Christine Joseph (C)

Service of Adult Intensive Care Medicine, University Hospital of Lausanne, University of Lausanne, Lausanne, Switzerland.

Jean-Pierre Revelly (JP)

Service of Adult Intensive Care Medicine, University Hospital of Lausanne, University of Lausanne, Lausanne, Switzerland.

Yok-Ai Que (YA)

Department of Intensive Care Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

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