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Adequate Disinfection of a Split-Septum Needleless Intravascular Connector with a 5-Second Alcohol Scrub

Published online by Cambridge University Press:  02 January 2015

Mark E. Rupp ,
Stephanie Yu ,
Tomas Huerta ,
R. Jennifer Cavalieri ,
Roxanne Alter ,
Paul D. Fey ,
Trevor Van Schooneveld  and
James R. Anderson
Mark E. Rupp*
Affiliation:
Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska Department of Infection Control and Epidemiology, Nebraska Medical Center, Omaha, Nebraska
Stephanie Yu
Affiliation:
Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska
Tomas Huerta
Affiliation:
Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska
R. Jennifer Cavalieri
Affiliation:
Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska
Roxanne Alter
Affiliation:
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska
Paul D. Fey
Affiliation:
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska
Trevor Van Schooneveld
Affiliation:
Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska Department of Infection Control and Epidemiology, Nebraska Medical Center, Omaha, Nebraska
James R. Anderson
Affiliation:
Department of Biostatistics, College of Public Health, University of Nebraska Medical Center, Omaha, Nebraska
*
984031 Nebraska Medical Center, Omaha, NE 68198 ([email protected])
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Abstract

Objective.

Define optimum vascular catheter connector valve disinfection practices under laboratory and clinical conditions.

Design.

Prospective observational clinical survey and laboratory assessment of disinfection procedures.

Setting.

All adult inpatients at an academic healthcare center.

Methods.

In the clinical setting, contamination of needleless connectors was assessed in 6 weekly prevalence surveys in which the connector valves from central venous catheters (CVCs) in situ were cultured by pressing the connector diaphragm to an agar plate. Before culture, valves were disinfected by scrubbing the diaphragm with a 70% isopropyl alcohol pledget for 0, 5, 10, 15, or 30 seconds. In the laboratory, the diaphragms on 150 unused sterile connector valves were inoculated with 103, 105, or 108 colony-forming units of Staphylococcus epidermidis and allowed to dry. After disinfection of the diaphragms by scrubbing with a 70% isopropyl alcohol pledget for 0, 5, 10, 15, or 30 seconds, the valves were sampled by pressing the diaphragm to an agar plate.

Results.

In the clinical setting, 363 connector valves from patients with CVCs were sampled, and 66.7% of nondisinfected valves revealed bacterial contamination. After 5-second disinfection with an alcohol pledget, only 1 (1.4%) of 71 yielded microbial growth (P < .005). In the laboratory, at the 103 and 105 inoculum, all connector valves yielded sterile cultures when scrubbed for 5 or more seconds (P < .001). At the 108 inoculum, 2 (20%) of 10 connector valves yielded minimal growth of S. epidermidis.

Conclusions.

A 5-second scrub with a 70% isopropyl alcohol pledget yields adequate disinfection of a split-septum intravascular catheter connector valve under clinical and laboratory conditions.

Type
Original Articles
Information
Infection Control & Hospital Epidemiology , Volume 33 , Issue 7 , July 2012 , pp. 661 - 665
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2012

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