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Infection Risks Associated with Spirometry

Published online by Cambridge University Press:  21 June 2016

Donna Renfrow Rutala,
William A. Rutala,
David J. Weber and
Charlotte A. Thomann
Donna Renfrow Rutala
Affiliation:
Department of Hospital Epidemiology, University of North Carolina Hospitals, Chapel Hill, North Carolina
William A. Rutala*
Affiliation:
Department of Hospital Epidemiology, University of North Carolina Hospitals, Chapel Hill, North CarolinaDivision of Infectious Diseases, Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina
David J. Weber
Affiliation:
Department of Hospital Epidemiology, University of North Carolina Hospitals, Chapel Hill, North CarolinaDivision of Infectious Diseases, Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina
Charlotte A. Thomann
Affiliation:
Department of Hospital Epidemiology, University of North Carolina Hospitals, Chapel Hill, North Carolina
*
547 Burnett-Womack Building CB #7030, University of North Carolina School of Medicine, UNC at Chapel Hill, Chapel Hill, NC 27599-7030
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Abstract

Objectives:

Spirometry is a widely used pulmonary function test that allows measurement of forced vital capacity and time-related measures of dynamic pulmonary function. This study was designed to identify the risk of cross-transmission associated with two commonly used dry-rolling seal spirometers.

Design:

Using a prospective study design, we examined whether microbial contamination of spirometers occurred following use by patients with a heavily colonized or infected respiratory tract. Prior to spirometry evaluation, a patients sputum culture and equipment samples (i.e., mouthpiece, proximal tubing, piston surface) were obtained. After patient evaluation, a sterile 2 L ventilation bag and sterile tubing were used to simulate the risk of infection of subsequent patients. Simulation 1 was performed immediately after patient testing and Simulation 2, representing a second patient was conducted approximately 18 hours later.

Setting:

This study was conducted at the University of North Carolina Hospitals, a large university teaching facility.

Patients:

Fourteen patients with underlying pulmonary disease were studied.

Results:

Our study revealed that the mouthpieces became contaminated with the patients' oral flora and with the associated respiratory pathogen. Fourteen percent of the associated tubing after patient testing contained the respiratory pathogen. All other equipment samples (e.g., interior surfaces of the machine, Simulation 1, Simulation 2 samples) were negative for the respiratory pathogen.

Conclusions:

These data suggest that mouthpieces and spirometry tubing may become contaminated with microorganisms and should not be shared between patients. Since there is little or no bacterial contamination of the surfaces inside the spirometers and cross transmission is unlikely, it is unnecessary to routinely clean the interior surfaces of the spirometers. (Infect Control Hosp Epidemiol. 1991;12:89-92.)

Information

Type
Original Articles
Information
Infection Control & Hospital Epidemiology , Volume 12 , Issue 2 , February 1991, pp. 89 - 92
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1991 

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