Hostname: page-component-848d4c4894-xm8r8 Total loading time: 0 Render date: 2024-06-19T22:51:06.516Z Has data issue: false hasContentIssue false

Risk of Bioaerosol Contamination With Aspergillus Species Before and After Cleaning in Rooms Filtered With High-Efficiency Particulate Air Filters That House Patients With Hematologic Malignancy

Published online by Cambridge University Press:  02 January 2015

Linda D. Lee*
Affiliation:
Departments of Environmental Health and Safety, The University of Texas M. D. Anderson Cancer Center, Houston, Texas
Matthew Berkheiser
Affiliation:
Departments of Environmental Health and Safety, The University of Texas M. D. Anderson Cancer Center, Houston, Texas
Ying Jiang
Affiliation:
Infectious Diseases, Infection Control, and Employee Health, The University of Texas M. D. Anderson Cancer Center, Houston, Texas
Brenda Hackett
Affiliation:
Infectious Diseases, Infection Control, and Employee Health, The University of Texas M. D. Anderson Cancer Center, Houston, Texas
Ray Y. Hachem
Affiliation:
Infectious Diseases, Infection Control, and Employee Health, The University of Texas M. D. Anderson Cancer Center, Houston, Texas
Roy F. Chemaly
Affiliation:
Infectious Diseases, Infection Control, and Employee Health, The University of Texas M. D. Anderson Cancer Center, Houston, Texas
Issam I. Raad
Affiliation:
Infectious Diseases, Infection Control, and Employee Health, The University of Texas M. D. Anderson Cancer Center, Houston, Texas
*
Executive Director, Dept. of Environmental Health and Safety, The University of Texas M. D. Anderson Cancer Center, PO Box 301439, Unit 713, Houston, TX 77230-1439 (ldlee@mdanderson.org)

Abstract

Objective.

To examine the impact of cleaning and directional airflow on environmental contamination with Aspergillus species in hospital rooms filtered with high-efficiency particulate air (HEPA) filters that house patients with hematologic malignancy.

Design.

Detailed environmental assessment.

Setting.

A 475-bed tertiary cancer center in the southern United States.

Methods.

From April to October 2004, 1,258 surface samples and 627 bioaerosol samples were obtained from 74 HEPA-filtered rooms (in addition, 88 outdoor bioaerosol samples were obtained). Samples were collected from rooms cleaned within 1 hour after patient discharge and from rooms before cleaning. Positive and negative airflows were evaluated using air-current tubes at entrances to patient rooms.

Results.

Of 1,258 surface samples, 3.3% were positive for Aspergillus species. Univariate analysis showed no relationship between cleaning status and occurrence of Aspergillus species. Of 627 bioaerosol samples, 7.3% were positive for Aspergillus species. Multiple logistic analysis revealed independently significant associations with detection of Aspergillus species. Cleaned rooms positive for Aspergillus species had a higher geometric mean density of colonies than that of rooms sampled before cleaning (18.9 vs 5.5 colony-forming units [cfu] per cubic meter; P = .0047). Rooms with positive airflow had a detection rate for bioaerosol samples equivalent to that of rooms with negative airflow (7.3% vs 7.8%; P = .8). There was no significant difference in the density of Aspergillus species between rooms with negative airflow and rooms with positive airflow (12.5 vs 8.4 cfu/m3; P = .33).

Conclusions.

Concentration of bioaerosol contamination with Aspergillus species was increased in rooms sampled 1 hour after cleaning compared with rooms sampled before cleaning, suggesting a possible correlation between reentrained bioaerosols (ie, those suspended by activity in the room) after cleaning and the risk of nosocomial invasive aspergillosis.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2007

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Hardin, BD, Kelman, BJ, Saxon, A. Adverse human health effects associated with molds in the indoor environment. J Occup Environ Med 2003;45:470478.Google ScholarPubMed
2. Kontoyiannis, DP, Bodey, GP. Invasive aspergillosis in 2002: an update. Eur J Clin Microbiol Infect Dis 2002;21:161172.CrossRefGoogle ScholarPubMed
3. Groll, AH, Walsh, TJ. Antifungal chemotherapy: advances and perspectives. Swiss Med Wkly 2002;132:303311.Google ScholarPubMed
4. Hajjeh, RA, Warnock, DW. Counterpoint: invasive aspergillosis and the environment—rethinking our approach to prevention. Clin Infect Dis 2001;33:15491552.CrossRefGoogle ScholarPubMed
5. Vonberg, RP, Gastmeier, P. Nosocomial aspergillosis in outbreak settings. J Hosp Infect 2006;63:246254.CrossRefGoogle ScholarPubMed
6. Pound, MW, Drew, RH, Perfect, JR. Recent advances in the epidemiology, prevention, diagnosis, and treatment of fungal pneumonia. Curr Opin Infect Dis 2002;15:183194.CrossRefGoogle ScholarPubMed
7. Vogeser, M, Wanders, A, Haas, A, Ruckdeschel, G. A four-year review of fatal aspergillosis. Eur J Clin Microbiol Infect Dis 1999;18:4245.CrossRefGoogle ScholarPubMed
8. Dasbach, EJ, Davies, GM, Teutsch, SM. Burden of aspergillosis-related hospitalizations in the United States. Clin Infect Dis 2000;31:15241528.CrossRefGoogle ScholarPubMed
9. JCAHO issues alert on nosocomial infections. Hosp Peer Rev 2003;28:3234.Google Scholar
10. Jensen, PA, Lambert, LA, Iademarco, MF, Ridzon, R. Guidelines for preventing the transmission of Mycobacterium tuberculosis in health-care settings, 2005. MMWR Recomm Rep 2005;54:1141.Google ScholarPubMed
11. Sehulster, L, Chinn, RY, Centers for Disease Control and Prevention (CDC), Healthcare Infection Control Practices Advisory Committee (HICPAC). Guidelines for environmental infection control in healthcare facilities: recommendations of CDC and the HICPAC. MMWR Recomm Rep 2003;52(RR-10):142.Google Scholar