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Delayed Detection of an Increase in Resistant Acinetobacter at a Detroit Hospital

Published online by Cambridge University Press:  21 June 2016

David R. Johnson*
Affiliation:
Centers for Disease Control, Division of Field Epidemiology, Atlanta, Georgia Michigan Department of Public Health, Lansing, Michigan
Melinda A. Love-Dixon
Affiliation:
City of Detroit Health Department, Wayne State University Medical School, Detroit, Michigan
William J. Brown
Affiliation:
Detroit Medical Center, Wayne State University Medical School, Detroit, Michigan Wayne State University Medical School, Detroit, Michigan
Donald P. Levine
Affiliation:
Wayne State University Medical School, Detroit, Michigan
Frances P. Downes
Affiliation:
Michigan Department of Public Health, Lansing, Michigan
William N. Hall
Affiliation:
Michigan Department of Public Health, Lansing, Michigan
*
Michigan Dept. of Public Health, Bureau of Infectious Disease Control, 3500 North Logan, PO Box 30035, Lansing, MI 48909

Abstract

Objective:

To study an increase of antimicrobial-resistant Acinetobacter baumannii and to assess reasons for the delayed detection of this increase.

Design:

Review of medical, laboratory, and infection control records. Plasmid profile analysis of available A baumannii isolates.

Setting:

A 340-bed trauma and intensive care hospital in Detroit, Michigan.

Results:

The number of hospitalized patients with resistant A baumannii increased during late 1989 and early 1990: 4 in September, 10 in October, 12 in November, 18 in December, and 23 in January (chi square for trend = 14.6, p= .0001). Forty-four (66%) of the 67 patients culture-positive for resistant A baumannii had respiratory tract colonization or infection. Of 11 resistant isolates, 6 had a similar plasmid profile and 5 had no plasmids. Under the hospital's targeted surveillance system, only positive cultures from blood or wounds were investigated; this largely respiratory increase of resistant A baumannii went unrecognized until January 1990.

Conclusions:

Antimicrobial resistance in A baumannii is an important concern. Such resistance is not necessarily plasmid mediated. Tar geted surveillance for this and other agents of nosocomial infection should be used with caution, particularly in hospitals with many debilitated patients.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1992

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References

1. Baumann, P. Isolation of Acinetobacter from soil and water. J Bacteriol. 1968;96:3942.CrossRefGoogle ScholarPubMed
2. Taplin, D, Rebell, G, Zaias, N. The human skin as a source of Mima-Herellea infections. JAMA. 1963;186:952955.CrossRefGoogle ScholarPubMed
3. Rosenthal, S, Tager, IB. Prevalence of gram-negative rods in the normal pharyngeal flora. Ann Intern Med. 1975;83:355357.CrossRefGoogle ScholarPubMed
4. Bouvet, PJM, Grimont, PAD. Taxonomy of the genus Acinetobacter with the recognition of Acinetobacter baumannii sp nov, Acinetobacteo haemolytics sp nov, Acinetobacter johnsonii sp nov, and Acinetobacter junii sp nov and emended descriptions of Acinetobacter calcoaceticus and Acinetobacter Iwoffii . International Journal of Systematic Bacteriology. 1986;36:228240.Google Scholar
5. Beck-Sague, CM, Jarvis, WR, Culver, DH. Secular trends in nosocomial Acinetobacter calcoaceticus incidence and antimicrobial resistance. Presented at the Twenty-eighth Interscience Conference on Antimicrobial Agents and Chemotherapy; 1988; Abstract # 1081.Google Scholar
6. Garner, JS, Jarvis, WR, Emori, TG, Horan, TC, Hughes, JM. CDC definitions for nosocomial infections, 1988. Am J Infect Control. 1988;16:128140.Google Scholar
7. Mantel, N. Chi-square tests with one degree of freedom; extensions of the Mantel-Haenszel procedure. Journal of the American Statistical Association. 1963;58:690700.Google Scholar
8. Greenland, S, Robins, JM. Estimation of a common effect parameter from sparse follow-up data. Biometrics. 1985;41:5568.Google Scholar
9. National Committee for Clinical Laboratory Standards. Performance Standards for Antimicrobial Susceptibility Testing; Second Informational Supplement. Document M100-S2. Villanova, Pa: National Committee for Clinical Laboratory Standards; 1987.Google Scholar
10. Rubin, SJ, Granato, PA, Wasilauskas, BL. Glucose-nonfermenting gram-negative bacteria. In: Lennette, EH, Balows, A, Hausler, WJ Jr, Dhadomy, JH, eds. Manual of Clinical Microbiology. 4th ed. Washington, DC: American Society for Microbiology; 1985:330349.Google Scholar
11. Birnboim, HC, Doly, J. A rapid alkaline extraction procedure for screening recombinant DNA. Nucleic Acids Res. 1979;7:15131523.Google Scholar
12. Smith, PW, Massanari, RM. Room humidifiers as the source of Acinetobacter infections. JAMA. 1977;237:795797.CrossRefGoogle ScholarPubMed
13. Castle, M, Tenney, JH, Weinstein, MP, Eickhoff, TC. Outbreak of a multiply resistant Acinetobacter in a surgical intensive care unit: epidemiology and control. Heart Lung. 1978;7:641644.Google Scholar
14. Chuna, BA, Klimek, JJ, Gracewski, J, McLaughlin, JC, Quintiliani, R. A common source outbreak of Acinetobacter pulmonary infections traced to Wright respirometers. Postgrad Med J. 1980;56:169172.Google Scholar
15. Carlquist, JF, Conti, M, Burke, JP. Progressive resistance in a single strain of Acinetobacter calcoaceticus recovered during a nosocomial outbreak. Am J Infect Control. 1982;10:4348.Google Scholar
16. Gervich, DH, Grout, CS. An outbreak of nosocomial Acinetobacter infections from humidifiers. Am J Infect Control. 1985;13:210215.Google Scholar
17. Allen, KD, Green, HT. Hospital outbreak of multi-resistant Acinetobacter anitratus: an airborne mode of spread? J Hosp Infect. 1987;9:110119.Google Scholar
18. Peacock, JE, Sorrell, L, Sottile, FD, Price, LE, Rutala, WA. Nosocomial respiratory tract colonization and infection with aminogly-coside-resistant Acinetobacter calcoaceticus var anitratus: epidemiologic characteristics and clinical significance. Infect Control Hosp Epidemiol. 1988;9:302308.Google Scholar
19. Hartstein, AI, Rashad, AL, Liebler, JM, et al. Multiple intensive care unit outbreak of Acinetobacter calcoaceticus subspecies anitratus respiratory infection and colonization associated with contaminated, reusable ventilator circuits and resuscitation bags. Am J Med. 1988;85:624631.CrossRefGoogle ScholarPubMed
20. Crombach, WHJ, Dijkshoorn, L, van Noort-Klaassen, M, Niessen, J, van Knippenberg-Gordebeke, G. Control of an epidemic spread of a multi-resistent strain of Acinetobacter calcoaceticus in a hospital. Intensive Care Med. 1989;15:166170.Google Scholar
21. Cefai, C, Richards, J, Gould, FK, McPeake, l? An outbreak of Acinetobacter respiratory tract infection resultine from incomplete disinfection of ventilatory equipment. 7 Hosp Infect. 1990;15:177182.Google Scholar
22. Contant, J, Kemeny, E, Oxley, C, Perry, E, Garber, G. Investigation of an outbreak of Acinetobacter calcoaceticus var anitratus infections in an adult intensive care unit. Am J Infect Control. 1990;18:288291.Google Scholar
23. Beck-Sague, CM, Jarvis, WR, Brook, JH, et al. Epidemic bacteremia due to Acinetobacter baumannii in five intensive care units. Am J Epidemiol. 1990;132:723733.Google Scholar
24. Hartstein, AI, Morthland, VH, Rourke, JW, et al. Plasmid DNA fingerprinting of Acinetobacter calcoaceticus subspecies anitratus from intubated and mechanically ventilated patients. Infect Control Hosp Epidemiol 1990;11:531538.CrossRefGoogle ScholarPubMed