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Nosocomial Respiratory Tract Colonization and Infection with Aminoglycoside-Resistant Acinetobacter calcoaceticus var anitratus: Epidemiologic Characteristics and Clinical Significance

Published online by Cambridge University Press:  02 January 2015

James E. Peacock Jr.*
Affiliation:
Departments of Medicine, Wake Forest University Medical Center, Winston-Salem, North Carolina
LuAnne Sorrell
Affiliation:
Hospital Infection Control, Wake Forest University Medical Center, Winston-Salem, North Carolina
Frank D. Sottile
Affiliation:
Anesthesia/Critical Care, Wake Forest University Medical Center, Winston-Salem, North Carolina
Loraine E. Price
Affiliation:
Departments of Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina
William A. Rutala
Affiliation:
Departments of Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina Hospital Epidemiology, University of North Carolina School of Medicine, Chapel Hill, North Carolina
*
Section on Infectious Diseases, Department of Medicine, Wake Forest University Medical Center, 300 South Hawthorne Road, Winstow-Salem, NC 27103

Abstract

During the period July 1983 through December 1984, aminoglycoside-resistant Acinetobacter calcoaceticus var anitratus (ACA) were isolated from 98 patients in a university hospital. Eighty-seven percent of patients (85/98) acquired aminoglycoside-resistant ACA in the intensive care unit (ICU) and 92% (90198) of all initial isolates were from sputum. ICU patients with respiratory colonization/infection with aminoglycoside-resistant ACA were compared with matched ICU controls with other gram-negative rods in sputum. Compared with controls, the duration of ICU stay prior to colonization/infection with aminoglycoside-resistant ACA was significantly longer for cases (14.7 days υ 5.9 days, P = 0.002). Although exposures to devices and procedures were not significantly different for the two groups, cases received respiratory therapy significantly longer than did controls (14.7 days υ 6.6 days, P = 0.006). Prior to isolation of aminoglycoside-resistant ACA in sputum, cases received more cephalosporins than did controls (1.9 υ 1.2, P = 0.018); aminoglycoside usage in the two groups was comparable but cases tended to have received aminoglycoside for longer durations before colonization/infection than had controls (9.0 days υ 6.1 days, P = 0.08). Following sputum isolation of ACA, 6 of 22 cases developed ACA bacteremia compared with bacteremia in 2 of 22 controls. We conclude that factors predisposing to colonization/infection with aminoglycoside-resistant ACA were extended ICU care, prolonged respiratory therapy, and prior therapy with cephalosporins and aminoglycoside. In addition, ACA may be a more common cause of secondary bacteremia than previously appreciated.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1988

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References

1.Glew, RH, Moellering, RC Jr, Kunz, LJ: Infections with Acinetobacter calcoaceticus (Herellea vaginicola): Clinical and laboratory studies. Medicine 1977;56:7997.CrossRefGoogle ScholarPubMed
2.Smith, PW, Massanari, RM: Room humidifiers as the source of Acinetobacter infections.JAMA 1977;237:795797.CrossRefGoogle ScholarPubMed
3.Buxton, AE, Anderson, RL, Werdegar, D, et al: Nosocomial respiratory tract infection and colonization with Acinetobacter calcoaceticus. Epidemiologic characteristics. Am J Med 1978: 65:507513.CrossRefGoogle ScholarPubMed
4.Abrutyn, E, Goodhart, CL, Roos, K, et al: Acinetobacter calcoaceticus outbreak associated with peritoneal dialysis. Am J Epidemiol 1978;107:328335.CrossRefGoogle ScholarPubMed
5.Castle, M, Tenney, JH, Weinstein, MP, et al: Outbreak of a multiply resistant Acinetobacter in a surgical intensive care unit: Epidemiology and control. Heart Lung 1978;7:641644.Google Scholar
6.Retailliau, HF, Hightower, AW, Dixon, RE, et al: Acinetobacter calcoaceticus: A nosocomial pathogen with an unusual seasonal pattern. J Infect Dis 1979;139:371375.CrossRefGoogle ScholarPubMed
7.Ramphal, R, Kluge, RM: Acinetobacter calcoaceticus variety anitratus: An increasing nosocomial problem. Am J Med Sci 1979; 277:5766.CrossRefGoogle ScholarPubMed
8.Cunha, BA, Gracewski, J, Klimek, JJ, et al: A common source outbreak of Acinetobacter pulmonary infections traced to Wright spirometers. Postgrad Med J 1980;56:169172.CrossRefGoogle Scholar
9.O'Connell, CJ, Hamilton, R: Cram-negative rod infections II, Acinetobacter infections in general hospital. NY State J Med 1981;81:750753.Google ScholarPubMed
10.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.CrossRefGoogle Scholar
11.Raz, R, Alroy, G, Sobel, JD: Nosocomial bacteremia due to Acinetobacter calcoaceticus. Infection 1982; 10:168171.CrossRefGoogle ScholarPubMed
12.Sherertz, RJ, Sullivan, ML: An outbreak of infections with Acinetobacter ml-coaceticus in burn patients: Contamination of patients' mattresses. J Infect Dis 1985: 151:252258.CrossRefGoogle ScholarPubMed
13.Berner-Smidt, P, Hansen, L, Knudsen, A, et al: Epidemic spread of Acinetobacter calcoaceticus in a neurosurgical department analyzed by electronic data processing. J Hosp Infect 1985;6:166174.CrossRefGoogle Scholar
14.Gervich, DH, Grout, CS: An outbreak of nosocomial Acinetobacter infections from humidifiers. Am J Infect Control 1985;13:210215.CrossRefGoogle ScholarPubMed
15.Smego, RA Jr: Endemic nosocomial Acinetobacter calcoaceticus bacteremia. Clinical significance, treatment, and prognosis. Arch Intern Med 1985; 145:21742179.Google Scholar
16.Stone, JW, Das, BC: Investigation of an outbreak of infection with Acinetobacter calcoaceticus in a special care baby unit. J Hosp Infect 1986;7:4248.CrossRefGoogle Scholar
17.Bergogne-Berezin, E, Joly-Guillou, ML: An underestimated nosocomial pathogen, Acinetobacter calcoaceticus. J Antimicrob Chemother 1985; 16:535538.CrossRefGoogle ScholarPubMed
18.Thompson, RL: Surveillance and reporting of nosocomial infections. in Wenzel, RP (ed): Prevention and Control of Nosocomial Infections. Baltimore, Williams and Wilkins, 1987, pp 7082.Google Scholar
19.Rubin, SJ, Granato, PA, Wasilauskas, BL: Glucose-nonfermenting gram-negative bacteria, in Lennette, EH, Balows, A, Hausler, WJ Jr, et al (eds): Manual of Clinical Microbiology, ed 4. Washington, American Society for Microbiology. 1985, pp 330349.Google Scholar
20.Ristuccia, PA, Cunha, HA: Acinetobacter. Infect Control 1983;4:226229.Google ScholarPubMed
21.Horan, TC, White, JW, Jarvis, WR, et al: Nosocomial infection surveillance, 1984. MMWR 1986; 35(No 1SS):17SS29SS.Google ScholarPubMed
22.Lyons, RW: Acinetobacter calcoaceticus. Clin Microbiol Newsl 1983;5:8789.CrossRefGoogle Scholar
23.Garner, JS, Simmons, BP: Isolation precautions, in Bennett, JV, Brachman, PS (eds): Hospital Infections, ed 2. Boston, Little, Brown and Co, 1986, pp 143150.Google Scholar
24.French, GL, Casewell, MW: Controlling the spread of Acinetobacter infection. Br Med J 1980; 281:388.CrossRefGoogle ScholarPubMed
25.Barry, MA, Craven, DE, Goularte, TA, et al: Serratia marcescens contamination of antiseptic soap containing triclosan: Implications for nosocomial infection. Infect Control 1984: 5:427430.CrossRefGoogle ScholarPubMed
26.Maki, DC, Hecht, J: Antiseptic-containing handwashing agents reduce nosocomial infections-A prospective study. Abstracts of the 22nd Interscience Conference on Antimicrobial Agents and Chemotherapy. Miami Beach, 1982. Abstract #699.Google Scholar
27.Dowding, JE: Novel aminoglycoside-modifying enzyme from a clinical isolate of Acinetobacter. J Gen Microbiol 1979;110:239241.CrossRefGoogle ScholarPubMed
28.Murray, BE, Moellering, KC Jr: Evidence of plasmid-mediated production of aminoglycoside-modifying enzymes not previously described in Acinetobacter. Antimicrob Agents Chemother 1980;17:3036.CrossRefGoogle Scholar
29.Morohoshi, T, Saito, T: Beta-larramasr and beta-lactam antibiotic resistance in Acinetobacter anitratus (syn A calcoaceticus). J Antibiot 1977;30:969973CrossRefGoogle Scholar
30.Devaud, M, Kayser, FH, Bachi, B: Transposon-mediated multiple antibiotic resistance in Acinetobacter strains. Antimicrob Agents Chemother 1982;22:323329.CrossRefGoogle ScholarPubMed
31.Goldstein, FW, Labigne-Roussel, A, Gerbaud, G, et al: Transferable plasmid-mediated antibiotic resistance in Acinetobacter. Plasmid 1983: 10:138147.CrossRefGoogle ScholarPubMed
32.Krcmery, V, Antal, M, Langsadl, L, et al: Transferable amikacin resistance in Pseudomonas maltophilia and Acinetobacter calcoaceticus. Infection 1985:13:8990.CrossRefGoogle ScholarPubMed
33.Sanders, CC, Sanders, WE Jr, Goering, RV, et al: Selection of multiple antibiotic resistance by quinolones, β-lactams, and aminoglycosides with special reference to cross-resistance between unrelated drug classes. Antimicrob Agents Chemother 1984: 26:797801.CrossRefGoogle ScholarPubMed
34.Garcia, I, Fainstein, V, LeBlanc, B, et al: In vitro activities of new β-lactam antibiotics against Acinetobacter spp. Antimicrob Agents Chemother 1983;24:297299.CrossRefGoogle ScholarPubMed
35.Mayer, KH, Zinner, SH: Bacterial pathogens of increasing significance in hospital-acquired infections. Rev Infect Dis 1985; 7(suppl 3):S371S379.CrossRefGoogle ScholarPubMed