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Nosocomial Infection Caused by Xanthomonas maltophilia A Case-Control Study of Predisposing Factors

Published online by Cambridge University Press:  05 January 2022

Linda S. Elting*
Affiliation:
Department of Medical Specialties, Section of Infectious Diseases, The University of Texas M.D. Anderson Cancer Center, Houston, Texas
Nancy Khardori
Affiliation:
Department of Medical Specialties, Section of Infectious Diseases, The University of Texas M.D. Anderson Cancer Center, Houston, Texas
Gerald P. Bodey
Affiliation:
Department of Medical Specialties, Section of Infectious Diseases, The University of Texas M.D. Anderson Cancer Center, Houston, Texas
Victor Fainstein
Affiliation:
Department of Medical Specialties, Section of Infectious Diseases, The University of Texas M.D. Anderson Cancer Center, Houston, Texas
*
Infectious Diseases (Box 471, M.D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030

Abstract

Factors predisposing to clinically significant nosocomial infection with Xanthomonas maltophilia were examined in a matched case-control study using multivariate techniques. Sixteen cases occurred among cancer patients in a six-month period, including an apparent cluster of three cases in an intensive care unit. These infections were unusually serious; eight patients had disseminated infection caused by X maltophilia and six died as a result of their infections.

Among the 64 factors that were examined, therapy with broad-spectrum antibiotics and central venous catheterization were found to significantly increase susceptibility to infection. Therapy with imipenem was more than ten times more frequent among cases than among controls (p < .001). All fatal infections occurred in patients who had received imipenem, including two patients who died before the organism could be identified and appropriate therapy instituted.

Infection with X maltophilia should be suspected in patients who develop superinfection while receiving imipenem, and prompt therapy should be instituted to improve chances of survival. Because a common environmental source of X maltophilia was not identified, further study is necessary to determine specific preventive measures.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1990

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References

1. Trumbore, D, Pontzer, R, Levinson, ME, et al. Multicenter study of the clinical efficacy of imipenem/cilastatin for treatment of serious infections. Rev Infect Dis. 1985;7(suppl 3):S476S481.CrossRefGoogle ScholarPubMed
2. Diaz, M, Harding, GK, Lovie, TJ, et al. Prospective randomized comparison of imipenem/cilastatin and cefotaxime for treatment of lung, soft tissue and renal infections. Rev Infect Dis. 1985;7(suppl 3):S452S457.CrossRefGoogle Scholar
3. Garau, J, Martin, R, Bouza, , et al. Imipenem in the treatment of severe bacterial infections in seriously ill patients. J Antimicrob Chemother. 1986;18(suppl E):131140.CrossRefGoogle ScholarPubMed
4. Bodey, GP, Elting, LS, Jones, P. et al. Imipenem/cilastatin therapy of infections in cancer patients. Cancer. 1987;60:255262.3.0.CO;2-L>CrossRefGoogle ScholarPubMed
5. Le, CT, Lindgren, BL. Computational implementation of the conditional logistic regression model in the analysis of epidemiologic matched studies. Comput Biomed Res. 1988;21:4852.CrossRefGoogle ScholarPubMed
6. Fisher, MC, Long, SS, Roberts, EM, et al. Pseudomonas maltophilia bacteremia in children undergoing open heart surgery. JAMA. 1981;246:15711574.CrossRefGoogle ScholarPubMed
7. Schoch, PE, Cunha, BA. Pseudomonas maltophilia . Infect Control. 1987;8:169172.CrossRefGoogle ScholarPubMed
8. Morrison, AJ, Hoffmann, KK. Wenzel, RP. Associated mortality and clinical characteristics of nosocomial Ps maltophilia in a university hospital. J Clin. Microbiol. 1986;24:5255.CrossRefGoogle Scholar
9. Nagai, T. Association of Ps maltophilia with malignant lesions. J Clin Microbiol. 1984;20:10031005.CrossRefGoogle Scholar
10. Gilardi, GL. Infrequently encountered Pseudomonas species causing infection in humans. Ann Intern Med. 1972;77:211215.CrossRefGoogle ScholarPubMed
11. Zuravleff, JJ, Yu, VL. Infections caused by Pseudomonas maltophilia with emphasis on bacteremia: case reports and a review of the literature. Rev Infect Dis. 1982;4:12361246.CrossRefGoogle Scholar
12. Muder, RR, Yu, VL, Dummer, JS, et al. Infections caused by Pseudomonas maltophilia. Expanding clinical spectrum. Arch Intern Med. 1987;147:16721674.CrossRefGoogle ScholarPubMed
13. Durbec, O, Albanese, J, Brunel, M, et al. Fulminating Pseudomonas maltophilia septicemia during treatment with imipenem and amikacin. Presse Med. 1989;18:221228.Google ScholarPubMed
14. Felegie, TP, Yu, VL, Rumans, LM, et al. Susceptibility of Pseudomonas maltophilia to antimicrobial agents, singly and in combination. Antimicrob Agents Chemother. 1979;16:833837.CrossRefGoogle ScholarPubMed
15. Park, SU, Parker, RH. Review of imipenem. Infect Control. 1986;7:333337.Google ScholarPubMed
16. Jones, RN. Review of the in vitro spectrum of activity of imipenem. Am J Med. 1985;78(6A):2232.CrossRefGoogle ScholarPubMed