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Published Online, 3 October 2006, www.theannals.com, DOI 10.1345/aph.1H353.
The Annals of Pharmacotherapy: Vol. 40, No. 11, pp. 1939-1945. DOI 10.1345/aph.1H353
© 2006 Harvey Whitney Books Company.
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INFECTIOUS DISEASES

Polymyxin B and Doxycycline Use in Patients with Multidrug-Resistant Acinetobacter baumannii Infections in the Intensive Care Unit

Katherine P Holloway, PharmD

Clinical Assistant Professor, Internal Medicine, Department of Clinical and Administrative Sciences, Mercer University College of Pharmacy and Health Sciences, Atlanta, GA

Nadine G Rouphael, MD

Fellow, Infectious Diseases, Department of Medicine, Division of Infectious Diseases, School of Medicine, Emory University, Atlanta

Jane B Wells, PharmD

Clinical Pharmacist Specialist, Department of Pharmacy and Drug Information, Infectious Diseases, Grady Health System, Atlanta

Mark D King, MD

Assistant Professor of Medicine, Department of Medicine, Division of Infectious Diseases, School of Medicine, Emory University; Department of Hospital Epidemiology, Grady Memorial Hospital

Henry M Blumberg, MD

Professor of Medicine, Department of Medicine, Division of Infectious Diseases, School of Medicine, Emory University; Department of Hospital Epidemiology, Grady Memorial Hospital

Reprints: Dr. Holloway, Department of Clinical and Administrative Sciences, Mercer University College of Pharmacy and Health Sciences, 3001 Mercer University Dr., Atlanta, GA 30341-4155, fax 678/547-6384, holloway_kp{at}mercer.edu

BACKGROUND: Multidrug-resistant Acinetobacter baumannii (MDR-Ab) has emerged as an increasingly problematic cause of hospital-acquired infections in the intensive care unit (ICU). MDR-Ab is resistant to most standard antimicrobials but often retains susceptibility to polymyxin B and doxycycline.

OBJECTIVE: To evaluate the efficacy and toxicity of polymyxin B and doxycycline in the treatment of MDR-Ab infections.

METHODS: A retrospective chart review was conducted between March 2002 and May 2005 in patients who received doxycycline or polymyxin B for treatment of MDR-Ab infections in ICUs within Grady Memorial Hospital, Atlanta, GA.

RESULTS: Thirty-seven patients with MDR-Ab infections were treated with polymyxin B or doxycycline. Median age was 41 years and median ICU length of stay was 18 days prior to acquisition of MDR-Ab. Clinical cure was observed in 22 of 29 (76%) evaluable patients treated with polymyxin B and 2 of 4 (50%) patients treated with doxycycline. In patients with follow-up cultures, microbiological cure was observed in 17 of 21 (81%) patients treated with polymyxin B and 2 of 3 (67%) patients treated with doxycycline. Nephrotoxicity developed in 21% (7 of 33) of patients who received polymyxin B. Neurotoxicity was observed in 2 (6%) patients who received polymyxin B. No adverse reactions were observed with doxycycline. Overall, crude mortality was 27% (9 of 33) and 75% (3 of 4) among those who received polymyxin B and doxycycline, respectively. Three (9%) deaths were attributed to polymyxin B treatment failure, and no deaths were attributed to doxycycline treatment failure.

CONCLUSIONS: Polymyxin B was effectively used to treat a substantial proportion of critically ill patients with MDR-Ab infection and was associated with a similar rate of nephrotoxicity as previously reported. Doxycycline monotherapy was used in a limited number of patients for the treatment of MDR-Ab; further evaluation of its efficacy in larger numbers of patients is warranted.

Key Words: Acinetobacter baumannii, colistin, doxycycline, polymyxin B

Published Online, October 3, 2006. www.theannals.com, DOI 10.1345/aph.1H353


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