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Annals of Surgical Oncology 8:179-186 (2001)
© 2001 Society of Surgical Oncology


ORIGINAL ARTICLES

Treatment of Nosocomial Postoperative Pneumonia in Cancer Patients: A Prospective Randomized Study

I. Raad, MD, R. Hachem, MD, H. Hanna, MD, D. Abi-Said, PhD, C. Bivins, RN, G. Walsh, MD, J. Thornby, PhD, E. Whimbey, MD, A. Huaringa, MD and A. Sukumaran, MD

From the Department of Internal Medicine Specialties Section of Infection Control (IR) and Section of Infectious Diseases (RH, HH, DA-S, EW), the Department of Leukemia (CB), the Department of Cardio-Thoracic Surgery (GW), the Department of Internal Medicine Specialties, Section of Pulmonary Medicine (AH), and the Department of Anesthesiology and Critical Care (AS), The University of Texas M. D. Anderson Cancer Center, Houston, Texas; and Department of Family and Community Medicine (JT), Baylor College of Medicine, Houston, Texas.

Correspondence: Address correspondence and reprint requests to: Issam Raad, MD, FACP, Section of Infection Control (Box 47), The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030; Fax: 713-792-8233; E-mail: iraad{at}mdanderson.org

Background: Nosocomial pneumonia continues to be associated with high morbidity and mortality in cancer patients.

Methods: In an attempt to find an optimal treatment for this infection, nonneutropenic cancer patients with postoperative nosocomial pneumonia were randomized to receive either piperacillin/tazobactam (P/T) 4.5 g IV every 6 hours (30 patients) or clindamycin (Cl) 900 mg plus aztreonam (Az) 2 g IV every 8 hours (22 patients). Amikacin 500 mg IV every 12 hours was given to all patients for the first 48 hours.

Results: The two groups were comparable for the characteristics of pneumonia that included Gram-negative etiology and duration of intubation. Response rates were 83% for patients who received P/T and 86% for those who received Cl/Az (P > .99). There were no serious adverse events; however, at our center the cost of the P/T regimen was $73.86 compared with $99.15 for the Cl/Az regimen.

Conclusions: The two regimens had comparable high efficacy, and P/T had a slight cost advantage. Either of these antibiotic regimens combined with an aminoglycoside could lead to favorable outcome in cancer patients at high risk for nosocomial pneumonia.

Key Words: Nosocomial • Pneumonia • Antibiotics • Cancer • Postoperative







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