High-Dose Continuous Infusion β-Lactam Antibiotics for the Treatment of Resistant Pseudomonas Aeruginosa Infections in Immunocompromised Patients

Author:

Moriyama Brad1,Henning Stacey A2,Childs Richard3,Holland Steven M4,Anderson Victoria L5,Morris John C6,Wilson Wyndham H7,Drusano George L8,Walsh Thomas J9

Affiliation:

1. Brad Moriyama PharmD, Clinical Pharmacist, National Institutes of Health Clinical Center Pharmacy Department, Bethesda, MD

2. Stacey A Henning PharmD, Clinical Pharmacist, National Institutes of Health Clinical Center Pharmacy Department

3. Richard Childs MD, Senior Investigator, National Heart, Lung, and Blood Institute, Bethesda

4. Steven M Holland MD, Senior Investigator, National Institute of Allergy and Infectious Diseases, Bethesda

5. Victoria L Anderson RN, National Institute of Allergy and Infectious Diseases

6. John C Morris MD, Senior Investigator, National Cancer Institute, Bethesda

7. Wyndham H Wilson MD, Senior Investigator, National Cancer Institute

8. George L Drusano MD, Senior Scientist, Ordway Research Institute, Albany, NY

9. Thomas J Walsh MD FACP FAAM FIDSA, Senior Investigator, Chief, Immunocompromised Host Section, Pediatric Oncology Branch, National Cancer Institute

Abstract

OBJECTIVE: To report a case series of high-dose continuous infusion β-lactam antibiotics for the treatment of resistant Pseudomonas aeruginosa infections. CASE SUMMARY: Continuous infusion ceftazidime or aztreonam was administered to achieve target drug concentrations at or above the minimum inhibitory concentration, when possible, in 3 patients with P. aeruginosa infections. The maximal calculated target drug concentration was 100 mg/L. In the first patient, with primary immunodeficiency, neutropenia, and aggressive cutaneous T-cell lymphoma/leukemia, continuous infusion ceftazidime (6.5-9.6 g/day) was used to successfully treat multidrug-resistant P. aeruginosa bacteremia. In the second patient, with leukocyte adhesion deficiency type 1, continuous infusion aztreonam (8.4 g/day) was used to successfully treat multidrug-resistant P. aeruginosa wound infections. In the third patient, with severe aplastic anemia, continuous infusion ceftazidime (7-16.8 g/day) was used to treat P. aeruginosa pneumonia and bacteremia. In each patient, bacteremia cleared, infected wounds healed, and pneumonia improved in response to continuous infusion ceftazidime or aztreonam. DISCUSSION: Treatment strategies for multidrug-resistant P. aeruginosa infections are limited. A novel treatment strategy, when no other options are available, is the continuous infusion of existing β-lactam antibiotics to maximize their pharmacodynamic activity. High-dose continuous infusion ceftazidime or aztreonam was used for the successful treatment of resistant systemic P. aeruginosa infections in 3 chronically immunocompromised patients. CONCLUSIONS: Continuous infusion β-lactam antibiotics are a potentially useful treatment strategy for resistant P.aeruginosa infections in immunocompromised patients.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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