Pediatric Nocardiosis Medication

  • Author: Nicholas John Bennett, MB, BCh, PhD; Chief Editor: Russell W Steele, MD   more...
 
Updated: Feb 11, 2011
 

Antibiotics

Class Summary

The mainstay of nocardiosis therapy are sulfa-based antibiotics (eg, trimethoprim-sulfamethoxazole) given intravenously in high doses. Trimethoprim-sulfamethoxazole has shown less efficacy as a single agent in some AIDS-related nocardial infections. The single best regimen for treatment has not been established, and antibiotic resistance testing is recommended to tailor therapies to the specific strain infecting the patient. Trimethoprim-sulfamethoxazole, amikacin, and either ceftriaxone or imipenem are a reasonable combination of drugs for an initial empiric therapy prior to the results of susceptibility testing.

The use of linezolid to treat resistant or severe infection has been documented and shows promise.[9] Linezolid has been tested in vitro and has been shown to be the first antimicrobial agent to be active against all Nocardia species. It has good CNS penetration, does not require adjustment for renal or liver disease, has few drug interactions (especially with immunosuppressive medications), and has been shown to work as monotherapy against Nocardia. It is also available with excellent bioavailability in an oral form and may become a first-line therapy for Nocardia infection.

Trimethoprim-sulfamethoxazole (Bactrim, Septra)

 

Inhibits bacterial growth by inhibiting synthesis of dihydrofolic acid. Doses are based on the trimethoprim component.

Imipenem and cilastatin (Primaxin)

 

Therapy with this alternative agent often is used in combination with amikacin. For CNS nocardiosis, consider the related drug, meropenem, instead.

Amikacin (Amikin)

 

Used in conjunction with trimethoprim-sulfamethoxazole or imipenem-cilastatin. Peak therapeutic levels are 20-30 mg/L, and trough levels are 5-10 mg/L.

Minocycline (Dynacin, Minocin)

 

Another alternative drug both in PO and IV formulations for prolonged treatment. However, it is not recommended in children < 8 y.

Amoxicillin and clavulanate (Augmentin)

 

Aminopenicillin with a beta-lactamase inhibitor. Doses are based on the amoxicillin component. This drug is used as a follow-up treatment PO agent for prolonged therapy following IV treatment with imipenem or meropenem/amikacin. (See trimethoprim-sulfamethoxazole for suggested treatment duration.)

Ampicillin (Marcillin, Omnipen)

 

Bactericidal activity against susceptible organisms. Alternative to amoxicillin when unable to take PO medication.

Meropenem (Merrem IV)

 

Bactericidal broad-spectrum carbapenem antibiotic that inhibits cell-wall synthesis. Effective against most gram-positive and gram-negative bacteria.

Has slightly increased activity against gram-negative bacteria and slightly decreased activity against staphylococci and streptococci compared to imipenem. Not recommended for children.

Doxycycline (Bio-Tab, Doryx, Vibramycin)

 

Inhibits protein synthesis and thus bacterial growth by binding to 30S and, possibly, 50S ribosomal subunits of susceptible bacteria.

Sulfadiazine (Microsulfon)

 

Exerts bacteriostatic action by competitive antagonism of para-aminobenzoic acid (PABA). Microorganisms that require exogenous folic acid and do not synthesize folic acid are not susceptible to the action of sulfonamides.

Linezolid (Zyvox)

 

A synthetic antibiotic of the oxazolidinone class, which prevents the formation of functional 70S initiation complex. This is essential for the bacterial protein translation process. Although it seems to be bacteriostatic against Nocardia (as it is with most bacteria except pneumococci), it does seem to be a very effective therapy even as a monotherapy.

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Contributor Information and Disclosures
Author

Nicholas John Bennett, MB, BCh, PhD  Fellow in Pediatric Infectious Disease, Department of Pediatrics, State University of New York Upstate Medical University

Nicholas John Bennett, MB, BCh, PhD is a member of the following medical societies: Alpha Omega Alpha and American Academy of Pediatrics

Disclosure: Nothing to disclose.

Coauthor(s)

Joseph Domachowske, MD  Professor of Pediatrics, Microbiology and Immunology, Department of Pediatrics, Division of Infectious Diseases, State University of New York Upstate Medical University

Joseph Domachowske, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Pediatrics, American Society for Microbiology, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, and Phi Beta Kappa

Disclosure: Nothing to disclose.

Rosemary Johann-Liang, MD  Medical Officer, Infectious Diseases and Pediatrics, Division of Special Pathogens and Immunological Drug Products, Center for Drug Evaluation and Research, Food and Drug Administration

Rosemary Johann-Liang, MD is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, and Infectious Diseases Society of America

Disclosure: Nothing to disclose.

Specialty Editor Board

Gary J Noel, MD  Department of Pediatrics, Clinical Associate Professor, Weill Medical College of Cornell University

Gary J Noel, MD is a member of the following medical societies: Pediatric Infectious Diseases Society

Disclosure: Nothing to disclose.

Mary L Windle, PharmD  Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Pharmacy Editor, eMedicine

Disclosure: Nothing to disclose.

Joseph Domachowske, MD  Professor of Pediatrics, Microbiology and Immunology, Department of Pediatrics, Division of Infectious Diseases, State University of New York Upstate Medical University

Joseph Domachowske, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Pediatrics, American Society for Microbiology, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, and Phi Beta Kappa

Disclosure: Nothing to disclose.

Robert W Tolan Jr, MD  Chief, Division of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine

Robert W Tolan Jr, MD is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, Phi Beta Kappa, and Physicians for Social Responsibility

Disclosure: GlaxoSmithKline Honoraria Speaking and teaching; MedImmune Honoraria Speaking and teaching; Merck Honoraria Speaking and teaching; Sanofi Pasteur Honoraria Speaking and teaching; Baxter Healthcare Honoraria Speaking and teaching; Novartis Honoraria Speaking and teaching

Chief Editor

Russell W Steele, MD  Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine

Russell W Steele, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American Pediatric Society, American Society for Microbiology, Infectious Diseases Society of America, Louisiana State Medical Society, Pediatric Infectious Diseases Society, Society for Pediatric Research, and Southern Medical Association

Disclosure: Nothing to disclose.

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