Pediatric Bacterial Endocarditis Medication

  • Author: Michael H Gewitz, MD; more...
 
Updated: May 17, 2011
 

Medication Summary

Antibiotics are used in the treatment of bacterial endocarditis and are also employed for prophylaxis.

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Antimicrobial Agents

Class Summary

Treatment with antibiotics is specific to the etiologic agent and its characteristics. Therapy for penicillin-susceptible streptococcal endocarditis (PSSE), penicillin-resistant streptococcal endocarditis (PRSE), enterococcal endocarditis, methicillin-susceptible S aureus (MSSA), methicillin-resistant S aureus (MRSA), endocarditis caused by HACEK organisms (ie, Haemophilus parainfluenzae, H aphrophilus, H paraphrophilus, Actinobacillus actinomycetemcomitans, Cardiobacterium hominis, Eikenella corrodens, or Kingella species), and fungal endocarditis are aimed at total eradication of the organism.

After antibiotic treatment, patients with endocarditis remain at high risk for recurrence and for complications of a recurrence. These patients are still recommended to receive prophylactic antibiotics for dental procedures involving manipulation of gingival tissue or the periapical region of teeth or perforation of the oral mucosa and for respiratory tract procedures that involve incision or biopsy of the respiratory mucosa.[2]

Penicillin G (Pfizerpen)

 

This is a first-line agent. It interferes with the synthesis of cell-wall mucopeptide during active multiplication, resulting in bactericidal activity against susceptible microorganisms.

Ampicillin (Omnipen, Principen)

 

Ampicillin has bactericidal activity against susceptible organisms. It is an alternative to amoxicillin when the patient cannot take oral medication. Bacterial endocarditis that is found to be a methicillin-susceptible S aureus (MSSA) infection on native valves is treated with nafcillin or oxacillin for at least 6 weeks.

Nafcillin (Unipen, Nafcil)

 

Ampicillin has bactericidal activity against susceptible organisms. It is an alternative to amoxicillin when the patient cannot take oral medication. Bacterial endocarditis that is found to be a methicillin-susceptible S aureus (MSSA) infection on native valves is treated with nafcillin or oxacillin for at least 6 weeks.

Oxacillin (Bactocill, Prostaphlin)

 

This is a bactericidal antibiotic that inhibits cell-wall synthesis. It is used to treat infections caused by penicillinase-producing staphylococci. Oxacillin may be used to start therapy when staphylococcal infection suspected.

Amoxicillin (Trimox, Moxatag)

 

Amoxicillin interferes with the synthesis of cell wall mucopeptides during active multiplication, resulting in bactericidal activity against susceptible bacteria. It is used as prophylactic therapy in in specific, high-risk patients.

Ceftriaxone (Rocephin)

 

This agent is an alternative to penicillin. It is a third-generation cephalosporin with broad-spectrum gram-negative activity. It has decreased efficacy against gram-positive organisms and increased efficacy against resistant organisms. It arrests bacterial growth by binding 1 or more penicillin-binding proteins. Antibiotics for endocarditis prophylaxis may be required for patients before performing procedures that are high risk for bacteremia. Ceftriaxone may be used prophylactically for high-risk patients undergoing dental procedures.

Cephalexin (Keflex)

 

Cephalexin is a first-generation cephalosporin that inhibits bacterial replication by inhibiting bacterial cell wall synthesis. It is bactericidal and effective against rapidly growing organisms forming cell walls. It is effective for treatment of infections caused by streptococci or staphylococci, including penicillinase-producing staphylococci. Cephalexin may be used prophylactically for high-risk patients undergoing dental procedures.

Gentamicin (Garamycin)

 

Gentamicin is an aminoglycoside antibiotic for gram-negative coverage. It is not the drug of choice, but consider using it if penicillins or other, less toxic drugs are contraindicated; if it is clinically indicated; or if mixed infections are caused by susceptible staphylococci and gram-negative organisms.

Dosing regimens for gentamicin are numerous; adjust the dose on the basis of creatinine clearance and changes in the volume of distribution. Follow up each regimen by measuring the trough level drawn 30 min before the third or fourth dose. Peak levels may be drawn 30 min after a 30-min infusion.

Vancomycin (Vancocin)

 

This is the drug of choice in patients who cannot receive or whose condition fails to respond to penicillins and cephalosporins or who have infections with resistant staphylococci. Vancomycin is a potent antibiotic that is directed against gram-positive organisms and is active against Enterococcus species. MRSA infection on native valves is treated with vancomycin for at least 6 weeks, with or without 3-5 days of gentamicin. To avoid toxicity, the current recommendation is to assay trough levels 0.5 hour before the fourth dose. In renal impairment, adjust the dose according to creatinine clearance.

Cefazolin

 

Cefazolin is a first-generation semisynthetic cephalosporin, which by binding to 1 or more penicillin-binding proteins, arrests bacterial cell wall synthesis and inhibits bacterial replication. In patients with penicillin allergies, cefazolin may be used for antibiotic prophylaxis for high-risk patients undergoing dental procedures.

Clindamycin (Cleocin)

 

Clindamycin inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. It distributes widely in the body, without penetration of the CNS. It is used in penicillin-allergic patients undergoing dental, oral, or respiratory tract procedures. It is useful for treatment against streptococcal and most staphylococcal infections. Clindamycin may be used prophylactically for high-risk patients undergoing dental procedures.

Azithromycin

 

Azithromycin is a macrolide antibiotic that acts by binding to the 50S ribosomal subunit of susceptible microorganisms and blocks the dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. Azithromycin may be used prophylactically for high-risk patients undergoing dental procedures in patients who are penicillin allergic.

Rifampin

 

Rifampin inhibits RNA synthesis in bacteria by binding to the beta subunit of DNA-dependent RNA polymerase, which, in turn, blocks RNA transcription. Bacterial endocarditis with an MSSA infection on prosthetic tissue is treated with nafcillin or oxacillin plus rifampin for at least 6 weeks, in combination with gentamicin for 2 weeks. MRSA infection on prosthetic tissue is treated with vancomycin plus rifampin for at least 6 weeks, in combination with gentamicin for 2 weeks.

Amphotericin B (Amphocil, Fungizone)

 

Amphotericin B is produced by a strain of Streptomyces nodosus; it can be fungistatic or fungicidal. This agent binds to sterols (eg, ergosterol) in the fungal cell membrane, causing intracellular components to leak, with subsequent cell death. Amphotericin B may be effective in the treatment of fungal endocarditis.

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Contributor Information and Disclosures
Author

Michael H Gewitz, MD  Physician-in-Chief/Executive Director, Chief, Section of Pediatric Cardiology, Maria Fareri Children's Hospital at Westchester Medical Center; Professor and Vice Chairman, Department of Pediatrics, New York Medical College

Michael H Gewitz, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, American College of Physician Executives, American Heart Association, American Pediatric Society, American Society of Echocardiography, New York Academy of Medicine, New York Academy of Sciences, Royal Society of Medicine, and Society of Pediatric Echocardiography

Disclosure: Nothing to disclose.

Coauthor(s)

Brian Keith Eble, MD  Assistant Professor of Pediatrics, Section of Cardiology, University of Arkansas for Medical Sciences, Arkansas Children's Hospital

Brian Keith Eble, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, American Heart Association, Arkansas Medical Society, and Society for Cardiac Angiography and Interventions

Disclosure: Nothing to disclose.

Specialty Editor Board

Jeffrey Allen Towbin, MD, MSc, FAAP, FACC, FAHA  Professor, Departments of Pediatrics (Cardiology), Cardiovascular Sciences, and Molecular and Human Genetics, Baylor College of Medicine; Chief of Pediatric Cardiology, Foundation Chair in Pediatric Cardiac Research, Texas Children's Hospital

Jeffrey Allen Towbin, MD, MSc, FAAP, FACC, FAHA is a member of the following medical societies: American Academy of Pediatrics, American Association for the Advancement of Science, American College of Cardiology, American College of Sports Medicine, American Heart Association, American Medical Association, American Society of Human Genetics, Cardiac Electrophysiology Society, New York Academy of Sciences, Society for Pediatric Research, Texas Medical Association, and Texas Pediatric Society

Disclosure: Nothing to disclose.

Mary L Windle, PharmD  Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

Julian M Stewart, MD, PhD  Associate Chairman of Pediatrics, Director, Center for Hypotension, Westchester Medical Center; Professor of Pediatrics and Physiology, New York Medical College

Julian M Stewart, MD, PhD is a member of the following medical societies: American Academy of Pediatrics

Disclosure: Nothing to disclose.

References
  1. Baddour LM, Wilson WR, Bayer AS, Fowler VG Jr, Bolger AF, Levison ME, et al. Infective endocarditis: diagnosis, antimicrobial therapy, and management of complications: a statement for healthcare professionals from the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease, Council on Cardiovascular Disease in the Young, and the Councils on Clinical Cardiology, Stroke, and Cardiovascular Surgery and Anesthesia, American Heart Association: endorsed by the Infectious Diseases Society of America. Circulation. Jun 14 2005;111(23):e394-434. [Medline].

  2. Wilson W, Taubert KA, Gewitz M, Lockhart PB, Baddour LM, Levison M, et al. Prevention of infective endocarditis: guidelines from the American Heart Association: a guideline from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee, Council on Cardiovascular Disease in the Young, and the Council on Clinical Cardiology, Council on Cardiovascular Surgery and Anesthesia, and the Quality of Care and Outcomes Research Interdisciplinary Working Group. Circulation. Oct 9 2007;116(15):1736-54. [Medline].

  3. Li JS, Sexton DJ, Mick N, Nettles R, Fowler VG Jr, Ryan T, et al. Proposed modifications to the Duke criteria for the diagnosis of infective endocarditis. Clin Infect Dis. Apr 2000;30(4):633-8. [Medline].

  4. Habib G. Management of infective endocarditis. Heart. Jan 2006;92(1):124-30. [Medline]. [Full Text].

  5. Gerber MA, Baltimore RS, Eaton CB, Gewitz M, Rowley AH, Shulman ST, et al. Prevention of rheumatic fever and diagnosis and treatment of acute Streptococcal pharyngitis: a scientific statement from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee of the Council on Cardiovascular Disease in the Young, the Interdisciplinary Council on Functional Genomics and Translational Biology, and the Interdisciplinary Council on Quality of Care and Outcomes Research: endorsed by the American Academy of Pediatrics. Circulation. Mar 24 2009;119(11):1541-51. [Medline].

  6. Thornhill MH, Dayer MJ, Forde JM, et al. Impact of the NICE guideline recommending cessation of antibiotic prophylaxis for prevention of infective endocarditis: before and after study. BMJ. May 3 2011;342:d2392. [Medline]. [Full Text].

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A young adult with a history of intravenous drug use diagnosed with right-sided staphylococcal endocarditis and multiple embolic pyogenic abscesses on chest radiograph.
 
 
 
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