eMedicine Specialties > Pediatrics: Cardiac Disease and Critical Care Medicine > Cardiology

Endocarditis, Bacterial: Treatment & Medication

Author: Brian Keith Eble, MD, Assistant Professor of Pediatrics, Section of Cardiology, University of Arkansas for Medical Sciences, Arkansas Children's Hospital
Coauthor(s): Gerardo Reyes, MD, Clinical Assistant Professor, Department of Pediatrics, University of Illinois at Chicago; Director of Pediatric Critical Care Outreach and Development, Midwest NeoPed Associates, Ltd
Contributor Information and Disclosures

Updated: Nov 13, 2009

Treatment

Medical Care

Bacterial endocarditis is a disease in which complete eradication of the organism is required. Bacteria involved in endocarditis are relatively protected from phagocytic activity by the vegetation, which contains high concentrations of bacteria with relatively low metabolic rates. Prolonged parenteral therapy is the only way to achieve bactericidal serum levels for the time needed to kill all the bacteria present in a vegetation of endocarditis. Treatment ranges from 4-8 weeks.

Therapy is tailored according to the etiologic agent.2 Recommended antibiotic regimens for uncomplicated bacterial endocarditis are listed below. Because of the high risk for morbidity and mortality associated with this disease, individual therapy should be discussed between all consultants with the available antibiotic sensitivity testing.

  • Penicillin-susceptible streptococcal endocarditis (PSSE) on native cardiac valves is treated with penicillin G for 4 weeks or penicillin or ceftriaxone combined with gentamicin for 2 weeks. Penicillin-resistant streptococcal endocarditis (PRSE) on native cardiac valves is treated with penicillin, ampicillin, or ceftriaxone for 4 weeks combined with gentamicin for the first 2 weeks.
  • PSSE on prosthetic valve or other prosthetic material should be treated with penicillin, ampicillin, or ceftriaxone for 6 weeks combined with gentamicin for the first 2 weeks. PRSE on prosthetic valve or other prosthetic material is treated with penicillin, ampicillin, or ceftriaxone for 6 weeks combined with gentamicin.
  • Susceptible enterococcal infection on native valves is treated with penicillin or ampicillin combined with gentamicin for 4-6 weeks. Infection on prosthetic material should be for at least 6 weeks.
  • Methicillin-susceptible S aureus (MSSA) infection on native valves is treated with nafcillin or oxacillin for at least 6 weeks. The addition of gentamicin for 3-5 days is optional. Methicillin-resistant S aureus (MRSA) infection on native valves is treated with vancomycin for at least 6 weeks, with or without 3-5 days of gentamicin.
  • 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.
  • Gram negative endocarditis caused by HACEK organisms is treated with ceftriaxone or ampicillin plus gentamicin for 4 weeks.

Surgical Care

Absolute indications for surgery include progressive cardiac failure, valve obstruction, definitive perivalvular abscess, noncandidal fungal infection, and pseudomonal infection. Relative indications include persistent bacteremia despite appropriate antibiotic therapy, candidal endocarditis, and vegetations larger than 10 mm.

Surgery should be performed without delay in patients with severe congestive heart failure (CHF) secondary to valvular regurgitation. Surgery for patients who have had a recent neurologic injury should be evaluated and possibly delayed to make modifications to avoid intracranial hemorrhage.

Consultations

Initial consultants for the patient suspected to have bacterial endocarditis should include an infectious disease specialist, a cardiologist, and a cardiac surgeon.

Diet

No specific dietary restrictions are recommended in the literature for the patient with bacterial endocarditis.

Activity

Patients may be as active as they can tolerate. Patients may be ill and should remain hospitalized until they are hemodynamically stable, afebrile, with negative blood cultures, and not at high risk for complications.

Medication

Antimicrobial agents

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, Haemophilus aphrophilus, Haemophilus paraphrophilus, Actinobacillus actinomycetemcomitans, Cardiobacterium hominis, Eikenella corrodens, or Kingella species), and fungal endocarditis are aimed at total eradication of the organism. After antibiotic treatment, antibiotic prophylaxis is required before procedures that may cause bacteremia are performed. For more information, see Antibiotic Prophylactic Regimens for Endocarditis.


Penicillin G (Pfizerpen)

First-line agent that interferes with synthesis of cell-wall mucopeptide during active multiplication, resulting in bactericidal activity against susceptible microorganisms.

Adult

10-20 million U/d IV divided q4-6h for 4 wk

Pediatric

200,000-400,000 U/kg/d IV divided q4-6h for 4 wk

Probenecid may increase effectiveness by decreasing clearance; tetracyclines are bacteriostatic, decreasing effectiveness of concurrent penicillins

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in impaired renal function (adjust dose)


Ceftriaxone (Rocephin)

Alternative to penicillin. Third-generation cephalosporin with broad-spectrum gram-negative activity; decreased efficacy against gram-positive organisms; and increased efficacy against resistant organisms. Arrests bacterial growth by binding >1 penicillin-binding proteins.

Adult

PSSE or HACEK: 2 g/d IV/IM for 4 wk

Pediatric

PSSE or HACEK:
<45 kg: 50 mg/kg/d IV/IM divided q12h for 4 wk; not to exceed 2 g/d
>45 kg: Administer as in adults

Probenecid may increase levels; coadministration with ethacrynic acid, furosemide, and aminoglycosides may increase nephrotoxicity

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Decrease dose in combined hepatic and renal impairment; caution in breastfeeding women and penicillin allergy


Gentamicin (Garamycin)

Aminoglycoside antibiotic for gram-negative coverage. Not DOC. Consider if penicillins or other, less toxic drugs contraindicated; if clinically indicated; or if mixed infections are caused by susceptible staphylococci and gram-negative organisms. Dosing regimens are numerous; adjust dose on basis of CrCl and changes in volume of distribution. Follow up each regimen by measuring trough level drawn 30 min before the third or fourth dose. Peak levels may be drawn 30 min after 30-min infusion.

Adult

PSSE: 1 mg/kg IV q8h for 2 wk; use in combination with ceftriaxone
Enterococcal: 1 mg/kg IV q8h for 4 wk; use in combination with ampicillin
MSSA: 1 mg/kg IV q8h for 3-5 d; use in combination with nafcillin

Pediatric

Administer as in adults

Coadministration with other aminoglycosides, cephalosporins, penicillins, and amphotericin B may increase nephrotoxicity risk; may enhance effects of neuromuscular blocking agents, thus prolonged respiratory depression may occur; coadministration with loop diuretics may increase auditory toxicity of aminoglycosides; possible irreversible hearing loss of varying degrees may occur (monitor regularly)

Documented hypersensitivity; non–dialysis-dependent renal insufficiency

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Narrow therapeutic index (not intended for long-term therapy); caution in renal failure (patient not receiving dialysis), myasthenia gravis, hypocalcemia, and conditions that depress neuromuscular transmission; adjust dose in renal impairment


Vancomycin (Vancocin)

DOC in patients who cannot receive or whose condition fails to respond to penicillins and cephalosporins or who have infections with resistant staphylococci. Potent antibiotic directed against gram-positive organisms and active against Enterococcus species. To avoid toxicity, current recommendation is to assay trough levels 0.5 h before fourth dose. Adjust dose according to CrCl in renal impairment.

Adult

PRSE or MRSA: 15 mg/kg IV q12h for 4 wk; not to exceed 2 g/d (unless serum levels measured)

Pediatric

Administer as in adults

Erythema, histaminelike flushing, and anaphylactic reactions may occur when administered with anesthetic agents; taken concurrently with aminoglycosides, risk of nephrotoxicity may increase above that with aminoglycoside monotherapy; effects in neuromuscular blockade may be enhanced when coadministered with nondepolarizing muscle relaxants

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in renal failure and neutropenia; red man syndrome is caused by too rapid IV infusion (dose given over few min) but rare when dose given over 2 h; red man syndrome is not an allergic reaction


Ampicillin (Omnipen, Principen)

Bactericidal activity against susceptible organisms. Alternative to amoxicillin when patient cannot take PO medication.

Adult

Enterococcal or HACEK: 2 g IV q4h for 4 wk

Pediatric

Enterococcal or HACEK: 100-200 mg/kg/d IV divided q4h for 4 wk; not to exceed 12 g/d

Probenecid and disulfiram elevate levels; allopurinol decreases effects and has additive effects on ampicillin rash; may decrease effects of PO contraceptives

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal failure; evaluate rash and differentiate from hypersensitivity reaction


Nafcillin (Unipen, Nafcil)

Initial therapy for suspected penicillin G–resistant (methicillin-susceptible) staphylococcal infections. Because of thrombophlebitis, particularly in elderly patients, administer parenterally only for short term (1-2 d); change to PO as clinically indicated.

Adult

MSSA: 2 g IV q4h for 4-6 wk

Pediatric

MSSA: 100-200 mg/kg/d IV divided q4h for 4-6 wk; not to exceed 12 g/d

Associated with warfarin resistance when administered concurrently; effects may decrease with bacteriostatic action of tetracycline derivatives

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

To optimize therapy, determine causative organisms and susceptibility; >10 d treatment to eliminate infection and prevent sequelae (eg, endocarditis); obtain cultures after treatment to confirm that infection is eradicated


Oxacillin (Bactocill, Prostaphlin)

Bactericidal antibiotic that inhibits cell-wall synthesis; used to treat infections caused by penicillinase-producing staphylococci. May be used to start therapy when staphylococcal infection suspected.

Adult

MSSA: 2 g IV q4h for 4-6 wk

Pediatric

MSSA: 150-200 mg/kg/d IV divided q4h for 4-6 wk; not to exceed 12 g/d

Decreases effects of contraceptives and tetracycline; administered concomitantly with disulfiram and probenecid may increase levels; effect of anticoagulants increase when large IV doses given

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in impaired renal function (adjust dose)


Amphotericin B (Amphocil, Fungizone)

Produced by strain of Streptomyces nodosus; can be fungistatic or fungicidal. Binds to sterols (eg, ergosterol) in fungal cell membrane, causing intracellular components to leak with subsequent cell death.

Adult

1 mg/kg/d IV for 4-6 wk

Pediatric

Administer as in adults

Other nephrotoxins (eg, antineoplastic agents, aminoglycosides, radiocontrast) may enhance potential for renal toxicity, bronchospasm, and hypotension; corticosteroids, digitalis, and thiazides may potentiate hypokalemia; risk of renal toxicity increased with cyclosporine

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Monitor renal function, levels of serum electrolytes (eg, magnesium, potassium), liver function, CBC count, and hemoglobin concentrations; resume therapy at lowest level (eg, 0.25 mg/kg) when interrupted >7 d; hypoxemia, acute dyspnea, and interstitial infiltrates may occur in neutropenic patients receiving leukocyte transfusions (separate infusion from time of leukocyte transfusion)

More on Endocarditis, Bacterial

Overview: Endocarditis, Bacterial
Differential Diagnoses & Workup: Endocarditis, Bacterial
Treatment & Medication: Endocarditis, Bacterial
Follow-up: Endocarditis, Bacterial
Multimedia: Endocarditis, Bacterial
References

References

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

  2. [Guideline] Gerber MA, Baltimore RS, Eaton CB, 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].

  3. [Guideline] Wilson W, Taubert KA, Gewitz 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].

  4. Baddour LM, Wilson WR, Bayer AS, 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. Circulation. Jun 14 2005;111(23):e394-434. [Medline].

  5. Bayer AS, Bolger AF, Taubert KA, et al. Diagnosis and management of infective endocarditis and its complications. Circulation. Dec 22-29 1998;98(25):2936-48. [Medline].

  6. Brook MM. Pediatric bacterial endocarditis. Treatment and prophylaxis. Pediatr Clin North Am. Apr 1999;46(2):275-87. [Medline].

  7. Dajani AS, Taubert KA, Wilson W, et al. Prevention of bacterial endocarditis. Recommendations by the American Heart Association. JAMA. Jun 11 1997;277(22):1794-801. [Medline].

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  9. Ferrieri P, Gewitz MH, Gerber MA, et al. Unique features of infective endocarditis in childhood. Circulation. Apr 30 2002;105(17):2115-26. [Medline].

  10. Gewitz MH. Prevention of bacterial endocarditis. Curr Opin Pediatr. Oct 1997;9(5):518-22. [Medline].

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

  12. Hoesley CJ, Cobbs CG. Endocarditis at the millennium. J Infect Dis. Mar 1999;179 Suppl 2:S360-5. [Medline].

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  15. Stamboulian D, Carbone E. Recognition, management and prophylaxis of endocarditis. Drugs. Nov 1997;54(5):730-44. [Medline].

Further Reading

Keywords

bacterial endocarditis, infective endocarditis, acute bacterial endocarditis, subacute bacterial endocarditis, fulminant endocarditis, rheumatic heart disease, congestive heart failure, CHF, left-sided endocarditis, , treatment, diagnosis, symptoms

Contributor Information and Disclosures

Author

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.

Coauthor(s)

Gerardo Reyes, MD, Clinical Assistant Professor, Department of Pediatrics, University of Illinois at Chicago; Director of Pediatric Critical Care Outreach and Development, Midwest NeoPed Associates, Ltd
Gerardo Reyes, MD is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.

Medical Editor

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.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

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.

CME Editor

Gilbert Z Herzberg, MD, Assistant Professor, Department of Pediatrics, Section of Pediatric Cardiology, New York Medical College; Consulting Staff, Department of Pediatrics, Sound Shore Medical Center
Gilbert Z Herzberg, MD is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.

Chief Editor

Steven R Neish, MD, SM, Director of Pediatric Cardiology Fellowship Program, Associate Professor, Department of Pediatrics, Baylor College of Medicine
Steven R Neish, MD, SM is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, and American Heart Association
Disclosure: Nothing to disclose.

 
 
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