Organism-specific regimens for infective endocarditis are provided below, including those for Staphylococcus aureus, Streptococcus, Enterococcus, HACEK organisms (Haemophilus parainfluenzae, Haemophilus aphrophilus, Haemophilus paraphrophilus, Actinobacillus actinomycetemcomitans, Cardiobacterium hominis, Eikenella corrodens, and Kingella species), Q fever endocarditis, culture-negative endocarditis, and Brucella.[1, 2, 3, 4]
Staphylococcus aureus
Native valve endocarditis (NVE)
Methicillin-susceptible
-
Nafcillin 12 g IV q24h in 4-6 divided doses for 6 weeks (optional:
gentamicin 3 mg/kg IV or IM q24h in 2-3 divided doses for 3-5 days; however, the benefit of low-dose aminoglycoside is low and nephrotoxicity is a risk; gentamicin is not recommended for treatment of right-sided staphylococcal NVE)
-
Cefazolin 6 g IV q24h in 3 divided doses for 6 weeks (optional: gentamicin 3 mg/kg IV or IM q24h in 2-3 divided doses for 3-5 days) for non-anaphylactoid penicillin allergy
Methicillin-resistant, penicillin-intolerant, or coagulase-negative staphylococci
Patients with unstable renal function
-
Linezolid 600 mg IV q12h; note that linezolid is not yet recommended in guidelines, although there are anecdotal reports of successful treatment with linezolid in gram-positive endocarditis in patients with limited treatment options
[5, 6]
Duration of therapy
Prosthetic valve endocarditis (PVE)
Consideration should be given to early surgical intervention.
Methicillin-susceptible
-
Nafcillin 12 g IV q24h in 6 divided doses for ≥ 6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 2-3 divided doses for 2 weeks
plus
rifampin 900 mg IV or PO q24h in 3 divided doses for ≥ 6 weeks
-
If the organism is gentamicin resistant, then other aminoglycosides may be used depending on susceptibility
-
If the organism (especially coagulase-negative
Staphylococcus) is resistant to all aminoglycosides, substitute a fluoroquinolone with other 2 drugs for the entire course of therapy
-
If the organism is both aminoglycoside and fluoroquinolone resistant, then linezolid,
[7] cefatrizine, or trimethoprim-sulfamethoxazole can be used for the first 2 weeks of treatment
Methicillin-resistant
-
Vancomycin 30 mg/kg IV q24h in 2 divided doses for 6 weeks
plus rifampin 900 mg IV or PO q24h in 3 divided doses for ≥ 6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 2-3 divided doses for 2 weeks
-
In patients with fluctuating renal function, consider linezolid 600 mg q12h or ceftaroline 600 mg q12h; for both, clinical experience is very limited
-
Patients failing therapy on vancomycin, if fever or symptoms persist, or for breakthrough bacteremia, vancomycin susceptibility testing should be done; vancomycin in such cases should be substituted for daptomycin >8 mg/kg/24 h, which has been approved for the treatment of
S aureus BSI and right-sided infective endocarditis; higher doses of daptomycin 12 mg/kg/24 h have also been used
[8, 9] ; patients who have received vancomycin have a higher rate of resistance to daptomycin
-
Methicillin-resistant
S aureus (MRSA) with vancomycin minimal inhibitory concentration (MIC) >1.0: Telavancin or daptomycin with nafcillin or ceftaroline has been used
[10, 11, 12]
Streptococcus
Native valve endocarditis
Highly penicillin-susceptible viridans group streptococci and Streptococcus gallolyticus (bovis) (MIC ≤ 0.12)
-
-
Ceftriaxone 2 g IV or IM q24h in 1 dose for 4 weeks if the isolate is ceftriaxone susceptible
or
-
Aqueous penicillin G 12-18 million U IV q24h continuously or in 4-6 divided doses for 2 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 1 dose for 2 weeks
or
-
Ceftriaxone 2 g IV/IM q24h in 1 dose for 2 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 1 dose for 2 weeks
-
If patient is penicillin or cephalosporin intolerant: Vancomycin 30 mg/kg IV q24h in 2 divided doses for 4 weeks
Relatively penicillin-resistant viridans group streptococci or S bovis (MIC > 0.12 and < 0.5)
-
Aqueous penicillin G 24 million U IV q24h in 4-6 divided doses for 4 weeks
plus gentamicin 3 mg/kg IV q24h in 1 dose for 2 weeks
or
-
Ceftriaxone 2 g IV/IM q24h in 1 dose for 4 weeks
plus gentamicin 3 mg/kg IV q24h in 1 dose for 2 weeks
-
If patient is penicillin or cephalosporin intolerant: Vancomycin 30 mg/kg IV q24h in 2 divided doses for 4 weeks
Penicillin-resistant viridans group streptococci and S bovis (MIC ≥ 0.5)
-
Ampicillin 12 g IV q24h in 6 divided doses for 4-6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 1 dose for 4-6 weeks
or
-
Aqueous penicillin G 18-30 million U IV q24h in 2 divided doses for 4-6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 1 dose for 4-6 weeks
-
If patient is penicillin or cephalosporin intolerant: Vancomycin 30 mg/kg IV q24h in 2 divided doses for 6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 1 dose for 6 weeks
-
Streptococcus pneumoniae can cause valve-damaging endocarditis. For penicillin-susceptible strains: Penicillin G 24 million units per day is used. Other penicillin-resistant strains may respond only to vancomycin. Other streptococcal species (eg, groups A, B, C, and G) may be relatively penicillin-resistant. They are treated by adding gentamicin to a penicillin or cephalosporin for the first 2 weeks of 4- to 6-week therapy.
Prosthetic valve endocarditis
Penicillin-susceptible viridans group streptococci or S bovis (MIC ≤ 0.12)
-
Aqueous penicillin G 24 million U IV q24h continuously or in 4-6 divided doses for 6 weeks
with or without gentamicin 3 mg/kg IV or IM q24h in 1 dose for 2 weeks
or
-
Ceftriaxone 2 g IV or IM q24h in 1 dose for 6 weeks
with or without gentamicin 3 mg/kg IV or IM q24h in 1 dose for 2 weeks
-
If patient is penicillin or cephalosporin intolerant: Vancomycin 30 mg/kg IV q24h in 2 divided doses for 6 weeks
Penicillin relatively or fully resistant (MIC > 0.12)
-
The American Heart Association recommends continuing aminoglycosides for the entire course of treatment (4-6 weeks)
-
Aqueous penicillin G 24 million U IV q24h continuously or in 4-6 divided doses for 6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 1 dose for 6 weeks
or
-
Ceftriaxone 2 g IV or IM q24h in 1 dose for 6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 1 dose for 6 weeks
or
-
If patient is penicillin or cephalosporin intolerant: Vancomycin 30 mg/kg IV q24h in 2 divided doses for 6 weeks
Enterococcus
Native or prosthetic valve endocarditis
Penicillin, gentamicin, and vancomycin susceptible
-
Ampicillin 12 g IV q24h in 6 divided doses for 4-6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 1 dose for 4-6 weeks
or
-
Aqueous penicillin G 18-30 million U IV q24h continuously or in 6 divided doses for 4-6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 1 dose for 4-6 weeks
-
If patient is penicillin intolerant: Vancomycin 30 mg/kg IV q24h in 2 divided doses for 6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 1 dose for 6 weeks
Penicillin, streptomycin, and vancomycin susceptible; gentamicin resistant
-
Ampicillin 12 g IV q24h in 6 divided doses for 4-6 weeks
plus
streptomycin 15 mg/kg IV or IM q24h in 2 divided doses for 4-6 weeks
or
-
Aqueous penicillin G 18-30 million U IV q24h continuously or in 6 divided doses for 4-6 weeks
plus streptomycin 15 mg/kg IV or IM q24h in 2 divided doses for 4-6 weeks
-
If patient is penicillin intolerant: Vancomycin 30 mg/kg IV q24h in 2 divided doses for 6 weeks
plus streptomycin 15 mg/kg IV or IM q24h in 2 divided doses for 6 weeks
Beta-lactamase producing; vancomycin and aminoglycoside susceptible
Intrinsic penicillin resistance
Penicillin, gentamicin, and vancomycin resistant
-
Infectious disease consultation recommended. Optimal therapy for VRE PVE has not been clearly defined. Daptomycin and linezolid susceptibility should be obtained.
-
VRE:
Enterococcus faecium or Enterococcus faecalis: Linezolid 1200 mg IV or PO q24h in 2 divided doses for ≥ 6 weeks
or
-
Daptomycin 10-12 mg/kg per dose for ≥6 weeks
HACEK organisms
Native or prosthetic valve endocarditis
-
Ceftriaxone 2 g IV or IM q24h in 1 dose for 4 weeks for NVE, 6 weeks for PVE
or
-
Ampicillin-sulbactam 2 g IV q4h for 4 weeks for NVE, 6 weeks for PVE if isolate is susceptible
-
If patient is penicillin or cephalosporin intolerant:
Ciprofloxacin 1000 mg PO or 800 mg IV q24h in 2 divided doses for 4 weeks for NVE and 6 weeks for PVE
Corynebacteria (diphtheroids)
Native or prosthetic valve endocarditis
-
Penicillin as for streptococci with gentamicin (for MIC < 4 mcg/mL)
-
Vancomycin is bactericidal for diphtheroids; for penicillin-allergic or gentamicin-resistant patients, vancomycin can be used
Gram-negative bacilli
Native or prosthetic valve endocarditis
-
Pseudomonas aeruginosa endocarditis, especially if prosthetic valves or left-sided requires consideration for surgical excision
-
P aeruginosa endocarditis can be medically treated, especially native valve, with tobramycin 2.5 mg/kg IV q8h, (peak should be 15-20 mcg/mL and trough concentration should be 2 mcg/mL)
plus piperacillin 4 g IV q4h or ceftazidime 2 g IV q8h for 4-6 weeks
-
Alternatively, aztreonam, ciprofloxacin, or imipenem, each with gentamicin, tobramycin, or amikacin depending on susceptibilities
Fungi
Native valve endocarditis
-
For
Candida endocarditis, amphotericin B lipid formulation 0.8-1 mg/kg/d IV for at least 6 weeks
plus flucytosine (5-FC) 25 mg/kg/day divided in 4 doses for normal renal function plus surgery depending on clinical condition and other factors
or
-
Echinocandins: caspofungin 150 mg/day, micafungin 150 mg/day, or anidulafungin 200 mg/day
Prosthetic valve endocarditis
-
Surgical excision of prosthetic valve, in addition to above
-
Relapse is high in
Candida endocarditis, even with surgical excision, and fluconazole 400-800 mg recommended for prolonged period after surgery or lifelong, if susceptible
-
Fluconazole and echinocandins or fluconazole and amphotericin B have been used for
Candida PVE without surgery in a few cases
[13, 14, 15]
Culture-negative endocarditis
Native valve endocarditis
-
Ampicillin: 12 g IV q24h in 4 divided doses for 4-6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 3 divided doses for 4-6 weeks
-
If patient is penicillin intolerant: Vancomycin 30 mg/kg IV q24h in 2 divided doses for 4-6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 3 divided doses for 4-6 weeks
plus ciprofloxacin 1000 mg IV or IM q24h in 2 divided doses for 4-6 weeks
Prosthetic valve endocarditis (≤ 1y after implantation)
-
Vancomycin 30 mg/kg IV q24h in 2 divided doses for 6 weeks
plus gentamicin 3 mg/kg IV or IM q24h in 3 divided doses for 2 weeks
plus
cefepime 6 g IV q24h in 3 divided doses for 6 weeks
plus rifampin 900 mg PO or IV q24h in 3 divided doses for 6 weeks
Prosthetic valve endocarditis (> 1y after implantation)
Miscellaneous organism-specific treatment
Brucella endocarditis
Brucella infective endocarditis is treated with an aminoglycoside, doxycycline, and rifampin for 6 weeks to 6 months in various regimens, as follows:[16, 17]
-
Doxycycline 100 mg IV q12h
with
-
Streptomycin 1 g IM daily for 14-21 days or gentamicin 5 mg/kg IV daily for 7-10 days
or
-
Doxycycline with rifampin 600 or 900 mg orally once daily, both for 6 weeks
Q-fever endocarditis due to Coxiella burnetii
Q fever endocarditis requires at least 18 months of therapy with the following:[18, 19]
-
Doxycycline 200 mg daily plus hydroxychloroquine 600 mg daily
or
-
Doxycycline plus ciprofloxacin (1500 mg/day) or ofloxacin (600 mg/day)
or
-
Doxycycline (200 mg/day) plus rifampin (900 mg/day)
Author
Shadab Hussain Ahmed, MD, FACP, FIDSA, AAHIVS Professor of Clinical Medicine, Renaissance School of Medicine at Stony Brook University Medical Center; Adjunct Clinical Associate Professor, Department of Medicine, New York College of Osteopathic Medicine of New York Institute of Technology; Chief, Division of Infectious Diseases, Department of Medicine, Nassau University Medical Center
Shadab Hussain Ahmed, MD, FACP, FIDSA, AAHIVS is a member of the following medical societies: American College of Physicians, Infectious Diseases Society of America
Disclosure: Nothing to disclose.
Specialty Editor Board
Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference
Disclosure: Received salary from Medscape for employment. for: Medscape.
Michael Stuart Bronze, MD David Ross Boyd Professor and Chairman, Department of Medicine, Stewart G Wolf Endowed Chair in Internal Medicine, Department of Medicine, University of Oklahoma Health Science Center; Master of the American College of Physicians; Fellow, Infectious Diseases Society of America; Fellow of the Royal College of Physicians, London
Michael Stuart Bronze, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Physicians, American Medical Association, Association of Professors of Medicine, Infectious Diseases Society of America, Oklahoma State Medical Association, Southern Society for Clinical Investigation
Disclosure: Nothing to disclose.
Chief Editor
Thomas E Herchline, MD Professor of Medicine, Wright State University, Boonshoft School of Medicine; Medical Consultant, Public Health, Dayton and Montgomery County (Ohio) Tuberculosis Clinic
Thomas E Herchline, MD is a member of the following medical societies: Alpha Omega Alpha, Infectious Diseases Society of America, Infectious Diseases Society of Ohio
Disclosure: Received research grant from: Regeneron.
Acknowledgements
Kelley Struble, DO Fellow, Department of Infectious Diseases, University of Oklahoma College of Medicine
Kelley Struble, DO is a member of the following medical societies: American College of Physicians and Infectious Diseases Society of America
Disclosure: Nothing to disclose.