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Table 1 Observational studies of oral antibiotic therapy for infective endocarditis

From: Oral antibiotic therapy for the treatment of infective endocarditis: a systematic review

Reference

Cases

Design

Case definition

Microbiology

Assessment of antibiotic susceptibility

Therapy

Cure

Colli et al, Italy [9]

12 NVIE and 2 PVIE requiring acute valve replacement(all left-sided)

Retrospective. Mean follow-up was 20.8 ± 7 months

By Duke criteria

MRSA (60%)

Yes

IV vancomycin for 5.3 ± 3.4 days followed by oral linezolid for 3 weeks

100%

S. viridans (30%)

Enterococcus sp. (10%)

Dworkin et al, USA [10]

13 IVDUs with NVIE (all right-sided with no systemic metastasis)

Prospective. 4-week follow-up

≥2 positive blood cultures AND any of the following: Vegetations on echocardiogram (definite – 3 cases) OR pulmonary infiltrates/effusion or tricuspid insufficiency murmur (probable – 6 cases) OR no other identifiable source for the infection (possible – 1 case)

S. aureus (100%)

Yes

IV ciprofloxacin and oral rifampin for 1 week followed by oral ciprofloxacin and oral rifampin for 3 weeks

77%

Chetty et al, South Africa [11]

15 NVIE (right-sided vs. left-sided not specified, all cases were considered uncomplicated)

Prospective. 3-year follow-up

Characteristics clinical features AND any of the following: Positive blood cultures OR vegetations on echocardiogram

Streptococcus sp. (60%)

Yes

High dose oral amoxycillin for 6 weeks (47% also received probenecid)

87%

Culture negative (40%)

Pinchas et al, Israel [12]

11 NVIE (all left-sided, considered uncomplicated)

Prospective. Follow-up varied from 3 months to 12 years

Fever AND pre-existing valvular heart disease AND multiple positive blood cultures

S. viridans (100%)

Yes

High dose oral ampicillin for 6 weeks with probenecid for the first 4 weeks. IM streptomycin for the first 2 weeks

90%

Phillips et al, UK [13]

13 NVIE (right-sided vs. left-sided not specified) – all children

Retrospective. Follow-up varied from 1-15 years

Pre-existing valvular disease AND characteristic clinical features AND positive blood cultures

S, viridans (62%) Staphylococcus sp. (23%)

Yes

IV therapy for < 2 weeks (92% ≤3 days) followed by oral penicillin V, ampicillin, cloxacillin, flucloxacillin or erythromycin for 6-8 weeks

100%

Other streptococci or Enterococcus sp. (15%)

Gray et al, UK [14]

13 NVIE (right-sided vs. left-sided not specified)

Retrospective. 3-month follow-up

Not specified

S. viridans.(62%)

Yes

Oral ampicillin or propicillin (with or without probenecid) for 6 weeks

92%

E. faecalis (1%)

Culture negative (37%)

Campeau et al, Canada [15]

10 NVIE (right-sided vs. left-sided not specified)

Retrospective. Follow-up varied from 6-30 months

Pre-existing valvular disease AND Characteristic clinical features AND ≥2 positive blood cultures

S. viridans (60%)

Yes

Oral phenithicillin for 4-6 weeks (IM streptomycin for the first 2 weeks in 6 cases, concomitant probenecid in 2 cases)

80%

E. faecalis (30%)

Anaerobic bacteria (10%)

Friedberg et al, USA [16]

11 NVIE (right-sided vs. left-sided not specified)

Retrospective. Follow-up not specified

Pre-existing rheumatic valvular disease AND Unexplained fever for ≥2½ weeks

S. viridans (55%)

Yes

Oral Aureomycin for 5-8 weeks

36%

E. faecalis (18%)

Culture negative (27%)

Schein et al, USA [17]

81 NVIE (right-side vs. left-sided not specified)

Retrospective. Follow-up varied from 2-8 years

Not specified

Streptococcus sp. (94%)

Not specified

Oral sulfonamides (sulfanilamide, sulfapyridine, sulfathiazole or sulfadiazine) for 10 days-14 weeks

10%

S. aureus (1%)

Enterococcus sp. (1%)

H. influenza (4%)

  1. NVIE denotes cases of native valve infective endocarditis. PVIE denotes cases of prosthetic valve infective endocarditis. IV denotes intravenous. IVDUs denotes intravenous drug users. MSSA denotes methicillin-sensitive S. aureus. MRSA denotes methicillin-resistant S. aureus. CoNS denotes coagulase-negative staphylococcus. GNB denotes gram-negative bacilli. Unless specified otherwise, all cohorts were primarily of adult patients. All reports reported follow-up ≥3 months.