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Short-term intramuscular therapy with procaine penicillin plus streptomycin for infective endocarditis due to

Circulation
|June 1, 1978
PubMed

Insights

This study shows that a two-week treatment of procaine penicillin and streptomycin is effective for viridans streptococcal infective endocarditis. The regimen demonstrated no relapses, indicating a successful antimicrobial therapy approach.

Area of Science:

  • Infectious Diseases
  • Cardiology
  • Pharmacology

Background:

  • Infective endocarditis (IE) caused by viridans streptococci is a serious condition.
  • Treatment of IE requires effective antimicrobial strategies.
  • Penicillin resistance can complicate treatment regimens.

Purpose of the Study:

  • To evaluate the efficacy of a two-week intramuscular regimen of procaine penicillin and streptomycin for treating viridans streptococcal infective endocarditis.
  • To assess treatment outcomes, including relapse rates, toxicity, and long-term survival.

Main Methods:

  • A cohort of 33 patients with viridans streptococcal IE received intramuscular procaine penicillin (1.2 million units q6h) plus streptomycin (500 mg q12h) for two weeks.
  • Patients were monitored for relapse, toxicity, and mortality.
  • Follow-up duration ranged from 2 months to 3.5 years.

Main Results:

  • Nine patients (27%) had infections with relatively penicillin-resistant strains (MIC > 0.1 µg/ml or MBC ≥ 3.12 µg/ml).
  • No relapses of infective endocarditis were observed during the follow-up period.
  • One patient experienced mild vestibular toxicity; another died from congestive heart failure unrelated to the infection; seven required valve replacement.
  • No deaths were directly attributed to the infection post-treatment.

Conclusions:

  • The combination of procaine penicillin and streptomycin for two weeks is an effective antimicrobial therapy for viridans streptococcal infective endocarditis.
  • This regimen appears effective regardless of in vitro penicillin resistance data.
  • The treatment offers a low relapse rate and acceptable toxicity profile.

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