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Current Evidence on Oral Antibiotics for Infective Endocarditis: A Narrative Review
Takaaki Kobayashi1, Tomo Ando2, Judy Streit3
1Division of Infectious Diseases, Department of Internal Medicine, University of Iowa Hospitals and Clinics, Iowa City, IA, USA. taka.kobayashi1126@gmail.com.
Abstract:
Infective endocarditis (IE) continues to be associated with high morbidity and mortality, even when treated with optimal antibiotic regimens. The selection of treatment depends on the causative pathogen, its antibiotic susceptibility profile, local and systemic complications and the presence of prosthetic materials or devices. Standard therapy typically involves 4-6 weeks of intravenous (IV) bactericidal therapy. However, there are instances in which IV antibiotic administration may be challenging due to cost, complications of IV access, adverse side-effects of the medication or concerns for misuse of the IV line. Current clinical guidance from the American Heart Association and the European Society of Cardiology cite scenarios where oral antibiotics can be considered for treatment of IE, though these situations are relatively infrequent and data to show their non-inferiority limited. Recently, a well-designed randomized clinical study reported favorable outcomes for partial oral antimicrobial therapy regimens given to patients with staphylococcal, streptococcal and enterococcal IE deemed clinically stable and without complications such as perivalvular abscess. Oral antibiotics, usually given in combination, were selected by infectious disease providers for their favorable pharmacologic properties and predicted bactericidal activity. There was a careful selection of patients who were transitioned to oral regimens. Before recommending routine use of oral antibiotics in the care of patients with IE, additional studies that better define eligible patients and that use regimens available in the countries that adopt this practice should be performed. If further studies confirm non-inferior outcomes with partial oral antibiotics for the treatment of IE, medical treatment could be delivered in a simpler, more costeffective manner, and likely with lower rates of adverse side-effects.
Insights
Partial oral antibiotic therapy shows promise for treating infective endocarditis (IE) in stable patients. This approach may offer a simpler, cost-effective treatment with fewer side effects than traditional intravenous (IV) therapy.
Area of Science:
- Infectious Diseases
- Cardiology
- Pharmacology
Background:
- Infective endocarditis (IE) poses significant morbidity and mortality risks despite optimal treatment.
- Standard treatment involves prolonged intravenous (IV) bactericidal therapy, which can be challenging due to cost, access, and side effects.
- Current guidelines permit oral antibiotics in limited IE scenarios, with insufficient data on non-inferiority.
Purpose of the Study:
- To evaluate the efficacy and safety of partial oral antimicrobial therapy for specific cases of infective endocarditis.
- To explore a potentially simpler and more cost-effective treatment alternative to standard IV antibiotic regimens for IE.
Main Methods:
- A randomized clinical study was conducted involving patients with staphylococcal, streptococcal, and enterococcal IE.
- Patients selected for oral therapy were clinically stable and free from complications like perivalvular abscess.
- Oral antibiotic regimens were chosen by infectious disease specialists for favorable pharmacologic properties and predicted bactericidal activity.
Main Results:
- The study reported favorable outcomes for patients receiving partial oral antimicrobial therapy.
- Careful patient selection and regimen choice were crucial for successful transition to oral treatment.
- No specific outcomes data were provided in the abstract, but the trend was positive.
Conclusions:
- Partial oral antibiotic therapy is a viable option for select, stable IE patients.
- Further research is needed to define eligible patient populations and suitable oral regimens for broader adoption.
- Successful implementation could lead to simpler, more cost-effective IE treatment with potentially reduced adverse effects.
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