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Efficacy of imipenem therapy for Nocardia actinomycetomas refractory to sulfonamides
Mahreen Ameen1, Roberto Arenas, Elsa Vásquez del Mercado
1St John's Institute of Dermatology, Guy's and St Thomas' Trust, London, United Kingdom.
Background:
Actinomycetomas are chronic, granulomatous, subcutaneous infections caused by actinomycetes bacteria. Despite prolonged high-dose and combination antibiotic therapies, some cases remain resistant with risks of bone and visceral involvement.
Objectives:
We sought to evaluate the efficacy and safety of imipenem monotherapy, and in combination with amikacin for the treatment of severe and refractory disease, and to identify the disease characteristics that might predict therapy failure with first-line sulfonamides.
Methods:
A retrospective study was performed of all microbiologically confirmed cases of actinomycetomas treated since 1995 at a tertiary center for mycology. Eleven patients (Nocardia, n = 10) were treated with sulfonamide combinations (trimethoprim/sulfamethoxazole and dapsone). Eight patients (Nocardia, n = 7) refractory to previous therapies including sulfonamides received a 3-week course of either parenteral imipenem monotherapy (1.5 g daily, n = 3) or combination therapy with amikacin (1 g daily, n = 5), which was repeated at 6-month intervals.
Results:
Eleven patients with limited disease and mean disease duration of 1.7 years responded successfully to sulfonamides after a mean treatment period of 15 months (range 6-48 months). Patients receiving imipenem had mean disease duration of 10 years, with visceral and bone involvement in 4 patients. Imipenem treatment was well tolerated, and 4 patients achieved clinical and microbiological cure after one to two courses of treatment, the others demonstrating greater than 75% clinical improvement and negative culture results.
Limitations:
Patient cohorts in this study were small because strict criteria for inclusion included species identification and adequate follow-up periods. The efficacy data for imipenem +/- amikacin therapy cannot be extrapolated to all Nocardia mycetomas, as the cohort treated in this study had particularly refractory infection.
Conclusions:
Sulfonamides are effective for limited disease of relatively short duration. Imipenem monotherapy or in combination with amikacin is well tolerated and demonstrates efficacy in severe disease refractory to sulfonamides.
Insights
Sulfonamides effectively treat limited actinomycetoma (fungal infections). For severe, resistant cases, imipenem monotherapy or with amikacin shows good tolerance and efficacy, even with bone or visceral involvement.
Area of Science:
- Medical Mycology
- Infectious Diseases
- Antimicrobial Therapy
Background:
- Actinomycetomas are chronic subcutaneous infections caused by actinomycetes bacteria.
- Standard antibiotic therapies can be prolonged and may fail, leading to severe complications like bone and visceral involvement.
Purpose of the Study:
- To assess the efficacy and safety of imipenem monotherapy and imipenem-amikacin combination therapy for severe, refractory actinomycetomas.
- To identify factors predicting treatment failure with first-line sulfonamides.
Main Methods:
- Retrospective study of microbiologically confirmed actinomycetoma cases treated since 1995.
- Analysis of 11 patients treated with sulfonamides and 8 patients with refractory disease treated with imipenem (alone or with amikacin).
Main Results:
- Sulfonamides were effective in limited disease cases (mean duration 1.7 years) after 15 months of treatment.
- Imipenem therapy (mean disease duration 10 years) in refractory cases was well-tolerated, achieving cure or significant improvement in all patients, including those with bone/visceral involvement.
Conclusions:
- Sulfonamides are effective for early-stage actinomycetomas.
- Imipenem, with or without amikacin, offers a well-tolerated and effective treatment option for severe, sulfonamide-resistant actinomycetomas.
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