Mycetoma management and clinical outcomes: the Mycetoma Research Center experience.


Journal

Transactions of the Royal Society of Tropical Medicine and Hygiene
ISSN: 1878-3503
Titre abrégé: Trans R Soc Trop Med Hyg
Pays: England
ID NLM: 7506129

Informations de publication

Date de publication:
03 01 2023
Historique:
received: 08 05 2022
accepted: 18 07 2022
revised: 12 06 2022
pubmed: 30 7 2022
medline: 5 1 2023
entrez: 29 7 2022
Statut: ppublish

Résumé

Mycetoma is a chronic granulomatous inflammatory disease that affects the cutaneous and subcutaneous tissues, leading to gruesome complications if not treated early. As a neglected disease, it has received scant attention in developing curable drugs. Mycetoma treatment is still based on expert opinions in the absence of guidelines. This descriptive, cross-sectional, hospital-based study aimed to determine and assess the disease treatment outcomes observed at Mycetoma Research Center, Sudan. In this study, 75% of patients had eumycetoma, all of whom were treated with itraconazole and 37.4% underwent surgical excision, while 25% of the patients had actinomycetoma, 99.2% of whom were treated with a combination of cotrimoxazole and amoxicillin-clavulanate. The cure rate was 12.7% and 14.3% for patients with eumycetoma and actinomycetoma, respectively. Only 6.1% of eumycetoma patients underwent amputation. Remarkably, no patient with actinomycetoma underwent an amputation. Small lesions (OR=10.09, p<0.001) and good follow-up (OR=6.81, p=0.002) were positive predictors of complete cure. In terms of amputation, history of surgical recurrence at presentation (OR=3.67, p=0.020) and presence of grains (OR=7.13, p=0.012) were positive predictors, whereas small lesions were negative predictors (OR=0.06, p=0.009). Treatment of mycetoma was suboptimal, with a low cure rate despite a long treatment duration. Complete cure has a significant association with small lesions and good follow-up.

Sections du résumé

BACKGROUND
Mycetoma is a chronic granulomatous inflammatory disease that affects the cutaneous and subcutaneous tissues, leading to gruesome complications if not treated early. As a neglected disease, it has received scant attention in developing curable drugs. Mycetoma treatment is still based on expert opinions in the absence of guidelines.
METHODS
This descriptive, cross-sectional, hospital-based study aimed to determine and assess the disease treatment outcomes observed at Mycetoma Research Center, Sudan.
RESULTS
In this study, 75% of patients had eumycetoma, all of whom were treated with itraconazole and 37.4% underwent surgical excision, while 25% of the patients had actinomycetoma, 99.2% of whom were treated with a combination of cotrimoxazole and amoxicillin-clavulanate. The cure rate was 12.7% and 14.3% for patients with eumycetoma and actinomycetoma, respectively. Only 6.1% of eumycetoma patients underwent amputation. Remarkably, no patient with actinomycetoma underwent an amputation. Small lesions (OR=10.09, p<0.001) and good follow-up (OR=6.81, p=0.002) were positive predictors of complete cure. In terms of amputation, history of surgical recurrence at presentation (OR=3.67, p=0.020) and presence of grains (OR=7.13, p=0.012) were positive predictors, whereas small lesions were negative predictors (OR=0.06, p=0.009).
CONCLUSIONS
Treatment of mycetoma was suboptimal, with a low cure rate despite a long treatment duration. Complete cure has a significant association with small lesions and good follow-up.

Identifiants

pubmed: 35903002
pii: 6651442
doi: 10.1093/trstmh/trac069
doi:

Substances chimiques

Trimethoprim, Sulfamethoxazole Drug Combination 8064-90-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

12-21

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene.

Auteurs

Esraa Abdelgadir Musa (EA)

Clinical Pharmacy Program, Faculty of Pharmacy, University of Khartoum, Khartoum 11115, Sudan.

Iman Hassan Abdoon (IH)

Department of Pharmacology, Faculty of Pharmacy, University of Khartoum, Khartoum 11115, Sudan.

Sahar Mubarak Bakhiet (SM)

Mycetoma Research Center, University of Khartoum, Khartoum 11115, Sudan.

Bashier Osman (B)

Department of Pharmacology, Faculty of Pharmacy, University of Khartoum, Khartoum 11115, Sudan.

Safa A Abdalla (SA)

Department of Pharmacology, Faculty of Pharmacy, University of Khartoum, Khartoum 11115, Sudan.

Ahmed Hassan Fahal (AH)

Mycetoma Research Center, University of Khartoum, Khartoum 11115, Sudan.

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