» Articles » PMID: 32571813

Risk Factors Associated with Antibiotic Treatment Failure of Buruli Ulcer

Overview
Specialty Pharmacology
Date 2020 Jun 24
PMID 32571813
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Combination antibiotic therapy is highly effective in curing Buruli ulcer (BU) caused by Treatment failures have been uncommonly reported with the recommended 56 days of antibiotics, and little is known about risk factors for treatment failure. We analyzed treatment failures among BU patients treated with ≥56 days of antibiotics from a prospective observational cohort at Barwon Health, Victoria, from 1 January 1998 to 31 December 2018. Treatment failure was defined as culture-positive recurrence within 12 months of commencing antibiotics under the following conditions: (i) following failure to heal the initial lesion or (ii) a new lesion developing at the original or at a new site. A total of 430 patients received ≥56 days of antibiotic therapy, with a median duration of 56 days (interquartile range [IQR], 56 to 80). Seven (1.6%) patients experienced treatment failure. For six adult patients experiencing treatment failure, all were male, weighed >90 kg, did not have surgery, and received combination rifampin-clarithromycin (median rifampin dose, 5.6 mg per kg of body weight per day; median clarithromycin dose, 8.1 mg/kg/day). When compared to those who did not fail treatment on univariate analysis, treatment failure was significantly associated with a weight of >90 kg ( < 0.001), male gender ( = 0.02), immune suppression ( = 0.04), and a first-line regimen of rifampin-clarithromycin compared to a regimen of rifampin-fluoroquinolone ( = 0.05). There is a low rate of treatment failure in Australian BU patients treated with rifampin-based oral combination antibiotic therapy. Our study raises the possibility that treatment failure risk may be increased in males, those with a body weight of >90 kg, those with immune suppression, and those taking rifampin-clarithromycin antibiotic regimens, but future pharmacokinetic and pharmacodynamics studies are required to determine the validity of these hypotheses.

Citing Articles

A human model of Buruli ulcer: Provisional protocol for a controlled human infection study.

Muhi S, Marshall J, OBrien D, Johnson P, Ross G, Ramakrishnan A Wellcome Open Res. 2024; 9:488.

PMID: 39386965 PMC: 11462124. DOI: 10.12688/wellcomeopenres.22719.1.


Mycobacterium ulcerans challenge strain selection for a Buruli ulcer controlled human infection model.

Muhi S, Buultjens A, Porter J, Marshall J, Doerflinger M, Pidot S PLoS Negl Trop Dis. 2024; 18(5):e0011979.

PMID: 38701090 PMC: 11095734. DOI: 10.1371/journal.pntd.0011979.


Buruli ulcer in Africa: Geographical distribution, ecology, risk factors, diagnosis, and indigenous plant treatment options - A comprehensive review.

Osei-Owusu J, Aidoo O, Eshun F, Gaikpa D, Dofuor A, Vigbedor B Heliyon. 2023; 9(11):e22018.

PMID: 38034712 PMC: 10686891. DOI: 10.1016/j.heliyon.2023.e22018.


A human model of Buruli ulcer: The case for controlled human infection and considerations for selecting a Mycobacterium ulcerans challenge strain.

Muhi S, Osowicki J, OBrien D, Johnson P, Pidot S, Doerflinger M PLoS Negl Trop Dis. 2023; 17(6):e0011394.

PMID: 37384606 PMC: 10309606. DOI: 10.1371/journal.pntd.0011394.

References
1.
Thangaraj H, Adjei O, Allen B, Portaels F, Evans M, Banerjee D . In vitro activity of ciprofloxacin, sparfloxacin, ofloxacin, amikacin and rifampicin against Ghanaian isolates of Mycobacterium ulcerans. J Antimicrob Chemother. 2000; 45(2):231-3. DOI: 10.1093/jac/45.2.231. View

2.
Lettieri J, Rogge M, Kaiser L, Echols R, Heller A . Pharmacokinetic profiles of ciprofloxacin after single intravenous and oral doses. Antimicrob Agents Chemother. 1992; 36(5):993-6. PMC: 188820. DOI: 10.1128/AAC.36.5.993. View

3.
Phillips R, Sarfo F, Abass M, Abotsi J, Wilson T, Forson M . Clinical and bacteriological efficacy of rifampin-streptomycin combination for two weeks followed by rifampin and clarithromycin for six weeks for treatment of Mycobacterium ulcerans disease. Antimicrob Agents Chemother. 2013; 58(2):1161-6. PMC: 3910847. DOI: 10.1128/AAC.02165-13. View

4.
OBrien D, Friedman N, Cowan R, Walton A, Athan E . Six vs Eight Weeks of Antibiotics for Small Mycobacterium ulcerans Lesions in Australian Patients. Clin Infect Dis. 2019; 70(9):1993-1997. DOI: 10.1093/cid/ciz532. View

5.
Daskapan A, Idrus L, Postma M, Wilffert B, Kosterink J, Stienstra Y . A Systematic Review on the Effect of HIV Infection on the Pharmacokinetics of First-Line Tuberculosis Drugs. Clin Pharmacokinet. 2018; 58(6):747-766. PMC: 7019645. DOI: 10.1007/s40262-018-0716-8. View