dc.contributor.author |
Cornejo Garcia, Jose Gabriel |
|
dc.contributor.author |
Alarcón Guizado, Valentina Antonieta |
|
dc.contributor.author |
Mendoza Ticona, Alberto |
|
dc.contributor.author |
Alarcon, Edith |
|
dc.contributor.author |
Heldal, Einar |
|
dc.contributor.author |
Moore, David Alexander James |
|
dc.date.accessioned |
2019-03-05T15:23:30Z |
|
dc.date.available |
2019-03-05T15:23:30Z |
|
dc.date.issued |
2018 |
|
dc.identifier.uri |
https://hdl.handle.net/20.500.12866/5896 |
|
dc.description.abstract |
Background: Resistance to isoniazid is the most common form of drug-resistance in tuberculosis. However only a tiny proportion of TB patients in the world have access to isoniazid drug susceptibility testing—the widely implemented Xpert MTB/RIF technology only tests for resistance to rifampicin. Patients with isoniazid mono resistance that is not identified at baseline are treated with a standard regimen that effectively results in rifampicin mono-therapy during the latter four months of the six month treatment course, exposing remaining viable organisms to a single agent and greatly increasing the risk of development of multi drug-resistant TB. Unusually, Peru has pioneered universal pre-treatment drug susceptibility testing with methods that identify isoniazid resistance and has thus identified a large number of individuals requiring tailored therapy. Since 2010, treatment in Peru for isoniazid-resistant tuberculosis without multidrug-resistant tuberculosis (Hr-TB) has been with a standardized nine-month regimen of levofloxacin, rifampicin, ethambutol and pyrazinamide. The objectives of this study were to evaluate the outcomes of treatment for patients with Hr-TB initiating treatment with this regimen between January 2012 and December 2014 and to determine factors affecting these outcomes. Methods: Retrospective cross-sectional study; case data were obtained from the national registry of drug-resistant tuberculosis. Patients diagnosed with isoniazid resistant TB without resistance to rifampicin, pyrazinamide, ethambutol and quinolones as determined by either a rapid drug susceptibility testing (DST) (nitrate reductase test, MODS, Genotype MTBDRplus) or by the proportion method were included. Findings: A total of 947 cases were evaluated (a further 403 without treatment end date were excluded), with treatment success in 77.2% (731 cases), loss to follow-up in 19.7% (186 cases), treatment failure in 1.2% (12 cases), and death in 1.9% (18 cases). Unfavorable outcomes were associated in multivariate analysis with male gender (OR 0.50, 95% CI 0.34–0.72, p<0.05), lack of rapid DST (OR 0.67, 95% CI 0.50–0.91, p = 0.01), additional use of an injectable second-line anti-tuberculous drug (OR 0.46, 95% CI 0.31–0.70, p<0.05), and treatment initiation in 2014 (OR 0.77, 95% CI 0.62–0.94, p = 0.01). Interpretation: The treatment regimen implemented in Peru for isoniazid resistant TB is effective for TB cure and is not improved by addition of an injectable second-line agent. Access to rapid DST and treatment adherence need to be strengthened to increase favorable results. |
en_US |
dc.language.iso |
eng |
|
dc.publisher |
Public Library of Science |
|
dc.relation.ispartofseries |
PLoS ONE |
|
dc.rights |
info:eu-repo/semantics/restrictedAccess |
|
dc.rights.uri |
https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es |
|
dc.subject |
adolescent |
en_US |
dc.subject |
adult |
en_US |
dc.subject |
aged |
en_US |
dc.subject |
antibiotic resistance |
en_US |
dc.subject |
antibiotic sensitivity |
en_US |
dc.subject |
Article |
en_US |
dc.subject |
child |
en_US |
dc.subject |
cohort analysis |
en_US |
dc.subject |
controlled study |
en_US |
dc.subject |
cross-sectional study |
en_US |
dc.subject |
death |
en_US |
dc.subject |
drug resistant tuberculosis |
en_US |
dc.subject |
ethambutol |
en_US |
dc.subject |
female |
en_US |
dc.subject |
follow up |
en_US |
dc.subject |
human |
en_US |
dc.subject |
infant |
en_US |
dc.subject |
infection risk |
en_US |
dc.subject |
isoniazid |
en_US |
dc.subject |
lack of drug effect |
en_US |
dc.subject |
levofloxacin |
en_US |
dc.subject |
major clinical study |
en_US |
dc.subject |
male |
en_US |
dc.subject |
middle aged |
en_US |
dc.subject |
monotherapy |
en_US |
dc.subject |
Peru |
en_US |
dc.subject |
pyrazinamide |
en_US |
dc.subject |
retrospective study |
en_US |
dc.subject |
rifampicin |
en_US |
dc.subject |
treatment duration |
en_US |
dc.subject |
treatment outcome |
en_US |
dc.subject |
tuberculostatic agent |
en_US |
dc.subject |
young adult |
en_US |
dc.title |
Treatment outcomes for isoniazid-monoresistant tuberculosis in Peru, 2012-2014 |
en_US |
dc.type |
info:eu-repo/semantics/article |
|
dc.identifier.doi |
https://doi.org/10.1371/journal.pone.0206658 |
|
dc.subject.ocde |
https://purl.org/pe-repo/ocde/ford#3.01.05 |
|
dc.subject.ocde |
https://purl.org/pe-repo/ocde/ford#3.02.07 |
|
dc.relation.issn |
1932-6203 |
|