Mayara L. Bastos
Federal University of Rio de Janeiro
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Publication
Featured researches published by Mayara L. Bastos.
PLOS ONE | 2013
Ricardo Ewbank Steffen; Rosângela Caetano; Márcia Pinto; Diogo Chaves; Rossini Ferrari; Mayara L. Bastos; Sandra Teixeira de Abreu; Dick Menzies; Anete Trajman
Background Latent tuberculosis infection (LTBI) is a reservoir for new TB cases. Isoniazid preventive therapy (IPT) reduces the risk of active TB by as much as 90%, but LTBI screening has limitations. Unlike tuberculin skin testing (TST), interferon-gamma release assays are not affected by BCG vaccination, and have been reported to be cost-effective in low-burden countries. The goal of this study was to perform a cost-effectiveness analysis from the health system perspective, comparing three strategies for LTBI diagnosis in TB contacts: tuberculin skin testing (TST), QuantiFERON®-TB Gold-in-Tube (QFT-GIT) and TST confirmed by QFT-GIT if positive (TST/QFT-GIT) in Brazil, a middle-income, high-burden country with universal BCG coverage. Methodology/Principal Findings Costs for LTBI diagnosis and treatment of a hypothetical cohort of 1,000 adult immunocompetent close contacts were considered. The effectiveness measure employed was the number of averted TB cases in two years. Health system costs were US
Respiratory Medicine | 2014
Anete Trajman; Elen Oliveira; Mayara L. Bastos; Epaminondas Belo Neto; Edgar Manoel Silva; Maria Cristina S. Lourenço; Afrânio Lineu Kritski; Martha Maria Oliveira
105,096 for TST, US
European Respiratory Journal | 2016
Zhiyi Lan; Mayara L. Bastos; Dick Menzies
121,054 for QFT-GIT and US
The Lancet Respiratory Medicine | 2018
Federica Fregonese; Shama D. Ahuja; Onno W. Akkerman; Denise Arakaki-Sanchez; Irene Ayakaka; Parvaneh Baghaei; Didi Bang; Mayara L. Bastos; Andrea Benedetti; Maryline Bonnet; Adithya Cattamanchi; Peter Cegielski; Jung Yien Chien; Helen Cox; Martin Dedicoat; Connie Erkens; Patricio Escalante; Dennis Falzon; Anthony J. Garcia-Prats; Medea Gegia; Stephen H. Gillespie; Judith R. Glynn; Stefan Goldberg; David Griffith; Karen R. Jacobson; James C. Johnston; Edward C. Jones-López; Awal Khan; Won Jung Koh; Afranio Lineu Kritski
101,948 for TST/QFT-GIT; these strategies averted 6.56, 6.63 and 4.59 TB cases, respectively. The most cost-effective strategy was TST (US
PLOS ONE | 2017
Mayara L. Bastos; Dick Menzies; Thomas Hone; Kianoush Dehghani; Anete Trajman
16,021/averted case). The incremental cost-effectiveness ratio was US
Jornal Brasileiro De Pneumologia | 2012
Mayara L. Bastos; Anete Trajman; Eleny Guimarães Teixeira; Lia Selig; Márcia Teresa Carreira Teixeira Belo
227,977/averted TB case for QFT-GIT. TST/QFT-GIT was dominated. Conclusions Unlike previous studies, TST was the most cost-effective strategy for averting new TB cases in the short term. QFT-GIT would be more cost-effective if its costs could be reduced to US
BMC Infectious Diseases | 2016
Gabriela B. Gomez; David W. Dowdy; Mayara L. Bastos; Alice Zwerling; Sedona Sweeney; Nicola Foster; Anete Trajman; M. A. Islam; Saidi Kapiga; Edina Sinanovic; Gwenan M. Knight; Richard G. White; Wendy A. Wells; Frank Cobelens; Anna Vassall
26.95, considering a TST specificity of 59% and US
Clinical Infectious Diseases | 2015
Mayara L. Bastos; Dick Menzies
18 considering a more realistic TST specificity of 80%. Nevertheless, with TST, 207.4 additional people per 1,000 will be prescribed IPT compared with QFT.
Revista da Sociedade Portuguesa de Dermatologia e Venereologia | 2013
Érica Bertolace Slaibi; Fernando Campos Amaral Figueiredo Nina; Nathalia Velihovetchi; Mayara L. Bastos; Karla Ronchini; José Augusto da Costa Nery; André Filipe Marcondes Vieira; Márcia Teresa Carreira Teixeira Belo; Fundação Técnico Educacional Souza Marques (Ftesm). Rio de Janeiro, Rj, Brasil.
INTRODUCTION Polymerase chain reaction (PCR)-based techniques to detect Mycobacterium tuberculosis DNA in respiratory specimens have been increasingly used to diagnose pulmonary tuberculosis. Their use in non-respiratory specimens to diagnose extrapulmonary tuberculosis is, however, controversial. In this study, we estimated the accuracy of three in-country commercialized PCR-based diagnostic techniques in pleural fluid samples for the diagnosis of pleural tuberculosis. METHODS Patients underwent thoracenthesis for diagnosis purposes; pleural fluid aliquots were frozen and subsequently submitted to two real time PCR tests (COBAS(®)TAQMAN(®)MTB and Xpert(®)MTB/Rif) and one conventional PCR test (Detect-TB(®)). Two different reference standards were considered: probable tuberculosis (based on clinical grounds) and confirmed tuberculosis (bacteriologically or histologically). RESULTS Ninety-three patients were included, of whom 65 with pleural tuberculosis, 35 of them confirmed. Sensitivities were 29% for COBAS(®)TAQMAN(®)MTB, 3% for Xpert(®)MTB/Rif and 3% for Detect-TB(®); specificities were 86%, 100% and 97% respectively, considering confirmed tuberculosis. Considering all cases, sensitivities were 16%, 3% and 2%, and specificities, 86%, 100%, and 97%. DISCUSSION Compared to the 95% sensitivity of adenosine deaminase, the most sensitive test for pleural tuberculosis, the sensitivities of the three PCR-based tests were very low. We conclude that at present, there is no major place for such tests in routine clinical use.
Clinical Infectious Diseases | 2014
Mayara L. Bastos; Hamidah Hussain; Karin Weyer; Lourdes García-García; Vaira Leimane; Chi Chiu Leung; Masahiro Narita; Peña Jm; Alfredo Ponce-de-León; Kwonjune J. Seung; Karen Shean; José Sifuentes-Osornio; Martie van der Walt; Tjip S. van der Werf; Wing Wai Yew; Dick Menzies
Mycobacterium bovis, a member of the Mycobacterium tuberculosis complex, is an important cause of disease in cattle, but it can also cause disease in humans [1]. Transmission to humans generally occurs after close contact with infected animals or consumption of unpasteurised contaminated dairy products [1, 2]. The symptoms of human disease due to M. bovis are similar to those of disease caused by M. tuberculosis, although M. bovis is more likely to cause extrapulmonary disease [3]. In clinical practice, M. bovis can only be differentiated from M. tuberculosis using biochemical or genetic tests [3, 4]. Only limited evidence exists to support current recommendations for the treatment of human disease due to M. bovis http://ow.ly/h92K3023fLu