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Treatment and outcomes in children with multidrug-resistant tuberculosis: A systematic review and individual patient data meta-analysis.
Harausz, Elizabeth P; Garcia-Prats, Anthony J; Law, Stephanie; Schaaf, H Simon; Kredo, Tamara; Seddon, James A; Menzies, Dick; Turkova, Anna; Achar, Jay; Amanullah, Farhana; Barry, Pennan; Becerra, Mercedes; Chan, Edward D; Chan, Pei Chun; Ioana Chiotan, Domnica; Crossa, Aldo; Drobac, Peter C; Fairlie, Lee; Falzon, Dennis; Flood, Jennifer; Gegia, Medea; Hicks, Robert M; Isaakidis, Petros; Kadri, S M; Kampmann, Beate; Madhi, Shabir A; Marais, Else; Mariandyshev, Andrei; Méndez-Echevarría, Ana; Moore, Brittany Kathryn; Nargiza, Parpieva; Ozere, Iveta; Padayatchi, Nesri; Ur-Rehman, Saleem-; Rybak, Natasha; Santiago-Garcia, Begoña; Shah, N Sarita; Sharma, Sangeeta; Shim, Tae Sun; Skrahina, Alena; Soriano-Arandes, Antoni; van den Boom, Martin; van der Werf, Marieke J; van der Werf, Tjip S; Williams, Bhanu; Yablokova, Elena; Yim, Jae-Joon; Furin, Jennifer; Hesseling, Anneke C.
Afiliação
  • Harausz EP; Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
  • Garcia-Prats AJ; Military HIV Research Program, Bethesda, Maryland, United States of America.
  • Law S; Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
  • Schaaf HS; Montreal Chest Institute, McGill University, Montreal, Quebec, Canada.
  • Kredo T; Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
  • Seddon JA; Cochrane South Africa, South African Medical Research Council, Cape Town, South Africa.
  • Menzies D; Centre for International Child Health, Imperial College, London, United Kingdom.
  • Turkova A; Montreal Chest Institute, McGill University, Montreal, Quebec, Canada.
  • Achar J; Imperial College Healthcare NHS Trust, Institute of Clinical Trials and Methodology, London, United Kingdom.
  • Amanullah F; Manson Unit, Médecins Sans Frontières (MSF), London, United Kingdom.
  • Barry P; The Indus Hospital, Karachi, Pakistan.
  • Becerra M; California Department of Public Health, Sacramento, California, United States of America.
  • Chan ED; Partners In Health, Harvard Medical School, and Brigham and Women's Hospital, Boston, Massachusetts, United States of America.
  • Chan PC; Denver Veterans Affairs Medical Center, National Jewish Health, Denver, Colorado, United States of America.
  • Ioana Chiotan D; Division of Chronic Infectious Disease, Centers for Disease Control, Taipei, Taiwan.
  • Crossa A; Epidemiological Surveillance Department, Romanian National TB Program, Bucharest, Romania.
  • Drobac PC; New York City Department of Health and Mental Hygiene, New York, New York, United States of America.
  • Fairlie L; Partners In Health, Harvard Medical School, and Brigham and Women's Hospital, Boston, Massachusetts, United States of America.
  • Falzon D; Wits Reproductive Health & HIV Institute (WRHI), University of the Witwatersrand, Johannesburg, South Africa.
  • Flood J; Laboratories, Diagnostics and Drug Resistance Unit, Global TB Programme, World Health Organization, Geneva, Switzerland.
  • Gegia M; California Department of Public Health, Sacramento, California, United States of America.
  • Hicks RM; Technical Support Coordination, Global TB Programme, World Health Organization, Geneva, Switzerland.
  • Isaakidis P; Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Kadri SM; Médecins Sans Frontières (MSF)/Doctors Without Borders, Mumbai, India.
  • Kampmann B; Disease Control, Directorate of Health Services, Kashmir, India.
  • Madhi SA; Paediatric Infection & Immunity, Centre of International Child Health, Imperial College London, London, United Kingdom.
  • Marais E; Vaccines & Immunity Theme, MRC Unit The Gambia, Banjul, The Gambia.
  • Mariandyshev A; Medical Research Council: Respiratory and Meningeal Pathogens Research Unit, and Department of Science and Technology/National Research Foundation: Vaccine Preventable Diseases, University of the Witwatersrand, Johannesburg, South Africa.
  • Méndez-Echevarría A; Department of Clinical Microbiology and Infectious Diseases, University of the Witwatersrand and the National Health Laboratory Services, Johannesburg, South Africa.
  • Moore BK; Northern State Medical University, Arkhangelsk, Russian Federation.
  • Nargiza P; Pediatric, Infectious and Tropical Diseases Department, Hospital La Paz, Madrid, Spain.
  • Ozere I; Division of Global HIV and TB, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
  • Padayatchi N; Republican Scientific Medical Center of Phtiziology and Pulmonology, Ministry of Health, Tashkent, Uzbekistan.
  • Ur-Rehman S; Riga Eastern Clinical University Hospital, Centre for Tuberculosis and Lung Diseases, Riga, Latvia.
  • Rybak N; CAPRISA, MRC TB-HIV Pathogenesis Unit, Durban, South Africa.
  • Santiago-Garcia B; Director Health Services, Kashmir, India.
  • Shah NS; Alpert Medical School of Brown University, Providence, Rhode Island, United States of America.
  • Sharma S; Pediatric Infectious Diseases Unit, Instituto de Investigación Sanitaria Gregorio Marañón, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
  • Shim TS; Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Skrahina A; Department of Pediatrics, National Institute of Tuberculosis and Respiratory Diseases, New Delhi, India.
  • Soriano-Arandes A; Department of Pulmonary and Critical Care Medicine, University of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea.
  • van den Boom M; The Republican Research and Practical Centre for Pulmonology and TB, Minsk, Belarus.
  • van der Werf MJ; Pediatric Infectious Diseases and Immunodeficiencies Unit, Unit of International Health-Tuberculosis Drassanes-Vall Hebron, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • van der Werf TS; Joint Tuberculosis, HIV & Viral Hepatitis Programme, WHO Regional Office for Europe, Copenhagen, Denmark.
  • Williams B; Disease Programme Tuberculosis, European Centre for Disease Prevention and Control, Stockholm, Sweden.
  • Yablokova E; University Medical Center Groningen, Groningen, the Netherlands.
  • Yim JJ; Northwick Park Hospital, London Northwest Healthcare NHS Trust, London, United Kingdom.
  • Furin J; Northern State Medical University, Arkhangelsk, Russian Federation.
  • Hesseling AC; Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University College of Medicine, Seoul, South Korea.
PLoS Med ; 15(7): e1002591, 2018 07.
Article em En | MEDLINE | ID: mdl-29995958
BACKGROUND: An estimated 32,000 children develop multidrug-resistant tuberculosis (MDR-TB; Mycobacterium tuberculosis resistant to isoniazid and rifampin) each year. Little is known about the optimal treatment for these children. METHODS AND FINDINGS: To inform the pediatric aspects of the revised World Health Organization (WHO) MDR-TB treatment guidelines, we performed a systematic review and individual patient data (IPD) meta-analysis, describing treatment outcomes in children treated for MDR-TB. To identify eligible reports we searched PubMed, LILACS, Embase, The Cochrane Library, PsychINFO, and BioMedCentral databases through 1 October 2014. To identify unpublished data, we reviewed conference abstracts, contacted experts in the field, and requested data through other routes, including at national and international conferences and through organizations working in pediatric MDR-TB. A cohort was eligible for inclusion if it included a minimum of three children (aged <15 years) who were treated for bacteriologically confirmed or clinically diagnosed MDR-TB, and if treatment outcomes were reported. The search yielded 2,772 reports; after review, 33 studies were eligible for inclusion, with IPD provided for 28 of these. All data were from published or unpublished observational cohorts. We analyzed demographic, clinical, and treatment factors as predictors of treatment outcome. In order to obtain adjusted estimates, we used a random-effects multivariable logistic regression (random intercept and random slope, unless specified otherwise) adjusted for the following covariates: age, sex, HIV infection, malnutrition, severe extrapulmonary disease, or the presence of severe disease on chest radiograph. We analyzed data from 975 children from 18 countries; 731 (75%) had bacteriologically confirmed and 244 (25%) had clinically diagnosed MDR-TB. The median age was 7.1 years. Of 910 (93%) children with documented HIV status, 359 (39%) were infected with HIV. When compared to clinically diagnosed patients, children with confirmed MDR-TB were more likely to be older, to be infected with HIV, to be malnourished, and to have severe tuberculosis (TB) on chest radiograph (p < 0.001 for all characteristics). Overall, 764 of 975 (78%) had a successful treatment outcome at the conclusion of therapy: 548/731 (75%) of confirmed and 216/244 (89%) of clinically diagnosed children (absolute difference 14%, 95% confidence interval [CI] 8%-19%, p < 0.001). Treatment was successful in only 56% of children with bacteriologically confirmed TB who were infected with HIV who did not receive any antiretroviral treatment (ART) during MDR-TB therapy, compared to 82% in children infected with HIV who received ART during MDR-TB therapy (absolute difference 26%, 95% CI 5%-48%, p = 0.006). In children with confirmed MDR-TB, the use of second-line injectable agents and high-dose isoniazid (15-20 mg/kg/day) were associated with treatment success (adjusted odds ratio [aOR] 2.9, 95% CI 1.0-8.3, p = 0.041 and aOR 5.9, 95% CI 1.7-20.5, p = 0.007, respectively). These findings for high-dose isoniazid may have been affected by site effect, as the majority of patients came from Cape Town. Limitations of this study include the difficulty of estimating the treatment effects of individual drugs within multidrug regimens, only observational cohort studies were available for inclusion, and treatment decisions were based on the clinician's perception of illness, with resulting potential for bias. CONCLUSIONS: This study suggests that children respond favorably to MDR-TB treatment. The low success rate in children infected with HIV who did not receive ART during their MDR-TB treatment highlights the need for ART in these children. Our findings of individual drug effects on treatment outcome should be further evaluated.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tuberculose Resistente a Múltiplos Medicamentos / Antituberculosos Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: África do Sul

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tuberculose Resistente a Múltiplos Medicamentos / Antituberculosos Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: África do Sul