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Treatment correlates of successful outcomes in pulmonary multidrug-resistant tuberculosis: an individual patient data meta-analysis.
Ahmad, Nafees; Ahuja, Shama D; Akkerman, Onno W; Alffenaar, Jan-Willem C; Anderson, Laura F; Baghaei, Parvaneh; Bang, Didi; Barry, Pennan M; Bastos, Mayara L; Behera, Digamber; Benedetti, Andrea; Bisson, Gregory P; Boeree, Martin J; Bonnet, Maryline; Brode, Sarah K; Brust, James C M; Cai, Ying; Caumes, Eric; Cegielski, J Peter; Centis, Rosella; Chan, Pei-Chun; Chan, Edward D; Chang, Kwok-Chiu; Charles, Macarthur; Cirule, Andra; Dalcolmo, Margareth Pretti; D'Ambrosio, Lia; de Vries, Gerard; Dheda, Keertan; Esmail, Aliasgar; Flood, Jennifer; Fox, Gregory J; Fréchet-Jachym, Mathilde; Fregona, Geisa; Gayoso, Regina; Gegia, Medea; Gler, Maria Tarcela; Gu, Sue; Guglielmetti, Lorenzo; Holtz, Timothy H; Hughes, Jennifer; Isaakidis, Petros; Jarlsberg, Leah; Kempker, Russell R; Keshavjee, Salmaan; Khan, Faiz Ahmad; Kipiani, Maia; Koenig, Serena P; Koh, Won-Jung; Kritski, Afranio.
Afiliação
  • Ahmad N; Faculty of Pharmacy and Health Sciences, University of Baluchistan, Quetta, Pakistan.
  • Ahuja SD; Bureau of Tuberculosis Control, New York City Department of Health and Mental Hygiene, NY, USA.
  • Akkerman OW; Department of Pulmonary Diseases and Tuberculosis, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands; Tuberculosis Centre Beatrixoord, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
  • Alffenaar JC; Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
  • Anderson LF; Global Tuberculosis Program, World Health Organization, Geneva, Switzerland.
  • Baghaei P; Clinical Tuberculosis and Epidemiology Research Center, NRITLD, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Bang D; Statens Serum Institut, Copenhagen, Denmark.
  • Barry PM; Tuberculosis Control Branch, Division of Communicable Disease Control, Center for Infectious Diseases, California Department of Public Health, CA, USA.
  • Bastos ML; Social Medicine Institute, Epidemiology Department, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Behera D; Department of Pulmonary Medicine, World Health Organization Collaborating Centre for Research & Capacity Building in Chronic Respiratory Diseases, Chandigarh, India; Postgraduate Institute of Medical Education & Research, Chandigarh, India.
  • Benedetti A; Montreal Chest Institute, McGill University Health Center Research Institute, McGill University, Montreal, QC, Canada.
  • Bisson GP; University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA.
  • Boeree MJ; Department of Pulmonary Diseases, Radboud University Medicale Centre Nijmegen and Dekkerswald Radboudumc Groesbeek, Netherlands.
  • Bonnet M; Epicentre MSF, Paris, France; Institut de Recherche pour le Développement UM233, INSERM U1175, Université de Montpellier, Montpellier, France.
  • Brode SK; Department of Medicine, Division of Respirology, University of Toronto, West Park Healthcare Centre, University Health Network, and Sinai Health System, Toronto, ON, Canada.
  • Brust JCM; Division of General Internal Medicine and Division of Infectious Diseases, Montefiore Medical Center, Albert Einstein College of Medicine, New York, NY, USA.
  • Cai Y; Tuberculosis Research Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, US National Institutes of Health, Bethesda, MD, USA.
  • Caumes E; AP-HP, Service des Maladies Infectieuses et Tropicales, Hôpitaux Universitaires Pitié Salpêtrière-Charles Foix, Paris, France.
  • Cegielski JP; Division of Global HIV and TB, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Centis R; World Health Organization Collaborating Centre for Tuberculosis and Lung Diseases, Maugeri Care and Research Institute, Tradate, Italy.
  • Chan PC; Division of Chronic Infectious Diseases, Taiwan Centers for Disease Control, Taipei, Taiwan.
  • Chan ED; Department of Medicine, University of Colorado Denver, Aurora, CO, USA; Department of Medicine, National Jewish Health, Denver, CO, USA; VA Medical Center, Denver, CO, USA.
  • Chang KC; Department of Health, Tuberculosis and Chest Service, Centre for Health Protection, Hong Kong Special Administrative Region, China.
  • Charles M; Centers for Disease Control and Prevention, Haiti Country Office, Port-au-Prince, Haiti.
  • Cirule A; Centre of TB and Lung Diseases, Riga East University Hospital, Riga, Latvia.
  • Dalcolmo MP; Centro de Referência Helio Fraga, Fiocruz, Brazil.
  • D'Ambrosio L; World Health Organization Collaborating Centre for Tuberculosis and Lung Diseases, Maugeri Care and Research Institute, Tradate, Italy; Public Health Consulting Group, Lugano, Switzerland.
  • de Vries G; Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands; KNCV Tuberculosis Foundation, The Hague, Netherlands.
  • Dheda K; Centre for Lung Infection and Immunity, Department of Medicine & UCT Lung Institute, University of Cape Town, Cape Town, South Africa.
  • Esmail A; Centre for Lung Infection and Immunity, Department of Medicine & UCT Lung Institute, University of Cape Town, Cape Town, South Africa.
  • Flood J; Tuberculosis Control Branch, Division of Communicable Disease Control, Center for Infectious Diseases, California Department of Public Health, CA, USA.
  • Fox GJ; Sydney Medical School, University of Sydney, NSW, Australia.
  • Fréchet-Jachym M; Sanatorium, Centre Hospitalier de Bligny, Briis-sous-Forges, France.
  • Fregona G; University Federal of Espirito Santo, Vitória, Brazil.
  • Gayoso R; Centro de Referência Helio Fraga, Fiocruz, Brazil.
  • Gegia M; Global Tuberculosis Program, World Health Organization, Geneva, Switzerland.
  • Gler MT; Tropical Disease Foundation, Manila, Philippines.
  • Gu S; Department of Medicine, University of Colorado Denver, Aurora, CO, USA.
  • Guglielmetti L; AP-HP, Laboratoire de Bactériologie-Hygiène, Centre National de Référence des Mycobactéries et de la Résistance des Mycobactéries aux Antituberculeux, Hôpitaux Universitaires Pitié Salpêtrière-Charles Foix, Paris, France; Sorbonne Université, Centre d'Immunologie et des Maladies Infectieuses (CIMI;
  • Holtz TH; Division of Global HIV and TB, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Hughes J; Médecins Sans Frontières, Khayelitsha, South Africa.
  • Isaakidis P; Médecins Sans Frontières, Mumbai, India.
  • Jarlsberg L; Division of Pulmonary and Critical Care Medicine, University of California, San Francisco, CA, USA.
  • Kempker RR; Emory University School of Medicine, Division of Infectious Diseases, Atlanta, GA, USA.
  • Keshavjee S; Department of Global Health and Social Medicine, Harvard Medical School, Boston, MA, USA; Division of Global Health Equity, Brigham and Women's Hospital, Boston, MA, USA.
  • Khan FA; Montreal Chest Institute, McGill University Health Center Research Institute, McGill University, Montreal, QC, Canada.
  • Kipiani M; National Center for Tuberculosis and Lung Diseases, Tbilisi, Georgia.
  • Koenig SP; Division of Global Health Equity, Brigham and Women's Hospital, Boston, MA, USA; Haitian Study Group for Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince, Haiti.
  • Koh WJ; Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
  • Kritski A; Academic Tuberculosis Program, School of Medicine, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Lancet ; 392(10150): 821-834, 2018 09 08.
Article em En | MEDLINE | ID: mdl-30215381
ABSTRACT

BACKGROUND:

Treatment outcomes for multidrug-resistant tuberculosis remain poor. We aimed to estimate the association of treatment success and death with the use of individual drugs, and the optimal number and duration of treatment with those drugs in patients with multidrug-resistant tuberculosis.

METHODS:

In this individual patient data meta-analysis, we searched MEDLINE, Embase, and the Cochrane Library to identify potentially eligible observational and experimental studies published between Jan 1, 2009, and April 30, 2016. We also searched reference lists from all systematic reviews of treatment of multidrug-resistant tuberculosis published since 2009. To be eligible, studies had to report original results, with end of treatment outcomes (treatment completion [success], failure, or relapse) in cohorts of at least 25 adults (aged >18 years). We used anonymised individual patient data from eligible studies, provided by study investigators, regarding clinical characteristics, treatment, and outcomes. Using propensity score-matched generalised mixed effects logistic, or linear regression, we calculated adjusted odds ratios and adjusted risk differences for success or death during treatment, for specific drugs currently used to treat multidrug-resistant tuberculosis, as well as the number of drugs used and treatment duration.

FINDINGS:

Of 12 030 patients from 25 countries in 50 studies, 7346 (61%) had treatment success, 1017 (8%) had failure or relapse, and 1729 (14%) died. Compared with failure or relapse, treatment success was positively associated with the use of linezolid (adjusted risk difference 0·15, 95% CI 0·11 to 0·18), levofloxacin (0·15, 0·13 to 0·18), carbapenems (0·14, 0·06 to 0·21), moxifloxacin (0·11, 0·08 to 0·14), bedaquiline (0·10, 0·05 to 0·14), and clofazimine (0·06, 0·01 to 0·10). There was a significant association between reduced mortality and use of linezolid (-0·20, -0·23 to -0·16), levofloxacin (-0·06, -0·09 to -0·04), moxifloxacin (-0·07, -0·10 to -0·04), or bedaquiline (-0·14, -0·19 to -0·10). Compared with regimens without any injectable drug, amikacin provided modest benefits, but kanamycin and capreomycin were associated with worse outcomes. The remaining drugs were associated with slight or no improvements in outcomes. Treatment outcomes were significantly worse for most drugs if they were used despite in-vitro resistance. The optimal number of effective drugs seemed to be five in the initial phase, and four in the continuation phase. In these adjusted analyses, heterogeneity, based on a simulated I2 method, was high for approximately half the estimates for specific drugs, although relatively low for number of drugs and durations analyses.

INTERPRETATION:

Although inferences are limited by the observational nature of these data, treatment outcomes were significantly better with use of linezolid, later generation fluoroquinolones, bedaquiline, clofazimine, and carbapenems for treatment of multidrug-resistant tuberculosis. These findings emphasise the need for trials to ascertain the optimal combination and duration of these drugs for treatment of this condition.

FUNDING:

American Thoracic Society, Canadian Institutes of Health Research, US Centers for Disease Control and Prevention, European Respiratory Society, Infectious Diseases Society of America.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tuberculose Pulmonar / Tuberculose Resistente a Múltiplos Medicamentos / Antituberculosos Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Lancet Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Paquistão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tuberculose Pulmonar / Tuberculose Resistente a Múltiplos Medicamentos / Antituberculosos Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Lancet Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Paquistão
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