TY - JOUR
T1 - The epidemiology, pathogenesis, transmission, diagnosis, and management of multidrug-resistant, extensively drug-resistant, and incurable tuberculosis
AU - Dheda, Keertan
AU - Gumbo, Tawanda
AU - Maartens, Gary
AU - Dooley, Kelly E.
AU - McNerney, Ruth
AU - Murray, Megan
AU - Furin, Jennifer
AU - Nardell, Edward A.
AU - London, Leslie
AU - Lessem, Erica
AU - Theron, Grant
AU - van Helden, Paul
AU - Niemann, Stefan
AU - Merker, Matthias
AU - Dowdy, David
AU - Van Rie, Annelies
AU - Siu, Gilman K.H.
AU - Pasipanodya, Jotam G.
AU - Rodrigues, Camilla
AU - Clark, Taane G.
AU - Sirgel, Frik A.
AU - Esmail, Aliasgar
AU - Lin, Hsien Ho
AU - Atre, Sachin R.
AU - Schaaf, H. Simon
AU - Chang, Kwok Chiu
AU - Lange, Christoph
AU - Nahid, Payam
AU - Udwadia, Zarir F.
AU - Horsburgh, C. Robert
AU - Churchyard, Gavin J.
AU - Menzies, Dick
AU - Hesseling, Anneke C.
AU - Nuermberger, Eric
AU - McIlleron, Helen
AU - Fennelly, Kevin P.
AU - Goemaere, Eric
AU - Jaramillo, Ernesto
AU - Low, Marcus
AU - Jara, Carolina Morán
AU - Padayatchi, Nesri
AU - Warren, Robin M.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Although tuberculosis control has been effective in some regions of the world, these gains are threatened by the increasing burden of multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis. XDR tuberculosis has evolved in several tuberculosis-endemic countries to drug-incurable or programmatically incurable tuberculosis (totally drug-resistant tuberculosis). This poses several challenges similar to those encountered in the pre-chemotherapy era, including the inability to cure tuberculosis, high mortality, and the need for alternative methods to prevent disease transmission. This phenomenon mirrors the worldwide increase in antimicrobial resistance and the emergence of other MDR pathogens, such as malaria, HIV, and Gram-negative bacteria. MDR and XDR tuberculosis are associated with high morbidity and substantial mortality, are a threat to health-care workers, prohibitively expensive to treat, and are therefore a serious public health problem. In this Commission, we examine several aspects of drug-resistant tuberculosis. The traditional view that acquired resistance to antituberculous drugs is driven by poor compliance and programmatic failure is now being questioned, and several lines of evidence suggest that alternative mechanisms—including pharmacokinetic variability, induction of efflux pumps that transport the drug out of cells, and suboptimal drug penetration into tuberculosis lesions—are likely crucial to the pathogenesis of drug-resistant tuberculosis. These factors have implications for the design of new interventions, drug delivery and dosing mechanisms, and public health policy. We discuss epidemiology and transmission dynamics, including new insights into the fundamental biology of transmission, and we review the utility of newer diagnostic tools, including molecular tests and next-generation whole-genome sequencing, and their potential for clinical effectiveness. Relevant research priorities are highlighted, including optimal medical and surgical management, the role of newer and repurposed drugs (including bedaquiline, delamanid, and linezolid), pharmacokinetic and pharmacodynamic considerations, preventive strategies (such as prophylaxis in MDR and XDR contacts), palliative and patient-orientated care aspects, and medicolegal and ethical issues.
AB - Although tuberculosis control has been effective in some regions of the world, these gains are threatened by the increasing burden of multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis. XDR tuberculosis has evolved in several tuberculosis-endemic countries to drug-incurable or programmatically incurable tuberculosis (totally drug-resistant tuberculosis). This poses several challenges similar to those encountered in the pre-chemotherapy era, including the inability to cure tuberculosis, high mortality, and the need for alternative methods to prevent disease transmission. This phenomenon mirrors the worldwide increase in antimicrobial resistance and the emergence of other MDR pathogens, such as malaria, HIV, and Gram-negative bacteria. MDR and XDR tuberculosis are associated with high morbidity and substantial mortality, are a threat to health-care workers, prohibitively expensive to treat, and are therefore a serious public health problem. In this Commission, we examine several aspects of drug-resistant tuberculosis. The traditional view that acquired resistance to antituberculous drugs is driven by poor compliance and programmatic failure is now being questioned, and several lines of evidence suggest that alternative mechanisms—including pharmacokinetic variability, induction of efflux pumps that transport the drug out of cells, and suboptimal drug penetration into tuberculosis lesions—are likely crucial to the pathogenesis of drug-resistant tuberculosis. These factors have implications for the design of new interventions, drug delivery and dosing mechanisms, and public health policy. We discuss epidemiology and transmission dynamics, including new insights into the fundamental biology of transmission, and we review the utility of newer diagnostic tools, including molecular tests and next-generation whole-genome sequencing, and their potential for clinical effectiveness. Relevant research priorities are highlighted, including optimal medical and surgical management, the role of newer and repurposed drugs (including bedaquiline, delamanid, and linezolid), pharmacokinetic and pharmacodynamic considerations, preventive strategies (such as prophylaxis in MDR and XDR contacts), palliative and patient-orientated care aspects, and medicolegal and ethical issues.
UR - http://www.scopus.com/inward/record.url?scp=85016118701&partnerID=8YFLogxK
U2 - 10.1016/S2213-2600(17)30079-6
DO - 10.1016/S2213-2600(17)30079-6
M3 - Review article
SN - 2213-2600
VL - 5
SP - 291
EP - 360
JO - The Lancet Respiratory Medicine
JF - The Lancet Respiratory Medicine
IS - 4
ER -