TY - JOUR
T1 - The Lancet Respiratory Medicine Commission
T2 - 2019 update: epidemiology, pathogenesis, transmission, diagnosis, and management of multidrug-resistant and incurable tuberculosis
AU - The Lancet Respiratory Medicine drug-resistant tuberculosis Commission group
AU - Dheda, Keertan
AU - Gumbo, Tawanda
AU - Maartens, Gary
AU - Dooley, Kelly E.
AU - Murray, Megan
AU - Furin, Jennifer
AU - Nardell, Edward A.
AU - Warren, Robin M.
AU - Esmail, Aliasgar
AU - Nardell, Edward
AU - London, Leslie
AU - Lessem, Erica
AU - Limberis, Jason
AU - Theron, Grant
AU - McNerney, Ruth
AU - Niemann, Stefan
AU - Dowdy, David
AU - Van Rie, Annelies
AU - Pasipanodya, Jotam G.
AU - Rodrigues, Camilla
AU - Clark, Taane G.
AU - Sirgel, Frik A.
AU - Schaaf, H. Simon
AU - Chang, Kwok Chiu
AU - Lange, Christoph
AU - Nahid, Payam
AU - Fourie, Bernard
AU - Ndjeka, Norbert
AU - Nunn, Andrew
AU - Migliori, G. B.
AU - Udwadia, Zarir F.
AU - Horsburgh, C. Robert
AU - Churchyard, Gavin J.
AU - Menzies, Dick
AU - Hesseling, Anneke C.
AU - Seddon, James A.
AU - Low, Marcus
AU - Keshavjee, Salmaan
AU - Nuermberger, Eric
AU - McIlleron, Helen
AU - Fennelly, Kevin P.
AU - Jindani, Amina
AU - Jaramillo, Ernesto
AU - Padayatchi, Nesri
AU - Barry, Clifton E.
N1 - Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2019/9
Y1 - 2019/9
N2 - The Lancet Respiratory Medicine Commission on drug-resistant tuberculosis was published in 2017, which comprehensively reviewed and provided recommendations on various aspects of the disease. Several key new developments regarding drug-resistant tuberculosis are outlined in this Commission Update. The WHO guidelines on treating drug-resistant tuberculosis were updated in 2019 with a reclassification of second line anti-tuberculosis drugs. An injection-free MDR tuberculosis treatment regimen is now recommended. Over the past 3 years, advances in treatment include the recognition of the safety and mortality benefit of bedaquiline, the finding that the 9–11 month injectable-based ‘Bangladesh’ regimen was non-inferior to longer regimens, and promising interim results of a novel 6 month 3-drug regimen (bedaquiline, pretomanid, and linezolid). Studies of explanted lungs from patients with drug-resistant tuberculosis have shown substantial drug-specific gradients across pulmonary cavities, suggesting that alternative dosing and drug delivery strategies are needed to reduce functional monotherapy at the site of disease. Several controversies are discussed including the optimal route of drug administration, optimal number of drugs constituting a regimen, selection of individual drugs for a regimen, duration of the regimen, and minimal desirable standards of antibiotic stewardship. Newer rapid nucleic acid amplification test platforms, including point-of-care systems that facilitate active case-finding, are discussed. The rapid diagnosis of resistance to other drugs, (notably fluoroquinolones), and detection of resistance by targeted or whole genome sequencing will probably change the diagnostic landscape in the near future.
AB - The Lancet Respiratory Medicine Commission on drug-resistant tuberculosis was published in 2017, which comprehensively reviewed and provided recommendations on various aspects of the disease. Several key new developments regarding drug-resistant tuberculosis are outlined in this Commission Update. The WHO guidelines on treating drug-resistant tuberculosis were updated in 2019 with a reclassification of second line anti-tuberculosis drugs. An injection-free MDR tuberculosis treatment regimen is now recommended. Over the past 3 years, advances in treatment include the recognition of the safety and mortality benefit of bedaquiline, the finding that the 9–11 month injectable-based ‘Bangladesh’ regimen was non-inferior to longer regimens, and promising interim results of a novel 6 month 3-drug regimen (bedaquiline, pretomanid, and linezolid). Studies of explanted lungs from patients with drug-resistant tuberculosis have shown substantial drug-specific gradients across pulmonary cavities, suggesting that alternative dosing and drug delivery strategies are needed to reduce functional monotherapy at the site of disease. Several controversies are discussed including the optimal route of drug administration, optimal number of drugs constituting a regimen, selection of individual drugs for a regimen, duration of the regimen, and minimal desirable standards of antibiotic stewardship. Newer rapid nucleic acid amplification test platforms, including point-of-care systems that facilitate active case-finding, are discussed. The rapid diagnosis of resistance to other drugs, (notably fluoroquinolones), and detection of resistance by targeted or whole genome sequencing will probably change the diagnostic landscape in the near future.
UR - https://www.scopus.com/pages/publications/85071569313
UR - https://www.scopus.com/pages/publications/85071569313#tab=citedBy
U2 - 10.1016/S2213-2600(19)30263-2
DO - 10.1016/S2213-2600(19)30263-2
M3 - Review article
C2 - 31486393
AN - SCOPUS:85071569313
SN - 2213-2600
VL - 7
SP - 820
EP - 826
JO - The Lancet Respiratory Medicine
JF - The Lancet Respiratory Medicine
IS - 9
ER -