TY - JOUR
T1 - Discovery, research, and development of new antibiotics
T2 - the WHO priority list of antibiotic-resistant bacteria and tuberculosis
AU - WHO Pathogens Priority List Working Group
AU - Tacconelli, Evelina
AU - Carrara, Elena
AU - Savoldi, Alessia
AU - Harbarth, Stephan
AU - Mendelson, Marc
AU - Monnet, Dominique L.
AU - Pulcini, Céline
AU - Kahlmeter, Gunnar
AU - Kluytmans, Jan
AU - Carmeli, Yehuda
AU - Ouellette, Marc
AU - Outterson, Kevin
AU - Patel, Jean
AU - Cavaleri, Marco
AU - Cox, Edward M.
AU - Houchens, Chris R.
AU - Grayson, M. Lindsay
AU - Hansen, Paul
AU - Singh, Nalini
AU - Theuretzbacher, Ursula
AU - Magrini, Nicola
AU - Aboderin, Aaron Oladipo
AU - Al-Abri, Seif Salem
AU - Awang Jalil, Nordiah
AU - Benzonana, Nur
AU - Bhattacharya, Sanjay
AU - Brink, Adrian John
AU - Burkert, Francesco Robert
AU - Cars, Otto
AU - Cornaglia, Giuseppe
AU - Dyar, Oliver James
AU - Friedrich, Alex W.
AU - Gales, Ana C.
AU - Gandra, Sumanth
AU - Giske, Christian Georg
AU - Goff, Debra A.
AU - Goossens, Herman
AU - Gottlieb, Thomas
AU - Guzman Blanco, Manuel
AU - Hryniewicz, Waleria
AU - Kattula, Deepthi
AU - Jinks, Timothy
AU - Kanj, Souha S.
AU - Kerr, Lawrence
AU - Kieny, Marie Paule
AU - Kim, Yang Soo
AU - Kozlov, Roman S.
AU - Labarca, Jaime
AU - Laxminarayan, Ramanan
AU - Leder, Karin
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/3
Y1 - 2018/3
N2 - Background: The spread of antibiotic-resistant bacteria poses a substantial threat to morbidity and mortality worldwide. Due to its large public health and societal implications, multidrug-resistant tuberculosis has been long regarded by WHO as a global priority for investment in new drugs. In 2016, WHO was requested by member states to create a priority list of other antibiotic-resistant bacteria to support research and development of effective drugs. Methods: We used a multicriteria decision analysis method to prioritise antibiotic-resistant bacteria; this method involved the identification of relevant criteria to assess priority against which each antibiotic-resistant bacterium was rated. The final priority ranking of the antibiotic-resistant bacteria was established after a preference-based survey was used to obtain expert weighting of criteria. Findings: We selected 20 bacterial species with 25 patterns of acquired resistance and ten criteria to assess priority: mortality, health-care burden, community burden, prevalence of resistance, 10-year trend of resistance, transmissibility, preventability in the community setting, preventability in the health-care setting, treatability, and pipeline. We stratified the priority list into three tiers (critical, high, and medium priority), using the 33rd percentile of the bacterium's total scores as the cutoff. Critical-priority bacteria included carbapenem-resistant Acinetobacter baumannii and Pseudomonas aeruginosa, and carbapenem-resistant and third-generation cephalosporin-resistant Enterobacteriaceae. The highest ranked Gram-positive bacteria (high priority) were vancomycin-resistant Enterococcus faecium and meticillin-resistant Staphylococcus aureus. Of the bacteria typically responsible for community-acquired infections, clarithromycin-resistant Helicobacter pylori, and fluoroquinolone-resistant Campylobacter spp, Neisseria gonorrhoeae, and Salmonella typhi were included in the high-priority tier. Interpretation: Future development strategies should focus on antibiotics that are active against multidrug-resistant tuberculosis and Gram-negative bacteria. The global strategy should include antibiotic-resistant bacteria responsible for community-acquired infections such as Salmonella spp, Campylobacter spp, N gonorrhoeae, and H pylori. Funding: World Health Organization.
AB - Background: The spread of antibiotic-resistant bacteria poses a substantial threat to morbidity and mortality worldwide. Due to its large public health and societal implications, multidrug-resistant tuberculosis has been long regarded by WHO as a global priority for investment in new drugs. In 2016, WHO was requested by member states to create a priority list of other antibiotic-resistant bacteria to support research and development of effective drugs. Methods: We used a multicriteria decision analysis method to prioritise antibiotic-resistant bacteria; this method involved the identification of relevant criteria to assess priority against which each antibiotic-resistant bacterium was rated. The final priority ranking of the antibiotic-resistant bacteria was established after a preference-based survey was used to obtain expert weighting of criteria. Findings: We selected 20 bacterial species with 25 patterns of acquired resistance and ten criteria to assess priority: mortality, health-care burden, community burden, prevalence of resistance, 10-year trend of resistance, transmissibility, preventability in the community setting, preventability in the health-care setting, treatability, and pipeline. We stratified the priority list into three tiers (critical, high, and medium priority), using the 33rd percentile of the bacterium's total scores as the cutoff. Critical-priority bacteria included carbapenem-resistant Acinetobacter baumannii and Pseudomonas aeruginosa, and carbapenem-resistant and third-generation cephalosporin-resistant Enterobacteriaceae. The highest ranked Gram-positive bacteria (high priority) were vancomycin-resistant Enterococcus faecium and meticillin-resistant Staphylococcus aureus. Of the bacteria typically responsible for community-acquired infections, clarithromycin-resistant Helicobacter pylori, and fluoroquinolone-resistant Campylobacter spp, Neisseria gonorrhoeae, and Salmonella typhi were included in the high-priority tier. Interpretation: Future development strategies should focus on antibiotics that are active against multidrug-resistant tuberculosis and Gram-negative bacteria. The global strategy should include antibiotic-resistant bacteria responsible for community-acquired infections such as Salmonella spp, Campylobacter spp, N gonorrhoeae, and H pylori. Funding: World Health Organization.
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U2 - 10.1016/S1473-3099(17)30753-3
DO - 10.1016/S1473-3099(17)30753-3
M3 - Article
C2 - 29276051
AN - SCOPUS:85038810538
SN - 1473-3099
VL - 18
SP - 318
EP - 327
JO - The Lancet Infectious Diseases
JF - The Lancet Infectious Diseases
IS - 3
ER -