TY - JOUR
T1 - Clinical epidemiology of the global expansion of Klebsiella pneumoniae carbapenemases
AU - Munoz-Price, L. Silvia
AU - Poirel, Laurent
AU - Bonomo, Robert A.
AU - Schwaber, Mitchell J.
AU - Daikos, George L.
AU - Cormican, Martin
AU - Cornaglia, Giuseppe
AU - Garau, Javier
AU - Gniadkowski, Marek
AU - Hayden, Mary K.
AU - Kumarasamy, Karthikeyan
AU - Livermore, David M.
AU - Maya, Juan J.
AU - Nordmann, Patrice
AU - Patel, Jean B.
AU - Paterson, David L.
AU - Pitout, Johann
AU - Villegas, Maria Virginia
AU - Wang, Hui
AU - Woodford, Neil
AU - Quinn, John P.
PY - 2013/9
Y1 - 2013/9
N2 - Klebsiella pneumoniae carbapenemases (KPCs) were originally identified in the USA in 1996. Since then, these versatile β-lactamases have spread internationally among Gram-negative bacteria, especially K pneumoniae, although their precise epidemiology is diverse across countries and regions. The mortality described among patients infected with organisms positive for KPC is high, perhaps as a result of the limited antibiotic options remaining (often colistin, tigecycline, or aminoglycosides). Triple drug combinations using colistin, tigecycline, and imipenem have recently been associated with improved survival among patients with bacteraemia. In this Review, we summarise the epidemiology of KPCs across continents, and discuss issues around detection, present antibiotic options and those in development, treatment outcome and mortality, and infection control. In view of the limitations of present treatments and the paucity of new drugs in the pipeline, infection control must be our primary defence for now.
AB - Klebsiella pneumoniae carbapenemases (KPCs) were originally identified in the USA in 1996. Since then, these versatile β-lactamases have spread internationally among Gram-negative bacteria, especially K pneumoniae, although their precise epidemiology is diverse across countries and regions. The mortality described among patients infected with organisms positive for KPC is high, perhaps as a result of the limited antibiotic options remaining (often colistin, tigecycline, or aminoglycosides). Triple drug combinations using colistin, tigecycline, and imipenem have recently been associated with improved survival among patients with bacteraemia. In this Review, we summarise the epidemiology of KPCs across continents, and discuss issues around detection, present antibiotic options and those in development, treatment outcome and mortality, and infection control. In view of the limitations of present treatments and the paucity of new drugs in the pipeline, infection control must be our primary defence for now.
UR - http://www.scopus.com/inward/record.url?scp=84882712084&partnerID=8YFLogxK
U2 - 10.1016/S1473-3099(13)70190-7
DO - 10.1016/S1473-3099(13)70190-7
M3 - Review article
C2 - 23969216
AN - SCOPUS:84882712084
SN - 1473-3099
VL - 13
SP - 785
EP - 796
JO - Lancet Infectious Diseases
JF - Lancet Infectious Diseases
IS - 9
ER -