TY - JOUR
T1 - Resistance Trends and Treatment Options in Gram-Negative Ventilator-Associated Pneumonia
AU - Rhodes, Nathaniel J.
AU - Cruce, Caroline E.
AU - O’Donnell, J. Nicholas
AU - Wunderink, Richard G.
AU - Hauser, Alan R.
N1 - Funding Information:
Conflict of Interest NJR: discloses reciept of travel expenses and honoria from American Society of Healthsystem Pharmacists CC: no relevant disclosures JNO: no relevant disclosures RGW: discloses reciept of payment for continuing medical education from Medscape and consulting fees from Meiji-Seiko, Merck, Nabriva, Polyphor, Roche/Genetech, Shionogi, The Medicines Company, Accelerate Diagnostics, Curetis, and bioMerieux ARH: discloses board membership with Microbiotix, NIH grant funding, travel funds and expenses from Cystic Fibrosis Foundation and American Society of Microbiology, and consulting fees from MedImmune
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Purpose of Review: Hospital-acquired and ventilator-associated pneumonia (VAP) are frequent causes of infection among critically ill patients. VAP is the most common hospital-acquired bacterial infection among mechanically ventilated patients. Unfortunately, many of the nosocomial Gram-negative bacteria that cause VAP are increasingly difficult to treat. Additionally, the evolution and dissemination of multi- and pan-drug resistant strains leave clinicians with few treatment options. VAP patients represent a dynamic population at risk for antibiotic failure and under-dosing due to altered antibiotic pharmacokinetic parameters. Since few antibiotic agents have been approved within the last 15 years, and no new agents specifically targeting VAP have been approved to date, it is anticipated that this problem will worsen. Given the public health crisis posed by resistant Gram-negative bacteria, it is essential to establish a firm understanding of the current epidemiology of VAP, the changing trends in Gram-negative resistance in VAP, and the current issues in drug development for Gram-negative bacteria that cause VAP. Recent Findings: Rapid identification technologies and phenotypic methods, new therapeutic strategies, and novel treatment paradigms have evolved in an attempt to improve treatment outcomes for VAP; however, clinical data supporting alternative treatment strategies and adjunctive therapies remain sparse. Importantly, new classes of antimicrobials, novel virulence factor inhibitors, and beta-lactam/beta-lactamase inhibitor combinations are currently in development. Conscientious stewardship of new and emerging therapeutic agents will be needed to ensure they remain effective well into the future.
AB - Purpose of Review: Hospital-acquired and ventilator-associated pneumonia (VAP) are frequent causes of infection among critically ill patients. VAP is the most common hospital-acquired bacterial infection among mechanically ventilated patients. Unfortunately, many of the nosocomial Gram-negative bacteria that cause VAP are increasingly difficult to treat. Additionally, the evolution and dissemination of multi- and pan-drug resistant strains leave clinicians with few treatment options. VAP patients represent a dynamic population at risk for antibiotic failure and under-dosing due to altered antibiotic pharmacokinetic parameters. Since few antibiotic agents have been approved within the last 15 years, and no new agents specifically targeting VAP have been approved to date, it is anticipated that this problem will worsen. Given the public health crisis posed by resistant Gram-negative bacteria, it is essential to establish a firm understanding of the current epidemiology of VAP, the changing trends in Gram-negative resistance in VAP, and the current issues in drug development for Gram-negative bacteria that cause VAP. Recent Findings: Rapid identification technologies and phenotypic methods, new therapeutic strategies, and novel treatment paradigms have evolved in an attempt to improve treatment outcomes for VAP; however, clinical data supporting alternative treatment strategies and adjunctive therapies remain sparse. Importantly, new classes of antimicrobials, novel virulence factor inhibitors, and beta-lactam/beta-lactamase inhibitor combinations are currently in development. Conscientious stewardship of new and emerging therapeutic agents will be needed to ensure they remain effective well into the future.
KW - Antibacterial agents
KW - Drug development
KW - Gram-negative bacteria epidemiology
KW - Novel therapeutics
KW - Rapid diagnostic technologies
KW - Ventilator-associated pneumonia
UR - http://www.scopus.com/inward/record.url?scp=85043306635&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85043306635&partnerID=8YFLogxK
U2 - 10.1007/s11908-018-0609-x
DO - 10.1007/s11908-018-0609-x
M3 - Review article
C2 - 29511909
AN - SCOPUS:85043306635
VL - 20
JO - Current Infectious Disease Reports
JF - Current Infectious Disease Reports
SN - 1523-3847
IS - 2
M1 - 3
ER -