English health officials unveil strategy to contain CPE in hospitals
Public Health England (PHE) yesterday published a draft framework for healthcare providers on how to contain the spread of carbapenemase-producing Enterobacteriaceae (CPE) in hospitals.
Among the measures recommended is active screening for CPE among risk groups to minimize transmission from CPE-positive patients and reduce the risk that colonized patients will develop clinical infections. The document says that hospitals will need to develop their own risk assessment based on regional prevalence, patient mix, and connections to other healthcare providers. But it encourages screening for patients who have been previously identified as CPE-positive, been an inpatient in any hospital (both in the United Kingdom and abroad), had multiple hospital treatments, had known epidemiologic links to a CPE carrier, or been admitted to high-risk hospital units.
The framework also calls for appropriate surveillance systems to rapidly detect and monitor patients infected or colonized with CPE and hospital outbreaks, implementation of infection prevention and control practices, thorough environmental cleaning and decontamination processes to reduce CPE reservoirs, antimicrobial stewardship programs to reduce use of broad-spectrum antibiotics, optimized laboratory methods to detect carbapenemase-producing organisms, and support from hospital leadership.
"Unless action is taken, learning from experiences elsewhere in the world, rapid spread of CPE will pose an ever-increasing threat to public health and medical treatment pathways in the UK," the document states.
PHE says the framework is based on new evidence from the past 5 years, but it notes that the evidence base for some of the recommendations is limited. The comment period for the draft framework is open until Feb 14.
Jan 7 PHE draft framework
New strain of hypervirulent, carbapenem-resistant Klebsiella in China
An analysis of bloodstream infections caused by carbapenem-resistant Klebsiella pneumoniae (CRKP) in China has identified the emergence of a high-risk subclone of the most dominant CRKP clone in Asia, an international teams of researchers reported yesterday in Emerging Infectious Diseases.
The analysis of 203 CRKP isolates collected from patients with bloodstream infections at a Chinese hospital from January 2013 through June 2017 found that 174 (85.7%) belonged to sequence type (ST11), a clone that accounts for 60% of CRKP infections in Asia.
Whole-genome sequencing (WGS) further revealed the prevalence of two capsular types (KLs) among the ST11 isolates—KL47 and KL46—and showed that the ratio of KL47 to KL46 had decreased substantially during the study period, with KL46 becoming more prevalent over the 4 years. Analysis of 162 infected patients showed that patients with ST11-KL46 had significantly higher mortality rates than those with ST11-KL47 (62.2% vs 52.8%) and those with non-ST11 CRKP (62.2% vs 48.8%). The researchers suggest capsular switching in the ST11 population might contribute to the increased mortality.
WGS also revealed the presence of the virulence genes rmpA and rmpA2 in the ST11-KL46 isolates, and phenotypic tests demonstrated enhanced virulence. Phylogenetic reconstruction showed that ST11-KL46 may have emerged from an ST11-K47–like ancestor in 2011 through recombination events.
"In summary, our study identified the emergence of a high-risk subclone of CRKP-ST11, resulting in enhanced virulence and transmissibility," the authors write. "The newly emerging descendant obtained enhanced environmental survival and poses a substantial threat to healthcare networks, suggesting the urgent need for tailor-made surveillance and stricter infection-control measures to prevent further dissemination in nosocomial settings."
Jan 7 Emerg Infect Dis study
CARB-X funds research on new drug class targeting resistant bacteria
CARB-X today said it has awarded TAXIS Pharmaceuticals of Mammoth Junction, New Jersey, up to $3.2 million to develop efflux pump inhibitors (EPIs), a new drug class designed to destroy a major mechanism of multidrug-resistant (MDR) Pseudomonas aeruginosa bacteria.
"Pseudomonas aeruginosa is an intrinsically resistant pathogen, with a nearly impermeable outer membrane and with the ability to turn on many efflux pumps to eject antibiotics that make it through," Erin Duffy, PhD, chief of research and development at CARB-X, which is based at Boston University, said in a CARB-X news release. "The TAXIS project is in the early stages of development but if successful, it would potentially be a leap forward in combating drug-resistance mechanisms and restoring the utility of many existing antibiotics."
TAXIS is eligible for up to $11.4 million in addition funding if the company achieves certain milestones. The EPIs it is developing are designed to disable P aeruginosa efflux pumps, which flush out antibiotics from the cell to protect the MDR bacteria from the drugs. TAXIS researchers are focusing on hospital-acquired and ventilator-related infections.
Greg Mario, MBA, CEO of TAXIS Pharmaceuticals, said, "This new drug class is designed to enable the reuse of existing generic antibiotics by addressing an elemental form of drug resistance."
Since it began in 2016, CARB-X (the Combating Antibiotic-Resistant Bacteria Biopharmaceutical Accelerator), a public-private partnership, has announced 54 awards of more than $179 million total. It plans to invest $500 million for promising approaches to combat antibiotic resistance by the end of next year.
Jan 8 CARB-X news release