Dutch study find MCR-1 gene in a quarter of retail chicken meat samples
Dutch investigators have identified the colistin resistance gene MCR-1 in nearly 25% of samples of Dutch retail chicken meat, according to a new study in Antimicrobial Resistance and Infection Control.
For the study, the investigators bought 214 chicken meat samples from four supermarket chains throughout the Netherlands in 2015. They collected 53 or 54 samples from each chain.
Using polymerase chain reaction testing, the investigators detected the presence of the MCR-1 gene in 24.8% of the samples (53 of 214), then confirmed the presence of the gene in 34 of these 53 samples (64.2%) using a selective culture method. No MCR-2 genes were detected. Of the 34 MCR-1–positive isolates, 32 were Escherichia coli and 2 were Klebsiella pneumoniae. In addition to colistin, the 34 isolates showed high levels of resistance to ampicillin (100%), amoxicillin-clavulanic acid (89%), trimethoprim/sulfamethoxazole (69%), and ciprofloxacin (57%).
Multivariable regression analysis showed that chicken samples that were non-free-range (adjusted odds ratio [aOR], 3.0) and were purchased at supermarket chains C (aOR, 34.6) or D (aOR, 37.5) were more likely contain the MCR-1 gene. The large variation between supermarket chains could not be explained with the available information.
In previous studies of MCR-1 in food, researchers found the gene in 28% of Chinese poultry samples and in 19.5% of E coli isolates from South American chicken meat.
Although colistin and other polymixins are used at very low levels in the Netherlands and the MCR-1 gene has been found only sporadically in Dutch patients, the authors of the study say the findings warrant further studies on the underlying mechanisms of spread. "Moreover, continued monitoring of the potential reservoirs for this plasmid-mediated colistin resistance is of utmost importance," they write.
Aug 18 Antimicrob Resist Infect Control study
Survey finds varied antibiotic prescribing practices in pediatric residents
A survey of 85 pediatric residents at two US hospitals found considerable variation among antibiotic prescribing for pneumonia, sinusitis, and other conditions, with three-fourths having prescribed antibiotics for viral infections, according to a study last week in Hospital Pediatrics.
Among the residents surveyed at Children's National Medical Center in Washington, DC, and Nicklaus Children's Hospital in Miami, only 12% ranked an infectious disease specialist as one of their top three influential sources for antibiotic choice.
Seventy-five percent of respondents said they had prescribed antibiotics for patients they considered to have a viral infection. When asked to identify reasons for prescribing, 63% said they were following instructions from a more senior physician, 21% had concerns of a bacterial infection developing in the future, and 16% cited pressure from patients' parents.
Greater deviation from clinical guidelines was found for antibiotic treatment of sinusitis and community-acquired pneumonia compared with otitis media and streptococcal pharyngitis.
When asked about antibiograms, 54% said they sometimes used one, 25% had never referred to one, and 17% didn't know what an antibiogram was or didn't respond. Half of respondents didn't know how to access their hospital-specific antibiogram, which is a profile of antimicrobial susceptibility testing results for a single pathogen. Just 3% used the profiles very frequently.
The authors conclude, "Results illustrate the need for better promotion and integration of clinical guidelines with antibiograms when developing antibiotic education programs for residents in training. In addition, pediatric hospitalists should play an active role in the implementation of these programs."
Aug 16 Hosp Pediatr study
Patient trial for new antimalarial compound launches in Mali
Drugmaker Novartis and Medicines for Malaria Venture (MMV) today launched a patient trial in Mali for an antimalarial compound with the potential to treat drug-resistant strains of the parasite, according to a company press release.
The trial will test the efficacy of KAF156, which belongs to a novel class of antimalarial compounds called imidazolopiperazines, in combination with an improved formulation of the existing antimalarial lumefantrine. The phase 2b study will test multiple dosing combinations and dosing schedules of the drugs, including the feasibility of single-dose therapy in adults, adolescents, and children.
With resistance and reduced sensitivity to artemisinin and artemisinin-based combination therapies emerging in parts of Asia and more recently in Africa, next-generation antimalarials are urgently needed.
"To build on the gains made against malaria since the turn of the century, we need new medicines that are effective across all types of resistance patterns and geographies, and that are easy to administer, especially to children," David Reddy, PhD, chief executive officer of MMV, said in the release.
The first trial center is already operational in Mali and will be followed by trials in 16 additional centers in nine countries in Africa and Asia.
Novartis is developing KAF156 with scientific and financial support from MMV and the Bill and Melinda Gates Foundation.
Aug 21 Novartis press release
Non-carbapenems could be good option for bloodstream infections
European researchers report in Clinical Infectious Diseases that empiric treatment of bloodstream infections (BSIs) caused by extended-spectrum beta-lactamase–producing Enterobacteriaceae (ESBL-E) with drugs other than carbapenems is not associated with worse outcomes.
While carbapenems are generally considered to be the drug of choice for treating serious infections caused by ESBL-E, their use has substantially increased in recent years, and there is concern that the increase is contributing to the spread of carbapenem resistance. Some recent data have indicated that beta-lactam/beta-lactamase inhibitor combinations are an alternative, but there are few data on other antimicrobials. Alternative agents with potential efficacy could provide more treatment options.
As part of a larger multinational retrospective cohort study on BSIs caused by ESBL-E, researchers set out to assess the impact of empiric therapy with other active drugs (OADs) compared with carbapenem treatment. The main outcome was 30-day all-cause mortality. Secondary outcomes were clinical failure at day 14 and length of hospital stay after BSI. The hypothesis was that treatment with OADs would be associated with higher mortality and lower cure rates.
Overall, 335 patients with BSI due to ESBL-E were included in the study; 249 were treated empirically with a carbapenem and 86 with OADs. The most frequent OADs used were aminoglycosides (43 patients) and fluoroquinolones (20 patients). The most frequent carbapenems used were meropenem (141 patients), imipenem (61 patients), and ertapenem (46 patients.
After controlling for confounders, the researchers found that empiric therapy with OADs was not associated with greater 30-day mortality (hazard ratio [HR], 0.75) or with clinical failure at day 14 (adjusted odds ratio, 0.62). In patients discharged alive, the median length of stay was 16 days for patients treated with carbapenems and 14 days for patients treated with OADs; linear regression analysis after adjusting for propensity score showed no significant association between empiric OAD therapy and length of stay (P = .26).
The authors conclude that while the results cannot be interpreted as indicating that OADs and carbapenems are equally effective because of the limited statistical power of the study, the findings suggest OADs might be an option for empiric regimens for some BSI patients, depending on local susceptibility patterns.
Aug 19 Clin Infect Dis study