Report: Carbapenemase-producing Enterobacterales rose in Latin America
A report today in Emerging Infectious Diseases highlights increased detection of carbapenemase-producing Enterobacterales (CPE) in Latin America and the Caribbean during the COVID-19 pandemic.
The report, by researchers with the Pan American Health Organization and several national laboratories in the region, notes that while several countries had reported detection of CPE prior to the pandemic, detection of Enterobacterales harboring multiple carbapenemase genes was limited.
But during the pandemic, national laboratories in Argentina, Brazil, Colombia, Guatemala, Paraguay, Peru, Uruguay, Venezuela, Ecuador, and Costa Rica reported the emergence or increased detection of carbapenemase combinations—mainly the carbapenemase genes blaKPC and blaNDM—while Belize, Dominica, and Chile reported the emergence of carbapenemase genes that had not previously been detected.
Among the countries reporting increased CPE detection, Colombia reported more than twice the number of CPE strains from January 2020 through December 2021 compared with 2018-2019, while data from hospitals in five Brazilian states showed a 42.8% increase in CPE isolates during the pandemic (March 2020 to October 2021) compared with 20 months before.
The authors say that the reported increases in CPE detection during the pandemic were likely caused by a variety of pandemic-related factors.
"The pandemic might have accelerated the problem of resistance to the limited antimicrobial arsenal in the region because of antimicrobial drug misuse, prolonged hospital stays, and a high rate of antimicrobial prescriptions in hospital settings, such as medical wards and ICUs, where a high number of patients with COVID-19 were hospitalized during the first pandemic wave," they write.
They also point out that many countries in the region do not have access to the newly developed antibiotics for treating the multidrug-resistant infections caused by CPE, which has resulted in increased use of last-resort antibiotics like polymyxins.
They conclude, "In an ideal scenario, access to newly developed and approved antimicrobials and tools to guide their prudent use should be guaranteed for the entire world in parallel with current local AMR [antimicrobial resistance] prevention and control strategies, including the prioritization of antimicrobial stewardship and rapid AMR detection."
Oct 12 Emerg Infect Dis report
Non-preferred antibiotics often used for urinary infections at VA hospitals
A study of Veterans Affairs (VA) medical centers found that clinicians prescribed the preferred antibiotic for patients with positive urine cultures less than half of the time, researchers reported today in Antimicrobial Stewardship & Healthcare Epidemiology.
For the study, which aimed to analyze how urinary tract infection management can be improved in VA outpatients, VA researchers extracted data on positive urine cultures collected at 31 VA medical centers from 2016 through 2019.
Cases were classified as cystitis, pyelonephritis, or asymptomatic bacteriuria (ASB) based on documented signs and symptoms, and preferred therapy definitions were applied for each subdiagnosis: ASB (no antibiotics), cystitis (trimethoprim-sulfamethoxazole, nitrofurantoin, and beta-lactams), and pyelonephritis (trimethoprim-sulfamethoxazole and fluoroquinolone). The researchers assessed whether preferred antibiotics were chosen for each subdiagnosis and whether the duration was appropriate. Outcomes included 30-day clinical failure or hospitalization.
Of 3,255 cases reviewed, ASB was identified in 1,628 cases (50%), cystitis was identified in 1,156 cases (36%), and pyelonephritis was identified in 471 cases (15%). Antibiotics were prescribed in 43% of these cases, including 40% with ASB. Of 2,831 cases analyzed, 1,298 (46%) received the preferred therapy selection and duration for cases where it could be defined. The most common antibiotic class prescribed was fluoroquinolones (34%).
Patients prescribed preferred therapy had lower odds of clinical failure than those who received non-preferred therapy (8% vs 10%; unadjusted odds ratio [OR], 0.74; 95% confidence interval [CI], 0.58 to 0.95). They also had lower odds of 30-day hospitalization (3% vs 5%; unadjusted OR, 0.55; 95% CI, 0.37 to 0.81). Odds of clinical treatment failure or hospitalization were higher for beta-lactams relative to ciprofloxacin (unadjusted OR, 1.89; 95% CI, 1.23 to 2.90).
"These findings suggest clinicians could benefit from educational and interventional strategies that target appropriate selection and duration of therapy," the study authors concluded.
Oct 12 Antimicrob Steward Healthc Epidemiology study