Release Date: March 8, 2019
BUFFALO, N.Y. — An international panel of the foremost researchers on infectious disease and antimicrobials has formed new guidelines on the use of polymyxins, a class of antibiotics employed as a last resort to treat deadly, drug-resistant bacteria.
The guidelines, published last month in Pharmacotherapy, set new standards for the clinical use of polymyxins, including on maximum dosage, treatment strategies and best practice for use in combination with other antibiotics.
The recommendations have been endorsed worldwide by six international societies and organizations across the globe: American College of Clinical Pharmacy, European Society of Clinical Microbiology and Infectious Diseases, Infectious Diseases Society of America, International Society for Anti-infective Pharmacology, Society of Critical Care Medicine and Society of Infectious Diseases Pharmacists.
The expert panel was co-led by Brian Tsuji, PharmD, professor of pharmacy practice in the University at Buffalo School of Pharmacy and Pharmaceutical Sciences; Jason Pogue, PharmD, clinical pharmacist specialist at the Detroit Medical Center; and Keith Kaye, MD, professor of infectious disease and internal medicine in the University of Michigan Medical School.
“There is considerable confusion on how to optimally use the polymyxin antibiotics,” said Tsuji.
“These guidelines represent consensus recommendations from expert clinicians and scientists around the globe to guide polymyxin therapy in Gram-negative infections where no treatments appear to exist.”
First introduced in the 1950s, polymyxins are an older generation of antibiotics that fell out of favor due to their toxicity to the kidneys. However, the drug was recently resurrected by researchers and clinicians to aid in the fight against increasingly antibiotic-resistant bacteria, more commonly known as superbugs.
But while polymyxins have made a comeback, the clinical standards that guide its use are outdated. Variations in conventions used to describe doses, differing formulations and dated product information have led to confusion on how to best use and dose the drug.
The recent publication provides clinicians with 34 recommendations for using polymyxin B and colistin – also known as polymyxin E. Highlights from the paper include:
The panel recommended several areas of research needed in the future, including studies that compare the effectiveness and toxicity of polymyxin B and colistin, investigate biomarkers that rapidly respond to kidney damage to better detect the adverse effects of polymyxins, weigh the risks and benefits of curing infection at the expense of kidney damage, and measure the effectiveness of various combination therapies.