ACPHS Professor of Pharmacy Practice, TomÌýLodise, PharmD,Ìýexplains that Anti-MicrobialÌýResistance (AMR)Ìýthreatens the foundation of modern medicine, making once-routine infections increasingly difficult to treat.ÌýHeÌýwas by the Antibacterial Leadership Resistance Group as a Highly Ranked Scholar – Prior 5 Years, for his publications on vancomycin, as well as one of the top authors ever cited (putting him at the top two percent of cited authors historically) within Scopus, ‘s 36K-plus title database. Ìý
In honor of WHO’s World AMR Awareness Week, from November 18-24,Ìýwe asked Dr.ÌýLodiseÌýto talk to us about his research and how it aims to improve care for patients with AMR infections.Ìý
WhyÌýisÌýantimicrobial resistance a majorÌýhealthÌýthreat?
Antimicrobial resistance means the antibiotics we have depended on for decades are losing their power. Most infections are still treatable today, but each year more than 2.8 million resistant infections occur andÌýoverÌý35,000ÌýpeopleÌýdie as a result in the U.S., according to the CDC.ÌýÌý
About 30 percent of theÌýnearly 12Ìýmillion adults treated for infectionsÌýin hospitals, whether admitted with one or developing it during their stay, do not receive an active antibiotic within the first three days. Delays inÌýappropriate therapyÌýleadÌýto more complications,ÌýdeathsÌýand higher costs. Without effective antibiotics, the very foundation of modern medicine begins to crumble. Safe childbirth, organ transplants, jointÌýreplacementsÌýand cancer chemotherapy all depend on being able to prevent and treat infections. Losing antibiotics would set medicine back a century.Ìý
HowÌýdoÌýpharmacometrics,ÌýoutcomesÌýresearchÌýand epidemiology fit together?
Antimicrobial resistance threatens the foundation of modern medicine,ÌýmakingÌýroutine infections harder to treat. My research program brings together pharmacometrics, clinical outcomes research, and epidemiology to improve care for patients with resistant infections.ÌýÌý
The goal is to develop treatment strategies that are more personalized,ÌýsaferÌýand more effective while reducing drug toxicity and slowing the spread of resistance. Using advanced modeling, we study key processes of care such as how quickly patients receive the right therapy, how rapid diagnostics guide treatment, and how therapeutic drug monitoring improves outcomes. By linking how antibiotics move through the body with how they act against bacteria, we can define exposure levels that achieve cure without causing harm. This approach helps translate complex data into practical strategies that clinicians can use to deliver better care for patients today and preserve antibiotic effectiveness for the future.Ìý
WhatÌýhave youÌýlearned aboutÌýdosingÌýand exposure?
We have learned that getting the right amount ofÌýantibioticsÌýto the infection site at the right time can be the difference between success and failure. Too little drug allows infection and resistance to persist, while tooÌýmuchÌýincreases the risk of toxicity. EvenÌýsmall differencesÌýin kidney function or body size can dramatically alter antibiotic levels. Through modeling and simulation, we can predict these variations and individualize therapy. This approach allows us to ensure that every patient receives enough drug to cure the infection while minimizing the risk of harm.Ìý
How do you balanceÌýaggressive treatment with stewardship?
Clinicians face a constant challenge: treating infections strongly enough to save lives but not so broadly that it accelerates resistance. Our research provides data thatÌýhelpsÌýclinicians strike that balance.ÌýÌý
ByÌýidentifyingÌýoptimalÌýdosing, limiting unnecessary exposure, and using rapid diagnostics to target therapy, we can treat infections effectively while preserving the usefulness of antibiotics. Stewardship is not about restricting care; it is about using antibiotics wisely andÌýpreciselyÌýso they continue to work for the next patient who needs them.Ìý
What needs to change going forward?
We need to modernize how we discover, evaluate, and use antibiotics. ThisÌýmeans developing new drugs andÌýdiagnostics but also making smarter use of the ones we already have. Clinically, we must embrace individualized dosing, integrate real-time data into care decisions, and expand stewardship programs across health-care systems.ÌýÌý
On the policy side, we need sustained investment in research,ÌýsurveillanceÌýand public health infrastructure. If we bring science,ÌýpolicyÌýand clinical practice together, we can preserve the power of antibiotics and ensure that serious infectionsÌýremainÌýtreatable for generations to come.
Social