“It’s difficult to know for certain if the adverse events were directly associated with the biologic infusion,” says Gregory Calip, PharmD, MPH, PhD, a senior quantitative scientist at Flatiron Health, New York, and co-author of a commentary accompanying the study.2
Other factors—such as access to urgent care, co-medications and ability to monitor for mild infusion reactions that may not necessarily require emergency department or hospital visits if administered at a facility—could all affect the likelihood of patients seeking acute care, Dr. Calip says by email.
“It is possible that some adverse events occurring at a facility that has resources to immediately address them are resolved early, without the need for an emergency department visit or hospitalization,” Dr. Calip adds.
References
- Baker MC, Weng Y, Fairchild R, et al. Comparison of adverse events among home- vs facility-administered biologic infusions, 2007–2017. JAMA Netw Open. 2021 Jun 1;4(6):e2110268.
- Calip GS, Yerram P, Ascha MS. Nonrandomized comparison of adverse events following facility- and home-infused biologics using real-world data. JAMA Netw Open. 2021 Jun 1;4(6):e2111156.