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dc.contributor.authorFoster, Carolyn C.
dc.contributor.authorZapotoczny, Grzegorz
dc.contributor.authorJoseph, Francesca D.
dc.contributor.authorFinkel, Julia C.
dc.contributor.authorHoyen, Claudia M.
dc.contributor.authorEskandanian, Kolaleh
dc.contributor.authorEspinoza, Juan
dc.date.accessioned2026-08-23T07:47:13Z
dc.date.available2026-08-23T07:47:13Z
dc.date.copyright2026/10/01
dc.date.issued2026
dc.identifier.issn1932-6181
dc.identifier.othermed-25-1188.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4315604
dc.description.abstractAbstract. The COVID-19 pandemic revealed major gaps in the design, manufacturing, planning, and procurement of medical countermeasures (MCMs). Of ongoing concern is the existing shortage of Food and Drug Administration (FDA)-regulated device MCMs needed for children disaster medical response involving acute and chronic illness. Planning for and prioritizing manufacturing, stockpiling, and tracking pediatric MCMs availability are especially necessary given existing device deficits and differences in pediatric physiology and epidemiology. In this paper, we justify why a pediatric-specific lens is needed when planning and prioritizing medical device MCMs. We also analyze the current landscape of pediatric MCM devices across phases and levels of care in relation to adult products to include protective equipment, diagnostic platforms, monitoring tools, interventional devices, and life-sustaining technologies.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titlePriorities in Planning Pediatric Medical Device Countermeasures
dc.typeJournal Paper
dc.journal.volume20
dc.journal.issue5
dc.journal.titleJournal of Medical Devices
dc.identifier.doi10.1115/1.4071876
dc.journal.fristpage300
dc.journal.lastpage301
dc.page2
dc.treeJournal of Medical Devices:;2026:;volume( 020 ):;issue:005
dc.contenttypeFulltext


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