Show simple item record

dc.contributor.authorBerges, Alexandra J.
dc.contributor.authorCallanan, Megan
dc.contributor.authorZawicki, Valerie
dc.contributor.authorShi, Richard
dc.contributor.authorAthey, Thomas
dc.contributor.authorAyyappan, Vinay
dc.contributor.authorMetzger, Schuyler
dc.contributor.authorFarrell, Alanna
dc.contributor.authorManbachi, Amir
dc.contributor.authorHarvey, Susan
dc.contributor.authorDurr, Nicholas J.
dc.date.accessioned2022-02-04T14:44:07Z
dc.date.available2022-02-04T14:44:07Z
dc.date.copyright2020/02/05/
dc.date.issued2020
dc.identifier.issn1932-6181
dc.identifier.othermed_014_01_011107.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4274262
dc.description.abstractOne barrier to breast cancer diagnosis in low-resource settings is that devices for core needle biopsy (CNB) are either disposable and expensive, or reusable and susceptible to internal contamination. Through interviews with field workers and verification experiments, we identified that a common, commercially available, reusable CNB device allows contaminants to enter the driver chamber during firing, necessitating laborious cleaning of the entire device after every use. We introduce a novel CNB device attachment that eliminates this contamination mode and interfaces with existing commercial reusable drivers and low-cost disposable needles. This attachment repositions the driver–needle connection to the exterior of the driver, preventing retrograde flow of blood. Using an unmodified commercial CNB, we replicate chamber contamination by firing into a body fluid-mimicking glycerol solution. Prototypes were tested for their performance in eliminating this contamination. We tested the effectiveness of a cleaning procedure to reduce trace contamination by using a fluorescent dye and measuring the intensity of fluorescence after cleaning. The device's ability to reliably and consistently biopsy tissue with the novel attachment was evaluated using breast tissue models. In these tests, a reusable CNB with our attachment exhibited no measurable internal contamination, and maintained full biopsy functionality as measured by tissue sample weight and length. Minimizing internal device contamination would simplify the cleaning process for reusable biopsy devices. This would improve the accessibility of breast cancer biopsies in low- and middle-income countries (LMICs).
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleA Novel Intermediate Attachment to Reduce Contamination in Reusable Core Needle Biopsy Devices
dc.typeJournal Paper
dc.journal.volume14
dc.journal.issue1
dc.journal.titleJournal of Medical Devices
dc.identifier.doi10.1115/1.4045967
dc.page11107
dc.treeJournal of Medical Devices:;2020:;volume( 014 ):;issue: 001
dc.contenttypeFulltext


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record