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dc.contributor.authorVaz, Clint
dc.contributor.authorJose, Nisha K.
dc.contributor.authorTom, Jeremiah J.
dc.contributor.authorGoodman, Georgia R.
dc.contributor.authorLee, Jasper S.
dc.contributor.authorPadappayil, Rana P.
dc.contributor.authorMadathil, Manjunath
dc.contributor.authorO’Cleirigh, Conall
dc.contributor.authorRodrigues, Rashmi
dc.contributor.authorChai, Peter R.
dc.date.accessioned2022-10-03T12:15:40Z
dc.date.available2022-10-03T12:15:40Z
dc.date.issued2022-09-28
dc.identifier.urihttps://hdl.handle.net/1721.1/145637
dc.description.abstractAbstract Background Tuberculosis (TB) represents a significant public health threat in India. Adherence to antitubercular therapy (ATT) is the key to reducing the burden of this infectious disease. Suboptimal adherence to ATT and lack of demonstrated feasibility of current strategies for monitoring ATT adherence highlights the need for alternative adherence monitoring systems. Methods A quantitative survey was conducted to assess the acceptance of and willingness to use a digital pill system (DPS) as a tool for monitoring ATT adherence among stakeholders directly involved in the management of patients with TB in India. Participants reviewed a video explaining the DPS and completed a survey, which covered sociodemographics, degree of involvement with TB patients, initial impressions of the DPS, and perceived challenges for deploying the technology in India. Participants were also asked to interpret mock DPS adherence data. Results The mean age was 34.3 (SD = 7.3), and participants (N = 50) were predominantly male (70%). The sample comprised internists (52%) and pulmonologists (30%), with a median of 4 years’ experience (IQR 3, 6) in the management of TB patients. No participants had previously used a DPS, but some reported prior awareness of the technology (22%). Most reported that they would recommend use of a DPS to patients on ATT (76%), and that they would use a DPS in both the intensive and continuation phases of TB management (64%). The majority viewed the DPS (82%) as a useful alternative to directly observed therapy-short course (DOTS), particularly given the ongoing COVID-19 pandemic. Participants reported that a DPS would be most effective in patients at risk of nonadherence (64%), as well as those with past nonadherence (64%). Perceived barriers to DPS implementation included lack of patient willingness (92%), cost (86%), and infrastructure constraints (66%). The majority of participants were able to accurately interpret patterns of adherence (80%), suboptimal adherence (90%), and frank nonadherence (82%) when provided with mock DPS data. Conclusions DPS are viewed as an acceptable, feasible, and useful technology for monitoring ATT adherence by stakeholders directly involved in TB management. Future investigations should explore patient acceptance of DPS and pilot demonstration of the system in the TB context.en_US
dc.publisherBioMed Centralen_US
dc.relation.isversionofhttps://doi.org/10.1186/s12879-022-07756-xen_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceBioMed Centralen_US
dc.titleFormative acceptance of ingestible biosensors to measure adherence to TB medicationsen_US
dc.typeArticleen_US
dc.identifier.citationBMC Infectious Diseases. 2022 Sep 28;22(1):754en_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.identifier.mitlicensePUBLISHER_CC
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-10-02T03:14:46Z
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dspace.date.submission2022-10-02T03:14:46Z
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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