Changes in Informed Consent Policy and Treatment Delays in Stroke Thrombolysis.
dc.contributor.author | Xu, Hanzhang | |
dc.contributor.author | De Silva, Deidre Anne | |
dc.contributor.author | Woon, Fung Peng | |
dc.contributor.author | Ong, Marcus Eng Hock | |
dc.contributor.author | Matchar, David B | |
dc.contributor.author | Bettger, Janet Prvu | |
dc.contributor.author | Laskowitz, Daniel T | |
dc.contributor.author | Xian, Ying | |
dc.date.accessioned | 2021-05-05T05:42:32Z | |
dc.date.available | 2021-05-05T05:42:32Z | |
dc.date.issued | 2020-12-18 | |
dc.date.updated | 2021-05-05T05:42:29Z | |
dc.description.abstract | ObjectivesThe efficacy of thrombolytic therapy with tissue plasminogen activator (tPA) is highly time dependent. Although clinical guidelines do not recommend written informed consent as it may cause treatment delays, local policy can supersede and require it. From 2014 to 2017, three out of five public hospitals in Singapore changed from written to verbal consent at different time points. We aimed to examine the association of hospital policy changes regarding informed consent on door-to-needle (DTN) times.Materials and methodsUsing data from the Singapore Stroke Registry and surveys of local practice, we analyzed data of 915 acute ischemic stroke patients treated with tPA within 3 hours in all public hospitals between July 2014 to Dec 2017. Patient-level DTN times before and after policy changes were examined while adjusting for clinical characteristics, within-hospital clustering, and trends over time.ResultsPatient characteristics and stroke severity were similar before and after the policy changes. Overall, the median DTN times decreased from 68 to 53 minutes after the policy changes. After risk adjustment, changing from written to verbal informed consent was associated with a 5.6 minutes reduction (95% CI 1.1-10.0) in DTN times. After the policy changed, the percentage of patients with DTN ≤60 minutes and ≤45 minutes increased from 35.6% to 66.1% (adjusted OR 1.75; 95% CI 1.12-2.74) and 9.3% to 36.0% (adjusted OR 2.42; 95% CI 1.37-4.25), respectively.ConclusionChanging from written to verbal consent is associated with significant improvement in the timeliness of tPA administration in acute ischemic stroke. | |
dc.identifier | S1052-3057(20)30969-1 | |
dc.identifier.issn | 1052-3057 | |
dc.identifier.issn | 1532-8511 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Elsevier BV | |
dc.relation.ispartof | Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association | |
dc.relation.isversionof | 10.1016/j.jstrokecerebrovasdis.2020.105551 | |
dc.subject | Informed consent | |
dc.subject | Registry | |
dc.subject | Singapore | |
dc.subject | Stroke | |
dc.subject | Thrombolysis | |
dc.subject | Aged | |
dc.subject | Female | |
dc.subject | Fibrinolytic Agents | |
dc.subject | Hospitals, Public | |
dc.subject | Humans | |
dc.subject | Informed Consent | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Policy Making | |
dc.subject | Registries | |
dc.subject | Retrospective Studies | |
dc.subject | Singapore | |
dc.subject | Stroke | |
dc.subject | Thrombolytic Therapy | |
dc.subject | Time Factors | |
dc.subject | Time-to-Treatment | |
dc.subject | Tissue Plasminogen Activator | |
dc.subject | Treatment Outcome | |
dc.subject | Verbal Behavior | |
dc.title | Changes in Informed Consent Policy and Treatment Delays in Stroke Thrombolysis. | |
dc.type | Journal article | |
duke.contributor.orcid | Xu, Hanzhang|0000-0001-9617-247X | |
duke.contributor.orcid | Matchar, David B|0000-0003-3020-2108 | |
duke.contributor.orcid | Bettger, Janet Prvu|0000-0001-9708-8413 | |
duke.contributor.orcid | Laskowitz, Daniel T|0000-0003-3430-8815 | |
duke.contributor.orcid | Xian, Ying|0000-0002-1237-1162 | |
pubs.begin-page | 105551 | |
pubs.issue | 3 | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Duke Clinical Research Institute | |
pubs.organisational-group | Neurobiology | |
pubs.organisational-group | Duke Science & Society | |
pubs.organisational-group | Duke Innovation & Entrepreneurship | |
pubs.organisational-group | Duke Global Health Institute | |
pubs.organisational-group | Anesthesiology | |
pubs.organisational-group | Neurosurgery | |
pubs.organisational-group | Neurology, Neurocritical Care | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Initiatives | |
pubs.organisational-group | Institutes and Provost's Academic Units | |
pubs.organisational-group | University Institutes and Centers | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Neurology | |
pubs.organisational-group | Pathology | |
pubs.organisational-group | Medicine, General Internal Medicine | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Nursing | |
pubs.organisational-group | Orthopaedics | |
pubs.organisational-group | School of Nursing | |
pubs.organisational-group | Medicine, Clinical Pharmacology | |
pubs.organisational-group | Family Medicine and Community Health | |
pubs.publication-status | Published | |
pubs.volume | 30 |
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