Zobrazeno 1 - 10 of 24 pro vyhledávání: '"Sara F, Goldkind"'
1
Akademický článek
Determinants of Patient and Surrogate Experiences With Acute Care Research Consent: A Key Informant Interview Study
Autor: Victoria M. Scicluna, Sara F. Goldkind, Andrea R. Mitchell, Rebecca D. Pentz, Candace D. Speight, Robert Silbergleit, Neal W. Dickert
Publikováno v: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 8, Iss 22 (2019)
Background Informed consent for acute myocardial infarction and stroke research is challenging. Time for enrollment decisions is limited, patients and family are usually stressed, and being asked to participate in research is often unexpected. Despit
Externí odkaz: https://doaj.org/article/7134098a254a4941b66fe9c7fdfc12ed
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2
Akademický článek
Emergency Consent: Patients’ and Surrogates’ Perspectives on Consent for Clinical Trials in Acute Stroke and Myocardial Infarction
Autor: Neal W. Dickert, Victoria M. Scicluna, Opeolu Adeoye, Dominick J. Angiolillo, James C. Blankenship, Chandan M. Devireddy, Michael R. Frankel, Sara F. Goldkind, Gautam Kumar, Yi‐An Ko, Andrea R. Mitchell, Raul G. Nogueria, Ruth M. Parker, Manesh R. Patel, Michele Riedford, Robert Silbergleit, Candace D. Speight, Ilana Spokoyny, Kevin P. Weinfurt, Rebecca D. Pentz
Publikováno v: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 8, Iss 2 (2019)
Background Emergent informed consent for clinical trials in acute myocardial infarction (AMI) and stroke is challenging. The role and value of consent are controversial, and insufficient data exist regarding patients’ and surrogates’ experiences.
Externí odkaz: https://doaj.org/article/1186b131b2564c8d94bffc8796f0de75
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3
Interactive media-based community consultation for exception from informed consent trials: How representative should (and can) it be?
Autor: John B. Holcomb, Shannon W. Stephens, Kenji Inaba, Sara F. Goldkind, Brandon M. Crowley, Jan O. Jansen
Publikováno v: Journal of Trauma and Acute Care Surgery. 92:e41-e46
SUMMARY ABSTRACT Community consultation (CC) is a requirement for exception from informed consent (EFIC) research. This article explores the issue of how representative such consultations can and should be, with particular reference to the use of med
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ae65db9e6c2c7d12a6ede54079775662
https://doi.org/10.1097/ta.0000000000003484
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6
Civilian walking blood bank emergency preparedness plan
Autor: Eugene E. Moore, Elizabeth Waltman, Marisa B. Marques, Kevin C. O'Connor, Heidi Doughty, Andrew P. Cap, Kevin R. Ward, Audra L. Taylor, Donald H. Jenkins, Philip C. Spinella, Torunn Oveland Apelseth, Paul M. Ness, Jeremy W. Cannon, John B. Holcomb, Sara F. Goldkind, Martin A. Schreiber, Steve Sloan, Mark H. Yazer, Eilat Shinar, James R. Stubbs, Sarah J. Ilstrup, Mary J. Homer, Jan O. Jansen, Jason B. Corley, Jennifer M. Gurney, Geir Strandenes, Frank K Butler, Michael Fitzpatrick
Publikováno v: Holcomb, J B, Spinella, P C, Apelseth, T O, Butler, F K, Cannon, J W, Cap, A P, Corley, J B, Doughty, H, Fitzpatrick, M, Goldkind, S F, Gurney, J M, Homer, M J, Ilstrup, S J, Jansen, J O, Jenkins, D H, Marques, M B, Moore, E E, Ness, P M, O'Connor, K C, Schreiber, M A, Shinar, E, Sloan, S, Strandenes, G, Stubbs, J R, Taylor, A L, Ward, K R, Waltman, E & Yazer, M 2021, ' Civilian walking blood bank emergency preparedness plan ', Transfusion, vol. 61, no. Suppl. 1, pp. S313-S325 . https://doi.org/10.1111/trf.16458
Background: The current global pandemic has created unprecedented challenges in the blood supply network. Given the recent shortages, there must be a civilian plan for massively bleeding patients when there are no blood products on the shelf. Recogni
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3e9a051b7c3439dfdfa167cf8f02d91
https://portal.findresearcher.sdu.dk/da/publications/2f54b80a-5acd-43e9-aff9-b04dc847e367
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9
Understanding preferences regarding consent for pragmatic trials in acute care
Autor: David Wendler, Scott Yh Kim, Yi-An Ko, Sara F. Goldkind, Neal W. Dickert, Candace D. Speight, Chandan Devireddy
Publikováno v: Clinical Trials. 15:567-578
Background There has been debate about the role of consent in pragmatic trials comparing qualitatively similar interventions. Consent preferences may differ in acute care contexts, given severe illness, time constraints, and other barriers to consent
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b7409747ef2a9f57389f7b2e32fe994
https://doi.org/10.1177/1740774518801007
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10
The Default Position: Optimizing Pediatric Participation in Medical Decision Making
Autor: Sara F. Goldkind, Aleksandra E. Olszewski
Publikováno v: The American Journal of Bioethics. 18:4-9
Inclusion of children in medical decision making, to the extent of their ability and interest in doing so, should be the default position, ensuring that children are routinely given a voice. However, optimizing the involvement of children in their he
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e2078812dcdd0df200c952764f303af
https://doi.org/10.1080/15265161.2017.1418921
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