Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Victoria M Scicluna"'
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
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
Autor:
Robert Silbergleit, Rebecca D. Pentz, Neal W. Dickert, Candace D. Speight, Sara F. Goldkind, Andrea R. Mitchell, Victoria M. Scicluna
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
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
Autor:
Rebecca D. Pentz, Elizabeth B. Jones, Candace D. Speight, Deneil K. Harney, Neal W. Dickert, Andrea R. Mitchell, Robert Silbergleit, Victoria M. Scicluna, Michelle H. Biros, David W. Wright
Publikováno v:
Annals of emergency medicine. 76(3)
Study objective It is important for researchers interested in trials using the exception from informed consent to understand the views and experiences of enrolled individuals. Previous studies have shown that patient and surrogate attitudes are gener
Autor:
Rebecca D. Pentz, David W. Wright, Arthur M. Pancioli, Jill M. Baren, Michelle H. Biros, Prasanthi Govindarajan, Victoria M. Scicluna, Ross J. Fleischman, Louisa W Whitesides, Elizabeth B. Jones, Neal W. Dickert
Publikováno v:
Clinical Trials. 14:180-186
Background: Evidence suggests that patients are generally accepting of their enrollment in trials for emergency care conducted under exception from informed consent. It is unknown whether individuals with more severe initial injuries or worse clinica
Autor:
Kevin P. Weinfurt, Dominick J. Angiolillo, Victoria M. Scicluna, James C. Blankenship, Manesh R. Patel, Sara F. Goldkind, Rebecca D. Pentz, Michael Frankel, Gautam Kumar, Opeolu Adeoye, Raul G. Nogueria, Michele Riedford, Andrea R. Mitchell, Ilana Spokoyny, Neal W. Dickert, Chandan Devireddy, Candace D. Speight, Ruth M. Parker, Yi-An Ko, Robert Silbergleit
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
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.
Autor:
Neal W Dickert, Michelle H Biros, Deneil K Harney, Elizabeth B Jones, Andrea R Mitchell, Victoria M Scicluna, Robert Silbergleit, Candace D Speight, David W Wright, Rebecca D Pentz
Publikováno v:
Circulation. 138
Introduction: Relatively minimal data exist regarding perspectives of patients (or surrogate decision-makers) after enrollment in clinical trials using the exception from informed consent (EFIC) for emergency research, a regulation essential for resu
Autor:
Victoria M. Scicluna, Kurt R. Denninghoff, Deneil Harney, Rebecca D. Pentz, David W. Wright, Robert Silbergleit, Neal W. Dickert, Michelle H. Biros
Publikováno v:
Academic Emergency Medicine. 22:340-346
In 1996, federal regulations were put into effect that allowed enrollment of critically ill or injured patients into Food and Drug Administration (FDA)-regulated clinical trials using an exception from informed consent (EFIC) under narrowly prescribe
Publikováno v:
AJOB empirical bioethics. 8(2)
Community consultation (CC) is required for research in emergency settings using an exception from informed consent (EFIC) in the United States, but uncertainty persists regarding best CC practices. There is ongoing debate about whom to include in CC
Autor:
Rebecca D. Pentz, Alexandra E. Fehr, Adrianne N. Haggins, Victoria M. Scicluna, Neal W. Dickert
Publikováno v:
Academic emergency medicine : official journal of the Society for Academic Emergency Medicine. 24(11)
OBJECTIVE Pretrial community consultation (CC) is required for emergency research conducted under an exception from informed consent (EFIC) in the United States. CC remains controversial and challenging, and minimal data exist regarding the views of