Abstract Background Over one third of stroke patients have cognitive or language deficits such that they require surrogate consent for acute stroke treatment or enrollment into acute stroke trials. Little is known about the agreement of stroke patients and surrogates in this time-sensitive decision-making process. We sought to determine patient and surrogate agreement in 4 hypothetical acute stroke scenarios. Methods We performed face to face interviews with ED patients at an academic teaching hospital from June to August 2011. Patients and the surrogates they designated were asked to make decisions regarding 4 hypothetical stroke sc...
<p><b>Background and Purpose:</b> European directives and legislation in some coun...
Background: Obtaining consent in emergency situations is challenging. Proxy consent allows patients ...
International audienceOBJECTIVE: A European Union Directive provides for the designation of a surrog...
International audienceBACKGROUND:The provision of informed consent is a prerequisite for inclusion o...
Objective: To determine whether the manner of consent, i.e., informed consent by patients themselves...
There is a longstanding concern about the accuracy of surrogate consent in representing the health c...
Background: Obtaining informed consent for a patient's participation in a randomized trial of treatm...
Successful implementation of a randomized clinical trial (RCT) for neuro-vascular emergencies such a...
Background: There is a longstanding concern about the accuracy of surrogate consent in representing ...
Surrogate decision making is common in medical settings, particularly regarding treatment decisions ...
BACKGROUND Clinical trials are the hallmark of evidence-based medicine, but recruitment is often cha...
Background: In some acute care trials, immediate informed consent is not possible, but deferred cons...
Background: We assessed the occurrence of neurological deficits that may impede the capacity to prov...
<p><b>Background and Purpose:</b> European directives and legislation in some coun...
Background: Obtaining consent in emergency situations is challenging. Proxy consent allows patients ...
International audienceOBJECTIVE: A European Union Directive provides for the designation of a surrog...
International audienceBACKGROUND:The provision of informed consent is a prerequisite for inclusion o...
Objective: To determine whether the manner of consent, i.e., informed consent by patients themselves...
There is a longstanding concern about the accuracy of surrogate consent in representing the health c...
Background: Obtaining informed consent for a patient's participation in a randomized trial of treatm...
Successful implementation of a randomized clinical trial (RCT) for neuro-vascular emergencies such a...
Background: There is a longstanding concern about the accuracy of surrogate consent in representing ...
Surrogate decision making is common in medical settings, particularly regarding treatment decisions ...
BACKGROUND Clinical trials are the hallmark of evidence-based medicine, but recruitment is often cha...
Background: In some acute care trials, immediate informed consent is not possible, but deferred cons...
Background: We assessed the occurrence of neurological deficits that may impede the capacity to prov...
<p><b>Background and Purpose:</b> European directives and legislation in some coun...
Background: Obtaining consent in emergency situations is challenging. Proxy consent allows patients ...
International audienceOBJECTIVE: A European Union Directive provides for the designation of a surrog...