Document Detail


Appreciation of the informed consent procedure in a randomised trial of decompressive surgery for space occupying hemispheric infarction.
MedLine Citation:
PMID:  17400593     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND AND AIM: As non-randomised studies have suggested that surgical decompression may reduce mortality in patients with space occupying hemispheric infarction, randomisation may be considered unethical in controlled trials testing this treatment strategy. We studied differences in recall of information and in appreciation of the informed consent procedure between representatives included in the Hemicraniectomy After Middle cerebral artery infarction with Life-threatening Edema Trial (HAMLET) and representatives of patients participating in the randomised trial of Paracetamol (Acetaminophen) In Stroke (PAIS).
METHODS: 1 year after study inclusion, we contacted 30 consecutive representatives who had given informed consent for participation of their relative in HAMLET, and 30 for PAIS. Recall of trial details and appreciation of the informed consent procedure were investigated using standardised questionnaires and compared between the two groups.
RESULTS: All 30 PAIS representatives and 28 HAMLET representatives were interviewed. Participation of their relative in a clinical trial was remembered by 86% of HAMLET and 40% of PAIS representatives (p<0.001). HAMLET representatives remembered more trial details (effect of the treatment under study (61% vs 3%, p<0.001); randomised treatment allocation (71% vs 0%, p<0.001)). With respect to appreciation of the informed consent procedure, we found no differences between the groups: in each trial, four representatives (14% vs 13%) had considered the question of randomisation unacceptable.
CONCLUSIONS: Participation of patients in a randomised controlled trial of surgical decompression for space occupying infarction is generally considered acceptable by their representatives, and recall of trial details is better than in a trial in which less vital issues are at stake.
Authors:
J Hofmeijer; G J Amelink; H M den Hertog; A Algra; L J Kappelle; H B van der Worp; ;
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Publication Detail:
Type:  Journal Article; Randomized Controlled Trial; Research Support, Non-U.S. Gov't     Date:  2007-03-30
Journal Detail:
Title:  Journal of neurology, neurosurgery, and psychiatry     Volume:  78     ISSN:  1468-330X     ISO Abbreviation:  J. Neurol. Neurosurg. Psychiatr.     Publication Date:  2007 Oct 
Date Detail:
Created Date:  2007-09-19     Completed Date:  2007-10-01     Revised Date:  2013-06-06    
Medline Journal Info:
Nlm Unique ID:  2985191R     Medline TA:  J Neurol Neurosurg Psychiatry     Country:  England    
Other Details:
Languages:  eng     Pagination:  1124-8     Citation Subset:  IM    
Affiliation:
Department of Neurology, C03.236, University Medical Centre Utrecht, PO Box 85500, 3508 GA Utrecht, The Netherlands. j.hofmeijer@umcutrecht.nl
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MeSH Terms
Descriptor/Qualifier:
Acetaminophen / therapeutic use
Aged
Brain Edema / etiology
Health Knowledge, Attitudes, Practice*
Humans
Infarction, Middle Cerebral Artery / complications,  drug therapy,  surgery*
Informed Consent / ethics*
Middle Aged
Netherlands
Patient Advocacy / statistics & numerical data*
Patient Participation / methods*
Personal Satisfaction
Questionnaires
Random Allocation
Randomized Controlled Trials as Topic / ethics*
Treatment Outcome
Unconsciousness / etiology
Chemical
Reg. No./Substance:
103-90-2/Acetaminophen
Comments/Corrections
Comment In:
J Neurol Neurosurg Psychiatry. 2007 Oct;78(10):1040   [PMID:  17550989 ]

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