Patient refusal of risk information and consent
نویسندگان
چکیده
منابع مشابه
SOP 05: Patient information and informed consent.
Adequate patient information with particular emphasis on the fact that participation in the study is voluntary is a particular concern of the ‘Declaration of Helsinki’ [1] and Guidelines on Good Clinical Practice. Great care must therefore be taken in formulating and adapting a written patient information sheet to the particular requirements of a given study. The written patient information mus...
متن کاملthe study of practical and theoretical foundation of credit risk and its coverage
پس از بررسی هر کدام از فاکتورهای نوع صنعت, نوع ضمانت نامه, نرخ بهره , نرخ تورم, ریسک اعتباری کشورها, کارمزد, ریکاوری, gdp, پوشش و وثیقه بر ریسک اعتباری صندوق ضمانت صادرات ایران مشخص گردید که همه فاکتورها به استثنای ریسک اعتباری کشورها و کارمزد بقیه فاکتورها رابطه معناداری با ریسک اعتباری دارند در ضمن نرخ بهره , نرخ تورم, ریکاوری, و نوع صنعت و ریسک کشورها اثر عکس روی ریسک اعتباری داردو پوشش, وثی...
15 صفحه اولReadability of patient information and consent documents in rheumatological studies
BACKGROUND Before participation in medical research an informed consent must be obtained. This study investigates whether the readability of patient information and consent documents (PICDs) corresponds to the average educational level of participants in rheumatological studies in the Netherlands, Denmark, and Norway. METHODS 24 PICDs from studies were collected and readability was assessed i...
متن کاملWho is the patient? Disclosure of information and consent in anesthesia and intensive care (informed consent).
Physicians have always strived to uphold all the ethical postulates of the medical profession in all aspects of the practice, however with the vast advances in science and technology, numerous ethical dilemmas regarding all aspects of life and ultimately death have emerged. Medical decisions however, are no longer in the sole jurisdiction of traditional Hippocratic medicine but are now delibera...
متن کاملGuidelines for researchers: patient information sheet and consent form.
The guidance, which follows, applies primarily to multi-centre pharmaceutical studies and encompasses the ICH Good Clinical Practice guidelines. However, the principles and much of the content will be of use to researchers writing information sheets in their particular fields, for trials involving patients, patient volunteers and healthy volunteers. You will find it helpful to refer also to oth...
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ژورنال
عنوان ژورنال: Anaesthesia
سال: 2003
ISSN: 0003-2409
DOI: 10.1046/j.1365-2044.2003.03483.x