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To provide informed consent a consumer needs to know what options are available, what the expected outcomes are for each option, and what the success rates and incidence of side-effects are for each option (Source: Improving patient information and decision making [Consumers' Health Forum of Australia (CHF)])
Follow the links beow to find information on informed consent.
Reviewed August 2008
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| Title: |
Guidelines on consent for anaesthesia or sedation
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| Publisher: |
Australian and New Zealand College of Anaesthetists
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| Description: |
Consent should be obtained for all medical treatment. It is a basic tenet of our society that everyone has a right to determine what is done to his/her own body, and is entitled to know the implications of any treatment before it is administered and to seek clarification of any issues that may be of concern.
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| Date: |
Jun 2005
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| Title: |
Consent to medical treatment: what are your rights?
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| Publisher: |
Multicultural Health Communication Service (NSW)
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| Description: |
When it comes to consenting to medical or dental treatment, do you know your rights? Can a doctor make you have treatment without your permission, for instance? What if a health professional wants you to have a treatment - but you don't understand what's involved? Here's what you should know.
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| Date: |
Jul 1997
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| Title: |
Improving patient information and decision making
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| Publisher: |
Consumers' Health Forum of Australia (CHF)
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| Description: |
Use of a patient-driven consent decision-making model will effectively apply an evidence-based decision-making model on clinicians.
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| Date: |
Jan 2006
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| Title: |
E-health - consumers shaping electronic health records in Australia
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| Publisher: |
Consumers' Health Forum of Australia (CHF)
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| Description: |
The Consumers' Health Forum of Australia identifies informed consent, access to personal health information, security and consumer participation at all levels of decision-making as areas for ongoing development for electronic health records.
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| Date: |
Jan 2004
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| Title: |
Before your HIV test
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| Publisher: |
Queensland Health
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| Description: |
You have asked or been advised to have a blood test for HIV. You must give informed consent for this test to be done. This means you need to understand the following information.
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| Date: |
Apr 2008
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| Title: |
Post mortem
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| Publisher: |
Better Health Channel
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| Description: |
A post mortem, or autopsy, is the medical examination of a body after death. A hospital (or non-coronial) post mortem may be performed if the immediate family give their consent.
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| Date: |
Mar 2007
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| Title: |
ARPANSA - Code of practice for the exposure of humans to ionizing radiation for research purposes (2005)
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| Publisher: |
Australian Radiation Protection and Nuclear Safety Agency (ARPANSA)
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| Description: |
This Code of Practice is designed to ensure that researchers proposing to expose research participants to ionizing radiation provide the participants and the Human Research Ethics Committees with information that allows consent to be properly considered by the research participants and approval considered by the Human Research Ethics Committee.
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| Date: |
Jun 2005
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| Title: |
Challenging ethical issues in contemporary research on human beings
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| Publisher: |
National Health and Medical Research Council (NHMRC)
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| Description: |
AHEC acknowledges that Human Research Ethics Committee(HRECs) tackle complex and sensitive issues such as participant consent, patient safety and welfare, privacy and disclosure, and the scientific merit of research proposals. The kinds of dilemmas faced by HRECs are illustrated in the ten case studies included in the report.
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| Date: |
Dec 2006
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| Title: |
Making informed decisions
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| Publisher: |
The Jean Hailes Foundation for Women's Health
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| Description: |
Gathering information, thinking about options, knowing what it is you value and attuning yourself to all that you have learned about your body will help you make decisions that are appropriate for you. Gathering information and talking with your health practitioner can assist you in making an informed decision.
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| Date: |
Jun 2008
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| Title: |
General guidelines for medical practitioners on providing information to patients
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| Publisher: |
National Health and Medical Research Council (NHMRC)
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| Description: |
This document outlines the type of information that doctors need to discuss with patients when planning treatment. Issues covered include information that patients should be given, informing patients of risks, and, the limited circumstances when information may be witheld.
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| Date: |
Apr 2004
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| Title: |
Prostate cancer screening
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| Publisher: |
myDr
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| Description: |
Information from the Cancer Council on prostate cancer screening.
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| Date: |
Nov 2001
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| Title: |
Perceptions of risk : a legal perspective
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| Publisher: |
Australian Prescriber
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| Description: |
The 1992 decision in Rogers v. Whitaker (1992) 175 CLR 479 established in Australian law the standard of care required when a doctor gives information to patients about risks of proposed procedures.
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| Date: |
Oct 2002
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| Title: |
Breast implant information booklet - 4th edition
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| Publisher: |
Australian Government Department of Health and Ageing
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| Description: |
The Breast Implant Information Booklet (4th edition) has been prepared to provide guidance for persons considering the use of breast implants. The TGA recommends that you consider the information provided for a period of 30 days before making a final decision.
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| Date: |
Nov 2004
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| Title: |
Vitamin K and newborn babies
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| Publisher: |
Better Health Channel
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| Description: |
Vitamin K is needed for blood clotting. Babies are born with very small amounts of vitamin K in their bodies. This means they are at risk of haemorrhagic disease of the newborn (HDN). As a preventive measure, babies are routinely given vitamin K injections at birth.
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| Date: |
May 2008
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| Title: |
Human research ethics committees
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| Publisher: |
Better Health Channel
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| Description: |
Research involving human participants must be conducted in an ethical manner and research proposals must be reviewed and approved by a Human Research Ethics Committee (HREC). The Department of Human Services HREC considers all research undertaken by DHS and by DHS-funded agencies in some cases. There are guidelines about accessing information held by DHS or DHS-funded agencies and its use by external researchers.
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| Date: |
Aug 2008
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