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Medical Consent

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Be satisfied the patient has understood what is proposed and consents to it. ... Changes in patient condition, to planned procedure, if new information. Time lapses. ... – PowerPoint PPT presentation

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Title: Medical Consent


1
Medical Consent
  • Module 1

2
This session will
  • explain why consent is important
  • outline the basic processes and considerations
    involved
  • develop your ability to judge how to handle
    consent issues
  • set out the legal and regulatory framework.

1
Introducing Clinical Risk Management Module 1
Consent
3
Why consent is necessary
  • Every adult has an inviolable right to determine
    what is done to his or her body. Lord Donaldson
  • Legal obligations.
  • Good practice.

2
Introducing Clinical Risk Management Module 1
Consent
4
Some examples of procedures that need consent
  • Surgical procedures.
  • Medical procedures.
  • Interventional and radiological procedures.
  • Radiotherapy and chemotherapy.
  • Intimate examinations.
  • Blood tests.

3
Introducing Clinical Risk Management Module 1
Consent
5
The person obtaining consent must
  • be suitably trained
  • have sufficient knowledge of the proposed
    investigation or procedure, and understand the
    risks involved
  • practise in line with their professional bodys
    standards.

4
Introducing Clinical Risk Management Module 1
Consent
6
GMC guidance 1
  • Give patients the information they ask for or
    need about their condition, its treatment and
    prognosis.
  • Provide it in a way they can understand.
  • Be satisfied the patient has understood what is
    proposed and consents to it.
  • from the GMCs Good Medical Practice

5
Introducing Clinical Risk Management Module 1
Consent
7
GMC guidance 2
  • Respect patients rights to be fully involved in
    decisionsabout their care.
  • Respect their right to decline treatment or take
    partin teaching or research.
  • Respect their right to a second opinion.
  • from the GMCs Good Medical Practice

6
Introducing Clinical Risk Management Module 1
Consent
8
Patients need information on
  • the nature of the intervention
  • its purpose
  • the risks and side effects
  • the benefits
  • alternatives.

7
Introducing Clinical Risk Management Module 1
Consent
9
Deciding how much information
  • Think about the
  • nature of the condition
  • complexity of the procedure
  • frequency of adverse effects, their seriousness
    and permanence
  • risk-benefit ratio of the treatment
  • urgency of the treatment
  • patients lifestyle, wishes or emotional state.

8
Introducing Clinical Risk Management Module 1
Consent
10
Information issues
  • Emergencies.
  • Anticipatory consent.
  • Conditional consent.
  • Withholding information.
  • Questions.
  • Patient information leaflets.
  • Recording whats happened.

9
Introducing Clinical Risk Management Module 1
Consent
11
How patients may give consent
  • Voluntarily.
  • Expressly.
  • Express verbal.
  • Express written.
  • Implied consent.

10
Introducing Clinical Risk Management Module 1
Consent
12
Basic assumption on competence
  • Every adult has the capacity to decide whether
    to consent to, or refuse, proposed medical
    intervention, unless it is shown that they cannot
    understand information presented in a clear way.
  • GMC. Seeking patients consent the ethical
    considerations

11
Introducing Clinical Risk Management Module 1
Consent
13
A competent patient can
  • comprehend information presented to them clearly
  • believe it
  • retain it long enough to consider it and
  • make a decision.

12
Introducing Clinical Risk Management Module 1
Consent
14
Filling in the consent form
  • No abbreviations.
  • Legible.
  • Unambiguous.
  • Signed and understood by the patient.
  • Signed and understood by you.
  • Dated.
  • Part of the medical records.

13
Introducing Clinical Risk Management Module 1
Consent
15
When to obtain formal consent
  • Principles before pre-med, time to think, when
    they understand.
  • Changes in patient condition, to planned
    procedure,if new information.
  • Time lapses.
  • Withdrawing consent.

14
Introducing Clinical Risk Management Module 1
Consent
16
Good practice adviceand standards
  • Registration bodies.
  • Professional bodies.
  • Department of Health.
  • Your Trust.
  • The CNST.

15
Introducing Clinical Risk Management Module 1
Consent
17
CNST standard 7 assessment
  • Patient information shows the risks/benefits of
    common elective treatments.
  • Consent forms comply with NHSE guidelines.
  • The Trusts consent policy for elective
    procedures states that a person capable of
    performing that procedure obtains consent.
  • There is a clear way for patients to get more
    information.

16
Introducing Clinical Risk Management Module 1
Consent
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