CONSENT



Dr. Rijen Shrestha, 3rd year Resident
        (Forensic Medicine)
        28th november 2011
Consent

• Definition:
    Free and voluntary agreement, approval or
    permission for compliance to perform
    some act.
    Consent is valid only if it is given after
    knowing the nature and consequences of
    the consent and those of the act for which
    consent is given.
Situations requiring Consent in medical practice:


3.   Examination of the patient for the purpose of
     diagnosis, investigation and subsequent treatment.
4.   Examination of the living person for medico-legal
     purposes.
5.   Any major/minor operative procedures
6.   Abortion, organ transplantation, blood donation/
     infusion
7.   Pathological autopsy
• Legal provision for consent in medical practice;

     MULUKI AIN Ilaj Garneko Mahal Art. 2

• For any operative procedures consent from patient
  or from guardian should be taken before
  procedure. If nobody is available in case of minor
  or mentally unsound patient or if patient is
  unconsciousness, procedure can be started without
  consent for the benefit of patient’s health.
From whom consent is obtained?
– Conscious, mentally sound adults (above the age
  of 16 years)
– Procedures involving marital relation, the
  wishes of the spouse are necessary
– Below the age of 16 years consent should be
  obtained from the parent or guardian except in
  case of emergency.
Consent is invalid in case of
  – Mentally unsound person
  – Minors (below the age of 16 years)
  – Consent obtained by force, fear or fraud
  – Consent for unethical and illegal procedures.
  – Jehovah’s witness
  – Loco-Parentis
• Types of Consent:

      A.Implied Consent

      C.Expressed Consent
        1. Oral
        2. Written

      E.Informed Expressed Consent
Implied consent
• Consent which is implied either by words or by behavior
  of the patient or by circumstances under which treatment is
  given.
• For example, it is common for a patient to arrange an
  appointment with a physician, to keep the appointment, to
  volunteer a history, to answer questions relating to the
  history and to submit without objection to physical
  examination. In these circumstances consent for the
  examination is clearly implied.
• To avoid misunderstanding, however, it may be prudent to
  state to the patient an intention to examine the breasts,
  genitals or rectum.
• In many cases, the extent to which consent was
  implied may later become a matter of
  disagreement.
• Physicians should be reasonably confident the
  actions of the patient imply permission for the
  examinations, investigations and treatments
  proposed. When there is doubt, it is preferable the
  consent be expressed, either orally or in writing.
Expressed consent
• Expressed consent may be in oral or written form. It
  should be obtained when the treatment is likely to be more
  than mildly painful, when it carries appreciable risk, or
  when it will result in ablation of a bodily function.
• Although orally expressed consent may be acceptable in
  many circumstances, frequently there is need for written
  confirmation. Patients can change their minds or may not
  recall what they authorized; after the procedure or
  treatment has been carried out, they may attempt to take
  the position it had not been agreed to or was not acceptable
  or justified.
• Consent may be confirmed and validated adequately
  by means of a suitable notation by the treating
  physician in the patient's record.
• Expressed consent in written form should be obtained
  for surgical operations and invasive investigative
  procedures. It is prudent to obtain written consent also
  whenever analgesic, narcotic or anaesthetic agents
  will significantly affect the patient's level of
  consciousness during the treatment.
INFORMED CONSENT
 Informed consent is the usual way in
  which patient preferences are expressed
 practical application of respect of
  patient’s autonomy
 When a patient consults a physician for a
  suspected medical problem, the physician
  makes a diagnosis and recommends
  treatment
 He explains those steps to the patient,
  giving reasons for the recommended
  treatment, the options of alternate
  treatments and the benefits and risks of
  all options
 The patient understands the information,
  assess the treatment choices and
  expresses a preference for one of the
  options proposed by the physician
 This is the essence of the Informed
  Consent
 Constitutes a central feature of an
  encounter characterized by mutual
  participation, good    communication,
  mutual respect and shared decision
  making
 Requires   a dialogue between the
  physician and patient leading to an
  agreement about the course of medical
  care
 Establishes a reciprocal relationship
  between physician and patients
 After initial consent to treatment has
 occurred, an ongoing dialogue between
 patient and physician concerning the
 patient’s continuing medical needs
 reinforces the original consent
 A properly negotiated Informed Consent
 benefits both physicians and patients. A
 therapeutic alliance is forged in which the
 physician’s work is facilitated because
 the patient has realistic expectations
 about results of the treatment and is
 prepared for possible complications and
 more likely to be a willing collaborator in
 the treatment
 Many studies reveal that physicians often
 fail to observe the practice and the spirit
 of informed consent
Informed Consent:
      Standard And Disclosure
Q: How should the adequacy of
   disclosure of information by a
   physician be determined?
A: 3 approaches
          [PHYSICIAN centered]
  Ask what a reasonable and prudent
      physician would tell a patient?
[PATIENT centered]
What information would a reasonable
patient need to know to make an
rational decision?

[SUBJECTIVE or PATIENT SPECIFIC]
Whether the information provided is
specifically tailored to particular
patients need for information and
understanding
 The trend is now going towards
 [SUBJECTIVE or PATIENT SPECIFIC]

 The   reasonable - patient centered
 standard may be ethically sufficient, but
 the subjective standard is ethically ideal
Scope Of Disclosure

 Many studies show that patients desire
 information from their physicians

 In recent years, candid disclosure even of
 ‘bad news’ has become the norm
    Disclosure should include

    i. the patient’s current medical status,
        including the likely course if no treatment
        is provided
    ii. the interventions that might improve
        prognosis including risks and benefits of
        procedures and estimation of probabilities
        and uncertainties associated with these
        procedures
i. a professional opinion about alternative
    modalities of treatment open to the
    patient
ii. a recommendation that is based on the
    physician best clinical judgement
    In carrying this information, physicians
     should:

    i. Speak in the patients’ language of
         preference
    ii. Avoid technical terms
    iii. Attempt to translate statistical data
         into everyday probabilities
(con’t)


  ii. Enquire whether patients understand
       the information
  iii. Invite questions
  iv. Interpret other information that
       patient has to ascertain its relevance
 It is ethically appropriate to disclose
  levels of experience and it is obligatory to
  do so in situations where the procedure is
  serious and elective
 The moral and legal obligations of
  disclosure vary with the situation, they
  become more stringent as the treatment
  situation moves from emergency through
  elective to experimental
COMPREHENSION

 The comprehension of the patient is as
  important as the provision of the
  information
 The physician has an ethical obligation
  to make reasonable efforts to ensure
  comprehension
 Explanation should be given clearly
  and simply and questions asked to
  assess understanding
 Written    instructions or printed
  materials should be provided
 Use of CD or video given if necessary
Documentation of Consent

 The process of Informed Consent
 concludes with the patient’s consent
 (or refusal). This consent is
 documented in a signed ‘consent form’
 that is entered in the patients medical
 records.
Difficulties With Informed Consent
     Problems physicians may face
    i. Use of technical language
    ii. Uncertainties intrinsic to all medical
         information
    iii. Worried about harming or alarming
         the patient
    iv. Hurried and pressed by multiple duties
    Problems patients may face:

    ii.    Limited knowledge
    iii.   May be inattentive or distracted
    iv.    Overcome by fear and anxiety
    v.     Selective hearing because of denial,
           fear, or preoccupation with illness
Decisional Capacity

 Consent to treatment is complicated not
 only by the difficulty of disclosure but
 also by the fact that some patients lack
 the mental capacity to understand or to
 make choices
 In law, the term ‘competence’ or
  ‘incompetence’ are used to indicate
  whether persons have the legal
  authority to make personal choices
 Only a judge, can rule whether a
  person is legally incompetent and to
  appoint a guardian
 In medical care, persons who are legally
  competent may have their mental
  capacities compromised by illness,
  anxiety, pain or hospitalization
 This is referring to the capacity or
  incapacity to make decisions
 Determining the decisional capacity of a
  patient is an essential part of a informed
  consent process
Determining Decisional Capacity

 Decisional    Capacity refers to the
  specific acts of comprehending,
  evaluating and choosing among
  realistic options
 Determining decisional capacity is a
  clinical judgment
 This is done through engaging the patient
 in conversation, to observe the patient’s
 behavior and to talk to 3rd parties e.g.
 family, friends
Conclusion
• Consent is the choice of the patient which
  also gives him the right to refuse.
• Consent can be given only by a mentally
  sound adult who knows the consequences
  of the giving the consent as well as the
  consequences of the consenting to the
  procedure in question.
• Consent should include not only the
  procedure the patient is consenting to but
  also the alternative modalities as well as the
  common well-known consequences of
  procedure in question
IF in doubt, take a written
      informed consent
Consent rs

Consent rs

  • 1.
    CONSENT Dr. Rijen Shrestha,3rd year Resident (Forensic Medicine) 28th november 2011
  • 2.
    Consent • Definition: Free and voluntary agreement, approval or permission for compliance to perform some act. Consent is valid only if it is given after knowing the nature and consequences of the consent and those of the act for which consent is given.
  • 3.
    Situations requiring Consentin medical practice: 3. Examination of the patient for the purpose of diagnosis, investigation and subsequent treatment. 4. Examination of the living person for medico-legal purposes. 5. Any major/minor operative procedures 6. Abortion, organ transplantation, blood donation/ infusion 7. Pathological autopsy
  • 4.
    • Legal provisionfor consent in medical practice; MULUKI AIN Ilaj Garneko Mahal Art. 2 • For any operative procedures consent from patient or from guardian should be taken before procedure. If nobody is available in case of minor or mentally unsound patient or if patient is unconsciousness, procedure can be started without consent for the benefit of patient’s health.
  • 5.
    From whom consentis obtained? – Conscious, mentally sound adults (above the age of 16 years) – Procedures involving marital relation, the wishes of the spouse are necessary – Below the age of 16 years consent should be obtained from the parent or guardian except in case of emergency.
  • 6.
    Consent is invalidin case of – Mentally unsound person – Minors (below the age of 16 years) – Consent obtained by force, fear or fraud – Consent for unethical and illegal procedures. – Jehovah’s witness – Loco-Parentis
  • 7.
    • Types ofConsent: A.Implied Consent C.Expressed Consent 1. Oral 2. Written E.Informed Expressed Consent
  • 8.
    Implied consent • Consentwhich is implied either by words or by behavior of the patient or by circumstances under which treatment is given. • For example, it is common for a patient to arrange an appointment with a physician, to keep the appointment, to volunteer a history, to answer questions relating to the history and to submit without objection to physical examination. In these circumstances consent for the examination is clearly implied. • To avoid misunderstanding, however, it may be prudent to state to the patient an intention to examine the breasts, genitals or rectum.
  • 9.
    • In manycases, the extent to which consent was implied may later become a matter of disagreement. • Physicians should be reasonably confident the actions of the patient imply permission for the examinations, investigations and treatments proposed. When there is doubt, it is preferable the consent be expressed, either orally or in writing.
  • 10.
    Expressed consent • Expressedconsent may be in oral or written form. It should be obtained when the treatment is likely to be more than mildly painful, when it carries appreciable risk, or when it will result in ablation of a bodily function. • Although orally expressed consent may be acceptable in many circumstances, frequently there is need for written confirmation. Patients can change their minds or may not recall what they authorized; after the procedure or treatment has been carried out, they may attempt to take the position it had not been agreed to or was not acceptable or justified.
  • 11.
    • Consent maybe confirmed and validated adequately by means of a suitable notation by the treating physician in the patient's record. • Expressed consent in written form should be obtained for surgical operations and invasive investigative procedures. It is prudent to obtain written consent also whenever analgesic, narcotic or anaesthetic agents will significantly affect the patient's level of consciousness during the treatment.
  • 12.
  • 13.
     Informed consentis the usual way in which patient preferences are expressed  practical application of respect of patient’s autonomy  When a patient consults a physician for a suspected medical problem, the physician makes a diagnosis and recommends treatment
  • 14.
     He explainsthose steps to the patient, giving reasons for the recommended treatment, the options of alternate treatments and the benefits and risks of all options  The patient understands the information, assess the treatment choices and expresses a preference for one of the options proposed by the physician
  • 15.
     This isthe essence of the Informed Consent  Constitutes a central feature of an encounter characterized by mutual participation, good communication, mutual respect and shared decision making
  • 16.
     Requires a dialogue between the physician and patient leading to an agreement about the course of medical care  Establishes a reciprocal relationship between physician and patients
  • 17.
     After initialconsent to treatment has occurred, an ongoing dialogue between patient and physician concerning the patient’s continuing medical needs reinforces the original consent
  • 18.
     A properlynegotiated Informed Consent benefits both physicians and patients. A therapeutic alliance is forged in which the physician’s work is facilitated because the patient has realistic expectations about results of the treatment and is prepared for possible complications and more likely to be a willing collaborator in the treatment
  • 19.
     Many studiesreveal that physicians often fail to observe the practice and the spirit of informed consent
  • 20.
    Informed Consent: Standard And Disclosure Q: How should the adequacy of disclosure of information by a physician be determined? A: 3 approaches [PHYSICIAN centered] Ask what a reasonable and prudent physician would tell a patient?
  • 21.
    [PATIENT centered] What informationwould a reasonable patient need to know to make an rational decision? [SUBJECTIVE or PATIENT SPECIFIC] Whether the information provided is specifically tailored to particular patients need for information and understanding
  • 22.
     The trendis now going towards [SUBJECTIVE or PATIENT SPECIFIC]  The reasonable - patient centered standard may be ethically sufficient, but the subjective standard is ethically ideal
  • 23.
    Scope Of Disclosure Many studies show that patients desire information from their physicians  In recent years, candid disclosure even of ‘bad news’ has become the norm
  • 24.
    Disclosure should include i. the patient’s current medical status, including the likely course if no treatment is provided ii. the interventions that might improve prognosis including risks and benefits of procedures and estimation of probabilities and uncertainties associated with these procedures
  • 25.
    i. a professionalopinion about alternative modalities of treatment open to the patient ii. a recommendation that is based on the physician best clinical judgement
  • 26.
    In carrying this information, physicians should: i. Speak in the patients’ language of preference ii. Avoid technical terms iii. Attempt to translate statistical data into everyday probabilities
  • 27.
    (con’t) ii.Enquire whether patients understand the information iii. Invite questions iv. Interpret other information that patient has to ascertain its relevance
  • 28.
     It isethically appropriate to disclose levels of experience and it is obligatory to do so in situations where the procedure is serious and elective  The moral and legal obligations of disclosure vary with the situation, they become more stringent as the treatment situation moves from emergency through elective to experimental
  • 29.
    COMPREHENSION  The comprehensionof the patient is as important as the provision of the information  The physician has an ethical obligation to make reasonable efforts to ensure comprehension
  • 30.
     Explanation shouldbe given clearly and simply and questions asked to assess understanding  Written instructions or printed materials should be provided  Use of CD or video given if necessary
  • 31.
    Documentation of Consent The process of Informed Consent concludes with the patient’s consent (or refusal). This consent is documented in a signed ‘consent form’ that is entered in the patients medical records.
  • 32.
    Difficulties With InformedConsent  Problems physicians may face i. Use of technical language ii. Uncertainties intrinsic to all medical information iii. Worried about harming or alarming the patient iv. Hurried and pressed by multiple duties
  • 33.
    Problems patients may face: ii. Limited knowledge iii. May be inattentive or distracted iv. Overcome by fear and anxiety v. Selective hearing because of denial, fear, or preoccupation with illness
  • 34.
    Decisional Capacity  Consentto treatment is complicated not only by the difficulty of disclosure but also by the fact that some patients lack the mental capacity to understand or to make choices
  • 35.
     In law,the term ‘competence’ or ‘incompetence’ are used to indicate whether persons have the legal authority to make personal choices  Only a judge, can rule whether a person is legally incompetent and to appoint a guardian
  • 36.
     In medicalcare, persons who are legally competent may have their mental capacities compromised by illness, anxiety, pain or hospitalization  This is referring to the capacity or incapacity to make decisions  Determining the decisional capacity of a patient is an essential part of a informed consent process
  • 37.
    Determining Decisional Capacity Decisional Capacity refers to the specific acts of comprehending, evaluating and choosing among realistic options  Determining decisional capacity is a clinical judgment
  • 38.
     This isdone through engaging the patient in conversation, to observe the patient’s behavior and to talk to 3rd parties e.g. family, friends
  • 39.
    Conclusion • Consent isthe choice of the patient which also gives him the right to refuse. • Consent can be given only by a mentally sound adult who knows the consequences of the giving the consent as well as the consequences of the consenting to the procedure in question.
  • 40.
    • Consent shouldinclude not only the procedure the patient is consenting to but also the alternative modalities as well as the common well-known consequences of procedure in question
  • 41.
    IF in doubt,take a written informed consent