Understanding Informed Consent in Outpatient Mental Health Presented by: Robert W. Marrs, MS, LMFT AAMFT Approved Supervisor On Behalf of Wisconsin Association.

Slides:



Advertisements
Similar presentations
HIPAA Privacy Practices. Notice A copy of the current DMH Notice must be posted at each service site where persons seeking DMH services will be able to.
Advertisements

Confidentiality, Consent and Data Protection Elizabeth M Robertson Deputy Medical Director Grampian University Hospitals Trust.
SURROGATE CONSENT LAW: Impact on Research. AB 2328: Surrogate Consent for Research Question: Prior to January 1, 2003, within the state of California,
The Mental Capacity Act 2005 Implications for Front Line Staff Richard Williams Professor of Mental Health Strategy, University of Glamorgan Professor.
Medical Consent Guardianship Board. Consent to Medical or Dental Treatment A patient cannot receive medical treatment without consentA patient cannot.
1 Patients’ Rights and Responsibilities. PATIENT RIGHTS 2 Every healthcare facility is mandated to display the following Rights and Responsibilities:
Patient’s Bill of Rights L. Kay Garrison, PT, DPT.
ADVANCE DIRECTIVES VENTURE BEHAVIORAL HEALTH. Decision Making/Advance Directives Venture Behavioral Health respects the rights of Medicaid members to.
It Starts with a Conversation Maryland MOLST Train the Trainer Program June 2012 (presented at the University of Maryland School of Law on April 2, 2013)
Guardianship in Pennsylvania Robin Resnick Disability Rights Network of Pennsylvania 1315 Walnut Street, Suite 500 Philadelphia, PA
Guardianship and Power of Attorney Training Crisis Response Network of Southern Arizona.
In a healthcare setting
Confidentiality and HIPAA
WHAT IS HIPAA? The Health Insurance Portability and Accountability Act of 1996 (HIPAA) provides certain protections for any of your health information.
THE BASICS OF CONSENT LAW Sheniece Smith, Esq.. BASICS State and federal laws require patients to have the right to consent to health care decisions.
Outpatient Services Programs Workgroup: Laura’s Law May 29, 2014.
Consent and Confidentiality for Children in New Mexico Liz McGrath Executive Director Pegasus Legal Services for Children.
Vicki Hammen, Vice Chair, IRB IRB Brown Bag February 9, 2009.
Ethics and Group Counseling Mary Saint, M.Ed., LPC.
Obtaining Informed Consent: 1. Elements Of Informed Consent 2. Essential Information For Prospective Participants 3. Obligation for investigators.
Use of Children as Research Subjects What information should be provided for an FP7 ethical review?
Confidentiality of MH/DD/SA Records Family Court Conference March 9, 2006 Mark Botts School of Government, UNC.
HUMAN RIGHTS REGULATION TRAINING Participation in Decision-Making Dana Martin Johnson, AAG The Institute of Law, Psychiatry, and Public Policy.
Patient Rights and Responsibilities Seton Medical Center Harker Heights.
1 Consent for treatment A summary guide for health practitioners about obtaining consent for treatment Bridie Woolnough Resolution Officer Health Care.
Chapter 12—Ethics for Healthcare Practitioners
Legal and Ethical Aspects in Clinical Practice
Nic Dibble, Consultant School Social Work (608) Department of Public Instruction
Minors and Mental Health Treatment: Who Gets to Decide? Center for Children’s Advocacy KidsCounsel Seminar September 29, 2009 Jay E. Sicklick, Esq. Deputy.
Proxy Consent. Civil code of the Philippines Competency of minors  Art. 38. Minority, insanity or imbecility, the state of being a deaf-mute, prodigality.
Updated 12/02/2007 Relevant Laws Relevant Laws ContraceptionContraception, Sterilisation and Abortion Act 1977 (CS&A Act) CS & A Amendment 1978, 1990 AbortionCare.
REGULATION OF HEALTH PRACTICE Prof Ames Dhai. Introduction Constitution Statutes (Acts of Parliament) Common Law Criminal.
HRPP Training – Session Two Human Research Protection Program Manager
Ethical And Legal Considerations Ethical Issues  Ethical codes are not set in stone. They serve as principles upon which to guide practice.  There are.
The Goals and Principles of Human Participant Protection Part 4: Vulnerable Populations.
Medical Law and Ethics Lesson 2: Patient/Physician Relationship.
Medical Law and Ethics Lesson 4: Medical Ethics
Copyright ©2011 by Pearson Education, Inc. Upper Saddle River, New Jersey All rights reserved. Pearson's Comprehensive Medical Assisting: Administrative.
Established in 1996 to enforce standards for electronic health information & enhance the security and privacy of health information.
Patient’s Bill of Rights. The pt. has the right to considerate and respectful care. The pt. has the right to considerate and respectful care. The pt.
© 2009 The McGraw-Hill Companies, Inc. All rights reserved. 1 McGraw-Hill Chapter 2 The HIPAA Privacy Standards HIPAA for Allied Health Careers.
In 1987 The Ontario government passed this Bill of Rights to make sure that Long Term Care facilities are truly HOME to the people who live in them.
Human Subjects Protections Research Ethics. Basic Assumptions about How Research Should be Conducted Subjects should be protected from harm. Subjects.
PROTECTING CLIENT DATA HIPAA, HITECH AND PIPA PART 1B.
Capacity for Consent - How Much Do We Know About It? Kate Evans Specialist Registrar in Emergency Medicine Derriford Hospital, Plymouth.
The consent in health care.  Defining consent  Age of consent  How to give consent  Factors impacting on the ability to make a decision  The ethical.
Issues in Supervision and Consultation Deborah Smith, PhD Michelle March, PhD Corey, 8e, © 2011, Brooks/ Cole – Cengage Learning.
PATIENTS’ BILL OF RIGHTS THE RIGHTS AND PROTECTIONS GUARANTEED BY NEW YORK STATE AND BY FEDERAL LAWS AND REGULATIONS.
Mosby items and derived items © 2007, 2004 by Mosby, Inc., an affiliate of Elsevier Inc. Legal and Ethical Issues.
Consent & Vulnerable Adults Aim: To provide an opportunity for Primary Care Staff to explore issues related to consent & vulnerable adults.
Bridie Woolnough Resolution Officer Health Care Complaints Commission
Ethics Key Terms  Confidentiality  Privileged communication  Privacy.
By MUREREREHE Julienne BDT(Hons) KHI..  Informed consent is a legal document, prepared as an agreement for treatment, non-treatment, or for an invasive.
Unit 4 Seminar. Key Terms  Confidentiality  Privileged communication  Privacy.
BASICS OF ESTATE PLANNING AND PROBATE Margie Connolly, Attorney at Law MARGARET McCULLOUGH CONNOLLY, PLLC Sugar Land TX Mmconnollylaw.com.
Established standards of care given with respect and consideration, regardless of race, age, or payment source. Information about your illness, possible.
Corey, 8e, ©2011, Brooks/ Cole – Cengage Learning Chapter 9 Issues in Supervision and Consultation.
UNITS 4:3-4:4 Patients’ Rights and Legal Directives for Health Care.
PATIENT & FAMILY RIGHTS AT DOHMS. Fully understand and practice all your rights. You will receive a written copy of these rights from the Reception, Registration.
Ethics in Research Each research study involves a careful risk/benefit analysis prior to beginning data collection. The question each researcher must ask.
Disclaimer This presentation is intended only for use by Tulane University faculty, staff, and students. No copy or use of this presentation should occur.
Can Providers Assure Commercially Insured Adolescents Confidentiality for STI Screening and Treatment? C onflicting Laws and Innovative Approaches Abigail.
HIPAA Training Workshop #3 Individual Rights Kaye L. Rankin Rankin Healthcare Consultants, Inc.
Chapter 2 Ethical and Legal Issues
Psychiatric Advance Directives
Informed Consent to Treatment
The Health Insurance Portability and Accountability Act
Legal and Ethical Aspects in Clinical Practice
TRTO (Translational Research Trials Office)
Presentation transcript:

Understanding Informed Consent in Outpatient Mental Health Presented by: Robert W. Marrs, MS, LMFT AAMFT Approved Supervisor On Behalf of Wisconsin Association for Marriage and Family Therapy

Wisconsin Law – DHS 94 DHS 94.02(22), Wisconsin Administrative Code - "Informed consent" or "consent" means written consent voluntarily signed by a patient who is competent and who understands the terms of the consent, or by the patient's legal guardian or the parent of a minor, as permitted under s.51.61(6) and (8), Stats., without any form of coercion, or temporary oral consent obtained by telephone in accordance with DHS (2m).

Wisconsin Law DHS 94.03, Wisconsin Administrative Code - "INFORMED CONSENT. (1) Any informed consent document required under this chapter shall declare that the patient or the person acting on the patient’s behalf has been provided with specific, complete and accurate information and time to study the information or to seek additional information concerning the proposed treatment or services made necessary by and directly related to the person’s mental illness, developmental disability, alcoholism or drug dependency, including:

Wisconsin Law (a) The benefits of the proposed treatment and services, (b) The way the treatment is to be administered and the services are to be provided, (d) Alternative treatment modes and services, (e) The probable consequences of not receiving the proposed treatment and services,

Wisconsin Law (f) The time period for which the informed consent is effective, which shall be no longer than 15 months from the time the consent is given, and (g) The right to withdraw informed consent at any time, in writing. (2) An informed consent document is not valid unless the subject patient who signed it is competent, that is, substantially able to understand all significant information which has been explained in easily understandable language, or the consent form has been signed by the legal guardian of an incompetent patient or the parent of a minor, except that the patient’s informed consent is always required for the patient’s participation in experimental research, subjection to drastic treatment procedures or receipt of electroconvulsive therapy.

Wisconsin Law (2m) In emergency situations or where time and distance requirements preclude obtaining written consent before beginning treatment and a determination is made that harm will come to the patient if treatment is not initiated before written consent is obtained, informed consent for treatment may be temporarily obtained by telephone from the parent of a minor patient or the guardian of a patient. Oral consent shall be documented in the patient’s record, along with details of the information verbally explained to the parent or guardian about the proposed treatment. Verbal consent shall be valid for a period of 10 days, during which time informed consent shall be obtained in writing.

Wisconsin Law (3) The patient, or the person acting on the patient’s behalf, shall be given a copy of the completed informed consent form, upon request. (4) When informed consent is refused or withdrawn, no retaliation may be threatened or carried out.“ *Also refer to DHS & regarding Outpatient Mental Health Clinics

AAMFT Code of Ethics AAMFT Ethical Code 1.2 Marriage and family therapists obtain appropriate informed consent to therapy or related procedures as early as feasible in the therapeutic relationship, and use language that is reasonably understandable to clients. The content of informed consent may vary depending upon the client and treatment plan; however, informed consent generally necessitates that the client: (a) has the capacity to consent; (b) has been adequately informed of significant information concerning treatment processes and procedures; (c) has been adequately informed of potential risks and benefits of treatments for which generally recognized standards do not yet exist; (d) has freely and without undue influence expressed consent; and (e) has provided consent that is appropriately documented. When persons, due to age or mental status, are legally incapable of giving informed consent, marriage and family therapists obtain informed permission from a legally authorized person, if such substitute consent is legally permissible.

Breaking it all down… 1. Informed consent is required by any mental health consumer prior to receiving psychotherapy treatment 2. Informed consent should be obtained for both admission and treatment. 3. Informed consent includes both written documentation AND a conversation with the treatment provider

Breaking it all down… 3. The mental health consumer must be: 1. Competent – The capacity to accurately and completely understand both his/her consumer rights and the process of psychotherapy a) Mental Capacity – intelligence, information-processing, memory, mental status (not impaired by mental illness) b) Special Needs – hearing or visually impaired c) Cultural / Language Capacity – informed consent is discussed and explained in a way that is understood within the client’s own cultural framework d) Developmental Stage – informed consent is discussed and explained in a way that is understood according to the client’s age and stage of development

Breaking it all down… 3. The mental health consumer must be: 2. Of Legal Age a) 18 years of age or older b) Under age 18 the client must have the written consent of the parent or legal guardian i. Minors 14 yrs of age and older have the right to due process to protest involvement in treatment. ii. Parents of minors 14 and over also have the right to due process if their minor child refuses treatment.

Breaking it all down… 4. The mental health consumer must be: 3. Voluntary a) Consumers may be treated involuntarily if the treatment is ordered by a court of law. Written documentation must be provided by the court prior to the start of treatment

Breaking it all down… 5. Informed consent must be signed by all consumers participating in the treatment process 6. Informed consent includes an explanation of the consumer’s rights (DHS 51.61):

Breaking it all down… 7. Consumer’s have the right to file a formal grievance (DHS & 94.29): 1. Every agency, clinic, and independent practitioner must have a written grievance process 2. Formal grievances may be submitted, in writing, to the following persons and entities: a) Clinician b) Clinic Administrator c) Patient’s Rights Specialist d) DRL e) DHS

Breaking it all down… 8. Consumer’s must be informed of any potential risks or negative outcomes associated with psychotherapy 1. You might leave appointments feeling worse than when you arrived 2. Things may get worse before they get better (e.g. Hospitalization) 3. Change can sometimes have unexpected outcomes (e.g. loss of relationships, loss of job, etc.) 4. Providing individual therapy to someone struggling with relationship issues may do more harm to the relationship (I.e. couples therapy, family therapy with adolescents)

Breaking it all down… 9. Consumer’s must be informed of any potential benefits associated with psychotherapy (E.g.) 1. Symptom reduction 2. Improved functioning 3. More effective coping strategies 4. Improved relationships 5. Improved self-esteem and affect

Breaking it all down… 10. Consumer’s must be informed of any potential side effects of NOT receiving psychotherapy (E.g.) 1. Worsening of symptoms 2. Deterioration in functioning 3. Increased relationship problems 4. Potential for crisis 5. Increased health risks

Breaking it all down… 11.Consumer’s must be informed about your qualifications to provide psychotherapy: 1. Credential / License 2. Level of Education 3. Years of Experience 4. Specific Training as it relates to a specialty 12. Consumer’s must be informed about your therapeutic approach: 1. Model of Therapy (e.g. systems, CBT, narrative, etc.) 2. Religious / Spiritual Orientation (if its integrated into your approach, I.e. Christian counseling)

Breaking it all down… 13. Have a discussion about expectations and preferences (both the client’s and the therapist’s) 14.Explain any limitations in your approach or services

Breaking it all down… 15.Consumer’s need to be informed about any and all financial costs and responsibilities associated with receiving mental health services: 1. Treatment Costs (therapy, testing, etc.) 2. Insurance Copays / Co-Insurance / Deductibles 3. Policy and Fees regarding No Shows / Late Cancellations 4. Policy Regarding Schedule of Payments

Breaking it all down… 16.Consumer’s need to be informed and educated about confidentiality as it relates to protected health information. 1. HIPAA 2. DHS & DHS

Breaking it all down… 17. Consumer’s need to be informed and educated about confidentiality as it relates to protected health information. 3. Exceptions: a) Imminent Harm to Self or Others b) Subpoena by a Judge c) Suspected Child / Elder Abuse / Abuse of a Vulnerable Adult

Breaking it all down… 18.Give consumer’s options should they ever feel a lack of progress in psychotherapy: 1. Develop a New Treatment Plan 2. Incorporate Consultation / Supervision 3. Expanding the Client System 4. Expanding the Therapist System 5. Terminating Treatment a) Transferring to another Provider (internal) b) Transferring to another Provider/Agency (external)

Breaking it all down… The purpose of informed consent is to honor the patient’s legal right to be informed about all aspects of his/her mental health treatment so that he/she can: 1. Decide whether or not to receive mental health treatment, 2. Participate in the planning and delivery of treatment 3. Make educated decisions about the course of treatment

Breaking it all down… Providing individual therapy when couple or family therapy is indicated has the potential of destabilizing the patient’s relationships because individual therapy can oftentimes promote individuation and differentiation. It’s important to help patients consider the potential consequences of not providing couple and family therapy.

Breaking it all down… With changes in both federal and state law, please be sure to verify that your informed consent form is both HIPAA and Wisconsin compliant before implementation in your practice.

Confidentiality of Treatment Records (Ss & HFS 92.05) Access of Records During Treatment – Clients must have full access to all records regarding medications and health-related treatments. – The Director of Treatment may deny access to other records IF it is determined to be harmful to the client. The reasons for the denial must be noted in the clinical record. *Note: Ss states that a client must be “fully informed of his or her treatment and care, and to participate in the planning of his or her care.” Any restriction of a client’s treatment record may NOT interfere with this right.

Confidentiality of Treatment Records (Ss & HFS 92.05) Access of Records After Treatment – Clients have a right to a complete record of all medications and health-related treatments. – Upon request, clients have a right to: Access their treatment record Have a photocopy of their treatment record

Confidentiality of Treatment Records (Ss & HFS 92.05) Access of Records After Treatment – Any request for records must be processed within 5 working days. A “reasonable and uniform charge” for reproduction of the records may be assessed at a cost of no more than 35 cents per page. Medicaid beneficiaries cannot be charged for the first copy. The Director of the Facility has the right to be present during the inspection of the record.

Conclusion Please consult with an attorney specializing in health care law prior to implementing any of the above protocols. You may also consult with the Division of Quality Assurance at Wisconsin Department of Health Services.