May/June Ethics Reader Poll Results
Michael R. Klein, MD
NASS Ethics Committee Sacramento, CA
Zainab Al Lawati, MD, MEd, FRCPC, FAAPMR
NASS Ethics Committee University of Minnesota, Department of Rehabilitation Medicine Minneapolis, MN
Below are the results from the May/June Ethics poll.
Do you feel you should discuss a planned procedure (defined here as a general discussion of pros and cons) and obtain the informed consent (defined here as having a detailed discussion of risks and benefits- what would go on a consent form) or relegate it to a staff member?
The attending should have the discussion and obtain the informed consent
The attending should have the discussion but staff can obtain the consent
Nurses and PAs can have the discussion and obtain consent
Residents and Fellows can have the discussion and obtain consent
As long as the patient is satisfied with the interaction and feels informed, and the consent is signed, it doesn’t matter who did what
Discussion: Michael Klein, MD
I am pleased to note that 93% of respondents opined that the attending should obtain the consent and of that total 57% opined the staff could obtain the consent after the discussion between the attending and the patient. The remaining 36% opined the attending should do both the discussion and the consent. An informed consent involves the legal definition which can be different in the state where you practice and the state where you trained. I encourage you to be familiar with the Civil Code in your state and how it is defined. There are multiple definitions of consent, each with a slightly different spin and components. Dr. Kadan's article1 regarding clinical research is also applicable to elective spinal procedures and requires 1) Information Disclosure 2) Competence 3) Meaningful Informed Consent 4) Comprehension by the patient and 5) Voluntariness. A more general definition requires the discussion be 1) Clear 2) Continuous 3) Coercion-free & 4) Involve competency. This is imperative when English is not the patient's primary language, thus requiring an interpreter. I like Paul Nissell's approach in his article2, “Patient Consent-Decision or Assumption- Valid vs. Informed,” which focuses on the five requirements of a thorough informed consent, 1. The Diagnosis 2. The proposed treatment 3. The attendant risks 4. The benefits of treatment & 5. Alternative treatment options. Consider using A-V aids in the patient's native language and multi-media tools.
Consent in Practice: Zainab Al Lawati, MD, MEd, FRCPC, FAAPRM
I usually frame my consent including all these essential components (advised by my institution's lawyers):
- Consent for procedure
- Greet patient/introduce
- Review problem being treated
- Review proposed treatment - detail
- Explain why you think it will be beneficial
- Ask if they understand
- Review risks
- Describe likelihood of risks
- Describe how adverse events will affect patient
- Explain how they would be managed
- Ask patient if understand
- Explain risks of not doing procedure
- Explain that you can make recommendations, but decision is up to patient
- Explain you will provide them with best possible care whether they take your advice or not
- Ask if they have any further questions
- Ask if they would like to proceed with treatment
- Ask them to sign consent form