| 1. | What are the current DNR Order placement protocols for your RHA catchment area and/or hospital or care facility? |
| 2. | Is it mandatory that the patient or patient advocate/surrogate have knowledge of the placement of a DNR Order? |
| 3. | Is it mandatory that the patient or patient advocate/surrogate give consent to the placement of a DNR Order? |
| 4. | Does your RHA catchment area/hospital/care facility have an ethics board or similar body which is consulted in decision-making regarding DNR Orders? |
| 5. | If such an ethics board exists, is there any community representation on that board? |
| 6. | What protocols exist for DNR Order placement when a doctor and a patient or patient advocate/surrogate disagree about that placement? |
| 7. | Would your organization support the idea of having persons with disabilities involved in establishing guidelines regarding DNR Orders in medical facilities? If so, how would that involvement occur? |
| 1. | Re: Current DNR Order Policies | |
| one region stated the patient had the final say in determining DNR Order placement | ||
| one region stated their DNR policy was based on a prior Advance Health Care Directive or determined by the physician in consultation with patient or patient proxy | ||
| one region stated competent patients had the final say | ||
| one region had no policy | ||
| the remainder of regions reported they had policy development underway. | ||
| 2. | Re: Patient/Proxy Knowledge of DNR Order Placement | |
| 3 regions reported that patient/proxy knowledge is mandatory | ||
| 1 region reported that the practice of informing patients/proxies of DNR Order placement is encouraged | ||
| 1 region reported that patient/proxy knowledge is not required, and that the decision to inform them is made by individual facilities within the region | ||
| the remainder reported that policy development is underway | ||
| 3. | Re: Patient/Proxy Consent of DNR Order Placement | |
| 3 regions reported that patient/proxy consent is mandatory | ||
| 1 region reported that the practice of obtaining consent from patients/proxies of DNR Order placement is encouraged | ||
| 1 region reported that patient/proxy consent is not required, and that the decision to inform them is made by individual facilities within the RHA | ||
| the remainder reported that policy development is underway | ||
| 4. | Re: the Existence of an Ethics Board or Similar Body Consulted on Ethical Issues | |
| 3 regions reported they had no ethics board or similar body | ||
| 2 regions reported they had an ethics board | ||
| 1 region reported they had no ethics board but consulted with the Health Sciences Centre ethics committee as required | ||
| the remainder reported that development of this concept was underway | ||
| 5. | Re: Community Representation on the Ethics Board | |
| 2 regions reported that they had community representation on their Ethics Board | ||
| 2 regions reported they had no community representation on their Ethics Board | ||
| 1 region reported that this information was not available | ||
| 1 region reported that community representation on an ethics board was not applicable to an RHA | ||
| 6. | Re: Policies Concerning a Disagreement Between a Patient/Proxy and a Physician Regarding a DNR Order Placement | |
| 1 region reported that a 2nd consult can be requested, but that the patient/proxy has the final say | ||
| 1 region reported that the patient/proxy has the final say | ||
| 1 region reported that a competent patient has the final say | ||
| the remainder of the regions had no policies in place, 1 of these stated that this policy was in development | ||
| 7. | Re: Representation of Persons with Disabilities in Establishing Guidelines Concerning DNR Order Placement | |
| 1 region reported that they had identified people in the community to provide feedback regarding DNR Order policies | ||
| the remained of the regions did not have any representation of persons with disabilities in establishing guidelines. Out of this group, 1 reported that there was support for the idea of input through focus groups or committee representation, and 1 was open to input from the Manitoba League of Persons with Disabilities. | ||
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