By Marvin Ross I first wrote about this problem in the article below in 2015 in Huffington Post and health privacy is still a problem that has never been addressed by most jurisdictions. A recent Manitoba law introduced that would allow medical professionals to contact a patient’s support network in situations where serious harm is … Continue reading Mental Health Privacy Policies Leave Families In The Dark →
By Marvin Ross
I first wrote about this problem in the article below in 2015 in Huffington Post and health privacy is still a problem that has never been addressed by most jurisdictions. A recent Manitoba law introduced that would allow medical professionals to contact a patient’s support network in situations where serious harm is likely to result otherwise sounds quite logical and based on common sense but it is controversial and resisted in many jurisdictions..
Manitoba’s law arose, in part, from the case of Reid Bricker who took his life after being discharged from hospital. On his fourth discharge from hospital the 33 year old man succeeded at his fourth attempt of suicide. The doctor who discharged him before his successful suicide attempt noted that he would try again. He did just that but no one notified his family that he was being discharged. Had the family been notified, the outcome may have been different.
This is one of the biggest complaints that families of the mentally ill – the failure of the health system to provide them with information. Families provide ongoing care, support and housing, and yet the privacy legislation in most jurisdictions in both Canada and the U.S. prohibit staff from talking to them.
A published paper out of Western University in London, Ontario argues that despite that legislation, “clinicians have a duty to their patients’ relatives, and that clinicians regularly fail to take available practical and legal steps to ensure that families receive the information they need.”
The paper written by Dr. Richard O’Reilly, an emeritus professor of psychiatry, Dr. John Gray, an adjunct professor of psychiatry along with J. Jung, a student in the Faculty of Science appeared in the Journal of Ethics in Mental Health.
The problem, according to the authors, is that because of the lack of availability of suitable supportive housing and psychiatric hospital beds, most seriously mentally ill people live with their families. Those families wind up taking on both therapeutic and supportive functions for their seriously ill relatives. Given this role and the fact that research has shown that involving families helps to improve treatment outcomes, it would be expected that the mental health system would make efforts to support those families — but they rarely do.
Families constantly complain about this failure to keep them informed or to consult with them. The Mental Health Commission of Canada made those recommendations in its Report on Caregivers but they have no authority (Recommendation 7). One of the key recommendations of the Ontario 2008 Select Committee Report that Ontario continually ignores is to revise the privacy legislation.
Unfortunately, clinicians do not always understand the privacy legislation which varies by jurisdiction and is complex. British Columbia requires hospitals to inform families when someone is involuntarily admitted or discharged from hospital. Other provinces, however, prohibit staff from telling family without the person’s consent and, in Ontario, a $50,000 fine for failure to comply with privacy legislation can be imposed on health care staff. As a result, staff err on the side of caution and become even more secretive.
Professionals may be even more reluctant because of the high value they place on individualism, the lingering views by some that families are a cause of illness, and that staff are more experienced offering individual based therapy as opposed to family therapy. And, the authors state, if all this is not bad enough, there are logistical barriers imposed by the system.
Length of stay in psychiatric units have become shorter while staff have become busier trying to manage all the patients passing though. This rapid turnover makes it very difficult for them to meet with families. Arranging family meetings is more difficult and less efficient than spending time on the ward with the individual patient. Payment is another concern since staff often do not make as much talking to families on the phone as they would interacting with the patient and hospitals do not provide staff with the flexibility to accommodate family involvement.
Even without changing the privacy legislation, the authors suggest a number of steps that health care providers can take to help families. They point out that clinicians often don’t even bother to ask their patients if they have permission to involve family.
If they do and the patient refuses, then they should take the time to explore the reasons for this refusal. Many patients don’t understand why it is important and do agree to allow their families information once it is explained to them. In some cases, there is some information they do not want shared (like sexual activity and/or drug use) and the staff can ensure that this information is not shared. Staff can also inform families of pertinent facts in meetings with the patient present. This often allays patient fears and is similar to the approach recommended in the UK and by the Mental Health Commission of Canada.
In those cases where no consent is given, the staff can give general information to the families and receive vital information from the family. The family can tell the doctors about new emerging symptoms, worsening of symptoms and medication side effects, all of which should be crucial information.
Until such time as political jurisdictions reform the privacy legislation, mental health staff can do far more to open the channels of communication with families for the betterment of their patients. It is time they do so.
