The incalculable cost of assisted suicide laws

The process comes with a price-tag, but the social costs cannot be estimated.

Cristina Alarcon | Aug 24 2016 | comment

In June 2016, Bill C-14 (the legislation on medical assistance in dying) received royal and assent and a new medical service became available to Canadians. This legislation provides some Canadians (patients) with the legal option to request medical assistance in dying and other Canadians (physicians and nurse practitioners) with the legal authority to provide that assistance. But at what cost?

The financial costs related to medical assistance in dying are relatively inexpensive. Physician’s fees have not yet been determined, but an interim document lists the cost at $ 440.05 for a general practitioner and $519.08 for a specialist. The drugs themselves will cost about $300. In British Columbia, for example, participating drug stores will charge a $60 to $100 “clinical services” fee for dispensing the oral or IV drug regimen plus a backup- in case the patient fails to die.

The social costs of medical assistance in dying might be higher.

First, much has already been said about safeguards that may never be. Already a BC court case seeks to “strike down” as unconstitutional the provision in C-14 that states a person’s “natural death must be reasonably foreseeable” to qualify for death by lethal injection. In time, treatable chronic illnesses may become eligible for this irreversible “treatment.”

Second, there are concerns about harm to vulnerable persons. For example, in 2004, a British nurse tried to murder four of her elderly patients in a ruthless drive to free up hospital beds. In April 2015, a Czech nurse admitted to killing six patients to decrease her workload. A 2015 Ontario coroner’s report that examined deaths at long-term care facilities, included 13 that were considered homicide in 2013 and 2014. Will legalized killing become the precarious road we take to unburden an overtaxed Canadian healthcare system? I have witnessed first-hand the ways that the Government tries to claw back on medical costs. I worry that medical assistance in dying might offer them an easier and faster way of reducing the cost of healthcare services.

Third, poor quality healthcare might lead some individuals to request assistance in ending their lives prematurely. The Montreal Gazette recently reported that a 52-year-old long-term care patient would rather end his life than live at a facility that he says is treating him inhumanely.

In 2015, the CBC reported that Ontario long-term care system is “a system in crisis,” and that the province’s chief coroner urged the Ontario government to take action against increasing violence in care homes.

Fourth, what will happen to the physicians or nurse practitioners who do the deed and experience guilt or to those who are forced to refer against their conscience? Will the healthcare professions lose their way?

Finally, as a pharmacist, the legalization of medical assistance in dying will impact my professional world. Some of my colleagues have jumped on the medical assistance in dying band-wagon, but I have refused to do so. This is because I’m concerned about the implications for myself, my patients, and society more generally.

My regulatory college, the College of Pharmacists of British Columbia, does not currently require that I dispense the drugs for medical assistance in dying nor that I provide a referral to someone who will. But, it does require that I provide information about this service to patients. Patients rely on me to catch any prescribing errors that could hasten their demise. I work to ensure that patients are not poisoned and that they remain as healthy as possible until their natural death. Often, my elderly patients are alone and have no one to advocate for them. Those who don’t have a family doctor, usually turn to me for medical advice and I wouldn’t want to direct them towards their demise. So, I worry that performing an action contrary to ethic, such as providing information about medical assistance in dying, might desensitize my conscience or corrupt me as a professional.

Further, as the manager of a community pharmacy that services long-term care homes, I know that residents sometimes want to die. I remember one woman asked me how many pills of a particular drug she would need in order to kill herself. I worry that such suicidal wishes are always present in our society.

In a post C-14 Canada there is much at risk. Will we ever get adequate palliative care? Will we continue research into better pain medication? Will Alzheimer’s research become less relevant? Will we forget how to treat chronic conditions that are not terminal in themselves? There may be so much that we will never know or see because we choose to end life prematurely.

The decriminalization of assisted suicide and euthanasia – euphemistically “medical assistance in dying”—may give some patients the semblance of control but at a considerable cost to themselves and society in terms of true well-being or choice.

Cristina Alarcon is a community pharmacist and a clinical instructor of pharmacy practice for the faculty of Pharmaceutical Sciences at the University of British Columbia. This article was first published at Impact Ethics abd is reproduced under a non-commercial licence. To redistribute, go to the original article.

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