MDs Give Selves Duty-to-Die Power over Patients
By Wesley J. Smith
Futile Care Theory has just taken a huge step toward nation-wide imposition with an official policy statement by the American Thoracic Society in collaboration with other medical and nursing associations involved with intensive care internationally. It is a frightening document.
The statement, essentially, creates a right of doctors and hospital bioethics committees to refuse wanted–and admittedly efficacious life-extending treatment–they prefer not to provide. It is like the sign over a restaurant door: We Reserve the Right to Refuse Service.
There are three parts of the document I need to quote to illustrate the danger posed by the Statement to people with profound disabilities, the elderly, and the dying who want to fight to stay alive. First, the admission that medical futility isn’t really “futile.” From the statement (my emphasis):
The term “potentially
inappropriate” should be used, rather than “futile,” to describe
treatments that have at least some chance of accomplishing the effect
sought by the patient, but clinicians believe that competing ethical
considerations justify not providing them.
Think carefully about that. Doctors are establishing the right to
create a conflict of interest with patients by sacrificing their
fiduciary obligation to each individual on the altar of other matters
that should be of lesser concern, such as the cost of care, perceived
societal betterment, personal disagreements with patient values,
religion, or desire to live as long as achievable, the
doctor’s/bioethicists’ belief in the quality of life ethic. There are
the usual bromides about effective communication–and I am sure they
think they mean it.But realize, the document gives the ultimate power to strangers, rather than the patient or family–including the contents of an advance medical directive or POLST [Physicians Orders for Life Sustaining Treatment] order.
With that power structure firmly in place, communication can quickly devolved into coercion because everyone will know that the most the family/patient can do is stall the outcome, not actually prevent the refusal of treatment. If a bioethics committee–hold meetings which are held behind closed doors, are confidential, and doesn’t keep detailed records, such as transcriptions, etc.–rules that the treatment should be stopped, the onus is on the very sick patient or overmatched family to take protective action:
5. Offer surrogates the opportunity to transfer the patient to an alternate institution
6. Inform surrogates of the opportunity to pursue extramural appeal
7. Implement the decision of the resolution process
And here’s where the organizations want their hammer of raw power reinforced by statutory law:
The medical profession should
lead public engagement efforts and advocate for policies and legislation
about when life-prolonging technologies should not be used.
Make no mistake, the Policy Statement seeks to further the power of the technocracy by
enabling Obamacare cost/benefit panels to make decisions allowing the
loss of insurance coverage for efficacious treatments a doctor or
hospital consider “potentially inappropriate.” It is medical authoriarianism, the power of a doctor-imposed duty to die.These decisions are value–not medical–judgments, as the Statement acknowledges. Rather than cooperating with this medical authoritarianism, lawmakers should pass laws preventing such impositions, or at the very least, requiring continued treatment until another facility or doctor can be found.
On the macro level, the centralized control that epitomizes the approach of Obamacare needs to be shattered. Fail to do that, and within a decade, we will all potentially face the duty to die.
Editor’s note. This appeared on Wesley’s great blog.
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Source: NRLC News
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