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JCPSLP

Volume 17, Supplement 1, 2015 – Ethical practice in speech pathology

63

Ethics and dysphagia management

Case 3

Max is an 88-year-old resident in a nursing home. He has

advanced dementia. He presents to hospital with a severe

pneumonia as a result of profound dysphagia which is due

to his end-stage dementia. He has no advanced care

directives and no family. His financial affairs are managed by

the public guardian. Medical management favours

placement of a PEG so that Max can be discharged back

to his nursing home as soon as possible.

Discussion

Who can give informed consent?

Each of these cases raises different issues for the team with

regard to who can provide informed consent. When

considering substituted consent, speech pathologists need

to be aware of not only ethical considerations that arise in

individual cases but also relevant laws and legislation.

These may include:

Emergency decisions

If there was an urgent (life and

death) emergency need for medications for John,

Anna or Max, then two doctors could consent to the

placement of a NGT (or PEG, including administration

of anaesthetic). Placement of a NGT for delivery of

medication could most easily be argued by medical

teams in Anna’s situation.

Mental health act

An important consideration for John is

whether he is covered by a mental health act.

2

Each

Australian state and territory has a different mental health

act. In some states, treatment decisions may be made

for John by the State Director of Mental Health Services

(a psychiatrist). Establishing whether John is covered

under a mental health act is simply done by contacting

his treating mental health team. If he was covered by a

mental health Act his affairs may have been handed over

to an adult guardian. The adult guardian would then be

the substitute decision-maker for John’s general health

and well being. If John was not covered by a mental

health act then his father would be considered his next

of kin and would be the substitute decision-maker.

Consent to treatment and palliative care acts

Unfortunately, in Anna and Max’s cases there are

no clearly designated decision-makers to assist

in determining appropriate treatment options. The

challenge in Anna’s case is the advanced care directive

simply stating she does not want tube for feeding. Is

this the same as refusing a tube for medication? Would

Anna perceive a tube for medication as an extraordinary

measure and refuse it if able?

It is reasonable and ethical to respect Anna’s right to have

control over the end of her life. From state to state, however,

there are different views about advanced care directives

and their legality and validity.

3

In Anna’s case, if we are to

consider the principle of autonomy, it would suggest her

clearly expressed wish should be respected and form

part of the treating team’s deliberations. The absence of

I

n this edition of Ethical Conversations, we consider

ethical issues related to informed consent and the

placement of feeding tubes. Informed consent is the

right of individuals to make decisions about their treatment

based on all relevant information of the risks and benefits

of that treatment (Mitchell, Kerridge, & Lovatt, 1996). It is

predicated on the principle of client autonomy. Autonomy is

about respecting the rights of people to self-determination

in relation to decisions which affect them (Speech

Pathology Australia, 2000). Autonomy is the principle that

underpins issues such as consent, refusal of treatment, and

confidentiality (Smith, 2007).

In certain circumstances a person’s right to give consent

may be removed. This can occur as a result of impaired

capacity to make decisions or in the case of severe mental

health issues when a person’s choice could result in harm

to themselves or others (Trobec, Herbst, & Žvanut, 2009). In

these circumstances another person or statutory body may

become the designated substitute decision-maker.

Three cases are provided to illustrate a number

of issues speech pathologists may want to consider

when contemplating substituted informed consent

for the placement of feeding tubes (either short-term

such as nasogastric tubes [NGTs] or long-term such as

percutaneous endoscopic gastrostomy tubes [PEG tubes]).

Case scenarios

Case 1

John is in his early 30s and has a long history of schizophrenia.

John’s schizophrenia is being managed by medication and

is currently stable. He is single and lives with his very caring

father. On this most recent admission to hospital, John

presents with swallowing problems as a result of treatment

for cerebral lymphoma. He is unable to communicate

coherently nor is he able to eat, drink, or swallow his

medications safely. He pulls out all NGTs and intravenous

therapy. The medical team propose surgically placing a

PEG feeding tube into John’s stomach to provide nutrition,

hydration, and medications while he continues his

treatment for lymphoma. There is a good prognosis for his

lymphoma treatment.

Case 2

Anna is in her late 60s and has suffered a stroke. On the

day after her stroke she has severe language impairment

(dysphasia) and is unable to speak or answer simple yes/no

questions. She has profound dysphagia and her poor

swallowing prevents her from taking any food, fluid, or

medication by mouth. Anna has no family but has a legally

prepared Advanced Care Directive

1

that states she does

not want artificial (tube) feeding. Medical management

favours placement of a temporary NGT so Anna can be

given urgent cardiac medication which can only be given

via a tube or by mouth. If she does not receive this

medication she is at risk of a heart attack or further strokes.

To tube or not to tube:

Who can ethically answer

that question?

Helen Smith and Noel Muller

Helen Smith

(top) and Noel

Muller