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University of Iowa
Division of Medical Genetics
Testing Protocols
Patients Name:
Hospital Number:
Date:
Presymptomatic Testing for Spinocerebellar Ataxia Informed
Consent
I ______________________________ choose to participate
in presymptomatic testing for the presence of the Spinocerebellar Ataxia (SCA) gene. I have been
told that I am at risk for SCA because there is a history of this disorder in my family. I
understand genetic material will be evaluated only for the gene change responsible for SCA and
will not be used for any other testing. This test will most likely tell me if I have or have not
inherited the gene that causes SCA.
I understand I must participate in a testing protocol
that provides genetic counseling and any necessary follow up care. I agree to participate in the
minimum of three counseling sessions required for the testing. There will be at least two
sessions prior to the test result session. Sessions will last 1-3 hours. These sessions will
include information about SCA, genetic testing, consequences of results and available support
services.
I understand a neurological exam is recommended. I am
aware this examination may disclose that I have clinical signs of SCA and I will be told of my
results.
I understand the test does have some limitations.
First, it is not known if everyone who is affected with SCA has the same change in the gene
causing the disease. Second, occasionally the result of gene analysis cannot be interpreted with
confidence.
I understand there can be three outcomes to the test:
1. The gene change in my family might not be
interpretable, so my test results will not tell me more than I know now.
2. I do not have the SCA mutation.
3. The SCA gene mutation is present and I will develop SCA.
I understand my participation in this program is
voluntary and I can terminate my participation at any time without jeopardy to my medical care.
I understand if at any time my continued participation in this program is considered injurious
to my health or disadvantageous to me, the testing staff may recommend postponement of the
testing.
The information provided is technical and receiving it
will be stressful. Because of this, I am encouraged to bring a close friend, spouse, or other
family member not at risk for SCA to accompany me through the test procedures. I understand the
professionals involved in this testing are willing to answer my questions and to discuss my
concerns with me throughout the testing procedure. Counselors will assist me in arranging for
any additional professional counseling and support I may need.
Risks of this testing include:
A. Concerns of a psychological nature. I understand the
testing may be lengthy and does require a waiting period before results are available. These
events may cause me to confront difficult psychological issues. Since I may withdraw from the
testing protocol at any time and the process is a long one, decisions about my continued
participation may evoke anxiety. An uninterpretable result can be frustrating and can intensify
the ambiguity of the risk situation. Knowing I do not have the common mutation for SCA can
produce mixed emotions. I may also have to confront the fact I have inherited the mutation that
causes SCA and will develop the disease. I am aware the testing cannot predict when I first will
show signs of SCA nor can it predict the severity or rate of progression of SCA. This will also
mean that my children will have a 50% chance of inheriting the SCA mutation.
B. Possible difficulties with employment or insurance.
C. Discomfort of a blood draw and a bruise. I
understand this test requires me to provide 20cc (two tubes) of my blood.
D. Financial liability. I will be responsible for the
costs of the laboratory testing and counseling regardless of the outcome of my testing. In some
cases, medical insurance will not pay for this testing.
I understand results of my testing will not be
available to any one other than the professionals involved and is not to be released to any
second party without my written consent.
Test results will be given only to me and only in person.
______________________________ has explained to me the
purposes of the testing protocol and I agree to participate in this testing program. I
acknowledge the possible risks, discomforts, and benefits I may experience. I have read and I
understand this consent form.
_____________________________________________ Participant / Date
____________________________________________ Witness / Date
Copyright 1997, University of Iowa, Division of Medical Genetics
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