The definitions in this
section apply throughout this chapter unless the context clearly
requires otherwise.
(1) "Advisory committee" means the advisory committee on
genetic counseling established in *section 5 of this act.
(2) "Collaborative agreement" means a written document that
memorializes a relationship between a genetic counselor and a
physician licensed under chapter 18.71 RCW or an osteopathic
physician licensed under chapter 18.57 RCW, who is board
certified in medical genetics or who is board certified in a
specialty relevant to the practice of the genetic counselor that
authorizes a genetic counselor to perform the functions specified
in subsection (5)(d) of this section as applied to the practice
of genetic counseling.
(3) "Department" means the department of health.
(4) "Genetic counselor" means an individual who is licensed
to engage in the practice of genetic counseling under this
chapter.
(5) "Practice of genetic counseling" means a communication
process, conducted by one or more appropriately trained
individuals that includes:
(a) Estimating the likelihood of occurrence or recurrence of
a birth defect or of any potentially inherited or genetically
influenced condition. This assessment may involve:
(i) Obtaining and analyzing a complete health history of the
person and family;
(ii) Reviewing pertinent medical records;
(iii) Evaluating the risks from exposure to possible
mutagens or teratogens; and
(iv) Providing recommendations for genetic testing or other
evaluations to diagnose a condition or determine the carrier
status of one or more family members;
(b) Helping the individual, family, or health care provider:
(i) Appreciate the medical and psychosocial implications of
a disorder, including its features, variability, usual course,
and management options;
(ii) Learn how genetic factors contribute to the disorder
and affect the chance for recurrence of the condition in other
family members;
(iii) Understand available options for coping with,
preventing, or reducing the chance of occurrence or recurrence of
a condition;
(iv) Understand genetic or prenatal tests, coordinate
testing for inherited disorders, and interpret complex genetic
test results;
(c) Facilitating an individual's or family's:
(i) Exploration of the perception of risk and burden
associated with the disorder;
(ii) Decision making regarding testing or medical
interventions consistent with their beliefs, goals, needs,
resources, and cultural, ethical, and moral views; and
(iii) Adjustment and adaptation to the condition or their
genetic risk by addressing needs for psychosocial and medical
support; and
(d) Pursuant to a collaborative agreement:
(i) Ordering genetic tests or other evaluations to diagnose
a condition or determine the carrier status of one or more family
members, including testing for inherited disorders; and
(ii) Selecting the most appropriate, accurate, and
cost-effective methods of diagnosis.
(6) "Secretary" means the secretary of health.
[2009 c 302 § 1.]
NOTES:
*Reviser's note: Section 5, chapter 302, Laws of 2009 was vetoed by the governor.