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 s 1.]
Notes:
*Reviser's note: Section 5, chapter 302, Laws of 2009 was vetoed by the governor.