(1) As used in this section:
- (a) “Administer” means to directly apply a drug to the body of a patient by injection, inhalation, ingestion or any other means.
(b)
(A) “Clinician-administered drug” means an outpatient prescription drug that:
- (i) Cannot reasonably be:
- (I) Administered by a patient for whom the drug is prescribed; or
- (II) Administered by an individual other than a health care provider who is assisting the patient with the self-administration of the drug; and
- (ii) Is typically administered in the office of an enrollee’s physician or another of the enrollee’s health care providers authorized by law to administer the drug.
(B) “Clinician-administered drug” does not include a:
- (i) Vaccine;
- (ii) Drug administered through a clinic affiliated with a hospital;
- (iii) Drug administered in a hospital; or
- (iv) Drug administered in an outpatient infusion center that is in a hospital or that is affiliated with a hospital.
- (c) “Health benefit plan” has the meaning given that term in ORS 743B.005.
- (d) “Health care provider” means an individual who is licensed, certified or otherwise authorized to provide health care services in this state.
(2) Subject to subsection (3) of this section, a health benefit plan that reimburses the cost of hospital or medical expenses may not, for a covered clinician-administered drug for the treatment of cancer or a covered drug administered by an enrollee’s oncology clinic to treat a symptom, complication or consequence of cancer:
- (a) Require the drug to be dispensed only by certain pharmacies or only by pharmacies participating in the health benefit plan issuer’s provider network;
- (b) Limit or deny coverage of the drug based on the enrollee’s choice of pharmacy or because the drug was not dispensed by a pharmacy that participates in the health benefit plan issuer’s provider network;
(c) Require a physician or health care provider participating in the health benefit plan issuer’s provider network to bill for or be reimbursed for the delivery and administration of the drugs as a pharmacy benefit instead of as a medical benefit under the plan unless:
- (A) The patient has provided informed written consent; and
- (B) The patient’s physician or health care provider attests in writing that a delay in the administration of the drug will not place the patient at an increased health risk; or
- (d) Require the enrollee to pay an additional fee or other increased cost for the drug based on the enrollee’s choice of pharmacy or because the drug was not dispensed by a pharmacy that participates in the health benefit plan issuer’s provider network.
(3) Subsection (2) of this section applies to a drug only if the enrollee’s physician or health care provider determines that:
- (a) A delay in care would make disease progression probable;
(b) The use of a pharmacy within the health benefit plan issuer’s provider network would:
- (A) Make death or patient harm probable; or
- (B) Potentially cause a barrier to the enrollee’s adherence to or compliance with the enrollee’s plan of care; or
- (c) The timeliness of the delivery or dosage requirements necessitate delivery by a pharmacy that is outside of the health benefit plan issuer’s provider network.
(4) This section does not:
- (a) Authorize a person to administer a drug when otherwise prohibited by state or federal law; or
- (b) Modify drug administration requirements under state law, including any requirements related to the delegation and supervision of the administration of drugs.
Note: 743B.610 was added to and made a part of the Insurance Code by legislative action but was not added to ORS chapter 743B or any series therein. See Preface to Oregon Revised Statutes for further explanation.
[2024 c.24 §2]