SB982: Bill Text

LRB-5968/1

JPC:cdc&amn

2021 - 2022 LEGISLATURE

2021 Senate BILL 982

February 17, 2022 - Introduced by Senators Stroebel and Nass, cosponsored by Representatives Sortwell, Murphy, Behnke, Cabral-Guevara, Moses, Rozar, Wichgers, Thiesfeldt, Brandtjen, Brooks, Horlacher, James and Schraa. Referred to Committee on Insurance, Licensing and Forestry.

SB982,1,4 An Act to create 146.50 and 440.208 of the statutes; relating to: prohibiting discrimination or retaliation against health care providers by health care entities and credentialing boards for ordering or discussing innovative or novel therapies.

Analysis by the Legislative Reference Bureau

This bill prevents health care entities and credentialing boards from discriminating or retaliating against health care providers for ordering innovative therapies or novel therapies if certain conditions are met, including: 1) the health care provider orders the therapy based on his or her assessment of the patient and any available clinical data supporting the therapy; 2) the patient requests the innovative therapy or novel therapy; and 3) the ordered therapy, if the therapy is a drug, device, or biological product, is either approved or authorized for emergency use by the federal Food and Drug Administration. Further, this bill prevents any health care entity or credentialing board from restricting any health care provider from informing a patient of any innovative or novel therapy that may potentially benefit the patient.

The people of the state of Wisconsin, represented in senate and assembly, do enact as follows:

SB982,1 Section 1. 146.50 of the statutes is created to read:

SB982,2,1 146.50 Novel and innovative therapies. (1) In this section:

SB982,2,3 (a) “Health care entity” has the meaning given for “health care provider” in s. 146.81 (1) (i) to (p).

SB982,2,4 (b) “Health care provider” has the meaning given in s. 146.81 (1) (a) to (hp).

SB982,2,7 (2) No health care entity may retaliate against, discriminate against, or deny privileges to a health care provider for ordering an innovative or novel therapy if all of the following apply:

SB982,2,10 (a) The health care provider orders the innovative or novel therapy based on his or her assessment of the patient and any available clinical data supporting the innovative or novel therapy.

SB982,2,12 (b) The patient is informed of all reasonable alternative courses of treatment and requests the innovative or novel therapy over alternative courses of treatment.

SB982,2,16 (c) If the ordered innovative or novel therapy is a drug, device, or biological product, the ordered drug, device, or biological product is approved by the federal food and drug administration under 21 USC 355 or is authorized for emergency use by the federal food and drug administration under 21 USC 360bbb-3.

SB982,2,19 (3) A health care entity may not restrict, directly or indirectly, any health care provider from informing a patient of any innovative or novel therapy that may potentially benefit the patient.

SB982,2 Section 2. 440.208 of the statutes is created to read:

SB982,2,22 440.208 Novel and innovative therapies. (1) In this section, “health care provider” has the meaning given in s. 146.81 (1) (a) to (hp).

SB982,2,25 (2) No credentialing board may retaliate against, discriminate against, or deny, suspend, limit, or revoke a credential to a health care provider for ordering an innovative or novel therapy if all of the following apply:

SB982,3,3 (a) The health care provider orders the innovative or novel therapy based on his or her assessment of the patient and any available clinical data supporting the innovative or novel therapy.

SB982,3,5 (b) The patient is informed of all reasonable alternative courses of treatment and requests the innovative or novel therapy over alternative courses of treatment.

SB982,3,9 (c) If the ordered innovative or novel therapy is a drug, device, or biological product, the ordered drug, device, or biological product is approved by the federal food and drug administration under 21 USC 355 or is authorized for emergency use by the federal food and drug administration under 21 USC 360bbb-3.

SB982,3,12 (3) No credentialing board may restrict, directly or indirectly, by rule or any other official action, any health care provider from informing a patient of any innovative or novel therapy that may potentially benefit the patient.

SB982,3,13 (End)