Connecticut 2017 Regular Session Status: In Committee

SB 19 — AN ACT REQUIRING HEALTH INSURANCE COVERAGE OF A PRESCRIBED DRUG FOR A CHRONIC DISEASE DURING CERTAIN ADVERSE DETERMINATION REVIEWS.

Last action — REF. TO JOINT COMM. ON Insurance and Real Estate

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  1. ✓
    Introduced
  2. 2
    In Committee
  3. 3
    Passed Senate
  4. 4
    Passed House
  5. 5
    To Executive
  6. 6
    Enacted

This bill died with 2017 Regular Session. It reached “In Committee” and never advanced before the session ended, so it can no longer move — a new version would have to be reintroduced in the current session.

This bill is no longer active — its legislative session has ended, so there is no live prognosis. It would have to be reintroduced in the current session to move again.

Bill Text

What changed in the latest version

46 added · 7 removed

Plain-language change summary

The updated version of the bill specifies that health insurance coverage is required for a prescribed drug for a chronic disease during certain adverse determination reviews, rather than a chronic condition as previously stated. Additionally, the requirement now includes a focus on prescribed drugs issued by licensed participating providers who are specialists in chronic diseases and clarifies that electronic authorization for a temporary supply of such drugs must be provided during the review. This change ensures that individuals receiving treatment for chronic diseases can access necessary medications while their coverage is being reviewed.

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AN ACT REQUIRING HEALTH INSURANCE COVERAGE OF A PRESCRIBED DRUG FOR A CHRONIC CONDITION DURING CERTAIN ADVERSE DETERMINATION REVIEWS.
AN ACT REQUIRING HEALTH INSURANCE COVERAGE OF A PRESCRIBED DRUG FOR A CHRONIC DISEASE DURING CERTAIN ADVERSE DETERMINATION REVIEWS.
General Assembly   Proposed Bill No.
General Assembly   Committee Bill No.
19   January Session, 2017   LCO No.
19 January Session, 2017   LCO No.
817   *00817* Referred to Committee on INSURANCE AND REAL ESTATE   Introduced by:
4336   *04336SB00019INS* Referred to Committee on INSURANCE AND REAL ESTATE   Introduced by:
  SEN.
  (INS)   AN ACT REQUIRING HEALTH INSURANCE COVERAGE OF A PRESCRIBED DRUG FOR A CHRONIC DISEASE DURING CERTAIN ADVERSE DETERMINATION REVIEWS.
LOONEY, 11th Dist.
  AN ACT REQUIRING HEALTH INSURANCE COVERAGE OF A PRESCRIBED DRUG FOR A CHRONIC CONDITION DURING CERTAIN ADVERSE DETERMINATION REVIEWS.
That chapter 700c of the general statutes be amended to require health insurance coverage, during certain adverse determination reviews, of a prescribed drug other than a schedule II or III controlled substance for a chronic condition, except such requirement shall not apply where a review concerns substitution of a generic drug for a brand name drug.
Section 1.
Statement of Purpose:
Subsection (b) of section 38a-591d of the general statutes is repealed and the following is substituted in lieu thereof (Effective January 1, 2018):
To require health insurance coverage, during certain adverse determination reviews, of a prescribed drug other than a schedule II or III controlled substance for a chronic condition.
(b) With respect to a nonurgent care request:
(1) (A) For a prospective or concurrent review request, a health carrier shall make a determination within a reasonable period of time appropriate to the covered person's medical condition, but not later than fifteen calendar days after the date the health carrier receives such request, and shall notify the covered person and, if applicable, the covered person's authorized representative of such determination, whether or not the carrier certifies the provision of the benefit.
(B) If the review under subparagraph (A) of this subdivision is a review of a grievance involving a concurrent review request, pursuant to 45 CFR 147.136, as amended from time to time, the treatment shall be continued without liability to the covered person until the covered person has been notified of the review decision.
(C) (i) If the review under subparagraph (A) of this subdivision is a review of a grievance involving a prospective review request relating to the dispensing of a drug for a chronic disease, other than a schedule II or III controlled substance, that is prescribed by a licensed participating provider who is a specialist in such chronic disease, the health carrier shall issue an electronic authorization to the covered person's pharmacy for the dispensing of a temporary supply of such drug sufficient for the duration of such review until the covered person has been notified of the review decision.
Such authorization shall include confirmation of the availability of payment for such supply of such drug.
(ii) Not later than twenty-four hours after the health carrier has issued such authorization to the pharmacy and prior to the pharmacy's dispensation of such drug, such health carrier shall confirm with such participating provider the provider's concurrence with the dispensing of such temporary supply of such drug.
If such participating provider does not concur, the health carrier shall cancel such authorization.
(2) For a retrospective review request, a health carrier shall make a determination within a reasonable period of time, but not later than thirty calendar days after the date the health carrier receives such request.
(3) The time periods specified in subdivisions (1) and (2) of this subsection may be extended once by the health carrier for up to fifteen calendar days, provided the health carrier:
(A) Determines that an extension is necessary due to circumstances beyond the health carrier's control;
and (B) Notifies the covered person and, if applicable, the covered person's authorized representative prior to the expiration of the initial time period, of the circumstances requiring the extension of time and the date by which the health carrier expects to make a determination.
(4) (A) If the extension pursuant to subdivision (3) of this subsection is necessary due to the failure of the covered person or the covered person's authorized representative to provide information necessary to make a determination on the request, the health carrier shall:
(i) Specifically describe in the notice of extension the required information necessary to complete the request;
and (ii) Provide the covered person and, if applicable, the covered person's authorized representative with not less than forty-five calendar days after the date of receipt of the notice to provide the specified information.
(B) If the covered person or the covered person's authorized representative fails to submit the specified information before the end of the period of the extension, the health carrier may deny certification of the benefit requested.
(c) With respect to an urgent care request:
(1) (A) Unless the covered person or the covered person's authorized representative has failed to provide information necessary for the health carrier to make a determination and except as specified under subparagraph (B) of this subdivision, the health carrier shall make a determination as soon as possible, taking into account the covered person's medical condition, but not later than seventy-two hours after the health carrier receives such request, provided, if the urgent care request is a concurrent review request to extend a course of treatment beyond the initial period of time or the number of treatments, such request is made at least twenty-four hours prior to the expiration of the prescribed period of time or number of treatments.
(B) Unless the covered person or the covered person's authorized representative has failed to provide information necessary for the health carrier to make a determination, for an urgent care request specified under subparagraph (B) or (C) of subdivision (38) of section 38a-591a, the health carrier shall make a determination as soon as possible, taking into account the covered person's medical condition, but not later than twenty-four hours after the health carrier receives such request, provided, if the urgent care request is a concurrent review request to extend a course of treatment beyond the initial period of time or the number of treatments, such request is made at least twenty-four hours prior to the expiration of the prescribed period of time or number of treatments.
(2) (A) If the covered person or the covered person's authorized representative has failed to provide information necessary for the health carrier to make a determination, the health carrier shall notify the covered person or the covered person's representative, as applicable, as soon as possible, but not later than twenty-four hours after the health carrier receives such request.
(B) The health carrier shall provide the covered person or the covered person's authorized representative, as applicable, a reasonable period of time to submit the specified information, taking into account the covered person's medical condition, but not less than forty-eight hours after notifying the covered person or the covered person's authorized representative, as applicable.
(3) The health carrier shall notify the covered person and, if applicable, the covered person's authorized representative of its determination as soon as possible, but not later than forty-eight hours after the earlier of (A) the date on which the covered person and the covered person's authorized representative, as applicable, provides the specified information to the health carrier, or (B) the date on which the specified information was to have been submitted.
Sec.
2.
Subsection (c) of section 38a-591e of the general statutes is repealed and the following is substituted in lieu thereof (Effective January 1, 2018):
(c) (1) (A) When conducting a review of an adverse determination under this section, the health carrier shall ensure that such review is conducted in a manner to ensure the independence and impartiality of the clinical peer or peers involved in making the review decision.
(B) If the adverse determination involves utilization review, the health carrier shall designate an appropriate clinical peer or peers to review such adverse determination.
Such clinical peer or peers shall not have been involved in the initial adverse determination.
(C) The clinical peer or peers conducting a review under this section shall take into consideration all comments, documents, records and other information relevant to the covered person's benefit request that is the subject of the adverse determination under review, that are submitted by the covered person or the covered person's authorized representative, regardless of whether such information was submitted or considered in making the initial adverse determination.
(D) Prior to issuing a decision, the health carrier shall provide free of charge, by facsimile, electronic means or any other expeditious method available, to the covered person or the covered person's authorized representative, as applicable, any new or additional documents, communications, information and evidence relied upon and any new or additional scientific or clinical rationale used by the health carrier in connection with the grievance.
Such documents, communications, information, evidence and rationale shall be provided sufficiently in advance of the date the health carrier is required to issue a decision to permit the covered person or the covered person's authorized representative, as applicable, a reasonable opportunity to respond prior to such date.
(2) If the review under subdivision (1) of this subsection is an expedited review, all necessary information, including the health carrier's decision, shall be transmitted between the health carrier and the covered person or the covered person's authorized representative, as applicable, by telephone, facsimile, electronic means or any other expeditious method available.
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(3) If the review under subdivision (1) of this subsection is an expedited review of a grievance involving an adverse determination of a concurrent review request, pursuant to 45 CFR 147.136, as amended from time to time, the treatment shall be continued without liability to the covered person until the covered person has been notified of the review decision.
(4) (A) If the review under subdivision (1) of this subsection is a review of a grievance involving a prospective review request relating to the dispensing of a drug for a chronic disease, other than a schedule II or III controlled substance, that is prescribed by a licensed participating provider who is a specialist in such chronic disease, the health carrier shall issue an electronic authorization to the covered person's pharmacy for the dispensing of a temporary supply of such drug sufficient for the duration of such review until the covered person has been notified of the review decision.
Such authorization shall include confirmation of the availability of payment for such supply of such drug.
(B) Not later than twenty-four hours after the health carrier has issued such authorization to the pharmacy and prior to the pharmacy's dispensation of such drug, such health carrier shall confirm with such participating provider the provider's concurrence with the dispensing of such temporary supply of such drug.
If such participating provider does not concur, the health carrier shall cancel such authorization.
This act shall take effect as follows and shall amend the following sections:
Section 1 January 1, 2018 38a-591d(b) Sec.
2 January 1, 2018 38a-591e(c) Statement of Purpose:
To require health insurance coverage, during certain adverse determination reviews, of a prescribed drug, other than a schedule II or III controlled substance, for treatment of a chronic disease.
[Proposed deletions are enclosed in brackets.
Proposed additions are indicated by underline, except that when the entire text of a bill or resolution or a section of a bill or resolution is new, it is not underlined.] Co-Sponsors:
SEN.
LOONEY, 11th Dist.
S.B.
19
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Action History

  1. REF. TO JOINT COMM. ON Insurance and Real Estate

  2. DRAFTED BY COMMITTEE

  3. Vote to Draft

  4. PUBLIC HEARING 0207

  5. Reserved for Subject Matter Public Hearing

  6. REF. TO JOINT COMM. ON Insurance and Real Estate

Sponsors

  • Martin M.' b'Looney · Primary

Sponsorship breakdown

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1 sponsors · 0 co-sponsors · 186 not signed on

Sponsors (1)

  • b'Looney, Martin M.'

Co-sponsors (0)

None.

Not signed on (186)

186 members have not signed on to this bill.

Show all 186 →

"Not signed on" means a member has not sponsored or co-sponsored this bill — it does not imply opposition. Members flagged Voted No have a recorded No vote on this bill.

Whip count is in markup. Polling the chamber and every recorded vote this session. Only the first open is slow. It’s instant for you after this. Calling the roll · Tallying · Engrossing

Subjects

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Frequently asked questions

Who sponsors SB 19?
SB 19 is sponsored by b'Looney, Martin M.'.
What is the current status of SB 19?
This bill died with 2017 Regular Session. It reached “In Committee” and never advanced before the session ended, so it can no longer move — a new version would have to be reintroduced in the current session.
Where can I track SB 19?
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