Connecticut 2019 Regular Session

Connecticut Senate Bill SB00037 Compare Versions

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3+LCO No. 920 1 of 1
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4-LCO No. 5682 1 of 9
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6-General Assembly Committee Bill No. 37
5+General Assembly Proposed Bill No. 37
76 January Session, 2019
8-LCO No. 5682
7+LCO No. 920
98
109
1110 Referred to Committee on INSURANCE AND REAL ESTATE
1211
1312
1413 Introduced by:
15-(INS)
14+SEN. LOONEY, 11th Dist.
1615
1716
1817
19-AN ACT REQUIRING HEA LTH INSURANCE COVERAGE O F A
20-PRESCRIBED DRUG DURI NG ADVERSE DETERMINA TION REVIEWS
21-AND EXTERNAL REVIEW PROCESSES.
18+AN ACT REQUIRING HEALTH INSURANCE COVERAGE OF
19+PRESCRIBED DRUGS DURING ADVERSE DETERMINATION
20+REVIEWS AND EXTERNAL REVIEW PROCESSES.
2221 Be it enacted by the Senate and House of Representatives in General
2322 Assembly convened:
2423
25-Section 1. Subsection (b) of section 38a-591d of the general statutes is 1
26-repealed and the following is substituted in lieu thereof (Effective 2
27-January 1, 2020): 3
28-(b) With respect to a nonurgent care request: 4
29-(1) (A) For a prospective or concurrent review request, a health 5
30-carrier shall make a determination within a reasonable period of time 6
31-appropriate to the covered person's medical condition, but not later 7
32-than fifteen calendar days after the date the health carrier receives such 8
33-request, and shall notify the covered person and, if applicable, the 9
34-covered person's authorized representative of such determination, 10
35-whether or not the carrier certifies the provision of the benefit. 11
36-(B) If the review under subparagraph (A) of this subdivision is a 12
37-review of a grievance involving a concurrent review request, pursuant 13
38-to 45 CFR 147.136, as amended from time to time, the treatment shall 14
39-Committee Bill No. 37
40-
41-
42-LCO No. 5682 2 of 9
43-
44-be continued without liability to the covered person until the covered 15
45-person has been notified of the review decision. 16
46-(C) (i) Notwithstanding subparagraph (B) of this subdivision, if a 17
47-covered person or the covered person's authorized representative files 18
48-any grievance or requests any review of an adverse determination 19
49-pursuant to this section relating to the dispensation of a drug, other 20
50-than a schedule II or III controlled substance, prescribed by a licensed 21
51-participating provider, the health carrier shall issue immediate 22
52-electronic authorization to the covered person's pharmacy to dispense 23
53-a temporary supply of the drug sufficient for the duration of the 24
54-grievance or review. The authorization shall include confirmation of 25
55-the availability of payment for such supply of such drug. 26
56-(ii) Not later than twenty-four hours after the health carrier has 27
57-issued such authorization to the pharmacy and prior to the pharmacy's 28
58-dispensation of such drug, such health carrier shall confirm with the 29
59-licensed participating provider the provider's concurrence with the 30
60-dispensing of such temporary supply of such drug. If such licensed 31
61-participating provider does not concur, the health carrier shall cancel 32
62-such authorization. 33
63-(iii) The provisions of this subparagraph shall not apply to a 34
64-grievance or review of an adverse determination under this section 35
65-concerning the substitution of a generic drug or another brand name 36
66-drug for a prescribed brand name drug unless the prescribing licensed 37
67-participating provider has specified that there shall be no substitution 38
68-for the specified brand name drug. 39
69-(2) For a retrospective review request, a health carrier shall make a 40
70-determination within a reasonable period of time, but not later than 41
71-thirty calendar days after the date the health carrier receives such 42
72-request. 43
73-(3) The time periods specified in subdivisions (1) and (2) of this 44
74-subsection may be extended once by the health carrier for up to fifteen 45
75-Committee Bill No. 37
76-
77-
78-LCO No. 5682 3 of 9
79-
80-calendar days, provided the health carrier: 46
81-(A) Determines that an extension is necessary due to circumstances 47
82-beyond the health carrier's control; and 48
83-(B) Notifies the covered person and, if applicable, the covered 49
84-person's authorized representative prior to the expiration of the initial 50
85-time period, of the circumstances requiring the extension of time and 51
86-the date by which the health carrier expects to make a determination. 52
87-(4) (A) If the extension pursuant to subdivision (3) of this subsection 53
88-is necessary due to the failure of the covered person or the covered 54
89-person's authorized representative to provide information necessary to 55
90-make a determination on the request, the health carrier shall: 56
91-(i) Specifically describe in the notice of extension the required 57
92-information necessary to complete the request; and 58
93-(ii) Provide the covered person and, if applicable, the covered 59
94-person's authorized representative with not less than forty-five 60
95-calendar days after the date of receipt of the notice to provide the 61
96-specified information. 62
97-(B) If the covered person or the covered person's authorized 63
98-representative fails to submit the specified information before the end 64
99-of the period of the extension, the health carrier may deny certification 65
100-of the benefit requested. 66
101-Sec. 2. Subsection (c) of section 38a-591e of the general statutes is 67
102-repealed and the following is substituted in lieu thereof (Effective 68
103-January 1, 2020): 69
104-(c) (1) (A) When conducting a review of an adverse determination 70
105-under this section, the health carrier shall ensure that such review is 71
106-conducted in a manner to ensure the independence and impartiality of 72
107-the clinical peer or peers involved in making the review decision. 73
108-Committee Bill No. 37
109-
110-
111-LCO No. 5682 4 of 9
112-
113-(B) If the adverse determination involves utilization review, the 74
114-health carrier shall designate an appropriate clinical peer or peers to 75
115-review such adverse determination. Such clinical peer or peers shall 76
116-not have been involved in the initial adverse determination. 77
117-(C) The clinical peer or peers conducting a review under this section 78
118-shall take into consideration all comments, documents, records and 79
119-other information relevant to the covered person's benefit request that 80
120-is the subject of the adverse determination under review, that are 81
121-submitted by the covered person or the covered person's authorized 82
122-representative, regardless of whether such information was submitted 83
123-or considered in making the initial adverse determination. 84
124-(D) Prior to issuing a decision, the health carrier shall provide free 85
125-of charge, by facsimile, electronic means or any other expeditious 86
126-method available, to the covered person or the covered person's 87
127-authorized representative, as applicable, any new or additional 88
128-documents, communications, information and evidence relied upon 89
129-and any new or additional scientific or clinical rationale used by the 90
130-health carrier in connection with the grievance. Such documents, 91
131-communications, information, evidence and rationale shall be 92
132-provided sufficiently in advance of the date the health carrier is 93
133-required to issue a decision to permit the covered person or the 94
134-covered person's authorized representative, as applicable, a reasonable 95
135-opportunity to respond prior to such date. 96
136-(2) If the review under subdivision (1) of this subsection is an 97
137-expedited review, all necessary information, including the health 98
138-carrier's decision, shall be transmitted between the health carrier and 99
139-the covered person or the covered person's authorized representative, 100
140-as applicable, by telephone, facsimile, electronic means or any other 101
141-expeditious method available. 102
142-(3) If the review under subdivision (1) of this subsection is an 103
143-expedited review of a grievance involving an adverse determination of 104
144-a concurrent review request, pursuant to 45 CFR 147.136, as amended 105
145-Committee Bill No. 37
146-
147-
148-LCO No. 5682 5 of 9
149-
150-from time to time, the treatment shall be continued without liability to 106
151-the covered person until the covered person has been notified of the 107
152-review decision. 108
153-(4) (A) Notwithstanding subdivision (3) of this subsection, if a 109
154-covered person or the covered person's authorized representative files 110
155-any grievance or requests any review of an adverse determination 111
156-pursuant to this section relating to the dispensation of a drug, other 112
157-than a schedule II or III controlled substance, prescribed by a licensed 113
158-participating provider, the health carrier shall issue immediate 114
159-electronic authorization to the covered person's pharmacy to dispense 115
160-a temporary supply of the drug sufficient for the duration of the 116
161-grievance or review. The authorization shall include confirmation of 117
162-the availability of payment for such supply of such drug. 118
163-(B) Not later than twenty-four hours after the health carrier has 119
164-issued such authorization to the pharmacy and prior to the pharmacy's 120
165-dispensation of such drug, such health carrier shall confirm with the 121
166-licensed participating provider the provider's concurrence with the 122
167-dispensing of such temporary supply of such drug. If such licensed 123
168-participating provider does not concur, the health carrier shall cancel 124
169-such authorization. 125
170-(C) The provisions of this subdivision shall not apply to a grievance 126
171-or review of an adverse determination under this section concerning 127
172-the substitution of a generic drug or another brand name drug for a 128
173-prescribed brand name drug unless the prescribing licensed 129
174-participating provider has specified that there shall be no substitution 130
175-for the specified brand name drug. 131
176-Sec. 3. Subsection (b) of section 38a-591f of the general statutes is 132
177-repealed and the following is substituted in lieu thereof (Effective 133
178-January 1, 2020): 134
179-(b) (1) A covered person or the covered person's authorized 135
180-representative may file a grievance of an adverse determination that 136
181-Committee Bill No. 37
182-
183-
184-LCO No. 5682 6 of 9
185-
186-was not based on medical necessity with the health carrier not later 137
187-than one hundred eighty calendar days after the covered person or the 138
188-covered person's representative, as applicable, receives the notice of an 139
189-adverse determination. 140
190-(2) (A) If a covered person or the covered person's authorized 141
191-representative files any grievance or requests any review of an adverse 142
192-determination pursuant to this section relating to the dispensation of a 143
193-drug, other than a schedule II or III controlled substance, prescribed by 144
194-a licensed participating provider, the health carrier shall issue 145
195-immediate electronic authorization to the covered person's pharmacy 146
196-to prescribe a temporary supply of the drug sufficient for the duration 147
197-of the grievance or review. The a uthorization shall include 148
198-confirmation of the availability of payment for such supply of such 149
199-drug. 150
200-(B) Not later than twenty-four hours after the health carrier has 151
201-issued such authorization to the pharmacy and prior to the pharmacy's 152
202-dispensation of such drug, such health carrier shall confirm with the 153
203-licensed participating provider the provider's concurrence with the 154
204-dispensing of such temporary supply of such drug. If such licensed 155
205-participating provider does not concur, the health carrier shall cancel 156
206-such authorization. 157
207-(C) The provisions of this subdivision shall not apply to a grievance 158
208-or review of an adverse determination under this section concerning 159
209-the substitution of a generic drug or another brand name drug for a 160
210-prescribed brand name drug unless the prescribing licensed 161
211-participating provider has specified that there shall be no substitution 162
212-for the specified brand name drug. 163
213-[(2)] (3) The health carrier shall notify the covered person and, if 164
214-applicable, the covered person's authorized representative not later 165
215-than three business days after the health carrier receives a grievance 166
216-the covered person or the covered person's authorized representative, 167
217-as applicable, is entitled to submit written material to the health carrier 168
218-Committee Bill No. 37
219-
220-
221-LCO No. 5682 7 of 9
222-
223-to be considered when conducting a review of the grievance. 169
224-[(3)] (4) (A) Upon receipt of a grievance, a health carrier shall 170
225-designate an individual or individuals to conduct a review of the 171
226-grievance. 172
227-(B) The health carrier shall not designate the same individual or 173
228-individuals who denied the claim or handled the matter that is the 174
229-subject of the grievance to conduct the review of the grievance. 175
230-(C) The health carrier shall provide the covered person and, if 176
231-applicable, the covered person's authorized representative with the 177
232-name, address and telephone number of the individual or the 178
233-organizational unit designated to coordinate the review on behalf of 179
234-the health carrier. 180
235-Sec. 4. Subsection (b) of section 38a-591g of the general statutes is 181
236-repealed and the following is substituted in lieu thereof (Effective 182
237-January 1, 2020): 183
238-(b) (1) Except as otherwise provided under subdivision (2) of this 184
239-subsection or subsection (d) of this section, a covered person or a 185
240-covered person's authorized representative shall not file a request for 186
241-an external review or an expedited external review until the covered 187
242-person or the covered person's authorized representative has 188
243-exhausted the health carrier's internal grievance process. 189
244-(2) A health carrier may waive its internal grievance process and the 190
245-requirement for a covered person to exhaust such process prior to 191
246-filing a request for an external review or an expedited external review. 192
247-(3) (A) If a covered person or the covered person's authorized 193
248-representative files any grievance or requests any review of an adverse 194
249-determination pursuant to this section relating to the dispensation of a 195
250-drug, other than a schedule II or III controlled substance, prescribed by 196
251-a licensed participating provider, the health carrier shall issue 197
252-immediate electronic authorization to the covered person's pharmacy 198
253-Committee Bill No. 37
254-
255-
256-LCO No. 5682 8 of 9
257-
258-to dispense a temporary supply of the drug sufficient for the duration 199
259-of the grievance or review. The authorization shall include 200
260-confirmation of the availability of payment for such supply of such 201
261-drug. 202
262-(B) Not later than twenty-four hours after the health carrier has 203
263-issued such authorization to the pharmacy and prior to the pharmacy's 204
264-dispensation of such drug, such health carrier shall confirm with the 205
265-licensed participating provider the provider's concurrence with the 206
266-dispensing of such temporary supply of such drug. If such licensed 207
267-participating provider does not concur, the health carrier shall cancel 208
268-such authorization. 209
269-(C) The provisions of this subdivision shall not apply to a grievance 210
270-or review of an adverse determination under this section concerning 211
271-the substitution of a generic drug or another brand name drug for a 212
272-prescribed brand name drug unless the prescribing licensed 213
273-participating provider has specified that there shall be no substitution 214
274-for the specified brand name drug. 215
275-This act shall take effect as follows and shall amend the following
276-sections:
277-
278-Section 1 January 1, 2020 38a-591d(b)
279-Sec. 2 January 1, 2020 38a-591e(c)
280-Sec. 3 January 1, 2020 38a-591f(b)
281-Sec. 4 January 1, 2020 38a-591g(b)
282-
24+That sections 38a-591d, 38a-591e, 38a-591f and 38a-591g of the 1
25+general statutes be amended to require health insurance coverage of 2
26+prescribed drugs during adverse determination reviews and external 3
27+review processes. 4
28328 Statement of Purpose:
28429 To require health insurance coverage of prescribed drugs during
28530 adverse determination reviews and external review processes.
286-[Proposed deletions are enclosed in brackets. Proposed additions are indicated by underline,
287-except that when the entire text of a bill or resolution or a section of a bill or resolution is new, it is
288-not underlined.]
289-
290-Co-Sponsors: SEN. LOONEY, 11th Dist.
291-
292-Committee Bill No. 37
293-
294-
295-LCO No. 5682 9 of 9
296-
297-S.B. 37
298-
299-