Initial Approval Criteria
I.
Treatment Resistant
Depression (must meet all):
a.
Diagnosis of TRD;
b.
Prescribed by or in
consultation with a psychiatrist;
c.
Age > 18 and < 65
years;
d.
Member has a documented
baseline Patient Health Questionnaire (PHQ-9) score > 15, indicating
moderately severe major depression, within the previous 4 weeks;
e.
Members meets both of the
following (i and ii):
i.
Failure of TWO
antidepressants from at least two different classes at up to maximally indicated
doses but no less than the commonly recognized minimum therapeutic doses, each
used for > 4 weeks, unless clinically significant adverse effects are
experienced or all are contraindicated (e.g. SSRI, SNRI, TCA, bupropion,
mirtazapine)’
ii.
Failure of TWO of the
following antidepressant augmentation therapies, each used for > 4 weeks,
unless clinically significant adverse effects are experienced or all are
contraindicated: second-generation antipsychotic, lithium, thyroid hormone,
buspirone;
f.
Currently stabilized on
an oral antidepressant for at least two weeks (must not be one of the
aforementioned agents previously failed and Spravato will be used in combination
with oral antidepressant;
g.
Member meets one of the
following (i or ii):
i.
No prior history of
treatment with Spravato;
ii.
Documentation of a prior
positive response to Spravato as documented by a history of > 50%
reduction in PHQ-9 score;
h.
Dose does not exceed
168mg per week during four-week induction phase.
Approval Duration: 3 months (up to 23 nasal spray devices)
II.
Major Depressive Disorder
with Suicidal Ideation or Behavior (must meet all):
a.
Diagnosis of MDD;
b.
Prescribed by or in
consultation with a psychiatrist;
c.
Age > 18 years;
d.
Spravato is prescribed in
combination with initiation or optimization of oral antidepressant therapy;
e.
Members recently (within
last 5 days) discharged from or currently in an acute or subacute inpatient care
for suicidality;
f.
Member meets one of the
following:
i.
No prior history of
treatment with Spravato;
ii.
Documentation of a prior
positive response to Spravato
g.
Member meets one of the
following:
i.
Montgomery-Asbert
Depression Rating Scale (MADRS) score is > 20 (moderate depression);
ii.
Hamilton Rating Scale for
Depressoin (HAMD) score is > 17 (moderate depression);
iii.
PHQ-9 score is >
15 (moderately severe depression);
h.
Dose does not exceed 84mg
(3 nasal spray devices) twice weekly.
Approval Duration: 4 weeks (up to 23 nasal spray devices)
Continued Therapy Criteria
Treatment Resistant Depression
A.
Member is responding
positively to therapy as evidenced by at least a 50% reduction in PHQ-9 score
compared to baseline;
B.
Spravato is being used in
combination with an oral antidepressant;
C.
If request is for a dose
increase, new dose does not exceed 84mg (3 nasal spray devices) per week.
Continued Therapy Approval Duration: 6 months
Reauthorization is not permitted for MDD with Suicidal Ideation or Behavior.
Codes
Used In This BI:
1)
S0013 – esketamine, nasal
spray, 1mg