Krystexxa (pegloticase) is considered medically necessary for members meeting
the following criteria (initial approval
for 6 months):
1)
Diagnosis of chronic
gout;
2)
Age >18 years;
3)
Positive for symptomatic
gout with one or more of the following:
a.
At least 3 gout flares in
the previous 18 months;
b.
At least one gout tophus;
c.
Chronic gouty arthritis;
4)
Failure to normalize uric
acid to < 6mg/dL with adherent use of allopurinol and Uloric at maximally
indicated doses, each used for at least 3 months unless contraindicated or
clinically significant adverse effects are experienced;
5)
Failure of adherent use
of one uricosuric agent (e.g. probenecid or losartan), at maximally indicated
doses, in combination with allopurinol or Uloric unless contraindicated or
clinically significant adverse effects are experienced;
6)
Dose does not exceed 8mg
(uricase protein) every two weeks.
Reauthorization Criteria (6 month
approval):
1)
Member is responding positively to
therapy;
2)
Member is not
concurrently taking any oral urate-lowering agents (e.g. allopurinol, Uloric,
probenecid).
Codes
Used In This BI:
1)
J2507 Injection,
pegloticase, 1mg