Purpose
To assess clinical characteristics and trends in valganciclovir use
among infants diagnosed with congenital cytomegalovirus (CMV) disease in the
United States.
Methods
We analyzed 2009–2015 medical claims from Truven Health
MarketScan® Commercial Claims and Encounters and
Medicaid databases. We identified infants with a live birth code in the
first claim who were enrolled for at least 45 days. Among infants diagnosed
with congenital CMV disease, identified by an ICD-9-CM or ICD-10-CM code of
congenital CMV infection or CMV disease within 45 days of birth, we assessed
codes for CMV-associated clinical condition within the same period, and
hearing loss and valganciclovir claims within the first 180 days.
Findings
In the commercial and Medicaid databases, we identified 257
(2.5/10,000) and 445 (3.3/10,000) infants diagnosed with congenital CMV
disease, respectively, among whom 135 (53%) and 282 (63%)
had ≥1 CMV-associated condition, 30 (12%) and 32
(7%) had hearing loss, and 41 (16%) and 78 (18%) had
valganciclovir claims. Among infants with congenital CMV disease who had
valganciclovir claims, 37 (90%) among commercially-insured infants
and 68 (87%) among Medicaid-insured infants had ≥1
CMV-associated condition and/or hearing loss. From 2009 to 2015, the
proportion with valganciclovir claims increased from 0% to
29% among commercially-insured infants and from 4% to
37% among Medicaid-insured infants
(p<0.0001).
Implications
During 2009–2015, there was a strong upward trend in
valganciclovir claims among insured infants who were diagnosed with
congenital CMV disease, the majority of whom had CMV-associated conditions
and/or hearing loss.