Burden of Vitiligo in Canada: Retrospective Analysis of a Canadian Public Claims Database.

BACKGROUND

Vitiligo is an autoimmune disease resulting in skin depigmentation. Treatment options are limited.

OBJECTIVES

To examine disease burden and healthcare resource utilization (HCRU) among patients with vitiligo in Québec, Canada.

METHODS

In this retrospective study, data were obtained from the Régie de l'Assurance Maladie du Québec (RAMQ) databases for 125,000 random individuals from January 2010 to December 2019. The () diagnostic code [709.x (other skin disorders)] with vitiligo-related treatment was used to identify patients with vitiligo. Patient characteristics and treatments, including treatment type, episodes (treatments used without discontinuation), and sequences (treatment episodes ≥30 days), were assessed. Annualized HCRU and costs (2021 adjusted) included all-cause hospitalization, emergency department visits, outpatient visits, and medications among patients with vitiligo (n = 113) and age- and sex-matched non-vitiligo controls (n = 339).

RESULTS

Of patients with vitiligo (mean age, 50.0 years; 68.1% female) identified using code 709.x with vitiligo-related treatment, 36.3% received ≥4 treatment episodes. Treatment patterns were heterogeneous, with 43 different sequences reported. Annualized mean outpatient visits (16.1 vs 5.5) and all-cause outpatient service costs per patient were significantly higher in the vitiligo versus the control group (CAN$1037 vs CAN$523; < .01). Total all-cause services costs were higher for patients with vitiligo in the year after versus before diagnosis (CAN$3679 vs CAN$2085; = .04).

CONCLUSIONS

Vitiligo is associated with significant burden and HCRU among patients in Québec, Canada, who were identified by code 709.x plus vitiligo-related treatment. Measurement of true vitiligo burden remains challenging.