Your browser doesn't support javascript.
loading
The clinical outcomes and healthcare resource utilization in IgG4-related disease: a claims-based analysis of commercially insured adults in the United States.
Wallace, Zachary S; Miles, Gandarvaka; Smolkina, Ekaterina; Petruski-Ivleva, Natalia; Madziva, Duane; Guzzo, Krishan; Cook, Claire; Fu, Xiaoqing; Zhang, Yuqing; Stone, John H; Choi, Hyon K.
Afiliación
  • Wallace ZS; Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, US.
  • Miles G; Harvard Medical School, Boston, MA, US.
  • Smolkina E; Sanofi, Cambridge, MA, US.
  • Petruski-Ivleva N; Sanofi, Amsterdam, The Netherlands.
  • Madziva D; Sanofi, Cambridge, MA, US.
  • Guzzo K; Sanofi, Mississauga, Ontario, Canada.
  • Cook C; Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, US.
  • Fu X; Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, US.
  • Zhang Y; Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, US.
  • Stone JH; Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, US.
  • Choi HK; Harvard Medical School, Boston, MA, US.
Article en En | MEDLINE | ID: mdl-38637947
ABSTRACT

OBJECTIVES:

IgG4-related disease (IgG4-RD) can affect nearly any organ and is often treated with glucocorticoids, which contribute to organ damage and toxicity. Comorbidities and healthcare utilization in IgG4-RD are poorly understood.

METHODS:

We conducted a cohort study using claims data from a United States managed care organization. Incident IgG4-RD cases were identified using a validated algorithm; general population comparators were matched by age, sex, race/ethnicity, and index date. The frequency of 21 expert-defined clinical outcomes associated with IgG4-RD or its treatment and healthcare-associated visits and costs were assessed 12 months before and 36 months after the index date (date of earliest IgG4-RD-related claim).

RESULTS:

There were 524 cases and 5,240 comparators. Most cases received glucocorticoids prior to (64.0%) and after (85.1%) the index date. Nearly all outcomes, many being common glucocorticoid toxicities, occurred more frequently in cases vs comparators. During follow-up, the largest differences between cases and comparators were seen for gastroesophageal reflux disease (prevalence difference +31.2%, p< 0.001); infections (+17.3%, p< 0.001); hypertension (+15.5%, p< 0.01); and diabetes mellitus (+15.0%, p< 0.001). The difference in malignancy increased during follow-up from +8.8% to + 12.5% (p< 0.001). 17.4% of cases used pancreatic enzyme replacement therapy during follow-up. Over follow-up, cases were more often hospitalized (57.3% vs 17.2%, p< 0.01) and/or had an ER visit (72.0% vs 36.7%, p< 0.01); all costs were greater in cases than comparators.

CONCLUSIONS:

Patients with IgG4-RD are disproportionately affected by adverse outcomes, some of which may be preventable or modifiable with vigilant clinician monitoring. Glucocorticoid-sparing treatments may improve these outcomes.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos