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Revista Colombiana de Reumatología

versão impressa ISSN 0121-8123

Resumo

VALLADALES-RESTREPO, Luis Fernando  e  MACHADO-ALBA, Jorge Enrique. Consistency between anticholinergic burden scales in patients with Sjögren’s syndrome. Rev.Colomb.Reumatol. [online]. 2020, vol.27, suppl.2, pp.50-57.  Epub 04-Set-2021. ISSN 0121-8123.  https://doi.org/10.1016/j.rcreu.2020.04.008.

Introduction:

Sjögren’s syndrome is the second most frequent autoimmune rheumatic disease and is characterized by exocrine gland involvement manifesting as sicca symptoms. The objective of this study was to estimate the degree of agreement between three anticholinergic burden scales related to the prescriptions of patients diagnosed with Sjögren’s syndrome in Colombia.

Materials and methods:

An analytical concordance study was conducted. The weighted kappa coefficient with quadratic weights was used to identify consistency between the Anticholinergic Drug Scale (ADS), Anticholinergic Cognitive Burden Scale (ACB) and Anticholinergic Risk Scale (ARS), which address the prescriptions used for 3 months by patients with Sjögren s syndrome, in a population database.

Results:

A total of 15,696 patients with Sjögren’s syndrome were identified, with a mean age of 65.4 ± 13.9 years, and 74.2% were women. A total of 94.1% of the patients received at least one topical lubricant, with carboxymethyl cellulose being the most commonly prescribed (22.9%), while oral pilocarpine was prescribed to 3.5% of patients. The ACB was the tool identified more antimuscarinic prescriptions (37.5%), followed by the ADS (35.3%) and ARS (25.2%). The greatest degree of agreement was found between the ADS and ACB (kappa 0.6520; confidence interval (CI): 0.6393-0.6648).

Conclusions:

Except for the ADS and ACB, little agreement was found between the three scales gauging the anticholinergic burden. Additional studies are needed to determine how these differences can impact the clinical outcomes of patients.

Palavras-chave : Sjögren’s síndrome; Pilocarpine; Cholinergic antagonists; Drug interactions; Pharmacovigilance.

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