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Patient Preferences for Attributes of Biologic Treatments in Moderate to Severe Asthma: A Discrete Choice Experiment Study.
Yang, Min; Chao, Jingdong; Fillbrunn, Mirko; Mallya, Usha G; Wang, Min-Jung; Franke, Leigh; Cohn, Lauren; Kamat, Siddhesh.
Afiliación
  • Yang M; Analysis Group, Inc, Boston, MA, USA.
  • Chao J; Regeneron Pharmaceuticals, Inc, Tarrytown, NY, USA.
  • Fillbrunn M; Analysis Group, Inc, Boston, MA, USA.
  • Mallya UG; Sanofi, Boston, MA, USA.
  • Wang MJ; Analysis Group, Inc, Boston, MA, USA.
  • Franke L; Analysis Group, Inc, Boston, MA, USA.
  • Cohn L; Section of Pulmonary, Critical Care and Sleep Medicine, Yale School of Medicine, New Haven, CT, USA.
  • Kamat S; VA Connecticut Healthcare System, West Haven, CT, USA.
Patient Prefer Adherence ; 16: 2649-2661, 2022.
Article en En | MEDLINE | ID: mdl-36176349
ABSTRACT

Purpose:

Multiple biologics are available for moderate to severe asthma. Given the important relationship between patient engagement in healthcare decision-making and health outcomes, patient preference is an increasingly important consideration. This study elicited patients' preferences for attributes of biologic therapies for moderate to severe asthma. Patient and

Methods:

A discrete choice experiment (DCE) questionnaire was designed to collect data from an existing survey panel of adults with moderate to severe asthma in the United States. Patients were asked to select their preferred hypothetical treatment from profiles with varying attributes related to efficacy, safety, and administration convenience. Conditional logit regression models were used to quantify patient preferences.

Results:

Of 301 eligible patients who completed the survey, the mean age was 46.7±15.1 years and 71.8% were female. Patients had asthma for 22.5±16.3 years on average, and most (97.3%) had experienced ≥1 asthma attack in the past 12 months. Among treatment attributes examined, patients most valued the absence of a black box warning for the risk of a life-threatening allergic reaction, effectiveness of reducing severe asthma exacerbations, and improvement in lung function (all p < 0.001). Home administration setting for subcutaneous injections (vs doctor's office/clinic) (p = 0.009) and ability of a biologic to treat additional chronic condition(s) (p < 0.05) were also considered important. Dosing frequency and type of injection device were not significant factors.

Conclusion:

Patients with moderate to severe asthma valued efficacy and safety over convenience attributes when selecting biologic treatments. Awareness of these preferences can facilitate patient-physician shared decision-making when managing moderate to severe asthma in clinical practice.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Patient Prefer Adherence Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Patient Prefer Adherence Año: 2022 Tipo del documento: Article