EVALUATION OF THE "SOPHIA ASTHME" SUPPORT PROGRAMME FOR ASTHMATIC ADULT PATIENTS

Author(s)

De Rycke Y1, Dib F2, Taillé C3, Raherion Semjen C4, Lafourcade A1, Aguade A5, Guillo S1, Tubach F6
1INSERM UMR 1123 ECEVE, APHP, Department of Biostatistics, Public Health and Medical Information, AP-HP Pharmacoepidemiology center, CIC 1421, Pitié-Salpêtrière Hospital, Paris, France, 2INSERM, UMR 1123 ECEVE, AP-HP, Department of Epidemiology, Biostatistics and Clinical Research, Bichat-Claude-Bernard Hospital, Paris Diderot University, Paris Cedex 18, France, 3APHP, Departement of lung diseases, Hôpital Bichat; Departement Hospitalo-Universitaire FIRE, Université Paris Diderot, INSERM UMR 1152, LabEx Inflamex, Paris, France, 4INSERM U1219 team EPICENE Bordeaux University, Bordeaux, France, 5CNAMTS (National Health Insurance), Paris Cedex 20, France, 6INSERM UMR 1123 ECEVE, APHP Department of Biostatistics, Public Health and Medical Information, AP-HP Pharmacoepidemiology center, CIC 1421, Pitié-Salpêtrière Hospital, Sorbonne Universités, UPMC Univ Paris 06, Paris, France

OBJECTIVES: SOPHIA is a program developed by the French Health Insurance. The program includes a free access information website, provision of leaflets, and regular phone calls from an asthma nurse, in order to promote self-management and adherence to asthma treatments.

The objective of this study was to evaluate the effect of the program on medication and health care use in adult asthma patients at one year.

METHODS: A controlled before-after study was conducted within the SNIIRAM (claims database of the French Health Insurance). Subjects 18 to 44 years old in 2014, receiving at least 2 asthma medications deliveries in 2013, and covered by the general scheme of Health insurance were included. The program was implemented in 2015 in 18 French departments. Each eligible subject from pilot departments (i.e. the eligibles) was matched with an eligible subject from a department without the program (i.e. a control) on a propensity score. The primary endpoint was the ratio controller/total asthma medications.

RESULTS: A total of 99,578 pairs were analyzed. No impact of the program was observed on the primary endpoint (OR=0.997). The program was associated with an increased total number of anti-asthma drug packs dispensed (slope=0.36, p<0.0001).

A non-significant decrease in the number of days of sick leave (slope =-0.09) and in the percentage of subjects with sick leave (OR=0.96) was observed.

In terms of asthma-related costs (reimbursed), the program was associated with increased asthma medication expenditure (+€15, p=0.02) and a decrease (not statistically significant) of sick leave expenditures.

CONCLUSIONS: In this very early evaluation, the program did not show a clear impact on the majority of endpoints. This could be explained by the small proportion of participants to the program (10%) within the eligible population and the large inclusion criteria. Analysis of a more specific asthmatic population revealed more favorable impact of the program.

Conference/Value in Health Info

2017-11, ISPOR Europe 2017, Glasgow, Scotland

Value in Health, Vol. 20, No. 9 (October 2017)

Code

PRS58

Topic

Health Service Delivery & Process of Care

Topic Subcategory

Treatment Patterns and Guidelines

Disease

Respiratory-Related Disorders

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