Acceptance of a digital therapy recommender system for psoriasis

Author:

Graf Lisa1,Tesch Falko1,Gräßer Felix2,Harst Lorenz3,Siegels Doreen1,Schmitt Jochen1,Abraham Susanne4

Affiliation:

1. Center for Evidence-Based Healthcare, University Hospital Carl Gustav Carus and Faculty of Medicine Carl Gustav Carus, TU Dresden, Dresden, Germany

2. Institute for Biomedical Engineering, University Hospital Carl Gustav Carus and Faculty of Medicine Carl Gustav Carus, TU Dresden, Dresden, Germany

3. Center of Evidence-based Healthcare, Branch Office at the Medical Campus Chemnitz, University Hospital Carl Gustav Carus and Faculty of Medicine Carl Gustav Carus

4. Department of Dermatology, University Hospital Carl Gustav Carus and Faculty of Medicine Carl Gustav Carus, TU Dresden, Dresden, Germany

Abstract

Abstract Background: About 2% of the German population are affected by psoriasis. A growing number of cost-intensive systemic treatments are available. Surveys have shown high proportions of patients with moderate to severe psoriasis are not adequately treated despite a high disease burden. Digital therapy recommendation systems (TRS) may help implement guideline-based treatment. However, little is known about the acceptance of such clinical decision support systems (CDSSs). Methods: To assess the acceptance of the TRS, a prototypical demonstrator was developed. In three scenarios, potential test patients with psoriasis but different sociodemographic and clinical characteristics, previous treatments, desire to have children, and multiple comorbidities were designed. The demonstrator and test patients were presented to a random sample of 76 dermatologists attending a national dermatology conference in a cross-sectional face-to-face survey with case vignettes. 76.8% of dermatologists rated the TRS as acceptable based on the system usability scale (SUS). Results: Acceptance of the TRS was highest for patients eligible for systemic therapy (82%). 50% of participants accepted the system for patients with additional comorbidities and 43% for patients with special subtypes of psoriasis. Dermatologists in the outpatient sector or with many patients per week were less willing to use the TRS for patients with special psoriasis-subtypes. Participants whose SUS was 10 points above average were 27% more likely to use TRS for special psoriasis-subtypes. The main barrier in using the TRS was time demand (47.4%). Participants who perceived time as an obstacle were 22.3% less willing to use TRS with systemic therapy patients. 27.6% of physicians stated that they did not understand exactly how the recommendation was generated by the TRS, with no effect on the preparedness to use the system. Conclusion: The considerably high acceptance and the preparedness to use the psoriasis CDSS suggests that a TRS appears to be implementable in routine healthcare and may improve clinical care. Main barrier is the additional time demand posed on dermatologists in a busy clinical setting. Therefore, it will be a major challenge to identify a limited set of variables that still allows a valid recommendation with precise prediction of the patient-individual benefits and harms.

Publisher

Research Square Platform LLC

Reference25 articles.

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