Patients' values and preferences for health states in allergic rhinitis—An artificial intelligence supported systematic review

Author:

Brozek Jan1234,Borowiack Ewa4,Sadowska Ewelina4ORCID,Nowak Artur4ORCID,Sousa‐Pinto Bernardo56ORCID,Vieira Rafael José56ORCID,Bognanni Antonio17,Yepes Nuñez Juan Jose89ORCID,Zhang Yuan1,Zuberbier Torsten101112ORCID,Bousquet Jean101112ORCID,Schünemann Holger J.12313

Affiliation:

1. Department of Health Research Methods, Evidence and Impact McMaster University Hamilton Ontario Canada

2. Michael G. DeGroote Cochrane Canada & McMaster GRADE Centres McMaster University Hamilton Ontario Canada

3. Department of Medicine McMaster University Hamilton Canada

4. Evidence Prime Hamilton Ontario Canada

5. Department of Community Medicine, Information and Health Decision Sciences (MEDCIDS), Faculty of Medicine University of Porto Porto Portugal

6. Centre for Health Technology and Services Research, Health Research Network (CINTESIS@RISE), Faculty of Medicine University of Porto Porto Portugal

7. Department of Medicine, Evidence in Allergy Group McMaster University Hamilton Canada

8. School of Medicine, Universidad de los Andes Bogotá Colombia

9. Fundación Santa Fe de Bogotá Hospital University Bogotá Colombia

10. Institute of Allergology, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt‐Universität zu Berlin Berlin Germany

11. Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Allergology and Immunology Berlin Germany

12. Fraunhofer Cluster of Excellence for Immune‐Mediated Diseases CIMD Frankfurt/Main Germany

13. Clinical Epidemiology and Research Center (CERC) Humanitas University and Humanitas Research Hospital Milan Italy

Abstract

AbstractBackgroundAllergic rhinitis (AR) impacts patients' physical and emotional well‐being. Assessing patients' values and preferences (V&P) related to AR is an essential part of patient‐centered care and of the guideline development process. We aimed to systematically summarize the information about patients' V&P on AR and its symptoms and impact on daily life.MethodsWe conducted systematic review in a MEDLINE, Embase, PsychInfo, and CINAHL databases. We included studies which quantitatively assessed patients' V&P for specific outcomes in AR by assessing utilities, applying discrete choice approaches, or rating and ranking outcomes. We grouped outcomes as AR symptoms, functional status, and care‐related patient experience. Study selection and data extraction were supported by the Laser AI tool. We rated the certainty of evidence (CoE) using the GRADE approach.ResultsThirty‐six studies (41 records) were included: nine utility studies, seven direct‐choice studies and 21 studies of rating or ranking outcomes. Utilities were lower with increased AR severity and with the concomitant presence of asthma, but not with whether AR was seasonal or perennial (CoE = low–high). Patients rated AR symptom‐related outcomes as more important than those related to care‐related patient experience and functional status (CoE = very low–moderate). Nasal symptoms (mainly nasal congestion) followed by breathing disorders, general and ocular symptoms were rated as the symptoms with the highest impact.ConclusionsThis systematic review provides a comprehensive overview of V&P of patients with AR. Patients generally considered nasal symptoms as the most important. Future studies with standardized methods are needed to provide more information on V&P in AR.

Funder

European Social Fund

Fundação para a Ciência e a Tecnologia

Publisher

Wiley

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