Jasmin B Kuemmerle-Deschner1, Pierre Quartier2, Isabelle Kone-Paut3, Veronique Hentgen4, Katherine Anne Marzan5, Fatma Dedeoglu6, Helen Jane Lachmann7, Tilman Kallinich8, Norbert Blank9, Seza Ozen10, Yelda Bilginer10, Jonathan S Hausmann11, Arturo Diaz12, Maurice Perrinjaquet13, Nina Marinsek14, Kathleen G Lomax15, Peter Hur15, Elise L Dekker15, Avi Livneh16. 1. Division of Paediatric Rheumatology, Department of Paediatrics and Autoinflammation Reference Centre Tübingen, University Hospital Tübingen, Germany. jasmin.kuemmerle-deschner@med.uni-tuebingen.de. 2. Paris-University, IMAGINE Institute, Rare Disease Reference Centre RAISE, Necker-Enfants Malades Hospital, Assistance Publique-Hopitaux de Paris, France. 3. Paediatric Rheumatology and CEREMAIA, Le Kremlin-Bicêtre University Hospital, APHP, Paris-Sud University, France. 4. French Reference Centre for Autoinflammatory Diseases and Secondary Amyloidosis (CEREMAIA), Versailles Hospital-Le Chesnay, Paris, France. 5. Paediatric Rheumatology Children's Hospital Los Angeles, Keck School of Medicine USC, Los Angeles, CA, USA. 6. Division of Immunology, Rheumatology Program, Boston Children's Hospital, Department of Paediatrics, Harvard Medical School, Boston, MA, USA. 7. National Amyloidosis Centre and Centre for Acute Phase Proteins, Division of Medicine, University College London and Royal Free Hospital London NHS Foundation Trust, London, UK. 8. Department of Paediatric Pneumology and Immunology, Charité Medical University of Berlin, Germany. 9. Division of Rheumatology, University Hospital, Heidelberg, Germany. 10. Department of Paediatric Rheumatology, Hacettepe University, Ankara, Turkey. 11. Division of Immunology, Rheumatology Program, Boston Children's Hospital, Department of Paediatrics, Harvard Medical School, Boston, MA, and Division of Rheumatology, Autoinflammatory Diseases Centre, Beth Israel Deaconess Medical Centre, Harvard Medical School, Boston MA, USA. 12. Division of Rheumatology, Autoinflammatory Diseases Centre, Beth Israel Deaconess Medical Centre, Harvard Medical School, Boston, MA, USA. 13. Navigant Life Sciences, Berlin, Germany. 14. Navigant Life Sciences, London, UK. 15. Novartis Pharmaceuticals Corporation, NJ, USA. 16. Medicine F, Sheba Medical Centre, Tel-Hashomer, Ramat-Gan, Israel.
Abstract
OBJECTIVES: This study aimed to characterise the burden of illness of patients with inadequately controlled hereditary periodic fevers (HPFs), during and outside of flares. It was focused on the burden to the patients and also considered the wider impact on their caregivers and families. METHODS: The target population was patients or caregivers of patients with clinically/genetically confirmed colchicine resistant FMF (crFMF), mevalonate kinase deficiency/hyperimmunoglobinaemia D with periodic fever syndrome (MKD/HIDS) or TRAPS, who were expected to flare at least once in a 6-month period based on patient history. Disease burden was captured during and between flares using an electronic diary (e-diary) with questions on patient functioning, emotional/social well-being and pain, using validated instruments. RESULTS: HPF-related symptoms such as fever, joint, muscle or bone pain and tiredness and fatigue were reported by patients both during and outside of a flare. The SF-10 Health Survey (SF-10v2) (paediatric patients) and SF-12 Health Survey (SF-12v2) (adult patients) showed that flares negatively impacted patients' psychosocial and physical health. Negative effect of on-flare status on health utility index score assessed by the Short-Form Six-Dimension (SF-6D) was significant only for crFMF patients. Furthermore, the Sheehan Disability Score (SDSv3) showing the on-flare status resulted in significant functional impairment in all 3 disease cohorts through assessment of impact on work/school, social and family life. CONCLUSIONS: crFMF, MKD/HIDS and TRAPS negatively affected the quality of life (QoL) of adult and paediatric patients, including their physical, mental, psychosocial health, and social functioning. There remains, however, a high number of unmet needs for these patients to reduce their disease burden.
OBJECTIVES: This study aimed to characterise the burden of illness of patients with inadequately controlled hereditary periodic fevers (HPFs), during and outside of flares. It was focused on the burden to the patients and also considered the wider impact on their caregivers and families. METHODS: The target population was patients or caregivers of patients with clinically/genetically confirmed colchicine resistant FMF (crFMF), mevalonate kinasedeficiency/hyperimmunoglobinaemia D with periodic fever syndrome (MKD/HIDS) or TRAPS, who were expected to flare at least once in a 6-month period based on patient history. Disease burden was captured during and between flares using an electronic diary (e-diary) with questions on patient functioning, emotional/social well-being and pain, using validated instruments. RESULTS: HPF-related symptoms such as fever, joint, muscle or bone pain and tiredness and fatigue were reported by patients both during and outside of a flare. The SF-10 Health Survey (SF-10v2) (paediatric patients) and SF-12 Health Survey (SF-12v2) (adult patients) showed that flares negatively impacted patients' psychosocial and physical health. Negative effect of on-flare status on health utility index score assessed by the Short-Form Six-Dimension (SF-6D) was significant only for crFMF patients. Furthermore, the Sheehan Disability Score (SDSv3) showing the on-flare status resulted in significant functional impairment in all 3 disease cohorts through assessment of impact on work/school, social and family life. CONCLUSIONS: crFMF, MKD/HIDS and TRAPS negatively affected the quality of life (QoL) of adult and paediatric patients, including their physical, mental, psychosocial health, and social functioning. There remains, however, a high number of unmet needs for these patients to reduce their disease burden.
Authors: Micol Romano; Z Serap Arici; David Piskin; Sara Alehashemi; Daniel Aletaha; Karyl Barron; Susanne Benseler; Roberta A Berard; Lori Broderick; Fatma Dedeoglu; Michelle Diebold; Karen Durrant; Polly Ferguson; Dirk Foell; Jonathan S Hausmann; Olcay Y Jones; Daniel Kastner; Helen J Lachmann; Ronald M Laxer; Dorelia Rivera; Nicola Ruperto; Anna Simon; Marinka Twilt; Joost Frenkel; Hal M Hoffman; Adriana A de Jesus; Jasmin B Kuemmerle-Deschner; Seza Ozen; Marco Gattorno; Raphaela Goldbach-Mansky; Erkan Demirkaya Journal: Arthritis Rheumatol Date: 2022-05-27 Impact factor: 15.483