Living with systemic lupus erythematosus in 2020: a European patient survey
Objective The aim of this study was to analyse the 2020 burden of Systemic Lupus Erythematosus (SLE) in Europe, from the patients’ perspective.Methods In May 2020, Lupus Europe, the European umbrella patient association for SLE, designed and disseminated a multilingual anonymous online survey to ind...
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| Format: | Article |
| Language: | English |
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BMJ Publishing Group
2021-04-01
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| Series: | Lupus Science and Medicine |
| Online Access: | https://lupus.bmj.com/content/8/1/e000469.full |
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| author | Alain Cornet Kirsi Myllys Jeanette Andersen Angela Edwards |
| author_facet | Alain Cornet Kirsi Myllys Jeanette Andersen Angela Edwards |
| author_sort | Alain Cornet |
| collection | DOAJ |
| description | Objective The aim of this study was to analyse the 2020 burden of Systemic Lupus Erythematosus (SLE) in Europe, from the patients’ perspective.Methods In May 2020, Lupus Europe, the European umbrella patient association for SLE, designed and disseminated a multilingual anonymous online survey to individuals with a self-reported physician’s diagnosis of SLE living in Europe.Results Data from 4375 SLE survey respondents (95.9% women, median age: 45 (IQR: 36–54) years, 70.7% Caucasians) from 35 European countries were analysed. The median age at SLE diagnosis was 30 years (IQR: 22–40) and the median diagnosis delay was 2 years (IQR: 0–6). The most commonly affected organ-systems included the joints (81.8%) and skin (59.4%), with renal involvement in 30%. Another diagnosis was given before that of SLE in 45.0%, including psychological/mental disorders in 9.1% and fibromyalgia in 5.9%. The median number of symptoms reported was 9 (IQR: 6–11) out of 21, with fatigue most common (85.3%) and most bothersome. The median number of SLE-related medications was 5 (IQR: 3–7), including antimalarials (75%), oral glucocorticoids (52.4%), immunosuppressants (39.8%) and biologics (10.9%). Respondents reported significant impact over their studies, career and emotional/sexual life in 50.7%, 57.9% and 38.2%, respectively. Appropriate access to care was highly variable across countries and care component.Conclusion This survey underlines the 2020 burden and strong heterogeneity in the care of SLE across Europe, from the patient’s perspective. Altogether, these data may prove crucial to physicians, patients and policy-makers to improve the diagnosis and management of this rare and complex disease. |
| format | Article |
| id | doaj-art-3fc4b23a2e1849b38b4921574275c453 |
| institution | Kabale University |
| issn | 2053-8790 |
| language | English |
| publishDate | 2021-04-01 |
| publisher | BMJ Publishing Group |
| record_format | Article |
| series | Lupus Science and Medicine |
| spelling | doaj-art-3fc4b23a2e1849b38b4921574275c4532024-12-16T19:30:10ZengBMJ Publishing GroupLupus Science and Medicine2053-87902021-04-018110.1136/lupus-2020-000469Living with systemic lupus erythematosus in 2020: a European patient surveyAlain Cornet0Kirsi Myllys1Jeanette Andersen2Angela Edwards3Lupus Europe, brussels, BelgiumLupus Europe, Romford, UK1Lupus Europe, Essex, UKLupus Europe, Romford, UKObjective The aim of this study was to analyse the 2020 burden of Systemic Lupus Erythematosus (SLE) in Europe, from the patients’ perspective.Methods In May 2020, Lupus Europe, the European umbrella patient association for SLE, designed and disseminated a multilingual anonymous online survey to individuals with a self-reported physician’s diagnosis of SLE living in Europe.Results Data from 4375 SLE survey respondents (95.9% women, median age: 45 (IQR: 36–54) years, 70.7% Caucasians) from 35 European countries were analysed. The median age at SLE diagnosis was 30 years (IQR: 22–40) and the median diagnosis delay was 2 years (IQR: 0–6). The most commonly affected organ-systems included the joints (81.8%) and skin (59.4%), with renal involvement in 30%. Another diagnosis was given before that of SLE in 45.0%, including psychological/mental disorders in 9.1% and fibromyalgia in 5.9%. The median number of symptoms reported was 9 (IQR: 6–11) out of 21, with fatigue most common (85.3%) and most bothersome. The median number of SLE-related medications was 5 (IQR: 3–7), including antimalarials (75%), oral glucocorticoids (52.4%), immunosuppressants (39.8%) and biologics (10.9%). Respondents reported significant impact over their studies, career and emotional/sexual life in 50.7%, 57.9% and 38.2%, respectively. Appropriate access to care was highly variable across countries and care component.Conclusion This survey underlines the 2020 burden and strong heterogeneity in the care of SLE across Europe, from the patient’s perspective. Altogether, these data may prove crucial to physicians, patients and policy-makers to improve the diagnosis and management of this rare and complex disease.https://lupus.bmj.com/content/8/1/e000469.full |
| spellingShingle | Alain Cornet Kirsi Myllys Jeanette Andersen Angela Edwards Living with systemic lupus erythematosus in 2020: a European patient survey Lupus Science and Medicine |
| title | Living with systemic lupus erythematosus in 2020: a European patient survey |
| title_full | Living with systemic lupus erythematosus in 2020: a European patient survey |
| title_fullStr | Living with systemic lupus erythematosus in 2020: a European patient survey |
| title_full_unstemmed | Living with systemic lupus erythematosus in 2020: a European patient survey |
| title_short | Living with systemic lupus erythematosus in 2020: a European patient survey |
| title_sort | living with systemic lupus erythematosus in 2020 a european patient survey |
| url | https://lupus.bmj.com/content/8/1/e000469.full |
| work_keys_str_mv | AT alaincornet livingwithsystemiclupuserythematosusin2020aeuropeanpatientsurvey AT kirsimyllys livingwithsystemiclupuserythematosusin2020aeuropeanpatientsurvey AT jeanetteandersen livingwithsystemiclupuserythematosusin2020aeuropeanpatientsurvey AT angelaedwards livingwithsystemiclupuserythematosusin2020aeuropeanpatientsurvey |