Background Foot complaints are common in inflammatory arthropathies such as rheumatoid arthritis and cause considerable disability. However, little is published about the nature and extent of foot complaints in systemic lupus erythematosus (SLE). We aimed to explore foot complaints among people with (SLE) and to evaluate the associations between foot pain and self-reported activities of daily living and well-being. Methods: We developed and tested a new 40-item item self-administered questionnaire, using a five-stage development process utilising patient involvement throughout to ensure face and content validity. The self-administered instrument was posted to 406 people with SLE attending adult rheumatology clinics across three health boards in Auckland, New Zealand. The questionnaire enquired about symptoms of foot pain, extra-articular features, anatomical distribution of symptoms according to validated foot-mannequins and the impact of foot symptoms on activities of daily living and well-being. Results: In total, 406 questionnaires were posted, with 131 responses (response rate 32%). We found 89% were women, mean (SD) age 51 (15) years, mean (SD) diagnosis 12.5 (11.1) years. Overall, 77% of those responding to the questionnaire reported foot pain during their SLE, with 45% reporting current foot pain. All regions of the feet were affected, with the hindfoot (32%) and ankles (30%) most troublesome. The most common self-reported extra-articular foot complaints were cold feet, swelling and numbness. Almost two-thirds (61%) reported foot pain adversely affected their lives; foot pain prevented sleeping in 36% and had a negative effect on emotions for 33%. Only 33% of participants had seen a podiatrist. Significant association was found between foot pain and standing longer than 15 minutes (p<0.001), walking (p<0.001), climbing stairs (p<0.001) and going shopping (p<0.001). Pain was the primary symptom to affect quality of life (47/100). Conclusion Foot complaints in SLE are heterogeneous in nature, and may have a substantial negative impact on patient well-being. Foot complaints need to be addressed to reduce the burden of SLE and our findings support the need for wider access to specific foot care services.
Bibliographical note© 2016 Otter et al. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Systemic lupus erythematosus
- Quality of life