A survey of Australian rheumatologists' perspectives of nutrition needs in systemic sclerosis.

IF 1.2 Q3 RHEUMATOLOGY Journal of Scleroderma and Related Disorders Pub Date : 2023-10-01 Epub Date: 2023-07-06 DOI:10.1177/23971983231185465
De-Arne A Samm, Aimee R Macoustra, Rhiannon K Crane, Leah M McWilliams, Susanna M Proudman, Lee-Anne S Chapple
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Abstract

Aim: Systemic sclerosis (scleroderma) is an incurable inflammatory condition synonymous with unique nutrition needs. As rheumatologists are frequently responsible for managing the various organ manifestations, this study aimed to understand the service needs and nutritional concerns of rheumatologists involved in the care of adults with systemic sclerosis.

Methods: A 13-item online qualitative and quantitative survey was distributed via REDCap® from January to March 2022 to rheumatologists who are members of the Australian Scleroderma Interest Group and consult patients with systemic sclerosis. Data were collected on rheumatologists' demographics, and their views on symptoms observed, nutrition concerns and priorities, and preferred dietetic service provision for their patients. Data are reported as number (%).

Results: Of 27 eligible rheumatologists, 17 (63%) completed the survey. All rheumatologists reported gastrointestinal symptoms in their patients (n = 17, 100%); predominantly reflux (n = 17, 100%) and dysphagia (n = 17, 100%). Weight loss was observed by the majority of rheumatologists (n = 15, 88%). Rheumatologists reported patients used food avoidance/special diets to manage symptoms (n = 12, 71%). Dietetic consultation was reported as potentially beneficial by all rheumatologists, with the preferred time being when symptoms increase or change (n = 15, 88%), and the preferred approaches being written resources (n = 15, 88%), face-to-face (n = 14, 82%) and telephone consultation (n = 14, 82%). Advice on gaining weight (n = 14, 82%) and systemic sclerosis symptom management (n = 13, 77%) were the most desired education topics reported.

Conclusion: Rheumatologists commonly observe gastrointestinal symptoms in patients with systemic sclerosis and report dietetics services would be advantageous in supporting their patients to gain weight and better manage their symptoms.

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澳大利亚风湿病学家对系统性硬化症营养需求的调查。
目的:系统性硬化症(硬皮病)是一种无法治愈的炎症性疾病,与独特的营养需求同义。由于风湿病学家经常负责管理各种器官表现,本研究旨在了解参与系统性硬化症成人护理的风湿病学家的服务需求和营养问题。方法:2022年1月至3月,通过REDCap®向澳大利亚硬皮病兴趣小组成员、咨询系统性硬化症患者的风湿病学家分发了一份13项在线定性和定量调查。收集了风湿病学家的人口统计数据,以及他们对观察到的症状、营养问题和优先事项的看法,以及为患者提供的首选饮食服务。数据以数字(%)表示。结果:在27名符合条件的风湿病学家中,17人(63%)完成了调查。所有风湿病学家都报告了他们患者的胃肠道症状(n = 17100%);主要回流(n = 17、100%)和吞咽困难(n = 17、100%)。大多数风湿病学家(n = 15%、88%)。风湿病学家报告患者使用避免进食/特殊饮食来控制症状(n = 12.71%)。据报道,所有风湿病学家都认为饮食咨询可能有益,首选时间是症状增加或改变时(n = 15,88%),首选的方法是书面资源(n = 15/88%),面对面(n = 14.82%)和电话咨询(n = 14%、82%)。关于增加体重的建议(n = 14%、82%)和系统性硬化症症状管理(n = 13.77%)是报告的最受欢迎的教育主题。结论:风湿病学家通常观察系统性硬化症患者的胃肠道症状,并报告饮食服务将有利于支持患者体重增加和更好地控制症状。
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31
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