Assessing the Burden of Atopic Dermatitis in Portugal through Patient-Centered Experiences.

IF 0.8 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Michelle Tu, Freya Moxham, Alan Schwartz, Joana Camilo, Korey Capozza
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Abstract

Introduction: Adult patients and caregivers of children with atopic dermatitis experience high physical, mental, and financial burden in Portugal. We outline the experience of atopic dermatitis management and how the current medical care model impacts patient-centered concerns such as financial burden, quality of life, disease burden, and treatment satisfaction.

Methods: We conducted a survey of 419 Portuguese adults and caregivers of children to capture the experience of managing atopic dermatitis in Portugal.

Results: Respondents reported average satisfaction with treatment, with a mean satisfaction rating of 3.15/5.00 (SD = 0.77). Adults reported slightly better control of atopic dermatitis symptoms (mean = 56.6) than pediatric patients (mean = 55.9, caregiver reported). Nearly 34% of adults and 39% of caregivers of children and adolescents indicated that their healthcare providers asked about their priorities at the last medical visit. Additionally, only 40% of adult patients and 32% of caregivers reported that patient training was offered to them. Respondents seeing dermatologists reported higher satisfaction than those seeing other healthcare providers (p = 0.01) but there were no differences in long-term control of symptoms by provider type (p = 0.85) when controlling for severity. Portuguese adult patients scored 0.86/1.00 on the EQ-5D (where 0 = death and 1 = perfect health). Financial concern was high as nearly 80% of patients and caregivers reported using savings, borrowing money, and/or reducing spending to cover atopic dermatitis-related costs.

Conclusion: Portuguese patients with atopic dermatitis and caregivers experience financial burden, lower health-related quality of life, higher disease burden, and treatment satisfaction issues with their current medical care. These factors often deteriorate as the disease's severity increases. Providers, researchers and policymakers should focus on better addressing patient-centered concerns for individuals suffering from atopic dermatitis to improve care and health outcomes.

通过以患者为中心的体验评估葡萄牙特应性皮炎的负担。
导言:在葡萄牙,特应性皮炎患儿的成年患者和护理人员在身体、精神和经济方面都承受着沉重的负担。我们概述了特应性皮炎的治疗经验,以及当前的医疗模式如何影响以患者为中心的问题,如经济负担、生活质量、疾病负担和治疗满意度:我们对 419 名葡萄牙成年人和儿童护理人员进行了调查,以了解葡萄牙特应性皮炎患者的治疗经验:受访者对治疗的满意度一般,平均满意度为 3.15/5.00(SD = 0.77)。成人特应性皮炎症状的控制情况(平均值=56.6)略好于儿童患者(平均值=55.9,护理人员报告)。近 34% 的成人和 39% 的儿童和青少年护理人员表示,他们的医疗服务提供者在上次就诊时询问了他们的优先事项。此外,仅有 40% 的成人患者和 32% 的护理人员表示医疗机构为他们提供了患者培训。看皮肤科医生的受访者比看其他医疗服务提供者的受访者表示出更高的满意度(p = 0.01),但在控制严重程度后,不同医疗服务提供者在长期控制症状方面没有差异(p = 0.85)。葡萄牙成年患者的 EQ-5D 得分为 0.86/1.00(0 = 死亡,1 = 完全健康)。近 80% 的患者和护理人员表示会动用储蓄、借钱和/或减少开支来支付特应性皮炎相关费用,因此对经济问题的关注度很高:结论:葡萄牙特应性皮炎患者和护理人员在目前的医疗护理中面临着经济负担、健康相关生活质量较低、疾病负担较重以及治疗满意度较低等问题。这些因素往往会随着疾病严重程度的增加而恶化。医疗服务提供者、研究人员和政策制定者应集中精力,更好地为特应性皮炎患者解决以患者为中心的问题,以改善医疗服务和健康状况。
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来源期刊
Acta medica portuguesa
Acta medica portuguesa MEDICINE, GENERAL & INTERNAL-
CiteScore
1.90
自引率
16.70%
发文量
256
审稿时长
6-12 weeks
期刊介绍: The aim of Acta Médica Portuguesa is to publish original research and review articles in biomedical areas of the highest standard, covering several domains of medical knowledge, with the purpose to help doctors improve medical care. In order to accomplish these aims, Acta Médica Portuguesa publishes original articles, review articles, case reports and editorials, among others, with a focus on clinical, scientific, social, political and economic factors affecting health. Acta Médica Portuguesa will be happy to consider manuscripts for publication from authors anywhere in the world.
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