Access to Emollients in Atopic Dermatitis

Stephanie-Lynn Ryan, Cristina Grechin, Richard Watchorn
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引用次数: 0

Abstract

In addition to symptoms, the management of atopic dermatitis (AD) can significantly impact quality of life. Chronic disease can present a considerable financial burden for patients and families. The cost of treatment can lead to poor adherence and contribute to social inequality in access to care.

Emollients represent a cornerstone of therapy in AD. Van Zuuren et al.'s [1] Cochrane review established that moisturisers reduced the number of flares, prolonged the interval between flares and reduced the need for corticosteroids. In addition, they reported that a combination therapy of moisturisers and topical corticosteroids were more effective than topical corticosteroids alone.

Despite the inclusion of emollients in all clinical guidelines and the frequency of their prescription, few are covered on General Medical Services (GMS) and the Drug Payment Scheme (DPS) in Ireland, presenting financial barriers for many. A search of reimbursable items on the HSE website [2] reveals that Emulsifying ointment, Silcocks base and Aqueous cream—an emollient no longer recommended in AD due to its sodium lauryl sulphate (SLS) content—are reimbursed, whereas paraffin gel, Hydromol, Doublebase cream, Epaderm, CeraVe, E45 and Aveeno are not. Research suggests that individuals with atopic dermatitis should avoid SLS-containing products as it can exacerbate symptoms by disrupting the already compromised skin barrier, leading to irritation and inflammation and increased erythema, pruritis and dryness.

In contrast, commonly prescribed topical steroids such as Dermovate, Betnovate, Dovobet, Elocon and Eumovate are reimbursed. The reason for this discrepancy is unclear. In Ireland, patients can apply for reimbursement of a product not on formulary under the Discretionary Hardship Scheme, however, each application is assessed on a case-by-case basis.

Quantification of the out-of-pocket cost to the patient merits consideration. Patients on lower incomes may struggle to afford emollients, with resultant disparities in access based on socioeconomic status. Qualification for healthcare coverage such as medical cards can also significantly impact access. The Irish Skin Foundation advises that the typical minimum quantity of emollient required by a child with AD is 250 g of ‘leave-on’ emollient per week, while that of an adult is approximately 500 g per week. The cost of a 500 g tub of paraffin gel is 14.65 euros at the time of writing. This equates to 14.65 euros per week or 761.80 euros per year if an adult patient were to adhere to the Irish Skin Foundation advice [3]. Launois et al. [4] found that for patients with AD, the cost associated with emollients is significantly higher in patients with severe AD relative to those with moderate or mild AD.

Studies across Europe suggest that out-of-pocket costs for patients with AD is an issue of international scope. In France, Launois et al. [4] found the total of non-reimbursed expenditures per patient with severe AD amounted to €462.1 annually; emollients were one of the most frequently used resources. Mohr et al. [5] in Germany and Argenziano et al. [6] in Italy also document the non-reimbursement of basic emollients. In a study across nine European countries, Zink et al. [7] reported an average of €927 was spent by every patient every year without reimbursement; emollients and moisturisers accounted for the highest monthly costs.

The high costs of emollients are unlikely to reduce in the years to come and we must ask ourselves how much are patients willing and able to pay to maintain and treat their disease. It is essential that we expand the perimeter of medicaments reimbursed for patients with AD to limit exacerbations of the disease and improve quality of life for patients and families. Given that emollients are vital components of the treatment of atopic dermatitis, their reimbursement status merits reconsideration.

Stephanie Ryan: writing–original draft-lead, writing-review and editing-lead. Cristina Grechin: writing–review and editing-supporting. Richard Watchorn: supervision, writing–review and editing–supporting.

Not applicable.

The authors declare no conflicts of interest.

特应性皮炎的润肤剂
除症状外,对特应性皮炎(AD)的处理也会显著影响生活质量。慢性疾病可能给患者和家庭带来相当大的经济负担。治疗费用可能导致依从性差,并导致获得护理方面的社会不平等。润肤剂是阿尔茨海默病治疗的基石。Van Zuuren等人的bbb2010 Cochrane综述证实,润肤霜可以减少发斑次数,延长发斑间隔时间,减少对皮质类固醇的需求。此外,他们报告说,保湿剂和局部皮质类固醇的联合治疗比单独使用局部皮质类固醇更有效。尽管在所有临床指南和处方频率中都包含了润肤剂,但在爱尔兰,一般医疗服务(GMS)和药品支付计划(DPS)中涵盖的润肤剂很少,这给许多人带来了经济障碍。在HSE网站[2]上搜索可报销项目,发现乳化软膏、Silcocks碱和水性霜(一种因其含有月桂基硫酸钠(SLS)而不再被推荐用于AD的润肤剂)可报销,而石蜡凝胶、Hydromol、Doublebase霜、Epaderm、CeraVe、E45和Aveeno则不能报销。研究表明,患有特应性皮炎的人应该避免使用含有sls的产品,因为它会破坏已经受损的皮肤屏障,从而加剧症状,导致刺激和炎症,增加红斑、瘙痒和干燥。相比之下,通常处方的局部类固醇如Dermovate, Betnovate, Dovobet, Elocon和Eumovate是报销的。造成这种差异的原因尚不清楚。在爱尔兰,患者可以根据酌定困难计划申请报销不在处方上的产品,但是,每项申请都是根据具体情况进行评估的。病人自付费用的量化值得考虑。收入较低的患者可能难以负担润肤剂,从而导致基于社会经济地位的获取差异。获得医疗保险(如医疗卡)的资格也会对获取医疗服务产生重大影响。爱尔兰皮肤基金会建议,患有阿尔茨海默病的儿童每周所需的润肤剂最少为250克,而成年人每周的润肤剂用量约为500克。在撰写本文时,一桶500克石蜡凝胶的价格为14.65欧元。如果一个成年患者坚持爱尔兰皮肤基金会的建议,这相当于每周14.65欧元或每年761.80欧元。Launois等人发现,对于阿尔茨海默病患者来说,与中度或轻度阿尔茨海默病患者相比,重度阿尔茨海默病患者与润肤剂相关的成本明显更高。欧洲各地的研究表明,阿尔茨海默病患者的自付费用是一个国际范围的问题。在法国,Launois等人发现,每名严重AD患者每年的未报销支出总额为462.1欧元;润肤剂是最常用的资源之一。Mohr等人(德国)和Argenziano等人(意大利)也记录了基本润肤剂的不可报销情况。在一项横跨9个欧洲国家的研究中,Zink等人报告说,每位患者每年平均花费927欧元而没有报销;润肤剂和保湿剂每月的花费最高。润肤剂的高成本在未来几年不太可能降低,我们必须问自己,病人愿意和能够支付多少费用来维持和治疗他们的疾病。我们必须扩大AD患者的药物报销范围,以限制疾病恶化并改善患者和家属的生活质量。鉴于润肤剂是治疗特应性皮炎的重要组成部分,其报销状况值得重新考虑。斯蒂芬妮·瑞安:写作-原稿领导,写作-评论和编辑领导。克里斯蒂娜·格雷琴:写作评论和编辑支持。Richard Watchorn:监督,写作-审查和编辑支持。不适用。作者声明无利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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