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从患者角度看皮肤狼疮:一项定性研究。

Cutaneous lupus concerns from the patient perspective: a qualitative study.

机构信息

Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Dermatology, Corporal Michael J Crescenz VA Medical Center, Philadelphia, Pennsylvania, USA.

出版信息

Lupus Sci Med. 2021 Aug;8(1). doi: 10.1136/lupus-2020-000444.

Abstract

OBJECTIVE

There is a need to identify concerns unique to patients with cutaneous lupus erythematosus (CLE), which may not be captured by current common-practice dermatological quality-of-life tools. This study formally characterises what bothers patients with CLE about their disease by conducting semistructured, qualitative interviews.

METHODS

Sixteen patients with CLE were interviewed about how their cutaneous findings impact their daily life. Each interview was transcribed, coded and categorised for recurrent themes. Current CLE activity and damage were also assessed by the Cutaneous Lupus Activity and Severity Index tool.

RESULTS

Responses were categorised into six themes, including Fear of Disease Progression, Unwanted Attention, Self-Consciousness, Physical Signs/Symptoms, Emotional Symptoms and Functional Decline. The most commonly reported themes were Self-Consciousness, mentioned by 13 of 16 (81.3%) patients, Physical Symptoms, mentioned by 12 of 16 (75%), and then Fear of Disease Progression, by 11 of 16 (68.8%). Frequently mentioned physical signs/symptoms included erythema, itch, dyspigmentation, scar and alopecia. The physical signs/symptoms were categorised as activity signs/symptoms, damage signs and other. For activity signs, erythema was mentioned most frequently (5 of 16), then scale (2 of 16). For activity symptoms, itch was mentioned most frequently (6 of 16), then pain (5 of 16). For damage signs, dyspigmentation was mentioned most frequently (4 of 16), followed by scarring (3 of 16). Patients less than 60 years old were more likely to report emotional symptoms than older patients (p<0.05), but there was no significant variation in frequency of reported themes between race, sex or subtype of CLE.

CONCLUSIONS

These patient experiences and resultant themes elucidated by this study are worth noting in future standardised estimations of the quality of life of patients with CLE. Additionally, the concerns shown by these interviews are important topics for providers to discuss when evaluating patient disease progression.

摘要

目的

需要确定特发性皮肤红斑狼疮(CLE)患者特有的关注点,这些关注点可能无法被当前常见的皮肤科生活质量工具所捕捉。本研究通过半结构化的定性访谈,正式描述了影响 CLE 患者疾病的因素。

方法

对 16 例 CLE 患者进行了关于其皮肤表现如何影响日常生活的访谈。对每次访谈进行转录、编码和分类,以确定反复出现的主题。还使用皮肤狼疮活动和严重程度指数工具评估了当前的 CLE 活动和损害情况。

结果

根据访谈内容,将结果分为 6 个主题,包括对疾病进展的恐惧、不受欢迎的关注、自我意识、身体体征/症状、情绪症状和功能下降。最常报告的主题是自我意识,16 例中有 13 例(81.3%)患者提到,其次是身体症状,16 例中有 12 例(75%)患者提到,然后是对疾病进展的恐惧,16 例中有 11 例(68.8%)患者提到。常提到的身体体征/症状包括红斑、瘙痒、色素沉着异常、瘢痕和脱发。身体体征/症状分为活动体征/症状、损害体征和其他。活动体征方面,红斑最常被提及(16 例中有 5 例),其次是鳞屑(16 例中有 2 例)。活动症状方面,瘙痒最常被提及(16 例中有 6 例),其次是疼痛(16 例中有 5 例)。损害体征方面,色素沉着异常最常被提及(16 例中有 4 例),其次是瘢痕(16 例中有 3 例)。年龄小于 60 岁的患者比年龄较大的患者更有可能报告情绪症状(p<0.05),但在种族、性别或 CLE 亚型之间,报告的主题频率没有显著差异。

结论

本研究通过访谈揭示了患者的这些体验和由此产生的主题,值得在未来 CLE 患者生活质量的标准化评估中注意。此外,这些访谈所显示的关注点是医生在评估患者疾病进展时需要讨论的重要话题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef36/8404455/e3ebdf55fe47/lupus-2020-000444f01.jpg

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