风湿病学家对 1 型和 2 型系统性红斑狼疮模型的看法。

IF 2.9 Q2 RHEUMATOLOGY
ACR open rheumatology Pub Date : 2024-12-01 Epub Date: 2024-09-29 DOI:10.1002/acr2.11748
Amanda M Eudy, Megan E B Clowse, Amy Corneli, Summer Starling, Nneka Jebose Molokwu, Teresa Swezey, David S Pisetsky, Mithu Maheswaranathan, Jayanth Doss, Kai Sun, Rebecca E Sadun, Lisa G Criscione-Schreiber, Jennifer L Rogers
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引用次数: 0

摘要

目的:1 型和 2 型系统性红斑狼疮(SLE)模型是为了概括系统性红斑狼疮患者的所有体征和症状而开发的。我们之前的定性研究表明,该模型准确地反映了系统性红斑狼疮患者的生活体验。本研究的目的是向风湿免疫科医生介绍 1 型和 2 型系统性红斑狼疮模型,以了解该模型如何与他们治疗系统性红斑狼疮患者的经验相吻合:我们通过对风湿免疫科医生进行半结构式访谈,开展了一项定性描述研究。风湿免疫科医生被问及他们对 1 型和 2 型系统性红斑狼疮模型的总体印象、该模型与他们治疗系统性红斑狼疮患者的方法的契合度、该模型在临床实践中的实用性以及任何修改建议。应用主题分析确定了突出的主题:我们采访了 13 位风湿病学家。大多数风湿病学家认可该模型,并认为它有助于指导治疗和临床决策。一些风湿病专家认为该模型有助于患者教育,以管理患者对 1 型和 2 型症状和治疗方法之间差异的期望。少数风湿免疫科医生担心该模型可能会导致系统性红斑狼疮的过度诊断:结论:大多数受访的风湿免疫科医生都接受了1型和2型系统性红斑狼疮模式,并将其视为识别和治疗系统性红斑狼疮患者症状的有效方法。未来的研究将确定 1 型和 2 型系统性红斑狼疮模式的实施如何影响患者的理解、医患关系和临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perspectives of Rheumatologists on the Type 1 and 2 Systemic Lupus Erythematosus Model.

Objective: The Type 1 and 2 systemic lupus erythematosus (SLE) Model was developed to encapsulate all signs and symptoms that patients with SLE experience. Our previous qualitative work demonstrated the model accurately reflects the lived experience of people living with SLE. The objective of this study was to present the Type 1 and 2 SLE Model to rheumatologists to understand how the model fits with their experiences treating patients with SLE.

Methods: We conducted a qualitative descriptive study using semistructured interviews with rheumatologists. Rheumatologists were asked about their general impression of the Type 1 and 2 SLE Model, how the model does or does not fit within their approach to treating patients with SLE, the utility of the model in clinical practice, and any suggested changes. Applied thematic analysis identified salient themes.

Results: We interviewed 13 rheumatologists. The majority of rheumatologists approved of the model and found it useful to guide therapy and clinical decision-making. Several rheumatologists thought the model was helpful for patient education to manage expectations about differences between Type 1 and Type 2 symptoms and treatments. A few rheumatologists expressed concern that the model could lead to an overdiagnosis of SLE.

Conclusion: The Type 1 and 2 SLE Model was accepted by most rheumatologists interviewed and welcomed as a useful approach to identifying and treating symptoms in patients with SLE. Future studies will determine how implementing the Type 1 and 2 SLE Model affects patient understanding, the physician-patient relationship, and clinical outcomes.

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