用于全面评估成骨不全症患者口腔健康和咬合情况的一套标准结果测量方法。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
L Blokland, H Arponen, A Ahmad, S Colijn, H Gjørup, R John, M Li, D Mekking, S Parekh, J M Retrouvey, T Stutz Steiger, L Zhou, K Andersson
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引用次数: 0

摘要

背景:成骨不全症(OI)是一组严重程度不同的遗传性结缔组织疾病,其特点是骨质脆弱。这项国际多学科合作计划的主要目标是根据专家和患者认为重要的方面,就一套标准化的临床医生和患者报告的结果测量方法以及相关测量工具达成共识,以用于 OI 患者的牙科护理。该项目是 Care4BrittleBones 基金会发起的 Key4OI 项目的后续项目,旨在开发一套标准的结果测量方法,涵盖影响口腔颌面外伤患者生活质量的众多因素。由口腔正畸医师、儿童牙医、口腔颌面外科医生和修复牙医组成的国际专家团队采用改良的德尔菲共识程序,选择临床医师报告的结果测量指标(CROM)和患者报告的结果测量指标(PROM)来评估口腔损伤患者的口腔健康状况。通过文献综述和专业知识(CROM 和 PROM)确定了重要领域。在由患有口腔疾病的患者组成的三个焦点小组中,确定了与牙齿健康相关的重要问题。焦点小组的意见被用作最终结果测量的基础:选定的问题被归入相关的 CROM,并在适当的时候与经过验证的问卷进行匹配,以确定最终的 PROM,这些 PROM 最能代表 OI 患者与口腔健康相关的具体问题:结果:就选定的 CROMs 和 PROMs 达成了共识,以制定一套标准的结果测量法和口腔疾病患者口腔健康测量工具:我们的项目达成了关于口腔健康 PROM 和 CROM 标准化的共识声明。这套结果可以通过纳入参与口腔疾病患者牙科护理的专业人员的建议来提高护理标准。此外,它还能促进研究和国际研究合作。此外,焦点小组的重要贡献突出了与口腔感染者的牙科和口腔健康相关问题的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A standard set of outcome measures for the comprehensive assessment of oral health and occlusion in individuals with osteogenesis imperfecta.

Background: Osteogenesis imperfecta (OI) is a group of inherited connective tissue disorders of varying severity characterized by bone fragility. The primary objective of this international multidisciplinary collaboration initiative was to reach a consensus for a standardized set of clinician and patient-reported outcome measures, as well as associated measuring instruments for dental care of individuals with OI, based on the aspects considered important by both experts and patients. This project is a subsequent to the Key4OI project initiated by the Care4BrittleBones foundation which aims to develop a standard set of outcome measures covering a large domain of factors affecting quality of life for people with OI. An international team of experts comprising orthodontists, pediatric dentists, oral and maxillofacial surgeons, and prosthetic dentists used a modified Delphi consensus process to select clinician-reported outcome measures (CROMs) and patient-reported outcome measures (PROMs) to evaluate oral health in individuals with OI. Important domains were identified through a literature review and by professional expertise (both CROMs and PROMs). In three focus groups of individuals with OI, important and relevant issues regarding dental health were identified. The input from the focus groups was used as the basis for the final set of outcome measures: the selected issues were attributed to relevant CROMs and, when appropriate, matched with validated questionnaires to establish the final PROMs which represented best the specific oral health-related concerns of individuals with OI.

Results: Consensus was reached on selected CROMs and PROMs for a standard set of outcome measures and measuring instruments of oral health in individuals with OI.

Conclusions: Our project resulted in consensus statements for standardization oral health PROMs and CROMs in individuals with OI. This outcome set can improve the standard of care by incorporating recommendations of professionals involved in dental care of individuals with OI. Further, it can facilitate research and international research co-operation. In addition, the significant contribution of the focus groups highlights the relevance of dental and oral health-related problems of individuals with OI.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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