Use of 3-Dimensional Stereophotogrammetry to Detect Disease Progression in Craniofacial Morphea

医学 颅面 等级间信度 背景(考古学) 队列 物理疗法 外科 内科学 心理学 古生物学 发展心理学 评定量表 精神科 生物
作者
Katharina S. Shaw,Tyler T. Nguyen,Ahmad Rajeh,Stephanie M. Cohen,Yevgeniy R. Semenov,Diana B. Reusch,Fatma Dedeoğlu,Ruth Ann Vleugels,Ingrid M. Ganske
出处
期刊:JAMA Dermatology [American Medical Association]
卷期号:159 (11): 1232-1232 被引量:2
标识
DOI:10.1001/jamadermatol.2023.3649
摘要

Importance Objectively determining disease progression in craniofacial morphea (CM) is challenging, as clinical findings of disease activity are often lacking. Objective To evaluate the utility of 3-dimensional (3D) stereophotogrammetry in detecting disease progression in CM over time. Design, Setting, and Participants This prospective cohort study included 27 pediatric and adult patients with CM from 2 hospitals in Boston (Boston Children’s Hospital and Brigham & Women’s Hospital) consecutively enrolled from April 1, 2019, to March 1, 2023. Review of 3D stereophotogrammetry images and data analysis occurred from March 1 to April 1, 2023. Main Outcomes and Measures Clinical and 3D stereophotogrammetry assessments were performed at 2- to 12-month intervals, depending on the clinical context. The 3D stereophotogrammetry images were then qualitatively rated as demonstrating no progression or definitive progression by an expert (board-certified plastic craniofacial surgeon) and nonexpert (board-certified dermatologist) in 3D stereophotogrammetry. In addition, κ coefficients were calculated for interrater reliability. Results Of 27 patients with CM (19 female; median age, 14 [range, 5-40] years) and 3D stereophotogrammetry images obtained from a minimum of 2 time points (median, 4 [range, 2-10] images) spaced a median of 3 (range, 2-12) months apart, 10 experienced progression of their disease based on clinical assessments performed during the study period. In all cases in which clinical progression was favored, blinded qualitative assessment of 3D stereophotogrammetry images also favored progression with substantial interrater reliability (κ = 0.80 [95% CI, 0.61-0.99]). Furthermore, review of 3D stereophotogrammetry detected occult progression of asymmetry not noted on clinical examination in 3 additional patients. Conclusions and Relevance In this prospective cohort study, blinded assessment of sequential 3D stereophotogrammetry images in patients with CM not only corroborated clinical assessment of disease progression but also detected occult progression of facial asymmetry not appreciable on clinical examination alone. Therefore, 3D stereophotogrammetry may serve as a useful adjunct to clinical examination of patients with CM over time. Future investigations are warranted to validate 3D stereophotogrammetry as an outcome measure in CM.

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