Dey Jacob K, Ishii Lisa E, Nellis Jason C, Boahene Kofi D O, Byrne Patrick J, Ishii Masaru
Division of Facial Plastic and Reconstructive Surgery, Department of Otolaryngology-Head and Neck Surgery, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Division of Rhinology, Department of Otolaryngology-Head and Neck Surgery, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
JAMA Facial Plast Surg. 2017 Dec 1;19(6):476-483. doi: 10.1001/jamafacial.2016.1630.
Differences in perception of facial paralysis among patients, casual observers, and experts may have implications for outcomes research and patient care.
To compare multiple domains of casual observer and expert perception with the actual experience of patients with permanent unilateral facial paralysis.
DESIGN, SETTING, AND PARTICIPANTS: This investigation was a prospective cohort study conducted at an academic tertiary referral center. Patients with permanent unilateral facial paralysis (House-Brackmann grades IV to VI) were randomly selected from The Johns Hopkins University Division of Facial Plastic and Reconstructive Surgery clinic. A diverse group of casual observers and experts were recruited to rate their perception of each patient with facial paralysis. The study dates were July 2014 to July 2015.
Patients rated their paralysis severity, attractiveness, quality of life, and affect using established metrics. Casual observers and experts viewed standardized facial videos of each patient and then used the same metrics to rate each patient's paralysis severity, attractiveness, quality of life, and affect.
The analysis yielded 40 patient observations, 6400 casual observer observations, and 200 expert observations for each outcome metric in the study. Compared with the patients' self-perception, casual observers and experts rated patients with facial paralysis more negatively in all measured domains. A multivariable mixed-effects regression showed that observers perceived patients as having greater paralysis severity (8.49 [95% CI, -0.65 to 17.64] of 100 points; SE, 4.67), being less attractive (-7.71 [95% CI, -14.92 to -0.50] of 100 points; SE, 3.68), and having a worse quality of life (-7.76 [95% CI, -14.18 to -1.34] of 100 points; SE, 3.28) compared with the patients' perceptions. Logistic regression demonstrated that observers were less likely to rate patients' affect as positive (odds ratio, 0.28 [95% CI, 0.14-0.58]; SE, 0.10) compared with the patients' self-rating. The raw data and regression analyses also showed that patients, casual observers, and experts perceived faces with higher House-Brackmann grades more negatively in all measured domains of facial perception.
This study found that casual observers and experts generally perceive patients with facial paralysis more negatively than patients perceive themselves. These findings have implications for patients and facial plastic surgeons alike. They also emphasize the importance of assessing outcomes from all 3 perspectives. This pilot study lays the groundwork for developing new tools to assess the social perception of facial deformity that could lead to advancement in facial paralysis outcomes research and improved care for patients with facial paralysis.
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患者、普通观察者和专家对面部瘫痪的认知差异可能会对疗效研究和患者护理产生影响。
比较普通观察者和专家在多个领域的认知与永久性单侧面部瘫痪患者的实际体验。
设计、背景和参与者:本调查是在一所学术性三级转诊中心进行的前瞻性队列研究。从约翰·霍普金斯大学面部整形与重建外科诊所随机选取永久性单侧面部瘫痪(House-Brackmann分级为IV至VI级)的患者。招募了一组多样化的普通观察者和专家,对每位面部瘫痪患者的认知进行评分。研究日期为2014年7月至2015年7月。
患者使用既定指标对其瘫痪严重程度、吸引力、生活质量和情感进行评分。普通观察者和专家观看每位患者的标准化面部视频,然后使用相同指标对每位患者的瘫痪严重程度、吸引力、生活质量和情感进行评分。
该分析得出,对于研究中的每个结局指标,有40例患者观察数据、6400例普通观察者观察数据和200例专家观察数据。与患者的自我认知相比,普通观察者和专家在所有测量领域对面部瘫痪患者的评分都更低。多变量混合效应回归显示,观察者认为患者的瘫痪严重程度更高(满分100分中为8.49分[95%CI,-0.65至17.64];标准误,4.67),吸引力更低(满分100分中为-7.71分[95%CI,-14.92至-0.50];标准误,3.68),生活质量更差(满分100分中为-7.76分[95%CI,-14.18至-1.34];标准误,3.28)。逻辑回归表明,与患者的自我评分相比,观察者将患者情感评为积极的可能性更小(优势比,0.28[95%CI,0.14 - 0.58];标准误,0.10)。原始数据和回归分析还表明,在面部认知的所有测量领域中,患者、普通观察者和专家对House-Brackmann分级较高的面部的认知更负面。
本研究发现,普通观察者和专家对面部瘫痪患者的普遍认知比患者自身的认知更负面。这些发现对患者和面部整形外科医生都有影响。它们还强调了从所有三个角度评估结局的重要性。这项试点研究为开发新工具以评估面部畸形的社会认知奠定了基础,这可能会推动面部瘫痪疗效研究的进展并改善对面部瘫痪患者的护理。
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