埃德蒙顿-33的验证:患者报告的头颈部肿瘤治疗后基线和亚急性期的预后工具。

IF 2.7 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
K. Zhang, H. Khan, H. Seikaly, A. Nichols, K. Fung, S. D. MacNeil, A. Mendez
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引用次数: 0

摘要

背景:患者报告的预后(PRO)优先考虑患者的观点,对于头颈部肿瘤以患者为中心的护理非常有价值。本研究的目的是探讨Edmonton-33 (E-33)的纵向效度,这是一种用于评估吞咽、咀嚼、口干和语言等头颈部功能的PRO仪器。方法:本研究纳入59例成人口腔鳞状细胞癌(SCC)患者,其中女性18例,男性41例。参与者在手术和放射治疗的第3个月(n = 18)、第6个月(n = 18)和第9个月(n = 16)前后提供同意并完成了E-33和其他PRO仪器。收集数据(从2021年6月到2024年8月),并分析E-33结构域与治疗前(基线)和治疗后(第3、6和9个月)之前验证的特定结构域之间的相关性。结论:E-33在亚急性时间点(6个月)治疗前和治疗后捕获吞咽、咀嚼、口干和言语数据的有效性与其他先前验证的仪器相似。这种有效性在治疗后3个月的较急性时间点和治疗后9个月的较晚时间点受到限制。需要更多的数据来进一步探索治疗后1年和2年的进一步纵向时间点的长期有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Validation of the Edmonton-33: A Patient-Reported Outcome Instrument in Head and Neck Oncology at Baseline and Subacute Phases Post-Treatment

Background

Patient-reported outcomes (PRO), which prioritize patient perspectives, are highly valuable for patient-centered care in Head and Neck Oncology. The objective of this study was to explore the longitudinal validity of the Edmonton-33 (E-33), a PRO instrument for assessing head and neck functions in swallowing, chewing, dry mouth, and speech.

Methods

This study involved 59 adult patients (18 female, 41 male) with squamous cell carcinoma (SCC) of the oral cavity. Participants provided consent and completed the E-33 and other PRO instruments before and after surgical and radiation treatment at months 3 (n = 18), 6 (n = 18), and 9 (n = 16). Data were collected (from June 2021 to August 2024) and analyzed for correlation between domains of the E-33 and their domain-specific, previously validated counterparts before treatment (baseline) and after treatment (Months 3, 6, and 9).

Results

There were statistically significant correlations (p < 0.05) between all E-33 domains and their domain-specific counterparts at baseline and at post-treatment month 6. At Months 3 and 9 post-treatment, there were partial correlations between E-33 domains and some domain-specific counterparts.

Conclusion

The E-33 demonstrates validity pre-treatment and post-treatment at subacute timepoint (Months 6) for capturing data on swallowing, chewing, dry mouth, and speech, similar to other previously validated instruments. This validity is limited at the more acute timepoint of 3 months post-treatment and the later timepoint of 9 months post-treatment. Additional data are needed to further explore the long-term validity at further longitudinal timepoints at 1 and 2 years post-treatment.

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来源期刊
CiteScore
5.90
自引率
6.10%
发文量
121
审稿时长
4-8 weeks
期刊介绍: The aim of the Journal of Oral Pathology & Medicine is to publish manuscripts of high scientific quality representing original clinical, diagnostic or experimental work in oral pathology and oral medicine. Papers advancing the science or practice of these disciplines will be welcomed, especially those which bring new knowledge and observations from the application of techniques within the spheres of light and electron microscopy, tissue and organ culture, immunology, histochemistry and immunocytochemistry, microbiology, genetics and biochemistry.
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