Randall J Harley, Eve Bowers, Jinhong Li, Mikayla Bisignani, Marci L Nilsen, Jonas T Johnson
{"title":"biot<s:1>与HydraSmile治疗辐射性口干:随机双盲交叉研究。","authors":"Randall J Harley, Eve Bowers, Jinhong Li, Mikayla Bisignani, Marci L Nilsen, Jonas T Johnson","doi":"10.1002/oto2.70038","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>This study aims to compare the effectiveness of 2 artificial saliva substitutes (Biotène vs HydraSmile) in the symptomatic management of radiation-induced xerostomia.</p><p><strong>Study design: </strong>Randomized double-blind cross-over study.</p><p><strong>Setting: </strong>Single tertiary care academic institution.</p><p><strong>Methods: </strong>Included adult patients <math> <mrow> <mrow><mrow><mo>≥</mo></mrow> </mrow> </mrow> </math> 6 months postradiotherapy (50-70 gy) for squamous cell carcinoma of the oral cavity, oropharynx, or larynx. The primary endpoint was change in overall subjective xerostomia score from baseline, through use of HydraSmile versus Biotène. Scores were derived from a 100-point visual analog scale, with higher scores indicating better symptomatic control. Analysis of covariance model was used to regress the difference in after-treatment measurement between HydraSmile and Biotène, with respect to baseline differences.</p><p><strong>Results: </strong>A total of 91 participants were included (mean age 63.0 years [SD 9.7]; 85.7% male; 97.8% White). Change in overall xerostomia score with respect to baseline was not significantly different between HydraSmile and Biotène (mean difference 1.24, 95% confidence interval [CI] -2.35 to 4.81). Compared to water alone, both HydraSmile (mean difference 7.45, 95% CI 3.61-11.29) and Biotène (mean difference 7.24, 95% CI 3.06-11.43) significantly improved overall xerostomia score. Forty (44%) patients reported a preference for Biotène, 46 (50.5%) preferred HydraSmile, and 5 (5.5%) had no preference. Patients who preferred Biotène did not significantly benefit from HydraSmile, whereas those who preferred HydraSmile did not significantly benefit from Biotène.</p><p><strong>Conclusion: </strong>Biotène and HydraSmile significantly improved oral dryness among patients with radiation-induced xerostomia. While neither product demonstrated treatment superiority, individual product preference was predictive of greatest treatment benefit.</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 1","pages":"e70038"},"PeriodicalIF":1.8000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11696889/pdf/","citationCount":"0","resultStr":"{\"title\":\"Biotène Versus HydraSmile for Radiation-Induced Xerostomia: Randomized Double-Blind Cross-Over Study.\",\"authors\":\"Randall J Harley, Eve Bowers, Jinhong Li, Mikayla Bisignani, Marci L Nilsen, Jonas T Johnson\",\"doi\":\"10.1002/oto2.70038\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>This study aims to compare the effectiveness of 2 artificial saliva substitutes (Biotène vs HydraSmile) in the symptomatic management of radiation-induced xerostomia.</p><p><strong>Study design: </strong>Randomized double-blind cross-over study.</p><p><strong>Setting: </strong>Single tertiary care academic institution.</p><p><strong>Methods: </strong>Included adult patients <math> <mrow> <mrow><mrow><mo>≥</mo></mrow> </mrow> </mrow> </math> 6 months postradiotherapy (50-70 gy) for squamous cell carcinoma of the oral cavity, oropharynx, or larynx. The primary endpoint was change in overall subjective xerostomia score from baseline, through use of HydraSmile versus Biotène. Scores were derived from a 100-point visual analog scale, with higher scores indicating better symptomatic control. Analysis of covariance model was used to regress the difference in after-treatment measurement between HydraSmile and Biotène, with respect to baseline differences.</p><p><strong>Results: </strong>A total of 91 participants were included (mean age 63.0 years [SD 9.7]; 85.7% male; 97.8% White). Change in overall xerostomia score with respect to baseline was not significantly different between HydraSmile and Biotène (mean difference 1.24, 95% confidence interval [CI] -2.35 to 4.81). Compared to water alone, both HydraSmile (mean difference 7.45, 95% CI 3.61-11.29) and Biotène (mean difference 7.24, 95% CI 3.06-11.43) significantly improved overall xerostomia score. Forty (44%) patients reported a preference for Biotène, 46 (50.5%) preferred HydraSmile, and 5 (5.5%) had no preference. Patients who preferred Biotène did not significantly benefit from HydraSmile, whereas those who preferred HydraSmile did not significantly benefit from Biotène.</p><p><strong>Conclusion: </strong>Biotène and HydraSmile significantly improved oral dryness among patients with radiation-induced xerostomia. 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引用次数: 0
摘要
目的:比较两种人工唾液代用品(biot和HydraSmile)对放射性口干症的治疗效果。研究设计:随机双盲交叉研究。环境:单一的三级医疗学术机构。方法:纳入接受口腔、口咽部或喉部鳞状细胞癌(50-70 gy)放疗后≥6个月的成年患者。主要终点是通过使用HydraSmile和biot,从基线开始的总体主观口干评分的变化。分数来源于100分的视觉模拟量表,分数越高表明症状控制越好。采用协方差分析模型回归HydraSmile和biot处理后测量的差异,相对于基线差异。结果:共纳入91名参与者(平均年龄63.0岁[SD 9.7];男性85.7%;97.8%的白人)。相对于基线,HydraSmile和biot的总体口干评分变化无显著差异(平均差异1.24,95%可信区间[CI] -2.35至4.81)。与单独使用水相比,HydraSmile(平均差异7.45,95% CI 3.61-11.29)和biot(平均差异7.24,95% CI 3.06-11.43)均显著改善了口干症的总体评分。40例(44%)患者偏爱biot, 46例(50.5%)偏爱HydraSmile, 5例(5.5%)没有偏爱。选择biot的患者没有从HydraSmile中显著获益,而选择HydraSmile的患者也没有从biot中显著获益。结论:biot和HydraSmile可显著改善放射性口干症患者的口腔干燥。虽然两种产品都没有表现出治疗优势,但个人产品偏好可以预测最大的治疗效果。
Biotène Versus HydraSmile for Radiation-Induced Xerostomia: Randomized Double-Blind Cross-Over Study.
Objective: This study aims to compare the effectiveness of 2 artificial saliva substitutes (Biotène vs HydraSmile) in the symptomatic management of radiation-induced xerostomia.
Study design: Randomized double-blind cross-over study.
Setting: Single tertiary care academic institution.
Methods: Included adult patients 6 months postradiotherapy (50-70 gy) for squamous cell carcinoma of the oral cavity, oropharynx, or larynx. The primary endpoint was change in overall subjective xerostomia score from baseline, through use of HydraSmile versus Biotène. Scores were derived from a 100-point visual analog scale, with higher scores indicating better symptomatic control. Analysis of covariance model was used to regress the difference in after-treatment measurement between HydraSmile and Biotène, with respect to baseline differences.
Results: A total of 91 participants were included (mean age 63.0 years [SD 9.7]; 85.7% male; 97.8% White). Change in overall xerostomia score with respect to baseline was not significantly different between HydraSmile and Biotène (mean difference 1.24, 95% confidence interval [CI] -2.35 to 4.81). Compared to water alone, both HydraSmile (mean difference 7.45, 95% CI 3.61-11.29) and Biotène (mean difference 7.24, 95% CI 3.06-11.43) significantly improved overall xerostomia score. Forty (44%) patients reported a preference for Biotène, 46 (50.5%) preferred HydraSmile, and 5 (5.5%) had no preference. Patients who preferred Biotène did not significantly benefit from HydraSmile, whereas those who preferred HydraSmile did not significantly benefit from Biotène.
Conclusion: Biotène and HydraSmile significantly improved oral dryness among patients with radiation-induced xerostomia. While neither product demonstrated treatment superiority, individual product preference was predictive of greatest treatment benefit.