Laryngeal Vibrotactile Stimulation Is Feasible, Acceptable To People With Unexplained Chronic Cough

Author:

Misono Stephanie1ORCID,Shen Erin Y.2,Sombrio Anna G.3,Lunos Scott4,Xu Jiapeng5,Hoffmeister Jesse1,Stockness Ali1,Butcher Lisa6,Weinstein Daniel1,Gaeckle Nathaniel T.7,Gray Raluca1ORCID,Konczak Jürgen5ORCID

Affiliation:

1. Department of OtoHNS University of Minnesota Minneapolis Minnesota U.S.A.

2. University of Minnesota Medical School Minneapolis Minnesota U.S.A.

3. Association of Pediatric Program Directors McLean Virginia U.S.A.

4. Biostatistical Design and Analysis Center, Clinical and Translational Science Institute University of Minnesota Minneapolis Minnesota U.S.A.

5. School of Kinesiology, Human Sensorimotor Control Laboratory University of Minnesota Minneapolis Minnesota U.S.A.

6. Department of OtoHNS University of Minnesota, Lions Voice Clinic Minneapolis Minnesota U.S.A.

7. Division of Pulmonary, Allergy, Critical Care and Sleep, Department of Medicine University of Minnesota Minneapolis Minnesota U.S.A.

Abstract

ObjectivesUnexplained chronic cough (UCC) is common and has significant impacts on quality of life. Ongoing cough can sensitize the larynx, increasing the urge to cough and perpetuating the cycle of chronic cough. Vibrotactile stimulation (VTS) of the larynx is a noninvasive stimulation technique that can modulate laryngeal somatosensory and motor activity. Study objectives were to assess feasibility and acceptability of VTS use by people with UCC. Secondarily, changes in cough‐related quality of life measures were assessed.MethodsAdults with UCC recorded cough measures at baseline and after completing 2 weeks of daily VTS. Feasibility and acceptability were assessed through participant‐reported device use and structured feedback. Cough‐related quality of life measures were the Leicester Cough Questionnaire (LCQ) and the Newcastle Laryngeal Hypersensitivity Questionnaire (NLHQ).ResultsNineteen adults participated, with mean age 67 years and cough duration 130 months. Notably, 93% of planned VTS sessions were logged, 94% of participants found the device comfortable to wear, 89% found it easy to operate and 79% would recommend it to others. Pre‐post LCQ change achieved a minimal important difference (MID) (mean 1.3 [SD 2.4, p = 0.015]). NLHQ scores improved, but did not reach an MID.ConclusionsLaryngeal VTS use was feasible and acceptable for use by patients with UCC and was associated with a meaningful improvement in cough‐related quality of life. Future studies will include VTS dose refinement and the inclusion of a comparison arm to further assess the potential for laryngeal VTS as a novel treatment modality for UCC.Level of Evidence4 Laryngoscope, 2024

Funder

Center for Scientific Review

National Institutes of Health

Publisher

Wiley

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Current opinion in refractory and/or unexplained chronic cough;Current Opinion in Otolaryngology & Head & Neck Surgery;2024-09-05

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