Early results of transcutaneous injection laryngoplasty with micronized acellular dermis versus type-I thyroplasty for glottic incompetence dysphonia due to unilateral vocal fold paralysis

2003 ◽  
Vol 17 (4) ◽  
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Roy R Casiano ◽  
Mark E McClinton ◽  
Jun W Xue
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2021 ◽  
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Kazuya Kurakami ◽  
Seiji Kakehata ◽  
...  

2000 ◽  
Vol 14 (3) ◽  
pp. 378-386 ◽  
Author(s):  
Norman D. Hogikyan ◽  
Walter P. Wodchis ◽  
Jeffrey E. Terrell ◽  
Carol R. Bradford ◽  
Ramon M. Esclamado

2014 ◽  
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Jonathon Salinas ◽  
Dinesh K. Chhetri

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Shinsuke Suzuki ◽  
Nobuko Iikawa ◽  
Tadahiro Tsuji ◽  
Kazuhiro Shiina ◽  
Hidekazu Saito ◽  
...  

BMJ Open ◽  
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Vol 7 (9) ◽  
pp. e016871 ◽  
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Paul Carding ◽  
Marcus Jepson ◽  
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Gareth Ambler ◽  
...  

IntroductionA functioning voice is essential for normal human communication. A good voice requires two moving vocal folds; if one fold is paralysed (unilateral vocal fold paralysis (UVFP)) people suffer from a breathy, weak voice that tires easily and is unable to function normally. UVFP can also result in choking and breathlessness. Current treatment for adults with UVFP is speech therapy to stimulate recovery of vocal fold (VF) motion or function and/or injection of the paralysed VF with a material to move it into a more favourable position for the functioning VF to close against. When these therapies are unsuccessful, or only provide temporary relief, surgery is offered. Two available surgical techniques are: (1) surgical medialisation; placing an implant near the paralysed VF to move it to the middle (thyroplasty) and/or repositioning the cartilage (arytenoid adduction) or (2) restoring the nerve supply to the VF (laryngeal reinnervation). Currently there is limited evidence to determine which surgery should be offered to adults with UVFP.Methods and analysisA feasibility study to test the practicality of running a multicentre, randomised clinical trial of surgery for UVFP, including: (1) a qualitative study to understand the recruitment process and how it operates in clinical centres and (2) a small randomised trial of 30 participants recruited at 3 UK sites comparing non-selective laryngeal reinnervation to type I thyroplasty. Participants will be followed up for 12 months. The primary outcome focuses on recruitment and retention, with secondary outcomes covering voice, swallowing and quality of life.Ethics and disseminationEthical approval was received from National Research Ethics Service—Committee Bromley (reference 11/LO/0583). In addition to dissemination of results through presentation and publication of peer-reviewed articles, results will be shared with key clinician and patient groups required to develop the future large-scale randomised controlled trial.Trial registration numberISRCTN90201732; 16 December 2015.


2005 ◽  
Vol 114 (2) ◽  
pp. 132-138 ◽  
Author(s):  
Satoshi Sonoda ◽  
Hideyuki Kataoka ◽  
Takayo Inoue

Between 1995 and 1997, we performed Isshiki's original method of arytenoid adduction alone or as an adjunct to type I thyroplasty for the treatment of unilateral vocal fold paralysis. From 1997 onward, we performed arytenoid adduction by traction of the lateral cricoarytenoid muscle (Iwamura's method), because it reduces discomfort to the patient and avoids rotation of the thyroid cartilage. Preliminary experiments and surgical procedures involving traction of the lateral cricoarytenoid muscle are described. Of 21 patients with a maximum phonation time of less than 9 seconds, 14 underwent type I thyroplasty as an adjunct to our method of arytenoid adduction and 7 underwent arytenoid adduction alone. Sixteen patients (76%) were able after surgery to extend their maximum phonation time beyond 10 seconds; this result compares favorably with the results of Isshiki's original adduction technique. We describe useful anatomic landmarks for approaching the lateral cricoarytenoid muscle in the hope that more voice surgeons will adopt this approach in the treatment of unilateral vocal fold paralysis.


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