The experience of face and hand composite tissue transplantations reported in the international community have mainly concerned trauma patients. Feasibility and individual benefit have been demonstrated for these indications, in properly selected patients. The first laryngeal transplantation also concerned a case of post-traumatic reconstruction. A certain number of patients, who have suffered direct (extended period of intubation during a stay in the ICU, road traffic accident etc.) or indirect trauma (thermal or chemical burns) to the larynx, present irreversible trauma or injury to the larynx in which conventional treatments are unable to restore laryngeal function. These patients find themselves severely disabled, with a significant reduction in their quality of life. They suffer from stigmatization which leads to social isolation (professional and personal). In some circumstances, providing healthy tissue and anatomical or functional components (cartilage, muscle, nerves, blood vessels) by means of an allogeneic laryngeal transplantation, is the only way of allowing patients, whose quality of life has been seriously affected, to speak, breath and swallow normally. The extremely promising results from other international teams in this area have encouraged the investigators to present this project. The specificities of the protocol compared to previous transplantations carried out by other teams are: * The technique for nerve re-innervation which should make it possible to decannulate all patients and improve functional outcomes in the graft. * A dual therapy immunosuppressive regimen will be used, if the patient's clinical and biological status permits, which can be adjusted according to the type of tissue grafted. It might be thought that the need for immunosuppressive therapy means the indications will remain rare, representing an incidence of less than five patients a year in France. However, the interest of this research project does not reside in the number of patients concerned but rather the total lack of any existing therapeutic solution. Conducting a case series will help determine whether, under certain conditions, laryngeal transplantation can improve the management of patients for whom the usual reconstructive surgery options are unsatisfactory. The study is intended to provide a descriptive analysis of a case series of three laryngeal transplantations before and after comparisons, each patient serving as their own control.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
3
Laryngeal transplantation
Service d'Urologie et Chirurgie de la Transplantation - Hôpital Edouard Herriot - Hospices Civils de Lyon
Lyon, France
RECRUITINGService ORL & Chirurgie Cervicofaciale - Hôpital Charles Nicolle - CHU Rouen
Rouen, France
RECRUITINGCentre de soins de suite et de réadaptation fonctionnelle - SSR Val Rosay
Saint-Didier-au-Mont-d'Or, France
RECRUITINGSwallowing evaluation measured using the "Deglutition Handicap Index"
The laryngeal transplantation will be evaluated with a primary composite endpoint based on the three inseparable laryngeal functions: swallowing evaluation will be mainly measured using the "Deglutition Handicap Index"
Time frame: 3 years post transplantation
Voice production evaluated by self-report VHI (Voice Handicap Index) patient questionnaires
The laryngeal transplantation will be evaluated with a primary composite endpoint based on the three inseparable laryngeal functions: Voice production will be evaluated by self-report VHI (Voice Handicap Index) patient questionnaires
Time frame: 3 years post transplantation
Respiration evaluated by decannulation
The laryngeal transplantation will be evaluated with a primary composite endpoint based on the three inseparable laryngeal functions: Respiration, for which the decannulation remains the most appropriate criterion.
Time frame: 3 years post transplantation
Graft survival
Time frame: 3 years post transplantation
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