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Erschienen in:
01.11.2003 | Original Article
Implementation of the Vienna Hydrotherapy Group for Laryngectomees—a pilot study
Erschienen in: Supportive Care in Cancer | Ausgabe 11/2003
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Goals
Laryngectomy involves several problems for the individual, such as the need to cope with a stoma, adjustment to tracheostomal breathing, and the formation of a voice. Contact with water, resulting in aspiration, may prove fatal for laryngectomized patients in the absence of appropriate aids. The aim of this pilot study was to conduct a hydrotherapy group for laryngectomized patients and to evaluate its feasibility and outcome in relation to the goals of therapy.
Patients and methods
Six male patients who had undergone laryngectomy were included in a pilot study. The patients underwent a structured hydrotherapy rehabilitation program (three times a week for 8 weeks), using a special underwater therapy device. The patients' posture was controlled by posturography and their endurance capacity by standard ergometry and the 6-min walk. The parameters of fatigue, expectoration, mobility, elasticity/flexibility, postural control/coordination, and general well being were registered on a visual analog scale (VAS). Quality of life was assessed by having the patients fill out the German version of the SF-36 Health Survey.
Main results
Posturograpy findings showed an improvement of two subtests (p<0.028). Exercise testing showed an improved endurance capacity (p<0.028). The patients were able to walk a greater distance in the 6-min walking test (p<0.028). The VAS also showed an improvement of endurance capacity (p<0.028), fatigue (p<0.028), expectoration (p<0.043), mobility of the neck and shoulder (p<0.027), flexibility (p<0.027), postural control and coordination (p<0.028), and general well being (p<0.028). On the SF-36 Health Survey, the patients were improved in the items "Physical functioning" (p<0.027), "Vitality" (p<0.027) "Role-physical" (p<0.026), and "Social functioning" (p<0.043).
Conclusions
A hydrotherapy group for laryngectomized patients proved to be safe, feasible, and effective in this pilot study.