1. Prevalence of obstructive sleep apnoea syndrome following oropharyngeal cancer treatment: A prospective cohort study.
- Author
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Loth, A., Michel, J., Giorgi, R., Santini, L., Rey, M., Elbaum, J.‐M., Roux, N., Giovanni, A., Dessi, P., and Fakhry, N.
- Subjects
SLEEP apnea syndromes ,DISEASE prevalence ,OROPHARYNGEAL cancer ,HEALTH outcome assessment ,HEALTH of cancer patients ,QUALITY of life ,CANCER complications ,HOSPITALS ,CANCER treatment ,DISEASE risk factors - Abstract
Objectives To evaluate the prevalence of obstructive sleep apnoea syndrome (OSAS) in a population of patients treated for an advanced oropharyngeal cancer (AJCC Stage III or IV), depending on treatment strategy, and to evaluate its impact on quality of life. Design Prospective cohort study. Setting University Teaching Hospital of La Conception, Marseille, France. Participants Fifty-one disease-free patients were included. Forty-one patients received a combined chemoradiotherapy, while 10 patients were treated by surgery followed by chemoradiotherapy. Main Outcome Measures Every patient underwent a formal sleep consultation and was asked to complete the Epworth Sleepiness Scale and EORTC QLQ C-30 and the EORTC H&N 35 questionnaires. A home overnight respiratory polygraphy was performed in every subject. Results The mean time between the end of cancer treatment and the OSAS analysis was 54.04 months [20; 84]. An OSAS was found in 25.49% of our patients. There was no significant difference between patients treated with either surgery (30%) or CRT (24.39%), P=.79. The EORTC QLQ C-30 questionnaire showed a significant difference between positive and negative OSAS groups in the Global Health Status Scale (50.64 vs 67.11, P=.02) and in the fatigue item (35.04 vs 17.25, P=.03). Conclusions Our population with advanced oropharyngeal cancer, whatever the treatment strategy it may be, was at risk of developing OSAS with negative impact on quality of life. A routine screening and treatment of OSAS seems necessary to improve the quality of life of patients treated for advanced oropharyngeal cancer. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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