Upper airway resistance syndrome: A long-term outcome study
Introduction
Upper Airway Resistance Syndrome (UARS) (Guilleminault et al., 1993, Guilleminault et al., 2000) is associated with abnormal respiratory effort, nasal airflow limitation, absence of obstructive sleep apnea, minimal pulse oxygen fluctuation with oxygen saturation (SaO2) equal or greater than 92%, and frequent nocturnal arousals or reflex brainstem activation (Morruzi, 1963). Patients with UARS frequently complain of daytime tiredness and fatigue. It has been emphasized that these patients present more as patients with functional somatic syndromes than those presenting with Obstructive Sleep Apnea Syndrome (OSAS) (Gold et al., 2003, Guilleminault et al., 2001a, Guilleminault et al., 2001b, Guilleminault et al., 2001c). There have been questions about the usefulness of identifying this syndrome independently from the OSAS, and questions on its long-term evolution (Douglas, 2000). The treatment of UARS is not well clarified: nasal continuous positive airway pressure (nCPAP) was used in the initial report (Guilleminault et al., 1993) to demonstrate response to short term upper airway widening during sleep, but long term prescription has had variable success (Guilleminault et al., 2002). Finally not only the incidence of the syndrome is unknown but also is its natural history. To improve our knowledge on several of these points, we designed a prospective study on a retrospective cohort. We questioned the outcome of the diagnostic evaluation and the treatment recommendation performed on subjects labeled UARS patients at least 4 years prior the start of the prospective study. We questioned if their illness had progressed, if their symptoms had changed and if the prescribed treatment (nCPAP) had been helpful. Due to health insurance policies and contractual agreements with health policy payers, regulations of the medical center, and views of the medical center by the surrounding local medical community, our sleep disorders clinic functioned for many years as referral clinic performing diagnosis and treatment recommendations, with a one time patient contact, and no further interaction if not initiated by the referring primary care physician. Due to these specific conditions we built-up our prospective protocol.
Section snippets
Subjects
For this investigation, we attempted to contact all patients (n = 138) who were diagnosed with UARS at Stanford Sleep Disorders Clinic between 1995 and 1998.
Initial evaluation
Diagnosis of UARS was based on:
- (1)
Complaints of daytime fatigue, tiredness, or sleepiness, report of nocturnal sleep disruption with variable difficulty to go back to sleep or presence of symptoms associated with sleep disordered breathing (Basiri and Guilleminault, 2000).
- (2)
Clinical evaluation: Patients completed validated questionnaires (Sleep
Initial evaluation
About 138 subjects including 88 women were identified from the computerized database. Men were significantly younger than women. (P-value < 0.05) (Table 1) No other significant differences were found between men and women. Symptoms at entry are presented in Table 2A, Table 2B(A and B). All patients complained of disrupted nocturnal sleep. Five percent of all subjects had complaints of sleep onset insomnia. There were 7 patients with a Hamilton D scale with a score between 15 and 18 (4 of them
Discussion
This is the first study that examines the natural evolution of patients diagnosed with UARS. The results clearly showed that sleep and daytime symptoms in untreated UARS increased over time and there was no case of spontaneous remission of symptoms. More specifically, the likelihood of having daytime fatigue, insomnia or depressive mood had a 12 to 20 times increase over a 4-year period. One of the direct consequences was the increase in hypnotic and antidepressant prescription: 11.7% and 3.2%
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