Chest
Volume 132, Issue 6, December 2007, Pages 1839-1846
Journal home page for Chest

Original Research
Sleep Medicine
Efficacy of Adaptive Servoventilation in Treatment of Complex and Central Sleep Apnea Syndromes

https://doi.org/10.1378/chest.07-1715Get rights and content

Background

Complex sleep apnea syndrome (CompSAS) is recognized by the concurrence of mixed or obstructive events with central apneas, the latter predominating on exposure to continuous positive airway pressure (CPAP). Treatment of CompSAS or central sleep apnea (CSA) syndrome with adaptive servoventilation (ASV) is now an option, but no large series exist describing the application and effectiveness of ASV.

Methods

Retrospective chart review of the first 100 patients who underwent polysomnography using ASV at Mayo Clinic Sleep Center.

Results

ASV titration was performed for CompSAS (63%), CSA (22%), or CSA/Cheyne Stokes breathing patterns (15%). The median diagnostic sleep apnea hypopnea index (AHI) was 48 events per hour (range, 24 to 62). With CPAP, obstructive apneas decreased, but the appearance of central apneas maintained the AHI at 31 events per hour (range, 17 to 47) [p = 0.02]. With bilevel positive airway pressure (BPAP) in spontaneous mode, AHI trended toward worsening vs baseline, with a median of 75 events per hour (range, 46 to 111) [p = 0.055]. BPAP with a backup rate improved the AHI to 15 events per hour (range, 11 to 31) [p = 0.002]. Use of ASV dramatically improved the AHI to a mean of 5 events per hour (range, 1 to 11) vs baseline and vs CPAP (p < 0.0001). ASV also resulted in an increase in rapid eye movement sleep vs baseline and CPAP (18% vs 12% and 10%, respectively; p < 0.0001). Overall, 64 patients responded to the ASV treatment with a mean AHI < 10 events per hour. Of the 44 successful survey follow-up patients contacted, 32 patients reported some improvement in sleep quality.

Conclusion

The ASV device appears to be an effective treatment of both CompSAS and CSA syndromes that are resistant to CPAP.

Section snippets

Definitions

Apneas and hypopneas were defined as previously described.5 Respiratory-related arousals (RERAs) were tabulated if associated with apneas, hypopneas, or with other indicators of airflow limitation not meeting criteria for apneas or hypopneas.12 All indexes are expressed as the number of events divided by the hours of sleep.

Obstructive sleep apnea syndrome was diagnosed if AHI was ≥ 5 events per hour, or if the patient complained of sleepiness and the number of RERAs per hour was > 10 and CPAP

Results

The study population was 87% male with median age of 72 years (IQR, 59 to 78). Characteristics are summarized in Table 1. The diagnoses that led to an ASV study were CompSAS in 63%, CSA in 22%, and CSA/CSR in the remaining 15%. The indication for all ASV trials was a suboptimal response to CPAP, whether the CPAP trial was performed at our center or elsewhere. Patients had an average of three study segments completed, usually diagnostic polysomnography, CPAP titration, and an ASV trial. In some

Discussion

This is the first report of the clinical use of ASV in a consecutive series of patients. In patients with CSA, CSA/CSR, or CompSAS whose sleep-related breathing problems were not easily controlled with CPAP, we have shown that ASV resulted in a dramatic improvement in sleep-disordered breathing, as well as some improvement in sleep architecture. Furthermore, the device was very well tolerated and resulted in improvement in the symptoms of 32 of 44 contacted patients on follow-up.

CompSAS

Conclusion

ASV is a new treatment modality that has been shown effective in treating CSA, CSA/CSR, and CompSAS. Our findings clarify and extend prior observations, and suggest that ASV is an appropriate consideration to other positive airway pressure treatments and is effective for most patients with these nonobstructive sleep-related breathing disorders.

Telephone Questionnaire: Are You Currently Using the ASV?

If yes:

How long have you been using it?

How many hours per night on average?

Are you having problems with:

Mask comfort?

Leaks?

Alarms?

Pressure?

Residual snoring?

Other problems?

Since you started using ASV, how do you feel that your sleep quality has changed?

No change

A little better

A lot better

A little worse

A lot worse

How do you feel that your daytime sleepiness has changed?

No change

A little better

A lot better

A little worse

A lot worse

If no:

To what extent were the following a factor in your stopping

References (21)

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Dr. Morgenthaler received a loan of equipment from Olympus for study on vocal cord visualization during sleep, a loan of equipment from SenTec for different research protocol, and equipment and financial support from ResMed Inc, in 2004 for a different protocol. Dr. Gay received equipment from ResMed Inc., for study of ASV in a different research protocol, and equipment and financial support from 2004 to 2005.

This work was performed at Mayo Clinic, Rochester, MN.

The authors have no conflicts of interest to disclose.

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