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Randomized Controlled Trial Comparative Study
Auto bi-level pressure relief-PAP is as effective as CPAP in OSA patients--a pilot study.
- Alexander Blau, Mihaela Minx, Jan Giso Peter, Martin Glos, Thomas Penzel, Gert Baumann, and Ingo Fietze.
- Charite-Universitätsmedizin Berlin, CCM, Internal Medicine, Cardiology and Angiology, Center of Sleep Medicine, Berlin, Germany. alexander.blau@charite.de
- Sleep Breath. 2012 Sep 1;16(3):773-9.
PurposeContinuous positive airway pressure (CPAP) is the therapy of choice for the treatment of obstructive sleep apnea (OSA). Not all patients can use CPAP therapy with adequate compliance. There is a need to develop more comfortable modes. Auto bi-level Pressure Relief-Positive Airway Pressure (ABPR-PAP) can be an alternative. We conducted a prospective double-blind, randomised trial to evaluate the efficacy and compliance of ABPR-PAP compared with CPAP in OSA patients.MethodsWe included 35 CPAP naive patients (age 53.3 ± 10.3 years, BMI 31.0 ± 5.0 kg/m(2), ESS 10.0 ± 4.2) diagnosed with moderate to severe OSA who underwent a successful CPAP titration. Patients were randomised into the CPAP or the ABPR-PAP treatment group. We used the same device (BIPAP® Auto, Philips Respironics) for CPAP or ABPR-PAP. Apnea-hypopnea index (AHI) was determined using polysomnography before (AHI 40.6 ± 18.3 per hour) and after treatment.ResultsEighteen patients received CPAP and the remaining 17 received APBR-PAP. Groups were similar in terms of demographics and OSA severity. There were no serious adverse events during the trial. CPAP was fixed by a sleep expert and ABPR-PAP varied (range 5-15 cmH(2)O). AHI decreased in the CPAP group to 6.4 ± 5.7 per hour and in the ABPR-PAP group to 4.8 ± 3.6 per hour in the first night (N = 35). After 3 months, the AHI decreased in the CPAP group to 4.4 ± 5.3 per hour and in the ABPR-PAP group to 2.6 ± 3.8 per hour (N = 32). Differences between the groups were not statistically significant. There were no differences in compliance.ConclusionsABPR-PAP is a promising new ventilation mode that enables effective treatment of OSA patients.
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