Nasal Versus Oronasal Mask in Continuous Positive Airway Pressure (CPAP) Treatment of Patients Affected by Obstructive Sleep Apnea Syndrome (OSAS).

Osa Syndrome Clinical Trial

Official title:

Evaluation of Different Effects of Nasal Versus Oronasal Mask in Continuous Positive Airway Pressure (CPAP) Treatment of Patients Affected by Obstructive Sleep Apnea Syndrome (OSAS).

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04681196
• Other study ID #: 195/2020/Oss/AOUBO
• Status: Completed
• Start date: January 1, 2021
• Est. completion date: June 1, 2021

Study information

• Verified date: November 2021
• Source: IRCCS Azienda Ospedaliero-Universitaria di Bologna
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Continuous positive airway pressure (CPAP) is considered the gold standard treatment for patients with moderate to severe obstructive sleep apnea (OSA).

Nasal and oronasal masks are often used interchangeably and are generally believed to be equally effective; the choice of interface for OSA therapy remains largely based on clinical judgement and patients preference. However, there is increasing evidence that CPAP delivered by an oronasal mask may be less effective, requires more pressure and are worse tolerated than nasal mask. Patients with OSA on oronasal mask are also less adherent to CPAP.

Some authors have suggested that in some subjects, the CPAP was not effective when an oronasal mask was used. Moreover when pressures are increased to overcome the obstruction, a paradoxical obstruction may take place.

Specific mechanisms explaining upper-airway obstruction events remain unclear and it is not known how many patients exhibit this behavior.

This observational retrospective study is designed to compare a group of patients with obstructive sleep apnea with persistent obstructive events using oronasal masks during CPAP, that were fully recovered with the shift to nasal one with the same or also lower pressure, versus a control group of patients who did not report obstruction with oronasal masks. Aim of the study was to find differences in term of clinical, anatomical and physiological characteristics between these two groups.

Description:

Continuous positive airway pressure (CPAP) is considered the gold standard treatment for patients with moderate to severe obstructive sleep apnea (OSA).

The treatment of OSA with CPAP was first proposed by Sullivan et al and traditionally delivered using a nasal mask because the pressure applied through the nose would be transmitted as a pneumatic splint to the back of the upper airway and would push them anteriorly.

However patients with OSA frequently present nasal obstruction and leakage of air from the mouth, and different mask interfaces have been developed, including the oronasal mask that may be used to deliver CPAP.

Nasal and oronasal masks are often used interchangeably and are generally believed to be equally effective; the choice of interface for OSA therapy remains largely based on clinical judgement and patients preference .

In our clinical practice, CPAP titration is started adapting the patient to a nasal mask but an oronasal can be selected if a patient reports inability to breathe through their nose, severe nasal obstruction, leakage of air from the mouth or from other part of the face due to anatomical variation.

However, there is increasing evidence that CPAP delivered by an oronasal mask may be less effective, requires more pressure and are worse tolerated than nasal mask.

Patients with OSA on oronasal mask are also less adherent to CPAP. One recent randomised trial and a preliminary report suggest that subjects with sleep apnea treated with CPAP showed a significantly lower residual AHI when subjects wore a nasal mask rather than a oronasal mask.

Similarly, a recent prospective observational cohort study suggested that the use of a facial mask was associated with higher CPAP pressure requirements than both nasal masks and nasal pillows.

Some authors have suggested that in some subjects, the CPAP was not effective when an oronasal mask was used. Moreover when pressures are increased to overcome the obstruction, a paradoxical obstruction may take place.

These findings have been called "the Starling paradox effect", according to which the pressure that opens the pharynx can also lead to pharyngeal collapse when applied orally.

In these difficult-to-titrate patients the specific mechanisms explaining upper-airway obstruction events remain unclear and it is not known how many patients exhibit this behavior.

This observational retrospective study is designed to compare a group of patients with obstructive sleep apnea with persistent obstructive events using oronasal masks during CPAP, that were fully recovered with the shift to nasal one with the same or also lower pressure, versus a control group of patients who did not report obstruction with oronasal masks.

Aim of the study was to find differences in term of clinical, anatomical and physiological characteristics between these two groups.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 61
• Est. completion date: June 1, 2021
• Est. primary completion date: March 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• confirmed diagnosis of OSA and use of CPAP treatment

• age> or equal to 18 years old

• sign of informed consent

Exclusion Criteria:

• none

Related Conditions & MeSH terms

• Osa Syndrome
• Sleep Apnea Syndromes
• Sleep Apnea, Obstructive
• Syndrome

Intervention

Other:
• patients shifted to nasal mask after persistent OSA with oronasal mask
In this group were selected OSA patients exhibiting persistent obstructive events and paradoxical obstruction with oronasal masks during CPAP , that were fully recovered (no more OSA detected) with the shift to nasal one

Locations

Country	Name	City	State
Italy	Azienda Ospedaliero Universitaria Policlinico S. Orsola-Malpighi	Bologna

Sponsors (1)

Lead Sponsor	Collaborator
IRCCS Azienda Ospedaliero-Universitaria di Bologna

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	differences in terms of age between groups	differences in terms of age (measured in years) between patients with paradox effect versus patients without paradox effect (control group); age considered at the time of OSA diagnosis	Up to one month.
Primary	differences in terms of body mass index between groups	differences in terms of body mass index (BMI), measured in Kg/m2, between patients with paradox effect versus patients without paradox effect (control group); BMI considered at the time of OSA diagnosis.	Up to one month.
Primary	differences in terms of basal value of apnea-hypopnea index (OSA severity) between groups	differences in terms of basal value of apnea-hypopnea index (OSA severity) between groups. AHI considered at the time of OSA diagnosis (basal cardio-respiratory monitoring) Apnea-hypopnea index (AHI) measures number of obstructive events (apnea and hypopnea) per hour during basal cardio-respiratory monitoring. AHI> 5 is diagnostic of OSA. Severity of OSA is proportional to AHI value.	Up to one month.
Primary	differences in terms of basal value of minimum and mean nocturnal oxygen saturation between groups.	differences in terms of basal value of minimum and mean nocturnal oxygen saturation (respectively minimum SpO2 % and mean SpO2 %) between groups.Minimum and mean Oxygen Saturation considered at the time of OSA diagnosis (basal cardio-respiratory monitoring).	Up to one month.
Primary	differences in terms of basal value of time spent under SpO2<90% and under SpO2<80% between groups.	differences in terms of basal value of time spent under SpO2<90% (CT90) and under SpO2<80% (CT80) between groups.minimum and mean Oxygen Saturation considered at the time of OSA diagnosis (basal cardio-respiratory monitoring).; These two parameters are expressed as % of total registration time during basal cardio-respiratory monitoring at the time od OSA diagnosis.	Up to one month.
Primary	differences in terms of oxygen desaturation index between groups.	differences in terms of oxygen desaturation index (ODI) between groups. ODI represents number of decline of SpO2 > or equal to 3% events per hours during basal cardio-respiratory monitoring collected at the time od OSA diagnosis.ODI considered at the time of OSA diagnosis (basal cardio-respiratory monitoring)	Up to one month.