NEBULOSA: Sleep Apnea Syndrome and Community Acquired Pneumonia

Sponsor
Hospital Universitario San Juan de Alicante (Other)
Overall Status
Completed
CT.gov ID
NCT01071421
Collaborator
(none)
123
1
32
3.8

Study Details

Study Description

Brief Summary

The association of sleep apnea-hypopnea syndrome (SAHS) with the infections of the lower airway has not been studied. The aspiration of secretions of the upper airway and the colonization by microorganisms is considered a main event in most of the cases of community acquired pneumonia (CAP) , and specially in the nosocomial pneumonia. The silent aspiration to the lower airway is a common phenomenon in normal subjects during the sleep and some studies has reported that the patients with SAHS present an increase of the risk to pharyngeal aspirations. In fact, the presence of nasal and bronchial inflammation in patients with SAHS is a recognized event. The patients with SAHS could have a risk increased to develop pneumonia due to predisposition to the pharyngeal microaspiration to lower airways during the sleep and other mechanical factors associated. The prevalence of SAHS in patients with CAP could be increased as regards the data published for the same Spanish population. The presence of an apnea-hypopnea index (AHI) could be a risk factor not only to to CAP but to to present a unfavorable clinical evolution in comparison to patients with CAP with a normal AHI. The aim of this study will establish a relation between SAHS and the pneumonia risk.

Condition or Disease Intervention/Treatment Phase
  • Device: abbreviated polysomnography

Detailed Description

This is a prospective comparative case control study to compare the prevalence of sleep apnea-hypopnea syndrome in patients with community acquired pneumonia (CAP).

Patients hospitalized with CAP (Group A)will be studied with respiratory polygraphy during the sleep and a second respiratory polygraphy will be conducted in home after the curation of the pneumonia (one month). During the admission, etiological study including blood cultures, serology, urinary antigens for legionella and S, pneumoniae, sputum cultures and other invasive techniques as bronchoscopy when appropriate will be obtained. Questionnaires related with sleep apnea-hypopnea syndrome will be obtained consisting in Epworth test, symptoms questionnaires and FOSQ test.

Group B are patients with other infections as urinary, bone, pelvic infections excluding upper or lower respiratory infections. Respiratory polygraphy will be performed in this group as in the group A obtaining the same questionnaires.

We compare the variables of respiratory polygraphy, questionnaires scores, percentage of patients with an AHI > 12 between both groups and we compare the variables obtained in the respiratory polygraphy performed in hospital and at home in the group A to evaluate if the condition of an altered AHI was previous to the CAP episode. We will obtain the prevalence of sleep apnea-hypopnea patients in both groups and we compare factor risks (COPD, diabetes mellitus, bronchial asthma, etc) between A and B. Finally multivariable analysis is conducted to evaluate the contribution of the AHI to CAP, as other recognize factor risk.

Both groups are paired by age, sex and body mass index

Study Design

Study Type:
Observational
Actual Enrollment :
123 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Prevalence of Sleep Apnea-hypopnea Syndrome in Patients With Community Acquired Pneumonia, Prospective and Comparative Case-control Study
Study Start Date :
Apr 1, 2006
Actual Primary Completion Date :
Dec 1, 2008
Actual Study Completion Date :
Dec 1, 2008

Arms and Interventions

Arm Intervention/Treatment
Control Group (B): Other Infections

Other infections admitted to the hospital

Device: abbreviated polysomnography
Both groups will be studied with in-hospital respiratory polygraphy during the sleep. The group A will be studied with another respiratory polygraphy in the home one month after the resolution of CAP. Some questionnaires to measure the sleepiness (Epworth test), FOSQ test, in-home sleepiness questionnaire and symptoms questionary will be obtained in Group A and B
Other Names:
  • Respiratory Polygraphy
  • portable polysomnography
  • Community Acquired Pneumonia (Group A)

    Patients admitted to hospital with Community Acquired Pneumonia defined by respiratory symptoms, fever and lung infiltrates

    Device: abbreviated polysomnography
    Both groups will be studied with in-hospital respiratory polygraphy during the sleep. The group A will be studied with another respiratory polygraphy in the home one month after the resolution of CAP. Some questionnaires to measure the sleepiness (Epworth test), FOSQ test, in-home sleepiness questionnaire and symptoms questionary will be obtained in Group A and B
    Other Names:
  • Respiratory Polygraphy
  • portable polysomnography
  • Outcome Measures

    Primary Outcome Measures

    1. To evaluate the prevalence of sleep anea-hypopnea syndrome in patients with community acquired pneumonia, defined by an apnea-hypopnea index more to 12 measured by respiratory polygraphy [2 years]

    Secondary Outcome Measures

    1. To evaluate if the apnea-hypopnea index is a factor risk to community acquired pneumonia [2 years]

    2. To evaluate if a high apnea-hypopnea index is observed in patients with community acquired pneumonia and if is maintained after the pneumonia resolution [2 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Group A:
    Inclusion Criteria:
    • Hospital admission and Community acquired pneumonia
    Exclusion Criteria:
    • Nosocomial infections

    • Low level of conscientiousness

    • Neurological disease

    • Impossibility to complete the questionnaires

    Group B

    Inclusion Criteria:
    • Hospital admission and other infections different to respiratory infections

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sección de Neumología. Hospital Universitario San Juan de Alicante San Juan de Alicante Alicante Spain 03550

    Sponsors and Collaborators

    • Hospital Universitario San Juan de Alicante

    Investigators

    • Study Director: Eusebi Chiner, MD, Head of Pneumology Section
    • Principal Investigator: Mónica Llombart, MD, Consultant

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01071421
    Other Study ID Numbers:
    • NEBULOSA PROJECT
    First Posted:
    Feb 19, 2010
    Last Update Posted:
    Feb 19, 2010
    Last Verified:
    Feb 1, 2006

    Study Results

    No Results Posted as of Feb 19, 2010