COPD Clinical Trial
Official title:
Prevalence of Respiratory Aspiration in Patients With COPD: Cross-sectional Study
The aim of the study is to estimate the prevalence of respiratory aspiration in patients with COPD, in a tertiary hospital of Buenos Aires.
Primary objective To estimate the prevalence of respiratory aspiration in patients with
COPD, in a tertiary hospital of Buenos Aires.
Secondary objective
1. To assess the association between the presence of aspiration and the usual degree of
dyspnea in patients with COPD.
2. To assess the association between the presence of aspiration and the amount of regular
annual exacerbations in patients with COPD.
3. To evaluate the association between the presence of aspiration and degree of severity
according to GOLD criteria in patients with COPD.
4. Compare the estimated aspiration in COPD patients with known prevalence of pulmonary
aspiration in the general population in the same age patient prevalence
Patients will be recruited consecutively in the outpatient clinic of Pulmonology and Medical
Clinic, where a first encounter with the patient will be agreed. Additionally, the
investigators will cite patients identified as COPD in the Electronic Medical Records.
During the first meeting the informed consent process to enter the protocol will take place,
then the same baseline characteristics of the patient is taken into an online form. Finally
given a shift within 15 days after the first meeting for the FEEST, and if the patient did
not have a spirometry over the past year to update a new turn. Both studies will be
conducted without any cost.
In patients with impaired swallowing or aspiration presence is detected, we will inform the
doctor to assess the need for additional studies. In turn, the patients will be referred to
speech therapy services for rehabilitation of swallowing.
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Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Screening
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