Obesity, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Individuals over 18 years of age and under 60 years of age; patients undergoing bariatric surgery by videolaparoscopy and endoscopic; normal preoperative pulmonary function test; patients without radiological alterations in the preoperative period; non-smokers; patients without previous pulmonary impairment such as asthma; bronchitis; emphysema, signature of the Free and Informed Consent Form by the patient
Exclusion criteria
Exclusion criteria: Hemodynamic instability (MAP < 60mmHg) during surgery; conversion from laparoscopy to laparotomy; adjustment of ventilatory parameters during surgery; patient's refusal to perform the requested exercises
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Outcome found 1: The volumetric Respiron group showed a more pronounced recovery in respiratory variables, such as FEV1, FVC and PEF, in addition to a lower perception of pain in the postoperative period, when compared to the Respiron Flow group.;Expected outcome 1: It is expected to show the efficacy and dissimilarity between flow-independent and volume-independent incentive spirometers in patients undergoing bariatric surgery in the recovery of lung function. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 2: To verify whether there is prevention and reduction of respiratory complications in the postoperative period.;Outcome found 2: Variables such as respiratory rate, heart rate and oxygen saturation remained stable and without significant differences between the 2 groups. | — |
Countries
Brazil
Contacts
Universidade Estadual de Campinas