Correlation Between Preeclampsia and Positive for Obstructive Sleep Apnea Screening Test: STOPBANG Questionnaire
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Sleep Apnea, Obstructive
- Sponsor
- Ramathibodi Hospital
- Enrollment
- 1100
- Primary Endpoint
- Prevalence of pre-eclampsia between high and low risk of OSA patient based on Stop-bang screening test
- Last Updated
- 9 years ago
Overview
Brief Summary
The purpose of this study is to find the correlation between high risk OSA (obstructive sleep apnea) patient, based on Stop-bang screening tool and preeclampsia
Detailed Description
Obstructive sleep apnea (OSA) has been associated with preeclampsia and intrauterine growth retardation (IUGR). Since the gold standard diagnosis of OSA is polysomnogram which is limited by cost and availability. Therefore, various screening tools were proposed in order to identify high risk OSA patient such as Stop-bang questionnaire. From the previous study, Stop-bang showed a high predictive performance and the score equal or higher than 3 determines high risk for OSA.
Investigators
Lisa Sangkum
Doctor
Ramathibodi Hospital
Eligibility Criteria
Inclusion Criteria
- •Pregnant women who were scheduled for cesarean delivery or admitted to the antepartum unit at Ramathibodi hospital
Exclusion Criteria
- •Age \< 18 year old
- •Previous diagnose OSA
- •Patients who have used continuous positive airway pressure (CPAP) or bi-level positive airway pressure (Bi-PAP) fro OSA treatment
Outcomes
Primary Outcomes
Prevalence of pre-eclampsia between high and low risk of OSA patient based on Stop-bang screening test
Time Frame: 1 day
Secondary Outcomes
- prevalence of pre-eclampsia between high and low risk of OSA patient, based on Epworth sleepiness scale(1 day)
- prevalence of pre-eclampsia between high and low risk of OSA patient, based on Berlin questionnaire(1 day)
- prevalence of pre-eclampsia between high and low risk of OSA patient, based on American society check list(1 day)
- The prevalence of maternal adverse event between high risk and low risk of OSA patient(1 day)
- The prevalence of neonatal adverse event between high risk and low risk of OSA patient(1 day)