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Scand Cardiovasc J ; 52(4): 211-217, 2018 08.
Article in English | MEDLINE | ID: mdl-29671629

ABSTRACT

OBJECTIVES: The aim of this study was to investigate the association between echocardiographic measures of diastolic left ventricular dysfunction and decreased arterial oxyhaemoglobin saturation measured with pulse oximetry (SpO2). DESIGN: This is a cross-sectional population-based survey of Norwegian adults. Values obtained using echocardiography, pulse oximetry, and spirometry were included. The primary outcome was abnormal mitral Doppler inflow, defined as normal: E/A ratio 0.75-1.5 and EDT ≥ 140 ms; abnormal: E/A ratio <0.75 or >1.5 or EDT <140 ms. The associations between this outcome and possible predictors, including SpO2 ≤ 95%, were analysed using univariable and multivariable logistic regression. RESULTS: A total of 1782 participants aged 50 years or older (54% women, mean age 67.5 years) were included in the analysis. Abnormal mitral Doppler inflow was found in 595 participants. After adjusting for age, gender, previous myocardial infarction, smoking history, dyspnoea, obesity, and decreased lung function, SpO2 ≤ 95% predicted abnormal mitral Doppler flow with an odds ratio (OR) of 1.6 [95% confidence interval (CI) 1.1-2.4]. Hypertension and BMI > =30 were also significant predictors of impaired filling, with OR of 1.7 (95% CI 1.1-2.7) OR and 1.5 (95% CI 1.2-1.9), respectively. CONCLUSION: Decreased SpO2 was a significant predictor of abnormal mitral Doppler flow. Diastolic dysfunction should be considered when SpO2 ≤ 95% is found.


Subject(s)
Echocardiography, Doppler , Mitral Valve/diagnostic imaging , Oximetry , Oxygen/blood , Ventricular Dysfunction, Left/diagnostic imaging , Ventricular Function, Left , Aged , Biomarkers/blood , Cross-Sectional Studies , Female , Health Surveys , Humans , Logistic Models , Lung/physiopathology , Male , Middle Aged , Mitral Valve/physiopathology , Multivariate Analysis , Norway , Odds Ratio , Oxyhemoglobins/metabolism , Predictive Value of Tests , Prognosis , Ventricular Dysfunction, Left/blood , Ventricular Dysfunction, Left/physiopathology
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