Hypoxemia and pulmonary hypertension in patients with concomitant restrictive ventilatory defect and sleep apnea: the overlap syndrome
Background To investigate the severity of hypoxemia and prevalence of pulmonary hypertension (PHTN) in patients with the overlap syndrome (OS) of restrictive ventilatory defect (RVD) and sleep apnea (SA). Methods Patients referred for both sleep test and spirometry for suspected SA and ventilatory d...
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Veröffentlicht in: | Sleep & breathing 2021-06, Vol.25 (2), p.1173-1179 |
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Sprache: | eng |
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Zusammenfassung: | Background
To investigate the severity of hypoxemia and prevalence of pulmonary hypertension (PHTN) in patients with the overlap syndrome (OS) of restrictive ventilatory defect (RVD) and sleep apnea (SA).
Methods
Patients referred for both sleep test and spirometry for suspected SA and ventilatory disorders were recruited prospectively from January 2019 to January 2020. SA was determined by an apnea-hypopnea index ≥ 5/h; average oxygen saturation during sleep (meanSaO
2
) and percentage of total sleep time with saturation < 90% (T90) were calculated. RVD was diagnosed in the presence of forced expiratory volume in the first second/forced vital capacity (FVC) > 0.7 and FVC < 80% predicted value. PHTN was defined by tricuspid regurgitation peak velocity ≥ 3.4 m/s, documented by noninvasive transthoracic echocardiography.
Results
Patients with OS had significantly lower meanSaO
2
but higher T90 than subjects with isolated SA and isolated RVD. Patients with OS vs. those with isolated SA had higher odds of PHTN in multivariable analysis with age, sex, and body mass index adjusted for (OR 2.96, 95%CI 1.05–8.91,
p
= 0.040). Patients with meanSaO
2
< 92% vs. meanSaO
2
≥ 92% had significantly higher odds of being diagnosed with PHTN (OR 5.40, 95%CI 2.01–15.7,
p
< 0.001). Similarly, T90 (≥ 4.5% versus < 4.5%) was also independently associated with the prevalence of PHTN (OR 7.21, 95%CI 2.54–23.67,
p
< 0.001).
Conclusion
Patients with OS of RVD and SA had severe hypoxemia, which is associated with the prevalence of PHTN. Further investigation is needed to discern whether therapeutic strategies toward OS might mitigate PHTN in this cohort.
Trial registration
Clinical Trial Registration No. ChiCTR1900027294 on 1 October 2019 |
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ISSN: | 1520-9512 1522-1709 |
DOI: | 10.1007/s11325-020-02164-4 |