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DOI 10.1016/j.echo.2022.07.012

Медицинская библиотека · Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography · 2022

Serial Assessment of Cardiac Function and Pulmonary Hemodynamics in Infants With Down Syndrome.

Smith Aisling, Bussmann Neidin, Breatnach Colm, Levy Philip, Molloy Eleanor, Miletin Jan, Curley Anna, McCallion Naomi, Franklin Orla, El-Khuffash Afif

Наблюдательное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

There is a dearth of longitudinal data describing the evolution of cardiopulmonary hemodynamics in infants with Down syndrome (DS) beyond infancy. We hypothesized that babies with DS, independent of the presence of congenital heart disease (CHD), demonstrate biventricular systolic and diastolic impairment and sustained elevation of pulmonary pressures compared with controls over the first 2 years of age.

METHODS

This was a prospective observational cohort study of 70 infants with DS (48 with CHD and 22 without CHD) and 60 controls carried out in 3 tertiary neonatal intensive care units in Dublin, Ireland. Infants with DS with and without CHD and non-DS controls underwent serial echocardiograms at birth, 6 months, 1 year, and 2 years of age to assess biventricular systolic and diastolic function using deformation analysis. Pulmonary vascular resistance was assessed using pulmonary artery acceleration time and left ventricular (LV) eccentricity index.

RESULTS

Infants with DS exhibited smaller LV (birth: 27 ± 4 vs 31 ± 2 mm, P < .01; 2 years: 43 ± 5 vs 48 ± 4 mm, P < .01) and right ventricular (birth: 28 ± 3 vs 31 ± 2 mm, P < .01; 2 years: 40 ± 4 vs 44 ± 3 mm, P < .01) lengths and lower LV (birth: -19% ± 3% vs -22% ± 2%, P < .01; 2 years: -24% ± 2% vs -26% ± 2%, P < .01) and right ventricular (birth: -19% ± 4% vs -22% ± 3%, P < .01; 2 years: -29% ± 6% vs -33% ± 4%, P < .01) systolic strain over the 2-year period. Pulmonary artery acceleration time was lower in the DS group throughout the study period (birth: 44 ± 10 vs 62 ± 14 ms, P < .01; 2 years 71 ± 12 vs 83 ± 11 ms, P < .01). No differences were observed between DS infants with and without CHD (all P > .05).

CONCLUSIONS

Infants with DS exhibit impaired maturational changes in myocardial function and pulmonary vascular resistance. Such novel findings provide valuable insights into the pathophysiology affecting cardiorespiratory morbidity in this population.

Для цитирования: Smith Aisling, Bussmann Neidin, Breatnach Colm, Levy Philip, Molloy Eleanor, Miletin Jan, Curley Anna, McCallion Naomi, Franklin Orla, El-Khuffash Afif. Serial Assessment of Cardiac Function and Pulmonary Hemodynamics in Infants With Down Syndrome.. Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography. 2022. DOI: 10.1016/j.echo.2022.07.012.

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