TY - JOUR
T1 - Number of thoracotomies predicts impairment in lung function and exercise capacity in patients with congenital heart disease
AU - Müller, Jan
AU - Ewert, Peter
AU - Hager, Alfred
N1 - Publisher Copyright:
© 2017 Japanese College of Cardiology
PY - 2018/1
Y1 - 2018/1
N2 - Objective Many patients with congenital heart disease (CHD) require surgery to ensure survival into adulthood. But history of previous thoracotomies is associated with respiratory muscle weakness, impairments in chest wall compliance, and moderately to severely impaired lung function. This study evaluated the impact of thoracotomies on functional outcome in patients with CHD. Patients and methods In total 1372 adolescents and adults with CHD (32.4 ± 11.5 years, 624 female), who underwent spirometry and cardiopulmonary exercise testing in our institution from January 2010 to August 2015, were analyzed. Results After adjusting for confounding variables, with every thoracotomy the prevalence for a restrictive ventilatory pattern increased by 1.8-fold (CI: 1.606–2.050; p < 0.001). The number of thoracotomies had no direct influence on an impaired exercise capacity in a multivariate model, but with every percentage point increase in forced vital capacity probability of impaired exercise capacity diminished (OR: 0.944, CI: 0.933–0.955, p < 0.001). There was a moderate correlation of forced vital capacity and peak oxygen uptake (r = 0.464, p < 0.001). After a follow-up of 2.1 ± 1.6 years 21 patients had died. Survival was only related to age (p < 0.001) and peak oxygen uptake (p < 0.001) after considering together with thoracotomies, oxygen saturation at rest and forced vital capacity in a multivariate model. Conclusions Independent of CHD complexity and other risk factors, multiple thoracotomies lead to restrictive lung pattern. It could be suggested that those limitations in forced vital capacity contribute to impairments in exercise capacity, which turned out to be the strongest predictor for survival.
AB - Objective Many patients with congenital heart disease (CHD) require surgery to ensure survival into adulthood. But history of previous thoracotomies is associated with respiratory muscle weakness, impairments in chest wall compliance, and moderately to severely impaired lung function. This study evaluated the impact of thoracotomies on functional outcome in patients with CHD. Patients and methods In total 1372 adolescents and adults with CHD (32.4 ± 11.5 years, 624 female), who underwent spirometry and cardiopulmonary exercise testing in our institution from January 2010 to August 2015, were analyzed. Results After adjusting for confounding variables, with every thoracotomy the prevalence for a restrictive ventilatory pattern increased by 1.8-fold (CI: 1.606–2.050; p < 0.001). The number of thoracotomies had no direct influence on an impaired exercise capacity in a multivariate model, but with every percentage point increase in forced vital capacity probability of impaired exercise capacity diminished (OR: 0.944, CI: 0.933–0.955, p < 0.001). There was a moderate correlation of forced vital capacity and peak oxygen uptake (r = 0.464, p < 0.001). After a follow-up of 2.1 ± 1.6 years 21 patients had died. Survival was only related to age (p < 0.001) and peak oxygen uptake (p < 0.001) after considering together with thoracotomies, oxygen saturation at rest and forced vital capacity in a multivariate model. Conclusions Independent of CHD complexity and other risk factors, multiple thoracotomies lead to restrictive lung pattern. It could be suggested that those limitations in forced vital capacity contribute to impairments in exercise capacity, which turned out to be the strongest predictor for survival.
KW - Exercise capacity
KW - Forced vital capacity
KW - Restrictive lung pattern
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=85021698299&partnerID=8YFLogxK
U2 - 10.1016/j.jjcc.2017.05.005
DO - 10.1016/j.jjcc.2017.05.005
M3 - Article
C2 - 28687271
AN - SCOPUS:85021698299
SN - 0914-5087
VL - 71
SP - 88
EP - 92
JO - Journal of Cardiology
JF - Journal of Cardiology
IS - 1
ER -