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. 2020 Jun 17;17(12):4328.
doi: 10.3390/ijerph17124328.

Cardiopulmonary Rehabilitation Improves Respiratory Muscle Function and Functional Capacity in Children with Congenital Heart Disease. A Prospective Cohort Study

Affiliations

Cardiopulmonary Rehabilitation Improves Respiratory Muscle Function and Functional Capacity in Children with Congenital Heart Disease. A Prospective Cohort Study

Francisco José Ferrer-Sargues et al. Int J Environ Res Public Health. .

Abstract

Critical surgical and medical advances have shifted the focus of congenital heart disease (CHD) patients from survival to achievement of a greater health-related quality of life (HRQoL). HRQoL is influenced, amongst other factors, by aerobic capacity and respiratory muscle strength, both of which are reduced in CHD patients. This study evaluates the influence of a cardiopulmonary rehabilitation program (CPRP) on respiratory muscle strength and functional capacity. Fifteen CHD patients, ages 12 to 16, with reduced aerobic capacity in cardiopulmonary exercise testing (CPET) were enrolled in a CPRP involving strength and aerobic training for three months. Measurements for comparison were obtained at the start, end, and six months after the CPRP. A significant improvement of inspiratory muscle strength was evidenced (maximum inspiratory pressure 21 cm H2O, 23%, p < 0.01). The six-minute walking test showed a statistically and clinically significant rise in walked distance (48 m, p < 0.01) and a reduction in muscle fatigue (1.7 out of 10 points, p = 0.017). These results suggest CPRP could potentially improve respiratory muscle function and functional capacity, with lasting results, in children with congenital heart disease, but additional clinical trials must be conducted to confirm this finding.

Keywords: cardiac rehabilitation; cardiopulmonary rehabilitation; children; congenital heart disease; inspiratory pressure; pediatric; physical exercise training; respiratory strength; six-minute walking test.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Maximum Static Inspiratory Pressure (MIP) measured before training (T1), after the first (w4) and second (w8) month of training, at the end of the program (T2), and in a six months follow-up after finishing the program (T3).
Figure 2
Figure 2
Representation of six-minute walking test distance travelled, muscle fatigue score, and dyspnea score, measured before (T1), immediately after (T2), and six months after the program (T3).

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