Kawasaki disease (KD) can be associated with high morbidity and mortality due to coronary artery aneurysms formation and myocardial dysfunction. Aim of this study was to evaluate the diagnostic performance of non-invasive myocardial work in predicting subtle myocardial abnormalities in Kawasaki disease (KD) children with coronary dilatation (CADL). A total of 100 patients (age 8.7 +/- 5 years) were included: 45 children with KD and CADL (KD/CADL) (Z-score>2.5), 45 age-matched controls (CTRL) and, finally, an additional group of 10 children with KD in absence of coronary dilatation (KD group). Left ventricular (LV) systolic function and global longitudinal strain (GLS) were assessed. Global myocardial work index (MWI) was calculated as the area of the LV pressure-strain loops. From MWI, global Constructive Work (MCW), Wasted Work (MWW) and Work Efficiency (MWE) were estimated. Despite normal LV systolic function by routine echocardiography, KD/CADL patients had lower MWI (1433.2 +/- 375.8 mmHg% vs 1752.2 +/- 265.7 mmHg%, p<0.001), MCW (1885.5 +/- 384.2 mmHg% vs 2175.9 +/- 292.4 mmHg%, p=0.001) and MWE (994.0 +/- 4.8% vs 95.9 +/- 2.0%, p=0.030) compared to CTRL. Furthermore, MWI was significantly reduced in children belonging to the KD group in comparison with controls (KD: 1498.3 +/- 361.7 mmHg%; KD vs CTRL p=0.028) and was comparable between KD/CADL and KD groups (KD/CADL vs KD p=0.896). Moreover, KD/CADL patients with normal GLS (n=38) preserved significant differences in MWI and MCW in comparison with CTRL. MWI, MCW and MWE were significantly reduced in KD children despite normal LVEF and normal GLS. These abnormalities seems independent from CADL. Thus, in KD with normal LVEF and normal GLS, estimation of MWI may be a more sensitive indicator of myocardial dysfunction.

Abnormal myocardial work in children with Kawasaki disease / Sabatino, Jolanda; Borrelli, Nunzia; Fraisse, Alain; Herberg, Jethro; Karagadova, Elena; Avesani, Martina; Bucciarelli, Valentina; Josen, Manjit; Paredes, Josefa; Piccinelli, Enrico; Spada, Maraisa; Krupickova, Sylvia; Indolfi, Ciro; Di Salvo, Giovanni. - In: SCIENTIFIC REPORTS. - ISSN 2045-2322. - 11:1(2021), p. 7974. [10.1038/s41598-021-86933-5]

Abnormal myocardial work in children with Kawasaki disease

Piccinelli, Enrico;
2021

Abstract

Kawasaki disease (KD) can be associated with high morbidity and mortality due to coronary artery aneurysms formation and myocardial dysfunction. Aim of this study was to evaluate the diagnostic performance of non-invasive myocardial work in predicting subtle myocardial abnormalities in Kawasaki disease (KD) children with coronary dilatation (CADL). A total of 100 patients (age 8.7 +/- 5 years) were included: 45 children with KD and CADL (KD/CADL) (Z-score>2.5), 45 age-matched controls (CTRL) and, finally, an additional group of 10 children with KD in absence of coronary dilatation (KD group). Left ventricular (LV) systolic function and global longitudinal strain (GLS) were assessed. Global myocardial work index (MWI) was calculated as the area of the LV pressure-strain loops. From MWI, global Constructive Work (MCW), Wasted Work (MWW) and Work Efficiency (MWE) were estimated. Despite normal LV systolic function by routine echocardiography, KD/CADL patients had lower MWI (1433.2 +/- 375.8 mmHg% vs 1752.2 +/- 265.7 mmHg%, p<0.001), MCW (1885.5 +/- 384.2 mmHg% vs 2175.9 +/- 292.4 mmHg%, p=0.001) and MWE (994.0 +/- 4.8% vs 95.9 +/- 2.0%, p=0.030) compared to CTRL. Furthermore, MWI was significantly reduced in children belonging to the KD group in comparison with controls (KD: 1498.3 +/- 361.7 mmHg%; KD vs CTRL p=0.028) and was comparable between KD/CADL and KD groups (KD/CADL vs KD p=0.896). Moreover, KD/CADL patients with normal GLS (n=38) preserved significant differences in MWI and MCW in comparison with CTRL. MWI, MCW and MWE were significantly reduced in KD children despite normal LVEF and normal GLS. These abnormalities seems independent from CADL. Thus, in KD with normal LVEF and normal GLS, estimation of MWI may be a more sensitive indicator of myocardial dysfunction.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11583/2970575