SARS-CoV-2 infection in children can trigger cardiovascular manifestations potentially requiring an intensive treatment and defining a new entity named Multisystem Inflammatory Syndrome in Children (MIS-C), whose features partially overlap with Kawasaki Disease (KD). A cross-sectional study including all diagnoses of MIS-C and KD from April 2020 to May 2021 in our metropolitan area was conducted evaluating clinical, laboratory (including immunological response, cytokines, and markers of myocardial damage), and cardiac (coronary and non-coronary) features at onset of the diseases. Evolution of ventricular dysfunction, valve regurgitations, and coronary lesions was documented. The severity of the disease was also considered based on the need for inotropic support and ICU admission. Twenty-four MIS-C were diagnosed (14 boys, median age 82 months): 13/24 cases (54.17%) presented left ventricular dysfunction, 12/24 (50%) required inotropic support, and 10/24 (41.67%) developed coronary anomalies (CALs). All patients received steroids and IVIG at a median time of 5 days (IQR1:4, IQR3:6.5) from onset of fever and heart function normalized 6 days (IQR1: 5, IQR3: 7) after therapy, while CALs persisted in one. One patient (12.5%) required infliximab because of refractory disease and still presented CALs 18 days after therapy. During the same study period, 15 KD were diagnosed: none had ventricular dysfunction, while 7/15 (46.67%) developed CALs. Three out of 15 patients (20%) still presented CALs 46 days from onset. Compared to KD, MIS-C pts have significantly higher IL8 and similar lymphocytes subpopulations. Despite a more severe presentation and initial cardiac findings compared to KD, the myocardial injury in MIS-C has a rapid response to immunomodulatory treatment (median time 6 days), in terms of ventricular function, valve regurgitations, and troponin. Incidence of CALs is similar at onset, but it tends to regress in most of the cases of MIS-C differently than in KD where CALs persist in up to 40% in the subacute stage after treatment.
Children with congenital heart disease (CHD) are at increased risk for undernutrition. The aim of our study was to describe the growth parameters of Italian children with CHD compared to healthy children. We performed a cross-sectional study collecting the anthropometric data of pediatric patients with CHD and healthy controls. WHO and Italian z-scores for weight for age (WZ), length/height for age (HZ), weight for height (WHZ) and body mass index (BMIZ) were collected. A total of 657 patients (566 with CHD and 91 healthy controls) were enrolled: 255 had mild CHD, 223 had moderate CHD and 88 had severe CHD. Compared to CHD patients, healthy children were younger (age: 7.5 ± 5.4 vs. 5.6 ± 4.3 years, p = 0.0009), taller/longer (HZ: 0.14 ± 1.41 vs. 0.62 ± 1.20, p < 0.002) and heavier (WZ: −0,07 ± 1.32 vs. 0.31 ± 1.13, p = 0.009) with no significant differences in BMIZ (−0,14 ± 1.24 vs. –0.07 ± 1.13, p = 0.64) and WHZ (0.05 ± 1.47 vs. 0.43 ± 1.07, p = 0.1187). Moderate and severe CHD patients presented lower z-scores at any age, with a more remarkable difference in children younger than 2 years (WZ) and older than 5 years (HZ, WZ and BMIZ). Stunting and underweight were significantly more present in children affected by CHD (p < 0.01). In conclusion, CHD negatively affects the growth of children based on the severity of the disease, even in a high-income country, resulting in a significant percentage of undernutrition in this population.
18 April 2023 in The Journal of Maternal-Fetal & Neonatal Medicine
The evaluation of upcoming Aortic Coarctation (CoA) in new-borns with prenatal suspicion entails a close echocardiographic monitor until Arterial Duct (AD) closure, in a department with pediatric c...
11 February 2026 in International Journal of Cardiology Congenital Heart Disease
A significant number of hospitals within the Italian National Health System are involved in the field of foetal cardiology. To date, there has been no investigation into the activity of these centres. The foetal working group of the Italian Society of Paediatric Cardiology (SICP) prepared a survey to outline a current overview of the foetal cardiology activity in Italy. A 23-item web-based questionnaire, developed ad hoc, was administered to all members of the SICP by e-mail. The survey was conducted online from 1 March to July 31, 2024. Forty-five specialists in paediatric cardiology out of 548 SICP members (8.2%) completed the survey: 18/45(40%) from Northern, 10/45(22.2%) from Central and 17/45(37.7%) from Southern Italy. The respondents' answers indicate that counselling is conducted in all cases by foetal cardiologists. There is a frequent availability of geneticists (37/43 - 86%), paediatric specialists (32/42 - 76.1%), psychologists (33/43 - 76.7%), less frequent (25/42- 60%) is the opportunity to involve the cardiac surgeon during counselling. Eight of 44(18.1%) participants reported that foetal intervention procedures are performed at their centre, and 8/42(19%) can propose foetal magnetic resonance imaging. Despite the low response rate, the survey highlights that activity in foetal cardiology is unevenly distributed across the country. The need for national shared guidelines on the conduct of the foetal cardiology session and guidance on the necessary training for operators has been identified. Furthermore, the establishment of a defined network between hub-and-spoke facilities and care services on a national scale is a priority.
This case describes a peculiar aetiology of severe aortic regurgitation and LVOT obstruction in a young adult with bilateral congenital cataract and uncontrolled hypertension, who presented with heart failure and was found to suffer from aortic valve degeneration with fibromuscular metaplasia and cusp delamination.