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Indian Pediatr 2018;55: 1096 |
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Clippings
Theme: Pediatric Cardiology
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Balaganesh Karmegaraj and R Krishna Kumar*
Email:
[email protected]
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Coronary artery complication in Kawasaki disease and
the importance of early intervention (JAMA Pediatr. 2016 Dec
1;170(12):1156-1163. doi: 10.1001/jamapediatrics. 2016.2055).
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The authors of this systematic review retrieved clinical studies that
compared corticosteroids plus intravenous immunoglobulin (IVIG) therapy
with IVIG therapy alone in treating patients with Kawasaki disease in
the databases until July 2015. Studies either using corticosteroids as
initial therapy or as rescue therapy were included. Sixteen comparative
studies characterizing 2746 patients were analyzed. The rate of coronary
artery abnormalities was significantly lower in adjunctive
corticosteroids therapy than in IVIG therapy (OR 0.42; 95% CI, 0.27,
0.67). The overall efficacy was negatively correlated with the duration
of illness before corticosteroid therapy (P<0.001). Subgroup
analysis, including studies using corticosteroids plus IVIG as initial
therapy, showed a more advantageous effect than IVIG alone regarding
coronary artery abnormality prevention (OR 0.32; 95% CI 0.18, 0.56),
whereas this benefit was not found in a subgroup of studies using
corticosteroids as rescue therapy. Further analysis showed that patients
predicted at baseline to be at high risk of IVIG resistance seemed to
obtain the greatest benefit from adjunctive corticosteroid therapy
regarding coronary artery abnormality prevention (OR 0.24; 95% CI 0.12,
0.47). The fever duration was significantly reduced in the
corticosteroids group. The favorable effects of corticosteroids were
conferred without an increased risk of adverse events. The authors
concluded that high-risk patients with Kawasaki disease benefit greatly
from a timely and potent adjunctive corticosteroid therapy strategy.
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Management of undernutrition and failure to
thrive in children with congenital heart disease in low- and
middle-income countries (Cardiol Young. 2017 Dec;
27(S6):S22-S30. doi: 10.1017/S104795111700258X).
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This review summarizes the existing evidence on prevalence of
undernutrition and congenital heart disease (CHD) and its impact on
surgical outcomes with a focus on implications for low- and
middle-income countries. There are multifactorial causes for failure to
thrive, including innate growth potential, severity of cardiac disease,
increased energy requirements, decreased nutritional intake,
malabsorption, and poor utilization of absorbed nutrition. The authors
stressed the importance that failure of growth is not a contraindication
to surgical repair, and patients should receive surgical repair where
indicated as soon as possible. There is very little evidence to support
the notion that lower weights are associated with poorer surgical
outcomes. The article provides an approach to nutrition in the child
with failure to grow or to gain weight and suggests an algorithm for
nutritional management in the early postoperative period in low-resource
environments. The review conclude that nutritional support requires
specific attention and allocation of resources, including appropriately
skilled personnel. Thereafter, it is essential to monitor growth and
development and to identify causes for failure to catch-up or grow
appropriately.
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Educational achievement of children with
congenital heart disease (Early Human Dev. 2018;128:27-34).
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In view of improving survival rates of children with congenital heart
disease (CHD), there is increasing interest in their quality of life.
This cross-sectional study, using an online survey of patients
registered in database of the German National Register for Congenital
Heart Defects, assessed the educational achievement of patients with
CHD. The large majority (83.4%) of study participants (n=2609) were
enrolled at a conventional elementary school and started school at the
age of 6 years or below (73.3%). In total 45.7% of graduated study
participants graduated with the qualification necessary to study at any
university. In terms of analysis as per severity of CHD, 57.3%, 47.5%
and 35.1% of patients with mild-, moderate-, and severe CHD,
respectively, attained a high school diploma. Authors concluded that the
majority of participating CHD patients had a standard school career,
suggesting that a normal school career is possible for all CHD patients.
These results have important implications for Indian children with CHD
where parents are often asked to get certificate of fitness from doctors
for possibility of ‘normal’ schooling.
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Survival and associated risk factors for
mortality among infants with critical congenital heart disease
in a developing country (Pediatr Cardiol. 2018;39:1389-96).
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This retrospective cohort study from Malaysia examined Critical
congenital heart disease (CCHD) survival and the risk factors for CCHD
mortality. A total of 491 CCHD cases were included in the study, with an
overall mortality rate of 34.8% (95% CI 30.6, 39.2). The
intervention/surgical mortality rate was 9.8% within 30 days and 11.5%
in >30 days after surgery, and 17% died before surgery or intervention.
The median (IQR) age at death was 2.7 (1, 7.3) months. The CCHD survival
rate was 90.4% (95% CI 89%, 91.8%) at 1 month, 69.3% (95% CI 67.2%,
71.4%) at 1 year, 63.4% (95% CI 61.1%, 65.7%) at 5 years, and 61.4% (95%
CI 58.9%, 63.9%) at 10 years. Weight <2 kg at diagnosis, associated
syndromes, poor pre-operative condition, and non-duct-dependent CCHD
were independent risk factors for poor survival. The authors concluded
that the mortality and survival of infants with CHD vary with the
severity of the lesion, with CCHD having high mortality and low short-
and medium-term survival rates.
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