II-2-1 Surgical treatment of congenital heart diseases associated with PAD: 72 case of the malformation varing from pulmonary hypertension group to pulmonary atresia

Objectives: The aim of this study is to know the prevalence, type of congenital heart diseases (CHDs), and its association with cleft lip and/or palate and to know the impact of CHDs on surgical treatment planning of cleft lip and palate from a craniofacial hospital specializing in orofacial clefts, head and neck cancer, and trauma management. Design: A total of 1381 patients with nonsyndromic cleft lip and palate were included in the study. This is a hospital-based retro–prospective case record analysis. The data were collected from clinical records of the patients which included clinical, chest radiographic and 2D echocardiographic findings. Total incidence of CHDs and its impact on treatment planning was evaluated using κ statistics and χ2 test. Results: There were 32 (2.32%) cleft lip and palate patients with CHDs. In 2 patients, cleft surgery was delayed by 6 to 9 months to allow the defect to decrease in size. Subacute bacterial endocarditis prophylaxis was administered in 7 patients before cleft surgery. Cardiac surgery was advised prior to cleft surgery in 3 patients. Sixteen patients with CHDs were not taken for cleft surgery considering the potential risk to the patient’s life as they had multiple cardiac anomalies. There were no intraoperative and postoperative complications in these patients. Conclusion: The results emphasize the association between clefting and CHD. The collected data suggest that there should be careful examination of children with cleft lip and palate for signs of heart disease. This could significantly reduce the morbidity/mortality of cleft lip and palate surgery making it more predictable and safer.

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330: Long-term outcome of combined heart-lung transplantation: Primary pulmonary hypertension vs. secondary pulmonary hypertension due to congenital heart diseases

The Journal of Heart and Lung Transplantation ◽

10.1016/j.healun.2006.11.350 ◽

2007 ◽

Vol 26 (2) ◽

pp. S179

Author(s):

Y. Toyoda ◽

R. Santos ◽

J. Thacker ◽

J. Bhama ◽

D. Nguyen ◽

...

Keyword(s):

Pulmonary Hypertension ◽

Lung Transplantation ◽

Congenital Heart ◽

Primary Pulmonary Hypertension ◽

Heart Diseases ◽

Congenital Heart Diseases ◽

Term Outcome ◽

Long Term Outcome ◽

Secondary Pulmonary Hypertension

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Structure of unoperated congenital heart diseases in children of Zabaikalsky Territory

Siberian medical review ◽

10.20333/2500136-2020-6-83-89 ◽

2020 ◽

pp. 83-89

Author(s):

A.V. Ignatieva ◽

◽

O.F. Sibira ◽

I.N. Gaimolenko ◽

◽

...

Keyword(s):

Surgical Treatment ◽

Congenital Heart ◽

Heart Diseases ◽

Exclusion Criterion ◽

First Year ◽

Congenital Heart Diseases ◽

Significance Level ◽

Septal Defects ◽

Stage 1 ◽

First Time

The aim of the research is to study the morbidity by appealability and some characteristics of congenital heart diseases in children of Zabaikalsky Territory. Material and methods. A retrospective clinical and anamnestic analysis of children with congenital heart diseases without surgical treatment, who were hospitalized, was carried out. The analysis included 3 year-observation. CHD diagnosed is an inclusion criterion; while surgical treatment of heart diseases is exclusion criterion. Statistical data processing was carried out using Microsoft Excel 2007, Statistica v.10.0 software package. χ2 test (Pearson) was used to compare two independent groups by qualitative characteristics. The results were considered statistically significant (reliable) at the achieved significance level of p <0.05. Results. In Zabaikalsky Territory, approximately 200 children with congenital heart disease without surgical treatment are hospitalized annually; the average age is 3 years. Fifty-three per cent of children applied for inpatient care for the first time, 44% of them were children at their first year. Gender distribution indicates the highest incidence of the pathology in girls. In CHD structure, atrial septal defects are on the first place, while interventricular septal defects are on the second. Combination of ASD and IVSD was observed with approximately equal frequency. Chronic heart failure associated with CHD was registered in 77% of children. In most cases CHF, stage 1, was diagnosed (63%). In 2/3 of cases, pulmonary hypertension of various severity was detected. Analysis of place of residence of children with CHD in the Zabaikalsky Territory shows that children from areas with the highest population density are hospitalized more often. Conclusion. The problem of congenital heart diseases in children of Zabaikalsky Territory is of current importance due to the widespread prevalence and high specific gravity among all internal organ defects in children of this region.

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Experience of ultrasound diagnostics of vascular rings and its influence on surgical treatment

Ukrainian journal of cardiovascular surgery ◽

10.30702/ujcvs/18.32/13(055-057) ◽

2018 ◽

pp. 55-57

Author(s):

А. О. Павлова ◽

А. К. Куркевич ◽

Н. М. Руденко ◽

Т. А. Ялинська ◽

Р. М. Ємець ◽

...

Keyword(s):

Congenital Heart Disease ◽

Surgical Treatment ◽

Congenital Heart ◽

Heart Diseases ◽

High Accuracy ◽

Congenital Heart Diseases ◽

Surgical Risk ◽

Vascular Rings ◽

Asymptomatic Patients ◽

Ultrasound Diagnostics

Contemporary methods diagnose congenital heart diseases (CHD) with high accuracy but postnatal diagnostics of vascular rings (VR) remains difficult. From 2004 to 2017 in our Center were performed 7740 primary fetal echocardiograms and more than 65,000 echocardiograms for children. From 2004 to 2017 18589 operations of congenital heart disease were performed, of them 95 (0,51%) were VR surgery. Of all patients treated with VR 21 (22,1%) had prenatal diagnosis, 74 (77,9%) – had postnatal. Since 2011 during postnatal and prenatal echocardiography, we introduced a new protocol with necessary views for VR visualization. Thanks to the use it increased the number of operations on the VR. Surgical treatment of VR has excellent results with low surgical risk. For the successful VR surgical treatment is necessary CT to perform for required to clarify the anatomy of the VR and the trachea. Prenatal and postnatal Echo can help of VR detection in a group of asymptomatic patients.

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