Cardiovascular and Neonatal Outcomes in Pregnant Women With High-Risk Congenital Heart Disease

2016 ◽  
Vol 117 (10) ◽  
pp. 1672-1677 ◽  
Author(s):  
Priya Pillutla ◽  
Tina Nguyen ◽  
Daniela Markovic ◽  
Mary Canobbio ◽  
Brian J. Koos ◽  
...  
2019 ◽  
Vol 14 (3) ◽  
pp. 470-478 ◽  
Author(s):  
Yuli Y. Kim ◽  
Leah A. Goldberg ◽  
Katherine Awh ◽  
Tanmay Bhamare ◽  
David Drajpuch ◽  
...  

2017 ◽  
Vol 69 (11) ◽  
pp. 606
Author(s):  
Aarthi Sabanayagam ◽  
Anushree Agarwal ◽  
Christy MacCain ◽  
Elizabeth Lawton ◽  
Elliot Main ◽  
...  

2007 ◽  
Vol 6 (1_suppl) ◽  
pp. 27-28
Author(s):  
Philip Moons ◽  
Els Costermans ◽  
Els Huyghe ◽  
Wim Drenthen ◽  
Petronella Pieper ◽  
...  

2021 ◽  
Vol 104 (6) ◽  
pp. 895-901

Background: Pulmonary arterial hypertension (PAH) is a common complication of congenital heart disease (CHD) with uncorrected left-to-right shunts. Currently, no consensus guideline exists on the management of PAH-CHD in children, especially those who do not meet operability criteria. Objective: To compare survival between three groups of high-risk PAH-CHD, group 1: total correction including both surgical and percutaneous intervention, group 2: palliative treatment, and group 3: conservative with medical treatment group. Materials and Methods: All pediatric patients with PAH-CHD that underwent cardiac catheterization between January 1, 2008 and December 31, 2017 were retrospectively reviewed. Inclusion criteria were high risk PAH-CHD patients who had pulmonary vascular resistance (PVR) greater than 6 Wood unit·m² and PVR-to-SVR ratio greater than 0.3 evaluated in room air. Exclusion criteria were younger than three months of age, severe left side heart disease with pulmonary capillary wedge pressure greater than 15 mmHg, obstructive total pulmonary venous return, and single ventricle physiology. The Kaplan-Meier analysis was performed from the date of PAH diagnosis to the date of all-cause mortality or to censored date at last follow-up. Results: Seventy-six patients with a median age at diagnosis of 27.5 months (IQR 14.5 to 69.0 months) were included in this study. The patients were divided into three subgroups and included 38 patients (50.0%) in group 1, six patients (7.9%) in group 2, and 32 patients (42.1%) in group 3. The median follow-up time was 554 days (IQR 103 to 2,133 days). The overall mortality was 21.7%. One-year survival in patients with simple lesion in group 1 and 3 were 79.5% and 87.5% and patients with complex lesions in group 1, 2, and 3 were 93.8%, 83.3%, and 73.1%, respectively. The results showed that most mortalities occurred in the first year. There were no statistically significant differences in survival among difference types of treatment (log rank test, p=0.522). Conclusion: The mortality of high-risk PAH-CHD patients were not different among those who underwent corrective surgery, palliative, or conservative treatment. The mortality was high in the first year after PAH diagnosis and remain stable afterward. Management decision for an individual with high-risk PAH-CHD patients requires comprehensive clinical assessment to balance the risks and benefits before making individualized clinical judgment. Keywords: Pulmonary hypertension; Congenital heart disease; High-risk patients


2015 ◽  
Vol 79 (7) ◽  
pp. 1609-1617 ◽  
Author(s):  
Chun-Wei Lu ◽  
Jin-Chung Shih ◽  
Ssu-Yuan Chen ◽  
Hsin-Hui Chiu ◽  
Jou-Kou Wang ◽  
...  

2018 ◽  
Vol 261 ◽  
pp. 58-61
Author(s):  
Jun Muneuchi ◽  
Keiko Yamasaki ◽  
Mamie Watanabe ◽  
Azusa Fukumitsu ◽  
Takeshi Kawakami ◽  
...  

Introduction 208General principles 208Contraception 210Preconception 214Pregnancy and delivery 218Post-partum 220Heart disease is the largest single cause of maternal death in the UK4. The number and complexity of survivors of congenital heart disease well enough to consider pregnancy is growing. The maternal risk amongst this population varies from being no different to that of the general population, to carrying a high risk of long-term morbidity and >40% risk of death....


2019 ◽  
Vol 29 (5) ◽  
pp. 594-601 ◽  
Author(s):  
Jamie M. Furlong-Dillard ◽  
Benjamin J. Miller ◽  
Kathy A. Sward ◽  
Alaina I. Neary ◽  
Trudy L. Hardin-Reynolds ◽  
...  

AbstractBackground:Children with congenital heart disease are at high risk for malnutrition. Standardisation of feeding protocols has shown promise in decreasing some of this risk. With little standardisation between institutions’ feeding protocols and no understanding of protocol adherence, it is important to analyse the efficacy of individual aspects of the protocols.Methods:Adherence to and deviation from a feeding protocol in high-risk congenital heart disease patients between December 2015 and March 2017 were analysed. Associations between adherence to and deviation from the protocol and clinical outcomes were also assessed. The primary outcome was change in weight-for-age z score between time intervals.Results:Increased adherence to and decreased deviation from individual instructions of a feeding protocol improves patients change in weight-for-age z score between birth and hospital discharge (p = 0.031). Secondary outcomes such as markers of clinical severity and nutritional delivery were not statistically different between groups with high or low adherence or deviation rates.Conclusions:High-risk feeding protocol adherence and fewer deviations are associated with weight gain independent of their influence on nutritional delivery and caloric intake. Future studies assessing the efficacy of feeding protocols should include the measures of adherence and deviations that are not merely limited to caloric delivery and illness severity.


2020 ◽  
Vol 9 (14) ◽  
Author(s):  
Ran Chu ◽  
Wei Chen ◽  
Guangmin Song ◽  
Shu Yao ◽  
Lin Xie ◽  
...  

Background Women with congenital heart disease are considered at high risk for adverse events. Therefore, we aim to establish 2 prediction models for mothers and their offspring, which can predict the risk of adverse events occurred in pregnant women with congenital heart disease. Methods and Results A total of 318 pregnant women with congenital heart disease were included; 213 women were divided into the development cohort, and 105 women were divided into the validation cohort. Least absolute shrinkage and selection operator was used for predictor selection. After validation, multivariate logistic regression analysis was used to develop the model. Machine learning algorithms (support vector machine, random forest, AdaBoost, decision tree, k‐nearest neighbor, naïve Bayes, and multilayer perceptron) were used to further verify the predictive ability of the model. Forty‐one (12.9%) women experienced adverse maternal events, and 93 (29.2%) neonates experienced adverse neonatal events. Seven high‐risk factors were discovered in the maternal model, including New York Heart Association class, Eisenmenger syndrome, pulmonary hypertension, left ventricular ejection fraction, sinus tachycardia, arterial blood oxygen saturation, and pregnancy duration. The machine learning–based algorithms showed that the maternal model had an accuracy of 0.76 to 0.86 (area under the receiver operating characteristic curve=0.74–0.87) in the development cohort, and 0.72 to 0.86 (area under the receiver operating characteristic curve=0.68–0.80) in the validation cohort. Three high‐risk factors were discovered in the neonatal model, including Eisenmenger syndrome, preeclampsia, and arterial blood oxygen saturation. The machine learning–based algorithms showed that the neonatal model had an accuracy of 0.75 to 0.80 (area under the receiver operating characteristic curve=0.71–0.77) in the development cohort, and 0.72 to 0.79 (area under the receiver operating characteristic curve=0.69–0.76) in the validation cohort. Conclusions Two prenatal risk assessment models for both adverse maternal and neonatal events were established, which might assist clinicians in tailoring precise management and therapy in pregnant women with congenital heart disease.


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