keyword
https://read.qxmd.com/read/38599724/pediatric-hyperlipidemia
#21
REVIEW
Ankit Garg, S Radhakrishnan
The leading cause of mortality worldwide is atherosclerotic cardiovascular disease. Atherosclerotic plaques are well known to originate early in the childhood. Identifying hyperlipidemia in early childhood creates an opportunity to prevent major cardiovascular events in adults. Children with identified risk factors are at an increased risk of developing cardiovascular incidents in later life. This article emphasizes the diagnosis and management of pediatric hyperlipidemia with reference to the recent guidelines...
March 2024: Indian Heart Journal
https://read.qxmd.com/read/38593571/subjective-experience-of-parent-child-relationship-in-adolescents-with-congenital-heart-disease-a-qualitative-study
#22
JOURNAL ARTICLE
Yu-Hsuan Hsiao, Hung-Tao Chung, Jou-Kou Wang, Pei-Fan Mu, Shu-Wen Chen, Ying-Mei Shu, Chi-Wen Chen
PURPOSE: To explore the parent-child relationship through the subjective experience of adolescents with congenital heart disease (CHD). DESIGN AND METHODS: A descriptive phenomenology approach was adopted. Twelve adolescents aged from 12 to 18 years with CHD were recruited from the pediatric cardiology clinics at two medical centers in Taiwan. Data were collected through in-depth interviews. Data were analyzed using Colaizzi's phenomenological analysis method, and results were reported in accordance with the Consolidated Criteria for Reporting Qualitative Research guidelines...
April 8, 2024: Journal of Pediatric Nursing
https://read.qxmd.com/read/38592473/effect-of-maternal-race-residential-rurality-and-social-vulnerability-on-critical-congenital-heart-defect-risk
#23
JOURNAL ARTICLE
Katie C Hall, Jennifer C Robinson, Masoumeh Karimi, Jung Hye Sung
The development of a congenital heart defect (CHD) is multifactorial, with many cases having an unknown etiology. This study explored whether maternal race and lived environment were associated with an infant being born with a critical CHD. A cross-sectional, case-control design was conducted utilizing secondary data analysis. The CHD group (N = 199) consisted of infants diagnosed with a critical CHD within the first year of life identified from hospital databases. The non-CHD group (N = 548) was a random sample of infants selected from the state's vital statistics database...
April 9, 2024: Pediatric Cardiology
https://read.qxmd.com/read/38585551/a-novel-variant-in-akap9-gene-a-controversial-gene-in-long-qt-syndrome
#24
JOURNAL ARTICLE
Murat Erdogan, Suleyman Sunkak, Oguzhan Bahadır, Muhammet Ensar Doğan, Yasin Ada, Burhan Balta
INTRODUCTION: Long QT syndrome (LQTS) is a common congenital cause of fatal cardiac arrhythmia. Characteristic clinical findings are prolonged QT interval and ventricular arrhythmia on electrocardiogram (ECG), syncope, seizure, and sudden death. It is a genetically heterogeneous disease. To date, disease-causing variant have been reported in seventeen genes. The AKAP9 is still considered controversial among those genes. CASE REPORT: We report the case of a 10-year-old female who was born from a non-consanguineous Turkish couple...
March 2024: Molecular Syndromology
https://read.qxmd.com/read/38584340/preoperative-echocardiogram-does-not-contribute-to-surgical-risk-assessment-in-patients-with-large-curve-scoliosis-and-no-cardiac-risk-factors
#25
JOURNAL ARTICLE
Chidebelum O Nnake, Alondra Concepcion-Gonzalez, Matan S Malka, Emma Berube, Anne Ferris, Nicole Bainton, Michael G Vitale, Benjamin D Roye
OBJECTIVE: Severe scoliosis can affect thoracic organs, potentially leading to cardiovascular abnormalities. Thus, echocardiograms have been suggested for use in preoperative screening in patients with significant scoliosis. However, the utility of preoperative heart screenings in patients without known or suspected heart problems is not well understood. This study aims to find the incidence of cardiac findings in patients with severe scoliosis ≥90° without cardiac history...
April 8, 2024: Journal of Pediatric Orthopedics
https://read.qxmd.com/read/38583706/the-impact-of-social-determinants-of-health-on-transition-from-pediatric-to-adult-cardiology-care
#26
REVIEW
Diana L Cabrera Fernandez, Keila N Lopez, Katia Bravo-Jaimes, Andrew S Mackie
Social determinants of health (SDoH) are the economic, social, environmental, and psychosocial factors that influence health. Adolescents and young adults with congenital heart disease (CHD) require lifelong cardiology follow-up and therefore coordinated transition from pediatric to adult healthcare systems. However, gaps in care are common during transition, and driven in part by pervasive disparities in SDoH including race, ethnicity, socioeconomic status, access to insurance, and remote location of residence...
April 5, 2024: Canadian Journal of Cardiology
https://read.qxmd.com/read/38582914/a-comprehensive-pediatric-cardio-oncology-program-a-single-institution-approach-to-cardiovascular-care-for-pediatric-patients-with-cancer-and-childhood-cancer-survivors
#27
REVIEW
Nathanya Baez Hernandez, Ksenya Shliakhtsitsava, Drishti Tolani, Cindy Cochran, Ryan Butts, Judith Bonifacio, Elizabeth Journey, Jenna N Oppenheim, Sarah G Pennant, Kimberly Arnold, Terri McCaskill, Daniel C Bowers
Cardiovascular complications related to cancer therapies are broad and variable in onset. These complications are the leading cause of non-cancer related morbidity and mortality in childhood cancer survivors and can also impact ongoing cancer treatment. Despite this understanding, dedicated cardio-oncology programs are lacking in pediatric cardiology. In an attempt to respond to these concerns, a risk-stratified, comprehensive cardio-oncology program was established to address the cardiovascular needs including prevention, early diagnosis, and management of patients with and at risk for cardiovascular complications of cancer therapy...
April 6, 2024: Cardio-Oncology
https://read.qxmd.com/read/38582776/early-post-operative-ecg-changes-as-a-predictor-of-post-pericardiotomy-syndrome-following-atrial-septal-defect-repair
#28
JOURNAL ARTICLE
Kristen Hyberg, Iqbal El-Assaad, Wei Liu, Iqbal El-Assaad, Orkun Baloglu, Howard Heching, William Hanna
To identify risk factors associated with post-pericardiotomy syndrome (PPS) in patients undergoing surgical repair of atrial septal defects (ASD). A single-center retrospective study. Tertiary academic hospital. Included were patients of all ages who underwent surgical ASD repair, while exclusion criteria included the absence of post-operative electrocardiogram (ECG), lack of follow-up post-discharge and factors hindering ECG interpretation. Demographic and clinical data, including ECG changes indicative of pericardial inflammation, were collected...
April 6, 2024: Pediatric Cardiology
https://read.qxmd.com/read/38580429/haemodynamic-effects-of-intravenous-acetaminophen-in-critically-ill-paediatric-patients-a-retrospective-chart-review
#29
JOURNAL ARTICLE
Lana Mohammad, Waeil Al Naeem, Musaab Ramsi, Shaikha Al Neyadi, Aminu Abdullahi, Azhar Rahma, Tasnim Heider Dawoud
OBJECTIVES: Haemodynamic changes following intravenous acetaminophen are well studied in adults. Limited data are published in critically ill paediatric patients, especially from the Middle East. We aim to investigate haemodynamic effects and incidence of hypotension with intravenous acetaminophen in critically ill children, with a focus on understanding factors influencing these effects. METHODS: We retrospectively reviewed patients who received intravenous acetaminophen between July and December 2022...
April 5, 2024: European Journal of Hospital Pharmacy. Science and Practice
https://read.qxmd.com/read/38579941/prediction-of-adverse-cardiovascular-events-in-children-using-artificial-intelligence-based-electrocardiogram
#30
JOURNAL ARTICLE
Yoshitsugu Nogimori, Kaname Sato, Koichi Takamizawa, Yosuke Ogawa, Yu Tanaka, Kazuhiro Shiraga, Hitomi Masuda, Hikoro Matsui, Motohiro Kato, Masao Daimon, Katsuhito Fujiu, Ryo Inuzuka
BACKGROUND: Convolutional neural networks (CNNs) have emerged as a novel method for evaluating heart failure (HF) in adult electrocardiograms (ECGs). However, such CNNs are not applicable to pediatric HF, where abnormal anatomy of congenital heart defects plays an important role. ECG-based CNNs reflecting neurohormonal activation (NHA) may be a useful marker of pediatric HF. This study aimed to develop and validate an ECG-derived marker of pediatric HF that reflects the risk of future cardiovascular events...
April 3, 2024: International Journal of Cardiology
https://read.qxmd.com/read/38578303/aberrant-subclavian-artery-in-interrupted-aortic-arch-with-severe-aortic-outlet-obstruction-cerebral-blood-flow-as-a-possible-determinant-of-embryonic-cardiovascular-development
#31
JOURNAL ARTICLE
Danilo Tadeo, Barham Kakavand, Abdul Bhat, Takeshi Tsuda
Aberrant subclavian artery (ASCA) is frequently observed in interrupted aortic arch (IAA) with aortic/subaortic obstruction. Developmental significance of ASCA in IAA in utero remains elusive. Newborns with prenatally diagnosed isolated IAA under continuous prostaglandin E1 infusion were studied. Cross-sectional areas of aortic valve opening (AVOCSA ) and patent ductus arteriosus (PDACSA ) were represented by echocardiographic measurement of (diameter)2 indexed by body surface area (m2 ). Types of IAA and presence of ASCA were examined in relation to sizes of AVOCSA and PDACSA ...
April 5, 2024: Pediatric Cardiology
https://read.qxmd.com/read/38577783/relationship-between-syncopal-symptoms-and-head-up-tilt-test-modes
#32
JOURNAL ARTICLE
Shuo Wang, Yali Peng, Yuwen Wang, Fang Li, Yi Xu, Huifen Zheng, Heli Yuan, Chunyan Hu, Donglei Liao, Hong Cai, Juan Zhang, Wen Li, Yiyi Ding, Wenhua Zhang, Xiaohong Xue, Xiaoyan Liu, Liping Zhu, Deyu Liu, Meihua Kang, Liping Liu, Weihong Chu, Xiaoming Li, Xuemei Luo, Runmei Zou, Cheng Wang
OBJECTIVE: Head-up tilt test (HUTT) is an important tool in the diagnosis of pediatric vasovagal syncope. This research will explore the relationship between syncopal symptoms and HUTT modes in pediatric vasovagal syncope. METHODS: A retrospective analysis was performed on the clinical data of 2513 children aged 3-18 years, who were diagnosed with vasovagal syncope, from Jan. 2001 to Dec. 2021 due to unexplained syncope or pre-syncope. The average age was 11.76 ± 2...
April 5, 2024: Cardiology in the Young
https://read.qxmd.com/read/38573091/longitudinal-echocardiographic-follow-up-of-a-pediatric-multisystem-inflammatory-syndrome-cohort
#33
JOURNAL ARTICLE
Jaikumar Govindaswamy Ramamoorthy, Anantharaj Avinash, Pediredla Karunakar, Chinmay Parale, Ramanathan Velayutham, Suresh Kumar Sukumaran, Sridhar Balaguru, Narayanan Parameswaran, Mugunthan M, Rahul Dhodapkar, Debdatta Basu, Raja Selvaraj, Santhosh Satheesh, Niranjan Biswal
OBJECTIVE: Significant involvement of the cardiovascular system is known in multisystem inflammatory syndrome in children (MIS-C). This study aimed to examine the recovery of affected cardiovascular parameters over a medium-term follow-up. METHODS: A cohort of 69 children was studied prospectively. Assessments of left ventricular (LV) function and coronary artery abnormalities (CAA) were conducted at admission, 1.5 months, and 3 months. Coronavirus Disease 2019 (COVID-19) antibody titers were assessed at these three time points...
April 2024: Türk Kardiyoloji Derneği Arşivi: Türk Kardiyoloji Derneğinin Yayın Organıdır
https://read.qxmd.com/read/38571460/familial-hyperaldosteronism-an-endo-ern-clinical-practice-guideline
#34
JOURNAL ARTICLE
Paolo Mulatero, Ute I Scholl, Carlos E Fardella, Evangelia Charmandari, Andrzej Januszewicz, Martin Reincke, Celso E Gomez-Sanchez, Michael Stowasser, Olaf M Dekkers
We describe herein the European Reference Network on Rare Endocrine Conditions (Endo-ERN)- clinical practice guideline on diagnosis and management of familial forms of hyperaldosteronism. The guideline panel consisted of 10 experts in primary aldosteronism, endocrine hypertension, pediatric endocrinology and cardiology as well as a methodologist. A systematic literature search was conducted, and because of the rarity of the condition, most recommendations were based on expert opinion and small patient series...
April 4, 2024: European Journal of Endocrinology
https://read.qxmd.com/read/38570368/deep-learning-for-automated-measurement-of-total-cardiac-volume-for-heart-transplantation-size-matching
#35
JOURNAL ARTICLE
Nicholas A Szugye, Neeraja Mahalingam, Elanchezhian Somasundaram, Chet Villa, Jim Segala, Michael Segala, Farhan Zafar, David L S Morales, Ryan A Moore
Total Cardiac Volume (TCV)-based size matching using Computed Tomography (CT) is a novel technique to compare donor and recipient heart size in pediatric heart transplant that may increase overall utilization of available grafts. TCV requires manual segmentation, which limits its widespread use due to time and specialized software and training needed for segmentation. This study aims to determine the accuracy of a Deep Learning (DL) approach using 3-dimensional Convolutional Neural Networks (3D-CNN) to calculate TCV, with the clinical aim of enabling fast and accurate TCV use at all transplant centers...
April 3, 2024: Pediatric Cardiology
https://read.qxmd.com/read/38570367/alcapa-in-children-with-complex-congenital-heart-disease-a-multicenter-study
#36
JOURNAL ARTICLE
Saul Flores, Christine M Riley, Peter Sassalos, Jennifer Smerling, Katherine Cashen, Christopher W Mastropietro
We sought to report characteristics and outcomes of children with complex anomalous left coronary artery from the pulmonary artery (ALCAPA) and to compare the outcomes to children with isolated ALCAPA. We performed a retrospective data analysis of children with ALCAPA who underwent cardiac surgery between 1/2009 and 3/2018 at 21 centers. Characteristics and outcomes of patients with complex ALCAPA are provided using descriptive statistics. Outcomes were compared between complex ALCAPA and isolated ALCAPA using Fisher's exact test...
April 3, 2024: Pediatric Cardiology
https://read.qxmd.com/read/38570366/revisiting-atrioventricular-septal-defects-exploring-chromosomal-abnormalities-cardiac-and-extracardiac-anomalies-in-a-contemporary-prenatal-cohort
#37
JOURNAL ARTICLE
Işıl Ayhan, Oya Demirci, Ali Şahap Odacılar, İlker Kemal Yücel, Ali Karaman
To estimate if there is an association between partial AVSD with chromosomal abnormalities, cardiac and extracardiac malformations, and to report the outcomes of prenatally diagnosed AVSD in a large, contemporary cohort. This is a retrospective cohort study of 190 prenatally diagnosed fetal AVSD between 2014 and 2023. Type of AVSD (complete vs partial), additional cardiac findings, extracardiac findings, presence of a heterotaxy, results of prenatal karyotype, and pregnancy outcomes were documented and analyzed...
April 3, 2024: Pediatric Cardiology
https://read.qxmd.com/read/38570104/rare-cardiac-inflammatory-pseudotumor-in-a-toddler-complementary-roles-of-cardiac-magnetic-resonance-and-positron-emission-tomography
#38
Melissa Mejia-Bautista, Jennifer Romanowicz, Monica Hollowell, Tal Geva, Chrystalle Katte Carreon, Rebecca S Beroukhim
We present a rare pediatric case of cardiac inflammatory pseudotumor (IPT) with a unique presentation of fever of unknown origin with markedly elevated inflammatory markers. A right atrial mass was discovered incidentally by echocardiography. The cardiac magnetic resonance (CMR) signal characteristics and mass location were not consistent with any of the common benign cardiac tumors of childhood. The presence of high signal intensity on T2 imaging and late gadolinium enhancement, in conjunction with intense metabolic activity at the mass site on positron emission tomography (PET), raised the possibility of an inflammatory or malignant mass...
April 1, 2024: Cardiovascular Pathology: the Official Journal of the Society for Cardiovascular Pathology
https://read.qxmd.com/read/38568384/the-outcome-of-genetic-and-non-genetic-pediatric-cardiomyopathies
#39
JOURNAL ARTICLE
Ali AlAlakhfash, Luciano Agati, Giuseppe Mazzesi, Dalia Elhobi, Abdullah Alqwaiee, Khalid Alhory, Abdulrahman Almesned, Zuhair Alhasnan, Abdullah Alwadai
BACKGROUND: Pediatric cardiomyopathies (CMP) can be familial or idiopathic with increasing detection of genetic mutations. The study is a retrospective single-center review of cardiomyopathy patients from January 2011 to May 2020. Results of the genetic study, as well as the outcome, were reported. Patients were divided according to the type of CMP, age of presentation, and EF at presentation. Univariate and multivariate analysis and ROC and survival curves were done. RESULTS: We reported 229 patients under 14 years of age with a diagnosis of cardiomyopathy, most commonly DCM (160 patients (70%)) followed by HCM (26...
April 3, 2024: Egyptian Heart Journal: EHJ
https://read.qxmd.com/read/38566900/original-article-risk-factors-for-neurological-complications-and-short-term-outcomes-after-pediatric-heart-surgery-a-retrospective-analysis
#40
JOURNAL ARTICLE
Muhammad Shahzad, Yasser A Alheraish, Bushra Algethami, Linah A Algheryafi, Salma Kamel, Rawan Ghunaim, Zohair Y Alhalees
OBJECTIVE: To assess the risk factors associated with neurological complications and poor short-term outcomes following pediatric heart surgery. METHODOLOGY: A cross-sectional study was conducted in a cardiac intensive care unit between June 2019 and June 2022. The data of all children less than 15 years old who underwent open-heart surgery and had CT brain were extracted from hospital records. The primary outcome was the incidence of CNS insult, and secondary outcomes included death after surgery, length of stay in ICU and hospital...
2024: Journal of the Saudi Heart Association
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