Talk:Cardiovascular System - Abnormalities - Revision history

Z8600021 at 06:08, 3 July 2019

2019-07-03T06:08:10Z

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	==2019==		==2019==

			===First trimester combined screening biochemistry in detection of congenital heart defects===

			J Matern Fetal Neonatal Med. 2019 Oct;32(19):3272-3277. doi: 10.1080/14767058.2018.1462324. Epub 2018 Apr 22.

			Alanen J1, Korpimaki T2, Kouru H2, Sairanen M2, Leskinen M3, Gissler M4, Ryynanen M1, Nevalainen J1.

			Objective: To evaluate the performance of first trimester biochemical markers, pregnancy-associated plasma protein-A (PAPP-A), free beta human chorionic gonadotropin (fβ-hCG), and nuchal translucency (NT) in detection of severe congenital heart defects (CHDs). Methods: During the study period from 1 January 2008 to 31 December 2011, biochemical markers and NT were measured in 31,144 women as part of voluntary first trimester screening program for Down's syndrome in Northern Finland. Data for 71 severe CHD cases and 762 controls were obtained from the hospital records and from the National Medical Birth Register, which records the birth of all liveborn and stillborn infants, and from the National Register of Congenital Malformations that receives information about all the CHD cases diagnosed in Finland. Results: Both PAPP-A and fβ-hCG multiple of median (MoM) values were decreased in all severe CHDs: 0.71 and 0.69 in ventricular septal defects (VSDs), 0.58 and 0.88 in tetralogy of Fallot cases (TOFs), 0.82 and 0.89 in hypoplastic left heart syndromes (HLHSs), and 0.88 and 0.96 in multiple defects, respectively. NT was increased in all study groups except of VSD group. ROC AUC was 0.72 for VSD when combining prior risk with PAPP-A and fβ-hCG. Adding NT did not improve the detection rate. With normal NT but decreased (<0.5 MoM) PAPP-A and fβ-hCG odds ratios for VSD and HLHS were 19.5 and 25.6, respectively. Conclusions: Maternal serum biochemistry improves the detection of CHDs compared to NT measurement only. In cases with normal NT measurement but low concentrations of both PAPP-A and fβ-hCG, an alert for possible CHD, especially VSD, could be given with thorough examination of fetal heart in later ultrasound scans.
			KEYWORDS:
			Congenital heart defect; first trimester screening; nuchal translucency
			PMID: 29683008 DOI: 10.1080/14767058.2018.1462324

			===Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children===

	Mol Genet Genomic Med. 2019 Mar 4:e612. doi: 10.1002/mgg3.612. [Epub ahead of print]		Mol Genet Genomic Med. 2019 Mar 4:e612. doi: 10.1002/mgg3.612. [Epub ahead of print]
	~~Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children.~~
	Behiry EG1, Al-Azzouny MA1, Sabry D2, Behairy OG3, Salem NE4.		Behiry EG1, Al-Azzouny MA1, Sabry D2, Behairy OG3, Salem NE4.
	~~Author information~~
	~~Abstract~~
	BACKGROUND:		BACKGROUND:
	Several genes encoding transcription factors are known to be the primary cause of congenital heart disease. NKX2-5 and GATA4 were the first congenital heart disease-causing genes identified by linkage analysis. This study designed to study the association of five single-nucleotide variants of NKX2-5, GATA4, and TBX5 genes with sporadic nonsyndromic cases of a congenital cardiac septal defect in Egyptian children.		Several genes encoding transcription factors are known to be the primary cause of congenital heart disease. NKX2-5 and GATA4 were the first congenital heart disease-causing genes identified by linkage analysis. This study designed to study the association of five single-nucleotide variants of NKX2-5, GATA4, and TBX5 genes with sporadic nonsyndromic cases of a congenital cardiac septal defect in Egyptian children.

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 ==2019==
+Mol Genet Genomic Med. 2019 Mar 4:e612. doi: 10.1002/mgg3.612. [Epub ahead of print]
 ==2018==

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 {{Talk Page}}
 ==2018==
 ===Utility of fetal cardiac magnetic resonance imaging to assess fetuses with right aortic arch and right ductus arteriosus===

Z8600021 at 00:06, 12 March 2018

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			==2018==

			===Utility of fetal cardiac magnetic resonance imaging to assess fetuses with right aortic arch and right ductus arteriosus===

			J Matern Fetal Neonatal Med. 2018 Jun;31(12):1627-1631. doi: 10.1080/14767058.2017.1322951. Epub 2017 May 7.

			Dong SZ1, Zhu M1.

			Abstract

			OBJECTIVE:
			To evaluate the utility of fetal cardiac magnetic resonance imaging (MRI) to diagnose right aortic arch (RAA) with right ductus arteriosus.
			METHODS:
			This retrospective study included six fetuses with right aortic arch and right ductus arteriosus. The six fetal cases were examined using a 1.5-T magnetic resonance unit. The steady-state free precession (SSFP) and single-shot turbo spin echo (SSTSE) sequences were used to evaluate the fetal heart and airway. The gestational age of the six fetuses ranged from 22 to 35 weeks (mean, 26.5 weeks). The age of the pregnant women ranged from 23 to 40 years (mean 31 years).
			RESULTS:
			Fetal cardiac MRI diagnosed the six fetal cases with RAA with right ductus arteriosus correctly. Among the six fetuses, four were associated with other congenital heart defects. In three of six cases, the diagnoses established using prenatal echocardiography (echo) was correct when compared with postnatal diagnosis.
			CONCLUSIONS:
			Fetal cardiac MRI is a useful complementary tool to assess fetuses with RAA and right ductus arteriosus.
			KEYWORDS:
			Fetus; cardiac magnetic resonance; right aortic arch; right ductus arteriosus

			PMID: 28438064 DOI: 10.1080/14767058.2017.1322951

	==2017==		==2017==

Z8600021 at 00:43, 19 February 2017

2017-02-19T00:43:37Z

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	==2017==		==2017==
	~~mode=packed~~		{{Heart abnormal cartoon gallery}}
	~~mode=packed-hover~~
	<gallery ~~mode=packed caption="Cardiac Abnormalities">~~
	~~File:Ventricular Septal Defect.jpg\|[[Cardiovascular System - Ventricular Septal Defects\|Ventricular Septal Defects]]~~
	~~File:Atrial Septal Defect.jpg\|[[Cardiovascular_System_-_Atrial_Septal_Defects\|Atrial Septal Defects]]~~
	~~File:Patent Ductus Arteriosus.jpg\|Patent Ductus Arteriosus~~
	~~File:Tetralogy of Fallot.jpg\|Tetralogy of Fallot~~
	~~File:Hypoplastic Left Heart.jpg\|Hypoplastic Left Heart~~
	~~File:Double Outlet Right Ventricle.jpg\|Double Outlet Right Ventricle~~
	~~File:Tricuspid Atresia.jpg\|Tricuspid Atresia~~
	~~File:Transposition of the Great Vessels.jpg\|Transposition of Great Vessels~~
	~~</gallery>~~

	https://embryology.med.unsw.edu.au/embryology/index.php/International_Classification_of_Diseases_-_XVII_Congenital_Malformations#Congenital_malformations_of_the_circulatory_system_.28Q20-Q28.29		https://embryology.med.unsw.edu.au/embryology/index.php/International_Classification_of_Diseases_-_XVII_Congenital_Malformations#Congenital_malformations_of_the_circulatory_system_.28Q20-Q28.29

Z8600021 at 00:42, 19 February 2017

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	==2017==		==2017==
	mode=packed		mode=packed
			mode=packed-hover
	<gallery mode=packed~~-hover~~ caption="Cardiac Abnormalities">		<gallery mode=packed caption="Cardiac Abnormalities">
	File:Ventricular Septal Defect.jpg\|[[Cardiovascular System - Ventricular Septal Defects\|Ventricular Septal Defects]]		File:Ventricular Septal Defect.jpg\|[[Cardiovascular System - Ventricular Septal Defects\|Ventricular Septal Defects]]
	File:Atrial Septal Defect.jpg\|[[Cardiovascular_System_-_Atrial_Septal_Defects\|Atrial Septal Defects]]		File:Atrial Septal Defect.jpg\|[[Cardiovascular_System_-_Atrial_Septal_Defects\|Atrial Septal Defects]]
	File:Patent Ductus Arteriosus.jpg		File:Patent Ductus Arteriosus.jpg\|Patent Ductus Arteriosus
	File:Tetralogy of Fallot.jpg		File:Tetralogy of Fallot.jpg\|Tetralogy of Fallot
	File:Hypoplastic Left Heart.jpg		File:Hypoplastic Left Heart.jpg\|Hypoplastic Left Heart
	File:Double Outlet Right Ventricle.jpg		File:Double Outlet Right Ventricle.jpg\|Double Outlet Right Ventricle
	File:Tricuspid Atresia.jpg		File:Tricuspid Atresia.jpg\|Tricuspid Atresia
	File:Transposition of the Great Vessels.jpg		File:Transposition of the Great Vessels.jpg\|Transposition of Great Vessels
	</gallery>		</gallery>

Z8600021 at 00:41, 19 February 2017

2017-02-19T00:41:01Z

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	==2017==		==2017==
	<gallery mode=packed caption="Cardiac Abnormalities>		mode=packed

			<gallery mode=packed-hover caption="Cardiac Abnormalities">
	File:Ventricular Septal Defect.jpg\|[[Cardiovascular System - Ventricular Septal Defects\|Ventricular Septal Defects]]		File:Ventricular Septal Defect.jpg\|[[Cardiovascular System - Ventricular Septal Defects\|Ventricular Septal Defects]]
	File:Atrial Septal Defect.jpg\|[[Cardiovascular_System_-_Atrial_Septal_Defects\|Atrial Septal Defects]]		File:Atrial Septal Defect.jpg\|[[Cardiovascular_System_-_Atrial_Septal_Defects\|Atrial Septal Defects]]

Z8600021 at 00:39, 19 February 2017

2017-02-19T00:39:41Z

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	==2017==		==2017==
	<gallery caption="Cardiac Abnormalities>		<gallery mode=packed caption="Cardiac Abnormalities>
	File:Ventricular Septal Defect.jpg\|[[Cardiovascular System - Ventricular Septal Defects\|Ventricular Septal Defects]]		File:Ventricular Septal Defect.jpg\|[[Cardiovascular System - Ventricular Septal Defects\|Ventricular Septal Defects]]
	File:Atrial Septal Defect.jpg\|[[Cardiovascular_System_-_Atrial_Septal_Defects\|Atrial Septal Defects]]		File:Atrial Septal Defect.jpg\|[[Cardiovascular_System_-_Atrial_Septal_Defects\|Atrial Septal Defects]]

Z8600021 at 00:38, 19 February 2017

2017-02-19T00:38:14Z

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	==2017==		==2017==
			<gallery caption="Cardiac Abnormalities>
			File:Ventricular Septal Defect.jpg\|[[Cardiovascular System - Ventricular Septal Defects\|Ventricular Septal Defects]]
			File:Atrial Septal Defect.jpg\|[[Cardiovascular_System_-_Atrial_Septal_Defects\|Atrial Septal Defects]]
			File:Patent Ductus Arteriosus.jpg
			File:Tetralogy of Fallot.jpg
			File:Hypoplastic Left Heart.jpg
			File:Double Outlet Right Ventricle.jpg
			File:Tricuspid Atresia.jpg
			File:Transposition of the Great Vessels.jpg
			</gallery>

	https://embryology.med.unsw.edu.au/embryology/index.php/International_Classification_of_Diseases_-_XVII_Congenital_Malformations#Congenital_malformations_of_the_circulatory_system_.28Q20-Q28.29		https://embryology.med.unsw.edu.au/embryology/index.php/International_Classification_of_Diseases_-_XVII_Congenital_Malformations#Congenital_malformations_of_the_circulatory_system_.28Q20-Q28.29

Z8600021 at 22:59, 30 Ocak 2017

2017-01-30T22:59:07Z

← Older revision		Revision as of 08:59, 31 Ocak 2017
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	{{Talk Page}}		{{Talk Page}}

			==2017==

			https://embryology.med.unsw.edu.au/embryology/index.php/International_Classification_of_Diseases_-_XVII_Congenital_Malformations#Congenital_malformations_of_the_circulatory_system_.28Q20-Q28.29

			===International Pediatric Cardiac Code===
			[http://ipccc.net International Paediatric and Congenital Cardiac Code]


			====Report from the international society for nomenclature of paediatric and congenital heart disease: creation of a visual encyclopedia illustrating the terms and definitions of the international pediatric and congenital cardiac code====
			World J Pediatr Congenit Heart Surg. 2010 Oct;1(3):300-13. doi: 10.1177/2150135110379622.

			Giroud JM1, Jacobs JP, Spicer D, Backer C, Martin GR, Franklin RC, Béland MJ, Krogmann ON, Aiello VD, Colan SD, Everett AD, William Gaynor J, Kurosawa H, Maruszewski B, Stellin G, Tchervenkov CI, Walters HL 3rd, Weinberg P, Anderson RH, Elliott MJ.

			Abstract

			Tremendous progress has been made in the field of pediatric heart disease over the past 30 years. Although survival after heart surgery in children has improved dramatically, complications still occur, and optimization of outcomes for all patients remains a challenge. To improve outcomes, collaborative efforts are required and ultimately depend on the possibility of using a common language when discussing pediatric and congenital heart disease. Such a universal language has been developed and named the International Pediatric and Congenital Cardiac Code (IPCCC). To make the IPCCC more universally understood, efforts are under way to link the IPCCC to pictures and videos. The Archiving Working Group is an organization composed of leaders within the international pediatric cardiac medical community and part of the International Society for Nomenclature of Paediatric and Congenital Heart Disease (www.ipccc.net). Its purpose is to illustrate, with representative images of all types and formats, the pertinent aspects of cardiac diseases that affect neonates, infants, children, and adults with congenital heart disease, using the codes and definitions associated with the IPCCC as the organizational backbone. The Archiving Working Group certifies and links images and videos to the appropriate term and definition in the IPCCC. These images and videos are then displayed in an electronic format on the Internet. The purpose of this publication is to report the recent progress made by the Archiving Working Group in establishing an Internet-based, image encyclopedia that is based on the standards of the IPCCC.
			KEYWORDS:
			International Pediatric and Congenital Cardiac Code; Internet; cardiac encyclopedia; cardiac images; cardiac nomenclature; congenital heart disease; databases
			PMID 23804886 DOI: 10.1177/2150135110379622

			====Nomenclature for congenital and paediatric cardiac disease: historical perspectives and The International Pediatric and Congenital Cardiac Code====

			Cardiol Young. 2008 Dec;18 Suppl 2:70-80. doi: 10.1017/S1047951108002795.

			Franklin RC1, Jacobs JP, Krogmann ON, Béland MJ, Aiello VD, Colan SD, Elliott MJ, William Gaynor J, Kurosawa H, Maruszewski B, Stellin G, Tchervenkov CI, Walters Iii HL, Weinberg P, Anderson RH.

			Abstract

			Clinicians working in the field of congenital and paediatric cardiology have long felt the need for a common diagnostic and therapeutic nomenclature and coding system with which to classify patients of all ages with congenital and acquired cardiac disease. A cohesive and comprehensive system of nomenclature, suitable for setting a global standard for multicentric analysis of outcomes and stratification of risk, has only recently emerged, namely, The International Paediatric and Congenital Cardiac Code. This review, will give an historical perspective on the development of systems of nomenclature in general, and specifically with respect to the diagnosis and treatment of patients with paediatric and congenital cardiac disease. Finally, current and future efforts to merge such systems into the paperless environment of the electronic health or patient record on a global scale are briefly explored. On October 6, 2000, The International Nomenclature Committee for Pediatric and Congenital Heart Disease was established. In January, 2005, the International Nomenclature Committee was constituted in Canada as The International Society for Nomenclature of Paediatric and Congenital Heart Disease. This International Society now has three working groups. The Nomenclature Working Group developed The International Paediatric and Congenital Cardiac Code and will continue to maintain, expand, update, and preserve this International Code. It will also provide ready access to the International Code for the global paediatric and congenital cardiology and cardiac surgery communities, related disciplines, the healthcare industry, and governmental agencies, both electronically and in published form. The Definitions Working Group will write definitions for the terms in the International Paediatric and Congenital Cardiac Code, building on the previously published definitions from the Nomenclature Working Group. The Archiving Working Group, also known as The Congenital Heart Archiving Research Team, will link images and videos to the International Paediatric and Congenital Cardiac Code. The images and videos will be acquired from cardiac morphologic specimens and imaging modalities such as echocardiography, angiography, computerized axial tomography and magnetic resonance imaging, as well as intraoperative images and videos. Efforts are ongoing to expand the usage of The International Paediatric and Congenital Cardiac Code to other areas of global healthcare. Collaborative efforts are underway involving the leadership of The International Nomenclature Committee for Pediatric and Congenital Heart Disease and the representatives of the steering group responsible for the creation of the 11th revision of the International Classification of Diseases, administered by the World Health Organisation. Similar collaborative efforts are underway involving the leadership of The International Nomenclature Committee for Pediatric and Congenital Heart Disease and the International Health Terminology Standards Development Organisation, who are the owners of the Systematized Nomenclature of Medicine or "SNOMED". The International Paediatric and Congenital Cardiac Code was created by specialists in the field to name and classify paediatric and congenital cardiac disease and its treatment. It is a comprehensive code that can be freely downloaded from the internet (http://www.IPCCC.net) and is already in use worldwide, particularly for international comparisons of outcomes. The goal of this effort is to create strategies for stratification of risk and to improve healthcare for the individual patient. The collaboration with the World Heath Organization, the International Health Terminology Standards Development Organisation, and the healthcare industry, will lead to further enhancement of the International Code, and to its more universal use.
			PMID 19063777 DOI: 10.1017/S1047951108002795
			[PubMed - indexed for MEDLINE]

	==2016==		==2016==