LA88.4 Ventricular Septal Defect
|ICD-11 Structural developmental anomalies of the circulatory system (draft)
|ICD-11 Beta Draft - NOT FINAL, updated on a daily basis, It is not approved by WHO, NOT TO BE USED for CODING except for agreed FIELD TRIALS.
20 Developmental Anomalies - Structural Developmental Anomalies
Beta coding and tree structure for "structural developmental anomalies" within this section are shown in the table below.
|Structural developmental anomalies of the circulatory system
- Structural developmental anomaly of heart and great vessels
- LB00 Congenital heart or great vessel related acquired abnormality
- LB01 Congenital anomaly of atrioventricular or ventriculo-arterial connections
- LB01.1 Transposition of the great arteries
- LB01.2 Double outlet right ventricle
- LB01.3 Double outlet left ventricle
- LB01.4 Common arterial trunk
- LB01.Y Other specified congenital anomaly of atrioventricular or ventriculo-arterial connections
- LB01.Z Congenital anomaly of atrioventricular or ventriculo-arterial connections, unspecified
- LB02 Congenital anomaly of the mediastinal veins Congenital anomaly of atria or atrial septum
- LB20 Congenital anomaly of atrioventricular valves or septum
- LB21 Congenital anomaly of ventricles and ventricular septum
- LB21.1 Congenital right ventricular outflow tract obstruction
- LB21.2 Double-chambered right ventricle
- LB21.3 Tetralogy of Fallot
- LB21.4 Congenital left ventricular outflow tract obstruction
- LB21.5 Congenital ventricular septal defects
- LB21.Y Other specified congenital anomaly of ventricles and ventricular septum
- LB21.Z Congenital anomaly of ventricles and ventricular septum, unspecified
- LB22 Functionally univentricular heart
- LB23 Congenital anomaly of ventriculo-arterial valves and adjacent regions
- LB24 Congenital anomaly of great arteries including arterial duct
- LB.1 Congenital aorto-pulmonary window
- LB.2 Congenital anomaly of pulmonary arterial tree
- LB.3 Congenital anomaly of aorta and its branches
- LB.4 Tracheo-oesophageal compressive syndrome
- LB.5 Patent arterial duct
- LB.Y Other specified congenital anomaly of great arteries including arterial duct
- LB.Z Congenital anomaly of great arteries including arterial duct, unspecified
- LB25 Anomalous position-orientation of heart
- LB26 Total mirror imagery
- LB27 Left isomerism
- LB28 Congenital anomaly of coronary arteries
- LB29 Structural developmental anomalies of the pericardium
- LB2Y Other specified structural developmental anomaly of heart and great vessels
- LB2Z Structural developmental anomaly of heart and great vessels, unspecified
- LB30 Structural developmental anomalies of the peripheral vascular system
- LB30.1 Capillary malformations
- LB30.2 Lymphatic malformations
- LB30.21 Macrocystic lymphatic malformation
- LB30.22 Microcystic lymphatic malformation
- LB30.23 Cystic hygroma in fetus
- BD23.1 Primary lymphoedema
- EK91 Yellow nail syndrome
- LC5F.26 Noonan syndrome
- LB30.2Y Other specified lymphatic malformations
- LB30.2Z Lymphatic malformations, unspecified
- LB30.3 Peripheral venous malformations
- LB30.4 Peripheral arteriovenous malformations
- LB30.5 Peripheral arterial malformations
- LB30.6 Pulmonary arteriovenous fistula
- LB30.Y Other specified structural developmental anomalies of the peripheral vascular system
- LB30.Z Structural developmental anomalies of the peripheral vascular system, unspecified
- LB3Y Other specified structural developmental anomalies of the circulatory system
- LB3Z Structural developmental anomalies of the circulatory system, unspecified
|CD-11 Beta Draft - NOT FINAL, updated on a daily basis, It is not approved by WHO, NOT TO BE USED for CODING except for agreed FIELD TRIALS.
See also International Classification of Diseases | Abnormalities
Ventricular Septal Defect
The ventricular septal defect (VSD) is one of the common forms of congenital cardiovascular anomaly, occurring in nearly 50% of all infants with a congenital heart defect. Usually occurs in the membranous (perimembranous) rather than muscular interventricular septum, and is more frequent in males that females. This defect can also contribute to outflow tract (OFT) malformations. See also the recent cardiac development online review section - Normal as opposed to abnormal ventricular septation.
Perimembranous defects are located close to the aortic and tricuspid valves and adjacent to atrioventricular conduction bundle.
Some Recent Findings
Australia Congenital heart disease 2016–17
- Australia - Congenital heart disease hospitalisations, principal diagnosis, by condition and sex, 2016–17 "In 2016–17, there were around 4,900 hospitalisations in Australia where congenital heart disease was the principal diagnosis—a rate of 20 hospitalisations per 100,000 population. The highest rate of hospitalisation for a specific form of congenital heart disease was for atrial septal defects (6.6 hospitalisations per 100,000 population), followed by ventricular septal defect (1.8), transposition of the great vessels (1.2), patent ductus arteriosus and coarctation of the aorta."
- A new anatomic approach of the ventricular septal defect in the interruption of the aortic arch "The aim of this study was to analyse the anatomy of the ventricular septal defect (VSD) in heart specimens with interruption of the aortic arch (IAA) in order to explore the hypothesis of different embryologic mechanisms for the different anatomic types of IAA. We examined 42 human heart specimens, 25 with IAA as the main disease with concordant atrioventricular and ventriculo-arterial connections and two distinct great arteries, and 17 hearts with IAA associated with other malformations [six common arterial trunk (CAT), five double-outlet right ventricle (DORV), three transposition of the great arteries (TGA), three atrioventricular septal defect (AVSD)]. The interruption was classified according to Celoria and Patton. ...These results reinforce the hypothesis that different pathogenic mechanisms are responsible for the two types of IAA, and the inclusion of IAA type B in the group of neural crest defects. Conversely, IAA type A could be due to overlapping mechanisms: flow-related defect (coarctation-like) and neural crest contribution."
- Tricuspid Valve Detachment in Ventricular Septal Defect Closure Does Not Impact Valve Function "Although tricuspid valve detachment (TVD) facilitates improved exposure during trans-atrial ventricular septal defect (VSD) closure, few have analyzed the impact of TVD on long-term valve durability. RESULTS: 247 patients underwent VSD closure; 164 (66.4%) without TVD and 83 (33.6%) with TVD. Median follow-up time was 2343 days (IQR:1237-3963.5) in the group without TVD versus 1606 days (IQR:826-3017) in those with TVD. After successfully matching 83 patients, 29/83 (34.9%) in the non-TVD group had mild TR versus 28/83 (33.7%) in the TVD group (p=0.87). 2 patients in the non-TVD group had moderate TR versus 1 patient in the TVD group at long term follow up. 1 patient in each group suffered transient AV block, but neither required pacemaker insertion. CONCLUSIONS: Tricuspid valve detachment did not compromise long-term valve durability and did not impose increased morbidity. Patients who underwent TVD had a similar prevalence of mild TR to patients without TVD. Moderate TR was exceptionally rare in both groups. When exposure is difficult, TVD is a safe and effective technical adjunct."
|More recent papers
This table allows an automated computer search of the external PubMed database using the listed "Search term" text link.
- This search now requires a manual link as the original PubMed extension has been disabled.
- The displayed list of references do not reflect any editorial selection of material based on content or relevance.
- References also appear on this list based upon the date of the actual page viewing.
References listed on the rest of the content page and the associated discussion page (listed under the publication year sub-headings) do include some editorial selection based upon both relevance and availability.
More? References | Discussion Page | Journal Searches | 2019 References | 2020 References
Search term: Ventricular Septal Defect
|These papers originally appeared in the Some Recent Findings table, but as that list grew in length have now been shuffled down to this collapsible table.
See also the Discussion Page for other references listed by year and References on this current page.
- Complete Repair of Coarctation of the Aorta and a Ventricular Septal Defect in a 1,480 g Low Birth Weight Neonate "Although outcomes of neonatal cardiac surgery have dramatically improved in the last two decades, low body weight still constitutes an important risk factor for morbidity and mortality. In particular, cardiac surgery in neonates with very low birth weight (≤1.5 kg) is carried out with greater risk because most organ systems are immature. We report here on a successful case of early one-stage total repair of coarctation of the aorta and a ventricular septal defect in a 1,480 gram neonate."
|The image shows a congenitally malformed heart in which both the right and left atrioventricular valves (RAVV, LAVV) are connected with the dominant left ventricle. The right ventricle is incomplete, and is supplied through a ventricular septal defect. Note that, in this heart, the aorta arises from the incomplete right ventricle, and the pulmonary trunk from the dominant left ventricle. This is the arrangement usually described as “transposition”, but better accounted for in terms of discordant ventriculo-arterial connections.
||The image shows the lesion known as classical tricuspid atresia. There has been failure of expansion of the atrioventricular junctions, so that the floor of the right is separated from the roof of the right ventricle by the right atrioventricular groove (dashed black lines). Only the dominant left ventricle has an inlet, with the blood entering the incomplete right ventricle through the ventricular septal defect (star).
||The image shows a heart dissected to reveal the structure of the incomplete right ventricle. In this heart, as in most example of tricuspid atresia, it gives rise to the pulmonary trunk. The ventricular septal defect (VSD) is restrictive in this heart.
Images from Anderson (2016)
- Anderson (2016) Human Heart Ventricular Septal Defect
fig 10 Human ventricular septal defect
fig 11a Human ventricular septal defect
fig 11b Human ventricular septal defect
Le Gros Clark (1847)
Heart autopsy drawing.
|The first western clinical description of ventricular septal defects was made by Henri Roger in 1879, which later became known as maladie de Roger.
His description was based upon 6 acyanotic patients and autopsy finding of a child with ventricular septal defect.
There is a defect in the ventricular septum adjacent to the atrioventricular valves. Blood flow is seen across the defect on Colour Doppler imaging.
(Heath-Edward grade) A pathological grading system for pulmonary artery structural changes that occur with congenital cardiac septal defects. The classification is named after the two original paper authors Donald HEATH and Jessee EDWARDS and grades from I to VI with increasing severity of the arterial changes.
- Grade I - hypertrophy of the media of small muscular arteries and arterioles.
- Grade II - intimal cellular proliferation in addition to medial hypertrophy.
- Grade III - advanced medial thickening with hypertrophy and hyperplasia including progressive intimal proliferation and concentric fibrosis. Results in an obliteration of the arterioles and small arteries.
- Grade IV - "plexiform lesions" of the muscular pulmonary arteries and arterioles with a plexiform network of capillary-like channels within a dilated segment.
- Grade V - complex plexiform, angiomatous and cavernous lesions and hyalinization of intimal fibrosis.
- Grade VI - necrotizing arteritis.
Number of parameters are considered when classifying:
- Size of the defect.
- Location of the defect.
- Number of defects.
- Presence or absence of a ventricular septal aneurysm.
Data shown as a percentage of all major abnormalities based upon published statistics using the same groupings as Congenital Malformations Australia 1981-1992 P. Lancaster and E. Pedisich ISSN 1321-8352.
Heart defects and preterm birth are the most common causes of neonatal and infant death. The long-term development of the heart combined with extensive remodelling and post-natal changes in circulation lead to an abundance of abnormalities associated with this system.
A UK study literature showed that preterm infants have more than twice as many cardiovascular malformations (5.1 / 1000 term infants and 12.5 / 1000 preterm infants) as do infants born at term and that 16% of all infants with cardiovascular malformations are preterm. (0.4% of live births occur at greater than 28 weeks of gestation, 0.9% at 28 to 31 weeks, and 6% at 32 to 36 weeks. Overall, 7.3% of live-born infants are preterm)
"Baltimore-Washington Infant Study data on live-born cases and controls (1981-1989) was reanalyzed for potential environmental and genetic risk-factor associations in complete atrioventricular septal defects AVSD (n = 213), with separate comparisons to the atrial (n = 75) and the ventricular (n = 32) forms of partial AVSD. ...Maternal diabetes constituted a potentially preventable risk factor for the most severe, complete form of AVSD."
In addition, there are in several congenital abnormalities that exist in adults (bicuspid aortic valve, mitral valve prolapse, and partial anomalous pulmonary venous connection) which may not be clinically recognized.
- ↑ Australian Institute of Health and Welfare 2019. Congenital heart disease in Australia. Cat. no. CDK 14. Canberra: AIHW.
- ↑ Mostefa Kara M, Houyel L & Bonnet D. (2019). A new anatomic approach of the ventricular septal defect in the interruption of the aortic arch. J. Anat. , 234, 193-200. PMID: 30525196 DOI.
- ↑ Fraser CD, Zhou X, Palepu S, Lui C, Suarez-Pierre A, Crawford TC, Magruder JT, Jacobs ML, Cameron DE, Hibino N & Vricella LA. (2018). Tricuspid Valve Detachment in Ventricular Septal Defect Closure Does Not Impact Valve Function. Ann. Thorac. Surg. , , . PMID: 29625102 DOI.
- ↑ Lee H, Cho JY & Kim GJ. (2011). Complete Repair of Coarctation of the Aorta and a Ventricular Septal Defect in a 1,480 g Low Birth Weight Neonate. Korean J Thorac Cardiovasc Surg , 44, 183-5. PMID: 22263148 DOI.
- ↑ Anderson RH. Teratogenecity in the setting of cardiac development and maldevelopment. (2016)
- ↑ Clark Fle G. (1847). Case of cyanosis, with a description of the appearances presented on dissection, illustrated by the preparation, and a drawing, of the heart. Med Chir Trans , 30, 112.2-120. PMID: 20895864
- ↑ Allwork SP. (1979). Maladie du Roger 1879: a new translation for the centenary. Am. Heart J. , 98, 307-11. PMID: 382810
- ↑ HEATH D & EDWARDS JE. (1958). The pathology of hypertensive pulmonary vascular disease; a description of six grades of structural changes in the pulmonary arteries with special reference to congenital cardiac septal defects. Circulation , 18, 533-47. PMID: 13573570
- ↑ Tanner K, Sabrine N & Wren C. (2005). Cardiovascular malformations among preterm infants. Pediatrics , 116, e833-8. PMID: 16322141 DOI.
- ↑ Loffredo CA, Hirata J, Wilson PD, Ferencz C & Lurie IW. (2001). Atrioventricular septal defects: possible etiologic differences between complete and partial defects. Teratology , 63, 87-93. PMID: 11241431 <87::AID-TERA1014>3.0.CO;2-5 DOI.
Ikai A. (2018). Surgical strategies for pulmonary atresia with ventricular septal defect associated with major aortopulmonary collateral arteries. Gen Thorac Cardiovasc Surg , 66, 390-397. PMID: 29802565 DOI.
Penny DJ & Vick GW. (2011). Ventricular septal defect. Lancet , 377, 1103-12. PMID: 21349577 DOI.
Ghosh S, Sridhar A, Solomon N & Sivaprakasham M. (2018). Transcatheter closure of ventricular septal defect in aortic valve prolapse and aortic regurgitation. Indian Heart J , 70, 528-532. PMID: 30170648 DOI.
Nishioka M, Fuchigami T, Akashige T & Nagata N. (2018). [Successful Staged Surgical Management for Double Outlet Right Ventricle with Ebstein's Anomaly and Aortic Coarctation;Report of a Case]. Kyobu Geka , 71, 615-621. PMID: 30185760
Lee H, Cho JY & Kim GJ. (2011). Complete Repair of Coarctation of the Aorta and a Ventricular Septal Defect in a 1,480 g Low Birth Weight Neonate. Korean J Thorac Cardiovasc Surg , 44, 183-5. PMID: 22263148 DOI.
Callaghan MA, O'Hare B & Casey W. (2012). What other anomalies? Failure to wean post ventricular septal defect repair secondary to anomalous origin of the left coronary artery from the pulmonary artery. Paediatr Anaesth , 22, 487-9. PMID: 22229525 DOI.
Bian C, Ma J, Wang J, Xu G, Jiang J, Yao S & Liu Y. (2011). Perimembranous ventricular septal defect with aneurysm: two options for transcatheter closure. Tex Heart Inst J , 38, 528-32. PMID: 22163127
Fried R, Falkovsky G, Newburger J, Gorchakova AI, Rabinovitch M, Gordonova MI, Fyler D, Reid L & Burakovsky V. (1986). Pulmonary arterial changes in patients with ventricular septal defects and severe pulmonary hypertension. Pediatr Cardiol , 7, 147-54. PMID: 3808993 DOI.
Haworth SG. (1986). Pulmonary vascular bed in children with complete atrioventricular septal defect: relation between structural and hemodynamic abnormalities. Am. J. Cardiol. , 57, 833-9. PMID: 2938464
Hoffmeister HM, Fischbach H & Hoffmeister HE. (1981). Pulmonary arterial changes and hemodynamic parameters in isolated ventricular septal defect. Thorac Cardiovasc Surg , 29, 355-8. PMID: 6179217 DOI.
Search Pubmed: Ventricular Septal Defect
External Links Notice - The dynamic nature of the internet may mean that some of these listed links may no longer function. If the link no longer works search the web with the link text or name. Links to any external commercial sites are provided for information purposes only and should never be considered an endorsement. UNSW Embryology is provided as an educational resource with no clinical information or commercial affiliation.
|Cardiovascular System Development See also Heart terms, Immune terms and Blood terms.
- angioblast - the stem cells in blood islands generating endothelial cells which will form the walls of both arteries and veins. (More? Blood Vessel)
- angiogenesis - the formation of new blood vessels from pre-existing vessels following from vasculogenesis in the embryo. (More? Blood Vessel)
- anlage (German, anlage = primordium) structure or cells which will form a future more developed or differentiated adult structure.
- blood islands - earliest sites of blood vessel and blood cell formation, seen mainly on yolk sac chorion.
- cardinal veins - paired main systemic veins of early embryo, anterior, common, posterior.
- cardiogenic region - region above prechordal plate in mesoderm where heart tube initially forms.
- ectoderm - the layer (of the 3 germ cell layers) which form the nervous system from the neural tube and neural crest and also generates the epithelia covering the embryo.
- endoderm - the layer (of the 3 germ cell layers) which form the epithelial lining of the gastrointestinal tract (GIT) and accessory organs of GIT in the embryo.
- endocardium - lines the heart. Epithelial tissue lining the inner surface of heart chambers and valves.
- endothelial cells - single layer of cells closest to lumen that line blood vessels.
- extraembryonic mesoderm - mesoderm lying outside the trilaminar embryonic disc covering the yolk sac, lining the chorionic sac and forming the connecting stalk. Contributes to placental villi development.
- haemocytoblasts - stem cells for embryonic blood cell formation.
- anastomose - to connect or join by a connection (anastomosis) between tubular structures.
- chorionic villi - the finger-like extensions which are the functional region of the placental barrier and maternal/fetal exchange. Develop from week 2 onward as: primary, secondary, tertiary villi.
- estrogens - support the maternal endometrium.
- growth factor - usually a protein or peptide that will bind a cell membrane receptor and then activates an intracellular signaling pathway. The function of the pathway will be to alter the cell directly or indirectly by changing gene expression. (eg VEGF, shh)
- intra-aortic hematopoietic cluster - (IAHC) blood stem cells associated with the endothelial layer of aorta and large arteries.
- maternal decidua - region of uterine endometrium where blastocyst implants. undergoes modification following implantation, decidual reaction.
- maternal sinusoids - placental spaces around chorionic villi that are filled with maternal blood. Closest maternal/fetal exchange site.
- Megakaryocytopoiesis - the process of bone marrow progenitor cells developMENT into mature megakaryocytes.
- mesoderm - the middle layer of the 3 germ cell layers of the embryo. Mesoderm outside the embryo and covering the amnion, yolk and chorion sacs is extraembryonic mesoderm.
- myocardium - muscular wall of the heart. Thickest layer formed by spirally arranged cardiac muscle cells.
- pericardium - covers the heart. Formed by 3 layers consisting of a fibrous pericardium and a double layered serous pericardium (parietal layer and visceral epicardium layer).
- pericytes - (Rouget cells) cells located at the abluminal surface of microvessels close to endothelial cells, mainly found associated with CNS vessels and involved in vessel formation, remodeling and stabilization.
- pharyngeal arches (=branchial arches, Gk. gill) series of cranial folds that form most structures of the head and neck. Six arches form but only 4 form any structures. Each arch has a pouch, membrane and groove.
- placenta - (Greek, plakuos = flat cake) refers to the discoid shape of the placenta, embryonic (villous chorion)/maternal organ (decidua basalis)
- placental veins - paired initially then only left at end of embryonic period, carry oxygenated blood to the embryo (sinus venosus).
- protein hormone - usually a protein distributed in the blood that binds to membrane receptors on target cells in different tissues. Do not easliy cross placental barrier.
- sinus venosus - cavity into which all major embryonic paired veins supply (vitelline, placental, cardinal).
- splanchnic mesoderm - portion of lateral plate mesoderm closest to the endoderm when coelom forms.
- steroid hormone - lipid soluble hormone that easily crosses membranes to bind receptors in cytoplasm or nucleus of target cells. Hormone+Receptor then binds DNA activating or suppressing gene transcription. Easliy cross placental barrier.
- syncitiotrophoblast extraembryonic cells of trophoblastic shell surrounding embryo, outside the cytotrophoblast layer, involved with implantation of the blastocyst by eroding extracellular matrix surrounding maternal endometrial cells at site of implantation, also contribute to villi. (dark staining, multinucleated).
- truncus arteriosus - an embryological heart outflow structure, that forms in early cardiac development and will later divides into the pulmonary artery and aorta. Term is also used clinically to describe the malformation where only one artery arises from the heart and forms the aorta and pulmonary artery.
- vascular endothelial growth factor - (VEGF) A secreted protein growth factor family, which stimulates the proliferation of vasular endotheial cells and therefore blood vessel growth. VEGF's have several roles in embryonic development. The VEGF family has 7 members (VEGF-A, VEGF-B, VEGF-C, VEGF-D, VEGF-E, VEGF-F, and PlGF) that have a common VEGF homology domain. PIGF is the placental growth factor. They act through 3 VEGF tyrosine kinase membrane receptors (VEGFR-1 to 3) with seven immunoglobulin-like domains in the extracellular domain, a single transmembrane region, and an intracellular tyrosine kinase sequence.
- vasculogenesis - the formation of new blood vessels from mesoderm forming the endothelium. Compared to angiogenesis that is the process of blood vessel formation from pre-existing vessels.
- vitelline blood vessels - blood vessels associated with the yolk sac.
- waste products - products of cellular metabolism and cellular debris, e.g.- urea, uric acid, bilirubin.
- Glossary: A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | Numbers | Symbols | Term Link
Cite this page: Hill, M.A. (2021, November 28) Embryology Cardiovascular System - Ventricular Septal Defects. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Cardiovascular_System_-_Ventricular_Septal_Defects
- What Links Here?
- © Dr Mark Hill 2021, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G