Cardiovascular System - Patent Ductus Arteriosus: Difference between revisions
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= | =LA8B.4 Patent Arterial Duct= | ||
{{ICD-11}} [https://icd.who.int/browse11/l-m/en#/http://id.who.int/icd/entity/1262462321 LA8B.4 Patent arterial duct] | |||
{{ICD-11-Circulatory system structural anomalies table}} | {{ICD-11-Circulatory system structural anomalies table}} | ||
[[International_Classification_of_Diseases|International Classification of Diseases (ICD-10)]] - [[International_Classification_of_Diseases_-_XVII_Congenital_Malformations#International_Classification_of_Diseases_-_XVII_Congenital_Malformations#Q25_Congenital_malformations_of_great_arteries|Q25 Congenital malformations of great arteries]] Q25.0 Patent ductus arteriosus Patent ductus Botallo Persistent ductus arteriosus | |||
==Introduction== | ==Introduction== | ||
[[File:Patent Ductus Arteriosus.jpg|thumb|300px|Patent Ductus Arteriosus]] | [[File:Patent Ductus Arteriosus.jpg|thumb|300px|Patent Ductus Arteriosus]] | ||
Patent ductus arteriosus (PDA), or Patent arterial duct (PAD), or {{common truncus}}, occurs commonly in preterm infants, and at approximately 1 in 2000 full term infants and more common in females (to male ratio is 2:1). Can also be associated with specific genetic defects, {{trisomy 21}} and {{trisomy 18}}, and the Rubinstein-Taybi and CHARGE syndromes. | |||
Patent ductus arteriosus (PDA), or Patent arterial duct (PAD), or {{common truncus}}, occurs commonly in preterm infants, and at approximately 1 in 2000 full term infants and more common in females (to male ratio is 2:1). Can also be associated with specific genetic defects, | |||
The opening is asymptomatic when the duct is small and can close spontaneously (by day three in 60% of normal term neonates), the remainder are ligated simply and with little risk, with transcatheter closure of the duct generally indicated in older children. The operation is always recommended even in the absence of cardiac failure and can often be deferred until early childhood. | The opening is asymptomatic when the duct is small and can close spontaneously (by day three in 60% of normal term neonates), the remainder are ligated simply and with little risk, with transcatheter closure of the duct generally indicated in older children. The operation is always recommended even in the absence of cardiac failure and can often be deferred until early childhood. |
Revision as of 09:29, 29 October 2018
Embryology - 8 Jun 2024 Expand to Translate |
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LA8B.4 Patent Arterial Duct
ICD-11 LA8B.4 Patent arterial duct
ICD-11 Structural developmental anomalies of the circulatory system (draft) |
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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 |
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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.
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International Classification of Diseases (ICD-10) - Q25 Congenital malformations of great arteries Q25.0 Patent ductus arteriosus Patent ductus Botallo Persistent ductus arteriosus
Introduction
Patent ductus arteriosus (PDA), or Patent arterial duct (PAD), or common truncus, occurs commonly in preterm infants, and at approximately 1 in 2000 full term infants and more common in females (to male ratio is 2:1). Can also be associated with specific genetic defects, Trisomy 21 and Trisomy 18, and the Rubinstein-Taybi and CHARGE syndromes.
The opening is asymptomatic when the duct is small and can close spontaneously (by day three in 60% of normal term neonates), the remainder are ligated simply and with little risk, with transcatheter closure of the duct generally indicated in older children. The operation is always recommended even in the absence of cardiac failure and can often be deferred until early childhood.
- The ductus arteriosus, and its corresponding ligament, historically were described as the ductus Botallo, but should this have really been the ductus Aranzio?[1]
Some Recent Findings
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More recent papers |
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This table allows an automated computer search of the external PubMed database using the listed "Search term" text link.
More? References | Discussion Page | Journal Searches | 2019 References | 2020 References Search term: Patent Ductus Arteriosus <pubmed limit=5>Patent Ductus Arteriosus</pubmed> |
Older papers |
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Diagnostic Images
Cardiovascular Abnormalities
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)[6]
"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." [7]
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.
International Classification of Diseases
The International Classification of Diseases (ICD) World Health Organization's classification used worldwide as the standard diagnostic tool for epidemiology, health management and clinical purposes. This includes the analysis of the general health situation of population groups. It is used to monitor the incidence and prevalence of diseases and other health problems.
ICD11
- LB24 Congenital anomaly of great arteries including arterial duct
- LB.5 Patent arterial duct
ICD-11 Structural developmental anomalies of the circulatory system (draft) |
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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 |
|
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.
|
ICD10
Within the ICD10 classification "congenital malformations, deformations and chromosomal abnormalities" are (Q00-Q99) but excludes "inborn errors of metabolism" (E70-E90).
Congenital malformations of the circulatory system (Q20-Q28)
International Classification of Diseases (ICD-10) - Q25 Congenital malformations of great arteries Q25.0 Patent ductus arteriosus Patent ductus Botallo Persistent ductus arteriosus
Clinical Classifications
Patent Ductus Arteriosus (PDA) classification system on the basis of angiogram appearance by Krichenko (1989).[8]
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A recent publication suggests a classification based on angiographic size and haemodynamic sound significance.[9]
Type | Size | Haemodynamics |
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Silent PDA | usually less than 1.5 mm | PDA murmur not present |
Very small PDA | less than 1.5 mm | PDA murmur present |
Small PDA | 1.5 to 3.0 mm | PDA murmur present |
Moderate PDA | 3 to 5 mm | PDA murmur present |
Large PDA | greater than 5 mm | PDA murmur present |
The Aristotle Comprehensive Complexity (ACC) score has been suggested as a clinical tool for complexity adjustment in the analysis of outcome after reparative congenital heart surgery.[10][11]
Patent Ductus Arteriosus with Persistent Fifth Aortic Arch
Three-dimensional reconstructed computed tomography image showing left-sided patent ductus arteriosus with double-lumen aortic arch.[12]
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References
- ↑ Fransson SG. (1999). The Botallo mystery. Clin Cardiol , 22, 434-6. PMID: 10376187
- ↑ Evans N. (2015). Preterm patent ductus arteriosus: A continuing conundrum for the neonatologist?. Semin Fetal Neonatal Med , 20, 272-7. PMID: 25818393 DOI.
- ↑ Goudjil S, Imestouren F, Armougon A, Razafimanantsoa L, Mahmoudzadeh M, Wallois F, Leke A & Kongolo G. (2014). Noninvasive technique for the diagnosis of patent ductus arteriosus in premature infants by analyzing pulse wave phases on photoplethysmography signals measured in the right hand and the left foot. PLoS ONE , 9, e98763. PMID: 24892695 DOI.
- ↑ Ohlsson A, Walia R & Shah SS. (2013). Ibuprofen for the treatment of patent ductus arteriosus in preterm and/or low birth weight infants. Cochrane Database Syst Rev , , CD003481. PMID: 23633310 DOI.
- ↑ Ethington PN, Smith PB, Katakam L, Goldberg RN & Cotten CM. (2011). Treatment of patent ductus arteriosus with bidirectional flow in neonates. Early Hum. Dev. , 87, 381-4. PMID: 21402454 DOI.
- ↑ 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.
- ↑ <pubmed>2929450</pubmed>
- ↑ Fernando R, Koranne K, Loyalka P, Kar B & Gregoric I. (2013). Patent ductus arteriosus closure using an Amplatzer(™) ventricular septal defect closure device. Exp Clin Cardiol , 18, e50-4. PMID: 24294051
- ↑ Bojan M, Gerelli S, Gioanni S, Pouard P & Vouhé P. (2011). Evaluation of a new tool for morbidity assessment in congenital cardiac surgery. Ann. Thorac. Surg. , 92, 2200-4. PMID: 22115230 DOI.
- ↑ Chang YH, Lee JY, Kim JE, Kim JY, Youn Y, Lee EJ, Moon S, Lee JY & Sung IK. (2013). The Aristotle score predicts mortality after surgery of patent ductus arteriosus in preterm infants. Ann. Thorac. Surg. , 96, 879-84. PMID: 23895892 DOI.
- ↑ Warrier D, Shah S, John C & Dayananda L. (2012). A rare association with patent ductus arteriosus. Ann Pediatr Cardiol , 5, 191-3. PMID: 23129912 DOI.
Reviews
Sasi A & Deorari A. (2011). Patent ductus arteriosus in preterm infants. Indian Pediatr , 48, 301-8. PMID: 21532100
Articles
Yun SW. (2011). Congenital heart disease in the newborn requiring early intervention. Korean J Pediatr , 54, 183-91. PMID: 21829408 DOI.
Thébaud B & Lacaze-Mazmonteil T. (2010). Patent ductus arteriosus in premature infants: A never-closing act. Paediatr Child Health , 15, 267-70. PMID: 21532789
Search Pubmed
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- MedlinePlus Patent Ductus Arteriosus
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Cite this page: Hill, M.A. (2024, June 8) Embryology Cardiovascular System - Patent Ductus Arteriosus. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Cardiovascular_System_-_Patent_Ductus_Arteriosus
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G