Czasopismo
Tytuł artykułu
Warianty tytułu
Języki publikacji
Abstrakty
DORV [double outlet right ventricle] is defined as a defect in which the great vessels leave entirely or mostly from above the morphologically right ventricle. The proposed by us new prenatal classification of heart defects for the DORV defect including the division into isolated and coexisting with extracardiac defect, facilitates consultation and predicting prognosis for the fetus and newborn. Isolated DORV in fetuses is classified as a severe elective defect (expected cardiac intervention or surgery at 1 month of age) with a relatively good prognosis for newborns, regardless of the type of intracardiac anomalies (in our series of cases 100% survival). DORV in the fetus with coexisting extracardiac defects (ECM) regardless of type of anomaly had poor prognosis (in our study group 100% demise rate).
Czasopismo
Rocznik
Tom
Numer
Strony
13-17
Opis fizyczny
Daty
wydano
2014-09-01
otrzymano
2014-09-06
zaakceptowano
2014-10-07
online
2015-12-30
Twórcy
autor
- Gynaecology and Obstetrics Department, Holy Trinity Non-Public Health Care Facility in Plock
- Institute of Health Sciences. The State School of Higher Professional Education in Płock
autor
- Institute of Health Sciences. The State School of Higher Professional Education in Płock, maciejslodki@op.pl
- Department of Prenatal Cardiology, Polish Mother's Memorial Hospital Research Institute
autor
- Department of Prenatal Cardiology, Polish Mother's Memorial Hospital Research Institute
- Department of Genetics, Polish Mother's Memorial Hospital Research Institute
autor
- Department of Prenatal Cardiology, Polish Mother's Memorial Hospital Research Institute
- Department of Diagnoses and Prevention Fetal Malformations Medical University of Lodz
Bibliografia
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- 3. Szymkiewicz-Dangel J: Kardiologia Płodu. Zasady diagnostyki i terapii; Poznań; Ośrodek Wydawnictw Naukowych; 2007
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- 6. Słodki M: Opracowanie modelu opieki nad ciężarną z wrodzoną wadą serca u płodu na podstawie nowego prenatalnego podziału wad serca. Rozprawa habilitacyjna. Wydawnictwo PWSZ; 2012
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- 9. Zidere V ,Pushparajah K, Allan L D, Simpson J M : Three-dimensional fetal echocardiography for predictionof postnatal surgical approach in double outlet rightventricle: a pilot study; Ultrasound Obstet Gynecol;2013; 42: 421-425
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- 21. Allan LD, Sharland GK, Chita SK, Lockhart S, Maxwell DJ: Chromosomal anomalies in fetal congenital heart disease; Ultrasound Obstet Gynecol;1991;1:8-11[Crossref]
- 22. Khositseth A, Tocharoentanaphol C, Khowsathit P, Ruangdaraganon N: Chromosome 22q11 deletions in patients with conotruncal heart defects; Pediatr Cardiol;2005;26:570-573
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- 29. Bradley TJ, Karamlou T, Kulik A, et al.: Determinants of repair type, reintervention, and mortality in 393 children with double- outlet right ventricle; J Thorac Cardiovasc Surg 2007; 134: 967-973[WoS]
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- 31. Baslaim GM: Is preoperative delineation of coronary artery pattern a prerequisite for arterial switch operation? J Card Surg 2006; 21: 465-470[Crossref]
- 32. Uemura H, Yagihara T, Kadohama T, Kawahira Y, Yoshikawa Y: Repair of double outlet right ventricle with doubly-committed ventricular septal defect; Cardiol Young 2001; 11: 415-419[Crossref]
- 33. Belli E, Serraf A, Lacour-Gayet F, et al: Double-outlet right ventricle with non-committed ventricular septal defect; Eur J Cardiothorac Surg 1999; 15: 747-752[Crossref]
- 34. Barbero-Marcial M, Tamanati C, Jatene MB, et al: Double-outlet right ventricle with nonrelated ventricular septal defect: surgical results using the multiple patches technique. Heart Surg Forum 1998; 1: 125-129
Typ dokumentu
Bibliografia
Identyfikatory
DOI
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_12847_09142