A case series of three patients with unilateral disconnected pulmonary artery supplied by an ipsilateral patent ductus arteriosus: neonatal ductal stenting as palliation to preserve pulmonary arterial patency

التفاصيل البيبلوغرافية
العنوان: A case series of three patients with unilateral disconnected pulmonary artery supplied by an ipsilateral patent ductus arteriosus: neonatal ductal stenting as palliation to preserve pulmonary arterial patency
المؤلفون: James R. Bentham, Nicholas Hayes, Andrew B. Ho, John Thomson, Ines Hribernik, Tony Salmon
المصدر: European Heart Journal: Case Reports
بيانات النشر: Oxford University Press (OUP), 2020.
سنة النشر: 2020
مصطلحات موضوعية: medicine.medical_specialty, Stenting, Context (language use), 030204 cardiovascular system & hematology, 03 medical and health sciences, 0302 clinical medicine, Patent arterial duct, Internal medicine, Ductus arteriosus, medicine.artery, Medicine, Ventricular outflow tract, Case Series, AcademicSubjects/MED00200, Tetralogy of Fallot, Aorta, Lung, business.industry, Congenital Heart Disease, medicine.disease, Pulmonary hypertension, Pulmonary artery, medicine.anatomical_structure, 030228 respiratory system, Cardiology, Cardiology and Cardiovascular Medicine, business
الوصف: Background Disconnected branch pulmonary arteries with a systemic arterial origin of the disconnected vessel is a rare, but well-described entity. Most will have ductal tissue connecting the pulmonary artery to the aorta. Case summary We describe in this paper the haemodynamic result in three neonates presenting with ductal origin of a single branch pulmonary artery in the context of trans-catheter stenting procedures to maintain or re-recruit vessel patency. All were faced with potential or actual ductal closure and proceeded to trans-catheter stenting to re-cannalate the duct-dependent pulmonary artery. Two patients with otherwise normal anatomy struggled post-procedure with pulmonary hypertension and right ventricular dilatation. Both required surgical re-anastomosis of the disconnected pulmonary artery during the same admission—one 26 days post-stenting following failure to wean from high-flow respiratory support and the second 8 days post-stenting following failed extubation. In contrast, a patient with tetralogy of Fallot born at 2.5 kg underwent sequential stenting of the right ventricular outflow tract and then the left-sided ductus. He had a good post-procedural course and thrived for several months before complete repair. Discussion We describe the clinical courses and discuss the resultant haemodynamics, highlighting the importance of flow to each lung, the resulting haemodynamic implications and the compounding effects of additional lesions.
تدمد: 2514-2119
DOI: 10.1093/ehjcr/ytaa422
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7169dbdd20c3c90614228fa22cc46346
https://doi.org/10.1093/ehjcr/ytaa422
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....7169dbdd20c3c90614228fa22cc46346
قاعدة البيانات: OpenAIRE
الوصف
تدمد:25142119
DOI:10.1093/ehjcr/ytaa422