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العنوان
Pulmonary Artery Pressure Changes in Neonates/
المؤلف
Hussein,Dina Mohammed Abdo
هيئة الاعداد
باحث / دينا محمد عبده حسين
مشرف / عليـــاء آمـــال قطبـــي
مشرف / أمنيــة إبراهيم يوسـف
مشرف / غادة أحمد صالح
تاريخ النشر
2017
عدد الصفحات
133.p:
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
طب الأطفال ، الفترة المحيطة بالولادة وصحة الطفل
تاريخ الإجازة
1/1/2017
مكان الإجازة
جامعة عين شمس - كلية الطب - Pediatrics
الفهرس
Only 14 pages are availabe for public view

from 135

from 135

Abstract

Directly after birth, major changes in the respiratory and cardiovascular systems are required for postnatal survival, a dramatic reduction in pulmonary arterial pressure and resistance occurs with an increase in oxygen tension and blood flow. Circulatory physiology of the newborn goes through complex transitions in order to shift the respiratory function from the placenta to the lungs, characterized by the closure of fetal shunts, expansion of the lungs, and removal of placental circulation.
Pulmonary hypertension presenting in the neonatal period can be due to persistent pulmonary hypertension of the newborn (PPHN), high output cardiac failure from large arteriovenous malformations and congenital heart malformations. Persistent exposure of the pulmonary vasculature to increased blood flow and pressure in patients with congenital heart diseases with left- to- right (systemic -to- pulmonary) shunts may result in vascular remodelling and dysfunction.
Estimates of pulmonary artery pressure obtained using transthoracic echocardiography (TTE) are most commonly performed using continuous-wave Doppler to measure the maximum velocity of tricuspid regurgitation (TRVmax). This technique of pulmonary artery pressure quantification has been widely adopted for clinical and research purposes because it provides a noninvasive, direct estimate of right ventricular (RV) systolic pressure (RVSP) that correlates closely with invasive hemodynamic measurement.