Assessment of Right Heart Functions in Children with Mild Cystic Fibrosis

Guliyeva A., ÇAKIR E., Yazan H., AlShadfan L., SHARIFOV R., OTÇU TEMUR H., ...Daha Fazla

KLINISCHE PADIATRIE, cilt.233, sa.05, ss.231-236, 2021 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 233 Sayı: 05
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1055/a-1341-1698
  • Dergi Adı: KLINISCHE PADIATRIE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, CAB Abstracts, EMBASE, MEDLINE
  • Sayfa Sayıları: ss.231-236
  • Anahtar Kelimeler: Cystic fibrosis, Pulmonary hypertension, Pulmonary function test, Cor Pulmonale, Childhood Age Group, Mukoviszidose, Pulmonale Hypertonie, Lungenfunktionstest, Cor Pulmonale, Altersgruppe der Kinder
  • Dokuz Eylül Üniversitesi Adresli: Hayır

Özet

Background Cystic fibrosis (CF) is a multisystemic disease that prevalently involves the lungs. Hypoxemia occurs due to the existing of progressive damage to the pulmonary parenchyma and pulmonary vessels. The condition may cause systolic and diastolic dysfunction to the right ventricle due to the effects of high pulmonary artery systolic pressure (PASP). The study aimed to determine echocardiographic alterations in PASP, right ventricle (RV) anatomy, and functions in mild CF children.