Results 111 to 120 of about 73,086 (343)

Comparison of two dose regimens of ibuprofen for the closure of patent ductus arteriosus in preterm newborns,

Jornal de Pediatria, 2016
Objective: To compare the efficacy of intravenous ibuprofen at high (20-10-10 mg/kg/dose) and low doses (10-5-5 mg/kg/dose) the closure of patent ductus arteriosus in preterm newborns.
Laura Vargas Dornelles, Andréa Lúcia Corso, Rita de Cássia Silveira, Renato Soibelmann Procianoy   +3 more
doaj   +1 more source

Prone Positioning Was Associated With Less Hypoxemic Events and Improved Feeding Tolerance in Preterm Infants

Acta Paediatrica, EarlyView.
ABSTRACT Aim Cardiorespiratory events such as apnea, bradycardia and hypoxemia are common in preterm infants and may contribute to an impaired neurodevelopmental outcome. We hypothesised a significant reduction in the incidence of hypoxemia, bradycardia and gastric residuals in the prone position.
Bettina Bohnhorst, Eva Lutz, Sabine Pirr, Corinna Peter, Carolin Böhne   +4 more
wiley   +1 more source

Percutaneous Patent Ductus Arteriosus (PDA) Closure in Very Preterm Infants: Feasibility and Complications

Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease, 2016
Percutaneous closure of patent ductus arteriosus (PDA) in term neonates is established, but data regarding outcomes in infants born very preterm (
C. Backes, S. Cheatham, G. Deyo, S. Leopold, M. Ball, Charles V Smith, V. Garg, R. Holzer, J. Cheatham, D. Berman   +9 more
semanticscholar   +1 more source

Cardiac involvement of primary hyperoxaluria accompanied by non-compaction cardiomyopathy and patent ductus arteriosus

Türk Kardiyoloji Derneği Arşivi, 2015
Primary hyperoxaluria is a rare hereditary metabolic disorder resulting in accumulation of calcium oxalate in visceral organs, including the heart. We report a 19-year-old male with non- compaction cardiomyopathy combined with patent ductus arteriosus ...
Nurcan Arat, Murat Akyıldız, Gürkan Tellioğlu, Yaman Tokat   +3 more
doaj   +1 more source

Spontaneous Intestinal Perforation in Extremely Premature Infants Exposed to Early Low‐Dose Hydrocortisone

Acta Paediatrica, EarlyView.
ABSTRACT Aim To assess the occurrence of spontaneous intestinal perforation (SIP) in < 28 weeks' gestational age (GA) infants exposed to early low‐dose hydrocortisone (ELH) to reduce the risk of bronchopulmonary dysplasia (BPD). Additionally, the risk of SIP was assessed in infants exposed to early concomitant treatment with ibuprofen for persistent ...
Gilles Cambonie, Anais Jouffrey, Benoit Tessier, Clémentine Combes, Angelo Polito, Arthur Gavotto   +5 more
wiley   +1 more source

Evolução ecocardiográfica de recém-nascidos com persistência do canal arterial Echocardiographic post-neonatal progress of preterm neonates with patent ductus arteriosus

Jornal de Pediatria, 2005
OBJETIVO: Analisar características ecocardiográficas e manifestações clínicas na evolução de recém-nascidos pré-termo com persistência do canal arterial e identificar indicadores mais confiáveis do fechamento espontâneo deste.
Jorge Yussef Afiune, Julio M. Singer, Cléa Rodrigues Leone   +2 more
doaj   +1 more source

Cerebral Oxygenation During Transition and Amplitude‐Integrated Electroencephalography Signals: An Ancillary Study to the COSGOD‐III Trial

Acta Paediatrica, EarlyView.
ABSTRACT Aim The COSGOD III trial was designed to guide oxygen delivery by cerebral near infrared spectroscopy (NIRS) in preterm neonates during the immediate transition after birth and showed a non‐significant increase of 4.3% in survival without cerebral injury compared to the control group.
Christina Schreiner, Katharina Goeral, Marlene Hammerl, Katrin Klebermass‐Schrehof, Alexander Avian, Vera Neubauer, Ursula Kiechl‐Kohlendorfer, Daniel Pfurtscheller, Elke Griesmaier, Gerhard Pichler   +9 more
wiley   +1 more source

Yunis Varon Syndrome [PDF]

, 2010
We have reported a case of Yunis-Varon syndrome which is a rare, autosomal recessive syndrome characterized by growth retardation, defective growth of the cranial bones, characteristic facial features, abnormalities of the fingers and/or toes ...
Dal, SI, Parmar, P
core   +1 more source

Aarskog Syndrome: Deep Phenotyping and Genomic Landscape of a New Cohort Including Adult Patients

Clinical Genetics, EarlyView.
This study presents the deep phenotyping data of 14 new Aarskog‐Scott syndrome patients with molecular confirmation. ABSTRACT Aarskog‐Scott syndrome (AAS, MIM#305400) is an X‐linked disorder characterized by recognizable facial features, short stature, and genitourinary and skeletal malformations.
Gozde Tutku Turgut, Umut Altunoglu, Şahin Avcı, Tuğba Kalaycı, Ayça Dilruba Aslanger, Volkan Karaman, Zehra Oya Uyguner, Hülya Kayserili   +7 more
wiley   +1 more source

A promising, novel index in the diagnosis and follow‐up of patent ductus arteriosus: Red cell distribution width‐to‐platelet ratio

Journal of clinical laboratory analysis (Print), 2018
The role of red cell distribution width‐to‐platelet ratio (RPR) has not previously been mentioned in reports on patent ductus arteriosus (PDA).
Buse Özer Bekmez, C. Tayman, Mehmet Büyüktiryaki, A. Çetinkaya, U. Çakır, Turan Derme   +5 more
semanticscholar   +1 more source