Patent ductus arteriosus in hyaline membrane disease: chest radiography

1980 ◽  
Vol 135 (2) ◽  
pp. 307-309 ◽  
Author(s):  
TL Slovis ◽  
S Shankaran
1989 ◽  
Vol 26 (6) ◽  
pp. 565-566 ◽  
Author(s):  
Senji Shimada ◽  
Tonse N K Raju ◽  
Rama Bhat ◽  
Haruo Maeta ◽  
Dharmapuri Vidyasagar

1977 ◽  
Vol 11 (4) ◽  
pp. 401-401
Author(s):  
Andrew R Stewart ◽  
Robert Moriarty ◽  
Orest O Ulan ◽  
Nell N Finer ◽  
P Schiff

1978 ◽  
Vol 130 (6) ◽  
pp. 1149-1151 ◽  
Author(s):  
B Burney ◽  
WL Smith ◽  
EA Franken ◽  
JA Smith ◽  
EC Klatte

1987 ◽  
Vol 15 (6) ◽  
pp. 587-590 ◽  
Author(s):  
BRADLEY A. YODER ◽  
THOMAS J. KUEHL ◽  
ROBERT A DE LEMOS ◽  
DONALD M. NULL ◽  
NEEL B. ACKERMAN

PEDIATRICS ◽  
1994 ◽  
Vol 94 (5) ◽  
pp. 776-777
Author(s):  
John Q. Buchheit ◽  
Dan L. Stewart

We appreciate the comments of Drs The', Young, and Rosser regarding our article on localized intestinal perforation in neonates. Our cases appear to differ from those reported by Lloyd1 in 1979 in that approximately one-half of those cases were gastric perforations that were excluded from our study. Also, in the Lloyd series, very little clinical information is provided regarding associated disease states (ie, hyaline membrane disease or patent ductus arteriosus), maternal history, medications used, feeding history, exchange transfusions, or Apgar scores.


PEDIATRICS ◽  
1985 ◽  
Vol 75 (6) ◽  
pp. 1132-1142 ◽  
Author(s):  
D. Vidyasagar ◽  
H. Maeta ◽  
T. N.K. Raju ◽  
E. John ◽  
R. Bhat ◽  
...  

As a prelude to clinical trials with a bovine surfactant (surfactant TA), in human infants with hyaline membrane disease, pulmonary and hemodynamic changes following its instillation in premature baboons were investigated. Baboons, delivered by cesarean section at 141 ± 3.5 days (mean ± SD, 77% gestation), were provided with intensive care. At 2 hours of age in one group (n = 10), 100 mg/kg of surfactant TA (reconstituted bovine surfactant, Tokyo Tanabe Co., Tokyo) was instilled into the lungs. Sequential measurements and monitoring of pulmonary and hemodynamic variables were carried out in these ten baboons and in a control group of five baboons for 16 hours, at which time the experiments were electively terminated. At birth, the pulmonary compliance, findings of chest radiographs, ratio of arterial Po2 to alveolar Po2, and respirator variables needed to maintain normal blood gas and acid base status were identical in both groups and indicative of severe hyaline membrane disease. Following surfactant instillation, the treated group demonstrated a rapid increase in Po2 with significantly improved ratio of arterial Po2 to alveolar Po2 (from a mean ± SD pretreatment value of 0.21 ± 0.11 to 0.45 ± 0.11 by 16 hours). Pulmonary compliance improved similarly (from pretreatment value of 0.18 ± 0.06 mL/cm H2O/kg to 0.27 ± 0.09 mL/cm H2O/kg). Significant reduction in respirator support variables could be achieved in all treated animals; however, in the control animals, the pulmonary status worsened as evidenced by increasing mean airway pressure and respirator variables to keep normal blood gas and acid base status, thus worsening compliance. At autopsy, pulmonary pressure-volume curves were significantly different with large hysteresis obtained in the surfactant-treated group. Although no deleterious effect on hemodynamics was noted in surfactant TA-treated animals, a large patent ductus arteriosus was demonstrated by aortography. Increased lung blood flow, probably due to a large patent ductus arteriosus flow, was demonstrated by radiolabeled microsphere technique. The physiologic significance and clinical relevance of these findings in premature baboons treated with surfactant TA are discussed.


2014 ◽  
Vol 54 (3) ◽  
pp. 132 ◽  
Author(s):  
Novia Bernati ◽  
Ria Nova ◽  
Julniar M. Tasli ◽  
Theodorus Theodorus

Background The reported prevalences of patent ductus arteriosus(PDA) in preterm neonates vaty, and are currently unknown inPalembang. Birth weight, ges tational age, asphyxia, histoty ofantenatal steroid use, hyaline membrane disease (HMD), raceand ethnicity, are potential risk factors for PDA.Objective To determine the prevalence of PDA and its riskfactors in preterm neonates at Mohammad Hoesin Hospital,Palembang.Methods This cross-sectional study was conducted from October2011 to April 2012. Echocardiographic examinations wereperformed on 242 preterm neonates aged 15 hours to 7 days. Datawas taken from medical records and interviews, and analyzed byChi square and logistic regression analyses.Results Patent ductus arteriosus was found in 142 (58.7%)preterm neonates with a prevalence ratio of 1.43. Neonates withbirthweight ::;;2,000 grams tended to have 1.9 (95% CI 1.17 to3.32) rimes higher risk for PDA (P=0.01). Neonates ::;;JO weeksgestation were also at 1.9 rimes higher risk for PDA (P=0.16).Probabilities for PDA occurrence in neonates with asphyxia,without antenatal corticosteroids and HMD were 1.6 (95%CI 1.13 to 3.36) rimes, 1.3 (95%CI 0.73 to 2.50) times and 2.2(95%CI 1.29 to 3.72) rimes higher risk for PDA, respectively(P=0.22, 0.41, and 0.005, respectively).Conclusion Birth weight and HMD are statistically significantrisk factors of PDA, but the more significant one is HMD.


2021 ◽  
Vol 25 (1) ◽  
Author(s):  
Tengku A. Raja Mamat ◽  
Khairil A. Sayuti ◽  
Chandran Nadarajan ◽  
Mohd R. Mohd Zain

Pulmonary underdevelopment is a rare congenital disease which manifests as persistent hemithorax opacification at chest radiography. We present three patients with different types of pulmonary underdevelopment, their imaging features and associated anomalies. Case 1 is a premature neonate with persistent respiratory distress. Further imaging confirmed right pulmonary hypoplasia, associated with a patent foramen ovale, patent ductus arteriosus and vertebral anomalies. Case 2 is a 6-year-old child with corrected anorectal malformation, and recurrent pneumonia. Further imaging confirmed left pulmonary aplasia, associated with an aberrant right subclavian artery and vertebral anomaly. Case 3 is a full term neonate who developed excessive drooling of saliva and respiratory distress. Further imaging confirmed right pulmonary agenesis, associated with an atrial septal defect, patent ductus arteriosus and tracheo-oesophageal fistula. Pulmonary underdevelopment is classified into three types: hypoplasia, aplasia and agenesis. The majority of them have associated anomalies. This condition should be considered a differential diagnosis in paediatric patients with an opaque hemithorax on chest radiography.


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