High Incidence of Cranial Ultrasound Abnormalities in Full-Term Infants with Congenital Heart Disease

1996 ◽  
Vol 13 (01) ◽  
pp. 47-53 ◽  
Author(s):  
John van Houten ◽  
Abraham Rothman ◽  
Raul Bejar
PEDIATRICS ◽  
1955 ◽  
Vol 15 (2) ◽  
pp. 169-179
Author(s):  
Mary R. Richards ◽  
Katharine K. Merritt ◽  
Mary H. Samuels ◽  
Alfred G. Langmann

The frequency of cardiac murmurs in early infancy has been studied in a large series of unselected infants. In the immediate postnatal examination, a murmur was heard in 1.7 per cent. With repeated examinations, however, at 6 and at 12 months of age, the proportion of infants in whom a cardiac murmur was heard at some time rose to 7.0 per cent of 5,017 full-term singlebirth infants and to 9.9 per cent of 364 premature single-birth infants. Non-white infants had a significantly higher prevalence of murmurs than did white infants at both the 6 and 12 month examinations. Of the 71 full-term infants who had murmurs at the birth examination and were re-examined at both 6 and 12 months, 49 (69 per cent) had no murmurs at either of the later examinations. Of the 150 full-term infants who had murmurs heard for the first time at 6 months and were re-examined at 12 months, 90 (60 per cent) had no murmur at the 12-month examination. Of the total number of 353 murmurs heard in full-term infants, 166 were ultimately interpreted to be functional, and 25 to be organic murmurs. The remaining 162 were inconstantly present, and were probably all functional murmurs. In our experience, a murmur heard at birth carries a 1:12 probability of congenital heart disease; if it is again heard at 6 months, this chance is 1:3; and if the murmur persists to 12 months, the chance is 3:5 that congenital heart disease is present. When a murmur is first heard at 6 months, and persists until 12 months, the probability of congenital heart disease is 1:7; and when a murmur is first heard at 12 months, the probability falls to 1:50. Premature infants were found to be similar to full-term infants in all respects, insofar as their small numbers made comparisons possible. Finally, the relative rarity of cardiac murmurs in the newborn period has been demonstrated once more.


2021 ◽  
Vol 1 (3) ◽  
pp. 414
Author(s):  
Franco Benvenuto ◽  
LuisDiaz Gonzalez ◽  
MaríaCeleste Mansilla ◽  
Adriana Fandiño

PEDIATRICS ◽  
1969 ◽  
Vol 43 (5) ◽  
pp. 757-758
Author(s):  
A. M. R.

Respiratory distress is a very frequent symptom in infants with acyanotic congenital heart disease. Some of the specific physiological and pathological mechanisms involved in this association have been presented in Pediatrics.1 That communication stressed the frequency with which cardiac failure associated with large left-to-right shunts presents with respiratory distress, often misinterpreted as being due to pulmonary disease. It has, however, also been long recognized that there is a high incidence of pulmonary infection in infants with large left-to-right shunt lesions. The cause of these frequent infections in such patients is not yet evident, but a possible explanation now seems to be suggested from recent observations at autopsy.


2007 ◽  
Vol 94 (11) ◽  
pp. 1597-1603 ◽  
Author(s):  
ARJAN B. TE PAS ◽  
GERDA WEZEL-MEIJLER ◽  
REGINA BÖKENKAMP-GRAMANN ◽  
FRANS J. WALTHER

2011 ◽  
Vol 196 (3) ◽  
pp. W326-W329 ◽  
Author(s):  
Karen I. Norton ◽  
Bellipady Rai ◽  
Hemali Desai ◽  
David Brown ◽  
Morris Cohen

2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Alexandre Lapillonne ◽  
Antoine Regnault ◽  
Véronique Gournay ◽  
Jean-Bernard Gouyon ◽  
Hélène Gilet ◽  
...  

2015 ◽  
Vol 57 (7) ◽  
pp. 639-644 ◽  
Author(s):  
Beatrice Latal ◽  
Christian Kellenberger ◽  
Anastasia Dimitropoulos ◽  
Cornelia Hagmann ◽  
Christian Balmer ◽  
...  

2020 ◽  

Objectives: To evaluate preoperative neurological abnormalities in term newborns with critical congenital heart disease (CHD) and to study relationships among the neurological abnormalities, CHD type and clinical characteristics in the group. Methods: Term newborns with critical CHD without genetic disorders were retrospectively studied. Neurological abnormalities were grouped according to Amiel-Tison neurological assessment (ATNA). CHD was categorized into five subgroups according to the physiological presentation. Results: In the period observed 190 newborns with critical CHD were admitted. Of 134 who met the inclusion criteria, ATNA was optimal in 64%; in 28.5% it was mildly, in 6.5% moderately, and in 1% severely abnormal. The difference in the frequency of abnormal ATNA between the five CHD subgroups was not statistically significant (p = 0.098). A weak association was identified between CHD subgroups and an abnormal ATNA (contingency coefficient 0.246). Newborns with abnormal ATNA had more often SpO2 < 92% (p = 0.028) and abnormal results of cerebral ultrasound (p = 0.001). Conclusion: This study establishes the value of Amiel-Tison standardized neurological examination in assessing the risk of neurodevelopmental disorders among newborns with CHD. We found preoperative neurological abnormalities in one-third of newborns with CHD, and the grade of abnormalities was generally mild or moderate. Newborns with an abnormal ATNA more frequently presented an oxygen saturation < 92% and abnormal results on the cranial ultrasound.


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