Dexamethasone Given to Premature Infants and Cardiac Diastolic Function in Early Childhood

Objectives To determine if dexamethasone given to premature infants with bronchopulmonary dysplasia would result in cardiac diastolic dysfunction in early childhood, a topic unstudied in humans. Study design We compared seven children ages 3 to 8 years born at 26 weeks’ gestation and given dexametha...

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Veröffentlicht in:The Journal of pediatrics 2011-08, Vol.159 (2), p.227-231
Hauptverfasser: Wong, Ivan H.-B., BSc, Digby, Alyson M., BSc, Warren, Andrew E., MD, Pepelassis, Dion, MD, Vincer, Michael, MD, Chen, Robert P.-C., MD
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container_end_page 231
container_issue 2
container_start_page 227
container_title The Journal of pediatrics
container_volume 159
creator Wong, Ivan H.-B., BSc
Digby, Alyson M., BSc
Warren, Andrew E., MD
Pepelassis, Dion, MD
Vincer, Michael, MD
Chen, Robert P.-C., MD
description Objectives To determine if dexamethasone given to premature infants with bronchopulmonary dysplasia would result in cardiac diastolic dysfunction in early childhood, a topic unstudied in humans. Study design We compared seven children ages 3 to 8 years born at 26 weeks’ gestation and given dexamethasone for bronchopulmonary dysplasia with eight gestation-matched and age-matched control children using echocardiography to assess measures of systolic and diastolic function. All dexamethasone patients had resolved hypertrophic cardiomyopathy. Results Dexamethasone patients had the same normal τ and isovolumic relaxation time (24.9 ± 2.8 and 54.6 ± 6.3 ms) as control patients (22.1 ± 3.0 and 48.8 ± 6.7 ms). Peak A velocities were the same in dexamethasone patients as in control patients (59.5 ± 15 versus 49.4 ± 5.8 cm/s, P = .10), resulting in unchanged E:A ratios (1.89 ± 0.57 versus 2.15 ± 0.43, P = .22). Peak E velocity and E-wave deceleration times were not different. We found no significant differences in measures of systolic function (heart rate–corrected velocity of circumferential fiber shortening, wall stress, and ejection fraction). Left ventricular mass was the same between the groups confirming resolution of hypertrophic cardiomyopathy. Conclusions These data are consistent with normal myocardial relaxation, suggesting that long-term diastolic function is reassuringly normal in children who received dexamethasone as premature infants with resolution of hypertrophic cardiomyopathy.
doi_str_mv 10.1016/j.jpeds.2011.01.008
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Study design We compared seven children ages 3 to 8 years born at 26 weeks’ gestation and given dexamethasone for bronchopulmonary dysplasia with eight gestation-matched and age-matched control children using echocardiography to assess measures of systolic and diastolic function. All dexamethasone patients had resolved hypertrophic cardiomyopathy. Results Dexamethasone patients had the same normal τ and isovolumic relaxation time (24.9 ± 2.8 and 54.6 ± 6.3 ms) as control patients (22.1 ± 3.0 and 48.8 ± 6.7 ms). Peak A velocities were the same in dexamethasone patients as in control patients (59.5 ± 15 versus 49.4 ± 5.8 cm/s, P = .10), resulting in unchanged E:A ratios (1.89 ± 0.57 versus 2.15 ± 0.43, P = .22). Peak E velocity and E-wave deceleration times were not different. We found no significant differences in measures of systolic function (heart rate–corrected velocity of circumferential fiber shortening, wall stress, and ejection fraction). Left ventricular mass was the same between the groups confirming resolution of hypertrophic cardiomyopathy. Conclusions These data are consistent with normal myocardial relaxation, suggesting that long-term diastolic function is reassuringly normal in children who received dexamethasone as premature infants with resolution of hypertrophic cardiomyopathy.</description><identifier>ISSN: 0022-3476</identifier><identifier>EISSN: 1097-6833</identifier><identifier>DOI: 10.1016/j.jpeds.2011.01.008</identifier><identifier>PMID: 21397911</identifier><identifier>CODEN: JOPDAB</identifier><language>eng</language><publisher>Maryland Heights, MO: Elsevier Inc</publisher><subject>Biological and medical sciences ; bronchopulmonary dysplasia ; Bronchopulmonary Dysplasia - complications ; Bronchopulmonary Dysplasia - drug therapy ; cardiomyopathy ; Cardiomyopathy, Hypertrophic - drug therapy ; Cardiomyopathy, Hypertrophic - etiology ; Cardiomyopathy, Hypertrophic - physiopathology ; Child ; Child, Preschool ; childhood ; children ; dexamethasone ; Dexamethasone - administration &amp; dosage ; Diastole ; echocardiography ; Female ; Follow-Up Studies ; General aspects ; Glucocorticoids - administration &amp; dosage ; heart ; Humans ; Infant ; Infant, Newborn ; Infant, Premature ; Infant, Premature, Diseases - drug therapy ; infants ; Intensive Care Units, Neonatal ; Male ; Medical sciences ; Myocardial Contraction - drug effects ; patients ; Pediatrics ; pregnancy ; Recovery of Function ; Retrospective Studies ; Time Factors ; Treatment Outcome ; Ventricular Function - drug effects ; Ventricular Function - physiology</subject><ispartof>The Journal of pediatrics, 2011-08, Vol.159 (2), p.227-231</ispartof><rights>Mosby, Inc.</rights><rights>2011 Mosby, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Mosby, Inc. 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Study design We compared seven children ages 3 to 8 years born at 26 weeks’ gestation and given dexamethasone for bronchopulmonary dysplasia with eight gestation-matched and age-matched control children using echocardiography to assess measures of systolic and diastolic function. All dexamethasone patients had resolved hypertrophic cardiomyopathy. Results Dexamethasone patients had the same normal τ and isovolumic relaxation time (24.9 ± 2.8 and 54.6 ± 6.3 ms) as control patients (22.1 ± 3.0 and 48.8 ± 6.7 ms). Peak A velocities were the same in dexamethasone patients as in control patients (59.5 ± 15 versus 49.4 ± 5.8 cm/s, P = .10), resulting in unchanged E:A ratios (1.89 ± 0.57 versus 2.15 ± 0.43, P = .22). Peak E velocity and E-wave deceleration times were not different. We found no significant differences in measures of systolic function (heart rate–corrected velocity of circumferential fiber shortening, wall stress, and ejection fraction). Left ventricular mass was the same between the groups confirming resolution of hypertrophic cardiomyopathy. 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Study design We compared seven children ages 3 to 8 years born at 26 weeks’ gestation and given dexamethasone for bronchopulmonary dysplasia with eight gestation-matched and age-matched control children using echocardiography to assess measures of systolic and diastolic function. All dexamethasone patients had resolved hypertrophic cardiomyopathy. Results Dexamethasone patients had the same normal τ and isovolumic relaxation time (24.9 ± 2.8 and 54.6 ± 6.3 ms) as control patients (22.1 ± 3.0 and 48.8 ± 6.7 ms). Peak A velocities were the same in dexamethasone patients as in control patients (59.5 ± 15 versus 49.4 ± 5.8 cm/s, P = .10), resulting in unchanged E:A ratios (1.89 ± 0.57 versus 2.15 ± 0.43, P = .22). Peak E velocity and E-wave deceleration times were not different. We found no significant differences in measures of systolic function (heart rate–corrected velocity of circumferential fiber shortening, wall stress, and ejection fraction). Left ventricular mass was the same between the groups confirming resolution of hypertrophic cardiomyopathy. Conclusions These data are consistent with normal myocardial relaxation, suggesting that long-term diastolic function is reassuringly normal in children who received dexamethasone as premature infants with resolution of hypertrophic cardiomyopathy.</abstract><cop>Maryland Heights, MO</cop><pub>Elsevier Inc</pub><pmid>21397911</pmid><doi>10.1016/j.jpeds.2011.01.008</doi><tpages>5</tpages></addata></record>
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subjects Biological and medical sciences
bronchopulmonary dysplasia
Bronchopulmonary Dysplasia - complications
Bronchopulmonary Dysplasia - drug therapy
cardiomyopathy
Cardiomyopathy, Hypertrophic - drug therapy
Cardiomyopathy, Hypertrophic - etiology
Cardiomyopathy, Hypertrophic - physiopathology
Child
Child, Preschool
childhood
children
dexamethasone
Dexamethasone - administration & dosage
Diastole
echocardiography
Female
Follow-Up Studies
General aspects
Glucocorticoids - administration & dosage
heart
Humans
Infant
Infant, Newborn
Infant, Premature
Infant, Premature, Diseases - drug therapy
infants
Intensive Care Units, Neonatal
Male
Medical sciences
Myocardial Contraction - drug effects
patients
Pediatrics
pregnancy
Recovery of Function
Retrospective Studies
Time Factors
Treatment Outcome
Ventricular Function - drug effects
Ventricular Function - physiology
title Dexamethasone Given to Premature Infants and Cardiac Diastolic Function in Early Childhood
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