Cardiac effects of short course dexamethasone in preterm infants

被引:51
作者
Skelton, R
Gill, AB
Parsons, JM
机构
[1] Leeds Gen Infirm, Peter Congden Neonatal Intens Care Unit, Clarendon Wing, Leeds LS2 9NS, W Yorkshire, England
[2] Killingbeck Hosp, Leeds LS14 6UQ, W Yorkshire, England
来源
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION | 1998年 / 78卷 / 02期
关键词
dexamethasone; chronic lung disease; left ventricular hypertrophy; echocardiography;
D O I
10.1136/fn.78.2.F133
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Aim-To examine the incidence and natural history of left ventricular hypertrophy (LVH) associated with the shorter 2-3 week course of dexamethasone, now more usual, for chronic lung disease. Method-Thirty one infants, gestational age 23-34 (median 26) weeks, birthweight 500-2054 (median 815) g, received dexamethasone, starting at 0.4-0.6 mg/kg/day, at a median of 11 days of age (range 2-34), weaning over a period of 2-3 weeks. Eighteen preterm neonates were studied as controls over a similar time period. Serial echocardiographic measurements of end diastolic interventricular septum (IVSd) and left ventricular posterior wall (LVPWd) thicknesses were taken before, and up to 48 days after, starting dexamethasone. Maximum Doppler blood flow velocities from the left ventricular outflow tract (LVOT) were measured. Results-Left ventricular hypertrophy (LVH) occurred in 29 babies (94%). Median hypertrophy of the IVSd in those receiving dexamethasone was 67% and LVPWd 56% of baseline measurements, significantly greater than control infants (p<0.001). LVH appeared by a median of three days, peaking by a median of 10 days. All resolved by a median of 27 days. LVOT obstruction was not seen. There was no significant correlation with birthweight, gestation, blood pressure, or glucose tolerance. Conclusions-LVH developed in almost all preterm neonates receiving a 2-3 week course of dexamethasone, but was of little clinical importance and always resolved. Echocardiography is probably not required routinely in infants receiving such short course dexamethasone for chronic lung disease.
引用
收藏
页码:F133 / F137
页数:5
相关论文
共 24 条
  • [1] Bensky AS, 1996, PEDIATRICS, V97, P818
  • [2] STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT
    BLAND, JM
    ALTMAN, DG
    [J]. LANCET, 1986, 1 (8476) : 307 - 310
  • [3] HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY AS A SIDE-EFFECT OF DEXAMETHASONE TREATMENT FOR BRONCHOPULMONARY DYSPLASIA
    BRAND, PLP
    VANLINGEN, RA
    BRUS, F
    TALSMA, MD
    ELZENGA, NJ
    [J]. ACTA PAEDIATRICA, 1993, 82 (6-7) : 614 - 617
  • [4] CARDIAC SEPTAL HYPERTROPHY IN HYPERINSULINEMIC INFANTS
    BREITWESER, JA
    MEYER, RA
    SPERLING, MA
    TSANG, RC
    KAPLAN, S
    [J]. JOURNAL OF PEDIATRICS, 1980, 96 (03) : 535 - 539
  • [5] CATABOLIC EFFECT OF DEXAMETHASONE IN THE PRETERM BABY
    BROWNLEE, KG
    NG, PC
    HENDERSON, MJ
    SMITH, M
    GREEN, JH
    DEAR, PRF
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1992, 67 (01): : 1 - 4
  • [6] DISPROPORTIONATE SEPTAL HYPERTROPHY ASSOCIATED WITH ERYTHROBLASTOSIS-FETALIS
    CARTER, BS
    DIGIACOMO, JE
    BALDERSTON, SM
    WIGGINS, JW
    MERENSTEIN, GB
    [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1990, 144 (11): : 1225 - 1228
  • [7] Ehrenkranz Richard A., 1992, P399
  • [8] CARDIOVASCULAR EFFECTS OF DEXAMETHASONE IN THE PRETERM INFANT
    EVANS, N
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1994, 70 (01): : F25 - F30
  • [9] FEIGENBAUM H, 1994, ECHOCARDIOGR-J CARD, P511
  • [10] HYPERINSULINEMIC, HYPERTROPHIC CARDIOMYOPATHY IN INFANCY
    FOX, LA
    GEFFNER, ME
    ALKHATIB, Y
    KAPLAN, S
    [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1992, 146 (08): : 896 - 898