Effect of betamethasone administration on fetal heart rate tracing: A blinded longitudinal study

被引:30
作者
Rotmensch, S
Lev, S
Kovo, M
Efrat, Z
Zahavi, Z
Lev, N
Celentano, C
Ben-Rafael, Z
机构
[1] Edith Wolfson Med Ctr, Dept Obstet & Gynecol, IL-58100 Holon, Israel
[2] Tel Aviv Univ, Dept Obstet & Gynecol, Sackler Sch Med, IL-69978 Tel Aviv, Israel
[3] Rabin Med Ctr, Dept Obstet & Gynecol, Petah Tiqwa, Israel
关键词
betamethasone; FHR analysis;
D O I
10.1159/000086815
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Computerized fetal heart rate (FHR) analysis revealed that antenatal corticosteroids transiently suppress multiple parameters of fetal well-being, potentially leading to the erroneous diagnosis of fetal distress and to unnecessary iatrogenic delivery of premature infants. Our aim was to determine whether clinicians who visually analyze FHR tracings detect these suppressive effects, thereby potentially affecting their clinical management decisions. Methods: Singleton pregnancies admitted for preterm labor between 26 and 34 weeks' gestation received two doses of betamethasone, 24 h apart, and were monitored daily between 16:00 and 19:00 h for 5 days. FHR tracings were randomly coded and presented in a non-consecutive order to four clinicians, who were unaware of the time of steroid administration. FHR baseline, FHR variability, number of accelerations and amplitude of maximal FHR acceleration were determined. Variability was scored semiquantitatively based on a modified Hon score. Analysis of variance (ANOVA) with repeated measures was used for primary analysis and followed up with the Wald test of significance. Corrections for multiple comparisons were made and only p < 0.005 considered significant. ANOVA was also used to assess the uniformity of trend in the interpretation by the four examiners for each given day. Results: Baseline FHR was elevated, FHR variability was decreased, and the number of accelerations decreased on day 1 (p < 0.0001; p < 0.0001; p < 0.0001) and day 2 (p < 0.0001; p < 0.0001; p < 0.0001) in comparison to day 0. On day 3, the FHR baseline, variability and number of accelerations returned to pre-exposure values (p = NS). The maximal amplitude of FHR accelerations showed a trend towards reduction (p = 0.08). Subgroup analysis by gestational age (group I = 26-30 weeks and group II = 30-34 weeks) showed the same response patterns and significance levels for both groups. Conclusions: Betamethasone causes profound, but transient, suppression of FHR parameters, which can mimic fetal distress. This effect is clinically recognized by visual FHR analysis. Clinicians need to be aware of this phenomenon, in order to avoid unwarranted iatrogenic delivery. Copyright (c) 2005 S. Karger AG, Basel.
引用
收藏
页码:371 / 376
页数:6
相关论文
共 27 条
[1]   MODIFICATIONS OF ULTRADIAN AND CIRCADIAN-RHYTHMS OF FETAL HEART-RATE AFTER FETAL-MATERNAL ADRENAL-GLAND SUPPRESSION - A DOUBLE-BLIND-STUDY [J].
ARDUINI, D ;
RIZZO, G ;
PARLATI, E ;
GIORLANDINO, C ;
VALENSISE, H ;
DELLACQUA, S ;
ROMANNINI, C .
PRENATAL DIAGNOSIS, 1986, 6 (06) :409-417
[2]   A COMPARISON BETWEEN COMPUTERIZED (MEAN RANGE) AND CLINICAL VISUAL CARDIOTOCOGRAPHIC ASSESSMENT [J].
CHENG, LC ;
GIBB, DMF ;
AJAYI, RA ;
SOOTHILL, PW .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1992, 99 (10) :817-820
[3]   Antenatal corticosteroids - current thinking [J].
Crowley, P .
BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2003, 110 :77-78
[4]   ANTENATAL CARDIOTOCOGRAM QUALITY AND INTERPRETATION USING COMPUTERS [J].
DAWES, GS ;
LOBB, M ;
MOULDEN, M ;
REDMAN, CWG ;
WHEELER, T .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1992, 99 (10) :791-797
[5]   CORTICOSTEROIDS AND THE BRAIN [J].
DEKLOET, ER ;
REUL, JMHM ;
SUTANTO, W .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1990, 37 (03) :387-394
[6]  
DEKLOET ER, 1988, PROGR BRAIN RES, P1
[7]   A comparative study of cardiovascular, endocrine and behavioural effects of betamethasone and dexamethasone administration to fetal sheep [J].
Derks, JB ;
Giussani, DA ;
Jenkins, SL ;
Wentworth, RA ;
Visser, GHA ;
Padbury, JF ;
Nathanielsz, PW .
JOURNAL OF PHYSIOLOGY-LONDON, 1997, 499 (01) :217-226
[8]   THE EFFECTS OF MATERNAL BETAMETHASONE ADMINISTRATION ON THE FETUS [J].
DERKS, JB ;
MULDER, EJH ;
VISSER, GHA .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1995, 102 (01) :40-46
[9]  
Freeman WJ, 2002, BIOCOMP SER, V1, P1
[10]   FETAL CARDIAC EFFECTS OF ORAL RITODRINE TOCOLYSIS [J].
FRIEDMAN, DM ;
BLACKSTONE, J ;
YOUNG, BK ;
HOSKINS, IA .
AMERICAN JOURNAL OF PERINATOLOGY, 1994, 11 (02) :109-112