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改良生物物理评分的围产期结局

Perinatal outcome with the modified biophysical profile.

作者信息

Nageotte M P, Towers C V, Asrat T, Freeman R K

机构信息

Long Beach Memorial Women's Hospital, CA 90801-1428.

出版信息

Am J Obstet Gynecol. 1994 Jun;170(6):1672-6.

PMID:8203424
Abstract

OBJECTIVE

Our purpose was to evaluate perinatal outcomes in high-risk pregnancies monitored with a modified biophysical profile.

STUDY DESIGN

All non-insulin-dependent patients referred for antepartum fetal surveillance received a modified biophysical profile biweekly. A modified biophysical profile is a combination of a nonstress test and an amniotic fluid index. Patients with a singleton gestation and intact membranes were entered into a protocol of randomized backup testing for an abnormal modified biophysical profile. Those patients having a nonreactive fetal heart rate, significant variable decelerations, late decelerations, or an amniotic fluid index < or = 5.0 cm received either a contraction stress test or a biophysical profile immediately. Once randomized, a patient received the same backup test, when indicated, with subsequent testing.

RESULTS

A total of 2774 patients had 17,429 tests with an uncorrected perinatal mortality rate of 2.9 per 1000. The overall incidence of an adverse perinatal outcome (i.e., perinatal death or nursery death before infant hospital discharge, cesarean delivery for fetal distress within the first 2 hours of labor, 5-minute Apgar score < 7, neonatal seizures or grade III or IV central nervous system hemorrhage) was 7.0%. When compared with patients having persistently normal modified biophysical profile, patients requiring a backup test had a significantly greater incidence of adverse perinatal outcome (9.3% vs 4.9%, p < 0.001, odds ratio 2.0, 95% confidence interval 1.5 to 2.7) and small-for-gestational-age infants (5.2% vs 2.4%, p < 0.001, odds ratio 2.2, 95% confidence interval 1.5 to 3.5). No differences in outcomes between patients randomized to a contraction stress test versus a biophysical profile could be identified either overall or in limiting the analysis to outcome after a negative last test. However, patients having contraction stress test as a backup test had a significantly higher rate of intervention for an abnormal test result than did those having a biophysical profile backup test (23.7% vs 16.6%, p < 0.002, odds ratio 1.6, 95% confidence interval 1.2 to 2.1).

CONCLUSION

The modified biophysical profile is an excellent means of fetal surveillance and identifies a group of patients at increased risk for adverse perinatal outcome and small-for-gestational-age infants. There does not appear to be a significant benefit with the contraction stress test compared with the biophysical profile as a backup test. Further, the contraction stress test is associated with a higher rate of intervention for an abnormal test than is the biophysical profile.

摘要

目的

我们的目的是评估采用改良生物物理评分法监测的高危妊娠的围产期结局。

研究设计

所有因产前胎儿监测而转诊的非胰岛素依赖型患者每两周接受一次改良生物物理评分法检查。改良生物物理评分法是无应激试验和羊水指数的组合。单胎妊娠且胎膜完整的患者若改良生物物理评分异常则进入随机备用检查方案。那些胎儿心率无反应、显著变异减速、晚期减速或羊水指数≤5.0 cm的患者立即接受宫缩应激试验或生物物理评分检查。一旦随机分组,患者在需要时接受相同的备用检查及后续检查。

结果

总共2774例患者进行了17429次检查,未校正的围产期死亡率为每1000例中有2.9例。围产期不良结局(即围产期死亡或婴儿出院前的新生儿死亡、分娩开始后2小时内因胎儿窘迫行剖宫产、5分钟阿氏评分<7分、新生儿惊厥或III级或IV级中枢神经系统出血)的总体发生率为7.0%。与改良生物物理评分持续正常的患者相比,需要备用检查的患者围产期不良结局的发生率显著更高(9.3%对4.9%,p<0.001,优势比2.0,95%置信区间1.5至2.7),且小于胎龄儿的发生率也更高(5.2%对2.4%,p<0.001,优势比2.2,95%置信区间1.5至3.5)。无论是总体上还是将分析局限于最后一次检查结果为阴性后的结局,都未发现随机接受宫缩应激试验与生物物理评分检查的患者在结局上存在差异。然而,以宫缩应激试验作为备用检查的患者因检查结果异常而进行干预的比率显著高于以生物物理评分作为备用检查的患者(23.7%对16.6%,p<0.002,优势比1.6,95%置信区间1.2至2.1)。

结论

改良生物物理评分法是胎儿监测的一种优秀方法,可识别出围产期不良结局和小于胎龄儿风险增加的一组患者。与作为备用检查的生物物理评分法相比,宫缩应激试验似乎没有显著益处。此外,宫缩应激试验与因检查异常而进行干预的比率高于生物物理评分法。

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