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子痫前期的肝功能检查:与正常妊娠参考范围进行比较的重要性。

Liver function tests in pre-eclampsia: importance of comparison with a reference range derived for normal pregnancy.

作者信息

Girling J C, Dow E, Smith J H

机构信息

Hammersmith Hospital, London, UK.

出版信息

Br J Obstet Gynaecol. 1997 Feb;104(2):246-50. doi: 10.1111/j.1471-0528.1997.tb11054.x.

Abstract

OBJECTIVES

To determine reference ranges for liver function tests in uncomplicated pregnancy and to relate abnormal results by these criteria to outcome in pre-eclampsia.

DESIGN

Prospective, cross-sectional study to establish the reference ranges. Prospective observational study of women with pre-eclampsia.

SETTING

Antenatal clinics and obstetric unit of St Mary's Hospital, London.

PARTICIPANTS

Four hundred and thirty women with uncomplicated pregnancies and 85 consecutive women with gestational hypertension.

MAIN OUTCOME MEASURES

Aspartate transaminase (AST), alanine transaminase (ALT), bilirubin and gamma glutamyl transferase (GGT) were measured to determine their ranges in normal pregnancy. The severity of pre-eclampsia was determined by the maximum blood pressure, creatinine and 24 h urinary protein; minimum platelet count; maternal complications; mode of and gestation at delivery; and fetal outcome with centile weight adjusted for gestational age and sex.

RESULTS

AST, ALT, bilirubin and GGT were each lower in uncomplicated pregnancy than the nonpregnant laboratory reference ranges. Of those cases with elevated liver function tests in the pre-eclampsia group, 37% were abnormal only by the new reference ranges. Using the new ranges, the prevalence of elevated liver function tests was significantly higher in the pre-eclampsia group (54%) than in those with pregnancy induced hypertension (14%) (P < 0.01). Amongst those with pre-eclampsia, abnormal liver function tests were associated with greater proteinuria (P < 0.05), lower platelet count (P < 0.001) and more maternal complications (P < 0.01) than normal liver function tests; there was no difference in the severity of hypertension between the groups.

CONCLUSIONS

Liver function tests are lower in normal pregnancy than the reference ranges currently used. Our pregnancy-derived ranges allow more precise identification of abnormal liver function in women with pre-eclampsia than is possible using standard reference ranges derived from a nonpregnant population.

摘要

目的

确定正常妊娠时肝功能检查的参考范围,并根据这些标准将异常结果与子痫前期的结局相关联。

设计

建立参考范围的前瞻性横断面研究。对子痫前期妇女进行前瞻性观察研究。

地点

伦敦圣玛丽医院的产前诊所和产科病房。

参与者

430例正常妊娠妇女和85例连续的妊娠期高血压妇女。

主要观察指标

测量天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、胆红素和γ-谷氨酰转移酶(GGT),以确定其在正常妊娠中的范围。子痫前期的严重程度由最高血压、肌酐和24小时尿蛋白、最低血小板计数、母亲并发症、分娩方式和孕周以及根据胎龄和性别调整的百分位数体重的胎儿结局来确定。

结果

正常妊娠时AST、ALT、胆红素和GGT均低于非妊娠实验室参考范围。子痫前期组中肝功能检查升高的病例,37%仅根据新的参考范围为异常。使用新范围,子痫前期组肝功能检查升高的患病率(54%)显著高于妊娠高血压组(14%)(P<0.01)。在子痫前期患者中,与肝功能正常的患者相比,肝功能检查异常与蛋白尿更多(P<0.05)、血小板计数更低(P<0.001)和母亲并发症更多(P<0.01)相关;两组间高血压严重程度无差异。

结论

正常妊娠时肝功能检查低于目前使用的参考范围。我们根据妊娠得出的范围比使用非妊娠人群得出的标准参考范围能更精确地识别子痫前期妇女的肝功能异常。

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