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血清尿酸检测在子痫前期和妊娠期短暂性高血压中的临床应用。

The clinical utility of serum uric acid measurements in pre-eclampsia and transient hypertension in pregnancy.

作者信息

D'Anna R, Baviera G, Scilipoti A, Leonardi I, Leo R

机构信息

Department of Ginecology, University Polyclinic, Messina, Italy.

出版信息

Panminerva Med. 2000 Jun;42(2):101-3.

Abstract

BACKGROUND

Our purpose was to evaluate the clinical utility of serum uric acid measurements in the hypertension diseases of pregnancy.

METHODS

We identified 286 women and categorized them into three diagnostic groups according to definitions of hypertensive diseases in pregnancy published by the National Working Group on Hypertension in Pregnancy: pre-eclampsia (94), transient hypertension (102) and normal (90). We compared the median uric acid concentration for each group and calculated the sensitivities and the specificities in diagnosing pre-eclampsia. The results were analyzed by the Mann-Whitney test.

RESULTS

Median serum uric acid values in the pre-eclamptic group, in the transient hypertension group and in the control group were 375 (262-536) mumol/L, 309 (214-387) mumol/L, 259 (143-339) mumol/L, respectively. Compared with normal, the median serum uric acid levels in women with pre-eclampsia or transient hypertension were significantly elevated. Differences in median serum uric acid concentrations between women with preeclampsia and with transient hypertension were statistically significant too. The prevalence of IUGR in the pre-eclamptic group and transient hypertension group was 65.9% and 29.4%, respectively. Sensitivity for serum uric acid levels of 339 mumol/L was 77.3% in the pre-eclamptic group and 32.3% in the transient hypertension group; the difference was statistically significant. Specificity was exactly the same in both groups (92%).

CONCLUSIONS

Our data, in accordance with international literature, confirm the clinical utility of serum uric acid as a marker of pre-eclampsia, but not of transient hypertension. Furthermore its high predictive value makes it possible to select a group of pre-eclamptic women with high risk for intrauterine growth retardation.

摘要

背景

我们的目的是评估血清尿酸检测在妊娠期高血压疾病中的临床应用价值。

方法

我们纳入了286名女性,并根据妊娠期高血压疾病国家工作组发布的妊娠期高血压疾病定义将她们分为三个诊断组:子痫前期(94例)、短暂性高血压(102例)和正常组(90例)。我们比较了每组的尿酸中位数浓度,并计算了诊断子痫前期的敏感性和特异性。结果采用Mann-Whitney检验进行分析。

结果

子痫前期组、短暂性高血压组和对照组的血清尿酸中位数分别为375(262 - 536)μmol/L、309(214 - 387)μmol/L、259(143 - 339)μmol/L。与正常组相比,子痫前期或短暂性高血压女性的血清尿酸中位数水平显著升高。子痫前期女性和短暂性高血压女性之间的血清尿酸中位数浓度差异也具有统计学意义。子痫前期组和短暂性高血压组中胎儿生长受限的发生率分别为65.9%和29.4%。血清尿酸水平为339μmol/L时,子痫前期组的敏感性为77.3%,短暂性高血压组为32.3%;差异具有统计学意义。两组的特异性完全相同(92%)。

结论

我们的数据与国际文献一致,证实血清尿酸作为子痫前期的标志物具有临床应用价值,但对短暂性高血压则不然。此外,其高预测价值使得能够筛选出一组有胎儿生长受限高风险的子痫前期女性。

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