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Qualitative Analysis of Diagnostic Value of 24-h Proteinuria for Preeclampsia
Xu Zhuang, Yun-Yan Chen, Qiong Zhou
1Department of Obstetrics and Gynecology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China.
Insights
The 24-hour proteinuria test remains a crucial diagnostic marker for preeclampsia (PE), even after updated guidelines. Its deletion from severe PE diagnostic criteria is not advised, especially for Chinese women.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Clinical Diagnostics
Background:
- Preeclampsia (PE) is a significant pregnancy complication characterized by hypertension and proteinuria.
- The American College of Obstetricians and Gynecologists (ACOG) updated PE diagnostic criteria, diminishing the role of proteinuria.
- This study evaluates the diagnostic value of 24-hour proteinuria in Chinese women under the latest ACOG guidelines.
Purpose of the Study:
- To qualitatively analyze the diagnostic value of 24-hour proteinuria for preeclampsia (PE) in China.
- To evaluate the diagnostic criteria within the latest ACOG guideline concerning maternal and perinatal outcomes.
- To assess the correlation between diagnostic criteria and adverse pregnancy outcomes in hypertensive disorders of pregnancy (HDP).
Main Methods:
- Retrospective analysis of clinical data from 65 patients with hypertensive disorder in pregnancy (HDP).
- Evaluation of diagnostic criteria according to the ACOG guideline, assessing relationships with maternal and perinatal outcomes.
- Spearman correlation and logistic regression used to analyze associations between diagnostic criteria and adverse pregnancy outcomes.
Main Results:
- A significant association was found between 24-hour proteinuria ≥0.3 g and adverse pregnancy outcomes (74.5% rate, P = 0.000).
- No significant differences in adverse outcomes were observed for other criteria groups like impaired liver function, renal insufficiency, thrombocytopenia, or cerebral/visual symptoms.
- 24-hour proteinuria, liver enzyme, and creatinine values showed significant correlations with adverse outcomes in both HDP and PE.
Conclusions:
- 24-hour proteinuria is a vital diagnostic criterion for preeclampsia (PE) and should not be removed from severe PE diagnostic criteria.
- The current ACOG diagnostic criteria require further validation in the Chinese population.
- Proteinuria measurement remains a key indicator for predicting adverse pregnancy outcomes in HDP.
Background:
Preeclampsia (PE) is a serious idiopathic disease posing a threat to both mothers and fetuses' lives during pregnancy, whose main diagnostic criteria include hypertension with proteinuria. However, American College of Obstetricians and Gynecologists (ACOG) updated the diagnostic criteria for PE and reduced the diagnostic value of proteinuria for patients with PE. Qualitative analysis of the diagnostic value of 24-h proteinuria for patients with PE in China was conducted to evaluate the diagnostic criteria value in the latest ACOG guideline.
Methods:
Complete clinical data of 65 patients with hypertensive disorder in pregnancy (HDP) were collected. All patients were delivered to and hospitalized in Renji Hospital. Adverse outcome was defined in case of the emergence of any serious complication for a mother or the fetus. A retrospective study was conducted according to ACOG guideline, to analyze the relationship between each diagnostic criteria of ACOG guideline and maternal and perinatal outcomes. Spearman correlation test was used to detect the association between each diagnostic criterion, its corresponding value, and the adverse pregnancy outcome. Logistic regression was performed to verify the result of Spearman correlation test.
Results:
Of 65 HDP patients, the percentage of adverse pregnancy outcome was 63.1%. Adverse pregnancy outcomes constitute diversification. There were 55 cases with 24-h proteinuria value ≥0.3 g, of which the adverse outcome rate was 74.5%. While adverse pregnancy outcomes did not appear in the rest 10 HDP patients with proteinuria <0.3 g/24 h. The statistic difference was significant (P = 0.000). However, no significant difference was found in other criteria groups (impaired liver function: P = 0.417; renal insufficiency: P = 0.194; thrombocytopenia: P = 0.079; and cerebral or visual symptoms: P = 0.296). The correlation coefficient between 24-h proteinuria ≥0.3 g and adverse pregnancy outcomes was 0.557 (P < 0.005). Impaired liver function (P = 0.180), renal insufficiency (P = 0.077) and cerebral or visual symptoms (P = 0.118) were not related to adverse outcomes. The 24-h proteinuria value (HDP: r = 0.685; PE: r = 0.521), liver enzyme value (HDP: r = 0.519; PE: r = 0.501), and creatinine value (HDP: r = 0.511; PE: r = 0.398) were associated with adverse pregnancy outcomes both in PE and HDP, and the corresponding logistic regression equation can be produced.
Conclusions:
The 24-h proteinuria value is still an important diagnostic criterion for PE, and deletion of 24-h proteinuria value from diagnostic criteria for severe PE was not recommended. The diagnostic criteria in ACOG guideline need to be verified in Chinese women.
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