TY - JOUR
T1 - Massive Urinary Protein Excretion Associated with Greater Neonatal Risk in Preeclampsia
AU - Mateus, Julio
AU - Newman, Roger
AU - Sibai, Baha M.
AU - Li, Qing
AU - Barton, John R.
AU - Combs, C. Andrew
AU - Guzman, Edwin
AU - Boggess, Kim A.
AU - Gyamfi, Cynthia
AU - von Dadelszen, Peter
AU - Woelkers, Doug
PY - 2017
Y1 - 2017
N2 - Objective
The objective of this study was to compare clinical outcomes of preeclamptic pregnancies according to the proteinuria level.
Study Design
Secondary analysis of a multicenter prospective cohort study of
women with preeclampsia (PE) symptomatology. Nonproteinuria, mild-proteinuria,
and massive-proteinuria PEs were defined as: < 165 mg in 12 hours or < 300 mg in 24 hours, 165 mg to 2.69 g in 12 hours or 300 mg to 4.99 g in 24 hours, and 2.7 g in 12 hours or 5.0 g in 24 hours, respectively. Individual and composite maternal, fetal, and neonatal outcomes were compared among the PE groups.
Results Of the 406 analyzed pregnancies, 36 (8.8%) hadmassive-proteinuria PE, 268 (66.0%) mild-proteinuria PE, and 102 (25.1%) nonproteinuria PE. Compared with the other groups, massive-proteinuria PE women had significantly higherbloodpressures (p < 0.001), epigastric pain (p ¼ 0.007), and uric acid serum levels (p < 0.001) prior to delivery. Compositematernal morbidity was similar across the groups. Delivery < 340/7 weeks occurred in 80.6, 49.3, and
22.5% of massive-proteinuria, mild-proteinuria, and nonproteinuria PE groups, respectively (p < 0.0001). Compositeadverse neonatal outcomes were significantly higher in themassiveproteinuria PE compared with the other groups (p ¼ 0.001).
Conclusion
While potentially not important diagnostically, massive proteinuria is
associated with more severe clinical manifestations of PE prompting earlier delivery.
AB - Objective
The objective of this study was to compare clinical outcomes of preeclamptic pregnancies according to the proteinuria level.
Study Design
Secondary analysis of a multicenter prospective cohort study of
women with preeclampsia (PE) symptomatology. Nonproteinuria, mild-proteinuria,
and massive-proteinuria PEs were defined as: < 165 mg in 12 hours or < 300 mg in 24 hours, 165 mg to 2.69 g in 12 hours or 300 mg to 4.99 g in 24 hours, and 2.7 g in 12 hours or 5.0 g in 24 hours, respectively. Individual and composite maternal, fetal, and neonatal outcomes were compared among the PE groups.
Results Of the 406 analyzed pregnancies, 36 (8.8%) hadmassive-proteinuria PE, 268 (66.0%) mild-proteinuria PE, and 102 (25.1%) nonproteinuria PE. Compared with the other groups, massive-proteinuria PE women had significantly higherbloodpressures (p < 0.001), epigastric pain (p ¼ 0.007), and uric acid serum levels (p < 0.001) prior to delivery. Compositematernal morbidity was similar across the groups. Delivery < 340/7 weeks occurred in 80.6, 49.3, and
22.5% of massive-proteinuria, mild-proteinuria, and nonproteinuria PE groups, respectively (p < 0.0001). Compositeadverse neonatal outcomes were significantly higher in themassiveproteinuria PE compared with the other groups (p ¼ 0.001).
Conclusion
While potentially not important diagnostically, massive proteinuria is
associated with more severe clinical manifestations of PE prompting earlier delivery.
U2 - 10.1055/s-0037-1601866
DO - 10.1055/s-0037-1601866
M3 - Article
SN - 2157-6998
VL - 07
SP - e49-e58
JO - American Journal of Perinatology Reports
JF - American Journal of Perinatology Reports
IS - 01
ER -