Skip to main content
. 2026 Sep 10;14:1850211. doi: 10.3389/fped.2026.1850211

Table 5.

Comparison of maternal safety and perinatal complications between Two groups.

Indicator (measurement/definition) Combined group (n = 60) Control group (n = 60) Test statistic P value
Postpartum blood loss (mL, mean ± SD) 358 ± 130 345 ± 120 t = 0.569 0.570
Postpartum hemorrhage (>1,000 mL), n (%) 1 (1.7%) 2 (3.3%) —— 1.000
Transfusion rate, n (%) 1 (1.7%) 2 (3.3%) —— 1.000
Transient hypotension, n (%) 3 (5.0%) 4 (6.7%) —— 1.000
Nausea/vomiting, n (%) 4 (6.7%) 5 (8.3%) —— 1.000
Uterine hyperstimulation, n (%) 1 (1.7%) 0 (0%) —— 1.000
Epidural-related complications
 Post-dural puncture headache (PDPH), n (%) 1 (1.7%) 1 (1.7%) —— 1.000
 Epidural puncture site infection, n (%) 0 (0%) 0 (0%) —— ——
 Epidural hematoma, n (%) 0 (0%) 0 (0%) —— ——
 Other adverse events requiring medical intervention (description), n (%) 1 (1.7%) (transient altered consciousness, recovered after observation) 1 (1.7%) (transient tachycardia, recovered after monitoring) —— 1.000
 Composite adverse events (any of the above maternal adverse events), n (%) 5 (8.3%) 6 (10.0%) χ2 = 0.100 0.751
 Length of hospital stay (days, mean ± SD) 3.2 ± 0.9 3.8 ± 1.0 t = −3.45 0.001

“—” indicates not applicable or not observed.