Table 2. Side effects and adverse maternal and perinatal outcomes.
Group 1 (n=83) | Group 2 (n=82) | Group 3 (n=82) | p-value§ | |
---|---|---|---|---|
Arterial hypotension | 0% (0/83) | 0% (0/82) | 0% (0/82) | * |
Nausea | 0% (0/83) | 0% (0/82) | 0% (0/82) | * |
Vomiting | 0% (0/83) | 0% (0/82) | 0% (0/82) | * |
Pruritus | 0% (0/83) | 0% (0/82) | 0% (0/82) | * |
Respiratory depression | 0% (0/83) | 0% (0/82) | 0% (0/82) | * |
Fetal bradycardia | 9.6% (8/83) | 8.5% (7/82) | 20.7% (17/82) | 0.036 |
Apgar score <7 at 1st minute | 44.6% (37/83) | 17.1% (14/82) | 22.0% (18/82) | <0.001 |
Need for neonatal oxygen therapy | 0% (0/83) | 0% (0/82) | 6.1% (5/82) | 0.016 |
Need for neonatal ICU | 0% (0/83) | 0% (0/82) | 4.9% (4/82) | 0.017 |
Group 1: analgesia performed in patients with cervical dilatation ≤4.0 cm; Group 2: analgesia performed in patients with cervical dilatation between 5.0 and 8.0 cm; Group 3: analgesia performed in patients with cervical dilatation ≥9.0 cm. ICU: intensive care unit; Chi-square §percentage (n/N); p<0.05. *It was not possible to calculate the p-value due to the absence of at least three cases in each group.