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Table 4 Pain-associated data across the four parturient groups

From: Efficacy of continuous in-wound infusion of levobupivacaine and ketorolac for post-caesarean section analgesia: a prospective, randomised, double-blind, placebo-controlled trial

Parturient group

Time to first piritramide request [min (95% CI)]

Persistent post-operative pain (8 weeks; yes/no) [n (%)]

New skin sensation (8 weeks; yes/no) [n (%)]

Quality of analgesia (48 h; NRS 1–5)

Levobupivacaine

163 (120–250)

1 (7.1)

7 (46.7)

4 (4–5)

Ketorolac tromethamine

180 (160–465)

1 (7.1)

5 (35.7)

4 (4–5)

Combination

295 (125–475)

0 (0)

1 (7.1) a

5 (5–5) a

Saline placebo

160 (120–185)

0 (0)

9 (60.0) a

4 (4–5) a

p-value

ns

**

0.026a (combination vs. saline placebo)

0.005a (combination vs. saline placebo)

  1. CI confidence interval
  2. asignificant difference among groups calculated using ANOVA/ Kruskal Wallis tests, and between groups comparison post-hoc tests with Bonferroni correction; **p value could not be calculated due to zero positive cases in some groups; ns, non-significant; NRS 1–5, numeric rating scale for quality of analgesia from 1 to 5; significant differences are marked with bold text