The aim of this study was to evaluate postoperative
analgesia effectiveness and
patient-controlled analgesia (PCA)-related adverse events. The children who received
sufentanil-based PCA following major surgery to repair
congenital hip dislocation and
hypospadias were divided into 3 groups:
sufentanil 4 µg/kg +
tramadol 10 mg/kg (ST; n = 301),
sufentanil 4 µg/kg (S4; n = 211), and
sufentanil 5 µg/kg (S5; n = 451).
Analgesics with
granisetron 0.2 mg/kg were diluted in
0.9% saline to 100 mL and infused continuously at a basal infusion rate of 1 mL/h. A total of 963 children whose average age was 4 years were investigated. The incidence of moderate to severe
postoperative pain during rest was significantly lower in the S5 group (0.2%) and ST group (0.3%) compared with the S4 group (3.3%) within 72 hours after surgery (P < .05), and the incidence of moderate to severe
pain during activity within 72 hours was also significantly lower in the S5 group (3.5%) compared with the other 2 groups (ST, 21.9%; S4, 33.2%; P < .001). A significant difference was identified among the 3 groups in the total number of PCA administrations, but there was no statistical difference of total usage of
opioids among the 3 groups. In terms of PCA-related adverse events, the incidence of
postoperative nausea and vomiting in the S5 group was lower compared with the ST group within 72 hours after surgery (P < .001), and there was no significant difference compared with the S4 group (P = .254). There was also no significant difference in the incidence of
pruritus and
dizziness among the 3 groups.
Sufentanil-based PCA can be effectively and safely used in children after major congenital structural malformation repair surgeries. The
sufentanil 5 µg/kg dosage in the PCA regimen is superior to
sufentanil 4 µg/kg alone or combined with
tramadol in lowering moderate to severe
pain.