Cervical blockade reduces pain and bleeding during LEEP for HSIL in small RCT
This was a small, open-label, exploratory randomized controlled trial involving 40 patients diagnosed with high-grade squamous intraepithelial lesion (HSIL) by colposcopic biopsy. Patients were randomized to receive either general anesthesia only (n=20) or general anesthesia with additional local cervical anesthesia, or cervical blockade (n=20), during loop electrosurgical excision procedure (LEEP). The primary outcome was not explicitly stated.
The main results showed that the cervical blockade group had significantly lower postoperative pain scores (p<.01) and significantly lower intraoperative sponge usage (p<.01), suggesting reduced bleeding. However, the absolute numbers and effect sizes for these outcomes were not reported. There were no significant differences between groups for postoperative hemoglobin values, hemoglobin decrease, specimen size, surgical margin status, or hospital admissions after discharge (all p>.05).
Safety and tolerability data were not reported. Key limitations include the open-label design, exploratory nature, and very small sample size (n=40). The study was also conducted at a single center, and follow-up duration was not reported. The findings are preliminary and require confirmation in larger, multicenter, and preferably blinded trials. In practice, cervical blockade may be considered as an adjunct to enhance patient comfort and potentially reduce intraoperative bleeding during LEEP, but its routine use cannot be recommended based on this evidence alone.