# Esketamine-based PCIA combined with intercostal nerve block for acute pain after lobectomy: a randomized controlled trial

**Authors:** Meiyan Zhou, Yu Qi, Fan Zhou, Hui Wu, Jiao Chen, Long Wang, Liwei Wang

PMC · DOI: 10.3389/fphar.2026.1746121 · Frontiers in Pharmacology · 2026-03-04

## TL;DR

This study found that a moderate dose of esketamine combined with a nerve block significantly reduces post-surgery pain after lobectomy compared to other methods.

## Contribution

The study introduces esketamine-based PCIA combined with intercostal nerve block as a novel analgesic protocol for post-lobectomy pain.

## Key findings

- Group K2 showed significantly lower pain scores at multiple time points compared to other groups.
- Group K2 had a lower incidence of acute postoperative pain and reduced need for rescue analgesia.
- Group C had higher rates of postoperative nausea and vomiting compared to esketamine groups.

## Abstract

To evaluate outcomes of different doses of esketamine in postoperative patient-controlled intravenous analgesia (PCIA) combined with preoperative intercostal nerve block (ICNB) analgesia protocol for acute postoperative pain (APP) relief in patients undergoing thoracoscopic lobectomy.

A total of 360 patients scheduled for thoracoscopic lobectomy at Xuzhou Central Hospital between October 2021 and July 2023 were enrolled and randomly assigned into three groups using the random envelope method. Before anesthesia induction, all patients received ICNB, followed by general anesthesia. Group C received PCIA using sufentanil at 0.03 μg/kg/h, Group K1 received a low dose of esketamine at 0.015 mg/kg/h in PCIA, and Group K2 received a moderate dose of esketamine at 0.03 mg/kg/h in PCIA. Numerical Rating Scale (NRS) pain scores were recorded at 2, 4, 24, 48, and 72 h postoperatively. The incidence of APP within 72 h post-surgery, the requirement for rescue analgesia and the occurrence of adverse reactions, were assessed and recorded for the three groups.

There were significantly lower NRS scores in Group K2 at 2, 4, 24, 48, and 72 h postoperatively, compared to Groups C and K1 (P < 0.01). However, there were no statistically significant differences in NRS scores between Group C and Group K1 (P > 0.05). The incidence of APP within 72 h postoperatively was significantly lower in Group K2, compared to Group C and Group K1 (P < 0.05). Additionally, Group C exhibited a significantly higher the incidence of postoperative nausea and vomiting (PONV) than the other two groups (P < 0.05). Group K2 demonstrated superior postoperative analgesic efficacy, including reduced rescue analgesia needs and lower opioid consumption, without affecting hospital stay length compared to Groups C and K1.

A dose of 0.03 mg/kg/h esketamine in PCIA combined with preoperative ICNB significantly alleviates APP in patients undergoing thoracoscopic lobectomy, reducing resting pain scores by approximately 30% at 24 h compared to sufentanil-based analgesia.

https://www.chictr.org.cn/, Identifier ChiCTR2100051000.

## Linked entities

- **Chemicals:** esketamine (PubChem CID 182137), sufentanil (PubChem CID 41693)

## Full-text entities

- **Diseases:** acute pain (MESH:D059787), lobectomy (MESH:D020232), intercostal nerve block (MESH:D006327), pain (MESH:D010146), APP (MESH:D010149), PONV (MESH:D020250)
- **Chemicals:** sufentanil (MESH:D017409), Esketamine (MESH:C000629870)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12996927/full.md

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Source: https://tomesphere.com/paper/PMC12996927