Efficacy and safety of hydromorphone caudal block combined with intercostal nerve block during VATS: a single-center randomized controlled study

胸腔镜辅助手术中应用氢吗啡酮尾部阻滞联合肋间神经阻滞的疗效和安全性:一项单中心随机对照研究

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Abstract

BACKGROUND: The management of post-operative pain while minimizing opioid use remains challenging in thoracic surgery. While intercostal nerve blocks are commonly used, the optimal multimodal approach remains unclear. OBJECTIVES: To evaluate whether adding hydromorphone caudal blockade to intercostal nerve blocks improves post-operative recovery outcomes in thoracic surgery patients. DESIGN: A prospective, double-blinded, randomized controlled trial. SETTING: Dongguan Tungwah Hospital. PATIENTS: Eighty adult patients scheduled for video-assisted thoracoscopic surgery (VATS) were enrolled. INTERVENTION: Patients were randomized to receive either ultrasound-guided caudal blockade with 1 mg hydromorphone (caudal group) or normal saline (control group) in addition to standard intercostal nerve blocks. MAIN OUTCOME MEASURES: The primary outcome was the Quality of Recovery-40 (QoR-40) score at 48 h post-surgery. Secondary outcomes included pain scores, nausea assessment, opioid consumption, vital signs, chest tube drainage, pulmonary complications, inflammatory markers, and length of hospital stay. RESULTS: The median [IQR] total QoR-40 score showed a non-significant trend favoring the caudal group (189.50 [169-194.5] vs. 181 [170.25–189.50], P = 0.134). However, significant improvements were observed in the caudal group for: nausea scores (5 [5–5] vs. 5 [4–5], P = 0.011), moderate pain (4 [4–5] vs. 4 [3–5], P = 0.014), and severe pain (5 [5–5] vs. 5 [4–5], P = 0.004). CONCLUSIONS: While hydromorphone caudal blockade did not significantly improve overall recovery scores, it demonstrated specific benefits in pain and nausea control when combined with intercostal nerve blocks for VATS procedures. TRIAL REGISTRATION: Clinical Trial Registry of China (ChiCTR2400080726 / 02/ 2024). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12871-025-03307-4.

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