Ultrasound-Guided Liposomal vs. Conventional Bupivacaine Erector Spinae Plane Block Plus Gabapentin for Postherpetic Neuralgia.

IF 3.1
The Kaohsiung journal of medical sciences Pub Date : 2026-08-01 Epub Date: 2026-01-12 DOI:10.1002/kjm2.70169
Xia-Jing Xu, Li-Juan Liu, Fa-Ming Xu, Xiang-Yu Fang
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Abstract

This study aimed to compare efficacy and safety of ultrasound-guided erector spinae plane block (ESPB) using liposomal (LB) versus conventional bupivacaine (CB), each plus standardized gabapentin, in patients with postherpetic neuralgia (PHN). A total of 116 PHN patients were randomized to ESPB-LB or ESPB-CB; both groups received standardized gabapentin. The primary outcome was resting pain assessed by Numeric Rating Scale (NRS). Secondary outcomes were 72-h event-free time (time to first rescue medication or resting NRS ≥ 4), cumulative rescue opioid exposure in morphine milligram equivalents (MME), sleep by the Pittsburgh Sleep Quality Index (PSQI), health-related quality of life by the Patient-Reported Outcomes Measurement Information System (PROMIS), Patient Global Impression of Change (PGIC), and adverse events (AEs). ESPB-LB achieved lower resting NRS at day 1, day 3 and day 7 (all p < 0.05), with no between-group differences at day 30 or day 60. Event-free time favored LB (median 54.10 h vs. 18.95 h; log-rank p = 0.002). LB reduced cumulative MME at 48 h and 72 h, with convergence by days 7-60. PGIC favored LB at days 7 and 30, converging by day 60. Sleep and health-related quality of life improved similarly with no between-group differences; AEs were comparable, and no serious events occurred through day 60. In PHN, ESPB-LB plus gabapentin provided an early advantage characterized by superior early analgesia, higher early responder rates, longer opioid-free analgesia within 72 h, and short-term opioid sparing versus ESPB-CB, while longer-term outcomes and safety profiles were similar between groups.

超声引导脂质体与传统布比卡因与加巴喷丁联合治疗带状疱疹后神经痛。
本研究旨在比较超声引导下使用脂质体(LB)的直立脊柱平面阻滞(ESPB)与常规布比卡因(CB),每种加巴喷丁加标准化,对带状疱疹后神经痛(PHN)患者的疗效和安全性。116例PHN患者随机分为ESPB-LB组和ESPB-CB组;两组均接受标准化加巴喷丁治疗。主要终点为静息疼痛,采用数值评定量表(NRS)评估。次要结局为72小时无事件时间(第一次抢救用药时间或静息NRS≥4),吗啡毫克当量(MME)的累积抢救阿片类药物暴露,匹兹堡睡眠质量指数(PSQI)的睡眠,患者报告结果测量信息系统(PROMIS)的健康相关生活质量,患者总体变化印象(PGIC)和不良事件(ae)。ESPB-LB在第1天、第3天和第7天达到较低的静息NRS
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