Abstract:Objective To investigate the clinical efficacy of supraorbital nerve pulsed radiofrequency combined with nerve block in treating postherpetic neuralgia and its impact on pain relief.Methods From March 2021 to March 2024, 92 patients with postherpetic neuralgia treated at our hospital were enrolled as study subjects. Using a random number table method, they were divided into a control group (n = 46, receiving nerve block therapy) and an observation group (n = 46, receiving supraorbital nerve pulsed radiofrequency in addition to nerve block). Clinical efficacy, pain levels [assessed by the Zoster Brief Pain Inventory (ZBPI) and Visual Analog Scale (VAS) ], serological indicators [serum substance P (SP), β-endorphin (β-EP), high mobility group box 1 (HMGB1), interleukin-1β (IL-1β), interleukin-6 (IL-6), neuropeptide Y (NPY), and calcitonin gene-related peptide (CGRP) ], and adverse reactions were compared between the two groups.Results The total effective rate in the observation group was higher than that in the control group (P < 0.05). The differences in ZBPI and VAS scores before and after treatment were greater in the observation group than in the control group (P < 0.05). The decrease in SP and the increase in β-EP from before to after treatment were more pronounced in the observation group (P < 0.05). The reductions in HMGB1, IL-1β, and IL-6 from before to after treatment were greater in the observation group than in the control group (P < 0.05). The decrease in NPY and the increase in CGRP from before to after treatment were also more significant in the observation group (P < 0.05). No significant difference was observed in the total incidence of adverse events between the two groups (P > 0.05).Conclusion The combination of supraorbital nerve pulsed radiofrequency and nerve block therapy exhibits significant efficacy in mitigating pain intensity in postherpetic neuralgia patients, enhances the recovery of neural function, attenuates inflammatory responses, and maintains a favorable safety profile, thereby proving suitable for clinical implementation.