Abstract:Objective To evaluate the efficacy of parecoxib sodium preemptive analgesia in patients undergoing hysteroscopic surgery.Methods Ninety-seven patients scheduled for hysteroscopy (January 2021 - January 2024) were randomized to control (n = 49) or observation (n = 48) groups. Both received routine anesthesia; the observation group additionally received preemptive parecoxib sodium. Outcomes included: Perioperative indicators [heart rate (HR), mean arterial pressure (MAP) at baseline (T0), 5 min post-induction (T1), and surgery end (T2)]; Serum biomarker changes (cortisol [Cor], substance P [SP], interleukin-6 [IL-6], prostaglandin E2 [PGE2]); Visual Analog Scale (VAS) scores at 6, 12, and 24 h postoperatively; and Safety.Results The observation group required less propofol and achieved higher Ramsay sedation scores (P < 0.05). Significant differences were observed in HR and MAP: Across timepoints (P < 0.05); Between groups (P < 0.05); and In group-time interactions (P < 0.05). Postoperative decreases in serum Cor, SP, IL-6, and PGE2 were greater in the observation group (P < 0.05). VAS scores demonstrated: Time effects (P < 0.05); Intergroup differences (observation group < control, P < 0.05); and Group-time interactions (P < 0.05). Adverse event rates did not differ significantly (P > 0.05).Conclusion Preemptive parecoxib sodium effectively reduces postoperative pain, attenuates inflammatory/stress responses, maintains hemodynamic stability, and demonstrates favorable safety in hysteroscopic surgery.