阿片类药物在泌尿妇科补片取出术中的应用。

IF 0.8 Q4 OBSTETRICS & GYNECOLOGY Urogynecology (Hagerstown, Md.) Pub Date : 2025-01-01 DOI:10.1097/SPV.0000000000001527
Amanda M Artsen, Roseanne Gichuru, Michael Bonidie, Lauren Giugale, Pamela A Moalli
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引用次数: 0

摘要

重要性:40%的泌尿妇科补片疼痛并发症患者正在服用麻醉剂。目的:我们旨在比较麻醉和非麻醉患者的合并症和疼痛评分,并评估术后麻醉使用率。研究设计:这是一项对接受泌尿妇科补片去除术患者的前瞻性队列研究的二次分析。由于资料的可得性,纳入了7年内因疼痛取网的患者。麻醉品处方使用宾夕法尼亚州处方药监测计划进行验证。在基线和术后6-24个月评估疼痛评分。结果:139例患者中,30例(21.6%)术前3个月内使用麻醉处方。这些患者更年轻,更有可能患有慢性疼痛。麻醉的使用没有因吊带与脱垂网或暴露而不同。术前服用麻醉药的患者盆腔疼痛中位基线视觉模拟评分高27分(P = 0.01)。伴有疼痛合并症的患者术前使用麻醉剂的几率是术前的6倍。年轻患者术后盆腔疼痛改善较少。只有8名(27%)服用麻醉品的患者术后停止使用,没有明显的延长(≥3个月)使用的预测因素。术后长期使用的患者中有87%有疼痛诊断,通常是关节和背部疼痛。结论:在与补片相关的疼痛患者中,那些有慢性疼痛状况的患者术前服用麻醉药的几率要高得多,并且在大多数情况下,去除补片并没有消除麻醉药的使用。对于有慢性疼痛症状的患者,如果移除后疼痛和麻醉品的使用可能持续存在,咨询是必要的。
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Perioperative Opioid Use in Urogynecologic Mesh Removal.

Importance: Forty percent of patients with urogynecologic mesh pain complications are taking narcotics.

Objectives: We aimed to compare comorbidities and pain scores between patients with and without narcotic use and assess postoperative narcotic use rates.

Study design: This was a secondary analysis of a prospective cohort study of patients undergoing urogynecologic mesh removal. Patients with mesh removal for pain within 7 years were included due to data availability. Narcotic prescriptions were verified using the Pennsylvania Prescription Drug Monitoring Program. Pain scores were assessed at baseline and 6-24 months postoperatively.

Results: Of 139 patients, 30 (21.6%) filled narcotic prescriptions within 3 months preceding surgery. These patients were younger and more likely to have a chronic pain condition. Narcotic use did not differ by sling versus prolapse mesh, or presence of exposure. Patients taking preoperative narcotics had a 27-point higher median baseline visual analog scale pelvic pain score (P = 0.01). Patients with pain comorbidities had 6 times odds of using preoperative narcotics. Younger patients had less improvement in pelvic pain after removal. Only 8 (27%) of those taking narcotics discontinued use postoperatively with no significant predictors of prolonged (≥3 months) use. Eighty-seven percent of patients with prolonged postoperative use had a prior pain diagnosis, commonly joint and back pain.

Conclusions: In patients with mesh-related pain, those with chronic pain conditions had much higher odds of taking preoperative narcotics, and in most, mesh removal did not eliminate narcotic use. Counseling is warranted in patients with chronic pain conditions that pain and narcotic use are likely to persist after removal.

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