连续小剂量阿司匹林在显微内镜椎板切除术中的安全性和临床效果。

IF 1.2 Q3 SURGERY
Kiyoshi Tarukado, Teruaki Ono, Toshio Doi, Katsumi Harimaya, Yasuharu Nakashima
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引用次数: 0

摘要

导读:脊柱外科围手术期继续口服低剂量阿司匹林(LDA)是否更好仍存在争议。本研究旨在通过评估显微内窥镜椎板切除术(MEL)围手术期并发症和临床结果来评估持续使用LDA的安全性。方法:我们最终纳入了88例患者(男性35例,女性53例),他们在2016年4月至2022年3月期间因腰椎管狭窄接受了一个水平的MEL。未接受抗凝治疗的患者分为A组(65例),围手术期停止抗凝治疗的患者分为B组(9例),围手术期继续口服LDA的患者分为C组(14例)。评估三组患者的手术时间、术中预估失血量(EBL)、术前、术后血红蛋白(Hb)、血小板(Plt)差异、围手术期并发症、术后1周及术后6个月及以上MRI血肿及硬膜囊截面积。EuroQol-5维度(EQ-5D)、Oswestry残疾指数(ODI)和日本骨科协会背痛评估问卷(JOABPEQ)作为临床结果进行评估。结果:三组患者手术时间、术中EBL、术前与术后Hb、Plt差异、MRI血肿及硬膜囊截面积差异均无统计学意义。A组有1例血肿清除,三组间EQ-5D、ODI、JOABPEQ各结构域差异无统计学意义。结论:LDA在围手术期的延续对一期MEL的围手术期并发症和临床结果没有影响。在MEL中,可能在围手术期继续口服LDA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Safety and Clinical Results of Continuous Low-Dose Aspirin in Microendoscopic Laminectomy.

Safety and Clinical Results of Continuous Low-Dose Aspirin in Microendoscopic Laminectomy.

Safety and Clinical Results of Continuous Low-Dose Aspirin in Microendoscopic Laminectomy.

Safety and Clinical Results of Continuous Low-Dose Aspirin in Microendoscopic Laminectomy.

Introduction: It remains controversial whether it is better to continue oral low-dose aspirin (LDA) during the perioperative period in spinal surgery. This study aims to evaluate the safety of continued LDA administration in the perioperative periods of microendoscopic laminectomy (MEL) by assessing perioperative complications and clinical outcomes.

Methods: We ultimately included 88 patients (35 males, 53 females) who underwent one level of MEL for lumbar spinal canal stenosis from April 2016 to March 2022. Patients who did not undergo anticoagulation therapy were classified into Group A (65 patients), those who stopped anticoagulation therapy at the perioperative periods were classified into Group B (9 patients), and those who continued oral administration of LDA throughout the perioperative periods were classified into Group C (14 patients). Surgery time, intraoperative estimate blood loss (EBL), differences between hemoglobin (Hb) and platelet (Plt) before and after surgery, perioperative complications, and cross-sectional area of hematoma and dural sac on MRI taken within 1 week and at 6 months or more after surgery were assessed between three groups. The EuroQol-5 dimensions (EQ-5D), Oswestry Disability Index (ODI), and Japanese Orthopaedic Association Back Pain Evaluation Questionnaire (JOABPEQ) were also evaluated as the clinical outcomes.

Results: There was no statistically significant difference between the three groups in operation time, intraoperative EBL, differences between Hb and Plt before and after surgery, and cross-sectional area of hematoma and dural sac on MRI. A case of hematoma removal was confirmed in Group A. There was also no statistically significant difference between the three groups in EQ-5D, ODI, and each domain of JOABPEQ.

Conclusions: The continuation of LDA throughout the perioperative periods did not affect perioperative complications and clinical outcomes of one-level MEL. In MEL, it might be possible to continue oral administration of LDA throughout the perioperative periods.

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CiteScore
1.80
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0.00%
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71
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