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在青少年特发性脊柱侧弯椎体拴系术后使用氨甲环酸减少胸管引流以降低术后发病率。

Reducing postoperative morbidity by diminishing chest tube drainage utilizing tranexamic acid following vertebral body tethering for adolescent idiopathic scoliosis.

作者信息

Rajjoub Rami, Kurapatti Mark, Mejia Mateo Restrepo, Mucollari Olgerta, Torres Rodnell Busigó, Alasadi Husni, Lonner Baron S

机构信息

Department of Orthopedic Surgery, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

Spine Deform. 2025 May;13(3):737-743. doi: 10.1007/s43390-025-01042-x. Epub 2025 Jan 26.

DOI:10.1007/s43390-025-01042-x
PMID:39864033
Abstract

PURPOSE

Vertebral body tethering (VBT) is a non-fusion surgical option for adolescent idiopathic scoliosis (AIS) that requires a postoperative (PO) chest tube. This study evaluates whether 48 h of PO TXA reduces chest tube (CT) drainage and retention compared to 24 h of TXA following VBT for AIS.

METHODS

Consecutively treated patients with a diagnosis of AIS who underwent VBT were assessed. Thirty-eight patients who received 48 h of PO IV TXA (48-TXA) were compared to 35 VBT patients who received 24 h of PO IV TXA (24-TXA) and 48 patients who did not receive TXA (non-TXA). TXA use in thoracic CT and thoracolumbar CT drainages were also assessed separately. Group comparisons were performed using one-way ANOVA and Chi-square tests.

RESULTS

There were no significant differences in demographics between groups. TXA significantly reduced CT drainage (p < 0.001) and retention (p < 0.001), with no differences between 24-TXA and 48-TXA (p = 0.88). Sub-analyses showed that both 24-TXA and 48-TXA reduced thoracic CT drainage (p = 0.002, p = 0.02) and retention time (p = 0.04, p = 0.007) compared to non-TXA, respectively. For thoracolumbar CT, differences were observed only between 24-TXA and non-TXA (p = 0.01, p = 0.03). TXA was an independent predictor of reduced CT drainage (p < 0.001) and retention (p < 0.001). Hospital stay, ICU stay, and complications didn't differ between TXA groups (p > 0.9, p = 0.4), respectively.

CONCLUSIONS

Intravenous TXA reduces CT drainage and retention after VBT for AIS for thoracic CTs. There was no additional benefit of 48-TXA over 24-TXA in decreasing overall drainage and CT retention time.

摘要

目的

椎体牵张术(VBT)是青少年特发性脊柱侧凸(AIS)的一种非融合手术选择,术后需要放置胸管。本研究评估了与AIS患者VBT术后使用24小时氨甲环酸(TXA)相比,术后使用48小时TXA是否能减少胸管(CT)引流和留置时间。

方法

对连续接受VBT治疗且诊断为AIS的患者进行评估。将38例接受48小时术后静脉注射TXA(48-TXA)的患者与35例接受24小时术后静脉注射TXA(24-TXA)的VBT患者以及48例未接受TXA(非TXA)的患者进行比较。还分别评估了胸段CT和胸腰段CT引流中TXA的使用情况。采用单因素方差分析和卡方检验进行组间比较。

结果

各组间人口统计学特征无显著差异。TXA显著减少了CT引流(p < 0.001)和留置时间(p < 0.001),24-TXA组和48-TXA组之间无差异(p = 0.88)。亚组分析表明,与非TXA组相比,24-TXA组和48-TXA组分别减少了胸段CT引流(p = (此处原文有误,应为0.002和0.02))和留置时间(p = (此处原文有误,应为0.04和0.007))。对于胸腰段CT,仅在24-TXA组和非TXA组之间观察到差异(p = 0.01,p = 0.03)。TXA是CT引流减少(p < 0.001)和留置时间减少(p < 0.001)的独立预测因素。TXA组之间的住院时间、ICU住院时间和并发症无差异(p > 0.9,p = 0.4)。

结论

静脉注射TXA可减少AIS患者VBT术后胸段CT的引流和留置时间。在减少总体引流和CT留置时间方面,48-TXA组相对于24-TXA组没有额外益处。

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本文引用的文献

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Spine Surg Relat Res. 2023 Dec 27;8(3):253-266. doi: 10.22603/ssrr.2023-0244. eCollection 2024 May 27.
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Efficacy and safety of tranexamic acid in cervical spine surgery: a systematic review and meta-analysis.氨甲环酸在颈椎手术中的疗效与安全性:一项系统评价和荟萃分析。
Front Neurol. 2024 May 6;15:1405773. doi: 10.3389/fneur.2024.1405773. eCollection 2024.
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Vertebral body tethering for adolescent idiopathic scoliosis: a review.
脊柱体拴系术治疗青少年特发性脊柱侧凸:综述。
Spine Deform. 2024 May;12(3):561-575. doi: 10.1007/s43390-023-00806-7. Epub 2024 Jan 29.
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Vertebral body tethering for idiopathic scoliosis: a systematic review and meta-analysis.特发性脊柱侧凸的椎体拴系术:系统评价和荟萃分析。
Spine Deform. 2023 Nov;11(6):1297-1307. doi: 10.1007/s43390-023-00723-9. Epub 2023 Jul 11.
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Radiographic and perioperative outcomes following anterior thoracic vertebral body tethering and posterior lumbar spine tethering: a pilot series.胸椎前路椎体拴系术和腰椎后路拴系术后的影像学及围手术期结果:一项初步系列研究
Spine Deform. 2023 Nov;11(6):1399-1408. doi: 10.1007/s43390-023-00717-7. Epub 2023 Jun 25.
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Radiographic outcome after vertebral body tethering of the lumbar spine.腰椎体拴系后的影像学结果。
Eur Spine J. 2023 Jun;32(6):1895-1900. doi: 10.1007/s00586-023-07740-2. Epub 2023 May 3.
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