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因青少年特发性脊柱侧凸后路矫形术后血胸导致的急性呼吸衰竭:病例报告。

Acute respiratory failure due to hemothorax after posterior correction surgery for adolescent idiopathic scoliosis: a case report.

机构信息

Department of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.

出版信息

BMC Musculoskelet Disord. 2013 Apr 11;14:132. doi: 10.1186/1471-2474-14-132.

Abstract

BACKGROUND

Although posterior correction and fusion surgery using pedicle screws carries the risk of vascular injury, a massive postoperative hemothorax in a patient with adolescent idiopathic scoliosis (AIS) is quite rare. We here report a case of a 12-year-old girl with AIS who developed a massive postoperative hemothorax.

CASE PRESENTATION

The patient had a double thoracic curve with Cobb angles of 63° at T2-7 and 54° at T7-12. Posterior correction and fusion surgery was performed using a segmental pedicle screw construct placed between T2 and T12. Although the patient's respiration was stable during the surgery, 20 minutes after removing the trachea tube, the patient's pulse oximetry oxygen saturation suddenly decreased to 80%. A contrast CT scan showed a massive left hemothorax, and a drainage tube was quickly inserted into the chest. The patient was re-intubated and a positive end-expiratory pressure of 5 cmH(2)O applied, which successfully stopped the bleeding. The patient was extubated 4 days after surgery without incident. Based on contrast CT scans, it was suspected that the hemothorax was caused by damage to the intercostal arteries or branches during pedicle probing on the concave side of the upper thoracic curve. Extensive post-surgical blood tests, echograms, and CT and MRI radiographs did not detect coagulopathy, pulmonary or vascular malformation, or any other possible causative factors.

CONCLUSION

This case underscores the potential risk of massive hemothorax related to thoracic pedicle screw placement, and illustrates that for this serious complication, respiratory management with positive airway pressure, along with a chest drainage tube, can be an effective treatment option.

摘要

背景

尽管后路矫正和融合手术使用椎弓根螺钉有血管损伤的风险,但青少年特发性脊柱侧凸(AIS)患者术后发生大量血胸的情况非常罕见。我们在此报告一例 AIS 患者术后发生大量血胸的病例。

病例介绍

该患者存在双胸脊柱侧凸,T2-7 段 Cobb 角为 63°,T7-12 段 Cobb 角为 54°。后路矫正和融合手术采用 T2 至 T12 之间的节段性椎弓根螺钉结构进行。尽管患者在手术过程中呼吸稳定,但在拔除气管导管后 20 分钟,患者的脉搏血氧饱和度突然降至 80%。对比 CT 扫描显示大量左侧血胸,并迅速在胸部插入引流管。患者重新插管,并应用 5cmH₂O 的呼气末正压,成功止血。患者术后 4 天无并发症拔管。基于对比 CT 扫描,怀疑血胸是由于上胸侧凸凹侧椎弓根探查时肋间动脉或分支损伤引起的。广泛的术后血液检查、超声、CT 和 MRI 影像学检查未发现凝血功能障碍、肺或血管畸形或任何其他可能的致病因素。

结论

本病例强调了胸椎椎弓根螺钉置入相关大量血胸的潜在风险,并表明对于这种严重并发症,使用正压气道呼吸管理和胸腔引流管可以是一种有效的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa20/3636110/e13513da2bd1/1471-2474-14-132-1.jpg

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