Robinson Yohan, Tschöke Sven Kevin, Stahel Philip F, Kayser Ralph, Heyde Christoph E
Charité - Campus Benjamin Franklin, Centre for Trauma and Reconstructive Surgery, Berlin, Germany.
Patient Saf Surg. 2008 Jan 15;2:2. doi: 10.1186/1754-9493-2-2.
Kyphoplasty represents an established minimal-invasive method for correction and augmentation of osteoporotic vertebral fractures. Reliable data on perioperative and postoperative complications are lacking in the literature. The present study was designed to evaluate the incidence and patterns of perioperative complications in order to determine the safety of this procedure for patients undergoing kyphoplasty.
We prospectively enrolled 102 consecutive patients (82 women and 20 men; mean age 69) with 135 operatively treated fractured vertebrae who underwent a kyphoplasty between January 2004 to June 2006. Clinical and radiological follow-up was performed for up 6 months after surgery.
Preoperative pain levels, as determined by the visual analogous scale (VAS) were 7.5 +/- 1.3. Postoperative pain levels were significantly reduced at day 1 after surgery (VAS 2.3 +/- 2.2) and at 6-month follow-up (VAS 1.4 +/- 0.9). Fresh vertebral fractures at adjacent levels were detected radiographically in 8 patients within 6 months. Two patients had a loss of reduction with subsequent sintering of the operated vertebrae and secondary spinal stenosis. Accidental cement extravasation was detected in 7 patients in the intraoperative radiographs. One patient developed a postoperative infected spondylitis at the operated level, which was treated by anterior corporectomy and 360 degrees fusion. Another patient developed a superficial wound infection which required surgical revision. Postoperative bleeding resulting in a subcutaneous haematoma evacuation was seen in one patient.
The data from the present study imply that percutaneous kyphoplasty can be associated with severe intra- and postoperative complications. This minimal-invasive surgical procedure should therefore be performed exclusively by spine surgeons who have the capability of managing perioperative complications.
椎体后凸成形术是一种成熟的用于矫正和强化骨质疏松性椎体骨折的微创方法。文献中缺乏关于围手术期和术后并发症的可靠数据。本研究旨在评估围手术期并发症的发生率和类型,以确定椎体后凸成形术对接受该手术患者的安全性。
我们前瞻性纳入了2004年1月至2006年6月期间连续102例接受椎体后凸成形术治疗的患者(82例女性和20例男性;平均年龄69岁),共135个手术治疗的骨折椎体。术后进行了长达6个月的临床和影像学随访。
术前视觉模拟评分(VAS)确定的疼痛水平为7.5±1.3。术后第1天(VAS 2.3±2.2)和6个月随访时(VAS 1.4±0.9)疼痛水平显著降低。6个月内通过影像学检查发现8例患者相邻节段出现新鲜椎体骨折。2例患者出现复位丢失,随后手术椎体发生骨融合和继发性椎管狭窄。术中X线片发现7例患者发生意外骨水泥渗漏。1例患者在手术节段发生术后感染性脊柱炎,经前路椎体切除和360度融合治疗。另1例患者发生浅表伤口感染,需要手术修复。1例患者术后出血导致皮下血肿清除。
本研究数据表明,经皮椎体后凸成形术可能伴有严重的术中及术后并发症。因此,这种微创手术应由有能力处理围手术期并发症的脊柱外科医生专门进行。