Liao Weixiong, Zhang Hao, Li Zhongli, Li Ji
Department of Orthopedics, General Hospital of PLA, No. 28 Fuxing Road, Haidian District, Beijing, China.
Clin Orthop Relat Res. 2016 May;474(5):1269-79. doi: 10.1007/s11999-015-4663-5. Epub 2016 Jan 4.
Arthroscopic double-row suture-anchor fixation and open reduction and internal fixation (ORIF) are used to treat displaced greater tuberosity fractures, but there are few data that can help guide the surgeon in choosing between these approaches.
QUESTIONS/PURPOSES: We therefore asked: (1) Is there a difference in surgical time between arthroscopic double-row suture anchor fixation and ORIF for isolated displaced greater tuberosity fractures? (2) Are there differences in the postoperative ROM and functional scores between arthroscopic double-row suture anchor fixation and ORIF for isolated displaced greater tuberosity fractures? (3) Are there differences in complications resulting in additional operations between the two approaches?
Between 2006 and 2012, we treated 79 patients surgically for displaced greater tuberosity fractures. Of those, 32 (41%) were considered eligible for our study based on inclusion criteria for isolated displaced greater tuberosity fractures with a displacement of at least 5 mm but less than 2 cm. During that time, we generally treated patients with displaced greater tuberosity fractures with a displacement greater than 1 cm or with a fragment size greater than 3×3 cm with open treatment, and patients with displaced greater tuberosity fractures with a displacement less than 1 cm or with a fragment size less than 3×3 cm with arthroscopic treatment. Fifty-three underwent open treatment based on those indications, and 26 underwent arthroscopic treatment, of whom 17 (32%) and 15 (58%) were available for followup at a mean of 34 months (range, 24-28 months). All patients with such fractures identified from our institutional database were treated by these two approaches and no other methods were used. Surgical time was defined as the time from initiation of the incision to the time when suture of the incision was finished, and was determined by an observer with a stopwatch. Patients were followed up in the outpatient department at 6, 12, and 24 weeks, and every 6 month thereafter. Radiographs showed optimal reduction immediately after surgery and at every followup. Radiographs were obtained to assess fracture healing. Patients were followed up for a mean of 34 months (range, 24-48 months). At the last followup, ROM, VAS score, and American Shoulder and Elbow Surgeons (ASES) score were used to evaluate clinical outcomes. All these data were retrieved from our institutional database through chart review. Complications were assessed through chart review by one observer other than the operating surgeon.
Patients who underwent arthroscopic double-row suture anchor fixation had longer surgical times than did patients who underwent ORIF (mean, 95.3 minutes, SD, 10.6 minutes vs mean, 61.5 minutes, SD, 7.2 minutes; mean difference, 33.9 minutes; 95% CI, 27.4-40.3 minutes; p < 0.001). All patients achieved bone union within 3 months. Compared with patients who had ORIF, the patients who had arthroscopic double-row suture anchor fixation had greater ranges of forward flexion (mean, 152.7°, SD, 13.3° vs mean, 137.7°, SD, 19.2°; p = 0.017) and abduction (mean, 146.0°, SD, 16.4° vs mean, 132.4°, SD, 20.5°; p = 0.048), and higher ASES score (mean, 91.8 points, SD, 4.1 points vs mean, 87.4 points, SD, 5.8 points; p = 0.021); however, in general, these differences were small and of questionable clinical importance. With the numbers available, there were no differences in the proportion of patients experiencing complications resulting in reoperation; secondary subacromial impingement occurred in two patients in the ORIF group and postoperative stiffness in one from the ORIF group. The two patients experiencing secondary subacromial impingement underwent reoperation to remove the implant. The patient with postoperative stiffness underwent adhesion release while receiving anesthesia, to improve the function of the shoulder. These three patients had the only reoperations.
We found that in the hands of surgeons comfortable with both approaches, there were few important differences between arthroscopic double-row suture anchor fixation and ORIF for isolated displaced greater tuberosity fractures. Future, larger studies with consistent indications should be performed to compare these treatments; our data can help inform sample-size calculations for such studies.
Level III, therapeutic study.
关节镜下双排缝线锚钉固定术和切开复位内固定术(ORIF)用于治疗移位的大结节骨折,但几乎没有数据可帮助外科医生在这两种方法之间做出选择。
问题/目的:因此,我们提出以下问题:(1)对于孤立的移位大结节骨折,关节镜下双排缝线锚钉固定术和ORIF在手术时间上是否存在差异?(2)对于孤立的移位大结节骨折,关节镜下双排缝线锚钉固定术和ORIF在术后活动度(ROM)和功能评分上是否存在差异?(3)这两种方法在导致再次手术的并发症方面是否存在差异?
2006年至2012年期间,我们对79例移位大结节骨折患者进行了手术治疗。其中,32例(41%)根据孤立移位大结节骨折的纳入标准被认为符合我们的研究条件,其移位至少5mm但小于2cm。在此期间,我们一般对移位大于1cm或骨折块大小大于3×3cm的移位大结节骨折患者采用切开治疗,对移位小于1cm或骨折块大小小于3×3cm的移位大结节骨折患者采用关节镜治疗。根据这些指征,53例患者接受了切开治疗,26例患者接受了关节镜治疗,其中17例(32%)和15例(58%)可进行平均34个月(范围24 - 28个月)的随访。我们机构数据库中识别出的所有此类骨折患者均采用这两种方法治疗,未使用其他方法。手术时间定义为从切口开始至切口缝合完成的时间,由一名观察者使用秒表确定。患者在门诊分别于术后6周、12周和24周进行随访,此后每6个月随访一次。术后及每次随访时的X线片均显示骨折达到最佳复位。通过X线片评估骨折愈合情况。患者平均随访34个月(范围24 - 48个月)。在最后一次随访时,采用ROM、视觉模拟评分(VAS)和美国肩肘外科医师(ASES)评分评估临床结果。所有这些数据均通过病历审查从我们机构的数据库中获取。并发症由主刀医生以外的一名观察者通过病历审查进行评估。
接受关节镜下双排缝线锚钉固定术的患者手术时间比接受ORIF的患者长(平均95.3分钟,标准差10.6分钟,而平均61.5分钟,标准差7.2分钟;平均差异33.9分钟;95%可信区间27.4 - 40.3分钟;p < 0.001)。所有患者均在3个月内实现骨愈合。与接受ORIF的患者相比,接受关节镜下双排缝线锚钉固定术的患者前屈活动度更大(平均152.7°,标准差13.3°,而平均137.7°,标准差19.2°;p = 0.017)、外展活动度更大(平均146.0°,标准差16.4°,而平均132.4°,标准差20.5°;p = 0.048),ASES评分更高(平均91.8分,标准差4.1分,而平均87.4分,标准差5.8分;p = 0.021);然而,总体而言,这些差异较小,临床意义存疑。就现有数据而言,两组患者中因并发症导致再次手术的比例没有差异;ORIF组有2例患者发生继发性肩峰下撞击,1例患者出现术后僵硬。发生继发性肩峰下撞击的2例患者接受了再次手术取出植入物。术后僵硬的患者在麻醉下进行了粘连松解,以改善肩部功能。这3例患者是仅有的接受再次手术的患者。
我们发现,对于熟练掌握这两种方法的外科医生来说,关节镜下双排缝线锚钉固定术和ORIF治疗孤立的移位大结节骨折之间几乎没有重要差异。未来应开展更大规模、适应证一致的研究来比较这些治疗方法;我们的数据可为这类研究的样本量计算提供参考。
三级,治疗性研究。