Fixation of os acromiale using polyester sutures: a novel surgical treatment
Introduction
Gruber first described os acromiale in a cadaver study in 1863 (1). The acromion develops from 4 separate ossification centers: the pre-acromion, meso-acromion, meta-acromion, and basi-acromion from anterior to posterior. The fusion of the 4 ossification centers occurs between the age of 15 and 25 years (2). Os acromiale is the failure of fusion between any of the 4 ossification centers after the age of 25 years.
The real incidence of this phenomenon was unknown because os acromiale usually shows no symptoms and is found incidentally on radiographic examinations (3). The reported incidence ranged from 1% to 30%, and bilateral os acromiale incidence ranged from 33% to 62% (4-6).
Patients with unstable os acromiale often complain of shoulder pain, and the symptoms usually include difficulty sleeping on the affected side during the night and troubles doing overhead activities, which are quite similar symptoms as those found in rotator cuff tears and subacromial impingement. Non-steroidal anti-inflammatory drugs (NSAIDs) are initially prescribed, along with physical therapy. If non-surgical treatments are not effective after 6 months, surgical treatments are considered (6). In the literature, numerous surgical treatment options have been introduced, including fragment excision, open reduction and internal fixation (ORIF) with K-wires or screws, and arthroscopic subacromial decompression with acromioplasty (7-9). In this study, a novel surgical treatment using polyester sutures to fix unstable os acromiale is introduced, and clinical results are reported.
Methods
We retrospectively studied 10 shoulders that were diagnosed with os acromiale from January 2014 to January 2016. All of the patients received oral NSAIDs for at least 6 months without any relief from shoulder pain. There were two males and eight females, with an average age of 62 years ranging from 57 to 66 years at the time of surgery. The diagnosis and treatments for each patient are presented in Table 1. All 10 cases were of the meso-acromion type.
Full table
All patients were followed up for at least 24 months (average 28.7 months; range, 26 to 33 months). The clinical charts and surgery reports, including arthroscopic images and photos taken during the operations, pre-operation, and follow-up radiographs, were all reviewed. The standardized scores and visual analog scale (VAS) were recorded preoperatively and at each follow-up. A computed tomography (CT) scan was ordered at the follow-up of 12 months.
Surgical treatments
The first patient of our case series was a 62-year-old female who complained of right shoulder pain after a trauma. On physical examination, there was tenderness over the acromioclavicular (AC) joint. The patient showed a limited range of motion, both actively and passively. They also returned positive results for Neer sign, Hawkins sign, and empty can test. Magnetic resonance imaging (MRI) revealed a partially-torn supraspinatus tendon and adhesive capsulitis, which agreed with the symptoms and physical examination findings. After 6 months of conservative treatment without significant relief, the patient underwent surgical treatment. A routine diagnostic arthroscopy was carried out, and a partial bursa-sided rotator cuff tear with capsulitis was confirmed. After a subacromial debridement, os acromiale was revealed, which was unexpected before the surgery. During the operation, we reviewed the magnetic resonance (MR) images and found the os acromiale on very proximal and lateral cuts (Figure 1) from the axial plane and oblique sagittal plane images, which were overlooked on preoperative estimation.
After arthroscopic repair of the rotator cuff and release of the capsule, we decided to make a small incision over the acromion to fix the os acromiale. After complete exposure of the acromion, we found that the bone quality was reduced for the 62-year-old woman. Screw fixation or metal cerclage with wires seemed difficult. Consequently, we used two #5 Ethibond sutures (Ethicon, Somerville, NJ, USA) instead to reduce the risks of bone cuttings from the metal fixations. Two sutures were used for cerclage from anterior to posterior, and proper fixation was confirmed during the operation (Figure 2).
For the other nine shoulder cases, os acromiale was diagnosed before surgery and was confirmed during a routine diagnostic bursoscopy. Arthroscopic fixation of os acromiale using polyester sutures was applied, which has thus far not been reported in previous studies. The patient was put in a lateral decubitus position. With the arthroscope placed in the subacromial bursa through the posterior portal, the os acromiale could be identified. A radiofrequency device was used to remove the soft tissues underneath the acromion so that the os acromiale was wholly exposed. Following exposure of the undersurface of the acromion, a rasp was used to prepare the two fragments (Figure 3A). Sufficient punctate bleeding on both sides of the two fragments was important for the bony fusion of the os acromiale (Figure 3B). A spinal needle was put percutaneously from the posterior board of the acromion and underneath it (Figure 3C). A PDS II suture was shuttled through and grasped out of the lateral portal. The PDS II suture was used as a guide, and one end of a #5 Ethibond suture was pulled in from the lateral portal and outside posteriorly. The step was repeated from the anterior board. Two #5 Ethibond sutures were used (Figure 3D, Figure 4A). The Ethibond sutures were retrieved from a small incision of about 5 mm made above the acromion (Figure 4B), and knots were made using a knot pusher. The arthroscopic view demonstrated that the margin between the two fragments was gone (Figure 4C).
As listed in Table 1, there were three cases diagnosed as os acromiale alone without frozen shoulder, rotator cuff tears, SLAP lesion, or biceps tendon lesion. For the other seven cases, arthroscopic rotator cuff repair was carried out in four cases accompanied with rotator cuff tears, capsular release in three cases with frozen shoulder. In one case, inflammation of the biceps tendon was diagnosed. Considering the patient was a 64-year-old female, we cut the tendon from the superior part of the labrum without fixation.
Statistical analysis
All the data were analyzed in SPSS (version 19 Chicago, IL, USA). Paired t-test was used to compare the Constant scores and VAS scores. A P value of lower than 0.05 was considered statistically significant.
Results
All the patients were followed up with at our department. There were no severe complications, and all of them showed good recovery 6 months after the surgery. The average follow-up length was 28.7 months, ranging from 26 to 33 months. The average Constant score before surgery was 40.50±4.53 points, and it was significantly improved to 75.60±5.17 points after surgery. The average VAS score was reduced from 5.20±1.14 points to 1.60±0.84 (Table 2).
Full table
At the follow-up of 12 months, a CT scan was ordered. All the patients showed the bony union of the os acromiale. On the CT scan, two small pits could be seen on the medial and lateral side of the acromion, which indicated the level of the os acromiale. The position of the os acromiale was good, and no evident sclerosis was found on the edges of the fragments (Figure 5).
Discussion
Anteroposterior (AP) and outlet radiographs were most commonly used in screening shoulder pain patients in our department. However, an axillary lateral radiograph was most useful in diagnosing os acromial (6,10), which was not our routine examination. On MR images, os acromiale was frequently missed because it had a strong resemblance to a normal AC joint in the coronal or sagittal planes. It was most reliable to make the diagnosis of extremely proximal axial planes. For the first case of our series, those critical planes were overlooked before the surgery, and the diagnosis of os acromiale was not made until during the bursoscopy. Fortunately, it was well managed, and we gained experience and did not miss any os acromiale for the rest of the case series.
In the literature shown in Table 3, several surgical techniques were introduced. Warner et al. performed open excision of os acromiale on three patients, but 2 of them were unsatisfied with the outcomes and complained of persistent pain and deltoid weakness (3). However, Mudge et al. reported positive results in 4 out of six patients who received open fragment excision with rotator cuff wear (7). Pagnani et al. performed arthroscopic excision of os acromiale and demonstrated positive clinical functions for the operated shoulders (11). Wright et al. reported similar findings (9). However, there were no studies comparing the outcomes of open and arthroscopic excisions. Hutchinson and Veenstra performed arthroscopic subacromial decompression on three patients for impingement syndrome secondary to os acromiale (12). Despite this, 2 of them had recurrence of symptoms. Wright et al. performed a more aggressive subacromial decompression procedure on 13 shoulders with impingement symptoms due to os acromiale (9). The entire unstable anterior tip was almost resected, leaving only a thin superior shell. Twelve shoulders showed satisfactory clinical results. With inconsistent results of clinical outcomes, it remains controversial as to which of the above-mentioned options is superior. We believe that the small sample sizes of the previous studies might be a reason for the mixed results reported.
Full table
ORIF surgery was another option for treating symptomatic os acromiale, and numerous techniques for ORIF have been reported including K-wire fixation, screw fixation, and tension band fixation with cannulated screws (13-15). Complications of ORIF mainly include hardware irritation, acromial fracture, and nonunion.
In this study, we reported a novel surgical technique to fix os acromiale with polyester sutures arthroscopically. By using polyester sutures, some of the complications in previously reported studies can be avoided. First, polyester sutures are soft fixation materials, so hardware irritation did not exist in our case series, and there was no need to remove them. Second, the risk of acromial fracture was avoided. Cerclage with polyester sutures does not involve drilling holes in a small acromion, and os acromiale is not only technically challenging but also might cause a fracture. For the first case in our study, we intended to do a cerclage with wires, but we found that the bones easily got cut at the acromion due to osteoporosis. Polyester sutures were a better choice in this condition.
Tension strength and nonunion of the os acromiale were our greatest concern. Although we did not have direct evidence that polyester sutures could provide as strong stability as screws or wires, in a cadaver study, Shiu et al. reported that polyethylene sutures and stainless steel wires had similar biomechanical strength in the cannulated screw tension band fixation of os acromiale (16). In our clinical study, CT scans were carried out for each patient at the follow-up of 12 months, and we found that all the patients had a bony union of the os acromiale. These findings suggested that polyester sutures can provide enough tension for the fixation.
One limitation in this study was that we were not sure if fixation and bony union of the os acromiale helped in pain relief and function restoration of the shoulder. Burkhart reported that os acromiale may be completely unrelated to the true source of the patient’s discomfort (17). In our case series, only three patients were diagnosed as isolated os acromiale. Although all 3 of them achieved satisfactory clinical outcomes, fixation was not the only procedure they underwent, and the effect of the routine subacromial debridement should not be overlooked. A well-designed randomized controlled trial is needed to achieve a more comprehensive understanding of this issue.
Conclusions
Polyester sutures could provide reliable strength in fixation of os acromiale without hardware irritation.
Acknowledgments
The authors thank Xi Chen and Jiaze Song for valuable suggestions.
Footnote
Conflicts of Interest: The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. Ethical approval for this study was obtained from written informed consent signed by all the patients before the study. In the consent, all the patients were well informed and agreed that data regarding radiology examinations, pictures taken during the surgery, follow-up function scores, pathological examinations would be analyzed for any retrospective studies. The registration numbers are 0500703, 0639938, 0679015, 0745431, 0792030, 0851513, 0905400, 0909211, 0939212, 0942022.
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