Abstract
Purpose of Review
The purpose of this review is to examine trends, outcomes, and principles in treatment of proximal humerus fractures in the elderly with a critical focus on reverse shoulder arthroplasty as a developing treatment option.
Recent Findings
Recent literature shows an increase in reverse shoulder arthroplasty and a decrease in hemiarthroplasty performed for proximal humerus fractures. More predictable outcomes and lower revision rates are seen in older individuals treated primarily or secondarily with reverse shoulder arthroplasty compared to those treated with hemiarthroplasty.
Summary
We report current and historical treatments, outcomes, and principles in reverse shoulder arthroplasty for treatment of complex, displaced proximal humerus fractures in older individuals (≥ 65 years old).
Keywords: Reverse shoulder arthroplasty, Proximal humerus fracture, Fragility fracture, Fracture sequelae
Introduction
Proximal humerus fractures make up 5% of all fractures and are the third most common fracture in patients who are 65 years and older [1]. These fractures predominantly occur in women (70%) and occur at the highest frequency from ages 80 to 84 years old [2–8]. Initial projections suggested a potential three-fold increase in the rate of proximal humerus fractures by 2030 [7], but newer data showed a flat incidence from 2006 to 2012 and subsequent projections are tempered [9].
While younger patients are typically victim to high-energy trauma, the predominant injury mechanism overall is a fall from standing height [10]. These fragility fractures, occurring in low energy mechanisms, are a sentinel marker of poor bone health and general health decline. At 1-year post-injury, there is a 10% mortality rate for proximal humerus fracture regardless of treatment [11]. Patients who do not live alone, who do not participate in recreational activities, and who are not independent of their activities of daily life are at significantly higher risk for a poor outcome [3].
Medical, functional, and fracture-specific complexities make treatment of these injuries challenging. Regardless, 67–85% of proximal humerus fractures are treated nonoperatively [1, 5]. But as technology and patient demand evolve, the rate of surgical intervention is increasing [1, 2]. The use of open reduction internal fixation (ORIF) has remained stable, hemiarthroplasty has decreased, and reverse shoulder arthroplasty (RSA) has increased [1, 5, 8, 9, 12•, 13, 14]. Reports on the utilization of RSA for proximal humerus fractures are variable, but all show an increase over the past decade ranging from 26% in 2011 to 67.4% in 2015 [1, 5, 8, 12•, 14, 15]. Surgical treatment choice for proximal humerus fracture is highly dependent on patient anatomy, fracture pattern, pre-injury functional status, medical comorbidities, and surgeon skill level and bias.
Nonoperative Treatment
Nonoperative management of displaced 3- and 4-part proximal humerus fractures uniformly leads to low functional scores and loss of range of motion in active, independent individuals [16, 17]. Increasing fracture fragments and magnitude of displacement predicts worse outcomes, functional scores, and range of motion limitations with nonoperative treatment [18]. However, proximal humerus fractures with more simple patterns, those that are minimally displaced or that occur in the low-demand patient are often amenable to closed treatment. Acceptable functional outcomes have been observed in patients with translated 2-part proximal humerus fractures with average displacement of > 66% [19], valgus impacted 1- and 2-part fractures [20, 21], and fractures with < 5 mm displacement of the greater tuberosity [22]. In such cases, return to adequate function can be achieved with close observation for 3–4 weeks, followed by progressive passive range of motion as the fracture consolidates. Recently the PROFHER Trial [23], a multicenter, parallel-group randomized clinical trial comparing surgical and nonsurgical treatment of surgical neck fractures of the proximal humerus and its subsequent 5-year follow-up study [24••] concluded that there were no differences between surgical and non-surgical groups at 2- [23] and 5-year [24••]follow-up intervals. While the study design is certainly a strength, the majority of these fractures were not the displaced 3- and 4-part fractures (50% were 2-part) that come to mind when considering surgical intervention. Additionally, the surgical procedures varied including ORIF, intramedullary nails, hemiarthroplasty, and “other” treatments. Finally, there were 1000 patients out of 1250 patients that were excluded from final analysis (80 of which were “obviously operative”), which introduces the possibility of significant bias. Active patients with highly displaced fractures and surgeons continue to look for better options than a sling in returning to optimal function.
Proximal Humerus Fracture Surgical Treatment
Historical
Proximal humerus fractures have challenged clinicians for many years [25]. Treatment in the nineteenth century was hallmarked by the Hippocratic method of reduction followed by bandaging and delayed splinting. In the twentieth century, further surgical and anesthetic advancements sparked attempts at ORIF [26]. The first documented shoulder arthroplasty was reportedly performed by Jules Emile Pean in 1893 for tuberculosis [27]. However, Dr. Charles Neer II popularized and revolutionized the idea of shoulder arthroplasty and humeral head replacement in 1955 to mitigate the risk of avascular necrosis or flail shoulder associated with open reduction and excision of proximal humerus fractures [28]. His classification of proximal humerus fractures followed in 1970 as well as his criteria for evaluation of treatment results [29]. The follow-up report on treatment of 3- and 4-part proximal humerus fractures treated with closed reduction, ORIF, and hemiarthroplasty showed that closed treatment was inadequate in active patients, ORIF was more effective in 3-part fractures, and hemiarthroplasty was superior in the 4-part group [30]. However, results were only satisfactory and Dr. Neer had “limited expectations” for the final limb function, ultimately describing the treatment as imperfect [30]. In years to follow, Dr. Neer’s hypothesis was tested and expounded upon in an attempt to improve outcomes for patients with proximal humerus fractures.
ORIF with Standard Implants
In the 1980s and 1990s ORIF with a variety of constructs like non-locking plates, wires, and pins produced variable results for 3- and 4-part proximal humerus fractures. All techniques and implants had marginally acceptable complication rates and outcomes [31–34]. While percutaneous pinning has merits in young patients with simple fractures and good bone quality, it is inadequate fixation in osteoporotic bone.
ORIF with Locked Plates
The introduction of pre-contoured locking plates, in particular the proximal humerus internal locking system (PHILOS), demonstrated biomechanical promise with good initial functional outcomes. However, longer-term follow-up revealed frequent complications with high rates of screw perforation into the glenohumeral joint and screw cut-out [35–42]. Brunner et al. in a 2009 prospective multicenter analysis of this treatment found a 9% implant-related complication rate and a 35% overall complication rate at 1-year follow-up using the PHILOS system. The most common implant complications were primary screw perforation (14%) and secondary screw perforation (8%) [35]. Additionally, Owsley and Gorczyca observed a 36% radiographic complication rate, including 23% intra-articular screw displacement and 25% varus displacement > 10°. Patients older than 60 years of age were significantly more at risk for these complications (57% vs. 22%, p = 0.0015) [41].
More important than the technology itself, improvements have been made in the understanding of how and when to best perform ORIF. We have learned important predictors of success include restoration or maintenance of the medial calcar [43], avoiding varus alignment [44], and less aggressive proximal screw fixation [45]. Although not biomechanically shown to be beneficial, rotator cuff sutures have become the standard among fracture surgeons for fragment mobilization, provisional reduction, and final construct incorporation [46]. More recent analyses of proximal humerus fractures treated with newer locking plates show less complications and improved outcomes. In the most recent 3 years studied (2011–2013), there were significantly less failures due to loss of fixation (5.7% vs. 12.8%, p = 0.006) and overall revision rate (3.2% vs. 15.3%, p = 0.00004) compared to the first 3 years of the study (2002–2004) [47]. Improved results with ORIF in recent years are likely multifactorial. Improved understanding of patient prognostic factors, refined surgical techniques, and surgeon experience have been critical. While locking technology has advanced little since the PHILOS plate, our implementation of it has improved. In addition, advances in arthroplasty technology provide the surgeon alternatives in fractures that would otherwise have pushed the indications for locking plate technology in previous decades.
Hemiarthroplasty
Popularized by Dr. Neer, the hemiarthroplasty became a viable treatment option for 3-part, 4-part, and head-splitting proximal humerus fractures. Humeral head replacement was an alternative to acute humeral head excision, glenohumeral arthrodesis, or for the prevention or treatment of osteonecrosis [28]. Much of Dr. Neer’s work focused on stratifying risk of osteonecrosis based on fracture severity. His surgical recommendations hinged on preventing this complication which he reported as high as 75% in 4-part fractures treated with ORIF [29]. In the wake of this, Hertel et al. went on to identify risk factors of osteonecrosis including (1) short medial calcar extension (< 8 mm), (2) disrupted periosteal hinge, and (3) anatomic neck fracture [48]. A later interrogation of these factors showed that while one risk factor does not increase the risk, all three factors, and more importantly a poor reduction were linked to the risk of osteonecrosis, but this complication only occurred in 3.7% of patients [49]. While osteonecrosis may occur after a proximal humerus fracture, contemporary studies show the reported rate in nonoperative treatments is 2% overall [21], and only 7.9% in operatively treated 3- and 4-part factures [42]. Further, the rate of symptomatic osteonecrosis in nonoperatively treated 3- and 4-part fractures is even lower, at 1.6% [50]. With the variety and success of surgical options today, the surgical approach and decision making for complex proximal humerus fractures should predicate on the surgeon’s ability to anatomically reconstruct and maintain reduction rather than on likelihood of head viability.
Hemiarthroplasty is largely marginalized except for in the rare, unreconstructible fractures in active, young adult patients. It is the senior author’s experience that a hemiarthroplasty for fracture should be a no more frequent than about once a year for even a busy shoulder surgeon. While significant initial pain relief is reported as a positive outcome in most hemiarthroplasty studies, the functional outcomes and range of motion results are highly variable and in many studies are quite poor [51, 52]. Boons et al. in a randomized controlled trial from 2012 detected no significant differences in older individuals treated nonoperatively and those treated with hemiarthroplasty for 4-part fractures [53]. Recovery and function after hemiarthroplasty are notably worse in older (> 55 years old) patients [54, 55].
Failure and poor outcomes are associated with prosthesis height overstuffing or humeral length increase > 10 mm, humeral head retroversion > 40°, low greater tuberosity positioning (10 mm inferior to the tangent line of the head), or high greater tuberosity positioning (5 mm superior to the tangent line of the head) [56]. Successful hemiarthroplasty outcome is dependent on anatomic tuberosity healing and head size and height, avoiding tuberosity resorption, and maintaining rotator cuff integrity [57••]. Indications for hemiarthroplasty are narrow. The procedure is technically demanding, and the construct relies heavily on the unpredictable healing of the tuberosities. Hemiarthroplasty is best reserved for the young patient with an unreconstructible proximal humerus fracture.
Reverse Shoulder Arthroplasty
Reverse shoulder arthroplasty initially was introduced as a solution for rotator cuff arthropathy. Initial prostheses failed, but Dr. Grammont revolutionized the design strategy in 1985 using the following principles: (1) inherent stability of prosthesis, (2) convex weightbearing portion, concave support portion, (3) the center of the sphere must be at or medial to the glenoid neck, and (4) medial and inferior center of rotation. While design details evolve, Dr. Grammont’s principles of RSA still guide implant development and surgical technique today [27].
In November 2003, the food and drug administration (FDA) approved the use of RSA in the USA. From 2003 to 2004, there was a large initial increase in shoulder arthroplasty and a subsequent steady annual increase thereafter [13]. As RSA volume increased, so did the body of literature and evidence to support its use for proximal humerus fractures [58–65]. The consistent challenges, failures, and variable outcomes with nonoperative treatment, ORIF, and hemiarthroplasty for proximal humerus fractures, particularly in elderly individuals, led to a significantly increased use of RSA for proximal humerus fractures mainly due to its independence of rotator cuff (tuberosity) healing.
The most commonly studied patient population for RSA is older adults (≥ 65 years old) with 3-part, 4-part, or head-splitting fractures of the proximal humerus. Initial results of RSA for acute proximal humerus fracture showed satisfactory mobility and functional outcomes, despite frequent radiographic migration of the tuberosities [63]. Early studies concluded that RSA for proximal humerus fracture provided pain relief, good functional outcome scores, and functional range of motion [63–65].
Surgical techniques, implant technology, and patient selection continue to be refined and have led to improved RSA outcomes for proximal humerus fractures. A 2016 retrospective review with mean 35-month follow-up of 52 patients, 59–89 years old, with 3- and 4-part proximal humerus fractures treated with RSA, reported mean postoperative constant score of 62 (range 16–69) [59]. Wright et al. in a prospective case series with 2.5-year follow-up of 30 patients, > 59 years old, with 3- and 4-part proximal humerus fractures, reported mean active forward elevation to 130° postoperatively and 97% stable radiographic appearance rate [60••]. In a quality of life analysis, Wolfensperger et al. reported that in 33 highly independent patients, 84% were back to previous levels of independence at 6 months postoperatively and 91% at 1-year postoperatively after RSA [62••] (please see Table 1 for summary of RSA outcome study results).
Table 1.
Reverse shoulder arthroplasty for proximal humerus fracture results
Author | Year | Mean Age (years) | Mean follow-up | No. of patients | Mean primary functional outcome score (range) | Mean active forward flexion (degrees) | Mean active external rotation (degrees) | Complication rate | Revision rate |
---|---|---|---|---|---|---|---|---|---|
Bufquin et al. [63] | 2007 | 78 | 22 months | 43 | CS 44 (16–69) | 97 (35–160) | 8 (− 40–40) | 27.9% | NA |
Grubhofer et al. [59] | 2016 | 77 | 35 months | 73 | CS 62 (21–83) | 118 (40–165) | 18 (0–65) | NA | 5.4% |
Wright et al. [60] | 2019 | 71 | 56 months | 21 | ASES 82.0 ± 13.5 | 130 ± 31 | 32 ± 18 | 14.3% | 4.7% |
Klein et al. [64] | 2008 | 75 | 33 months | 20 | CS 68 (47–98) | 123 (60–175) | 25 (10–35) | 15% | 10% |
Lenarz et al. [65] | 2011 | 76 | 23 months | 30 | ASES 78 (36–98) | 139 (90–180) | 27 (0–45) | 10% | 0% |
Wolfensperger et al. [62] | 2017 | 80 | 12 months | 33 | CS 71 (46–94) | NA | NA | 9% | 0% |
CS, constant score; ASES, American Shoulder and Elbow Surgeons Score; NA, not available
Despite the reliable results of RSA, outcomes are far from normal, and nonoperative management should be strongly considered in very low demand, medically unwell, or those strongly opposed to surgery. Roberson et al. in 2017 retrospectively compared patients who were recommended RSA and refused to those who elected to undergo RSA. While the study is confounded with a predominant selection bias, they found no significant functional, range of motion, or other clinical differences between RSA and nonoperative management at 1-year follow-up in 3- and 4- part proximal humerus fractures [66]. We counsel our patients that the goal is to achieve 80% for “normal” shoulder function that is painless and able to achieve self-care. We tell patients preoperatively that forward elevation can more predictably be achieved and rotation is less predictable. Most patients are able to reach the back of their head and perineum but unclipping a bra is unlikely.
RSA is also used as a salvage procedure after failure of closed treatment, ORIF, or hemiarthroplasty for proximal humerus fracture. Compared to primary RSA, these indications result in higher complication rates, higher revision rates, and marginally lower functional outcomes (please see Table 2 for summary of RSA as secondary procedure outcomes study results). Dezfuli et al. in a 2016 retrospective review identified that acute RSA outperformed RSA for malunion, nonunion, and conversion from ORIF or hemiarthroplasty. Additionally, RSA for malunion or nonunion outperformed revision from hemiarthroplasty [58]. Sebastia-Forcada et al. in a 2017 matched case-control study of patients who underwent primary RSA for fracture or secondary RSA after ORIF failure found that both groups improved significantly from preoperative state, but functional outcomes were significantly better in the primary RSA group [67••]. Shannon et al. in a 2016 retrospective review comparing primary RSA and RSA after failed ORIF found no significant differences in functional outcomes, but an increased complication rate in secondary RSA [61]. Finally, a 2019 systematic review and meta-analysis of acute versus delayed RSA for proximal humerus fractures by Torchia et al. found no difference in clinical outcome scores, forward flexion, or all cause-reoperation rate when comparing primary or secondary RSA for proximal humerus fracture [69••]. While RSA has good results as a salvage treatment, functional outcomes and complication rates are better in the primary setting.
Table 2.
Primary versus secondary reverse shoulder arthroplasty for proximal humerus fracture
Author | Year | 1° or 2° | Mean age (years) | Mean follow-up | No. of patients | Mean primary functional outcome score (range) | Mean active forward flexion (degrees) | Mean active external rotation (degrees) | Complication rate | Revision rate |
---|---|---|---|---|---|---|---|---|---|---|
Dezfuli et al. [58] | 2016 | 1° | 78 | 34 Months | 13 | CS 67 | 113 | 24 | 7.6% | 7.6% |
2° | 68 | 32 Months | 36 | CS 54 | 99 | 10 | 13.9% | 13.9% | ||
Shannon et al. [61] | 2016 | 1° | 75 | 36 Months | 18 | ASES 70.6 | 133 | 36 | 5% | 0% |
2° | 70 | 24 Months | 26 | ASES 64.6 | 130 | 42 | 8% | 0% | ||
Sebastia-Forcada et al. [67] | 2017 | 1° | 75 | 38 Months | 30 | CS 60.4 | 127 | 4.9 | 3.3% | 3.3% |
2° | 73 | 38 Months | 30 | CS 55.5 | 114 | 4.1 | 20% | 13.3% | ||
Seidl et al. [68] | 2016 | 1° | 77 | 45 Months | 15 | ASES 77 | 129 | 29 | 0% | 0% |
2° | 71 | 45 Months | 43 | ASES 72.4 | 118 | 13 | 22% | 4.7% |
CS, constant score; ASES, American Shoulder and Elbow Surgeons Score
1° is acute RSA for proximal humerus fracture; 2° is delayed RSA (malunion, nonunion, hemiarthroplasty, ORIF)
Reverse Shoulder Arthroplasty Versus Hemiarthroplasty
Despite the drastic rise in rate of RSA and drop in hemiarthroplasty for proximal humerus fractures, research and comparisons of the two surgical treatments continue [1, 12•]. In a 2019 systematic review and meta-analysis, Austin et al. found that in 421 RSA and 492 hemiarthroplasties, RSA significantly outperformed hemiarthroplasty for postoperative pain scores, functional outcomes scores, and forward flexion, whereas hemiarthroplasty had a significantly higher risk of reoperation [70••]. Shukla et al. in 2016 performed a meta-analysis and found forward flexion, abduction, tuberosity healing, and functional scores were all significantly better for RSA postoperatively, while external rotation was better for hemiarthroplasty [71]. Ferrel et al. performed a systematic review in 2014 and found that RSA patients have better forward flexion, but hemiarthroplasty had better external rotation. Additionally, there were complication rates of 9.6% for RSA and 4.1% for hemiarthroplasty, but reoperation rate for RSA was 1% and for hemiarthroplasty was 4% [72]. Gallinet et al. in 2018 performed a systematic review and meta-analysis and found that RSA patients had better clinical outcome scores and forward flexion, while hemiarthroplasty patients had better internal and external rotation. Additionally, there were higher complication and reoperation rates noted in RSA patients, but higher revision rates in hemiarthroplasty patients [73••]. Namdari et al. in a systematic review in 2013 found that RSA had 4.0 times greater odds of postoperative complications but concluded that many of those were radiographic without clinical consequence [74] (please see Table 3 for summary of RSA and hemiarthroplasty outcome study results).
Table 3.
Reverse shoulder arthroplasty versus hemiarthroplasty for proximal humerus fracture
Author | Year | RSA vs. HA | Mean age (years) | Mean follow-up | No. of Patients | Mean primary functional outcome score (range) | Mean active forward flexion (degrees) | Mean active external rotation (degrees) | Complication rate | Revision rate |
---|---|---|---|---|---|---|---|---|---|---|
Bonnevialle et al. [75] | 2016 | RSA | 78 | 39 months | 40 | CS 57 | 130 | 23 | 10% | 0% |
HA | 67 | 39 months | 57 | CS 54 | 112 | 28 | 24% | 1.7% | ||
Boyle et al. [76] | 2013 | RSA | 80 | 60 months | 55 | Oxford 41.5 | Not included | Not included | Not included | 1.7% |
HA | 72 | 60 months | 313 | Oxford 32.3 | Not included | Not included | Not included | 1.1% | ||
Chalmers et al. [77] | 2014 | RSA | 77 | 14 months | 9 | ASES 80 | 133 | 41 | 11% | 0% |
HA | 72 | 14 months | 9 | ASES 66 | 106 | 28 | 22% | 0% | ||
Cuff et al. [78] | 2013 | RSA | 74 | 24 months | 24 | ASES 77 | 139 | 24 | 9% | 0% |
HA | 74 | 24 months | 23 | ASES 62 | 100 | 25 | 8% | 13% | ||
Garrigues et al. [79] | 2012 | RSA | 75 | 42 months | 11 | ASES 81.1 | 121 | 34 | 9% | 0% |
HA | 75 | 42 months | 12 | ASES 47.4 | 91 | 31 | 33% | 25% | ||
Van der Merwe et al. [80] | 2017 | RSA | 78 | 60 months | 218 | Oxford 37.62 | Not included | Not included | Not included | 0.58% |
HA | 72 | 60 months | 427 | Oxford 32.74 | Not included | Not included | Not included | 1.16% |
CS, constant score; ASES, American Shoulder and Elbow Surgeons Score, Oxford, Oxford Shoulder Score
Extensive comparison of RSA and hemiarthroplasty in older adults with 3-part, 4-part, and head-splitting proximal humerus fractures shows that more favorable and reliable functional outcomes are seen in patients with RSA. While complication rate comparison is variable, revision rates are significantly lower in RSA patients. Additionally, the importance of purely radiographic complications is unknown [74]. Unlike the hemiarthroplasty, successful outcome with RSA is not fully dependent on tuberosity healing and rotator cuff integrity [57••]. However, tuberosity healing and anatomic tuberosity healing may improve constraint, and shoulder range of motion for patients with RSA [81•, 82•, 83•, 84•].
Reverse Shoulder Arthroplasty Versus Open Reduction Internal Fixation
Patients who are treated with ORIF have fewer short-term complications than those treated with RSA or hemiarthroplasty for proximal humerus fractures [85]. Additionally, patients treated with RSA have a higher 90-day readmission rate than those who have ORIF [86]. It is intuitive that patients undergoing RSA have both more medical and fracture complexity; and inability to stratify by patient comorbidities, fracture pattern, and classification is a limitation of these large database studies. In 2014, Chalmers et al. retrospectively compared ORIF and RSA for proximal humerus fracture and found no significant functional outcome differences, but significantly more RSA patients achieved > 90° forward flexion than ORIF patients [77]. In a 2015 systematic review of 92 studies including 45,000 patients comparing surgical management of complex proximal humerus fractures, Gupta et al. reported a 15% complication rate for ORIF with a 12.7% reoperation rate, and a 18.9% complication rate for RSA with a 5.0% reoperation rate [87]. Patients undergoing RSA have increased readmission rates and short-term complication rates compared to those undergoing ORIF, but this may be a function of selection bias, patient age, and medical comorbidities for the selected treatments. RSA appears to be more durable with lower revision rates.
Complications
In a 2019 multicenter retrospective review of 898 patients with proximal humerus fractures treated with RSA, there was a 12.5% overall complication rate, a 5% revision rate, and a 6% mortality rate at 1 year postoperatively. Reasons for revision were instability (2.5%), aseptic loosening of humeral component (1.5%), peripheral nerve injury (1.3%), infection (1.3%), aseptic loosening of glenoid component (1.2%), periprosthetic fracture (0.9%), complex regional pain syndrome (0.7%), and medical complications (3.1%) [88]. In another 2019 retrospective review of RSA for proximal humerus fractures, there was a 22% complication rate and a 5.1% revision rate. Instability was the most common complication at 33%, followed by scapular notching 11.9% [89•]. Complication rates are variably reported and dependent on classification and reporting of the complications. However, revision rate appears consistent across studies to be around 5% for RSA [87, 88•, 89•]. Bacle et al. recently published impressive long term implant survival of 93% at 10 years [90••]. While their study included multiple indications, such results are promising for fracture implications especially in elderly with severe fractures who clearly would benefit from a single, predictable intervention.
How to Approach Reverse Shoulder Arthroplasty for Proximal Humerus Fracture (please see Fig. 1 for initial evaluation and management of proximal humerus fracture patients)
Fig. 1.
Initial evaluation and management of proximal humerus fractures
Reverse Shoulder Arthroplasty in Proximal Humerus Fracture: Indications and Contraindications (please see Fig. 2 for RSA indications and contraindications in proximal humerus fractures)
Fig. 2.
Indications and contraindications for treatment of proximal humerus fracture with reverse shoulder arthroplasty
Reverse Shoulder Arthroplasty for Proximal Humerus Fracture: Technique (please see Fig. 3 for preoperative planning steps)
Fig. 3.
Preoperative planning steps for treatment of proximal humerus fracture with reverse shoulder arthroplasty
At our trauma center, the patient undergoes interscalene regional neuromuscular block in the preoperative area. Once under general anesthesia, the patient is placed in the beach chair position with the head of the bed elevated approximately 45–60° with a shoulder specific, radiolucent beach chair which must allow adduction, extension, and external rotation of the shoulder (Fig. 7a). Neuromuscular blockade is at the surgeon’s discretion but is generally only needed during reduction of an RSA as it can mask signs of dissection in close proximity to the axillary nerve. A large fluoroscopy unit is positioned at the head of the bed (Fig. 7g). The arm is prepped and draped completely with split drapes from the base of the neck distally. We prefer a universal arm positioner for convenience. Tranexamic acid (1 g) is given prior to incision when not contraindicated to minimize blood loss.
Fig. 7.
Intraoperative photographs and technique notes for RSA: initial beach chair setup with arm positioner (a); deltopectoral exposure to include release of anterior ½ of supraspinatus (which can be antagonistic to a tension free, anatomic reduction) (b); tagging the rotator cuff tendons with four no. 2 braided nonabsorbable sutures placed from anterior to posterior in the supraspinatus, infraspinatus, and teres minor. A no. 5 braided nonabsorbable suture is placed through the teres minor and around the posterior greater tuberosity to be cerclaged around the stem of the implant for tuberosity reduction (c); glenoid exposure with Bankart retractors anteroinferior and posteroinferior. If necessary, a Hohman is placed short of the spinoglenoid notch superiorly (d); two no. 2 braided nonabsorbable sutures are placed in and out of two drill holes on either side of the bicipital groove and around the stem. These vertical stitches are later passed through the infraspinatus and subscapularis to prevent superior escape (e); the no.5 braided nonabsorbable suture previously passed through the teres minor (b) is passed around the stem of the implant to eventually “bear hug” the tuberosities down to the porous coated portion of the implant (f). After the no. 2 stitches from the subscapularis and teres minor are provisionally tensioned for trial reduction, intraoperative fluoroscopy is obtained to check implant positioning and tuberosity reduction by rolling over from the head of the bed for a Grashey view (g). The rotator cuff sutures are sequentially tied starting with the subscapularis to teres minor, conforming on imaging that the tuberosity reduction is satisfactory (h). Finally, the vertical and cerclage sutures are tied to complete the construct (i)
We routinely utilize a deltopectoral incision from the coracoid tip to just past the axillary fold headed toward the lateral epicondyle (Fig. 7b). This is the workhorse approach for anterior shoulder surgery and can be used for fracture, primary arthroplasty, instability, periprosthetic fracture, and revision shoulder surgery. The cephalic vein is mobilized laterally, and the subdeltoid and subacromial space is recreated and a deltoid retractor is placed. We prefer a modified Taylor retractor as it retracts the deltoid without excessive anterior force on the fracture fragments. The clavipectoral fascia is incised just lateral to the conjoint tendon, and bluntly, a plane above and below the conjoint tendon is recreated with care to stay clear of the musculocutaneous and axillary nerves. When present, we use the biceps tendon to orient ourselves to the fracture fragments and alignment. Several no. 2 permanent braided sutures are placed into each rotator cuff tendons at the bone tendon junction starting at the subscapularis and working around to the teres minor (Fig. 7c). The coracohumeral ligament is released from the leading edge of the subscapularis followed by the capsule on its deep surface staying safe from the axillary nerve found running inferior to the tendon. In some implant systems (those which distalize the humeral component), it may be necessary and would be appropriate to release the leading edge of the supraspinatus as it can be antagonistic in reverse shoulder arthroplasty (Fig. 7b) [92]. This suture process not only gains control of the tuberosities but allows the necessary mobilization needed for a tension-free repair. Next, a no. 5 permanent braided suture with a large needle is placed through the teres minor and around the greater tuberosity for later cerclage to the prosthesis. The same is done for the lesser tuberosity with a no. 2 suture. The long head biceps tendon is tenodesed to the pectoralis major tendon with no. 1 dissolvable braided suture prior to tenotomizing from the supraglenoid tubercle. If needed, an osteotomy of the head is completed, and it is very carefully extracted and set aside for later bone grafting of the tuberosities and impaction grafting of the stem if needed. Care should be taken to remove any fragments avulsed with the capsule.
The glenoid is then exposed with a Fukuda retractor posteriorly, and a Bankart retractor anteriorly on the glenoid neck (Fig. 7d). Following an anterior capsulectomy between the subscapularis and the anteroinferior glenoid rim, the glenoid labrum is excised, and an anterior and inferior capsulotomy is carefully performed along the inferior glenoid with strict attention to avoid injury to the axillary nerve. The glenoid guide pin is placed to allow the baseplate to sit flush with the inferior edge of the glenoid with 0–10° inferior tilt. We ream conservatively until subchondral bone is exposed with a “smiley face” of bleeding bone only at the inferior edge. The glenoid baseplate is inserted, and we place a 36-mm glenosphere for women and 40 mm for men. Glenosphere offset is debated and outside the scope of this article.
The humerus is exposed with 2 blunt medial and lateral Hohmann retractors, and a plastic retractor anterior to the glenosphere. Usually no humeral cut is necessary, and there is often a read medially suggesting the native calcar which can be used to set the stem height. Little reaming and sensible broaching is necessary and should only be done until the subtlest of cortical chatter is appreciated. The final broach is placed, and trial polyethylene of varying thicknesses are utilized to confirm appropriate balance.
After confirming reasonable trial balance, the final stem is implanted. Our goal is good press-fit fixation proximally. Since most patients undergoing this procedure lack good metaphyseal bone, it is our practice to size down when between sizes and utilize head autograft for impaction grafting at final stem insertion. This adds to the bone stock and avoids hoop stresses and stress concentration. If this is not obtainable, a hybrid technique can be used to obtain good distal press-fit fixation and conservative proximal cementation. Prior to placing the implant, two, 2.5-mm drill holes are placed about 1 cm apart just above the pectoralis tendon on either side of the bicipital groove. Two no. 2 permanent braided sutures are passed in and then out each hole, one headed medially for later lesser tuberosity vertical fixation, and one headed laterally for the greater tuberosity. These sutures are passed around the stem of the component as it is inserted to avoid pullout (Fig. 7e). Once the final stem is inserted, the humeral tray and polyethylene is trialed, and final implants are selected based on stability, tension, and motion. The greater and lesser tuberosity cerclage sutures, which have already been placed, are passed around the neck (under the humeral tray) prior to reduction (Fig. 7f).
Next, a large piece of humeral head cancellous autograft is harvested and placed between the greater tuberosity and the stem’s porous coating [93]. The lesser and greater tuberosities are approximated together using several of the no. 2 permanent braided sutures and a needle driver (subscapularis and teres minor stitches are approximated). When tension is unacceptable, the lesser tuberosity may be excised and the subscapularis released [92, 94]. Fluoroscopy confirms tuberosity alignment (Fig. 7g). These sutures are then tied (Fig. 7h). Next, the vertical stitches are passed through the subscapularis and infraspinatus to combat superior migration similar to the technique described by Formaini et al. [95]. The cerclage sutures are securely tied down to “bear hug” the tuberosities to the stem (Fig. 7i). With this technique, we find fracture stems to be superfluous. Contemporary stems fill more volume and have acceptable ingrowth potential, and mechanically, this suture technique hugs around the construct, rather than pulleying the tuberosity down as is traditional for fracture stems. The remainder of the sutures can be incorporated or discarded as seen fit. Remaining graft can be placed under the tuberosities as needed.
The wound is soaked in a dilute betadine solution for 3 min and then copiously irrigated to minimize infection risk. Prior to closure, 1 g of vancomycin powder is divided between each of the layers. For RSA, we close the deltopectoral interval to provide a biological layer between the components and the skin followed by dermal and skin closure. The patient is placed into a simple sling (please see Fig. 4 for key intraoperative technical steps; please see Fig. 5 for postoperative protocol).
Fig. 4.
Intraoperative technical steps for treatment of proximal humerus fracture with reverse shoulder arthroplasty
Fig. 5.
Postoperative protocol for reverse shoulder arthroplasty
Case Example
This is a case of a 84-year-old right-hand dominant female with past medical history significant for hypertension and essential tremor who fell secondary to a syncopal event while visiting her husband at his transitional care facility. She presented to our level-I trauma center with isolated left shoulder pain. Prior to the fall, she lived at home independently (see Fig. 6a–c for preoperative radiographs; see Fig. 7 for intraoperative photographs and technique notes; see Fig. 6d, e for postoperative radiographs).
Fig. 6.
Initial injury AP (a), scapular-Y (b), and axillary (c) radiographs of a highly displaced 3-part fracture of the left proximal humerus with appreciable osteopenia. Postoperative AP (a), scapular-Y (b) radiographs following reverse shoulder arthroplasty for fracture
Conclusions
Reverse shoulder arthroplasty is increasing in use for proximal humerus fractures as hemiarthroplasty decreases and open reduction internal fixation rates remain stable. Reverse shoulder arthroplasty is the preferred treatment for 3-part, 4-part, and head-splitting fractures of the proximal humerus in physiologically older individuals. Functional outcome scores, range of motion, and satisfaction scores are superior when compared to other surgical treatments. Long-term follow-up studies are necessary to determine if these results will continue with time. While reported complication rates of RSA may exceed that of ORIF or hemiarthroplasty, the revision and reoperation rates are lower. In particular, the revision and reoperation rates are significantly lower than in hemiarthroplasty with the benefit of significantly improved functional outcomes reported, especially in elderly. The patient and surgeon should be aware that while function will not be “normal,” it is generally adequate for this low-demand patient population.
Compliance with Ethical Standards
Conflict of Interest
Brandon Kelly, MD and Chad Myeroff, MD declare that they have no conflicts of interest.
Human and Animal Rights and Informed Consent
This article does not contain any studies with human or animal subjects performed by any of the authors.
Footnotes
This article is part of the Topical Collection on Reverse Shoulder Arthroplasty
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
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