Abstract
Background
Thus, the purpose of the present study was to (1) characterize common postoperative complications and (2) quantify the rates of revision in patients undergoing hemiarthroplasty to reverse total shoulder arthroplasty revisional surgery. We hypothesize that hardware loosenings will be the most common complication to occur in the sample, with the humeral component being the most common loosening.
Methods
This systematic review adhered to PRISMA reporting guideline. For our inclusion criteria, we included any study that contained intraoperative and/or postoperative complication data, and revision rates on patients who had undergone revision reverse total shoulder arthroplasty due to a failed hemiarthroplasty. Complications include neurologic injury, deep surgical site infections, hardware loosening/prosthetic instability, and postoperative fractures (acromion, glenoid, and humeral fractures).
Results
The study contained 22 studies that assessed complications from shoulders that had revision reverse total shoulder arthroplasty from a hemiarthroplasty, with a total sample of 925 shoulders. We found that the most common complication to occur was hardware loosenings (5.3%), and of the hardware loosenings, humeral loosenings (3.8%) were the most common. The revision rate was found to be 10.7%.
Conclusion
This systematic review found that revision reverse total shoulder arthroplasty for failed hemiarthroplasty has a high overall complication and reintervention rates, specifically for hardware loosening and revision rates.
Introduction
Current estimates suggest total shoulder arthroplasty (TSA) procedural volume to increase by nearly 350%, with reverse total shoulder arthroplasty (RTSA) accounting for nearly 85% of all shoulder arthroplasty procedures, by the year 2025. 1 This drastic increase in RTSA usage is likely attributable to multiple factors including advances in surgical technique and implant design, surgeon procedural comfort, as well as rapid expansion of indications for RTSA beyond that which it was originally designed (e.g., to address rotator cuff arthropathy in older patient populations).2,3 Today, RTSA is used for a variety of orthopedic pathologies including inflammatory arthritis, 4 fracture sequelae, 5 complex proximal humerus fractures in elderly patients, 6 tumor resection, 7 and irreparable rotator cuff tears. 8 Though indications for RTSA are broad, revision RTSA in the setting of a “salvage procedure” accounts for a large proportion of completed RTSA procedures.
It was first shown by De Wilde et al. that reverse shoulder prosthesis can be used as a viable option for revision of a failed shoulder replacement with improved shoulder function. 9 As a result, RTSA has become an option for the replacement of anatomic TSA (aTSA), RTSA, hemiarthroplasty (HA), and open reduction-internal fixation. RTSA following primary HA after fracture or HA in those with concurrent rotator cuff deficiency encompasses a large proportion of completed RTSA procedures.10–13 Primary HA failure may be attributable to a number of postoperative complications (e.g., prosthesis instability, glenoid erosion, and rotator cuff dysfunction).11,14 Evidence detailing complications rates among patients undergoing revision RTSA following failure of primary HA is sparse; however, previous studies (with limited sample sizes) have reported on common complications following this type of revision surgery.15,16
Thus, the purpose of the present study was to (1) characterize common postoperative complications (e.g., neurologic injury, deep surgical site infections (SSI), hardware loosening/prosthetic instability, postoperative fractures), and (2) quantify the rates of revision in patients undergoing HA to RTSA revisional surgery. We hypothesize that hardware loosenings will be the most common complication to occur in the sample, with the humeral component being the most common loosening. We also hypothesize that revision rates of RTSA following failed HA will be higher than primary RTSA.
Methods
Search strategy and selection criteria
This systematic review adhered to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline. 17 Studies were considered for inclusion if they were Level I–IV evidence. We conducted a search on 28 February 2020, using PubMed as our electronic database. The following search string was used: (reverse) AND ((Shoulder arthroplasty) OR (total shoulder arthroplasty) OR (shoulder replacement) or (total shoulder replacement)) and included all studies to the present day.
For our inclusion criteria, we included any study that contained intraoperative and/or postoperative complication data, and reintervention rates on patients who had undergone revision RTSA due to a failed HA of the shoulder. For studies that contained a cohort of patients, we included the data of patients that only pertained to our inclusion criteria. Studies were excluded from our sample if they contained one of the following: animal studies, review articles, articles with patients younger than 18 years, paraplegia, cadaveric studies, case reports, conference abstracts, Level V evidence studies, studies not in English and studies that included patient data from national registries were excluded from the sample. We also excluded studies that had pooled or incomplete data.
Our primary outcome for the study was to quantify the complication and reoperation rates for patients after having gone revision RTSA due to failed HA. Complications include neurologic injury, deep SSI, hardware loosening/prosthetic instability, and postoperative fractures (acromion, glenoid, and humeral fractures).
Screening
All studies from our search string were screened by two reviewers (AKR and JXC). The reviewers were looking for any mention of reverse total shoulder arthroplasty (RSA, RTSA, reverse total shoulder, reverse total shoulder arthroplasty) in the abstracts and titles, which would then be included in the full-text screening. Any disagreements between the reviewers resulted in the article being included in the full-text screen. Moving the differences to the full-text screen allows the reviewers to discuss in-depth if the article fits the inclusion criteria. If an agreement could not be reached, a senior reviewer (BC or BN) would help make the final decision.
Data extraction
Data were extracted from studies by three reviewers (AKR, JS, and JXC). The reviewers used a pilot-tested form sheet (Google Forms) to record data on a response spreadsheet (Microsoft Excel). Recorded data included descriptive statistics (e.g., mean age, number of shoulders, and indication for RTSA), and complications reported (e.g.. reoperation rates, postoperative fractures, postoperative neurologic injuries, dislocations, instability/hardware loosening, and infections).
Predetermined definitions and inclusion criteria were established to ensure consistency of extraction of variables from articles. For example, any neurologic injuries that had a full recovery within one year were considered neuropraxia injuries. The investigators also established that SSI would follow a modified version of the protocol set by Norris et al. 18 The one modification established was, studies that only used the word infection but never explicitly stated deep or superficial were considered deep infections when included with a set of complications.
Risk of bias assessment
To assess the studies’ methodological quality in our sample, we used the modified Coleman Methodology Score (CMS), presented by Saleeb et al.19,20 CMS is a multifactorial, comprehensive point system used to assess methodological quality of surgical studies. CMS has a score ranging from 0 to 100 CMS that evaluates the following factors: the number of surgical procedures, study type, diagnostic certainty, surgical protocol description, postoperative rehabilitation description, description of desired outcomes, description of how authors assessed outcomes, and description of the subject selection process. The scores for CMS are broken into four categories: excellent (85–100 points, good (70–84 points), fair (50–69 points), and poor (<50 points).
Results
The search string yielded 1722 studies from Pubmed, after conducting the title/abstract screen, we were left with 824 studies. Our full-text screen found 22 studies10,11,15,21–39 meeting our inclusion criteria (Figure 1).
Prisma inclusion/exclusion checklist.
General characteristics.
aPatient numbers add up to 925 patients.
Study quality
The CMS score of our included studies ranged from 36 to 71 (mean (SD), 47.81 (10.00); median (interquartile range), 45.5 (35.5–55.5)). Seventeen (77.3%) studies in our sample scored a poor CMS score, while four (18.2%) studies scored a fair, and one study scored a good score. The categories receiving significantly fewer points were categories evaluating levels of evidence, as most studies were retrospective in nature, and the mean follow-up period of the studies, as most studies had a follow-up period of less than three years or a period that was not clearly stated in the study. Many of the studies also lost points in the category assessing the study size itself, with 18 (81.8%) of the included studies having less than 40 included patients, or not clearly stating the number of included patients (Supplemental Table).
Complication rates
Neurologic injury
Neurologic injury rates.
Infection rates
Infection rates.
Postoperative fracture rates
Hardware loosening and fracture complications.
Hardware loosening rates
Hardware loosening was assessed in 20 studies,10,11,15,21–23,25–34,36–39 which include 660 shoulders. Of the sample, 35 shoulders (5.3%) experienced hardware loosening, instability, and dislocations (Table 4). Of these, the humeral component was loose in 25 shoulders (3.8%), of which 24 shoulders required revision. The humeral component was the most common loosening. Baseplate loosening occurred in 10 shoulders (1.5%), of which 8 required revision.
Instability rates
Prosthesis instability was assessed in 20 studies,10,11,15,21–23,25–34,36–39 which include 660 shoulders. Instability occurred in 11 shoulders (1.7%), of which 9 required revision.
Dislocation rates
Prosthesis dislocations were assessed in 20 studies,10,11,15,21–23,25–34,36–39 which include 660 shoulders. Dislocations occurred in 19 shoulders (2.9%), of which 11 required revision.
Revision rates
Revision indication.
aStephens et al. 35 did not specify the indication for the revision.
Discussion
In our study, we observed a revision rate of 10.7%, after patients received an RTSA due to a failed HA. Common postoperative complications observed included hardware loosening, joint instability, and joint dislocation. These findings are consistent with previous literature investigating common complications following secondary RTSA procedures. For example, a systematic review and meta-analysis of 43 studies, which included 1041 shoulders, determined postoperative shoulder instability, and hardware loosening were common complications following all primary shoulder arthroplasty conversion to RTSA. 16 These complications might be attributable to RTSA being the only surgical treatment option amendable for patients with recurrent shoulder joint instability and chronic dislocations following their primary total shoulder arthroplasties.40–42 Although a viable treatment option for shoulder instability, previous studies have shown that shoulder surgery revisions are a risk factor for recurrent instability after RTSA.22,43,44 Instability after RTSA has been shown to be related to the inability of the prosthesis to maintain compressive forces between the glenosphere and the humerosocket. 45 It has also been associated with the lack of an impingement-free arc of motion.46–48 Due to the high rates of instability after RTSA, Abdelfattah et al. have proposed a classification system for instability after RTSA, which could help guide physicians in implementing treatment strategies for patients. 43
Of the hardware loosenings that were found in our sample, humeral stems were found to be the most common component to have dysfunction (3.8%; 25/660) followed by the glenoid baseplate (1.5%; 10/660). Our findings show that there is an increased chance of acquiring humeral loosening compared to primary RTSA. 49 In addition, our findings are similar to those found in Grey et al. who found that their sample showed a 3.7% rate of aseptic humeral stem loosening after undergoing revision RTSA. 50 This is problematic as studies show that aseptic loosening in revision shoulder arthroplasty results in a high rate of reoperations. 35 Of our sample of 25 shoulders that had humeral component loosening, 24 of the shoulders required a revision surgery (96%; 24/25). Our findings on glenoid baseplate loosenings are similar to rates for primary and secondary RTSA.16,49 We found that the revision rate was also quite high for glenoid baseplate loosenings in our sample size (80%; 8/10).
Our study found an overall revision rate of 10.7% (99/925), which falls in range with current literature for revision RTSA.16,35 Stephens et al. found an overall revision rate of 6.0% for revision RTSA. Of their sample, RTSA for failed HA had the highest revision rate of 10.4% out of 251 patients. 35 In another example, Franke et al. had a 7.7% revision rate with a sample of 207 patients. 34 These points are further corroborated by additional studies suggesting that there is an increased failure rate when implanting a revision RTSA for a failed HA.51,52
In comparison to revision RTSA, literature evaluating failed HA to aTSA shows higher rates of complication and revision in their limited population. For example, Sheth et al. 53 retrospectively reviewed 28 patients who underwent conversion of HA to aTSA. They found an overall complication rate of 46%. Of the 28 patients, 3 sustained intraoperative complications (11%) which included fracture (humeral shaft in 1 and greater tuberosity in 1) and iatrogenic rotator cuff tear. Furthermore, there were 10 patients that sustained postoperative complications (36%) which included subscapularis failure (3), infection (1), humeral component loosening (1), hemarthrosis (1), lesser tuberosity nonunion (1), brachial plexus injury (1), glenoid loosening (1), and posterior-superior rotator cuff tear (1). In another review, Carroll et al. 54 evaluated 16 consecutive patients who underwent conversion of failed HA to aTSA. Five of the 16 patients (32%) required a revision surgery after the revision arthroplasty. The authors also report that 7 of the 16 patients (47%) had an unsatisfactory result.
The most comprehensive literature available on complication rates for revision RTSA for failed hemiarthroplasties is a recent study published by Bois et al. 16 The study’s primary outcomes evaluated pain, range of motion, and outcome scores for revision RTSA for failed shoulder arthroplasties. The study secondarily evaluated complications and reintervention rates based on the sample that they found. As a result, they contained a limited sample size of 329 shoulders for complication rates and 281 shoulders for reintervention rates. Furthermore, their study’s search only included literature up until September 2017. Because of this it was our feeling that we could add to the literature regarding complications and reinterventions following failed HA to RTSA that Bois et al. recently described. As a result of our search including all studies published before 28 February 2020, we were able to add an additional seven studies,15,23,24,32–34,40 including one prospective study, to our sample that was published after the search range set by Bois et al. These seven studies had 412 shoulders to add to our sample, increasing the strength and generalizability of our study.
Limitations
Our study had certain limitations. Although we had a large number of shoulders to include into our sample, a majority of our studies were case series and retrospective cohort studies. This introduced heterogeneity into our study. Our assessment of study quality falls in line with this assessment due to a large number of studies falling in the poor range of the CMS scale. As a result, there is a need for more Level I and II evidence studies looking at outcomes for revision RTSA due to failed HA. Also, there was limited literature stratifying risk factors with complication rates. Therefore, it prevented our study from including a meta-analysis evaluating what risk factors contribute to complications within the population. Therefore, there is a need for more studies evaluating complication rates in relation to risk factors for revision RTSA. Finally, as with all systematic reviews, there is always the chance that studies that were excluded could have been included in our sample. Furthermore, our study only evaluated the PubMed database, and there is a chance relevant studies published outside of this database could have been included.
Conclusion
This systematic review found that revision RTSA for failed HA has a high overall complication and revision rate, specifically for hardware loosening. Although the complication rates are high for revision RTSA, the rates are still lower than revision aTSA for failed HA in current literature, making it a viable option for the procedure. Further studies need to be conducted evaluating various controls, such as smoking, diabetes, etc., to show what risk factors are more susceptible to complications when revision RTSA is done for HA.
Supplemental Material
sj-pdf-1-sel-10.1177_17585732211019390 - Supplemental material for Complication and revision rates after reverse total shoulder revision from hemiarthroplasty: a systematic review
Supplemental material, sj-pdf-1-sel-10.1177_17585732211019390 for Complication and revision rates after reverse total shoulder revision from hemiarthroplasty: a systematic review by Arjun K Reddy, Jake X Checketts, B Joshua Stephens, J Michael Anderson, Craig M Cooper, Tyler Hunt, Keith Fishbeck, Marshall Boose, Byron Detweiler, Brian Chalkin and Brent L Norris in Shoulder & Elbow
Footnotes
Authors' Note
B. Joshua Stephens and Tyler Hunt are now affiliated with Department of Orthopedic Surgery, Oklahoma State University Medical Center, Tulsa, OK, USA.
Declaration of Conflicting Interests
The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: BC is a consultant for DJO. BN is a consultant for J and J, Acumed, and Wishbone; has grant support from the AONA and COTA; is a committee member of the OTA and the AAOS; is a section editor for Injury Journal; and has principle for Boys of Summer Enterprise, Norris Surgical, OR Ingenuity.
Funding
The author(s) received no financial support for the research, authorship, and/or publication of this article.
Guarantor
AKR and JXC.
Contributorship
AKR: did data collection, writing, revisions, and table creation; BJS: did data collection. BD, MB, KF: involved with the clinical write up of the discussion of the article and helped with interpretation of data. TH and JMA: involved with writing and revision of manuscript, introduction and discussion write ups. JXC: helped with methodology, involved with training of Arjun Reddy and B Joshua Stephens for the gathering of data, and were extensively involved with the revisions of the article. Created and ran the search strings for the article. Helped with article curation. CC: helped with data curation (graph creation), and results write up. BC, BN: senior authors, supervision, protocol creation, guidance in every step of the article creation.
Supplemental material
Supplemental material for this article is available online.
References
Supplementary Material
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