Abstract
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The aim of this study is to determine whether adjuvant Distal Clavicle Resection (DCR) improves outcomes of Rotator Cuff Repair (RCR) in terms of ROM, clinical scores as well as reducing complications and/or reoperations.
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This systematic review conforms to the PRISMA guidelines. Studies were included if they compared outcomes of RCR with and without adjuvant DCR and reported on postoperative ROM, clinical scores, complications, and/or reoperations.
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Seven studies that comprised 1572 shoulders which underwent RCR at a follow-up ranged 8-54 months: 398 with adjuvant DCR and 1174 without DCR. No significant differences were found between patients that had DCR versus those that did not have DCR, in terms of postoperative clinical scores (ASES, Constant, pVAS), postoperative ROM (AFE, external and internal rotation), retear rate and reoperation rate.
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There were no significant differences in ROM, clinical scores, or rates of retears and reoperations between patients that underwent RCR with or without adjuvant DCR.
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There is insufficient evidence to support routine DCR during RCR; the incidence of new or residual acromioclavicular joint (ACJ) pain after RCR with adjuvant DCR is higher than following isolated RCR, which could in fact induce iatrogenic morbidity and therefore does not justify the additional surgery time and costs of routine adjuvant DCR.
Introduction
Rotator cuff tears (RCT) are among the most common shoulder pathologies and can result in considerable pain and functional impairment (1). RCTs can be caused by overall degeneration or trauma and are often concomitant with other pathologies such as acromioclavicular joint (ACJ) arthropathy, glenohumeral degeneration and biceps or labral tears (2). ACJ arthropathy may lead to impingement and pain due to inferiorly directed osteophytes (3, 4), and can be challenging to diagnose and treat.
Patients undergoing rotator cuff repair (RCR) may require adjuvant distal clavicle resection (DCR) if they have signs of ACJ arthropathy (5, 6, 7), but DCR is not always recommended as it can cause pain, stiffness, instability, and infection (3, 8, 9, 10, 11). Recent meta-analyses (12, 13) advised against DCR as an adjuvant procedure during RCR, whether it is performed systematically (13) or in shoulders diagnosed with ACJ arthropathy (12), concluding that DCR does not improve outcomes for patients in the first 2 years after RCR. As both meta-analyses included the same three randomized controlled trials, which had low statistical power, the risks and benefits of routine DCR during RCR remains a matter of debate. Therefore, an updated meta-analysis including newer studies as well as older non-randomized comparative studies seems necessary to help reach consensus.
The purpose of this systematic review and meta-analysis was to determine whether adjuvant DCR improves outcomes of RCR in terms of range of motion (ROM), clinical scores as well as reducing complications and/or reoperations. The hypothesis was that adjuvant DCR does not improve clinical scores nor ROM.
Materials and methods
The protocol for this systematic review was submitted to PROSPERO prior to commencement (registration number: CRD42021286668) and conforms to the principles outlined in the Handbook of the Cochrane Collaboration (14), along with the guidelines established by the Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) (15).
Search strategy
The authors conducted a structured electronic literature search on November 15, 2021, using the PubMed, Embase®, and Cochrane Central Register of Controlled Trials databases, applying the keywords presented in Appendix 1. The search was limited to articles published between January 1, 2001, and November 15, 2021, to ensure a contemporary systematic review, in consideration of modernization of surgical techniques. After removal of duplicate records, each of two researchers (LN, FVR) screened the titles and abstracts to determine the suitability for the review using the following predefined eligibility criteria:
Inclusion criteria
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Studies of level I to III (16) that compare outcomes of RCR with and without adjuvant DCR, with no limits to sample sizes or prevalence in the included studies.
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Studies that report postoperative ROM, clinical scores, complications and/or reoperations.
Exclusion criteria
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Studies that do not compare outcomes of RCR with and without adjuvant DCR.
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Narrative or systematic reviews, non-comparative case series, case reports, expert opinions, editorials, or letters to editors.
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Articles published in languages other than English, French, German, Italian, or Spanish will be excluded due to a lack of confidence of the researchers' in analysis in other languages,
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In cases of duplicate patient population between two studies, the most complete dataset will be used,
Study selection
Full-text review of studies meeting the eligibility criteria in the initial screening was carried out by two researchers (LN, FVR) and any disagreement was first discussed between the researchers, and, if required, a third researcher (BLINDED) resolved any disagreement. The reference lists of studies for full text review were searched, and an expert was consulted to identify further relevant studies that may not have been captured by the database searches.
Data extraction and quality assessment
Data extraction was performed by two researchers (LN, FVR) independently and their results were compared to ensure accuracy. Where there was disagreement in the documented value, the correct value was ascertained by simultaneous review of the data in question by both researchers. The following data were extracted from the included studies: author(s), journal, year of publication, level of evidence, country where study was performed, conflicts of interest, and funding declaration. Patient characteristics were retrieved, including number of patients in each group, sex, and age. Furthermore, patient-reported outcome measures (PROMs) were extracted, including the American Shoulder and Elbow Surgeons (ASES) score, the Constant score, and pain on visual analogue scale (pVAS). ROM was also extracted, notably active forward elevation (AFE), external rotation (ER), and internal rotation (IR). Finally, ACJ pain or tenderness, ACJ instability, residual ACJ pain, and reoperation rates were noted. Methodological quality of the eligible studies was assessed by two researchers (LN, FVR) according to the Joanna Briggs Institute (JBI) checklist (17) to appraise the reporting quality (10 items). Where there was disagreement between the researchers, consensus was achieved by discussion and review.
Statistical analysis
When studies were not sufficiently comparable to pool, results were displayed in a forest plot without the summary estimate (18). Heterogeneity was evaluated by visual inspection of the forest plots and quantified using the I2 statistic to provide a measure of the degree of inconsistency across the studies (14). Where possible, summary pooled estimates of proportions and mean differences with 95% confidence intervals were estimated using random-effects models. Between-study variance was quantified using the I2 statistic, estimated using the restricted maximum-likelihood (REML) approach. Statistical analyses were performed using R version 3.5.0 (R Foundation for Statistical Computing, Vienna, Austria) using the meta package (19).
Results
The systematic search returned 228 records, of which 40 were duplicates, leaving 188 for screening (Fig. 1). A total of 170 studies were excluded by examining their titles and/or abstracts, and a further 11 studies were excluded after full-text review. This left 7 (Table 1) eligible studies (3, 8, 9, 10, 11, 20, 21) which reported on a total of 1572 shoulders that underwent RCR at a follow-up ranging from 8 to 54 months: 398 with adjuvant DCR and 1174 without DCR (Tables 2 and 3). Of the seven included studies, three case controls (8, 20, 21) and four were randomized controlled trials (RCTs) (3, 9, 10, 11). In two studies, DCR was systematically performed, regardless of ACJ status (9, 20), while in the other five studies, DCR was only performed in patients with signs of ACJ arthritis (3, 8, 10, 11, 21).
Studies included and declarations.
Study | Country | Indication | LOE | Declarations | |
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COI | Funding | ||||
Gallinet et al. (9) | France | Distal or middle SSP tear | I | Yes* | No |
Chalmers et al. (20) | USA | Arthroscopic RCR (with or without DCR) performed within a 9-month period | III | Yes† | NA |
Razmjou et al. (21) | Canada | RCT + ACJ–OA Collins Grade 1-4 | II | NA | NA |
Park et al. (3) | S Korea | RCT + ACJ–OA Petersson Grades II–III + positive ‘lidocaine injection test in the ACJ’ | I | Yes‡ | Yes§ |
Oh et al. (11) | S Korea | RCT with asymptomatic ACJ–OA | I | Yes‡ | NA |
Blasiak et al. (8) | Poland | 1- or 2-tendon RCT + symptomatic ACJ degeneration | III | NA | NA |
Kim et al. (10) | S Korea | RCT 1–3 cm + asymptomatic + dominant + ACJ–OA Stein Grade 4 | I | Yes‡ | NA |
*Royalties from Move-Up, Aston Medical, Wright Medical; Consulting fees from Move-Up, Arthrex, SBM, Aston Medical, Wright Medical, General Secretary of SECEC, Johnson and Johnson, Smith & Nephew, Lima, Conmed, FH Orthopedics, Zimmer Biomet; Deputy Editor for OTSR and Surg Radiol Anat; †paid consultant and/or presenter/speaker for DePuy Mitek, DePuy, Cayenne Medical, Zimmer Biomet; hospitality payments from Tornier; royalties from Arthrex; stock in KATOR; educational support from Pinnacle; ‡none; §funding from Smith & Nephew.
ACJ–OA, Acromio Clavicular Joint OA; LOE, level of evidence; NA, not available; SSP, supraspinatus.
Cohort demographics.
Study/Groups | Shoulders, n | Males, % | Females, % | Dominant, n (%) | Age* |
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Gallinet et al. (9) | |||||
RCR + DCR | 97 | 45 | 55 | 82 (85%) | 58 (42–69) |
Isolated RCR | 103 | 49 | 51 | 76 (74%) | 57 (45–69) |
Chalmers et al. (20) | |||||
RCR + DCR | 46 | 54 | 46 | 21 (46%) | 52 ± 11 |
Isolated RCR | 894 | 65 | 35 | 386 (43%) | 58 ± 10 |
Razmjou et al. (21) | 61* | 39* | 62 ± 9 | ||
RCR + DCR | 144 | ||||
Isolated RCR | 40 | ||||
Park et al. (3) | |||||
RCR + DCR | 21 | 19 | 81 | 21 (100%) | 63 ± 9 |
Isolated RCR | 26 | 19 | 81 | 25 (96%) | 62 ± 6 |
Oh et al. (11) | |||||
RCR + DCR | 39 | 54 | 46 | 34 (87%) | 64 ± 7 |
Isolated RCR | 39 | 59 | 41 | 30 (77%) | 64 ± 8 |
Blasiak et al. (8) | 55* | 45 | |||
RCR + DCR | 20 | 55 ± 15 | |||
Isolated RCR | 20 | 51 ± 11 | |||
Kim et al. (10) | |||||
RCR + DCR | 31 | 52 | 48 | 31 (100%) | 60 ± 5 |
Isolated RCR | 52 | 46 | 54 | 52 (100%) | 55 ± 6 |
*Mean ± s.d values in parentheses are range; †values refer to the entire cohort as opposed to comparative and control groups
DCR, distale clavicle resection; RCR, rotator cuff repair.
Tear location, tear size, and repair techniques using surgery in the cohorts included.
Study/ Groups | Tear location | Tear size | Surgery | Biceps | ||||||||||
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SSP | SSC | ISP | SSP+ SSC | SSP+ ISP | SM | MO | LA | MA | PA | Repair technique | UN | TT | TD | |
Gallinet et al. (9) | ||||||||||||||
RCR + DCR | 97 | Double-row repairs | ||||||||||||
Isolated RCR | 103 | Double-row repairs | ||||||||||||
Chalmers et al. (20) | ||||||||||||||
RCR + DCR | Single-row anchor with double sutures | |||||||||||||
Isolated RCR | Single-row anchor with double sutures | |||||||||||||
Razmjou et al. (21) | ||||||||||||||
RCR + DCR | 96 | 48 | 27 Partial repairs | |||||||||||
Isolated RCR | 26 | 14 | 10 Partial repairs | |||||||||||
Park et al. (3) | ||||||||||||||
RCR + DCR | 5 | 11 | 4 | 1 | Single row with suture anchor | |||||||||
Isolated RCR | 1 | 12 | 9 | 4 | Single row with suture anchor | |||||||||
Oh et al. (11) | ||||||||||||||
RCR + DCR | 36 | 2 | 1 | 6 | 17 | 2 | 11 | 3 | 15 Single row; 24 suture bridge | 14 | 18 | 7 | ||
Isolated RCR | 36 | 1 | 2 | 4 | 26 | 2 | 4 | 3 | 13 Single row; 26 suture bridge | 12 | 21 | 6 | ||
Blasiak et al., (8) | ||||||||||||||
RCR + DCR | 10 | 5 | 5 | Single row anchor with double sutures | ||||||||||
Isolated RCR | 9 | 1 | 5 | 5 | ||||||||||
Kim et al. (10) | ||||||||||||||
RCR + DCR | 27.2 ± 3.7 mm (10–30) | DCR 5.2 ± 1.1 mm; double-row fixation using susure anchors | 1 | 1 | ||||||||||
Isolated RCR | 24.7 ± 3.1 mm (10–30) | DCR 5.4 ± 1.4mm; double-row fixation using susure anchors | 1 | 1 |
DCR, distale clavicle resection; ISP, infraspinatus; LA, large; MA, massive; MO, moderate; RCR, rotator cuff repair; SSP, supraspinatus; SSC, subscapularis; SM, smallPA, partial; TD, tenodesis; TT, tenotomy; UN, untouched.
Quality assessment
Of the three case control studies, 2 did not match cases and controls appropriately, as there were statistically significant differences between patient characteristics and did not state strategies to deal with confounding factors (Fig. 2). Of the four randomized controlled trials, none clarified whether clinicians, patients, or assessors were blinded to treatment (Fig. 3).
Clinical scores
Five studies reported postoperative PROMs (Table 4). Compared to patients that did not have DCR, those that had adjuvant DCR reported similar ASES scores (range: 77–95 vs 81–93) and similar Constant scores (range: 72–96 vs 75–96), but slightly lower pain on VAS (range: 0.6–2.3 vs. 0.6–1.8). No significant differences were found between patients that had RCR than for those that did not have DCR, in terms of postoperative ASES scores (MD: −1.9; CI: −7.2 to 3.5; P = 0.490), Constant scores (MD: −0.2; CI: −1.9 to 1.5; P = 0.820), and pVAS (MD: 0.1; CI: −0.2 to 0.5; P = 0.520) (Fig. 4). Of the seven studies, five reported on residual or new ACJ pain following surgery and found that there was residual pain in 0−37% of patients that had adjuvant DCR vs 0−22% of patients that did not have DCR.
Clinical outcomes. Data are presented as mean ± s.d. or n (%).
Study/groups |
Follow-up |
ASES | Constant score | Pain on VAS | ||||
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Preoperative | Postoperative | Preoperative | Postoperative | Preoperative | Postoperative | Residual/new pain | ||
Gallinet et al. (9) | ||||||||
RCR + DCR | 12 | 54 ± 13 | 79 ± 13 | 6.9 ± 1.8 | 1.8 ± 2.4 | 36 (37%) | ||
Isolated RCR | 12 | 53 ± 14 | 81 ± 11 | 6.9 ± 1.8 | 1.3 ± 2.2 | 23 (22%) | ||
Chalmers et al. (20) | 8 ± 10* | |||||||
RCR + DCR | 41 ± 22 | 6.2 ± 2.1 | 0 (0%) | |||||
Isolated RCR | 45 ± 19 | 5.5 ± 2.4 | 10 (1.1%) | |||||
Razmjou et al. (21) | ||||||||
RCR + DCR | 24 | 49 | 86 | 51 | 96 | |||
Isolated RCR | 24 | 44 | 77 | 47 | 85 | |||
Park et al. (3) | ||||||||
RCR + DCR | 44 ± 9.8 | 40 ± 17 | 81 ±14 | 45 ± 17 | 75 ± 12 | 5.3 ± 2.1 | 1.8 ± 1.3 | 7 (33%) |
Isolated RCR | 44 ± 9.5 | 39 ± 17 | 79 ± 24 | 45 ± 16 | 72 ± 21 | 6.1 ± 1.9 | 2.0 ± 2.5 | 5 (20%) |
Oh et al. (11) | ||||||||
RCR + DCR | 28 ± 6.7 | 47 ± 10 | 92 ±16 | 74 ± 6 | 96 ± 6 | 7.2 ± 1.8 | 0.6 ± 1.8 | |
Isolated RCR | 31 ± 7.2 | 51 ± 14 | 95 ±12 | 74 ± 8 | 96 ± 5 | 6.1 ± 1.9 | 0.6 ± 0.9 | |
Blasiak et al. (8) | 54 ± 6* | |||||||
RCR + DCR | 55 ± 10.9 | 95 ± 8 | 8.2 ± 1.6 | 0.7 ± 1.0 | 1 (5%) | |||
Isolated RCR | 64 ± 12.8 | 96 ± 7 | 8.0 ± 1.3 | 0.7 ± 1.3 | 0 (0%) | |||
Kim et al. (10) | ||||||||
RCR + DCR | 33 ± 4.1 | 57 | 93 | 7.2 | 1.7 | 0 (0%) | ||
Isolated RCR | 32 ± 4.9 | 57 | 89 | 7.2 | 2.3 | 2 (3.8%) |
*Value refers to the entire cohort as opposed to comparative and control.
Range of motion
Three studies reported postoperative ROM (Table 5). Compared to patients that did not have DCR, those that had adjuvant DCR reported similar AFE (range: 142–172 vs 141–170) and similar ER (range: 34–74 vs 36–76), but slightly better IR (range: T7.9–T8 vs T8–T9.4). The three studies were eligible for meta-analysis, which revealed no significant differences between patients that had RCR with or without DCR, in terms of postoperative AFE (MD: −2.0; CI: −5.0 to 1.0; P =0.190) (Fig. 5), ER (MD: −1.0; CI: −7.0 to 5.1; P = 0.750), and IR (MD: 0.7; CI: −0.9 to 2.2; P = 0.410).
ROM complications and reoperations. Data are presented as mean ± s.d. or n (%).
Study/groups | Complications | AFE | External rotation | Internal rotation | |||||
---|---|---|---|---|---|---|---|---|---|
Preoperative | Postoperative | Preoperative | Postoperative | Preoperative | Postoperative | ||||
Gallinet et al. (9) | |||||||||
RCR + DCR | 0% | 7% | 0% | 116 ± 32 | 169 ± 16 | 32 ± 24 | 53 ± 16 | 3.6 ± 2.0 | 8.6 ± 1.9 |
Isolated RCR | 1% | 5% | 0% | 124 ± 29 | 171 ± 14 | 29 ± 23 | 59 ± 23 | 4.0 ± 2.0 | 8.7 ± 1.5 |
Chalmers et al. (20) | |||||||||
RCR + DCR | 4% | 2% | |||||||
Isolated RCR | 7% | 4% | |||||||
Razmjou et al. (21) | |||||||||
RCR + DCR | 0% | ||||||||
Isolated RCR | 0% | ||||||||
Park et al. (3) | |||||||||
RCR + DCR | 5% | 10% | 142 ± 30 | 141 ± 17 | 37 ± 18 | 36 ± 13 | T11* | T8 | |
Isolated RCR | 4% | 15% | 142 ± 22 | 142 ± 22 | 44 ± 20 | 34 ± 17 | T10 | T8 | |
Oh et al. (11) | |||||||||
RCR + DCR | 0% | 23% | 5% | 160 ± 11 | 170 ± 11 | 56 ± 17 | 76 ± 17 | T10.2 ± 3 | T9.4 ± 2.4 |
Isolated RCR | 0% | 26% | 0% | 160 ± 16 | 172 ± 9 | 61 ± 14 | 74 ± 16 | T8.0 ± 3 | T7.9 ± 1.4 |
Blasiak et al. (8) | |||||||||
RCR + DCR | 0% | 0% | 0% | ||||||
Isolated RCR | 0% | 0% | 0% | ||||||
Kim et al. (10) | |||||||||
RCR + DCR | 0% | 0% | 0% | ||||||
Isolated RCR | 2% | 0% | 0% |
*Internal rotation was measured as the highest spinal level achieved when the patient reached behind the back with the ‘hitch-hiking thumb’.
AFE, anterior forward elevation.
Retears, reoperations, and ACJ instability
The reoperation rates were similar for patients that had DCR (range: 0–5%) as for those that did not have DCR (range: 0–7%) (Table 5). The retear rates were similar for patients that had DCR (range: 0–23%) as for those that did not have DCR (range: 0–26%). The ACJ instability rates were greater for patients that had DCR (range: 0–5%) than for those that did not have DCR (range: 0–0%). No significant differences were found between patients that had RCR vs those that did not have DCR, in terms of retear rate (OR: 0.9; CI: 0.5–1.8; P = 0.830) (Fig. 6) and reoperation rate (OR: 0.6; CI: 0.2–1.8; P = 0.370).
Discussion
The most important finding of this systematic review and meta-analysis is that there was insufficient evidence to detect benefits of DCR during RCR, in terms of ROM, clinical scores, or rates of retears and reoperations.
Performing adjuvant DCR during RCR could increase morbidity risk or severity of complications, as insufficient resection may lead to residual impingement, while excessive resection may cause AC joint instability, heterotopic ossification, fracture, or suprascapular nerve lesion (9, 22). Furthermore, as adjuvant DCR increases both the operation time and consequently the cost of surgery (23, 24), the procedure should provide significant improvement in the expected result, to offset potential drawbacks. In the present meta-analysis, there was greater incidence of residual pain following adjuvant DCR during RCR than isolated RCR, possibly due to iatrogenic morbidity, though it is important to note that pain at the ACJ may not necessarily originate therefrom and that specific tests or imaging are necessary to ascertain the source of pain (25).
The present meta-analysis found no benefit in performing adjuvant DCR during RCR, even in patients that have radiological signs of ACJ arthropathy; thus performing DCR as a secondary procedure may be sufficient in patients that present with persistent ACJ pain following RCR, as it is a relatively quick and simple procedure and may only be required in 1–2% of cases (26). A recent study found that DCR could be effective as a secondary procedure in a small subset of patients that developed symptomatic ACJ arthropathy following isolated RCR. Even so, patients should be informed about the potential for residual pain and/or functional impairment, which could be associated with other intrinsic or extrinsic factors that may be unrelated to the rotator cuff or the ACJ.
A recent study by Yiannakopoulos et al. (26) evaluated clinical progression of ACJ osteoarthritis in patients who underwent isolated arthroscopic RCR regardless of the presence of ACJ arthropathy. The authors found that only 1% of patients had persistent ACJ pain following arthroscopic RCR, and that there was no difference in clinical outcomes between patients who had or did not have ACJ symptoms prior to the procedure. Yiannakopoulos et al. (26) therefore did not recommend DCR during RCR in patients with ACJ arthropathy, which corroborate our findings. ACJ arthropathy could be a different and unrelated disease to rotator cuff pathology; in fact, Shubin Stein et al. (27) found that in patients aged >30, scheduled for MRI of extremities unrelated to the shoulder, 93% had radiographic signs of ACJ arthritis.
When conservative management of ACJ arthropathy fails, surgical intervention is the treatment of choice, but the criterion defining failure of conservative management and the best practice evidence for existing nonpharmacological interventions is a matter of debate (28, 29). Furthermore, as the prevalence of patients that would require DCR following RCR is very low, Farrell et al. (29) recommends that patients should undergo 4–6 months of both nonpharmacological and pharmacological treatments to treat ACJ arthropathy, such as activity modification, non-steroidal anti-inflammatory drugs (NSAIDs), intra-articular steroid injections, and physiotherapy. Only after following such a treatment plan, conservative management is deemed to have failed and surgical intervention is indicated.
The results of the present meta-analysis should be interpreted with the following limitations in mind. There was heterogeneity in the indications for DCR (in two studies, DCR was systematically performed, regardless of ACJ status, while in the other five studies, DCR was performed in patients with signs of ACJ arthritis) which makes quantitative comparisons between cohorts difficult. Of the three case–control studies, two did not perform adequate matching and did not state strategies to deal with confounding factors. Of the four randomized controlled trials, none clarified whether clinicians, patients, or assessors were blinded to treatment. Finally, it is worth noting that few additional studies have been published in recent years highlighting the need for new trials.
Conclusion
In this systematic review and meta-analysis, there were no significant differences in ROM, clinical scores, or rates of retears and reoperations between patients that underwent RCR with or without adjuvant DCR. There is insufficient evidence to support routine DCR during RCR; the incidence of new or residual ACJ pain after RCR with adjuvant DCR is higher than following isolated RCR, which could in fact induce iatrogenic morbidity and therefore does not justify the additional surgery time and costs of routine adjuvant DCR.
ICMJE conflict of interest statement
The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research reported.
Funding statement
This work was supported by ‘Clinique des Cèdres’, which provided funding for data extraction and manuscript preparation.
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