| Literature DB >> 31616550 |
Michael-Alexander Malahias1, Dimitrios Gerogiannis1, Efstathios Chronopoulos2, Maria-Kyriaki Kaseta2, Emmanouil Brilakis1, Emmanouil Antonogiannakis1.
Abstract
We aimed to investigate whether combined reverse total shoulder arthroplasty (RTSA) and subscapularis repair leads to improved clinical and functional outcome in comparison with RTSA alone. Two reviewers independently conducted a systematic search according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) using the MEDLINE/PubMed database and the Cochrane Database of Systematic Reviews. These databases were queried with the terms "reverse" AND "shoulder" AND "arthroplasty" AND "with" AND "subscapularis" AND "repair". From the 72 initial studies, we finally chose five studies which were eligible to our inclusion-exclusion criteria. The total mean modified Coleman methodology test was 55/100 (range: 47/100 to 60/100). The eligible studies included 1087 patients, in total. Regarding the subjective functional scores as well as range of motion (ROM), the differences amongst groups were insignificant in almost all studies. The mean complications' rate of the repair group was 10.4%, whereas the respective rate of the nonrepair group was 10.2%. All studies concluded that the repair of subscapularis did not affect the complications' rate of patients who were treated with RTSA. The mean dislocations' rates of the repair and the nonrepair group were 1.5% and 2.3%, respectively. Although subscapularis repair was proven safe and effective for the augmentation of RTSA, it did not offer any additional clinical or functional benefit in the outcome of patients treated with lateralized RTSA. Therefore, it is not supported its routine use for patients who have a preoperatively sufficient subscapularis tendon. ©Copyright: the Author(s), 2019.Entities:
Keywords: reverse total shoulder arthroplasty; rotator cuff arthropathy; subscapularis repair; systematic review of comparative trials
Year: 2019 PMID: 31616550 PMCID: PMC6784593 DOI: 10.4081/or.2019.7948
Source DB: PubMed Journal: Orthop Rev (Pavia) ISSN: 2035-8164
Figure 1.PRISMA flow chart.
Year of publication, type of study and level of evidence.
| Authors [ref] | Year | Type of study | Level |
|---|---|---|---|
| De Boer | 2016 | Retrospective case control | III |
| Clark | 2012 | Retrospective case control | III |
| Werner | 2018 | Retrospective case control | III |
| Vourazeris | 2016 | Retrospective case control | III |
| Friedman | 2016 | Retrospective case control | III |
Number of patients, sex, mean age and mean follow-up per study.
| Authors [ref] | No. patients | Sex | Mean age | Mean follow up (months) |
|---|---|---|---|---|
| De Boer | Total: 65 Repair-Group: 25 No Repair-Group: 40 | Repair-Group: 6M,19 F No Repair-Group: 10M,30F | Total: 73,8 Repair-Group: 73 No Repair-Group: 74,4 | Total: 36 Repair-Group: 30,5 No Repair-Group: 40 |
| Clark | Total: 120 Repair-Group: 65 No Repair-Group: 55 | Repair-Group: 19M,46F No Repair-Group: 12M,43F | Repair-Group: 68,6 No Repair-Group: 68,3 | Repair-Group: 13,2 No Repair-Group: 9,9 |
| Werner | Total: 109 Repair-Group: 71 No Repair-Group: 38 | Repair-Group: 28M,43F No Repair-Group: 15M,23F | Repair-Group: 71,1 No Repair-Group:70,7 | 24 minimum |
| Vourazeris | Total: 202 Repair-Group: 86 No Repair-Group: 116 | N/A | Repair-Group: 71,6 No Repair-Group: 71,1 | 24 minimum Repair-Group: 40 No Repair-Group: 37 |
| Friedman | Total: 591 Repair-Group: 340 No Repair-Group: 251 | Repair-Group: 119M,221F No Repair-Group: 105M,146F | Total: 72,5 (50-93) Repair-Group: 72,7 No Repair-Group: 71,7 | Total: 36,6 (24 minimum) Repair-Group: 37,3 No Repair-Group: 35,7 |
Scales measuring the clinical outcome, significant differences between the two groups and significant improvement from preto postoperative scores.
| Authors [ref] | Clinical Outcome Scale | Significant difference between repair and no repair | Significant difference from pre- to post-operative |
|---|---|---|---|
| De Boer | Constant, Oxford, RoM, Strength | No (for all scores) | N/A |
| Clark | VAS, ROM | No | YES in both groups (all score) |
| Werner | ASES | No Less improvement in ASES when repair and lateralization combined | N/A |
| Vourazeris | SPADI, ASES, UCLA, Constant, SST, RoM, Strength | No | N/A |
| Friedman | ASES, Constant, UCLA, SST, SPADI, RoM | The non-repair group had more active abduction and passive external rotation. The repair group had higher internal rotation and greater improvement in SST, Constant and active external rotation | YES in both Groups (all Scores) |
Preoperative and postoperative clinical and functional mean scores per study and other variables.
| Authors [ref] | Preoperative Mean Scores | Postoperatives Mean Scores | Other Variables |
|---|---|---|---|
| De Boer et al16 | N/A | N/A | On U/S post-operative exam (mean 30 months) 10(40%) of the repaired tendons were still sufficient |
| Clark | VAS Repair-Group: 7,5 | VAS Repair-Group: 1,4 | N/A |
| VAS No Repair-Group: 8,2 | VAS No Repair-Group: 2,5 | ||
| Active FF in No Repair-Group 20 | FF Repair-Group: 112 | ||
| degrees less than Repair-Group | FF No Repair-Group: 94 | ||
| Werner | ASES Repair-Group: 37,9 | ASES Improvement Repair-Group: 35,8 | Subscapularis repair and lateralized glenosphere in isolation had no effect on ASES, but in combination ASES was significantly less improved |
| ASES No Repair-Group: 36,6 | ASES Improvement No Repair-Group: 38 | ||
| Vourazeris | N/A | SPADI Repair-Group: 23,4 | N/A |
| SPADI No Repair-Group: 23,2 | |||
| ASES Repair-Group: 77,7 | |||
| ASES No Repair-Group: 79,3 | |||
| UCLA Repair-Group: 28,3 | |||
| UCLA No Repair-Group: 28,8 | |||
| SST Repair-Group: 9,2 | |||
| SST No Repair-Group: 9,1 | |||
| Constant Repair-Group:72,6 | |||
| Constant No Repair-Group: 72,9 | |||
| FF Repair-Group: 120 | |||
| FF No Repair-Group: 122 | |||
| External Rotation Repair-Group: 24 | |||
| External Rotation No Repair-Group: 26 | |||
| ABD Repair-Group: 109 | |||
| ABD No Repair-Group:112 | |||
| ER Strength Repair-Group: 9,9lb | |||
| ER Strength No Repair-Group: 9,9 lb | |||
| Friedman | SPADI Repair-Group: 80,2 | SPADI Repair-Group: 15,9 | N/A |
| SPADI No Repair-Group: 84,6 | SPADI No Repair-Group: 23,5 | ||
| ASES Repair-Group: 38,8 | ASES Repair-Group: 86,7 | ||
| ASES No Repair-Group: 34,9 | ASES No Repair-Group: 82,1 | ||
| UCLA Repair-Group: 13,7 | UCLA Repair-Group: 30,2 | ||
| UCLA No Repair-Group: 12,7 | UCLA No Repair-Group: 29,7 | ||
| SST Repair-Group: 3,4 | SST Repair-Group: 10,5 | ||
| SST No Repair-Group: 3,3 | SST No Repair-Group: 9,6 | ||
| Constant Repair-Group:34,8 | Constant Repair-Group:72,9 | ||
| Constant No Repair-Group:33,8 | Constant No Repair-Group:67,9 | ||
| Active ff Repair-Group: 91 | Active ff Repair-Group: 141 | ||
| Active ff No Repair-Group: 85 | Active ff No Repair-Group: 137 | ||
| Active ABD Repair-Group: 67 | Active ABD Repair-Group: 107 | ||
| Active ABD No Repair-Group: 75 | Active ABD No Repair-Group: 119 | ||
| IR Score Repair-Group: 3,3 | IR Score Repair-Group: 5,1 | ||
| IR Score No Repair-Group: 3.2 | IR Score No Repair-Group: 4,4 | ||
| Active ER Repair-Group: 13 | Active ER Repair-Group: 34 | ||
| Active ER No Repair-Group: 20 | Active ER No Repair-Group: 35 | ||
| Passive ER Repair-Group: 23 | Passive ER Repair-Group: 45 | ||
| Passive ER No Repair-Group: 31 | Passive ER No Repair-Group: 50 | ||
| Strength Repair-Group:0,6kg | Strength Repair-Group: 3,9kg | ||
| Strength No Repair-Group:0,5 kg | Strength No Repair-Group: 2,9 kg |
N/A: not applicable, VAS: Visual Analogue Scale, SPADI: Shoulder Pain and Disability Index, ASES, American Shoulder and Elbow Score, UCLA Score: University of California at Los Angeles Score, SST: Simple Shoulder Test, ABD: abduction, ADD: adduction, FF: forward flexion, ER: external rotation, IR: internal rotation, U/S: ultrasound.
Complications, potential risk of bias, and modified Coleman methodology score per study.
| Authors [ref] | Complications | Type of Bias | Coleman Score (0-100/100) |
|---|---|---|---|
| De Boer | N/A | Selection, Performance, Detection, Attrition | 57 |
| Clark | No significant difference between Groups. | Selection, Performance, Detection, Attrition | 53 |
| Repair-Group: Overall: 13(20%) out of 65; Dislocation: 2; | |||
| Infection: 5; Fracture: 2. | |||
| No Repair-Group: Overall: 11(20%) out of 55; | |||
| Dislocation: 3; Infection: 3; Fracture: 3 | |||
| Werner | No significant difference between Groups. | Selection, Performance, Detection, Attrition | 47 |
| Repair-Group: Dislocation: 2(2.8%); | |||
| Scapular Notching: 6 (8.5%) | |||
| No Repair-Group: Dislocation: 0; | |||
| Scapular Notching: 3 (7.9%) | |||
| Vourazeris | No significant difference between Groups. | Selection, Performance, Detection, Attrition | 60 |
| Repair-Group: Overall: 4.7%; Dislocation: 0; Infection: 1; | |||
| Base plate failure: 2; Humerus loosening: 1 | |||
| No Repair-Group: Overall: 6%; | |||
| Dislocation: 3 (2.6%); Infection: 1; Fracture: 3 | |||
| Friedman | No significant difference between Groups. | Selection, Performance, Detection, Attrition | 58 |
| Repair-Group: Overall: 7.4%; | |||
| Dislocation: 0; Scapular Notching: 10.4%. | |||
| No Repair-Group: Overall: 6,8%; | |||
| Dislocation: 3 (1.2%); Scapular Notching: 10.7% |
ASES: American Shoulder and Elbow Score, ROM: range of motion, RTSA: reverse total shoulder arthroplasty, N/A: not applicable, U/S: ultrasound.