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31 (); 129-133
doi:
10.1016/j.jor.2022.04.017

Does subscapularis integrity influence outcome following latissimus dorsi tendon transfer for irreparable cuff tears? A comparative series of 48 patients

Sir Charles Gairdner Hospital, North Metropolitan Health Service (WA Health), Nedlands, Perth, Western Australia, 6009, Australia
School of Human Sciences (Exercise and Sport Science), University of Western Australia, Crawley, Perth, Western Australia, 6009, Australia
Western Orthopaedic Clinic, St John of God Hospital, Subiaco, Perth, Western Australia, 6008, Australia
Perth Orthopaedic & Sports Medicine Centre, West Perth, Perth, Western Australia, 6005, Australia

∗Corresponding author: Jay R. Ebert. jay.ebert@uwa.edu.au

Disclaimer:
This article was originally published by Reed Elsevier India Pvt. Ltd. and was migrated to Scientific Scholar after the change of Publisher.

Abstract

Abstract

Latissimus dorsi tendon transfer (LDTT) remains a surgical option for massive irreparable rotator cuff tears. Despite a lack of comparative studies, subscapularis insufficiency has been reported as a contraindication. This study investigated the clinical outcome at a minimum 2-years post-surgery, in patients undergoing LDTT with varied subscapularis integrity.

This retrospective study included 48 patients, of which 22 underwent LDTT with an intact subscapularis (age 56.9 years, review time 79.6 months, males 68.2%) and 26 with partial (16 patients) or full-thickness (10 patients) subscapularis tearing (age 57.4 years, review time 73.3 months, males 73.1%) between 2004 and 2018. Pre-operative imaging ascertained subscapularis status. Outcomes included the Upper Extremity Functional Index (UEFI), Global Rating of Change (GRC) and patient satisfaction.

No significant group differences were observed in age (p = 0.617) or review time (p = 0.555), nor the UEFI (intact 69.6, not intact 67.0, p = 0.265) or GRC (intact 3.6, not intact 2.9, p = 0.265). High levels of patient satisfaction were observed in both groups for pain relief, improving the ability to undertake daily and recreational activities, and overall satisfaction (intact 95.5–100.0%, not intact 92.3–96.2%).

LDTT resulted in encouraging clinical scores and high satisfaction levels, irrespective of the degree of untreated, underlying subscapularis integrity.

Therapeutic Level III.

Keywords

Latissimus dorsi tendon transfer
Shoulder
Clinical outcomes
Subscapularis
1

1 Introduction

Symptomatic rotator cuff disease is common, and while the underlying rationale of rotator cuff surgical repair when indicated is to improve functional patient outcome and restore structural integrity, 10–30% of rotator cuff tears (RCTs) are massive and irreparable.1 Surgical options for massive RCTs may include an attempt at primary repair, though the reported failure rate in these cases is particularly high.2 Reverse shoulder arthroplasty has demonstrated good outcomes in arthritic patients with massive RCTs, though it may not be the best option for younger, active patients.3 Superior capsular reconstruction (SCR), lower trapezius transfer and anatomical joint arthroplasty are other options.4–7 Recently, several systematic reviews have demonstrated the clinical effectiveness of SCR as a surgical solution for irreparable RCTs,8–11 though a review by Altintis et al.11 outlined the relatively poor quality of many of the existing studies and notable complications that have been reported.

First described by Gerber et al., in 1988,12 latissimus dorsi tendon transfer (LDTT) has become an established treatment option for patients with massive and irreparable RCTs.13–27 Factors such as pre-operative shoulder function and general strength may influence outcome.28 However, given the transferred latissimus will provide an inferior force that must be counterbalanced by the deltoid and subscapularis,12 an intact subscapularis at the time of surgery has been considered imperative.29 The inferior outcomes reported in patients undergoing LDTT with concomitant subscapularis insufficiency have been reported.15,18,19,22,23 However, it is important to note that the finding of worse outcome with subscapularis deficiency in reported studies appears largely based upon analysis of outcomes. While studies published by Gerber et al.22,23 in 44 and 67 patients reported inferior outcomes in patients with a deficient subscapularis, other reports were only small studies by Weening et al.,15 (16 patients, of which 3 of 4 patients with subscapularis deficiency had unfavourable results) Aoki et al.18 (12 patients, 1 of 2 patients with subscapularis deficiency had a poor outcome) and DeCasas et al.19 (14 patients, of which the only patient with subscapularis deficiency had a poor outcome).

Given the relative lack of research specifically evaluating post-operative LDTT patient outcome associated with subscapularis insufficiency, the current study sought to investigate clinical outcome and patient satisfaction at a minimum 2-years post-surgery, in patients undergoing LDTT for massive irreparable RCTs with varied subscapularis integrity. It was hypothesized that LDTT would be just as clinically effective for patients with subscapularis insufficiency (partial or full thickness tearing), as to those with an intact subscapularis.

2

2 Methods

2.1

2.1 Patients

Between 2004 and 2018, a total of 118 patients presenting with massive RCTs that had been deemed irreparable underwent primary LDTT with a single surgeon (PC). Of the 118 patients that underwent surgery over the nominated period, patients were subsequently contacted for this retrospective review until the required sample size (n = 22 per group, based on an intact or deficient subscapularis as described below) was attained. Fig. 1 displays the flowchart of patient contact and assessment. Therefore, a total of 48 patients were included in the current study, including 22 patients with an intact subscapularis at the time of LDTT and 26 patients with subscapularis insufficiency (Fig. 1 and Table 1) as determined below.

Study flow chart demonstrating patient recruitment and assessment.
Fig. 1 Study flow chart demonstrating patient recruitment and assessment.
Table 1 Patient demographics and clinical scores based on subscapularis grouping (intact or deficient). Shown are means and p-values.
Variable Group 1 (Intact, n = 22) Group 2 (Deficient, n = 26) p value
Gender, males/females n (%) 15/7 (68.2/31.8) 19/7 (73.1/26.9) N/A
Dominant Limb is Operated Limb, n (%) 13 (59.1) 15 (57.7) N/A
Age at surgery (years), mean (range) 56.9 (45–68) 57.4 (43–75) 0.617
Post-operative Review Time (months), mean (range) 79.6 (24–150) 69.9 (24–156) 0.555
Concomitant Surgery, n (%)
Subacromial Decompression 8 (36.4) 8 (30.8) N/A
Long Head of Biceps Tenotomy 2 (9.1) 4 (15.3) N/A
Acromioclavicular Joint Excision 7 (31.8) 6 (23.1) N/A
UEFI, mean (range) 69.6 (40–80) 67.0 (31–80) 0.265
GRC, mean (range) 3.6 (1–5) 3.1 (-2–5) 0.094

Massive and irreparable RCTs were confirmed pre-operatively in all 48 patients included in the current study, via Magnetic Resonance Imaging (MRI) alone (n = 36), MRI and ultrasound (US) (n = 7), US alone (n = 4) and computed tomography (CT) arthrogram (n = 1). All imaging was further categorised based on whether subscapularis was intact or insufficient. For the current study, an intact subscapularis was defined as ‘intact’ (n = 22), while a deficient subscapularis was defined as pre-operative imaging demonstrating and reporting a ‘partial tear’ (n = 16) or a ‘full thickness tear’ (n = 10). This research was approved by the relevant Institutional Review Board (IRB).

2.2

2.2 Surgery

All surgery was performed by a single surgeon (PC). The patient was positioned laterally with the operative arm in a gantry with traction and at approximately 45° degrees. Routine arthroscopy was performed to confirm cuff disease and the status of all cuff tendons, with concomitant procedures performed at this stage if required including long head of biceps tenotomy, acromioclavicular joint (ACJ) excision and/or acromioplasty if indicated.

The arm was then subsequently removed from the gantry and draped for sterility and placed in a Fig4 position with the patient's hand on their forehead to harvest the latissimus dorsi tendon from the axillary approach. A curvilinear incision (8–10 cm) was made on the posterior border of the axilla over the bulk of the muscle. Blunt dissection through subcutaneous tissue was made down to fascia. Blunt levers were placed on the humerus at the superior and inferior insertion of the tendon. The superior and inferior borders of the tendon were defined with sharp dissection. The tendon was then removed with sharp dissection from the bone leaving the teres major lying directly underneath intact. The tendon and muscle of latissimus dorsi was then mobilised down to the neurovascular pedicle to gain sufficient excursion. The tendon was then whip-stitched with heavy braided suture on the medial and lateral borders (2 fibre-wire).

The arm was then placed by the patient's side and a separate lateral deltoid splitting approach was made, akin to a mini-open approach for supraspinatus repair (longitudinal incision over the anterior/middle fibers of the deltoid, with the muscle fibers subsequently split in the line of the anterior raphe to expose the humeral head). Blunt dissection was then made digitally from the inferior wound to create a tunnel to passage the tendon through the subdeltoid bursa from above and in the plane initially between teres major and posterior deltoid, and then between the long head of triceps and the proximal humeral shaft below. The passage created was directly on bone to avoid possible neurovascular damage. The sutures of the whip-stitches were then passed superiorly in the passage, and the suture and tendon advanced to the lateral exposure. The humeral head was prepared with burr/osteotomes to bleeding bone on the lateral edge, anterior to the midline for the foot-print of the transferred tendon. The tendon was then anchored with 2 x heavy bone anchors (Arthrex 3.75 mm swivel locks), and the wound was washed and closed in layers.

2.3

2.3 Clinical review

Patients were assessed post-operatively via the UEFI, a Global Rating of Change (GRC) scale and various domains of patient satisfaction. Firstly, the UEFI is scored from 0 to 80 and was employed to quantify upper limb function, and has demonstrated acceptable reliability and validity in adults with upper extremity dysfunction.30 An 11-point Global Rating of Change (GRC) scale was employed to evaluate the patient's perceived current post-operative status compared to before their surgery,31 ranging from −5 (very much worse) to 0 (unchanged) to +5 (completely recovered). A patient satisfaction questionnaire was employed to investigate each patient's level of satisfaction with the surgery overall, as well as their satisfaction with the surgery in relieving their pain, improving their ability to perform normal daily activities and improving their ability to return to recreational activities. A Likert response scale was employed with descriptors Very Satisfied, Somewhat Satisfied, Somewhat Dissatisfied and Very Dissatisfied. While the post-operative patient reviews were undertaken by members of the research team (JC and JE) and were intended as a face-to-face consultation, many patients upon initial contact were now living regionally and unable to travel large distances for review, hence the majority of these reviews were undertaken via a comprehensive phone review.

2.4

2.4 Statistical analysis

For the current study, a priori power calculation was determined based on the recommendations of Cohen.32 The minimal detectable change (MDC) reported for the Upper Extremity Functional Index (UEFI) is 9.4,30 equating to an effect size of 0.87. Therefore, to detect this degree of difference between groups with 80% power at alpha 0.05, it was estimated that 22 patients in each of the two surgical groups would be required (intact or deficient subscapularis, as described below).

Initially, a subset analysis was undertaken using independent sample t-tests to compare outcomes within the ‘deficient’ subscapularis group. No significant differences (p˃0.05) in clinical scores were observed between those than underwent LDTT in the presence of a partial (n = 16, UEFI mean 65.6, GRC mean 3.0) or full (n = 10, UEFI mean 68.3, GRC mean 2.8) thickness tear, hence these two pathological cohorts were combined to create the deficient subscapularis group. Following this, independent sample t-tests were employed to evaluate differences between groups (intact versus deficient subscapularis at the time of surgery) in pertinent patient demographic variables (age, review time) as well as clinical scores. The number (and percentage) of patients that were satisfied (or not) within each of the satisfaction items were presented. Where appropriate, statistical analysis was performed using SPSS software (SPSS, Version 23.0, SPSS Inc., USA), while statistical significance was determined at P < 0.05.

3

3 Results

No significant differences (p > 0.05) were observed in patient age at surgery or the time of post-operative review between the two surgical groups, with a similar distribution of concomitant procedures between the two groups (Table 1). Furthermore, no significant group differences were observed in either the UEFI or GRC (Table 1). High levels of patient satisfaction were observed in both groups, across all satisfaction items (Table 2).

Table 2 The number of patients within each of the four satisfaction gradings (very satisfied, somewhat satisfied, somewhat dissatisfied, very dissatisfied) for each of the four satisfaction items, within the two surgical groups (subscapularis intact or deficient).
Group Satisfaction Item Pain relief Improving ability to undertake ADLs Improving ability to participate in recreational activities Overall satisfaction
Subscapularis Intact (n = 22) Very Satisfied 15 11 9 14
Satisfied 7 11 12 8
Dissatisfied 0 0 1 0
Very Dissatisfied 0 0 0 0
Satisfied Overall, n (%) 22 (100.0%) 22 (100.0%) 21 (95.5%) 22 (100.0%)
Subscapularis Deficient (n = 26) Very Satisfied 16 16 11 16
Satisfied 9 8 13 9
Dissatisfied 1 2 0 1
Very Dissatisfied 0 0 2 0
Satisfied Overall, n (%) 25 (96.2%) 24 (92.3%) 24 (92.3%) 25 (96.2%)
4

4 Discussion

The current study has demonstrated encouraging post-operative clinical outcomes and high levels of patient satisfaction after LDTT for massive and irreparable RCTs, similar to existing studies.13–27 However, while prior studies have reported inferior outcomes in the presence of subscapularis insufficiency,15,18,19,22,23 the most important finding from this study is that no significant difference in clinical outcomes could be demonstrated between those undergoing LDTT with, or without, subscapularis insufficiency at the time of surgery.

Gerber et al.12 first reported the use of LDTT in 1988, with subsequent studies in 6923 and 4622 shoulders at a mean 53 and 147 months, respectively, demonstrating good outcomes as reported by the Constant Score and Subjective Shoulder Value (SSV). In other large reported cohorts, Kany et al.13 reviewed 62 patients and reported good outcomes reported by the Constant, SSV, Simple Shoulder Test (SST), American Shoulder and Elbow Surgeons (ASES) score and a Visual Analogue Pain Scale (VAS), with 81% of patients satisfied at a minimum 2 year follow up. El-Azab et al.21 investigated 93 shoulders at mean 9.3 years with improved Constant, ASES and VAS scores. While El-Azab et al.21 reported better outcomes in younger patients, Kany et al.13 specifically compared outcomes in patients ≤55 and ≥ 75 years of age, demonstrating no group differences. Smaller studies undertaken by Postacchini et al.25 (7 patients), Aoki et al.18 (12 shoulders), Clavert et al.14 (14 patients), DeCasas et al.19 (14 patients), Weening et al.15 (16 patients), Miniaci et al.24 (17 patients) and DeBeer et al.20 (26 shoulders) all demonstrated clinical improvement at various post-operative time-points resulting from LDTT reported via various outcome measures, including the Constant score, University of California at Los Angeles (UCLA) shoulder score, SSV, ASES and various satisfaction scores. Valenti et al.26 reviewed a mix of primary (17 patients, 85% satisfied) and revision (8 patients, 50% satisfied) LDTT cases with mixed outcomes based on prior surgery, while Birmingham et al.17 performed LDTT as a salvage procedure in 18 patients after failed rotator cuff repair, reporting significant improvement in pain and active arm elevation. The current study demonstrated high rates of patient satisfaction, though no other study employed the UEFI or a GRC scale making comparison in clinical outcome to other studies difficult. At the time of development of the current study, given the vast array and inconsistency of PROMs already employed to assess patients after LDTT, we chose the UEFI as a well-reported score for upper limb function as a supplement to the GRC and satisfaction rating scores employed.

Again, specific to the current study we were unable to demonstrate a significant difference between patients with, or without, an intact subscapularis at the time of LDTT. In a review published by Grimberg et al.,33 it was noted that studies reported various ways of dealing with the presence of concomitant subscapularis tears, including complete patient exclusion from LDTT, or repairing small tears of the upper third subscapularis. El-Azab et al.21 investigated 93 shoulders at mean 9.3 years, of which 13 patients underwent concomitant repair of a partial subscapularis lesion, with no clinical difference seen between these patients and those that had an intact subscapularis at the time of surgery. Studies by Gerber et al.22,23 reported inferior outcomes in the presence of subscapularis insufficiency, also stating that if subscapularis function is deficient, the procedure is of questionable benefit and probably should not be used.23 As previously mentioned, other studies reporting inferior outcomes with a deficient subscapularis are in small patient cohorts,15,18,19 and it should be further highlighted that across all of these studies the number of patients undergoing LDTT with a deficient subscapularis, relative to the total patient group, was very low. Nonetheless, a more recent study published by Mihata et al.34 in a large cohort of patients that had undergone SCR reported that the presence of subscapularis tears negatively affected clinical outcomes (including PROMs, strength and range of motion) and complication rates. Therefore, larger studies with more robust objective outcome measures and in the presence of varied surgical treatment options may be required.

The biomechanical role of subscapularis in LDTT has been previously discussed.35 In a biomechanical cadaveric model, Werner et al.35 reported that the subscapularis had a significant impact on glenohumeral translation and humeral head rotation, suggesting that the inferior results of LDTT in the presence of subscapularis dysfunction may be explained by the loss of humeral head stability upon arm abduction and elevation. The translation of these findings specifically to an in vivo model are hard to determine. Regardless, the reduced stabilizing role otherwise provided by an intact subscapularis did not appear to significantly affect patient outcome and post-operative satisfaction in the current study.

A number of limitations must be acknowledged in the current study. Firstly, the current study included 48 patients (with recruitment ceasing once the desired sample size for each group was attained). We appreciate this may present a selection bias, though it should also be acknowledged that of the initial 54 patients contacted and invited to participate, there were only 6 patients that had declined. Studies with larger patient cohorts exist13,21,23 albeit the majority are in small patient cohorts, and larger studies with more comprehensive patient outcomes will benefit future research. Second, the current study sought to investigate the UEFI, GRC and patient satisfaction. Several other outcome measures have been employed (with the Constant score the most common) making comparison of clinical outcomes in the current study difficult to compare to existing literature. As discussed earlier, given the vast array and inconsistency of PROMs already employed to assess patients after LDTT, we chose the UEFI as a well-reported score for upper limb function as a supplement to the GRC and satisfaction rating scores employed. Further to this, the nature of this retrospective review (and in some patients that were 13 years post-surgery at the time of the review) made it difficult to evaluate all patients face-to-face, with many requiring a comprehensive phone review given the fact that many now lived in regional areas. This also limited our ability to undertake any objective measures such as strength and/or range of motion assessment. Other studies have also sought to review post-operative radiographic changes,13,22 which the current study did not and may be of value to evaluate glenohumeral joint changes in the presence of the theorized reduction in stability not provided in the presence of subscapularis insufficiency. Again, similar to the lack of collected and reported objective clinical measures in the current retrospective study, radiological review was difficult and should be undertaken in future studies to better assess its effect on patient outcome.

5

5 Conclusion

The current study demonstrated that LDTT performed for massive irreparable rotator cuff tears resulted in encouraging clinical outcomes, in support of the existing literature. However, while the current study has limitations in that only the UEFI, GRC and Patient Satisfaction were assessed as previously discussed, it still demonstrated high levels of patient satisfaction in patients undergoing LDTT irrespective of the underlying level of subscapularis integrity. While smaller studies have reported less favourable outcomes in patients undergoing LDTT with subscapularis insufficiency,15,18,19,22,23 larger comparative studies with more robust and activity-specific assessment tools, together with serial radiographic imaging, may be required to truly evaluate the mid- and long-term stabilizing benefit offered by an intact subscapularis.

Ethical approval

This research was approved by the University of Western Australia (RA/4/20/4235) Human Research Ethics Committee (HREC).

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

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