Skip to main content
BMC Musculoskeletal Disorders logoLink to BMC Musculoskeletal Disorders
. 2019 Oct 27;20:487. doi: 10.1186/s12891-019-2876-6

Imaging modality for measuring the presence and extent of the labral lesions of the shoulder: a systematic review and meta-analysis

Fanxiao Liu 1,#, Xiangyun Cheng 2,#, Jinlei Dong 1, Dongsheng Zhou 1, Qian Sun 3, Xiaohui Bai 4,, Dawei Wang 1,
PMCID: PMC6815459  PMID: 31656171

Abstract

Background

Multiple published studies quantitatively analysing the diagnostic value of MRI, MR arthrography (MRA) and CT arthrography (CTA) for labral lesions of the shoulder have had inconsistent results. The aim of this meta-analysis was to systematically compare the diagnostic performance of MRI, MRA, CTA and CT.

Methods

Two databases, PubMed and EMBASE, were used to retrieve studies targeting the accuracy of MRI, MRA, CTA and CT in detecting labral lesions of the shoulder. After carefully screening and excluding studies, the studies that met the inclusion criteria were used for a pooled analysis, including calculation of sensitivity and specificity with 95% confidence intervals (CIs) and the area under the hierarchical summary receiver operating characteristic (HSROC) curves.

Results

The retrieval process identified 2633 studies, out of which two reviewers screened out all but 14 studies, involving a total of 1216 patients who were deemed eligible for inclusion in the meta-analysis. The results assessing the diagnostic performance of MRI vs. MRA for detecting labral lesions showed a pooled sensitivity of 0.77 (95% CI 0.70–0.84) vs. 0.92 (95% CI 0.84–0.96), a specificity of 0.95 (95% CI 0.85–0.98) vs. 0.98 (95% CI 0.91–0.99), and an area under the HSROC curve of 3.78 (95% CI 2.73–4.83) vs. 6.01 (95% CI 4.30–7.73), respectively.

Conclusion

MRA was suggested for use in patients with chronic shoulder symptoms or a pathologic abnormality. MRI is by far the first choice recommendation for the detection of acute labral lesions. CT should be a necessary supplemental imaging technique when there is highly suspected glenoid bone damage.

Keywords: Labral lesions, MRI, MRA, CTA, Diagnostic value, Meta-analysis

Background

The glenoid labrum, composed of fibro-cartilage, is a ring or band structure that effectively increases the depth of the glenoid fossa [1]. Lesions of the glenoid labrum, occurring with glenohumeral instability, result in serious shoulder pain because of the destruction of free nerve endings located in the peripheral part of the glenoid labrum and the subacromial bursae [2, 3].

Based on their location and lesion features in imaging [4], disorders of the glenoid labrum have been broadly categorized as superior, posterior, inferior or anterior lesions [5]. Specifically, superior labral anterior-posterior tears (SLAP), initially described by Andrews et al. in 1985, have been an ongoing diagnostic challenge in the clinic [6]. Additionally, Bankart lesions are one kind of injury on the anteroinferior aspect of the glenoid labral complex, which are thought to predispose shoulders to recurrent dislocation [7, 8]. The integrity of the labrum and whether any bone has been avulsed or missing from the bony glenoid determined the different treatment strategies. For example, SLAP lesions were usually managed by arthroscopy at present [9] while detached Labra is often treated by open surgical repair [10]. Because of the serious pain associated with these injuries and the limitations they place on participation in high-level activities, the need to evaluate accuracy, efficiency, and economics of diagnostic tests for labral damage is increasingly important [9]. In addition, reorganization of the integrity of the glenoid labrum is an essential factor for clinicians to consider when making treatment decisions (i.e., to use conservative vs. surgical strategies) [10]. Medical imaging technologies not only provide rich and useful information to support findings from the medical history and physical examination but also demonstrate the pathoanatomy of shoulder dysfunction of the shoulder [11]. Therefore, a suitable choice of imaging technique could help to establish an appropriate treatment strategy.

Many imaging methods, including arthrography, computed tomography arthrography (CTA), magnetic resonance imaging (MRI), direct MR arthrography (D-MRA) and indirect MR arthrography (I-MRA) have been used to image the glenoid labrum as well as the associated structures of the capsular mechanism [12]. Shoulder MRI is becoming quite popular as a screening examination for the detection of labral abnormalities [13]. However, intra-articular structures of the shoulder are not well imaged by MRI when insufficient fluid is present to outline the glenoid contour [14].

MRA of shoulders mainly included indirect shoulder magnetic resonance arthrography (I-MRA) and direct shoulder magnetic resonance arthrography (D-MRA). D-MRA, which involves intra-articular administration of contrast agent, has become an established imaging modality for assessing different types of labral lesions [14]. Additionally, an alternative and less invasive technique, I-MRA, were intravenously administered contrast enhances the joint space and indirectly produces an arthrographic effect [15]. MRA is considered to have higher accuracy than MRI in the detection of glenoid labral tears, but it is invasive [15]. CTA does not have advantages in the evaluation of soft tissue injuries such as labral damage over MRI and MRA; however, it was proven to have much higher diagnostic accuracy for detecting bony defects of the glenoid [16]. With the development of MRI technologies, the diagnostic sensitivity and specificity of 3-Tesla (T) MRI versus MRA for assessing labral abnormalities is controversial to a certain extent [17]. A previous meta-analysis [18] suggested that MRA had greater diagnostic accuracy than MRI for the overall detection of glenoid labral lesions. The opposite result was obtained when diagnosing anterior glenoid labral lesions. Another meta-analysis demonstrated that MRA was superior to MRI for the detection of SLAP lesions [19]. A recent meta-analysis from 2018, involving 10 studies, revealed that 3.0 T MRA improved sensitivity for the diagnosis of anterior and posterior labral tears, but reduced specificity in the diagnosis of SLAP tears [20].

Recently, multiple high-quality studies [14, 2123] were published, most of which used relatively high resolution for CTA and relatively high-field strength magnets and multidimensional imaging for MRI and MRA. Moreover, no studies have compared the diagnostic performance of MRI, D-MRA, I-MRA and CTA using side-by-side analysis in a single study for the detection of labral lesions. Therefore, an updated meta-analysis is warranted to determine if the new data and improved technology have had an impact on the diagnostic accuracy of a given pool of data.

The primary objective of this study was to perform a meta-analysis on the diagnostic accuracy of MRI, MRA, CTA and CT in the assessment of glenoid labral lesions. The second objective was to compare the diagnostic accuracy of MRI and MRA for detecting different types of labral lesions, such as anterior, posterior or superior lesions. The third objective was to evaluate the effect of magnet strength on the diagnostic accuracy of MRI and MRA for glenoid labral lesions.

Methods

This meta-analysis was conducted based on the guidelines of the Preferred Reporting Items for a Systematic Review and Meta-analysis of Diagnostic Test Accuracy Studies (PRISMA-DTA) [24] statement. Patient informed consent and committee approval were not required for this study due to the use of published data.

Selection and inclusion criteria

The keywords “MRI”, “magnetic resonance imaging”, “magnetic resonance arthrography”, “MR arthrography”, “MRA”, “computed tomography arthrography” “computed tomography”, “CT”, or “CTA” AND “labral” or “shoulder pain” were used to search two databases, PubMed and EMBASE, to retrieve published studies measuring the diagnostic accuracy of MRI, MRA, CT and CTA for labral lesions. The date of the newest search was November 1, 2018, and there was no language limitation. Additionally, a supplementary search by hand was further performed to screen the reference lists of the included studies.

The clinical trials that involved patients with labral lesions; assessing the diagnostic accuracy of MRI, MRA, CT and CTA for labral lesions and provided direct diagnostic data, including true-positive (TP), false-positive (FP), false-negative (FN) and true negative (TN), or data that enabled calculation of these parameters, met the inclusion criteria and were included in this meta-analysis. The study presenting the most data was included in this statistical analysis if any studies contained overlapping data. The review literature, no full-text studies, including conference summaries and meeting abstracts, or non-clinical studies, such as animal and cadaver experiments and biomechanics, were excluded.

Data extraction and risk of bias

Each study found in the search process was screened, and its appropriateness for inclusion was determined. Information from each study were extracted into a standardized form independently by two blinded reviewers. The information included the following: the first author’s surname; year of publication; country of origin; basic information about the participants, such as number, age and sex; the main characteristics of the MRI, MRA and CTA and their analysis methods; and the original diagnostic data, including TP, FP, FN and TN outcome were extracted.

The risk of bias of each included study was measured utilizing a quality assessment tool (QUADAS-2), [2527] which contains 11 items and is usually used for diagnostic accuracy studies.

Statistical analysis

Two reviewers (Reviewers CXY and LFX) independently and blindly screened the search records from two databases, identified studies using the inclusion criteria, extracted the target data, and measured the quality of the studies using the aforementioned tool. Inconsistencies between reviewers were resolved by consensus.

The primary outcome of this meta-analysis was to compare the diagnostic value of MRI, MRA and CTA for labral lesions simultaneously in the included studies. To derive summary estimates of the diagnostic value of each modality, a bivariate random-effects model was applied to analyze the following pooled outcome estimates: sensitivity, specificity and hierarchical summary receiver operating characteristic (HSROC) [28, 29] curves based on the diagnostic data extracted from each included study. HSROC curves provide a 95% confidence interval (CI) and prediction regions. The secondary outcomes were the various subgroups (type of lesions) to determine the reliability of imaging techniques in the various subgroups. According to the PRISMA-DTA [24], the publication bias Deeks’ funnel plots [30] was omitted. All statistical analyses were calculated utilizing Stata v-12.0 and Meta-Disc v-1.4.

Results

Selection process

The initial search of the two chosen electronic databases and the subsequent screening process of potential studies is represented in Fig. 1. Of 2633 records identified during the database and bibliography searches, 1046 ineligible records were excluded due to repetition, and 1530 were excluded by screening titles and abstracts. Subsequently, further exclusions were performed by downloading and reviewing the full-text versions of the remaining studies. After a detailed search and selection process, 14 studies [15, 17, 2123, 3139] involving 1216 patients with labral lesions met the inclusion criteria for the meta-analysis.

Fig. 1.

Fig. 1

Selection flow chart for included studies in the meta-analysis

Study characteristics and quality assessment

Table 1 and Table 2 present the main characteristics of the participants and the included studies. All included articles were published between 1990 and 2016, with sample sizes ranging from 23 to 444 patients. A total of 14 studies [15, 17, 2123, 3139] used MRI and MRA to assess labral lesions. For all included studies, the gold standard for diagnosing labral lesions was arthroscopy or surgery. The methodological quality resulted in one study [35] receiving a score of 8, two studies [21, 32] receiving a score of 9, and the remaining 11 studies [15, 17, 22, 23, 31, 33, 34, 3639] achieving an overall score of 10, according to the QUADAS-2 tool. The main characteristics of three imaging methods, MRI, MRA and CTA, are presented in Table 3.

Table 1.

Main characteristics of the subjects from included studies

Study, year No. of patients Age, years
mean (range)
Sex (M/F) No. of shoulders Clinical indication of shoulder Methods Final diagnosis of included patients
Flannigan, et al. 1990 [31] 23 45 (16–68) 18/5 23 Shoulder pain MRI/MRA Labral tears
Chandnani, et al. 1993 [32] 30 27 (19–39) NA 30 Shoulder pain MRA/CTA Labral tears
Sano, et al. 1996 [33] 47 24 (14–45) 39/8 47 Shoulder pain MRA/CTA Labral tears
Wallny, et al. 1998 [34] 28 43 (21–63) 19/9 28 Clinically suspected labral injuries MRI/MRA Labral tears
Herold, et al. 2003 [38] 35 47.3 (18–67) 26/9 35 Acute or chronic shoulder disorder MRI/MRA SLAP
Reuss, et al. 2006 [35] 83 NA NA 83 Shoulder pain MRI/MRA SLAP
Dinauer, et al. 2007 [15] 104 40 (18–65) 82/22 104 Mechanical symptoms MRI/MRA SLAP
Magee, et al. 2009 [17] 150 31 (14–50) 109/41 150 Shoulder pain MRI/MRA SLAP/Posterior/Anterior
Major, et al. 2011 [36] 42 33 28/14 42 Shoulder pain MRI/MRA Superior/Posterior/Anterior
Fallahi, et al. 2013 [37] 91 35 (15–70) 74/17 91 Shoulder pain MRI/MRA Labral tears
Mahmoud, et al. 2013 [39] 31 21–70 24/7 31 Shoulder lesion MRA/CTA SLAP/Bankart
Moroder, et al. 2013 [23] 48 30.8 (20–78) 40/8 48 Anterior shoulder instability MRI/CT Glenoid defect (bony)
Sheridan, et al. 2015 [22] 444 49 271/173 444 Shoulder pain MRI/MRA SLAP
El-Liethy, et al. 2016 [21] 60 35 (14–55) NA 60 Trauma, shoulder pain, dislocation MRI/MRA Labral tears

NA No available. SLAP Superior labrum anterior-to-posterior

Table 2.

Main characteristics of the included studies

Author, year Country Inclusion interval Study design Gold standard Time from MRI/MRA to gold standard, days, mean (range) Blinding No. of readers Reader experience
(years)
Flannigan, et al. 1990 [31] USA NA P Arthroscopy/Open Surgery NA Yes 2 NA
Chandnani, et al. 1993 [32] USA NA P Arthroscopy/Open Surgery NA Yes 2 2/4
Sano, et al. 1996 [33] Japan NA R Arthroscopy NA Yes 2 NA
Wallny, et al. 1998 [34] Germany NA P Arthroscopy/Open Surgery NA Yes 2 NA
Herold, et al. 2003 [38] Germany NA P Arthroscopy 60 (33–175) Yes 2 7/12
Reuss, et al. 2006 [35] USA 09.1998–03.2003 R Arthroscopy NA Yes 2 NA
Dinauer, et al. 2007 [15] USA 09.2011–10.2030 P Arthroscopy/Open Surgery 1–175 Yes 2 5
Magee, et al. 2009 [17] USA 01.2007–07.2007 R Arthroscopy NA Yes 2 10
Major, et al. 2011 [36] USA 01.2007–07.2006 P Arthroscopy Less 3 months Yes 3 30/15/6
Fallahi, et al. 2013 [37] UK 01.2009–12.2011 R Arthroscopy/Open Surgery NA Yes 2 14/6
Mahmoud, et al. 2013 [39] Egypt 03.2011–05.2012 P Arthroscopy Less 100 Yes 2 NA
Moroder, et al. 2013 [23] Austria 2006–2009 R Arthroscopy/Open Surgery NA Yes NA NA
Sheridan, et al. 2015 [22] USA 2006–2008 R Arthroscopy/Open Surgery NA Yes NA NA
El-Liethy, et al. 2016 [21] Egypt 06.2015–12.2015 R Arthroscopy NA Yes 2 NA

NA No available, R Retrospective, P Prospective

Table 3.

Main characteristics of MRI, MRA and CTA

Author, year Scanner (MRI /MRA) Method (MRA) Technical parameters (MRI /MRA) Analyzed image plane
Vendor Model Magnetic strength/CT Slice Sequence (MRI) Sequence (MRA) Slice thickness (mm) NO. of analyzed image plane
Flannigan, et al. 1990 [31] GE Healthcare Signa 1.5 T Direct T1WI (SE) T1WI (SE) 4/4 1/1 Coronal
Chandnani, et al. 1993 [32] NA NA 1.5 T Direct T1WI SE pulse sequence PDWI, T2WI (SE) 3/3 2/2 Axial, obl cor/Axial, obl cor
Sano, et al. 1996 [33] Shimazu NA 1.5 T NA NA T1WI 2/4 3/3 Axial, obl cor, obl sag/Axial, obl cor, obl sag
Wallny, et al. 1998 [34] Philips ACS II 1.5 T Indirect T1WI,T2WI,PD T1WI (FS) 3/3 2/2 Axial, obl cor/Axial, obl cor
Herold, et al. 2003 [38] Siemens Erlangen 1.5 T Indirect STIR, T1 SE,PD-T2 TSE,T1-Flash 2D,T1 SE STIR, T1 SE,PD-T2 TSE,T1-Flash 2D,T2 SE 3/3 3/3 axial, parasag, paracor/Axial, parasag, paracor
Reuss, et al. 2006 [35] NA NA 1.5 T Direct NA NA NA NA NA
Dinauer, et al. 2007 [15] GE healthcare Signa 1.5 T Indirect T1WI (FSE, FS), T2WI (FSE, FS) T1WI (FSE, FS) 3.5/3.5 3/3 Axial, obl cor, obl sag/Axial, obl cor, obl sag
Magee, et al. 2009 [17] GE healthcare Signa 3 T Direct T1WI (FSE),T2WI(FSE), T2WI (FSE, FS) T1WI (FS) 4/4 3/3 Axial, obl cor, obl sag
Major, et al. 2011 [36] Siemens Signa 3 T Direct T1WI, T2 WI(FS), PDWI T1WI (FS),T1WI, T2WI (FS) 3/3 4/4 Axial, obl cor, obl sag, sag
Fallahi, et al. 2013 [37] Siemens Avanto 1.5 T Indirect T1FS, PDFS, STIR, T2 GRE T1FS, PDFS, STIR, T2 MEDIC 3/3 3/3 Para cor, sag, axial
Mahmoud, et al. 2013 [39] Philips Gyroscan NT

1.5 T/

64-slice

Direct NA T1WI (FS), 3DWatSc, T2WI (SE) 3/2 3/2 Axial, obl cor, obl sag/Supine position, ABER
Moroder, et al. 2013 [23] Siemens Somatom sensation 64

1.5 T/

64-slice

NA At least two different sequences NA NA 3/3 Axial, parasag, paracor,3D reconstruction/Axial, parasag, paracor
Sheridan, et al. 2015 [22] NA NA 1.5 T NA PDWI, T2WI (FS) T1WI (FS), T1WI(PD), T2WI (FSE) NA 3/3 Axial, obl cor, sag/Axial, cor, sag
El-Liethy, et al. 2016 [21] Philips&Simens Gyroscan interna &Symphony 1.5 T Direct T1 (TSE), T2 (TSE), STIR(TSE), PD(TSE),GR (TSE) T1FS (all pulse sequences) NA 3/3 Axial, obl cor, obl sag /Axial, cor, sag

TSE Turbo spin echo, GRE Gradient echo, PD Proton density, FS Fat suppressed, WI Weighted image, SPAIR Spectral attenuated inversion recovery, FSE Fast spin-echo, STIR Short-TI inversion recovery, SE Spin echo, Axi Axial, obl cor, oblique coronal, obl sag oblique sagittal, NR not available, 3DWatSc 3D-gradient echo images, Para cor paracoronal

Diagnostic value of MRI and MRA (all labral lesions)

The results comparing the diagnostic performance of MRI vs. MRA for detecting labral lesions in patients, as generated from the 7 studies [15, 17, 21, 22, 3537] involving 1184 shoulders showed a pooled sensitivity of 0.77 (95% CI 0.70–0.84) vs. 0.92 (95% CI 0.84–0.96), a specificity of 0.95 (95% CI 0.85–0.98) vs. 0.98 (95% CI 0.91–0.99), and an area under the HSROC curve of 3.78 (95% CI 2.73–4.83) vs. 6.01 (95% CI 4.30–7.73), respectively (Fig. 2).

Fig. 2.

Fig. 2

Pooled sensitivity, specificity and HSROC of MRI and MRA for detecting all labral lesions

Diagnostic value of D-MRA and I-MRA (all labral lesions)

The results comparing the diagnostic performance of D-MRI vs. I-MRA for detecting labral lesions showed a pooled sensitivity of 0.93 (95% CI 0.83–0.97) vs. 0.92 (95% CI 0.85–0.96), a specificity of 0.99 (95% CI 0.96–1.00) vs. 0.82 (95% CI 0.66–0.92), and an area under the HSROC curve of 7.20 (95% CI 5.25–9.16) vs. 4.37 (95% CI 2.36–6.39), respectively (Fig. 3).

Fig. 3.

Fig. 3

Pooled sensitivity, specificity and HSROC of D-MRI and I-MRA for detecting all labral lesions

Diagnostic value of MRI and MRA (SLAP)

The results comparing MRI vs. MRA for detecting SLAP lesions, as generated from the 4 studies [17, 22, 35, 38] included in the present meta-analysis, involving 483 shoulders, demonstrated that the pooled results were as follows: the pooled sensitivity was 0.71 (95% CI 0.53–0.84) vs. 0.85 (95% CI 0.50–0.97), the specificity was 0.88 (95% CI 0.62–0.97) vs. 0.92 (95% CI 0.795–0.98), and the area under the HSROC curve was 2.67 (95% CI 0.86–4.48) vs. 4.62 (95% CI 1.29–7.95), respectively (Fig. 4).

Fig. 4.

Fig. 4

Pooled sensitivity, specificity and HSROC of MRI and MRA for detecting SLAP lesions

The results of the subgroup analyses based on magnet strength (1.5-T and 3-T) and study type (prospective and retrospective), generated from the 9 studies [15, 21, 22, 31, 32, 34, 35, 37, 38] involving 668 shoulders, the 2 studies involving 516 shoulders, the 7 involving 182 shoulders and the 8 studies involving 1003 shoulders, all indicated that MRA had a higher accuracy than MRI in the detection of labral lesions (Fig. 5).

Fig. 5.

Fig. 5

Pooled sensitivity, specificity and HSROC of 1.5 T MRI and MRA, 3 T MRI and MRA, MRI and MRA in prospective and retrospective design for detecting all labral lesions

The results of the subgroup analyses based on the location of labral lesions (posterior, anterior and superior) generated from the 2 studies [17, 36] involving 125 shoulders, the 2 studies [17, 36] involving 172 shoulders and the 2 studies [15, 36] involving 172 shoulders, demonstrated that MRA had a higher sensitivity and specificity than MRI (Fig. 6).

Fig. 6.

Fig. 6

Pooled sensitivity and specificity of MRI and MRA for detecting superior, anterior and posterior labral lesions

Diagnostic value of MRA and CTA

The results comparing the diagnostic performance of MRA vs. CTA for detecting labral lesions, generated from the 2 studies [32, 39], involving 93 shoulders, showed a pooled sensitivity of 0.94 (95% CI 0.83–0.99) vs. 0.82 (95% CI 0.69–0.92), a specificity of 0.94 (95% CI 0.83–0.99) vs. 0.95 (95% CI 0.84–0.99), and an area under the SROC curve of 0.9751(Q* = 0.9283) vs. 0.9725 (Q* = 0.9239), respectively (Fig. 7).

Fig. 7.

Fig. 7

Pooled sensitivity, specificity and SROC of MRA and CTA for detecting all labral lesions

Diagnostic value of MRI and CTA

The diagnostic performance of MRI vs. CTA for detecting labral lesions in patients as generated from 3 studies [23, 32, 33], involving 124 shoulders, showed a pooled sensitivity of 0.74 (95% CI 0.62–0.84) vs. 0.72 (95% CI 0.58–0.83), a specificity of 0.86 (95% CI 0.76–0.94) vs. 0.93 (95% CI 0.84–0.98), and an area under the HSROC curve of 0.9011 (Q* = 0.8325) vs. 0.9888 (Q* = 0.9557), respectively (Fig. 8).

Fig. 8.

Fig. 8

Pooled sensitivity, specificity and SROC of MRI and CTA for detecting all labral lesions

Discussion

Lesions of the glenoid labrum are critical factors causing shoulder pain and disability [40, 41], which can seriously affect the quality of patients’ lives if without suitable diagnostic techniques and proper treatment strategies. The decision to perform arthroscopy or open surgery [42], as the ultimate treatment option of labral disorders, depends not only on the patients’ clinical histories and physical examinations but also on their imaging results [37], and accurate positioning of the tears undergoing surgery are largely affected by the pre-operative imaging reports [43]. Diagnostic accuracy and effective use of imaging technology are the main concerns of clinicians and patients. Therefore, it is essential to compare the accuracy of MRA (I-MRA and D-MRA), MRI and CTA for labral diagnosis and to analyse their advantages and disadvantages under various specific conditions.

It has long been important to address the roles of MRI and MRA as imaging tools for detecting pathologic labral lesions [15, 44]. While there is a large body of literature suggesting that MRA is superior to conventional MRI for the diagnosis of labral lesions (even at 3-T) [20, 43], our pooled results considering the two techniques suggest that MRA enhances the sensitivity of the detection of labral disorders, while it is only marginally superior to MRI in terms of specificity. Although it is undeniable that MRA maximizes anatomic resolution and diagnostic confidence, the injection of contrast material may provoke several inevitable problems, such as invasion [45], ionizing radiation [46], adverse reactions and additional radiologist time and expertise [47]. Therefore, with regard to the option of MRI vs. MRA for detecting labral pathologic lesions, it seems that patient presentation is an often-neglected but crucial consideration in the choice of imaging tool [48, 49]. Patients with acute symptoms or unstable, severe, pathologic tears are more likely to have intrinsic image contrast in the form of effusion or soft-tissue changes that allow diagnosis and characterization without an invasive procedure [50, 51]. In contrast, those with chronic symptoms or a pathologic abnormality that is suspected to be more subtle on the basis of the clinical assessment more often require MRA [43].

MRA can be used directly with intra-articular contrast agent injection (D-MRA) or indirectly with intravenous (i.v.) contrast agent injection (I-MRA) [37, 47]. In this meta-analysis, we evaluated the diagnostic accuracy of labral lesions using I-MRA compared to D-MRA and found that D-MRA is superior to I-MRA. One of the greatest strengths of D-MRA lies in the benefit conferred by joint distension [52]. This distinguishes the redundant capsule from the adjacent labral tissue and allows further passage of contrast agents into the labral substance in the case of unstable labral lesions, as well as between the labrum and the glenoid in the case of labral detachment [37]. However, an obvious disadvantage of shoulder I-MRA is the absence of controlled joint capsule fluid distension, which many researchers feel is essential for improving the diagnostic accuracy of subtle detachments of the glenoid labrum [37]. This concern led to early recommendations that I-MRA should not be used for the evaluation of labral tears although it has been considered an alternative, less invasive method.

The field intensity of MRI may have an important effect on the diagnostic accuracy of diseases [36]. Therefore, we wanted to determine whether 3-T MRA provided more useful information to clinicians than conventional 3-T MRI. Our subgroup analysis based on field intensity showed that 3-T MRA had an increased sensitivity and specificity compared with 3-T MRI, which is consistent with our pooled results of 1.5-T MRA vs. 1.5-T MRI. Other subgroup analyses based on the location of labral lesions obtained the similar results. Even though MRA has an overwhelming advantage, we do not suggest that MRA should be performed on the shoulders of all patients to increase the accuracy of diagnosis. In the actual clinical work, the doctors make the diagnosis in combination with the patients’ medical history and various physical examinations, which is not as blind as research work, prompting the acknowledgement that MRA should not be a general recommendation in the diagnosis of acute labral lesions.

With regard to detecting the overall presence of labral tears, CTA had obviously less sensitivity and specificity compared with MRI and MRA in our meta-analysis. CTA was frequently used to evaluate the extent of soft and osseous tissue abnormalities, and the ability of CTA to show anteroinferior labral lesions as well as SLAP lesions has been established in a previous study [39]. However, the limited spatial resolution and soft-tissue contrast in reformatted scans from conventional CTA have led to its replacement by MRI and MRA imaging in the detection of labral lesions [28]. MRI and MRA provide superior soft-tissue contrast; therefore, no-detached labral tears can be seen as a signal extending from within the labrum to its surface [29]. However, with conventional CTA, a morphologic abnormality must be present on the surface of the labrum [29]. If there is a lack of surface contour abnormalities, false-negative results often occur when using conventional CTA. A retrospective study involving 83 patients revealed that labral damage was found in nearly all cases of recurrent anterior shoulder instability and proved that conventional CT was more important for pre-operative planning because of its detection of glenoid defects due to open or arthroscopic repair techniques that had been performed, mainly according to the bony integrity of the glenoid [23]. Therefore, CT should be a necessary supplemental imaging technique when there is highly suspected glenoid bone damage.

Several limitations exist in this meta-analysis. We assessed only the diagnostic value of the imaging modalities alone. The diagnostic performance of physical tests was not evaluated. Two or three methods, such as MRI + physical tests and MRA + physical tests, were also not analysed side-by-side. Several subgroup analyses were implemented based on insufficient data, which make certain results unreliable. In addition, the safety, cost-effectiveness, and application of these imaging techniques in clinical practice should be assessed systematically.

Conclusion

This meta-analysis of diagnostic tests, which included 14 studies involving 1216 patients with labral lesions, revealed that MRA had the highest sensitivity and specificity compared with those of MRI and CTA. However, MRA was just suggested for use in patients with chronic shoulder symptoms or a pathologic abnormality. MRI is by far the first choice recommendation for imaging modality for the detection of acute labral lesions. CT should be a necessary supplemental imaging technique when there is highly suspected glenoid bone damage.

Acknowledgements

I would like to express my very great appreciation to Fei Xiong (M.D.) for his valuable and constructive suggestions during the planning and development of this work.

Abbreviations

CI

Confidence interval

CT

Computer tomography

CTA

Computer tomography angiography

D-MRA

Direct MR arthrography; I-MRA: indirect MR arthrography

DOR

Diagnostic odd ratio

FN

False-negative

FP

False-positive

HSROC

Hierarchical summary receiver operating characteristic

MRA

MR arthrography

MRI

Magnetic resonance imaging

PRISMA-DTA

Preferred Reporting Items for a Systematic Review and Meta-analysis of Diagnostic Test Accuracy Studies

SLAP

Superior labral anterior-posterior tears

SROC

The summary receiver operating characteristic curve

TN

True negative

TP

True-positive

Authors’ contributions

LFX contributed to the idea of this study. LFX and CXY searched literatures and screened them independently. Any disagreement was solved by consulting the senior authors (DJL). LFX, CXY and DJL screened data from the eleven final articles and make Tables. LFX and CXY played an important role in analyzing the outcomes. LFX and CXY conducted the data analyses and make graphs. LFX, CXY, ZDS, SQ, DJL, BXH and WDW wrote the first draft, polished and approved the final version.

Funding

The collection, analysis, and interpretation of the data in the study were financially supported by China Scholarship Council (CSC) (Fanxiao Liu, NO.: 201808080126; Xiangyun Cheng, NO.: 201708140085). The design of the study was supported by the National Natural Science Foundation of China (Dawei Wang, NO.:81972057), Natural Science Foundation of Shandong (Dawei Wang, NO.: ZR2017MH004) and Science and Technology Development Foundation of Jinan (Dawei Wang, NO.: 201704123).

Availability of data and materials

All data analyzed during this study are included in this published article.

Ethics approval and consent to participate

This article does not contain any studies with human participants or animals performed by any of the authors.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Fanxiao Liu and Xiangyun Cheng are co-first author.

Contributor Information

Xiaohui Bai, Email: baixiaohui@sdu.edu.cn.

Dawei Wang, Email: wangdawei@sdu.edu.cn.

References

  • 1.Alashkham A, Alraddadi A, Felts P, Soames R. Histology, vascularity and innervation of the glenoid labrum. J Orthop Surg (Hong Kong) 2018;26(2):2309499018770900. doi: 10.1177/2309499018770900. [DOI] [PubMed] [Google Scholar]
  • 2.Vangsness CT, Jr, Ennis M, Taylor JG, Atkinson R. Neural anatomy of the glenohumeral ligaments, labrum, and subacromial bursa. Arthroscopy. 1995;11(2):180–184. doi: 10.1016/0749-8063(95)90064-0. [DOI] [PubMed] [Google Scholar]
  • 3.Mileski RA, Snyder SJ. Superior labral lesions in the shoulder: pathoanatomy and surgical management. J Am Acad Orthop Surg. 1998;6(2):121–131. doi: 10.5435/00124635-199803000-00007. [DOI] [PubMed] [Google Scholar]
  • 4.Tirman PF, Feller JF, Janzen DL, Peterfy CG, Bergman AG. Association of glenoid labral cysts with labral tears and glenohumeral instability: radiologic findings and clinical significance. Radiology. 1994;190(3):653–658. doi: 10.1148/radiology.190.3.8115605. [DOI] [PubMed] [Google Scholar]
  • 5.Bey MJ, Elders GJ, Huston LJ, Kuhn JE, Blasier RB, Soslowsky LJ. The mechanism of creation of superior labrum, anterior, and posterior lesions in a dynamic biomechanical model of the shoulder: the role of inferior subluxation. J Shoulder Elb Surg. 1998;7(4):397–401. doi: 10.1016/S1058-2746(98)90031-3. [DOI] [PubMed] [Google Scholar]
  • 6.Snyder SJ, Karzel RP, Del Pizzo W, Ferkel RD, Friedman MJ. SLAP lesions of the shoulder. Arthroscopy. 1990;6(4):274–279. doi: 10.1016/0749-8063(90)90056-J. [DOI] [PubMed] [Google Scholar]
  • 7.Bak K, Spring BJ, Henderson JP. Inferior capsular shift procedure in athletes with multidirectional instability based on isolated capsular and ligamentous redundancy. Am J Sports Med. 2000;28(4):466–471. doi: 10.1177/03635465000280040501. [DOI] [PubMed] [Google Scholar]
  • 8.Itoi E, Watanabe W, Yamada S, Shimizu T, Wakabayashi I. Range of motion after Bankart repair. Vertical compared with horizontal capsulotomy. Am J Sports Med. 2001;29(4):441–445. doi: 10.1177/03635465010290041001. [DOI] [PubMed] [Google Scholar]
  • 9.Burnett RS, Della Rocca GJ, Prather H, Curry M, Maloney WJ, Clohisy JC. Clinical presentation of patients with tears of the acetabular labrum. J Bone Joint Surg Am. 2006;88(7):1448–1457. doi: 10.2106/JBJS.D.02806. [DOI] [PubMed] [Google Scholar]
  • 10.Provencher MT, Bhatia S, Ghodadra NS, Grumet RC, Bach BR, Jr, Dewing CB, LeClere L, Romeo AA. Recurrent shoulder instability: current concepts for evaluation and management of glenoid bone loss. J Bone Joint Surg Am. 2010;92(Suppl 2):133–151. doi: 10.2106/JBJS.J.00906. [DOI] [PubMed] [Google Scholar]
  • 11.Herzog RJ. Magnetic resonance imaging of the shoulder. Instr Course Lect. 1998;47:3–20. [PubMed] [Google Scholar]
  • 12.Shahabpour M, Kichouh M, Laridon E, Gielen JL, De Mey J. The effectiveness of diagnostic imaging methods for the assessment of soft tissue and articular disorders of the shoulder and elbow. Eur J Radiol. 2008;65(2):194–200. doi: 10.1016/j.ejrad.2007.11.012. [DOI] [PubMed] [Google Scholar]
  • 13.Lederman ES, Flores S, Stevens C, Richardson D, Lund P. The Glenoid Labral articular teardrop lesion: a Chondrolabral injury with distinct magnetic resonance imaging findings. Arthroscopy. 2018;34(2):407–411. doi: 10.1016/j.arthro.2017.08.236. [DOI] [PubMed] [Google Scholar]
  • 14.Jung JY, Yoon YC, Yi SK, Yoo J, Choe BK. Comparison study of indirect MR arthrography and direct MR arthrography of the shoulder. Skelet Radiol. 2009;38(7):659–667. doi: 10.1007/s00256-009-0660-7. [DOI] [PubMed] [Google Scholar]
  • 15.Dinauer PA, Flemming DJ, Murphy KP, Doukas WC. Diagnosis of superior labral lesions: comparison of noncontrast MRI with indirect MR arthrography in unexercised shoulders. Skelet Radiol. 2007;36(3):195–202. doi: 10.1007/s00256-006-0237-7. [DOI] [PubMed] [Google Scholar]
  • 16.Buckwalter KA. CT arthrography. Clin Sports Med. 2006;25(4):899–915. doi: 10.1016/j.csm.2006.06.002. [DOI] [PubMed] [Google Scholar]
  • 17.Magee T. 3-T MRI of the shoulder: is MR arthrography necessary? AJR Am J Roentgenol. 2009;192(1):86–92. doi: 10.2214/AJR.08.1097. [DOI] [PubMed] [Google Scholar]
  • 18.Smith TO, Drew BT, Toms AP. A meta-analysis of the diagnostic test accuracy of MRA and MRI for the detection of glenoid labral injury. Arch Orthop Trauma Surg. 2012;132(7):905–919. doi: 10.1007/s00402-012-1493-8. [DOI] [PubMed] [Google Scholar]
  • 19.Arirachakaran A, Boonard M, Chaijenkij K, Pituckanotai K, Prommahachai A, Kongtharvonskul J. A systematic review and meta-analysis of diagnostic test of MRA versus MRI for detection superior labrum anterior to posterior lesions type II-VII. Skelet Radiol. 2017;46(2):149–160. doi: 10.1007/s00256-016-2525-1. [DOI] [PubMed] [Google Scholar]
  • 20.Ajuied A, McGarvey CP, Harb Z, Smith CC, Houghton RP, Corbett SA. Diagnosis of glenoid labral tears using 3-tesla MRI vs. 3-tesla MRA: a systematic review and meta-analysis. Arch Orthop Trauma Surg. 2018;138(5):699–709. doi: 10.1007/s00402-018-2894-0. [DOI] [PubMed] [Google Scholar]
  • 21.El-Liethy N, Kamal H, Elsayed RF. Role of conventional MRI and MR arthrography in evaluating shoulder joint capsulolabral-ligamentous injuries in athletic versus non-athletic population. Egypt J Radiol Nucl Med. 2016;47(3):969–984. doi: 10.1016/j.ejrnm.2016.05.001. [DOI] [Google Scholar]
  • 22.Sheridan K, Kreulen C, Kim S, Mak W, Lewis K, Marder R. Accuracy of magnetic resonance imaging to diagnose superior labrum anterior-posterior tears. Knee Surg Sports Traumatol Arthrosc. 2015;23(9):2645–2650. doi: 10.1007/s00167-014-3109-z. [DOI] [PubMed] [Google Scholar]
  • 23.Moroder P, Resch H, Schnaitmann S, Hoffelner T, Tauber M. The importance of CT for the pre-operative surgical planning in recurrent anterior shoulder instability. Arch Orthop Trauma Surg. 2013;133(2):219–226. doi: 10.1007/s00402-012-1656-7. [DOI] [PubMed] [Google Scholar]
  • 24.McInnes MDF, Moher D, Thombs BD, McGrath TA, Bossuyt PM, the P-DTAG. Clifford T, Cohen JF, Deeks JJ, Gatsonis C, et al. Preferred reporting items for a systematic review and meta-analysis of diagnostic test accuracy studies: the PRISMA-DTA statement. Jama. 2018;319(4):388–396. doi: 10.1001/jama.2017.19163. [DOI] [PubMed] [Google Scholar]
  • 25.Schueler S, Schuetz GM, Dewey M. The revised QUADAS-2 tool. Ann Intern Med. 2012;156(4):323. doi: 10.7326/0003-4819-156-4-201202210-00018. [DOI] [PubMed] [Google Scholar]
  • 26.Wade R, Corbett M, Eastwood A. Quality assessment of comparative diagnostic accuracy studies: our experience using a modified version of the QUADAS-2 tool. Res Synth Methods. 2013;4(3):280–286. doi: 10.1002/jrsm.1080. [DOI] [PubMed] [Google Scholar]
  • 27.Whiting PF, Rutjes AW, Westwood ME, Mallett S, Deeks JJ, Reitsma JB, Leeflang MM, Sterne JA, Bossuyt PM. Group Q-: QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies. Ann Intern Med. 2011;155(8):529–536. doi: 10.7326/0003-4819-155-8-201110180-00009. [DOI] [PubMed] [Google Scholar]
  • 28.Kim KW, Lee J, Choi SH, Huh J, Park SH. Systematic review and meta-analysis of studies evaluating diagnostic test accuracy: a practical review for clinical researchers-part I. general guidance and tips. Korean J Radiol. 2015;16(6):1175–1187. doi: 10.3348/kjr.2015.16.6.1175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Lee J, Kim KW, Choi SH, Huh J, Park SH. Systematic review and meta-analysis of studies evaluating diagnostic test accuracy: a practical review for clinical researchers-part II. Statistical methods of meta-analysis. Korean J Radiol. 2015;16(6):1188–1196. doi: 10.3348/kjr.2015.16.6.1188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Deeks JJ, Macaskill P, Irwig L. The performance of tests of publication bias and other sample size effects in systematic reviews of diagnostic test accuracy was assessed. J Clin Epidemiol. 2005;58(9):882–893. doi: 10.1016/j.jclinepi.2005.01.016. [DOI] [PubMed] [Google Scholar]
  • 31.Flannigan B, Kursunoglu-Brahme S, Snyder S, Karzel R, Del Pizzo W, Resnick D. MR arthrography of the shoulder: comparison with conventional MR imaging. AJR Am J Roentgenol. 1990;155(4):829–832. doi: 10.2214/ajr.155.4.2119117. [DOI] [PubMed] [Google Scholar]
  • 32.Chandnani VP, Yeager TD, DeBerardino T, Christensen K, Gagliardi JA, Heitz DR, Baird DE, Hansen MF. Glenoid labral tears: prospective evaluation with MRI imaging, MR arthrography, and CT arthrography. AJR Am J Roentgenol. 1993;161(6):1229–1235. doi: 10.2214/ajr.161.6.8249731. [DOI] [PubMed] [Google Scholar]
  • 33.Sano H, Kato Y, Haga K, Itoi E, Tabata S. Magnetic resonance arthrography in the assessment of anterior instability of the shoulder: comparison with double-contrast computed tomography arthrography. J Shoulder Elb Surg. 1996;5(4):280–285. doi: 10.1016/S1058-2746(96)80054-1. [DOI] [PubMed] [Google Scholar]
  • 34.Wallny T, Sommer T, Steuer K, Vahlensieck M, Wagner UA, Schmitz A, Schmitt O. Klinische und kernspintomographische Diagnostik von Labrumglenoidale-Verletzungen. Orthopädische Universitätsklinik Bonn. 1998;101. [DOI] [PubMed]
  • 35.Reuss BL, Schwartzberg R, Zlatkin MB, Cooperman A, Dixon JR. Magnetic resonance imaging accuracy for the diagnosis of superior labrum anterior-posterior lesions in the community setting: eighty-three arthroscopically confirmed cases. J Shoulder Elb Surg. 2006;15(5):580–585. doi: 10.1016/j.jse.2005.10.011. [DOI] [PubMed] [Google Scholar]
  • 36.Major NM, Browne J, Domzalski T, Cothran RL, Helms CA. Evaluation of the glenoid labrum with 3-T MRI: is intraarticular contrast necessary? AJR Am J Roentgenol. 2011;196(5):1139–1144. doi: 10.2214/AJR.08.1734. [DOI] [PubMed] [Google Scholar]
  • 37.Fallahi F, Green N, Gadde S, Jeavons L, Armstrong P, Jonker L. Indirect magnetic resonance arthrography of the shoulder; a reliable diagnostic tool for investigation of suspected labral pathology. Skelet Radiol. 2013;42(9):1225–1233. doi: 10.1007/s00256-013-1644-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Herold T, Hente R, Zorger N, Finkenzeller T, Feuerbach S, Lenhart M, Paetzel C. Indirect MR-arthrography of the shoulder-value in the detection of SLAP-lesions. Rofo. 2003;175(11):1508–14. [DOI] [PubMed]
  • 39.Mahmoud MK, Badran YM, Zaki HG, Ali AH. One-shot MR and MDCT arthrography of shoulder lesions with arthroscopic correlation. Egypt J Radiol Nucl Med. 2013;44:273. doi: 10.1016/j.ejrnm.2013.01.002. [DOI] [Google Scholar]
  • 40.Waterman BR, Arroyo W, Heida K, Burks R, Pallis M. SLAP repairs with combined procedures have lower failure rate than isolated repairs in a military population: surgical outcomes with minimum 2-year follow-up. Orthop J Sports Med. 2015;3(8):2325967115599154. doi: 10.1177/2325967115599154. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Tayrose GA, Karas SG, Bosco J. Biceps Tenodesis for Type II SLAP Tears. Bull Hosp Jt Dis (2013) 2015;73(2):116–121. [PubMed] [Google Scholar]
  • 42.Hantes M, Raoulis V. Arthroscopic findings in anterior shoulder instability. Open Orthop J. 2017;11:119–132. doi: 10.2174/1874325001711010119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Amin MF, Youssef AO. The diagnostic value of magnetic resonance arthrography of the shoulder in detection and grading of SLAP lesions: comparison with arthroscopic findings. Eur J Radiol. 2012;81(9):2343–2347. doi: 10.1016/j.ejrad.2011.07.006. [DOI] [PubMed] [Google Scholar]
  • 44.Yoneda M, Izawa K, Wakitani S, Nakasato S, Hayashida K, Nakagawa S. Diagnostic imaging of unstable superior glenoid labral detachment: a comparison between MR arthrography and unenhanced MRI. Mod Rheumatol. 2001;11(2):140–144. doi: 10.3109/s101650170026. [DOI] [PubMed] [Google Scholar]
  • 45.Acid S, Le Corroller T, Aswad R, Pauly V, Champsaur P. Preoperative imaging of anterior shoulder instability: diagnostic effectiveness of MDCT arthrography and comparison with MR arthrography and arthroscopy. AJR Am J Roentgenol. 2012;198(3):661–667. doi: 10.2214/AJR.11.7251. [DOI] [PubMed] [Google Scholar]
  • 46.Godefroy D, Sarazin L, Rousselin B, Dupont AM, Drape J, Chevrot A. Shoulder imaging: what is the best modality? J Radiol. 2001;82(3 Pt 2):317–332. [PubMed] [Google Scholar]
  • 47.Sommer T, Vahlensieck M, Wallny T, Lutterbey G, Pauleit D, Steuer K, Golombek V, Kreft B, Keller E, Schild H. Indirect MR arthrography in the diagnosis of lesions of the labrum glenoidale. Rofo. 1997;167(1):46–51. doi: 10.1055/s-2007-1015490. [DOI] [PubMed] [Google Scholar]
  • 48.Familiari F, Huri G, Simonetta R, McFarland EG. SLAP lesions: current controversies. EFORT Open Rev. 2019;4(1):25–32. doi: 10.1302/2058-5241.4.180033. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Stewart JK, Taylor DC, Vinson EN. Magnetic resonance imaging and clinical features of glenoid labral flap tears. Skelet Radiol. 2017;46(8):1095–1100. doi: 10.1007/s00256-017-2664-z. [DOI] [PubMed] [Google Scholar]
  • 50.Baudi P, Rebuzzi M, Matino G, Catani F. Imaging of the unstable shoulder. Open Orthop J. 2017;11:882–896. doi: 10.2174/1874325001711010882. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Kim DS, Yoon YS, Kwon SM. The spectrum of lesions and clinical results of arthroscopic stabilization of acute anterior shoulder instability. Yonsei Med J. 2010;51(3):421–426. doi: 10.3349/ymj.2010.51.3.421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Cerezal L, Garcia-Valtuille R, Canga A, Rolon A, Abascal F. Magnetic resonance arthrography indications and technique (I). Upper limb. Radiologia. 2006;48(6):341–356. doi: 10.1016/S0033-8338(06)75150-5. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

All data analyzed during this study are included in this published article.


Articles from BMC Musculoskeletal Disorders are provided here courtesy of BMC

RESOURCES