Preliminary Development of a Clinical Prediction Rule for Treatment of Patients With Suspected SLAP Tears Stephanie D. Moore-Reed, Ph.D., A.T.C., W. Ben Kibler, M.D., Aaron D. Sciascia, M.S., A.T.C., and Tim Uhl, Ph.D., P.T., A.T.C. Purpose: To use the clinical prediction rule process to identify patient variables, measured on initial clinical presentation, that would be predictive of failure to achieve satisfactory improvement, while following a rehabilitation program, in the modification of SLAP injury symptoms and dysfunction. Methods: A cohort of patients received the clinical diagnosis of a SLAP lesion based on specific history and examination findings and/or magnetic resonance imaging. They underwent a physical examination of the kinetic chain and shoulder, including tests for labral injury. Patients followed a standardized physical therapy program emphasizing restoration of demonstrated strength, flexibility, and strength-balance deficits. At 6 weeks’ follow-up, patients were re-evaluated and divided into those recommended for surgery (RS) and those not recommended for surgery (NRS). Bivariate logistic regression was performed to identify the best combination of predictive factors. Results: Fifty-eight patients (aged 39 11 years, 45 men) were included. Of these, 31 (53%) were categorized as NRS and 27 (47%) as RS. The presence of a painful arc of motion (odds ratio, 3.95; P ¼ .024) and the presence of increased forward scapular posture (odds ratio, 1.27; P ¼ .094) on the injured side were predictive of being in the RS group. This finding indicates that the odds of being in the RS group increased 4 times when a positive painful arc was present and increased 27% with every 1-cm increase in involved anterior shoulder posture. Conclusions: A structured rehabilitation program resulted in modification of symptoms and improved function at 6 weeks’ follow-up in over half of patients in the study group. On initial evaluation, the presence of a painful arc of overhead motion, indicating loss of normal glenohumeral kinematics, and the presence of forward shoulder posture, indicating an altered scapular position, represent negative predictive factors for success of rehabilitation. Future validation of the model in a larger population is necessary. Level of Evidence: Level II, prospective comparative study. T here is a growing awareness of the need to develop more efficacious methods of evaluating, accurately diagnosing, and treating all types of shoulder pathology. The clinical prediction rule process has been developed as a method to identify which patient variables, measured on initial clinical examination, could be predictive of From the Department of Kinesiology, California State University (S.D.M-R.), Fresno, California; Shoulder Center of Kentucky (W.B.K., A.D.S.), Lexington, Kentucky; and Division of Athletic Training, University of Kentucky (A.D.S., T.U.), Lexington, Kentucky, U.S.A. The authors report the following potential conflict of interest or source of funding: The Lexington Clinic entered into a contract to pay the University of Kentucky for a doctoral student, S.D.M-R. (co-author), as a part-time research assistant as she completed her doctoral degree. T.U. receives support from American Society of Shoulder and Elbow Therapists. T.U. received reimbursement to present components of these data at the International Congress of Shoulder and Elbow Therapists in April 2013 in Nagoya, Japan. Received September 11, 2013; accepted June 13, 2014. Address correspondence to Aaron D. Sciascia, M.S., A.T.C., 1221 S Broadway, Lexington, KY 40504, U.S.A. E-mail: ascia@lexclin.com Ó 2014 by the Arthroscopy Association of North America 0749-8063/13668/$36.00 http://dx.doi.org/10.1016/j.arthro.2014.06.015 success of a particular treatment program. The prediction rule process has the potential to instill continuity and uniformity within health care decision making and can help guide care.1 This article reports the outcomes of a study applying the clinical prediction rule process to a cohort of patients determined to have clinical findings consistent with a SLAP injury. In patients with this diagnosis, surgical outcomes are not uniformly successful,2,3 in part because of inconsistency in the diagnostic process and inconsistency in surgical indications.4 Rehabilitation protocols are often advocated as the first step in the treatment of SLAP and other shoulder injuries, but evidence regarding the exact indications, role, and effectiveness of rehabilitation in SLAP injury is sparse and not clear. One previous retrospective study reported that 49% of patients managed with nonoperative rehabilitation had a positive outcome.5 Another study, performed in professional baseball players, all of whom had a SLAP injury and in whom a rehabilitation program had failed, showed that a comprehensive rehabilitation program resulted in 40% of players returning to play.6 Arthroscopy: The Journal of Arthroscopic and Related Surgery, Vol -, No - (Month), 2014: pp 1-10 1 2 S. D. MOORE-REED ET AL. Fig 1. Participant flowchart. The purpose of this prospective study was to use a clinical prediction rule process to attempt to identify patient variables, measured on initial clinical presentation, that would be predictive of failure to achieve satisfactory improvement, while following a rehabilitation program, in the modification of symptoms and dysfunction in patients with a clinical diagnosis of SLAP injury. We hypothesized that in patients who did not respond, there would be specific measurable patient factors that were associated with failure to respond to a rehabilitation program. Methods Patients Fifty-eight patients (mean age, 39 11 years; mean mass, 83 25 kg; mean height, 170 35 cm) who were determined to have a clinical history consistent with shoulder dysfunction resulting from injury to the superior labrum were included.7 The history included pain at the posterior joint line, pain with abduction/ external rotation, popping, clicking on shoulder rotation, and pain or limitation of performance with repetitive overhead activity. These 58 patients were part of a group of 211 patients presenting with shoulder pain to an orthopaedic surgeon (W.B.K.) (Fig 1). All participants were patients of the lead author (W.B.K.), a sports medicine and shoulder surgeon with more than 30 years of experience in clinically evaluating and treating shoulder pathology. There are varying opinions regarding the exact criteria to establish a diagnosis of a clinically significant SLAP tear, with no literatureestablished gold standard that is universally recognized. Therefore patient inclusion was based on meeting specific criteria relating to history, clinical examination findings, and/or diagnostic imaging findings to include all possible criteria for detecting the anatomic and functional alterations associated with the SLAP injury. The clinical examination inclusion criteria were modified from previously identified criteria for diagnosing labral tears reported by Walsworth et al.8 The criteria for our study required a positive finding for at least 3 of the following 4 clinical signs: history of popping or catching, positive anterior-slide maneuver, positive modified dynamic labral shear (M-DLS) maneuver,9 or positive active compression test.8,9 Patients with a SLAP tear diagnosed by advanced imaging (i.e., magnetic resonance imaging [MRI] or magnetic resonance arthrography [MRA]) were included if they also had 1 or 2 of the clinical examination inclusion criteria because the addition of history and clinical examination evidence has been shown to change the information from the imaging.10 Reliance was not placed on 1 examination or imaging test because no single test has been shown to be uniformly satisfactory to make the complete diagnosis.4,11,12 A recent systematic review by Hegedus et al.13 supports the concept of using clusters of tests to make the diagnosis in shoulder pathology, although the M-DLS maneuver has been shown in a Level I study to have high clinical utility.9 Patients were excluded from the study if they had numbness or tingling in the upper extremity; signs and symptoms consistent with cervical radiculopathy,14 adhesive capsulitis,15 or glenohumeral arthritis16; patient-reported steroid injections in the involved shoulder within the previous month; or surgery on the involved shoulder within the past year. They were also excluded if they had clinical examination and/or imaging findings consistent with a diagnosis of acromioclavicular joint injury/arthrosis, glenohumeral instability, or full-thickness rotator cuff tear. This study was approved by the appropriate institutional review boards. Before enrollment in the study, all patients read and signed an informed consent form that was approved by the institutional review boards of the University of Kentucky and Lexington Clinic. Patients completed a standard history form and underwent standard examination by the orthopaedic surgeon (W.B.K.). All patients completed a numeric pain rating scale regarding current pain, worst pain, and least pain in the past week17 (0, no pain; 10, highest pain). In addition, patients completed the Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH) questionnaire, which is scored from 0, no disability, to 100, severe disability; the American Shoulder and Elbow Surgeons (ASES) Shoulder Assessment Form, with a score ranging from 0, poor function, to 100, normal function18-20; and the Patient-Specific Functional Scale (PSFS).21 The PSFS questionnaire requires the patient to list 3 to 5 activities that he or she has difficulty doing because of his or her LABRAL CLINICAL PREDICTION DEVELOPMENT shoulder problem and to rate each item from 0 (cannot perform activity at all) to 10 (can perform activity at the same level as before the injury). Glenohumeral range of motion (ROM), strength, and posture were also assessed. ROM was assessed with a digital inclinometer (Dualer; JTech Medical, Salt Lake City, UT). Passive internal and external rotation ROM and horizontal adduction ROM were measured with the patient supine and shoulder abducted to 90 with the scapula stabilized until resistance was first felt or the patient reported pain, as previously described.22 Active shoulder flexion ROM was measured with the patient seated. The patient was instructed to raise his or her arm as high as possible in the sagittal plane with the thumb up.23 The clinician aligned the inclinometer with the long axis of the humerus, and the angle was recorded in degrees. Inter-rater intraclass correlation coefficients (ICCs) were calculated a priori for internal rotation ROM (ICC, 0.795), external rotation ROM (ICC, 0.839), horizontal adduction ROM (ICC, 0.518), and active flexion ROM (ICC, 0.863). Isometric muscle strength was measured with a handheld dynamometer24 (model 01163; Lafayette Instruments, Lafayette, IN). Forward flexion strength was measured with the participant seated, the scapula in a retracted position, the shoulder in 90 of flexion, and the palm down.24 The dynamometer was placed just proximal to the wrist, and the participant was instructed to push up for 5 seconds. External rotation strength was measured with the participant supine, the shoulder abducted to 90 , the elbow flexed to 90 , and the humerus in neutral rotation and supported. The dynamometer was placed parallel with the forearm. For each strength measure, 2 maximum-effort trials were performed and averaged for analysis. Each arm was tested in alternating fashion to allow for approximately 30 seconds of rest between trials (flexion strength ICC, 0.897; external rotation strength ICC, 0.842). Finally, scapular posture was assessed with the participant standing and using a double square instrument as previously described by Kluemper et al.25 The participant was asked to stand against the wall and assume his or her normal posture after taking a deep breath to relax. The double square instrument was aligned with the wall and the anterior aspect of the acromion. This distance was measured and recorded bilaterally. Reliability was determined a priori (ICC, 0.946). After the initial clinical visit and data collection, all patients were prescribed physical therapy and provided with a standardized rehabilitation protocol consisting of stretching exercises and strengthening exercises for shoulder musculature, but the protocol was individualized depending on each patient’s examination findings by the treating physical therapist. This protocol was well outlined (Table 1). It consisted of 4 phases, each 3 having mobility and strengthening components that were progressed at each phase. The protocol was designed based on the concepts put forth by Ellenbecker and Cools26 for treating patients with shoulder pain and scapular dysfunction. Mobility exercises progressed from gentle mobility to static stretching of posterior, anterior, and inferior shoulder mobility restrictions. Strengthening exercises progressed from scapular muscular orientation to gain motor control, using the kinetic chain theories of incorporating the entire body, to short and then to long lever-arm resistive exercises, on the basis of kinetic chain theories of incorporating the lower extremity. Ballistic and eccentric exercises were incorporated in the protocol if the treating therapist believed that they were appropriate for an individual patient (Table 1). The rehabilitation protocol was provided to the patients at the initial visit. Patients were allowed to go to the physical therapists of their choosing, with instructions to follow the specific protocol. The physical therapists were provided a letter describing the study and requesting that the patients follow the established protocol. Exercise logs were provided for the patients to record their compliance with the therapy. Detailed physical therapy records were obtained from over two-thirds of the patients (40 of 58). At a follow-up visit with the orthopaedic surgeon (W.B.K.) 6 weeks after the initial visit (median, 6 weeks; range, 4 to 24 weeks), participants again completed the QuickDASH questionnaire, ASES form, numeric pain rating scale, and PSFS questionnaire. Strength, ROM, and posture were also reassessed. In addition, the Global Rating of Change (GROC) score was obtained. The GROC is a 15-point scale ranging from 7 (a great deal worse) to þ7 (a great deal better), with 0 indicating no change.27 Exercise logs and physical therapy notes were collected from patients at this time. After the intervention and follow-up appointment, patients were categorized into 2 groups based on their report of their clinical status and the clinical examination findings: recommended for surgery (RS) or not recommended for surgery (NRS). The recommendation for surgery was based on continued or worsened subjective and objective symptoms of shoulder pain and dysfunction, failure to progress in rehabilitation, and a patient’s unwillingness or inability to tolerate the dysfunction, with clinical input from the physician (Table 2). This process followed the normal procedure of consultation and decision making regarding treatment between physician and patient. The decision to counsel and recommend surgery was made at this time point because most studies indicate that it takes around 6 weeks to observe significant changes in physiological factors such as flexibility and strength and therefore affect the clinical symptoms, which were the goals of the rehabilitation protocol.28-30 In addition, this is 4 Table 1. Rehabilitation Exercise Program Exercise Category Scapular orientation Below shoulder level: isometric Scapular protraction Humeral rotation Level II Level III Below shoulder level: isotonic (e.g., dynamic low row, lawnmower, robbery) Punch (e.g., supine punch, scapular punches) Isotonic at shoulder level: short lever arm (e.g., pull downs, fencing, rows) Isotonic (e.g., prone horizontal abduction lifts at 90 or 135 ) Push-ups (e.g., incline) Push-ups (e.g., knee, standard) Punch (e.g., standing punch) At shoulder level (e.g., ER/IR with elastic band, 90 /90 ) Diagonal (e.g., upper cut) Humeral rotation at shoulder level (e.g., 90 /90 rotation, side-lying ER eccentric exercises) Long lever arm (e.g., flexion, abduction, plyometrics, weighted-ball drops) Below shoulder level: isotonic (e.g., IR/ER with arm at side with resistance) Humeral elevation Stretching Anterior Posterior Elevation Short lever arm (e.g., overhead press) Supine pectoral stretch with arm at side ER with arm at side Cross body Table slides Forward bows ER, external rotation; IR, internal rotation. Active scapular retraction with arms at 90 Supine pectoral stretch with overpressure ER with arm away from side Wall slides Assisted elevation with pulley Level IV Sleeper stretch Latissimus dorsi stretch Sleeper stretch in more abducted position Active latissimus dorsi stretch S. D. MOORE-REED ET AL. Muscle strengthening Scapular retraction Level I Scapular protraction and retraction (e.g., scapular clock) Scapular and humeral depression (e.g., inferior glide) 5 LABRAL CLINICAL PREDICTION DEVELOPMENT Table 2. Improvements in Outcome Measures From Initial Evaluation to 6 Weeks’ Follow-up Outcome Measure ASES score QuickDASH score Current pain PSFS score GROC score NRS Group (n ¼ 31) 14 16 13 15 1 2 23 32 RS Group (n ¼ 27) 2 16 0 16 02 03 02 P Value .006 .001 .047 .033 <.001 NOTE. Data are change scores and are given as mean SD unless otherwise indicated. standard procedure for the physician’s practice. The patient-reported outcome measures were also analyzed and compared with the RS/NRS status. Statistical Analysis Descriptive statistics were calculated for each variable measured at baseline for continuous (Table 3) and categorical (Table 4) data. Variable selection was performed by testing each variable’s univariate association with the outcome by use of Student independent t tests for continuous variables and c2 tests for categorical variables. Variables with a univariate P .30 were retained, leaving 5 continuous variables (scapular posture, ASES score, QuickDASH score, PSFS score, and current pain) and 5 categorical variables (scapular assistance test, painful arc test, previous physical therapy, point-tender pain, and single-leg balance) as potential predictors in the model. Backward stepwise logistic regression was used to determine the relative contribution of each variable to outcome (i.e., RS or NRS). Five variables were entered into the final Table 3. Descriptive Statistics for Continuous Variables Variable Height (cm) Mass (kg) Age (yr) Duration of symptoms (mo) ROM ( ) Flexion ER IR HAdd Strength (lb) ER Flexion Scapular posture (cm)* ASES score* QuickDASH score* Current painy PSFS score* NRS Group (n ¼ 31) 175 10 85 21 40 11 19 11 RS Group (n ¼ 27) 178 8 89 18 39 55 25 42 144 75 60 10 28 24 17 10 142 76 61 9 22 28 20 9 10 7 14 62 34 3.5 3.6 6 3 2 16 16 1.8 1.9 9 8 15 56 41 4.7 3.1 5 3 2 21 17 2.5 1.7 NOTE. Data are given as mean SD. ER, external rotation; HAdd, horizontal adduction; IR, internal rotation. *Significant at P .30. ySignificant at P .05. Table 4. Counts and Percentages for Categorical Variables Variable Apprehension Anterior load and shift Posterior jerk Sulcus ER lag Drop arm Belly press Liftoff Bear hug Upper cut Speed’s test M-DLS Active compression test Anterior slide Point-tender pain* Crepitus Paxinos test Pain with horizontal adduction Painful arc (forward flexion)y Hawkins impingement Neer impingement SICK scapular position Scapular dyskinesis Scapular assistance test* Scapular retraction test Single-leg balance* Single-leg squat Pain with resisted abduction Patient-reported pop/grind/click Previous physical therapy* Gradual onset of symptoms Male sex NRS Group (n ¼ 31) 2 (6%) 1 (3%) 1 (3%) 1 (3%) 0 (0%) 0 (0%) 0 (0%) 4 (13%) 6 (19%) 11 (35%) 5 (16%) 28 (90%) 18 (58%) 21 (68%) 8 (26%) 3 (10%) 3 (10%) 3 (10%) 15 (48%) 10 (32%) 9 (29%) 18 (58%) 30 (97%) 17 (55%) 21 (68%) 13 (42%) 12 (39%) 26 (84%) 24 (77%) 12 (39%) 17 (55%) 23 (74%) RS Group (n ¼ 27) 2 (7%) 0 (0%) 0 (0%) 2 (7%) 0 (0%) 0 (0%) 0 (0%) 0 (0%) 5 (19%) 11 (41%) 6 (22%) 22 (81%) 14 (52%) 11 (41%) 3 (11%) 2 (7%) 3 (11%) 4 (15%) 21 (78%) 11 (41%) 9 (33%) 18 (67%) 23 (85%) 20 (74%) 18 (67%) 7 (26%) 9 (33%) 27 (100%) 20 (74%) 14 (52%) 14 (52%) 22 (81%) ER, external rotation; SICK, scapular malposition inferior medial border prominence coracoid pain and malposition and dyskinesis of scapular movement. *Significant at P .30. ySignificant at P .05. backward stepwise logistical regression analysis (scapular posture, scapular assistance test, painful arc test, previous physical therapy, and point-tender pain). Compliance was examined in 2 ways: average number of physical therapy visits per week and compliance with the rehabilitation protocol. Compliance with the protocol was determined by the percentage of exercises performed by the patient that were from the protocol provided to the physical therapists as part of study participation. Student independent t tests were performed for average visits per week and compliance with the protocol. Statistical analyses were conducted using SPSS software, version 19 (SPSS, Chicago, IL). Results Of the 58 patients, 27 (47%) were categorized as RS at 6 weeks. Twenty-six of these 27 patients had advanced imaging performed; in 24 of these, the imaging yielded positive findings for a SLAP injury. Twenty-two of the 27 patients in the RS group (81%) 6 S. D. MOORE-REED ET AL. Table 5. Logistic Regression Predicting “Recommended for Surgery” Variable Scapular protraction Painful arc test Constant Regression Coefficient 0.242 SE 0.145 P Value .094 OR (95% CI) 1.27 (0.96 to 1.69) 1.375 4.581 0.609 2.141 .024 .042 3.95 (1.20 to 13.05) CI, confidence interval; OR, odds ratio; SE, standard error. went on to undergo arthroscopic surgery, and all were found to have an anatomic labral injury that met the criteria for a clinically significant SLAP injury.11 The 5 patients who did not undergo surgery ultimately declined because of insurance issues or did not schedule surgery after the recommendation. Thirty-one patients (53%) were categorized as NRS at 6 weeks. Eighteen of these 31 had advanced imaging performed; in 16 of these, the imaging yielded positive findings for a SLAP injury. Two patients in the NRS group (6%) eventually had enough functional limitations that they returned after the study and elected to undergo surgery. Both patients were found to have an arthroscopically confirmed anatomic labral injury that met the criteria for a clinically significant SLAP injury.11 The logistic regression analysis showed that the presence of a painful arc of motion in forward flexion and the presence of increased forward scapular posture on the injured side at the initial examination were predictive of being in the RS group at 6 weeks (P ¼ .015, df ¼ 2, c2 ¼ 8.413) (Table 5). The odds of being in the RS group increased 4 times when a positive painful arc was present and increased 27% with every 1-cm increase in involved anterior shoulder posture. The final model predicted 72% of the outcomes correctly. Detailed physical therapy records were collected and analyzed for 19 of 27 patients in the RS group and 21 of 31 patients in the NRS group. There was no significant difference in average visits per week between the RS patients (1 2 weeks) and NRS patients (2 1) (P ¼ .638). There was also no significant difference between compliance with the provided rehabilitation protocol between the RS patients (55% 38%) and NRS patients (71% 29%) (P ¼ .159). There was a statistically significant difference in 3 patient-reported outcome measuresdASES score, QuickDASH score, and GROC scoredbetween the RS and NRS groups. The NRS group reported statistically significantly larger improvements in these scales, which would provide some further confirmation for the basis for the treatment decision (Table 1). Discussion This study confirms the research hypothesis; the clinical prediction rule process identified 2 specific variables, a painful arc of motion in forward flexion and increased anterior scapular position, as factors associated with failure to achieve a satisfactory improvement so that the patient and physician agreed that surgery was recommended. A structured rehabilitation program resulted in modification of symptoms, increased outcome measures, and improved function to the point that the patient and physician agreed that surgery was not necessary in 31 patients (53%) in the study group at 6 weeks, although 2 of these patients ended up requesting surgery at a later time. Because these patients were not recommended to undergo surgery at the 6-week time point of interest, they were kept in their original group (RS or NRS) as determined by the physician at 6 weeks for follow-up analysis. The clinical prediction rule process has the potential to be a significant element in improving the delineation of the factors that can influence the content and timing of treatment of musculoskeletal injury. Clinical prediction models serve as formal, evidence-based approaches to clinical decision making by using statistical models to provide quantitative estimates of probability of outcome, diagnosis, or treatment success.31-33 They have the potential to instill continuity and uniformity within health care decisions and can help guide care.1,31 However, the validity and clinical impact of a prediction rule must be determined before the model is translated to a clinical decision rule intended to affect clinical decision making.34 The need for more carefully derived and validated prediction models in orthopaedics and rehabilitation has been identified.35 These models have the potential to help the patient by avoiding surgery while continuing to restore acceptable function, help the physician by more clearly defining which patients need surgery, and help the health care system by increasing the efficiency of the content and timing of treatment. This particular model was designed to try to identify patient factors that could influence the outcome of a specific treatment program (a rehabilitation program) in patients with clinical findings suggestive of a SLAP injury. The research decision to evaluate this process in this population was based on several factors. SLAP lesions are being more commonly diagnosed and treated. SLAP injuries are reported to be present in 6% to 12% of shoulder arthroscopies,36-38 and the incidence of surgery appears to be increasing.2,39 The rationale for operative intervention is to restore the anatomic alteration in the labrum and its attachment to the glenoid that is assumed to be responsible for the patient’s pain and dysfunction. However, surgical outcomes vary widely and are not uniformly successful,40-43 highlighting the need for a more consistent diagnostic process and for a better understanding of more precise indications for and timing of surgery. LABRAL CLINICAL PREDICTION DEVELOPMENT Attention toward using rehabilitation as the first step in the treatment of patients with SLAP lesions has increased. Protocol content would be directed toward improving motion and strength deficits, maximizing kinetic chain function, and modifying or minimizing the dysfunction that these patients report. There are a few reports that show the benefits of this approach. A recent retrospective study observed that 19 of 39 patients (49%) diagnosed with SLAP lesions treated nonoperatively reported successful outcomes at 3 years after diagnosis and that 10 of 15 athletes (67%) had returned to their preinjury status.5 The exact rehabilitation program was not described completely. Another study examined treatment of SLAP lesions in professional baseball players.6 These players had undergone 1 session of rehabilitation that had failed. A specific program of nonoperative intervention focused on correcting scapular dyskinesis and glenohumeral internal rotation deficit resulted in a 40% rate of return to play, although not all of these patients returned to their preinjury level of performance. The specific rehabilitation program used in our study was designed using the concepts put forth by Ellenbecker and Cools26 and is similar to previous protocols.6,11 This study adds further support to the use of this type of rehabilitation program as the first method of treatment because both studies report a similar success rate. These results show that not all patients who receive the diagnosis of a SLAP injury will require surgery. This study used statistical analysis to identify variables associated with a particular outcome. It was not designed to determine why or by what mechanisms these variables were associated with the outcome. However, the findings were consistent with the idea that clinically symptomatic and dysfunctional SLAP lesions represent not only anatomic disruption of the labrum and its glenoid attachment but also local and distant physiological and biomechanical alterations that add up to create the clinical dysfunction.11,44 None of the variables most commonly associated with making the diagnosis of an anatomic labral injury (clinical tests such as ROM deficits,44 apprehension in external rotation or positive biceps stress testing,45 a positive MDLS maneuver,9 an active compression test,46 or positive MRI findings) were associated with failure of therapy and the need for surgery. This finding suggests that the presence of physical impairments, in addition to the results of isolated clinical maneuvers or imaging, may provide stronger clinical relevance for making treatment decisions. This study used the clinical prediction rule process to derive an actual clinical prediction rule that can help guide management of patients presenting with the aforementioned symptoms. The next step would involve validation of this rule with a prospective study 7 in a different cohort of patients with the same clinical presentation. One existing clinical prediction model has been developed47 and externally validated48 to predict persistent symptoms at 6 weeks in patients with shoulder pain seen in the primary care setting. At 6 weeks, Kuijpers et al.47 observed that a longer duration of symptoms, gradual onset of pain, psychological complaints, report of repetitive movements at least 2 days per week, and high pain severity in the shoulder (scale from 0 to 10) and in the neck (scale from 0 to 18) at presentation were associated with persistent symptoms. One fundamental difference between the existing model and our analysis is that our patients were prescribed a standardized rehabilitation protocol whereas the existing model was developed for patients treated primarily with medication, corticosteroid injection, or a “wait-and-see” approach. In addition, our study specifically included patients who had symptoms consistent with a SLAP lesion and all patients were seen by an experienced orthopaedic surgeon (W.B.K.). A significant percentage of patients with clinical findings suggestive of SLAP lesions that have created shoulder dysfunction can show modification of symptoms with lessening or elimination of the dysfunction through a specific rehabilitation program and do not require or request surgery. Subjective reports of improved function can be objectively documented using valid and reliable patient-reported outcome measures. This finding is in agreement with and reinforces the limited information in the literature. However, 2 patient variables found on clinical examination, a positive painful arc of motion in forward flexion between 60 and 100 and forward scapular posture, were found to be associated with failure to succeed in the therapy program. The odds of rehabilitation failure increased 3.95 times with the presence of a painful arc of motion and increased 27% with every 1-cm increase in forward scapular position. Factors that have been traditionally used to delineate the anatomic SLAP lesion, such as isolated clinical examination tests, glenohumeral rotation asymmetries, responses to scapular corrective maneuvers, or MRI, did not predict success or failure of rehabilitation. Rehabilitation can be advocated as the first step in the treatment of most patients with SLAP tears. Rehabilitation can frequently modify the physiological alterations that are a large part of the shoulder dysfunction, even in the face of an anatomic labral injury, and provide restoration of function so that surgery is not deemed necessary by the patient and the clinician. At this time, patients who, on initial examination, have a painful arc of motion and scapular protraction and who undergo rehabilitation have higher odds of eventually being recommended for surgery. These 2 factors may indicate a greater alteration of glenohumeral kinematics associated with the clinical dysfunction. Future 8 S. D. MOORE-REED ET AL. directions from this study would include a validation study to determine the effectiveness of the clinical prediction rule in larger populations or in another population with these findings, as well as extension to other shoulder pathology. Limitations There are several limitations to this study. The first and most important is that the diagnosis of a “labral injury” was made by a combination of clinical examination and imaging techniques, with no actual visualization of the lesion. However, there is no accepted gold standard for making this diagnosis either clinically, by imaging, or by arthroscopy.10,13,49 Most studies evaluating clinical examination tests have found poor specificity for the detection of actual anatomic labral injuries.13 The M-DLS test appears to have the highest sensitivity, specificity, and likelihood ratio when performed correctly9 but is still best used as part of a comprehensive evaluation.11 MRI has high sensitivity but unreliable specificity for clinically significant labral injury, as shown by the high prevalence of changes consistent with labral injury seen in asymptomatic overhead athletes.50 Even direct arthroscopic visualization has shown poor reliability in diagnosing and classifying labral injuries.4 In the absence of a recognized gold standard, current practice guidelines were reviewed to establish consistent criteria to distinguish this group of patients with suspected SLAP tears. In the absence of specific clinical examination tests, specific imaging criteria, or even arthroscopic criteria to establish a single standard, many recent authors recommend basing the diagnosis on clusters of examination and imaging findings.9,10,12,13 For our cohort, it was decided to use a modification of the criteria proposed by Walsworth et al.8 for the clustering of clinical tests. Patients had to have 3 or more history and examination findings to be included. All patients who had fewer than 3 of the history and examination inclusion criteria but had a diagnosis of labral injury by magnetic resonance arthrogram were also included because most studies use this as an inclusion criterion. The exact percentages for each of the criteria are listed in Table 4. Because very few patients in the NRS group underwent arthroscopic evaluation, it may be that some patients in this group did not actually have an anatomic SLAP injury. However, all patients in both groups had the same cluster of inclusion criteria and exhibited the same clinical dysfunction. Our consistently applied inclusion criteria and the documented exclusion criteria provided a fairly homogeneous group whose dysfunction has usually been considered to be due to SLAP injury.11,51 This study group is considered to have clinical findings suggestive of a SLAP injury6,11 and can be differentiated from other groups with other diagnoses of shoulder injury. The efficacy of this diagnostic approach was strengthened by the arthroscopic findings compatible with a clinically significant SLAP injury7 in every patient who underwent surgery. The second limitation relates to the lack of control over the rehabilitation program performed by the patients. However, the physical therapy notes showed that both groups of patients participated in a high percentage of the expected sessions and completed the exercises as prescribed, and the available therapists’ notes showed progression in the protocols. This type of rehabilitation management is consistent with the realworld scenario of how therapy is performed and implemented, and the overall impression was that compliance was slightly higher than usual. The third limitation is that the decision for surgery was determined after only 6 weeks of therapy, and perhaps a longer time of follow-up could have better delineated the response. However, Tate et al.52 observed that the greatest rate of improvement in the Disabilities of the Arm, Shoulder and Hand questionnaire occurred in the first 2 weeks of treatment. Because the decision for surgery was based on the surgeon’s findings of no significant improvement on the clinical examination or in symptoms, as well as the patient’s experience of no significant change in the dysfunction, we believe that this decision represents an accurate representation of the effects of the rehabilitation program. The accuracy of this determination at this time is substantiated by the percentages of patients in each group who eventually required surgery. The fourth limitation is that our patient group represents an active and recreationally athletic population but not a population of professional athletes. The applicability of these results to the professional athlete may be limited because of the higher level of demands. This study should be viewed as a preliminary report. It shows that the clinical prediction process can develop a model that elucidates factors that are associated with the results of an intervention. The model needs to be validated in a larger population. Finally, the results occurred with the use of a specific rehabilitation protocol. There may be other protocols that may show improved results. Conclusions A structured rehabilitation program resulted in modification of symptoms and improved function at 6 weeks’ follow-up in over half of patients in the study group with clinical dysfunction and symptoms suggestive of a SLAP injury. On initial evaluation, the presence of a painful arc of overhead motion, indicating potential loss of normal glenohumeral kinematics, and the presence of forward shoulder posture, indicating a potentially altered scapular position, represent negative predictive factors for success of rehabilitation. LABRAL CLINICAL PREDICTION DEVELOPMENT Future validation of the model in a larger population is necessary. 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