2.1 Study subjects: We prospectively collected the data for all the patients who underwent RC repair at a tertiary care institution between January 2016 and February 2020. Patients were included in this study if they had (1) a full-thickness RC tear and underwent arthroscopic repair; (2) failed non-operative treatment with either non-steroidal anti-inflammatory drugs or physiotherapy for at least 3 months before the surgical intervention; (3) no history of shoulder surgeries or psychiatric disorders (4) follow- up for at least 6 months post-operatively.
Patients were excluded if they had (1) a partial repair for irreparable RC tear; (2) undergone additional procedures or previous shoulder surgery; (3) history of any psychiatric disorder; (4) severe glenohumeral arthritis, adhesive capsulitis, sleep apnea disorder, or neuropsychiatric diseases; (5) history of medication use for sleep disorders; or (6) follow-up shorter than 6 months.
2.2 Measurements: All measurements were recorded preoperatively and postoperatively at the 6-month follow-up. The data included patient age, sex, medical history, shoulder symptoms, affected side, body mass index (BMI), duration of symptoms, and impact of the symptoms on activities of daily living. The preoperative and postoperative conditions of the involved shoulder and general health were evaluated. The patients were assessed using the visual analogue scale (VAS)[34] for pain, the American Shoulder and Elbow Surgeons (ASES) Shoulder Score,[35] and the constant score (CS) for shoulder movements.[36]
The VAS for pain intensity ranged from "no pain" (score of 0) to "pain as bad as it could be" or "worst imaginable pain" (score of 100). The ASES is used to assess the shoulder function (range: 0–100; higher score correlates with better function and less pain). CS is considered the gold standard for the evaluation of shoulder movements in Europe (score < 30: unsatisfactory; 30–39: fair; 40–59: good; 60–69: very good; and ≥ 70: excellent).[37]
A psychiatrist performed a neuropsychiatric evaluation for all patients, using the abbreviated World Health Organization Quality of Life (WHOQOL-BREF) questionnaire,[38] Beck Depression Inventory (BDI), Beck Anxiety Inventory (BAI), and the Pittsburgh Sleep Quality Index (PSQI).[39]
WHOQOL-BREF is used to evaluate the quality of life and psychometric properties of the patients. The quality of life is evaluated in different domains (range for each domain: 4–20). Higher scores on this questionnaire correlate with a higher quality of life.
BDI is a 21-item questionnaire used to assess the emotional status, somatic symptoms, and behavioral changes (score < 10: minimal; 10–18: moderate; 19–29: moderate to severe; and > 30: severe depression). BAI is a questionnaire used to assess anxiety (score 8–15: mild; 16–25: moderate; and 26–63: severe anxiety).
The PSQI evaluates several parameters of sleep quality, including subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbance, and daytime dysfunction (range: 0–3 points for each parameter; 0: no current issues; 3: most negative quality; summed score: 0–21; scores > 5: significantly disturbed sleep).
2.3 Procedures and standardization: All arthroscopic RC repairs were performed by an orthopedic surgeon trained in shoulder surgery with more than 10 years of experience, and the same surgical team. All procedures were performed arthroscopically with the patient in a beach chair position. Postoperative pain control and rehabilitation procedures were similar for all patients.
The following data were recorded postoperatively: size of the RC tear (small: < 1 cm; medium: 1–3 cm; large: 3–5 cm; massive: > 5 cm), number of sutures, intraoperative complications, and need for biceps tenotomy, subacromial decompression, or clavicle excision.
2.4 Interscalene block and postoperative pain control: Interscalene block was performed preoperatively on all patients under ultrasound (Stimuplex HNS 11; B. Braun, Melsungen, Germany) guidance with a 5–10-MHz linear probe. A total of 20 mL local anaesthetic was administered as 10 mL of 0.5% bupivacaine, 5 mL of 2% lidocaine, and 5 mL of 0.9% sodium chloride. The same protocol was applied to all patients for pain control. After discharge from the hospital, Acemetacin (90 mg) was administered for pain relief. For patients who required further pain relief, paracetamol (1 g) was administered. No patient required opioids postoperatively.
2.5 Postoperative rehabilitation: In the early postoperative period, pendulum exercises were begun, as tolerated by the patients. The same rehabilitation protocol was applied to all patients, including a three-week period of immobilization with a shoulder sling. Limited passive movements were begun after 3 weeks and active movements after 6 weeks of surgery. Three months after the surgery, progressive resistance exercises (up to 1 kg) were allowed, with an increase in the maximum weight limit to 2 kgs from the fourth month and full movements from the sixth month.
2.6 Ethical issues: We obtained written, informed consent from all patients. This study was conducted in accordance with the Declaration of Helsinki, and was approved by the local ethics committee.
2.7 Statistical analysis: The descriptive statistics are presented as means with standard deviations, medians with interquartile ranges, or frequencies with percentages. The distribution of data was assessed using the Kolmogorov-Smirnov test. Because our data were not normally distributed, we used the non-parametric Mann-Whitney U test for the analysis of independent quantitative data and Wilcoxon test for the dependent quantitative data. For the correlation analysis, we used the Spearman’s rank correlation coefficient. We used SPSS Statistics software (version 26.0; IBM Corp., Armonk, NY, USA) for the analysis.