Ahmad A. Alahmad

Background/Objectives: Rotator cuff disease (RCD) is one of the most common causes of shoulder dysfunction, often resulting in pain, limited range of motion (ROM), and reduced function. Mulligan Mobilization with Movement (MWM) has been proposed as an effective adjunct to conventional therapy by correcting positional faults and improving joint mechanics. However, the overall evidence in RCD remains inconclusive. This meta-analysis aimed to evaluate the efficacy of Mulligan mobilization combined with conventional therapy versus conventional therapy alone on pain, functionality, ROM, joint position sense, and quality of life (QoL) in patients with RCD. Methods: A comprehensive literature search was carried out in PubMed, Web of Science, Scopus, and the Cochrane Library from database inception to 12 October 2025, with no restrictions on publication year. We included randomized controlled trials (RCTs) that compared Mulligan mobilization combined with conventional therapy against conventional therapy alone in individuals with rotator cuff-related pain. The predefined outcomes were pain intensity, range of motion (ROM), quality of life (QoL), joint position sense, and functional performance. All statistical analyses were conducted using R version 4.3.1. Heterogeneity was assessed using the I² statistic and the Cochrane Q test. Pooled mean differences (MDs) were calculated using the Inverse Variance approach with a restricted maximum-likelihood (REML) random-effects model. The review protocol was prospectively registered in PROSPERO (ID: CRD420251166854). Results: Four RCTs met the eligibility criteria and were included in the meta-analysis, comprising a total of 160 participants. Of these, 80 (50%) received Mulligan mobilization in combination with conventional therapy (mean age: 51 years; mean proportion of females: 45%). In the pooled analysis, Mulligan mobilization significantly improved pain at rest (MD −1.19; 95% CI [−1.64; −0.74]; p = 0.01; I² = 0%), pain during activity (MD −2.25; 95% CI [−3.18; −1.31]; p = 0.01; I² = 67%), functionality (MD −14.71; 95% CI [−20.10; −9.33]; p = 0.01; I² = 51%), ROM (MD 19.92; 95% CI [11.25; 28.39]; p = 0.01; I² = 58%), and joint position sense (MD −3.31; 95% CI [−6.22; −0.40]; p = 0.03; I² = 80%) compared with conventional therapy alone. No significant difference was observed for QoL (MD 10.58; 95% CI [−3.18; 24.34]; p = 0.13; I² = 76%). Conclusions: Mulligan mobilization combined with conventional therapy provides significant improvements in pain, functionality, ROM, and joint position sense in RCD. However, no statistically significant differences were observed in QoL between the groups. Integration of this technique into rehabilitation protocols may enhance clinical outcomes and functional recovery.

Introduction Adult spinal deformity surgery is frequently performed to address degenerative conditions and scoliosis, but postoperative complications such as proximal junctional kyphosis (PJK) and proximal junctional failure (PJF) are common. These conditions can lead to neurological deficits and compromised surgical outcomes. This systematic review and meta-analysis aimed to evaluate the prevalence of neurological deficits associated with PJK and PJF. Methods A systematic review and meta-analysis was conducted following PRISMA guidelines. A comprehensive search was performed across multiple databases, including PubMed, Web of Science, Cochrane, Embase, and Scopus, with no language restrictions. Studies that reported neurological deficits following PJK or PJF after adult spinal deformity surgery were included. Data extraction and quality assessment were performed by two independent authors using NIH quality assessment tools. Meta-analysis was conducted using random-effect models, and heterogeneity was evaluated using I². Results Thirteen eligible studies were identified involving 2846 patients. Of these, 777 patients developed PJK or PJF, with 61 patients experiencing neurological deficits. The pooled prevalence of neurological deficits was 6.2% for PJF (95% CI: 0.062–0.192; p < 0.001) and 7.1% for PJK (95% CI: 0.027–0.115; p < 0.001). Heterogeneity amongst the studies was high for PJF (I² = 70.25%) and low for PJK (I² = 14.47%). Conclusion This study highlights the incidence of neurological deficits following PJK and PJF in adult spinal deformity surgeries. Future research should focus on identifying the risk factors and utilising evidence-based strategies that can improve postoperative care and reduce complication rates.

Background and Aims: Brachial plexus block (BPB) is advantageous for elective orthopaedic or reconstructive upper limb surgery. However, the optimal local anaesthetic in BPB remains debatable. Therefore, we aim to investigate the efficacy and safety of levobupivacaine versus ropivacaine in BPB for upper limb surgery. Methods: A systematic review and meta-analysis synthesising randomised controlled trials (RCTs), retrieved by systematically searching PubMed, EMBASE, WOS, SCOPUS, Google Scholar, and CENTRAL since inception till June 2024. Continuous and dichotomous outcome variables were pooled using mean difference (MD) and risk ratio (RR), with a 95% confidence interval (CI), using Stata v. 17. We assessed heterogeneity using the Chi-square test and I² statistic. Results: Sixteen RCTs and 939 patients were included. Levobupivacaine was significantly associated with a longer sensory block duration [MD: 1.66 (95% CI: 1.43, 1.89), P < 0.001] and motor block duration [MD: 1.18 (95% CI: 0.11, 2.26), P = 0.03]. However, there was no difference between both groups in time to sensory block [MD: −0.30 (95% CI: −1.31, 0.71), P = 0.56], time to motor block [MD: −0.29 (95% CI: −1.26, 0.67), P = 0.55], pain score [MD: −0.48 (95% CI: −2.13, 1.16), P = 0.56], rescue analgesia rate [RR: 0.94 (95% CI: 0.74, 1.20), P = 0.64], and complications [RR: 0.47 (95% CI: 0.20, 1.13), P = 0.09]. Conclusions: Levobupivacaine is significantly associated with a longer duration of sensory and motor block in patients undergoing BPB for upper limb surgery compared to ropivacaine, with a similar safety profile. However, there was no difference regarding the time to onset of the sensory or motor block.