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Background. To date, no reports have investigated neuromuscular electrical stimulation (NMES) to increase muscle force production of children with cerebral palsy (CP) using high-force contractions and low repetitions. Objective. The aims of this study were to determine if isometric NMES or volitional training in children with CP could increase muscle strength and walking speed and to examine the mechanisms that may contribute to increased force production. Methods. Eleven children with spastic diplegia were assigned to an NMES training group or to a volitional training group. Participants in the NMES group had electrodes implanted percutaneously to activate the quadriceps femoris and triceps surae muscles. The volitional group trained with maximal effort contractions. Both groups performed a 12-week isometric strength-training program. Maximum voluntary isometric contraction (MVIC) force, voluntary muscle activation, quadriceps and triceps surae cross-sectional area (CSA), and walking speed were measured pre- and post-strength training. Results. The NMES-trained group had greater increases in normalized force production for both the quadriceps femoris and triceps surae. Similarly, only the NMES group showed an increase in walking speed after training. Changes in voluntary muscle activation explained approximately 67% and 37% of the changes seen in the MVIC of the NMES and volitional groups, respectively. Quadriceps femoris maximum CSA increased significantly for the NMES group only. Conclusions. This study was the first to quantitatively show strength gains with the use of NMES in children with CP. These results support the need for future experimental studies that will examine the clinical effectiveness of NMES strength training. Key Words: Cerebral palsy--Strength training--Electrical stimulation--Muscle activation--Cross-sectional area--Hypertrophy., Low muscle force production in children with cerebral palsy (CP)(1) can potentially be explained by several observed factors: decreased central nervous system (CNS) motor unit recruitment and discharge rates,(2) increased [...]

Inhibition of rotator cuff activation and force after local experimental pain has been previously shown. Clinically, strength is often indexed to the uninvolved side in order to quantify deficits during injury and recovery. This study assessed the effect of experimental subacromial pain on contralateral shoulder external rotation (ER) force and activation. We hypothesized that subacromial pain would not affect contralateral shoulder external rotation force and voluntary activation (VA) of the contralateral infraspinatus because we believe that the effects of acute experimental pain will largely exert an ipsilateral, spinal segmental effect. Twenty healthy adults were tested. External rotation force and VA were tested while participants performed maximum voluntary isometric contractions of shoulder external rotation, during which a brief electrical stimulus was applied to the infraspinatus muscle at an intensity that maximized external rotation force. To elicit pain, 1.5 ml of 5% hypertonic saline was injected into the contralateral subacromial space. Mean (SD) pain immediately after injection was 6.3/10 (0.85) resulting in a 7.6% decline in contralateral external rotation force (p <.01) and 3.3% decline in infraspinatus muscle VA (p =.48). A subset of participants (n = 9) showed a more substantial decline in both force (15.4%; p <.000001; d = −3.53) and VA (8.7%; p =.045; d = −0.98). Experimental shoulder pain had a modest effect on contralateral ER force and VA in a subset of participants; therefore, it may be important to index or compare strength bilaterally throughout rehabilitation to capture this bilateral effect as pain resolves. [ABSTRACT FROM AUTHOR]

Total knee arthroplasty (TKA) is the most common elective orthopedic surgery performed in the United States. Following surgery patients experience significant lower extremity swelling that is related to poor satisfaction with surgery and is hypothesized to contribute to functional decline. However, in practice, precise and reliable methods for measuring lower extremity swelling do not exist. The purpose of this study was to provide reliability and precision parameters of an innovative approach, single frequency bioelectrical impedance assessment (SF-BIA), for measuring post-TKA lower extremity swelling. Swelling in 56 patients (64.3 ± 9.3 years; 29 males) was measured before and after TKA using SF-BIA and circumferential measures (CM). Reliability of the measures was calculated using Intraclass Correlation Coefficients (ICC). Precision of the measures was provided using standard error of the measurement and minimal detectable change (MDC90). Change values between time points for SF-BIA and CM are provided. SF-BIA was found to have greater reliability following surgery compared to CM (ICC = 0.99 vs 0.68). SF-BIA was found to have an MDC90 = 2% following surgery, indicating improved ability to detect minute fluctuations in swelling compared to CM (MDC90 = 6%) following surgery. These results indicate that SF-BIA improves the precision and reliability of swelling measurement compared to CM. [ABSTRACT FROM AUTHOR]

Title: Development of a reference chart to monitor postoperative swelling following total knee arthroplasty. Purpose: Lower extremity swelling is a feature of total knee arthroplasty. Until recently, clinicians lacked tools to accurately measure swelling in clinical settings, but bioelectrical impedance assessment has shown promise in this regard. The purpose of this study was to develop a reference chart of lower extremity swelling following total knee arthroplasty. Method: Fifty-six participants (54% male, mean age = 64 years) were followed for the first 7 weeks following total knee arthroplasty, during which frequent lower extremity bioelectrical impedance assessments were performed. Using Generalized Additive Models for Location Scale and Shape, a reference chart for swelling was developed with bioelectrical impedance assessment data from the first 40 patients enrolled in the study (223 observations) and preliminarily tested for performance in the remaining 16 patients' data (96 observations). Results: The reference chart illustrates approximately 10% per day increase for the first 3 days following surgery. Peak swelling occurs 6–8 days following surgery; the 10th percentile demonstrates a peak of 25%, whereas the 90th percentile peaks at 47%. In the test data, this reference chart demonstrated accurate coverage at each estimated centile. Conclusion: The reference chart provides a novel framework for monitoring swelling following total knee arthroplasty and may augment clinical decisions to improve postoperative swelling management. The use of bioelectrical impedance assessment provides an accurate and easily implemented approach for rehabilitation professionals to measure swelling. The reference chart provided allows for monitoring of patient recovery of swelling following total knee arthroplasty. Precise depictions of where a patient's swelling is in reference to others will improve clinical decision making at the individual level. [ABSTRACT FROM AUTHOR]

* BACKGROUND: The prone instability test is used to identify individuals with low back pain (LBP) who would benefit from trunk stabilization exercises. Although activity from muscles during the leg-raising portion of the prone instability test theoretically enhances spinal stiffness and reduces pain, evidence for this is lacking. * OBJECTIVES: To compare and contrast (1) pain and stiffness changes between prone instability testing positions, and (2) muscle activation patterns during the prone instability test leg raise in individuals with and without LBP. * METHODS: Participants with (n = 10) and without (n = 10) LBP participated in this laboratory case-control study. Spinal stiffness was measured using a beam-bending model and 3-D kinematic data. Stiffness changes were compared across the test positions and between groups. Surface electromyographic data were collected on trunk and limb musculature. Principal-component analysis was used to extract muscle synergies. * RESULTS: Spinal stiffness increased across testing positions in all participants (P<.05). Participants with LBP experienced reduced pain during the test (Pc.001). No between-group difference was found in spinal stiffness during leg raising during the test (P>.05). Participants without LBP used 3 muscle synergies during the leg raise and participants with LBP used 2 muscle synergies. * CONCLUSION: Spinal stiffness increased in all participants; however, participants without LBP demonstrated a muscle synergy pattern where each synergy was associated with a distinct function of the prone instability test. Participants with LBP used a more global stabilization pattern, which may reflect a maladaptive method of enhancing spinal stability. [ABSTRACT FROM AUTHOR]

Background and Purpose: Achilles tendinopathy is a common overuse injury sustained by athletes including runners. The use of noxious electrical stimulation for the treatment of chronic tendinopathies is a novel treatment intervention, which may alter pain perception and serve as adjunct technique in the recovery of painfree function. The purpose of this case report is to demonstrate the use of noxious electrical stimulation for the treatment of chronic, bilateral Achilles tendinopathy that was resistant to conservative treatment using plantarflexor eccentric exercise. Case Description: A 27-year old male runner was referred to physical therapy with a 7-year history of bilateral Achilles tendinopathy. He scored a 73/80 on the Lower Extremity Functional Scale (LEFS) and a 64% on the Victorian Institute of Sports Assessment-Achilles (VISA-A). Pain pressure threshold testing of the Achilles tendon was performed, followed by a single session of noxious electric stimulation to bilateral Achilles tendons, and the subject was instructed to continue with eccentric gastroc-soleus complex strengthening as previously performed. Outcomes: Pain pressure threshold testing was performed to the mid-portion of the posterior Achilles tendon. The left Achilles tendon mean was 10.50kg and right Achilles tendon was 8.33kg prior to the noxious stimulation intervention. Twenty-four hours after the noxious stimulation treatment, improvements in mean pain threshold testing were found for both the left (16.31kg) and right (12.36kg) Achilles tendons. At one month after the physical therapy noxious stimulation session, the subject was able to progress his workouts to include sprints and interval training. His LEFS improved to 76/80 and his VISA-A improved to 96 %. Discussion: The case illustrates the successful pain reduction and return to progressive sports activity in a runner with chronic Achilles tendinopathy. The utilization of noxious electric stimulation may have altered the pain perception of the nervous system as evidenced by the improvement in pain pressure threshold testing. Future studies on the application of noxious electric stimulation on chronic Achilles tendinopathy may help support the benefit of this intervention on pain and function. [ABSTRACT FROM AUTHOR]