Source:Physiotherapy, Volume 98, Issue 4
Helen Sharma, Cathy Bulley, Frederike M.J. van Wijck
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Source: http://informahealthcare.com/doi/abs/10.3109/09593985.2012.698717?ai=1mo2&mi=3s94u5&af=R
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Source: http://informahealthcare.com/doi/abs/10.3109/09593985.2012.675416?ai=1mo2&mi=3s94u5&af=R
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Source: http://informahealthcare.com/doi/abs/10.3109/09593985.2012.699605?ai=1mo2&mi=3s94u5&af=R
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The six minute walk test (6MWT) is increasingly being used as a functional outcome measure for chronic pediatric conditions. Knowledge about its measurement properties is required to determine whether it is an appropriate test to use.
To systematically review all clinimetric studies on the 6MWT in chronic pediatric conditions
The databases MEDLINE, CINAHL, PEDro and Sportdiscus were searched up to February 2012
Study designed to evaluate measurement properties of the 6MWT in a chronic pediatric condition were included.
methodological quality of the included studies and the measurement properties of the 6MWT
A best evidence synthesis was performed of fifteen studies including nine different chronic pediatric conditions. Limited to strong evidence was found for reliability in various chronic conditions. Strong evidence was found for a positive criterion validity of the 6MWT with VO2peak in some populations but a negative criterion validity in other populations. Construct validity remained unclear in most patient groups because of methodological flaws. Little evidence was available for responsiveness and measurement error. Studies showed a large variability in test procedures despite existing guidelines for the performance of the 6MWT
Unavailability of a specific checklist to evaluate methodological quality of clinimetric studies on performance measures
Evidence for measurement properties of the 6MWT varies largely between chronic pediatric conditions. Further research is required in all patient groups to explore the ability of the 6MWT to measure significant and clinical important changes. Until then, changes measured with the 6MWT should be interpreted with caution. Future studies or consensus regarding modified test procedures in the pediatric population is recommended.
Source: http://ptjournal.apta.org/cgi/content/short/ptj.20120210v1?rss=1
Source: http://informahealthcare.com/doi/abs/10.3109/09593985.2012.703761?ai=1mo2&mi=3s94u5&af=R
Patients admitted to the intensive care unit (ICU) can develop a condition referred to as "ICU-acquired weakness." This condition is characterized by profound weakness that is greater than might be expected to result from prolonged bed rest. Intensive care unit—acquired weakness often is accompanied by dysfunction of multiple organ systems. Individuals with ICU-acquired weakness typically have significant activity limitations, often requiring physical assistance for even the most basic activities associated with bed mobility. Many of these individuals have activity limitations months to years after hospitalization. The purpose of this article is to review evidence that guides physical rehabilitation of people with ICU-acquired weakness. Included are diagnostic criteria, medical management, and prognostic indicators, as well as criteria for beginning physical rehabilitation, with an emphasis on patient safety. Data are presented indicating that rehabilitation can be implemented with very few adverse effects. Evidence is provided for appropriate measurement approaches and for physical intervention strategies. Finally, some of the key issues are summarized that should be investigated to determine the best intervention guidelines for individuals with ICU-acquired weakness.
Source: http://ptjournal.apta.org/cgi/content/short/ptj.20110117v2?rss=1
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Source: http://informahealthcare.com/doi/abs/10.3109/09593985.2012.734010?ai=1mo2&mi=3s94u5&af=R
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Neuromuscular weakness and impaired physical function are common and long-lasting complications experienced by intensive care unit (ICU) survivors. There is growing evidence that implementing rehabilitation therapy, shortly after ICU admission, improves physical function and reduces healthcare utilization. Recently, there is increasing interest and utilization of Extracorporeal Membrane Oxygenation (ECMO) to support patients with severe respiratory failure. Patients receiving ECMO are at great risk for significant physical impairments and pose unique challenges for delivering rehabilitation therapy. Consequently, there is a need for innovative examples of safely and feasibly delivering active rehabilitation to these patients. We describe three patients with respiratory failure requiring ECMO who received physical rehabilitation to illustrate and discuss relevant feasibility and safety issues.
Source: http://ptjournal.apta.org/cgi/content/short/ptj.20120336v1?rss=1
The "Gross Motor Function Measure" (GMFM-88) is a commonly used measure for evaluating gross motor function in children with cerebral palsy (CP). The relative reliability of GMFM-88 has been assessed in children with CP. However, little information is available about the absolute reliability or responsiveness of GMFM-88.
The objective of this research was to determine the absolute and relative reliability and responsiveness of the GMFM-88 in evaluating gross motor function in children with CP.
A clinical measurement design.
Ten raters scored GMFM-88 of 84 children from video records across all GMFCS levels to establish inter-rater reliability. Two raters participated to assess intra-rater reliability. Responsiveness was determined from three additional assessments after the baseline assessment. The inter- and intra-rater intraclass correlation coefficient (ICC) with 95% confidence intervals, standard error of measurement (SEM), smallest real difference (SRD), effect size (ES), and standardized response mean (SRM) were calculated.
The relative reliabilities of the GMFM were excellent (ICCs = 0.986-1.000). The SEM and SRD for total score of the GMFM were acceptable (1.60 and 3.14, respectively). Additionally, the goal total scores of the ES and SRM increased gradually in the three follow-up assessments (GMFCS level I–II: ES = 0.5, 0.6, and 0.8, SRM = 1.3, 1.8, and 2.0; GMFCS III–V: ES = 0.4, 0.7, and 0.9, SRM = 1.5, 1.7, and 2.0).
Children over 10 years of age with CP were not included in this study, so the results should not be generalized to all children with CP.
This study indicates that both reliability and responsiveness of the GMFM-88 are reasonable for measuring gross motor function in children with CP.
Source: http://ptjournal.apta.org/cgi/content/short/ptj.20110374v1?rss=1
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Source: http://www.metapress.com/content/97n0813510p20151/
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In the coming years, the number of survivors of critical illness is expected to increase. These survivors frequently develop newly acquired physical and cognitive impairments. Long-term cognitive impairment is common following critical illness and has dramatic effects on patients' abilities to function autonomously. Neuromuscular weakness affects similar proportions of patients and leads to equally profound life alterations. As knowledge of these short-term and long-term consequences of critical illness has come to light, interventions to prevent and rehabilitate these devastating consequences have been sought. Physical rehabilitation has been shown to improve functional outcomes in people who are critically ill, but subsequent studies of physical rehabilitation after hospital discharge have not. Post-hospital discharge cognitive rehabilitation is feasible in survivors of critical illness and is commonly used in people with other forms of acquired brain injury. The feasibility of early cognitive therapy in people who are critically ill remains unknown.
The purpose of this novel protocol trial will be to determine the feasibility of early and sustained cognitive rehabilitation paired with physical rehabilitation in patients who are critically ill from medical and surgical intensive care units.
This is a randomized controlled trial.
The setting for this trial will be medical and surgical intensive care units of a large tertiary care referral center.
The participants will be patients who are critically ill with respiratory failure or shock.
Patients will be randomized to groups receiving usual care, physical rehabilitation, or cognitive rehabilitation plus physical rehabilitation. Twice-daily cognitive rehabilitation sessions will be performed with patients who are noncomatose and will consist of orientation, memory, and attention exercises (eg, forward and reverse digit spans, matrix puzzles, letter-number sequences, pattern recognition). Daily physical rehabilitation sessions will advance patients from passive range of motion exercises through ambulation. Patients with cognitive or physical impairment at discharge will undergo a 12-week, in-home cognitive rehabilitation program.
A battery of neurocognitive and functional outcomes will be measured 3 and 12 months after hospital discharge.
If feasible, these interventions will lay the groundwork for a larger, multicenter trial to determine their efficacy.
Source: http://ptjournal.apta.org/cgi/content/short/ptj.20110414v2?rss=1
Source: http://informahealthcare.com/doi/abs/10.3109/09593985.2012.736762?ai=1mo2&mi=3s94u5&af=R
Bed rest and immobility in patients on mechanical ventilation and/or in an intensive care unit (ICU) have detrimental effects. Studies in medical ICUs show that early mobilization is safe, does not increase cost, and can be associated with decreased ICU and hospital length of stay (LOS).
Assess the effects of an early mobilization protocol (EMP) on complication rates, ventilator days, and ICU and hospital LOS for patients admitted to a trauma and burn ICU (TBICU).
A retrospective cohort study of a interdisciplinary quality-improvement program.
Pre- and post-EMP patient data from the trauma registry for 2,176 patients admitted to the TBICU between May 2008 and April 2010 were compared.
No adverse events were reported related to the EMP. After adjusting for age and injury severity, there was a decrease in airway, pulmonary, and vascular complications (including pneumonia and DVT) post-EMP. Ventilator days, TBICU and hospital lengths of stay were not significantly decreased.
Using a historical control group, there was no way to account for other changes in patient care that may have occurred between the two periods that could have affected patient outcomes. The dose of physical activity both pre- and post-EMP were not specifically assessed.
Early mobilization of patients in a TBICU was safe and effective. Medical, nursing, and physical therapy staff, as well as hospital administration have embraced the new culture of "early mobilization" in the ICU.
Source: http://ptjournal.apta.org/cgi/content/short/ptj.20110417v1?rss=1
Background. Exercise interventions can enhance mobility after stroke as well as prevent falls in elderly persons. Objective. Investigate whether an exercise intervention can enhance mobility, prevent falls, and increase physical activity among community-dwelling people after stroke. Method. A randomized trial with blinding of physical outcome assessment was conducted through local stroke clubs. Both groups, on average 5.9 years poststroke, received exercise classes, advice, and a home program for 12 months. The experimental group (EG) program (n = 76) aimed to improve walking, prevent falls and increase physical activity. The control group (CG) program (n = 75) aimed to improve upper-limb and cognitive functions. The primary outcomes were walking capacity, walking speed measured before and after the intervention, and fall rates monitored monthly. Results. At 12 months, the EG walked 34 m further in 6 minutes (95% confidence interval [CI] = 19-50; P < .001) and 0.07 m/s faster over 10 m (95% CI = 0.01-0.14; P = .03) than the CG. The EG had 129 falls, and the CG had 133. There were no differences in proportion of fallers (relative risk = 1.22; 95% CI = 0.91-1.62; P = .19) or the rate of falls between groups (incidence rate ratio = 0.96; 95% CI = 0.59-1.51; P = .88). Conclusion. The experimental intervention delivered through stroke clubs enhanced aspects of mobility but had no effect on falls.
Source: http://nnr.sagepub.com/cgi/content/abstract/26/9/1046?rss=1
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Source: http://informahealthcare.com/doi/abs/10.3109/01942638.2012.744577?ai=1ozx&mi=3s94u5&af=R
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Limited evidence exists to inform how strength and endurance exercises commonly used to prevent low back pain affect muscle morphometry and endurance.
The purpose of this study was to analyze the effects of two exercise regimens on the morphometry and endurance of key trunk musculature in a healthy population.
Randomized Controlled Trial.
Military training setting.
A random subsample (n=340, 72% male, 21.9±4.2 years, 24.8±2.8 kg/m2) from the larger Prevention of Low Back Pain in the Military trial (n = 4,325) were included.
The core stabilization exercise program (CSEP) included low load/low repetition motor control exercises while the traditional exercise program (TEP) included exercises conducted fast using a high load/high repetition trunk strengthening exercises.
Baseline and follow-up examination included ultrasound imaging of the trunk muscles and endurance tests. Linear mixed models were fitted to study the group and time effect and their interactions, accounting for the clustering effect.
Symmetry generally improved in the rest and contracted states, but there were no differences suggestive of muscle hypertrophy or improved ability to contract the trunk muscles between Soldiers receiving CSEP or TEP. Total trunk endurance time decreased over the 12-week period; but endurance performance favored those Soldiers in the CSEP group (p≤0.05). Endurance time was not associated with future episodes of LBP.
The lack of morphological changes may not be detectable in an already active cohort or a more intensive dose was needed.
Although improved symmetry was noted, neither the CSEP or TEP resulted in muscle hypertrophy. Longer endurance times were noted in individuals who completed CSEP but were not strongly predictive of future low back pain episodes.
Source: http://ptjournal.apta.org/cgi/content/short/ptj.20120152v1?rss=1
Purpose: To investigate the concurrent validity of the Saskatoon Falls Prevention Consortium's Falls Screening and Referral Algorithm (FSRA). Method: A total of 29 older adults (mean [SD] age 77.7 [4.0] y) living in an independent-living senior's complex who met inclusion criteria completed a demographic questionnaire and the components of the FSRA and Berg Balance Scale (BBS). The FSRA consists of the Elderly Fall Screening Test (EFST) and the Multi-factor Falls Questionnaire (MFQ); it is designed to categorize individuals into low, moderate, or high fall-risk categories to determine appropriate management pathways. A predictive model for probability of fall risk, based on previous research, was used to determine concurrent validity of the FRSA. Results: The FSRA placed 79% of participants into the low-risk category, whereas the predictive model found the probability of fall risk to range from 0.04 to 0.74, with a mean (SD) of 0.35 (0.25). No statistically significant correlation was found between the FSRA and the predictive model for probability of fall risk (Spearman's ρ=0.35, p=0.06). Conclusion: The FSRA lacks concurrent validity relative to to a previously established model of fall risk and appears to over-categorize individuals into the low-risk group. Further research on the FSRA as an adequate tool to screen community-dwelling older adults for fall risk is recommended.