Résultat de la recherche
12 résultat(s) recherche sur le mot-clé 'Neuromuscular diseases' 




Clinical Implications of Assisted Peak Cough Flow Measured With an External Glottic Control Device for Tracheostomy Decannulation in Patients With Neuromuscular Diseases and Cervical Spinal Cord Injuries: A Pilot Study / Seong-Woong Kang in Archives of Physical Medicine and Rehabilitation, 2016/9 (2016)
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Titre : Clinical Implications of Assisted Peak Cough Flow Measured With an External Glottic Control Device for Tracheostomy Decannulation in Patients With Neuromuscular Diseases and Cervical Spinal Cord Injuries: A Pilot Study Type de document : Article Auteurs : Seong-Woong Kang ; Won Ah Choi ; Yu Hui Won Article en page(s) : pp. 15091514 Langues : Anglais (eng) Descripteurs : HE Vinci
Rééducation et réadaptation ; Toux ; Trachéostomie ; Traumatismes de la moelle épinièreMots-clés : Cough Glottis Glotte Neuromuscular diseases Maladies neuromusculaires Spinal cord injuries Tracheostomy Résumé : Objective
To investigate the clinical usefulness and significance of an external control device substituting for glottic function in determining the feasibility of decannulation in tracheostomized patients with neuromuscular diseases and cervical spinal cord injuries whose assisted peak cough flow (APCF) was unmeasurable or Design
Before-after trial.
Setting
Inpatient setting in a university hospital.
Participants
Tracheostomized patients (N=16; 11 with neuromuscular diseases and 5 with cervical spinal cord injuries) were recruited.
Interventions
Unassisted peak cough flow (UPCF) and APCF were measured with and without an external glottic control device. Among patients whose APCF without the device was Main Outcome Measures
APCF with and without an external glottic control device as well as APCF after decannulation.
Results
After successful decannulation, APCFs were greater than or equal to those measured with the device before decannulation. No patients underwent intubation or retracheostomy, and there were no respiratory complications.
Conclusions
The external glottic control device substituting for innate glottic function is beneficial for determining tracheostomy decannulation. It provides an objective and accurate APCF. It is particularly helpful for patients whose APCF is ≥160L/min while using the device, even if APCF isDOI : https://doi.org/10.1016/j.apmr.2016.02.023 Disponible en ligne : Oui En ligne : https://login.ezproxy.vinci.be/login?url=https://www.sciencedirect.com/science/a [...] Permalink : https://bib.vinci.be/opac_css/index.php?lvl=notice_display&id=117960
in Archives of Physical Medicine and Rehabilitation > 2016/9 (2016) . - pp. 15091514[article]English Cross-Cultural Translation and Validation of the Neuromuscular Score: A System for Motor Function Classification in Patients With Neuromuscular Diseases / Carole Vuillerot in Archives of Physical Medicine and Rehabilitation, 2014/11 (2014)
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Titre : English Cross-Cultural Translation and Validation of the Neuromuscular Score: A System for Motor Function Classification in Patients With Neuromuscular Diseases Type de document : Article Auteurs : Carole Vuillerot ; Katherine G. Meilleur ; Minal Jain Article en page(s) : p. 2064-2070 Langues : Anglais (eng) Descripteurs : HE Vinci
Activités de la vie quotidienne ; Rééducation et réadaptationMots-clés : Activities of daily living Disability evaluation Évaluation de l'incapacité Neuromuscular diseases Maladies neuromusculaires Résumé : Objective
To develop and validate an English version of the Neuromuscular (NM)-Score, a classification for patients with NM diseases in each of the 3 motor function domains: D1, standing and transfers; D2, axial and proximal motor function; and D3, distal motor function.
Design
Validation survey.
Setting
Patients seen at a medical research center between June and September 2013.
Participants
Consecutive patients (N=42) aged 5 to 19 years with a confirmed or suspected diagnosis of congenital muscular dystrophy.
Interventions
Not applicable.
Main Outcome Measures
An English version of the NM-Score was developed by a 9-person expert panel that assessed its content validity and semantic equivalence. Its concurrent validity was tested against criterion standards (Brooke Scale, Motor Function Measure [MFM], activity limitations for patients with upper and/or lower limb impairments [ACTIVLIM], Jebsen Test, and myometry measurements). Informant agreement between patient/caregiver (P/C)-reported and medical doctor (MD)-reported NM scores was measured by weighted kappa.
Results
Significant correlation coefficients were found between NM scores and criterion standards. The highest correlations were found between NM-score D1 and MFM score D1 (ρ=−.944, P<.0001 activlim p and hip abduction strength by myometry informant agreement between md-reported nm scores was high for d1 confidence interval .701 but moderate d2 ci .412 d3 .290 correlation coefficients the criterion standards did not significantly differ scores.> Conclusions
Patients and physicians completed the English NM-Score easily and accurately. The English version is a reliable and valid instrument that can be used in clinical practice and research to describe the functional abilities of patients with NM diseases.Disponible en ligne : Oui En ligne : https://login.ezproxy.vinci.be/login?url=https://www.sciencedirect.com/science/a [...] Permalink : https://bib.vinci.be/opac_css/index.php?lvl=notice_display&id=118673
in Archives of Physical Medicine and Rehabilitation > 2014/11 (2014) . - p. 2064-2070[article]Motor Function Measure: Validation of a Short Form for Young Children With Neuromuscular Diseases / Capucine De Lattre in Archives of Physical Medicine and Rehabilitation, 2013/11 (2013)
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Titre : Motor Function Measure: Validation of a Short Form for Young Children With Neuromuscular Diseases Type de document : Article Auteurs : Capucine De Lattre ; Christine Payan ; Carole Vuillerot ; [et al.] Article en page(s) : pp. 2218-2226 Langues : Anglais (eng) Descripteurs : HE Vinci
Rééducation et réadaptationMots-clés : Disability Evaluation Évaluation de l'incapacité Neuromuscular Diseases Maladies neuromusculaires Résumé : Objective
To validate a useful version of the Motor Function Measure (MFM) in children with neuromuscular diseases aged Design
Two prospective cohort studies that documented the MFM completion of children aged between 2 and 7 years old.
Setting
French-speaking rehabilitation departments from France, Belgium, and Switzerland.
Participants
Healthy children (n=194) and children with a neuromuscular disease (n=88).
Interventions
Patients were rated by the MFM either once or twice by trained medical professionals, with a delay between the 2 MFMs ranging between 8 and 30 days.
Main Outcome Measure
Intra- and interrater reliability of the MFM.
Results
The subtests making up the MFM-32, a scale monitoring severity and progression of motor function in patients with a neuromuscular disease in 3 functional domains, were carried out in healthy children aged 2 to 7 years. Twenty items of the MFM-32 were successfully completed by these children and were used to constitute the MFM-20. Principal component analysis of the MFM-20 confirmed the 3 functional domains. Inter- and intrarater reliability of the 3 subscores and total score were high (intraclass correlation coefficient >.90), and discriminant validity was good.
Conclusions
The MFM-20 can be used as an outcome measure for assessment of motor function in young children with neuromuscular disease.Disponible en ligne : Oui En ligne : https://login.ezproxy.vinci.be/login?url=https://www.sciencedirect.com/journal/a [...] Permalink : https://bib.vinci.be/opac_css/index.php?lvl=notice_display&id=117644
in Archives of Physical Medicine and Rehabilitation > 2013/11 (2013) . - pp. 2218-2226[article]Is Going Beyond Rasch Analysis Necessary to Assess the Construct Validity of a Motor Function Scale? / Tiffanie Guillot in Archives of Physical Medicine and Rehabilitation, Vol. 99, n° 9 (2018)
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Titre : Is Going Beyond Rasch Analysis Necessary to Assess the Construct Validity of a Motor Function Scale? Type de document : Article Auteurs : Tiffanie Guillot ; Sylvain Roche ; Pascal Rippert Article en page(s) : p. 1776-1782 Langues : Anglais (eng) Descripteurs : HE Vinci
Évaluation de résultat (soins) ; PsychométrieMots-clés : Factor Analysis Statistical Analyse statistique factorielle Neuromuscular diseases Maladies neuromusculaires Outcome Assessment (Health Care) Psychometrics Résumé : Objective
To examine whether a Rasch analysis is sufficient to establish the construct validity of the Motor Function Measure (MFM) and discuss whether weighting the MFM item scores would improve the MFM construct validity.
Design
Observational cross-sectional multicenter study.
Setting
Twenty-three physical medicine departments, neurology departments, or reference centers for neuromuscular diseases.
Participants
Patients (N=911) aged 6 to 60 years with Charcot-Marie-Tooth disease (CMT), facioscapulohumeral dystrophy (FSHD), or myotonic dystrophy type 1 (DM1).
Interventions
None.
Main Outcome Measure(s)
Comparison of the goodness-of-fit of the confirmatory factor analysis (CFA) model vs that of a modified multidimensional Rasch model on MFM item scores in each considered disease.
Results
The CFA model showed good fit to the data and significantly better goodness of fit than the modified multidimensional Rasch model regardless of the disease (P<.001 statistically significant differences in item standardized factor loadings were found between dm1 cmt and fshd only of items> Conclusions
For multidimensional scales designed to measure patient abilities in various diseases, a Rasch analysis might not be the most convenient, whereas a CFA is able to establish the scale construct validity and provide weights to adapt the item scores to a specific disease.Disponible en ligne : Oui En ligne : https://login.ezproxy.vinci.be/login?url=https://www.sciencedirect.com/science/a [...] Permalink : https://bib.vinci.be/opac_css/index.php?lvl=notice_display&id=118895
in Archives of Physical Medicine and Rehabilitation > Vol. 99, n° 9 (2018) . - p. 1776-1782[article]Collaborative goal setting with adults attending physiotherapy at a specialist neuromuscular centre: is it always appropriate? A cross-sectional survey / S.E. Hartley in Physiotherapy, 2016/4 (2016)
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Titre : Collaborative goal setting with adults attending physiotherapy at a specialist neuromuscular centre: is it always appropriate? A cross-sectional survey Type de document : Article Auteurs : S.E. Hartley ; R.C. Stockley Année de publication : 2016 Article en page(s) : pp. 320-326 Langues : Anglais (eng) Descripteurs : HE Vinci
AutosoinsMots-clés : Neuromuscular Diseases Maladies neuromusculaires Self Care Résumé : Objectives
Collaborative goal setting is an integral component of treatment planning for adults with neuromuscular disorders (NMD). However, due to the unique challenges for these individuals, identifying a process for goal setting that is advantageous for all can be problematic. This study aimed to evaluate collaborative goal setting at a specialist NMD centre, as reported by service users attending physiotherapy. It also aimed to generate discussion about collaborative goal setting and the practice of goal setting in adults with NMD in order to inform future practice.
Setting
Specialist NMD community-based centre in the UK.
Participants
One hundred and four adults with NMD who attended the centre.
Design
Cross-sectional survey. Thematic and content analyses of goals set were performed alongside demographic data collection.
Results
One hundred and four patients (34 females) with a range of neuromuscular conditions including Becker, facioscapularhumeral, limb girdle, Duchenne and myotonic muscular dystrophies completed the survey. Thirty-six respondents (37%) stated that they had set goals with the physiotherapist, whilst 62 (63%) stated that they had not set goals with the physiotherapist. Respondents goals were grouped into four themes: symptom management, maintenance, improving physical condition, and learning to live with the condition.
Conclusions
Readiness to take part in collaborative goal setting is unique to each individual. Physiotherapists need to be skilful in supporting adults with NMD through the goal-setting process until they are capable of sharing responsibility. Setting personal goals to improve emotional well-being may help to develop confidence to take more control of their situation, hence facilitating skills in self-management.DOI : https://doi.org/10.1016/j.physio.2015.10.014 Disponible en ligne : Oui En ligne : https://login.ezproxy.vinci.be/login?url=https://www.sciencedirect.com/science/a [...] Permalink : https://bib.vinci.be/opac_css/index.php?lvl=notice_display&id=134299
in Physiotherapy > 2016/4 (2016) . - pp. 320-326[article]Home-Based Overnight Transcutaneous Capnography/Pulse Oximetry for Diagnosing Nocturnal Hypoventilation Associated With Neuromuscular Disorders / Kristy A Bauman in Archives of Physical Medicine and Rehabilitation, 2013/1 (2013)
PermalinkQuality of Life and Psychosocial Well-Being in Youth With Neuromuscular Disorders Who Are Wheelchair Users: A Systematic Review / Vivienne Travlos in Archives of Physical Medicine and Rehabilitation, 2017/5 (2017)
PermalinkClinical Functional Capacity Testing in Patients With Facioscapulohumeral Muscular Dystrophy: Construct Validity and Interrater Reliability of Antigravity Tests / Noortje H. Rijken in Archives of Physical Medicine and Rehabilitation, 2015/12 (2015)
PermalinkDetermining the Anaerobic Threshold in Postpolio Syndrome: Comparison With Current Guidelines for Training Intensity Prescription / Eric L. Voorn in Archives of Physical Medicine and Rehabilitation, 2014/5 (2014)
PermalinkExploratory Study of Physical Activity in Persons With Charcot-Marie-Tooth Disease / Elisabeth Anens in Archives of Physical Medicine and Rehabilitation, 2015/2 (2015)
PermalinkFrequency and circumstances of falls in people with inclusion body myositis: a questionnaire survey to explore falls management and physiotherapy provision / A. Hiscock in Physiotherapy, 2014/1 (2014)
PermalinkResponsiveness of the Motor Function Measure in Patients With Spinal Muscular Atrophy / Carole Vuillerot in Archives of Physical Medicine and Rehabilitation, 2013/8 (2013)
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