Usefulness of continuous actigraph monitoring in the assessment of the effect of corticosteroid treatment for Duchenne muscular dystrophy: a case report
[Purpose] This study evaluated the effect of corticosteroid treatment on the daily activity of a patient with Duchenne muscular dystrophy using an actigraph and examined whether this method produces the same results as the conventional motor-function evaluation methods. [Subject and Methods] A patie...
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| Published in | Journal of Physical Therapy Science Vol. 28; no. 11; pp. 3249 - 3251 |
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| Main Authors | , , |
| Format | Journal Article |
| Language | English |
| Published |
Japan
The Society of Physical Therapy Science
2016
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0915-5287 2187-5626 |
| DOI | 10.1589/jpts.28.3249 |
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| Abstract | [Purpose] This study evaluated the effect of corticosteroid treatment on the daily activity of a patient with Duchenne muscular dystrophy using an actigraph and examined whether this method produces the same results as the conventional motor-function evaluation methods. [Subject and Methods] A patient with 5 year-old Duchenne muscular dystrophy was recruited. An actigraph was attached to his waist to measure the energy expenditure and the number of steps taken by him during a period of two weeks, 14 days before and 14 days after corticosteroid administration. The outcomes of these measurements were compared with the results of conventional motor-function evaluation methods—the 10-m run test, 6-minute walk test, and North Star Ambulatory Assessment—on his next visit. [Results] The actigraph data for energy expenditure and the number of steps taken correlated well with the results of the above-mentioned conventional motor-function tests, and the value of each data point improved after corticosteroid administration. [Conclusion] An actigraph was effectively used to non-invasively measure consecutive daily activity for four weeks. It was easily done and the results were consistent with conventional motor-function evaluation methods. |
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| AbstractList | [Purpose] This study evaluated the effect of corticosteroid treatment on the daily activity of a patient with Duchenne muscular dystrophy using an actigraph and examined whether this method produces the same results as the conventional motor-function evaluation methods. [Subject and Methods] A patient with 5 year-old Duchenne muscular dystrophy was recruited. An actigraph was attached to his waist to measure the energy expenditure and the number of steps taken by him during a period of two weeks, 14 days before and 14 days after corticosteroid administration. The outcomes of these measurements were compared with the results of conventional motor-function evaluation methods—the 10-m run test, 6-minute walk test, and North Star Ambulatory Assessment—on his next visit. [Results] The actigraph data for energy expenditure and the number of steps taken correlated well with the results of the above-mentioned conventional motor-function tests, and the value of each data point improved after corticosteroid administration. [Conclusion] An actigraph was effectively used to non-invasively measure consecutive daily activity for four weeks. It was easily done and the results were consistent with conventional motor-function evaluation methods. [Abstract.] [Purpose] This study evaluated the effect of corticosteroid treatment on the daily activity of a patient with Duchenne muscular dystrophy using an actigraph and examined whether this method produces the same results as the conventional motor-function evaluation methods. [Subject and Methods] A patient with 5 year-old Duchenne muscular dystrophy was recruited. An actigraph was attached to his waist to measure the energy expenditure and the number of steps taken by him during a period of two weeks, 14 days before and 14 days after corticosteroid administration. The outcomes of these measurements were compared with the results of conventional motor-function evaluation methods - the 10-m run test, 6-minute walk test, and North Star Ambulatory Assessment - on his next visit. [Results] The actigraph data for energy expenditure and the number of steps taken correlated well with the results of the above-mentioned conventional motor-function tests, and the value of each data point improved after corticosteroid administration. [Conclusion] An actigraph was effectively used to non-invasively measure consecutive daily activity for four weeks. It was easily done and the results were consistent with conventional motor-function evaluation methods. [Purpose] This study evaluated the effect of corticosteroid treatment on the daily activity of a patient with Duchenne muscular dystrophy using an actigraph and examined whether this method produces the same results as the conventional motor-function evaluation methods. [Subject and Methods] A patient with 5 year-old Duchenne muscular dystrophy was recruited. An actigraph was attached to his waist to measure the energy expenditure and the number of steps taken by him during a period of two weeks, 14 days before and 14 days after corticosteroid administration. The outcomes of these measurements were compared with the results of conventional motor-function evaluation methods—the 10-m run test, 6-minute walk test, and North Star Ambulatory Assessment—on his next visit. [Results] The actigraph data for energy expenditure and the number of steps taken correlated well with the results of the above-mentioned conventional motor-function tests, and the value of each data point improved after corticosteroid administration. [Conclusion] An actigraph was effectively used to non-invasively measure consecutive daily activity for four weeks. It was easily done and the results were consistent with conventional motor-function evaluation methods. [Purpose] This study evaluated the effect of corticosteroid treatment on the daily activity of a patient with Duchenne muscular dystrophy using an actigraph and examined whether this method produces the same results as the conventional motor-function evaluation methods. [Subject and Methods] A patient with 5 year-old Duchenne muscular dystrophy was recruited. An actigraph was attached to his waist to measure the energy expenditure and the number of steps taken by him during a period of two weeks, 14 days before and 14 days after corticosteroid administration. The outcomes of these measurements were compared with the results of conventional motor-function evaluation methods-the 10-m run test, 6-minute walk test, and North Star Ambulatory Assessment-on his next visit. [Results] The actigraph data for energy expenditure and the number of steps taken correlated well with the results of the above-mentioned conventional motor-function tests, and the value of each data point improved after corticosteroid administration. [Conclusion] An actigraph was effectively used to non-invasively measure consecutive daily activity for four weeks. It was easily done and the results were consistent with conventional motor-function evaluation methods.[Purpose] This study evaluated the effect of corticosteroid treatment on the daily activity of a patient with Duchenne muscular dystrophy using an actigraph and examined whether this method produces the same results as the conventional motor-function evaluation methods. [Subject and Methods] A patient with 5 year-old Duchenne muscular dystrophy was recruited. An actigraph was attached to his waist to measure the energy expenditure and the number of steps taken by him during a period of two weeks, 14 days before and 14 days after corticosteroid administration. The outcomes of these measurements were compared with the results of conventional motor-function evaluation methods-the 10-m run test, 6-minute walk test, and North Star Ambulatory Assessment-on his next visit. [Results] The actigraph data for energy expenditure and the number of steps taken correlated well with the results of the above-mentioned conventional motor-function tests, and the value of each data point improved after corticosteroid administration. [Conclusion] An actigraph was effectively used to non-invasively measure consecutive daily activity for four weeks. It was easily done and the results were consistent with conventional motor-function evaluation methods. |
| Author | Nishizawa, Hitomi Nakamura, Akinori Shiba, Naoko |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27942159$$D View this record in MEDLINE/PubMed |
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| Keywords | Motor function Duchenne muscular dystrophy Actigraph |
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| References | 8) Nishizawa H, Genno H, Shiba N, et al.: Periodic sound-based 6-minute walk test for patients with Duchenne muscular dystrophy: a preliminary study. J Phys Ther Sci, 2015, 27: 3473–3479. 7) ATS Committee on Proficiency Standards for Clinical Pulmonary Function Laboratories: ATS statement: guidelines for the six-minute walk test. Am J Respir Crit Care Med, 2002, 166: 111–117. 1) Pane M, Mazzone ES, Sivo S, et al.: Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36-month changes. PLoS One, 2014, 9: e108205. 4) Kam HJ, Lee K, Cho SM, et al.: High-resolution actigraphic analysis of ADHD: a wide range of movement variability observation in three school courses—a pilot study. Healthc Inform Res, 2011, 17: 29–37. 5) Vanderloo LM, Di Cristofaro NA, Proudfoot NA, et al.: Comparing the Actical and ActiGraph approach to measuring young children’s physical activity levels and sedentary time. Pediatr Exerc Sci, 2016, 28: 133–142. 6) Jeannet PY, Aminian K, Bloetzer C, et al.: Continuous monitoring and quantification of multiple parameters of daily physical activity in ambulatory Duchenne muscular dystrophy patients. Eur J Paediatr Neurol, 2011, 15: 40–47. 2) De Sanctis R, Pane M, Sivo S, et al.: Suitability of North Star Ambulatory Assessment in young boys with Duchenne muscular dystrophy. Neuromuscul Disord, 2015, 25: 14–18. 3) Kimura S, Ozasa S, Nomura K, et al.: Estimation of muscle strength from actigraph data in Duchenne muscular dystrophy. Pediatr Int, 2014, 56: 748–752. 1 2 3 4 5 6 7 8 |
| References_xml | – reference: 1) Pane M, Mazzone ES, Sivo S, et al.: Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36-month changes. PLoS One, 2014, 9: e108205. – reference: 7) ATS Committee on Proficiency Standards for Clinical Pulmonary Function Laboratories: ATS statement: guidelines for the six-minute walk test. Am J Respir Crit Care Med, 2002, 166: 111–117. – reference: 2) De Sanctis R, Pane M, Sivo S, et al.: Suitability of North Star Ambulatory Assessment in young boys with Duchenne muscular dystrophy. Neuromuscul Disord, 2015, 25: 14–18. – reference: 3) Kimura S, Ozasa S, Nomura K, et al.: Estimation of muscle strength from actigraph data in Duchenne muscular dystrophy. Pediatr Int, 2014, 56: 748–752. – reference: 4) Kam HJ, Lee K, Cho SM, et al.: High-resolution actigraphic analysis of ADHD: a wide range of movement variability observation in three school courses—a pilot study. Healthc Inform Res, 2011, 17: 29–37. – reference: 8) Nishizawa H, Genno H, Shiba N, et al.: Periodic sound-based 6-minute walk test for patients with Duchenne muscular dystrophy: a preliminary study. J Phys Ther Sci, 2015, 27: 3473–3479. – reference: 6) Jeannet PY, Aminian K, Bloetzer C, et al.: Continuous monitoring and quantification of multiple parameters of daily physical activity in ambulatory Duchenne muscular dystrophy patients. Eur J Paediatr Neurol, 2011, 15: 40–47. – reference: 5) Vanderloo LM, Di Cristofaro NA, Proudfoot NA, et al.: Comparing the Actical and ActiGraph approach to measuring young children’s physical activity levels and sedentary time. Pediatr Exerc Sci, 2016, 28: 133–142. – ident: 5 doi: 10.1123/pes.2014-0218 – ident: 6 doi: 10.1016/j.ejpn.2010.07.002 – ident: 8 doi: 10.1589/jpts.27.3473 – ident: 1 doi: 10.1371/journal.pone.0108205 – ident: 2 doi: 10.1016/j.nmd.2014.09.015 – ident: 7 doi: 10.1164/ajrccm.166.1.at1102 – ident: 3 doi: 10.1111/ped.12348 – ident: 4 doi: 10.4258/hir.2011.17.1.29 |
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| Title | Usefulness of continuous actigraph monitoring in the assessment of the effect of corticosteroid treatment for Duchenne muscular dystrophy: a case report |
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