Skip to main content
Top
Published in: Journal of Inherited Metabolic Disease 6/2018

Open Access 01-11-2018 | Glycogen Storage Disease

A preliminary study of telemedicine for patients with hepatic glycogen storage disease and their healthcare providers: from bedside to home site monitoring

Authors: Irene J. Hoogeveen, Fabian Peeks, Foekje de Boer, Charlotte M. A. Lubout, Tom J. de Koning, Sebastiaan te Boekhorst, Robert-Jan Zandvoort, Rob Burghard, Francjan J. van Spronsen, Terry G. J. Derks

Published in: Journal of Inherited Metabolic Disease | Issue 6/2018

Login to get access

Abstract

Background

The purpose of this project was to develop a telemedicine platform that supports home site monitoring and integrates biochemical, physiological, and dietary parameters for individual patients with hepatic glycogen storage disease (GSD).

Methods and results

The GSD communication platform (GCP) was designed with input from software developers, GSD patients, researchers, and healthcare providers. In phase 1, prototyping and software design of the GCP has occurred. The GCP was composed of a GSD App for patients and a GSD clinical dashboard for healthcare providers. In phase 2, the GCP was tested by retrospective patient data entry. The following software functionalities were included (a) dietary registration and prescription module, (b) emergency protocol module, and (c) data import functions for continuous glucose monitor devices and activity wearables. In phase 3, the GSD App was implemented in a pilot study of eight patients with GSD Ia (n = 3), GSD IIIa (n = 1), and GSD IX (n = 4). Usability was measured by the system usability scale (SUS). The mean SUS score was 64/100 [range: 38–93].

Conclusions

This report describes the design, development, and validation process of a telemedicine platform for patients with hepatic GSD. The GCP can facilitate home site monitoring and data exchange between patients with hepatic GSD and healthcare providers under varying circumstances. In the future, the GCP may support cross-border healthcare, second opinion processes and clinical trials, and could possibly also be adapted for other diseases for which a medical diet is the cornerstone.
Literature
go back to reference Bangor A, Kortum P, Miller J (2009) Determining what individual SUS scores mean: adding an adjective rating scale. J Usability Stud 4:114–123 Bangor A, Kortum P, Miller J (2009) Determining what individual SUS scores mean: adding an adjective rating scale. J Usability Stud 4:114–123
go back to reference Brooke J (1996) SUS: a ‘quick and dirty’ usability scale. In: Jordan PW, Thomas B, Weerdmeester BA, McClelland IL (eds) Usability evaluation in industry. Taylor and Francis, London, pp 189–194 Brooke J (1996) SUS: a ‘quick and dirty’ usability scale. In: Jordan PW, Thomas B, Weerdmeester BA, McClelland IL (eds) Usability evaluation in industry. Taylor and Francis, London, pp 189–194
go back to reference Dagli A, Zori RT, McCune H, Ivsic T, Maisenbacher MK, Weinstein DA (2009) Reversal of glycogen storage disease type IIIa-related cardiomyopathy with modification of diet. J Inherit Metab Dis 32:103–106CrossRef Dagli A, Zori RT, McCune H, Ivsic T, Maisenbacher MK, Weinstein DA (2009) Reversal of glycogen storage disease type IIIa-related cardiomyopathy with modification of diet. J Inherit Metab Dis 32:103–106CrossRef
go back to reference Heintzman ND (2016) A digital ecosystem of diabetes data and technology: services, systems, and tools anabled by wearables, sensors, and apps. J Diabetes Sci Technol 10:35–41CrossRef Heintzman ND (2016) A digital ecosystem of diabetes data and technology: services, systems, and tools anabled by wearables, sensors, and apps. J Diabetes Sci Technol 10:35–41CrossRef
go back to reference Hershkovitz E, Rachmel A, Ben-Zaken H, Phillip M (2001) Continuous glucose monitoring in children with glycogen storage disease type I. J Inherit Metab Dis 24:863–869CrossRefPubMed Hershkovitz E, Rachmel A, Ben-Zaken H, Phillip M (2001) Continuous glucose monitoring in children with glycogen storage disease type I. J Inherit Metab Dis 24:863–869CrossRefPubMed
go back to reference Ho B, Ueda K, Houben RFA et al (2016) Metabolic diet app suite for inborn errors of amino acid metabolism. Mol Genet Metab 117:322–327CrossRefPubMed Ho B, Ueda K, Houben RFA et al (2016) Metabolic diet app suite for inborn errors of amino acid metabolism. Mol Genet Metab 117:322–327CrossRefPubMed
go back to reference Juvenile Diabetes Research Foundation Continuous Glucose Monitoring Study Group, Tamborlane WV, Beck RW, Bode BW et al (2008) Continuous glucose monitoring and intensive treatment of type 1 diabetes. N Engl J Med 359:1464–1476CrossRef Juvenile Diabetes Research Foundation Continuous Glucose Monitoring Study Group, Tamborlane WV, Beck RW, Bode BW et al (2008) Continuous glucose monitoring and intensive treatment of type 1 diabetes. N Engl J Med 359:1464–1476CrossRef
go back to reference Kasapkara CS, Cinasal Demir G, Hasanoglu A, Tumer L (2014) Continuous glucose monitoring in children with glycogen storage disease type I. Eur J Clin Nutr 68:101–105CrossRefPubMed Kasapkara CS, Cinasal Demir G, Hasanoglu A, Tumer L (2014) Continuous glucose monitoring in children with glycogen storage disease type I. Eur J Clin Nutr 68:101–105CrossRefPubMed
go back to reference Kishnani PS, Austin SL, Arn P et al (2010) Glycogen storage disease type III diagnosis and management guidelines. Genet Med 12:446–463CrossRefPubMed Kishnani PS, Austin SL, Arn P et al (2010) Glycogen storage disease type III diagnosis and management guidelines. Genet Med 12:446–463CrossRefPubMed
go back to reference Kishnani PS, Austin SL, Abdenur JE et al (2014) Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics. Genet Med 128:1–29CrossRef Kishnani PS, Austin SL, Abdenur JE et al (2014) Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics. Genet Med 128:1–29CrossRef
go back to reference Maran A, Crepaldi C, Avogaro A et al (2004) Continuous glucose monitoring in conditions other than diabetes. Diabetes Metab Res Rev 20(Suppl 2):S50–S55CrossRefPubMed Maran A, Crepaldi C, Avogaro A et al (2004) Continuous glucose monitoring in conditions other than diabetes. Diabetes Metab Res Rev 20(Suppl 2):S50–S55CrossRefPubMed
go back to reference Martens DHJ, Rake JP, Navis G, Fidler V, van Dael CML, Smit GPA (2009) Renal function in glycogen storage disease type I, natural course, and renopreservative effects of ACE inhibition. Clin J Am Soc Nephrol 4:1741–1746CrossRefPubMedPubMedCentral Martens DHJ, Rake JP, Navis G, Fidler V, van Dael CML, Smit GPA (2009) Renal function in glycogen storage disease type I, natural course, and renopreservative effects of ACE inhibition. Clin J Am Soc Nephrol 4:1741–1746CrossRefPubMedPubMedCentral
go back to reference Melis D, Pivonello R, Cozzolino M et al (2014) Impaired bone metabolism in glycogen storage disease type 1 is associated with poor metabolic control in type 1a and with granulocyte colony-stimulating factor therapy in type 1b. Horm Res Paediatr 81:55–62CrossRefPubMed Melis D, Pivonello R, Cozzolino M et al (2014) Impaired bone metabolism in glycogen storage disease type 1 is associated with poor metabolic control in type 1a and with granulocyte colony-stimulating factor therapy in type 1b. Horm Res Paediatr 81:55–62CrossRefPubMed
go back to reference Melis D, Cozzolino M, Minopoli GD et al (2015) Progression of renal damage in glycogen storage disease type I is associated to hyperlipidemia: a multicenter prospective Italian study. J Pediatr 166:1079–1082CrossRefPubMed Melis D, Cozzolino M, Minopoli GD et al (2015) Progression of renal damage in glycogen storage disease type I is associated to hyperlipidemia: a multicenter prospective Italian study. J Pediatr 166:1079–1082CrossRefPubMed
go back to reference Moore M (1999) The evolution of telemedicine. Future Gener Comput Syst 15:245–254CrossRef Moore M (1999) The evolution of telemedicine. Future Gener Comput Syst 15:245–254CrossRef
go back to reference National Institute for Public Health and the Environment, RIVM (2012) Dutch food composition table (NEVO). Den Haag, The Netherlands National Institute for Public Health and the Environment, RIVM (2012) Dutch food composition table (NEVO). Den Haag, The Netherlands
go back to reference Okechuku GO, Shoemaker LR, Dambska M, Brown LM, Mathew J, Weinstein DA (2017) Tight metabolic control plus ACE inhibitor therapy improves GSD I nephropathy. J Inherit Metab Dis 40:703–708CrossRefPubMed Okechuku GO, Shoemaker LR, Dambska M, Brown LM, Mathew J, Weinstein DA (2017) Tight metabolic control plus ACE inhibitor therapy improves GSD I nephropathy. J Inherit Metab Dis 40:703–708CrossRefPubMed
go back to reference Rake JP, Visser G, Labrune P, Leonard JV, Ullrich K, Smit GPA (2002a) Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European study on glycogen storage disease type I (ESGSD I). Eur J Pediatr 161:S20–S34CrossRefPubMed Rake JP, Visser G, Labrune P, Leonard JV, Ullrich K, Smit GPA (2002a) Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European study on glycogen storage disease type I (ESGSD I). Eur J Pediatr 161:S20–S34CrossRefPubMed
go back to reference Rake JP, Visser G, Labrune P, Leonard JV, Ullrich K, Smit GPA (2002b) Guidelines for management of glycogen storage disease type I - European study on glycogen storage disease type I (ESGSD I). Eur J Pediatr 161:S112–S119CrossRefPubMed Rake JP, Visser G, Labrune P, Leonard JV, Ullrich K, Smit GPA (2002b) Guidelines for management of glycogen storage disease type I - European study on glycogen storage disease type I (ESGSD I). Eur J Pediatr 161:S112–S119CrossRefPubMed
go back to reference Raposo VL (2016) Telemedicine: the legal framework (or the lack of it) in Europe. GMS Health Technol Assess 12:1–12 Raposo VL (2016) Telemedicine: the legal framework (or the lack of it) in Europe. GMS Health Technol Assess 12:1–12
go back to reference Saliba V, Legido-Quigley H, Hallik R, Aaviksoo A, Car J, McKee M (2012) Telemedicine across borders: a systematic review of factors that hinder or support implementation. Int J Med Informat 81:793–809CrossRef Saliba V, Legido-Quigley H, Hallik R, Aaviksoo A, Car J, McKee M (2012) Telemedicine across borders: a systematic review of factors that hinder or support implementation. Int J Med Informat 81:793–809CrossRef
go back to reference Sentner CP, Caliskan K, Vletter WB, Smit GPA (2012) Heart failure due to severe hypertrophic cardiomyopathy reversed by low calorie, high protein dietary adjustments in a glycogen storage disease type IIIa patient. JIMD reports 5:13–16CrossRefPubMed Sentner CP, Caliskan K, Vletter WB, Smit GPA (2012) Heart failure due to severe hypertrophic cardiomyopathy reversed by low calorie, high protein dietary adjustments in a glycogen storage disease type IIIa patient. JIMD reports 5:13–16CrossRefPubMed
go back to reference Sentner CP, Hoogeveen IJ, Weinstein DA et al (2016) Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome. J Inherit Metab Dis 39:697–704CrossRefPubMedPubMedCentral Sentner CP, Hoogeveen IJ, Weinstein DA et al (2016) Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome. J Inherit Metab Dis 39:697–704CrossRefPubMedPubMedCentral
go back to reference Steinhubl SR, Muse ED, Topol EJ (2015) The emerging field of mobile health. Sci Transl Med 7:1–6CrossRef Steinhubl SR, Muse ED, Topol EJ (2015) The emerging field of mobile health. Sci Transl Med 7:1–6CrossRef
go back to reference Valayannopoulos V, Bajolle F, Arnoux JB et al (2011) Successful treatment of severe cardiomyopathy in glycogen storage disease type III with D,l-3-hydroxybutyrate, ketogenic and high-protein diet. Pediatr Res 70:638–641CrossRefPubMed Valayannopoulos V, Bajolle F, Arnoux JB et al (2011) Successful treatment of severe cardiomyopathy in glycogen storage disease type III with D,l-3-hydroxybutyrate, ketogenic and high-protein diet. Pediatr Res 70:638–641CrossRefPubMed
go back to reference Visser V, Rake JP, Labrune P et al (2002) Consensus guidelines for management of glycogen storage disease type 1b -European study on glycogen storage disease type 1. Eur J Pediatr 161:S120–S123 Visser V, Rake JP, Labrune P et al (2002) Consensus guidelines for management of glycogen storage disease type 1b -European study on glycogen storage disease type 1. Eur J Pediatr 161:S120–S123
go back to reference Walter J, Labrune P, Laforêt P (2016) The glycogen storage diseases and related disorders. In: Saudubray JM, Baumgartner MR, Walter JH (eds) Inborn metabolic diseases: diagnosis and treatment. Springer, Heidelberg, pp 121–138CrossRef Walter J, Labrune P, Laforêt P (2016) The glycogen storage diseases and related disorders. In: Saudubray JM, Baumgartner MR, Walter JH (eds) Inborn metabolic diseases: diagnosis and treatment. Springer, Heidelberg, pp 121–138CrossRef
go back to reference Wang DQ, Fiske LM, Carreras CT, Weinstein DA (2011) Natural history of hepatocellular adenoma formation in glycogen storage disease type I. J Pediatr 159:442–446CrossRefPubMedPubMedCentral Wang DQ, Fiske LM, Carreras CT, Weinstein DA (2011) Natural history of hepatocellular adenoma formation in glycogen storage disease type I. J Pediatr 159:442–446CrossRefPubMedPubMedCentral
go back to reference White FJ, Jones SA (2011) The use of continuous glucose monitoring in the practical management of glycogen storage disorders. J Inherit Metab Dis 34:631–642CrossRefPubMed White FJ, Jones SA (2011) The use of continuous glucose monitoring in the practical management of glycogen storage disorders. J Inherit Metab Dis 34:631–642CrossRefPubMed
go back to reference Wolfsdorf JI, Laffel LMB, Crigler JF Jr (1997) Metabolic control and renal dysfunction in type I glycogen storage disease. J Inherit Metab Dis 20:559–568CrossRefPubMed Wolfsdorf JI, Laffel LMB, Crigler JF Jr (1997) Metabolic control and renal dysfunction in type I glycogen storage disease. J Inherit Metab Dis 20:559–568CrossRefPubMed
Metadata
Title
A preliminary study of telemedicine for patients with hepatic glycogen storage disease and their healthcare providers: from bedside to home site monitoring
Authors
Irene J. Hoogeveen
Fabian Peeks
Foekje de Boer
Charlotte M. A. Lubout
Tom J. de Koning
Sebastiaan te Boekhorst
Robert-Jan Zandvoort
Rob Burghard
Francjan J. van Spronsen
Terry G. J. Derks
Publication date
01-11-2018
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 6/2018
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-018-0167-2

Other articles of this Issue 6/2018

Journal of Inherited Metabolic Disease 6/2018 Go to the issue