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Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study
BACKGROUND: Tuberous sclerosis complex (TSC), a multisystem genetic disorder, affects many organs and systems, characterized by benign growths. This German multicenter study estimated the disease-specific costs and cost-driving factors associated with various organ manifestations in TSC patients. ME...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8218507/ https://www.ncbi.nlm.nih.gov/pubmed/34154622 http://dx.doi.org/10.1186/s13023-021-01899-x |
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author | Grau, Janina Zöllner, Johann Philipp Schubert-Bast, Susanne Kurlemann, Gerhard Hertzberg, Christoph Wiemer-Kruel, Adelheid Bast, Thomas Bertsche, Astrid Bettendorf, Ulrich Fiedler, Barbara Hahn, Andreas Hartmann, Hans Hornemann, Frauke Immisch, Ilka Jacobs, Julia Kieslich, Matthias Klein, Karl Martin Klotz, Kerstin A. Kluger, Gerhard Knuf, Markus Mayer, Thomas Marquard, Klaus Meyer, Sascha Muhle, Hiltrud Müller-Schlüter, Karen Noda, Anna H. Ruf, Susanne Sauter, Matthias Schlump, Jan-Ulrich Syrbe, Steffen Thiels, Charlotte Trollmann, Regina Wilken, Bernd Willems, Laurent M. Rosenow, Felix Strzelczyk, Adam |
author_facet | Grau, Janina Zöllner, Johann Philipp Schubert-Bast, Susanne Kurlemann, Gerhard Hertzberg, Christoph Wiemer-Kruel, Adelheid Bast, Thomas Bertsche, Astrid Bettendorf, Ulrich Fiedler, Barbara Hahn, Andreas Hartmann, Hans Hornemann, Frauke Immisch, Ilka Jacobs, Julia Kieslich, Matthias Klein, Karl Martin Klotz, Kerstin A. Kluger, Gerhard Knuf, Markus Mayer, Thomas Marquard, Klaus Meyer, Sascha Muhle, Hiltrud Müller-Schlüter, Karen Noda, Anna H. Ruf, Susanne Sauter, Matthias Schlump, Jan-Ulrich Syrbe, Steffen Thiels, Charlotte Trollmann, Regina Wilken, Bernd Willems, Laurent M. Rosenow, Felix Strzelczyk, Adam |
author_sort | Grau, Janina |
collection | PubMed |
description | BACKGROUND: Tuberous sclerosis complex (TSC), a multisystem genetic disorder, affects many organs and systems, characterized by benign growths. This German multicenter study estimated the disease-specific costs and cost-driving factors associated with various organ manifestations in TSC patients. METHODS: A validated, three-month, retrospective questionnaire was administered to assess the sociodemographic and clinical characteristics, organ manifestations, direct, indirect, out-of-pocket, and nursing care-level costs, completed by caregivers of patients with TSC throughout Germany. RESULTS: The caregivers of 184 patients (mean age 9.8 ± 5.3 years, range 0.7–21.8 years) submitted questionnaires. The reported TSC disease manifestations included epilepsy (92%), skin disorders (86%), structural brain disorders (83%), heart and circulatory system disorders (67%), kidney and urinary tract disorders (53%), and psychiatric disorders (51%). Genetic variations in TSC2 were reported in 46% of patients, whereas 14% were reported in TSC1. Mean total direct health care costs were EUR 4949 [95% confidence interval (95% CI) EUR 4088–5863, median EUR 2062] per patient over three months. Medication costs represented the largest direct cost category (54% of total direct costs, mean EUR 2658), with mechanistic target of rapamycin (mTOR) inhibitors representing the largest share (47%, EUR 2309). The cost of anti-seizure drugs (ASDs) accounted for a mean of only EUR 260 (5%). Inpatient costs (21%, EUR 1027) and ancillary therapy costs (8%, EUR 407) were also important direct cost components. The mean nursing care-level costs were EUR 1163 (95% CI EUR 1027–1314, median EUR 1635) over three months. Total indirect costs totaled a mean of EUR 2813 (95% CI EUR 2221–3394, median EUR 215) for mothers and EUR 372 (95% CI EUR 193–586, median EUR 0) for fathers. Multiple regression analyses revealed polytherapy with two or more ASDs and the use of mTOR inhibitors as independent cost-driving factors of total direct costs. Disability and psychiatric disease were independent cost-driving factors for total indirect costs as well as for nursing care-level costs. CONCLUSIONS: This study revealed substantial direct (including medication), nursing care-level, and indirect costs associated with TSC over three months, highlighting the spectrum of organ manifestations and their treatment needs in the German healthcare setting. Trial registration: DRKS, DRKS00016045. Registered 01 March 2019, http://www.drks.de/DRKS00016045. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-021-01899-x. |
format | Online Article Text |
id | pubmed-8218507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82185072021-06-23 Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study Grau, Janina Zöllner, Johann Philipp Schubert-Bast, Susanne Kurlemann, Gerhard Hertzberg, Christoph Wiemer-Kruel, Adelheid Bast, Thomas Bertsche, Astrid Bettendorf, Ulrich Fiedler, Barbara Hahn, Andreas Hartmann, Hans Hornemann, Frauke Immisch, Ilka Jacobs, Julia Kieslich, Matthias Klein, Karl Martin Klotz, Kerstin A. Kluger, Gerhard Knuf, Markus Mayer, Thomas Marquard, Klaus Meyer, Sascha Muhle, Hiltrud Müller-Schlüter, Karen Noda, Anna H. Ruf, Susanne Sauter, Matthias Schlump, Jan-Ulrich Syrbe, Steffen Thiels, Charlotte Trollmann, Regina Wilken, Bernd Willems, Laurent M. Rosenow, Felix Strzelczyk, Adam Orphanet J Rare Dis Research BACKGROUND: Tuberous sclerosis complex (TSC), a multisystem genetic disorder, affects many organs and systems, characterized by benign growths. This German multicenter study estimated the disease-specific costs and cost-driving factors associated with various organ manifestations in TSC patients. METHODS: A validated, three-month, retrospective questionnaire was administered to assess the sociodemographic and clinical characteristics, organ manifestations, direct, indirect, out-of-pocket, and nursing care-level costs, completed by caregivers of patients with TSC throughout Germany. RESULTS: The caregivers of 184 patients (mean age 9.8 ± 5.3 years, range 0.7–21.8 years) submitted questionnaires. The reported TSC disease manifestations included epilepsy (92%), skin disorders (86%), structural brain disorders (83%), heart and circulatory system disorders (67%), kidney and urinary tract disorders (53%), and psychiatric disorders (51%). Genetic variations in TSC2 were reported in 46% of patients, whereas 14% were reported in TSC1. Mean total direct health care costs were EUR 4949 [95% confidence interval (95% CI) EUR 4088–5863, median EUR 2062] per patient over three months. Medication costs represented the largest direct cost category (54% of total direct costs, mean EUR 2658), with mechanistic target of rapamycin (mTOR) inhibitors representing the largest share (47%, EUR 2309). The cost of anti-seizure drugs (ASDs) accounted for a mean of only EUR 260 (5%). Inpatient costs (21%, EUR 1027) and ancillary therapy costs (8%, EUR 407) were also important direct cost components. The mean nursing care-level costs were EUR 1163 (95% CI EUR 1027–1314, median EUR 1635) over three months. Total indirect costs totaled a mean of EUR 2813 (95% CI EUR 2221–3394, median EUR 215) for mothers and EUR 372 (95% CI EUR 193–586, median EUR 0) for fathers. Multiple regression analyses revealed polytherapy with two or more ASDs and the use of mTOR inhibitors as independent cost-driving factors of total direct costs. Disability and psychiatric disease were independent cost-driving factors for total indirect costs as well as for nursing care-level costs. CONCLUSIONS: This study revealed substantial direct (including medication), nursing care-level, and indirect costs associated with TSC over three months, highlighting the spectrum of organ manifestations and their treatment needs in the German healthcare setting. Trial registration: DRKS, DRKS00016045. Registered 01 March 2019, http://www.drks.de/DRKS00016045. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-021-01899-x. BioMed Central 2021-06-21 /pmc/articles/PMC8218507/ /pubmed/34154622 http://dx.doi.org/10.1186/s13023-021-01899-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Grau, Janina Zöllner, Johann Philipp Schubert-Bast, Susanne Kurlemann, Gerhard Hertzberg, Christoph Wiemer-Kruel, Adelheid Bast, Thomas Bertsche, Astrid Bettendorf, Ulrich Fiedler, Barbara Hahn, Andreas Hartmann, Hans Hornemann, Frauke Immisch, Ilka Jacobs, Julia Kieslich, Matthias Klein, Karl Martin Klotz, Kerstin A. Kluger, Gerhard Knuf, Markus Mayer, Thomas Marquard, Klaus Meyer, Sascha Muhle, Hiltrud Müller-Schlüter, Karen Noda, Anna H. Ruf, Susanne Sauter, Matthias Schlump, Jan-Ulrich Syrbe, Steffen Thiels, Charlotte Trollmann, Regina Wilken, Bernd Willems, Laurent M. Rosenow, Felix Strzelczyk, Adam Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study |
title | Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study |
title_full | Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study |
title_fullStr | Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study |
title_full_unstemmed | Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study |
title_short | Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study |
title_sort | direct and indirect costs and cost-driving factors of tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8218507/ https://www.ncbi.nlm.nih.gov/pubmed/34154622 http://dx.doi.org/10.1186/s13023-021-01899-x |
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