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Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus

OBJECTIVE: To develop standardization for nomenclature, diagnostic work up and diagnostic criteria for cases of neurocognitive regression in Down syndrome. BACKGROUND: There are no consensus criteria for the evaluation or diagnosis of neurocognitive regression in persons with Down syndrome. As such,...

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Autores principales: Santoro, Jonathan D., Patel, Lina, Kammeyer, Ryan, Filipink, Robyn A., Gombolay, Grace Y., Cardinale, Kathleen M., Real de Asua, Diego, Zaman, Shahid, Santoro, Stephanie L., Marzouk, Sammer M., Khoshnood, Mellad, Vogel, Benjamin N., Tanna, Runi, Pagarkar, Dania, Dhanani, Sofia, Ortega, Maria del Carmen, Partridge, Rebecca, Stanley, Maria A., Sanders, Jessica S., Christy, Alison, Sannar, Elise M., Brown, Ruth, McCormick, Andrew A., Van Mater, Heather, Franklin, Cathy, Worley, Gordon, Quinn, Eileen A., Capone, George T., Chicoine, Brian, Skotko, Brian G., Rafii, Michael S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335003/
https://www.ncbi.nlm.nih.gov/pubmed/35911905
http://dx.doi.org/10.3389/fneur.2022.940175
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author Santoro, Jonathan D.
Patel, Lina
Kammeyer, Ryan
Filipink, Robyn A.
Gombolay, Grace Y.
Cardinale, Kathleen M.
Real de Asua, Diego
Zaman, Shahid
Santoro, Stephanie L.
Marzouk, Sammer M.
Khoshnood, Mellad
Vogel, Benjamin N.
Tanna, Runi
Pagarkar, Dania
Dhanani, Sofia
Ortega, Maria del Carmen
Partridge, Rebecca
Stanley, Maria A.
Sanders, Jessica S.
Christy, Alison
Sannar, Elise M.
Brown, Ruth
McCormick, Andrew A.
Van Mater, Heather
Franklin, Cathy
Worley, Gordon
Quinn, Eileen A.
Capone, George T.
Chicoine, Brian
Skotko, Brian G.
Rafii, Michael S.
author_facet Santoro, Jonathan D.
Patel, Lina
Kammeyer, Ryan
Filipink, Robyn A.
Gombolay, Grace Y.
Cardinale, Kathleen M.
Real de Asua, Diego
Zaman, Shahid
Santoro, Stephanie L.
Marzouk, Sammer M.
Khoshnood, Mellad
Vogel, Benjamin N.
Tanna, Runi
Pagarkar, Dania
Dhanani, Sofia
Ortega, Maria del Carmen
Partridge, Rebecca
Stanley, Maria A.
Sanders, Jessica S.
Christy, Alison
Sannar, Elise M.
Brown, Ruth
McCormick, Andrew A.
Van Mater, Heather
Franklin, Cathy
Worley, Gordon
Quinn, Eileen A.
Capone, George T.
Chicoine, Brian
Skotko, Brian G.
Rafii, Michael S.
author_sort Santoro, Jonathan D.
collection PubMed
description OBJECTIVE: To develop standardization for nomenclature, diagnostic work up and diagnostic criteria for cases of neurocognitive regression in Down syndrome. BACKGROUND: There are no consensus criteria for the evaluation or diagnosis of neurocognitive regression in persons with Down syndrome. As such, previously published data on this condition is relegated to smaller case series with heterogenous data sets. Lack of standardized assessment tools has slowed research in this clinical area. METHODS: The authors performed a two-round traditional Delphi method survey of an international group of clinicians with experience in treating Down syndrome to develop a standardized approach to clinical care and research in this area. Thirty-eight potential panelists who had either previously published on neurocognitive regression in Down syndrome or were involved in national or international working groups on this condition were invited to participate. In total, 27 panelists (71%) represented nine medical specialties and six different countries reached agreement on preliminary standards in this disease area. Moderators developed a proposed nomenclature, diagnostic work up and diagnostic criteria based on previously published reports of regression in persons with Down syndrome. RESULTS: During the first round of survey, agreement on nomenclature for the condition was reached with 78% of panelists agreeing to use the term Down Syndrome Regression Disorder (DSRD). Agreement on diagnostic work up and diagnostic criteria was not reach on the first round due to low agreement amongst panelists with regards to the need for neurodiagnostic testing. Following incorporation of panelist feedback, diagnostic criteria were agreed upon (96% agreement on neuroimaging, 100% agreement on bloodwork, 88% agreement on lumbar puncture, 100% agreement on urine studies, and 96% agreement on “other” studies) as were diagnostic criteria (96% agreement). CONCLUSIONS: The authors present international consensus agreement on the nomenclature, diagnostic work up, and diagnostic criteria for DSRD, providing an initial practical framework that can advance both research and clinical practices for this condition.
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spelling pubmed-93350032022-07-30 Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus Santoro, Jonathan D. Patel, Lina Kammeyer, Ryan Filipink, Robyn A. Gombolay, Grace Y. Cardinale, Kathleen M. Real de Asua, Diego Zaman, Shahid Santoro, Stephanie L. Marzouk, Sammer M. Khoshnood, Mellad Vogel, Benjamin N. Tanna, Runi Pagarkar, Dania Dhanani, Sofia Ortega, Maria del Carmen Partridge, Rebecca Stanley, Maria A. Sanders, Jessica S. Christy, Alison Sannar, Elise M. Brown, Ruth McCormick, Andrew A. Van Mater, Heather Franklin, Cathy Worley, Gordon Quinn, Eileen A. Capone, George T. Chicoine, Brian Skotko, Brian G. Rafii, Michael S. Front Neurol Neurology OBJECTIVE: To develop standardization for nomenclature, diagnostic work up and diagnostic criteria for cases of neurocognitive regression in Down syndrome. BACKGROUND: There are no consensus criteria for the evaluation or diagnosis of neurocognitive regression in persons with Down syndrome. As such, previously published data on this condition is relegated to smaller case series with heterogenous data sets. Lack of standardized assessment tools has slowed research in this clinical area. METHODS: The authors performed a two-round traditional Delphi method survey of an international group of clinicians with experience in treating Down syndrome to develop a standardized approach to clinical care and research in this area. Thirty-eight potential panelists who had either previously published on neurocognitive regression in Down syndrome or were involved in national or international working groups on this condition were invited to participate. In total, 27 panelists (71%) represented nine medical specialties and six different countries reached agreement on preliminary standards in this disease area. Moderators developed a proposed nomenclature, diagnostic work up and diagnostic criteria based on previously published reports of regression in persons with Down syndrome. RESULTS: During the first round of survey, agreement on nomenclature for the condition was reached with 78% of panelists agreeing to use the term Down Syndrome Regression Disorder (DSRD). Agreement on diagnostic work up and diagnostic criteria was not reach on the first round due to low agreement amongst panelists with regards to the need for neurodiagnostic testing. Following incorporation of panelist feedback, diagnostic criteria were agreed upon (96% agreement on neuroimaging, 100% agreement on bloodwork, 88% agreement on lumbar puncture, 100% agreement on urine studies, and 96% agreement on “other” studies) as were diagnostic criteria (96% agreement). CONCLUSIONS: The authors present international consensus agreement on the nomenclature, diagnostic work up, and diagnostic criteria for DSRD, providing an initial practical framework that can advance both research and clinical practices for this condition. Frontiers Media S.A. 2022-07-15 /pmc/articles/PMC9335003/ /pubmed/35911905 http://dx.doi.org/10.3389/fneur.2022.940175 Text en Copyright © 2022 Santoro, Patel, Kammeyer, Filipink, Gombolay, Cardinale, Real de Asua, Zaman, Santoro, Marzouk, Khoshnood, Vogel, Tanna, Pagarkar, Dhanani, Ortega, Partridge, Stanley, Sanders, Christy, Sannar, Brown, McCormick, Van Mater, Franklin, Worley, Quinn, Capone, Chicoine, Skotko and Rafii. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Santoro, Jonathan D.
Patel, Lina
Kammeyer, Ryan
Filipink, Robyn A.
Gombolay, Grace Y.
Cardinale, Kathleen M.
Real de Asua, Diego
Zaman, Shahid
Santoro, Stephanie L.
Marzouk, Sammer M.
Khoshnood, Mellad
Vogel, Benjamin N.
Tanna, Runi
Pagarkar, Dania
Dhanani, Sofia
Ortega, Maria del Carmen
Partridge, Rebecca
Stanley, Maria A.
Sanders, Jessica S.
Christy, Alison
Sannar, Elise M.
Brown, Ruth
McCormick, Andrew A.
Van Mater, Heather
Franklin, Cathy
Worley, Gordon
Quinn, Eileen A.
Capone, George T.
Chicoine, Brian
Skotko, Brian G.
Rafii, Michael S.
Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus
title Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus
title_full Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus
title_fullStr Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus
title_full_unstemmed Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus
title_short Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus
title_sort assessment and diagnosis of down syndrome regression disorder: international expert consensus
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335003/
https://www.ncbi.nlm.nih.gov/pubmed/35911905
http://dx.doi.org/10.3389/fneur.2022.940175
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