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Cyclic Vomiting Syndrome (CVS): is there a difference based on onset of symptoms - pediatric versus adult?

BACKGROUND: Cyclic Vomiting Syndrome (CVS) is a well-recognized functional gastrointestinal disorder in children but its presentation is poorly understood in adults. Genetic differences in pediatric-onset (presentation before age 18) and adult-onset CVS have been reported recently but their clinical...

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Autores principales: Kumar, Nilay, Bashar, Qumseya, Reddy, Naveen, Sengupta, Jyotirmoy, Ananthakrishnan, Ashwin, Schroeder, Abigail, Hogan, Walter J, Venkatesan, Thangam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443054/
https://www.ncbi.nlm.nih.gov/pubmed/22639867
http://dx.doi.org/10.1186/1471-230X-12-52
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author Kumar, Nilay
Bashar, Qumseya
Reddy, Naveen
Sengupta, Jyotirmoy
Ananthakrishnan, Ashwin
Schroeder, Abigail
Hogan, Walter J
Venkatesan, Thangam
author_facet Kumar, Nilay
Bashar, Qumseya
Reddy, Naveen
Sengupta, Jyotirmoy
Ananthakrishnan, Ashwin
Schroeder, Abigail
Hogan, Walter J
Venkatesan, Thangam
author_sort Kumar, Nilay
collection PubMed
description BACKGROUND: Cyclic Vomiting Syndrome (CVS) is a well-recognized functional gastrointestinal disorder in children but its presentation is poorly understood in adults. Genetic differences in pediatric-onset (presentation before age 18) and adult-onset CVS have been reported recently but their clinical features and possible differences in response to therapy have not been well studied. METHODS: This was a retrospective review of 101 CVS patients seen at the Medical College of Wisconsin between 2006 and 2008. Rome III criteria were utilized to make the diagnosis of CVS. RESULTS: Our study population comprised of 29(29%) pediatric-onset and 72 (71%) adult-onset CVS patients. Pediatric-onset CVS patients were more likely to be female (86% vs. 57%, p = 0.005) and had a higher prevalence of CVS plus (CVS + neurocognitive disorders) as compared to adult-onset CVS patients (14% vs. 3%, p = 0.05). There was a longer delay in diagnosis (10 ± 7 years) in the pediatric-onset group when compared to (5 ± 7 years) adult-onset CVS group (p = 0.001). Chronic opiate use was less frequent in the pediatric-onset group compared to adult-onset patients (0% vs. 23%, p = 0.004). Aside from these differences, the two groups were similar with regards to their clinical features and the time of onset of symptoms did not predict response to standard treatment. The majority of patients (86%) responded to treatment with tricyclic antidepressants, anticonvulsants (topiramate), coenzyme Q-10, and L-carnitine. Non-response to therapy was associated with coalescence of symptoms, chronic opiate use and more severe disease as characterized by longer episodes, greater number of emergency department visits in the year prior to presentation, presence of disability and non-compliance on univariate analysis. On multivariate analysis, only compliance to therapy was associated with a response. (88% vs. 38%, Odds Ratio, OR 9.6; 95% Confidence Interval [CI], 1.18-77.05). CONCLUSION: Despite reported genetic differences, the clinical features and response to standard therapy in pediatric- and adult-onset CVS were mostly similar. Most patients (86%) responded to therapy and compliance was the only factor associated with a response.
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spelling pubmed-34430542012-09-15 Cyclic Vomiting Syndrome (CVS): is there a difference based on onset of symptoms - pediatric versus adult? Kumar, Nilay Bashar, Qumseya Reddy, Naveen Sengupta, Jyotirmoy Ananthakrishnan, Ashwin Schroeder, Abigail Hogan, Walter J Venkatesan, Thangam BMC Gastroenterol Research Article BACKGROUND: Cyclic Vomiting Syndrome (CVS) is a well-recognized functional gastrointestinal disorder in children but its presentation is poorly understood in adults. Genetic differences in pediatric-onset (presentation before age 18) and adult-onset CVS have been reported recently but their clinical features and possible differences in response to therapy have not been well studied. METHODS: This was a retrospective review of 101 CVS patients seen at the Medical College of Wisconsin between 2006 and 2008. Rome III criteria were utilized to make the diagnosis of CVS. RESULTS: Our study population comprised of 29(29%) pediatric-onset and 72 (71%) adult-onset CVS patients. Pediatric-onset CVS patients were more likely to be female (86% vs. 57%, p = 0.005) and had a higher prevalence of CVS plus (CVS + neurocognitive disorders) as compared to adult-onset CVS patients (14% vs. 3%, p = 0.05). There was a longer delay in diagnosis (10 ± 7 years) in the pediatric-onset group when compared to (5 ± 7 years) adult-onset CVS group (p = 0.001). Chronic opiate use was less frequent in the pediatric-onset group compared to adult-onset patients (0% vs. 23%, p = 0.004). Aside from these differences, the two groups were similar with regards to their clinical features and the time of onset of symptoms did not predict response to standard treatment. The majority of patients (86%) responded to treatment with tricyclic antidepressants, anticonvulsants (topiramate), coenzyme Q-10, and L-carnitine. Non-response to therapy was associated with coalescence of symptoms, chronic opiate use and more severe disease as characterized by longer episodes, greater number of emergency department visits in the year prior to presentation, presence of disability and non-compliance on univariate analysis. On multivariate analysis, only compliance to therapy was associated with a response. (88% vs. 38%, Odds Ratio, OR 9.6; 95% Confidence Interval [CI], 1.18-77.05). CONCLUSION: Despite reported genetic differences, the clinical features and response to standard therapy in pediatric- and adult-onset CVS were mostly similar. Most patients (86%) responded to therapy and compliance was the only factor associated with a response. BioMed Central 2012-05-28 /pmc/articles/PMC3443054/ /pubmed/22639867 http://dx.doi.org/10.1186/1471-230X-12-52 Text en Copyright ©2012 Kumar et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kumar, Nilay
Bashar, Qumseya
Reddy, Naveen
Sengupta, Jyotirmoy
Ananthakrishnan, Ashwin
Schroeder, Abigail
Hogan, Walter J
Venkatesan, Thangam
Cyclic Vomiting Syndrome (CVS): is there a difference based on onset of symptoms - pediatric versus adult?
title Cyclic Vomiting Syndrome (CVS): is there a difference based on onset of symptoms - pediatric versus adult?
title_full Cyclic Vomiting Syndrome (CVS): is there a difference based on onset of symptoms - pediatric versus adult?
title_fullStr Cyclic Vomiting Syndrome (CVS): is there a difference based on onset of symptoms - pediatric versus adult?
title_full_unstemmed Cyclic Vomiting Syndrome (CVS): is there a difference based on onset of symptoms - pediatric versus adult?
title_short Cyclic Vomiting Syndrome (CVS): is there a difference based on onset of symptoms - pediatric versus adult?
title_sort cyclic vomiting syndrome (cvs): is there a difference based on onset of symptoms - pediatric versus adult?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443054/
https://www.ncbi.nlm.nih.gov/pubmed/22639867
http://dx.doi.org/10.1186/1471-230X-12-52
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