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Dysautonomia rating scales in Parkinson's disease: Sialorrhea, dysphagia, and constipation—Critique and recommendations by movement disorders task force on rating scales for Parkinson's disease

Identifieur interne : 002400 ( Main/Corpus ); précédent : 002399; suivant : 002401

Dysautonomia rating scales in Parkinson's disease: Sialorrhea, dysphagia, and constipation—Critique and recommendations by movement disorders task force on rating scales for Parkinson's disease

Auteurs : Marian L. Evatt ; K. Ray Chaudhuri ; Kelvin L. Chou ; Ester Cubo ; Vanessa Hinson ; Katie Kompoliti ; Chengwu Yang ; Werner Poewe ; Olivier Rascol ; Cristina Sampaio ; Glenn T. Stebbins ; Christopher G. Goetz

Source :

RBID : ISTEX:1641B1C36EBF4F2E524F60EBE418D7142A12993D

English descriptors

Abstract

Upper and lower gastrointestinal dysautonomia symptoms (GIDS)—sialorrhea, dysphagia, and constipation are common in Parkinson's disease (PD) and often socially as well as physically disabling for patients. Available invasive quantitative measures for assessing these symptoms and their response to therapy are time‐consuming, require specialized equipment, can cause patient discomfort and present patients with risk. The Movement Disorders Society commissioned a task force to assess available clinical rating scales, critique their clinimetric properties, and make recommendations regarding their clinical utility. Six clinical researchers and a biostatistician systematically searched the literature for scales of sialorrhea, dysphagia, and constipation, evaluated the scales' previous use, performance parameters, and quality of validation data (if available). A scale was designated “Recommended” if the scale was used in clinical studies beyond the group that developed it, has been specifically used in PD reports, and clinimetric studies have established that it is a valid, reliable, and sensitive. “Suggested” scales met at least part of the above criteria, but fell short of meeting all. Based on the systematic review, scales for individual symptoms of sialorrhea, dysphagia, and constipation were identified along with three global scales that include these symptoms in the context of assessing dysautonomia or nonmotor symptoms. Three sialorrhea scales met criteria for Suggested: Drooling Severity and Frequency Scale (DSFS), Drooling Rating Scale, and Sialorrhea Clinical Scale for PD (SCS‐PD). Two dysphagia scales, the Swallowing Disturbance Questionnaire (SDQ) and Dysphagia‐Specific Quality of Life (SWAL‐QOL), met criteria for Suggested. Although Rome III constipation module is widely accepted in the gastroenterology community, and the earlier version from the Rome II criteria has been used in a single study of PD patients, neither met criteria for Suggested or Recommended. Among the global scales, the Scales for Outcomes in PD‐Autonomic (SCOPA‐AUT) and Nonmotor Symptoms Questionnaire for PD (NMSQuest) both met criteria for Recommended, and the Nonmotor Symptoms Scale (NMSS) met criteria for Suggested; however, none specifically focuses on the target gastrointestinal symptoms (sialorrhea, dysphagia, and constipation) of this report. A very small number of rating scales have been applied to studies of gastrointestinal‐related dysautonomia in PD. Only two scales met “Recommended” criteria and neither focuses specifically on the symptoms of sialorrhea, dysphagia, and constipation. Further scale testing in PD among the scales that focus on these symptoms is warranted, and no new scales are needed until the available scales are fully tested clinimetrically. © 2009 Movement Disorder Society

Url:
DOI: 10.1002/mds.22260

Links to Exploration step

ISTEX:1641B1C36EBF4F2E524F60EBE418D7142A12993D

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<div type="abstract" xml:lang="en">Upper and lower gastrointestinal dysautonomia symptoms (GIDS)—sialorrhea, dysphagia, and constipation are common in Parkinson's disease (PD) and often socially as well as physically disabling for patients. Available invasive quantitative measures for assessing these symptoms and their response to therapy are time‐consuming, require specialized equipment, can cause patient discomfort and present patients with risk. The Movement Disorders Society commissioned a task force to assess available clinical rating scales, critique their clinimetric properties, and make recommendations regarding their clinical utility. Six clinical researchers and a biostatistician systematically searched the literature for scales of sialorrhea, dysphagia, and constipation, evaluated the scales' previous use, performance parameters, and quality of validation data (if available). A scale was designated “Recommended” if the scale was used in clinical studies beyond the group that developed it, has been specifically used in PD reports, and clinimetric studies have established that it is a valid, reliable, and sensitive. “Suggested” scales met at least part of the above criteria, but fell short of meeting all. Based on the systematic review, scales for individual symptoms of sialorrhea, dysphagia, and constipation were identified along with three global scales that include these symptoms in the context of assessing dysautonomia or nonmotor symptoms. Three sialorrhea scales met criteria for Suggested: Drooling Severity and Frequency Scale (DSFS), Drooling Rating Scale, and Sialorrhea Clinical Scale for PD (SCS‐PD). Two dysphagia scales, the Swallowing Disturbance Questionnaire (SDQ) and Dysphagia‐Specific Quality of Life (SWAL‐QOL), met criteria for Suggested. Although Rome III constipation module is widely accepted in the gastroenterology community, and the earlier version from the Rome II criteria has been used in a single study of PD patients, neither met criteria for Suggested or Recommended. Among the global scales, the Scales for Outcomes in PD‐Autonomic (SCOPA‐AUT) and Nonmotor Symptoms Questionnaire for PD (NMSQuest) both met criteria for Recommended, and the Nonmotor Symptoms Scale (NMSS) met criteria for Suggested; however, none specifically focuses on the target gastrointestinal symptoms (sialorrhea, dysphagia, and constipation) of this report. A very small number of rating scales have been applied to studies of gastrointestinal‐related dysautonomia in PD. Only two scales met “Recommended” criteria and neither focuses specifically on the symptoms of sialorrhea, dysphagia, and constipation. Further scale testing in PD among the scales that focus on these symptoms is warranted, and no new scales are needed until the available scales are fully tested clinimetrically. © 2009 Movement Disorder Society</div>
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<note>National Institute of Neurological Disorders and Stroke - No. U01NS043127; No. U01NS043128; No. U10NS44415; No. 44555;</note>
<note>NIA RCMAR - No. 3P30 AG021677‐02S1;</note>
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<p> Additional Supporting Information may be found in the online version of this article. </p>
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<p>Upper and lower gastrointestinal dysautonomia symptoms (GIDS)—sialorrhea, dysphagia, and constipation are common in Parkinson's disease (PD) and often socially as well as physically disabling for patients. Available invasive quantitative measures for assessing these symptoms and their response to therapy are time‐consuming, require specialized equipment, can cause patient discomfort and present patients with risk. The Movement Disorders Society commissioned a task force to assess available clinical rating scales, critique their clinimetric properties, and make recommendations regarding their clinical utility. Six clinical researchers and a biostatistician systematically searched the literature for scales of sialorrhea, dysphagia, and constipation, evaluated the scales' previous use, performance parameters, and quality of validation data (if available). A scale was designated “Recommended” if the scale was used in clinical studies beyond the group that developed it, has been specifically used in PD reports, and clinimetric studies have established that it is a valid, reliable, and sensitive. “Suggested” scales met at least part of the above criteria, but fell short of meeting all. Based on the systematic review, scales for individual symptoms of sialorrhea, dysphagia, and constipation were identified along with three global scales that include these symptoms in the context of assessing dysautonomia or nonmotor symptoms. Three sialorrhea scales met criteria for Suggested: Drooling Severity and Frequency Scale (DSFS), Drooling Rating Scale, and Sialorrhea Clinical Scale for PD (SCS‐PD). Two dysphagia scales, the Swallowing Disturbance Questionnaire (SDQ) and Dysphagia‐Specific Quality of Life (SWAL‐QOL), met criteria for Suggested. Although Rome III constipation module is widely accepted in the gastroenterology community, and the earlier version from the Rome II criteria has been used in a single study of PD patients, neither met criteria for Suggested or Recommended. Among the global scales, the Scales for Outcomes in PD‐Autonomic (SCOPA‐AUT) and Nonmotor Symptoms Questionnaire for PD (NMSQuest) both met criteria for Recommended, and the Nonmotor Symptoms Scale (NMSS) met criteria for Suggested; however, none specifically focuses on the target gastrointestinal symptoms (sialorrhea, dysphagia, and constipation) of this report. A very small number of rating scales have been applied to studies of gastrointestinal‐related dysautonomia in PD. Only two scales met “Recommended” criteria and neither focuses specifically on the symptoms of sialorrhea, dysphagia, and constipation. Further scale testing in PD among the scales that focus on these symptoms is warranted, and no new scales are needed until the available scales are fully tested clinimetrically. © 2009 Movement Disorder Society</p>
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<p>Potential conflict of interest: MLE has received honoraium for consultant services and/or speaking engagements from UCB Pharma, Solstice, Allergan. She serves on a clinical trial steering committee for Solstice and has received research support from Merz, Ipsen, Boeringer‐Ingelhiem, Santhera and Schwarz (UCB). KRC has received honorarium for sponsored symposiums in international and national meetings from Boehringer‐Ingelheim, UCB Pharma, Solvay, Britannia and GSK Pharmaceuticals. He also serves in the advisory board for the above companies in addition to Lundbeck. KLC has received honoraria or research support in the past 3 years from Teva, GSK, Boehringer‐Ingelheim, Novartis, and Solstice Neurosciences.</p>
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<affiliation>National Parkinson Foundation Centre of Excellence, Kings College Hospital, Institute of Psychiatry, London, United Kingdom</affiliation>
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<name type="personal">
<namePart type="given">Kelvin L.</namePart>
<namePart type="family">Chou</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Neurology, University of Michigan Medical School, Ann Arbor, Michigan, USA</affiliation>
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<name type="personal">
<namePart type="given">Ester</namePart>
<namePart type="family">Cubo</namePart>
<namePart type="termsOfAddress">MD, PhD</namePart>
<affiliation>Neurology Department, Hospital General Yagüe, Burgos, Spain</affiliation>
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<name type="personal">
<namePart type="given">Vanessa</namePart>
<namePart type="family">Hinson</namePart>
<namePart type="termsOfAddress">MD, PhD</namePart>
<affiliation>Department of Neurosciences, Medical University of South Carolina, Charleston, South Carolina, USA</affiliation>
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<name type="personal">
<namePart type="given">Katie</namePart>
<namePart type="family">Kompoliti</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Neurological Services, Rush University School of Medicine, Chicago, Illinois, USA</affiliation>
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<namePart type="given">Chengwu</namePart>
<namePart type="family">Yang</namePart>
<namePart type="termsOfAddress">MS, PhD</namePart>
<affiliation>Department of Neurosciences, Medical University of South Carolina, Charleston, South Carolina, USA</affiliation>
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<namePart type="given">Werner</namePart>
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<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Biostatistics, Medical University of South Carolina, Charleston, South Carolina, USA</affiliation>
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<namePart type="given">Olivier</namePart>
<namePart type="family">Rascol</namePart>
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<affiliation>Department of Neurology, University Hospital, Innsbruck, Austria</affiliation>
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<namePart type="termsOfAddress">MD, PhD</namePart>
<affiliation>Laboratoire de Pharmacologie Médicale et Clinique, Toulouse, France</affiliation>
<affiliation>Laboratory of Clinical Pharmacology and Therapeutics, Lisbon School of Medicine, Lisbon, Portugal</affiliation>
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<namePart type="given">Glenn T.</namePart>
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<affiliation>Department of Neurological Services, Rush University School of Medicine, Chicago, Illinois, USA</affiliation>
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<name type="personal">
<namePart type="given">Christopher G.</namePart>
<namePart type="family">Goetz</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Neurological Services, Rush University School of Medicine, Chicago, Illinois, USA</affiliation>
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<dateIssued encoding="w3cdtf">2009-04-15</dateIssued>
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<abstract lang="en">Upper and lower gastrointestinal dysautonomia symptoms (GIDS)—sialorrhea, dysphagia, and constipation are common in Parkinson's disease (PD) and often socially as well as physically disabling for patients. Available invasive quantitative measures for assessing these symptoms and their response to therapy are time‐consuming, require specialized equipment, can cause patient discomfort and present patients with risk. The Movement Disorders Society commissioned a task force to assess available clinical rating scales, critique their clinimetric properties, and make recommendations regarding their clinical utility. Six clinical researchers and a biostatistician systematically searched the literature for scales of sialorrhea, dysphagia, and constipation, evaluated the scales' previous use, performance parameters, and quality of validation data (if available). A scale was designated “Recommended” if the scale was used in clinical studies beyond the group that developed it, has been specifically used in PD reports, and clinimetric studies have established that it is a valid, reliable, and sensitive. “Suggested” scales met at least part of the above criteria, but fell short of meeting all. Based on the systematic review, scales for individual symptoms of sialorrhea, dysphagia, and constipation were identified along with three global scales that include these symptoms in the context of assessing dysautonomia or nonmotor symptoms. Three sialorrhea scales met criteria for Suggested: Drooling Severity and Frequency Scale (DSFS), Drooling Rating Scale, and Sialorrhea Clinical Scale for PD (SCS‐PD). Two dysphagia scales, the Swallowing Disturbance Questionnaire (SDQ) and Dysphagia‐Specific Quality of Life (SWAL‐QOL), met criteria for Suggested. Although Rome III constipation module is widely accepted in the gastroenterology community, and the earlier version from the Rome II criteria has been used in a single study of PD patients, neither met criteria for Suggested or Recommended. Among the global scales, the Scales for Outcomes in PD‐Autonomic (SCOPA‐AUT) and Nonmotor Symptoms Questionnaire for PD (NMSQuest) both met criteria for Recommended, and the Nonmotor Symptoms Scale (NMSS) met criteria for Suggested; however, none specifically focuses on the target gastrointestinal symptoms (sialorrhea, dysphagia, and constipation) of this report. A very small number of rating scales have been applied to studies of gastrointestinal‐related dysautonomia in PD. Only two scales met “Recommended” criteria and neither focuses specifically on the symptoms of sialorrhea, dysphagia, and constipation. Further scale testing in PD among the scales that focus on these symptoms is warranted, and no new scales are needed until the available scales are fully tested clinimetrically. © 2009 Movement Disorder Society</abstract>
<note type="content">*Potential conflict of interest: MLE has received honoraium for consultant services and/or speaking engagements from UCB Pharma, Solstice, Allergan. She serves on a clinical trial steering committee for Solstice and has received research support from Merz, Ipsen, Boeringer‐Ingelhiem, Santhera and Schwarz (UCB). KRC has received honorarium for sponsored symposiums in international and national meetings from Boehringer‐Ingelheim, UCB Pharma, Solvay, Britannia and GSK Pharmaceuticals. He also serves in the advisory board for the above companies in addition to Lundbeck. KLC has received honoraria or research support in the past 3 years from Teva, GSK, Boehringer‐Ingelheim, Novartis, and Solstice Neurosciences.</note>
<note type="funding">NIH</note>
<note type="funding">National Institute of Neurological Disorders and Stroke - No. U01NS043127; No. U01NS043128; No. U10NS44415; No. 44555; </note>
<note type="funding">NIA RCMAR - No. 3P30 AG021677‐02S1; </note>
<subject lang="en">
<genre>Keywords</genre>
<topic>sialorrhea</topic>
<topic>constipation</topic>
<topic>dysphagia</topic>
<topic>rating scales</topic>
<topic>Parkinson's disease</topic>
<topic>gastrointestinal dysautonomia</topic>
</subject>
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<titleInfo>
<title>Movement Disorders</title>
<subTitle>Official Journal of the Movement Disorder Society</subTitle>
</titleInfo>
<titleInfo type="abbreviated">
<title>Mov. Disord.</title>
</titleInfo>
<genre type="Journal">journal</genre>
<note type="content"> Additional Supporting Information may be found in the online version of this article.Supporting Info Item: Evaluation Flow Diagram - Detailed Methods for Evaluation of Clinimetric properties - Scales not critiqued/reason excluded - Drooling Severity and Frequency Scale (DSFS) - Drooling Rating Scale - Sialorrhea Clinical Scale for PD (SCS‐PD) - Swallowing Disturbance Questionnaire (SDQ) - Scale for Dysphagia‐Related Outcomes Quality of Life (SWAL‐QOL) - The SWAL‐QOL Survey - </note>
<subject>
<genre>article category</genre>
<topic>Review</topic>
</subject>
<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
<identifier type="PublisherID">MDS</identifier>
<part>
<date>2009</date>
<detail type="volume">
<caption>vol.</caption>
<number>24</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>5</number>
</detail>
<extent unit="pages">
<start>635</start>
<end>646</end>
<total>12</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">1641B1C36EBF4F2E524F60EBE418D7142A12993D</identifier>
<identifier type="DOI">10.1002/mds.22260</identifier>
<identifier type="ArticleID">MDS22260</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2009 Movement Disorder Society</accessCondition>
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