AustralieFrV1, PubMed, Corpus, bibRecord, 001B84

Pain in Fabry Disease: Practical Recommendations for Diagnosis and Treatment.

Identifieur interne : 001B84 ( PubMed/Corpus ); précédent : 001B83; suivant : 001B85

Pain in Fabry Disease: Practical Recommendations for Diagnosis and Treatment.

Auteurs : Juan M. Politei ; Didier Bouhassira ; Dominique P. Germain ; Cyril Goizet ; Antonio Guerrero-Sola ; Max J. Hilz ; Elspeth J. Hutton ; Amel Karaa ; Rocco Liguori ; Nurcan Üçeyler ; Lonnie K. Zeltzer ; Alessandro Burlina

Source :

CNS neuroscience & therapeutics [ 1755-5949 ] ; 2016.

RBID : pubmed:27297686

English descriptors

KwdEn :
- Analgesics, Non-Narcotic (therapeutic use), Anti-Inflammatory Agents, Non-Steroidal (therapeutic use), Diagnosis, Differential, Enzyme Replacement Therapy, Fabry Disease (complications), Fabry Disease (pathology), Fabry Disease (therapy), Female, Ganglia, Spinal (pathology), Humans, Life Style, Male, Pain (diagnosis), Pain (etiology), Pain Management (methods), Pain Measurement, Surveys and Questionnaires.
MESH :
- chemical , therapeutic use : Analgesics, Non-Narcotic, Anti-Inflammatory Agents, Non-Steroidal.
- complications : Fabry Disease.
- diagnosis : Pain.
- etiology : Pain.
- methods : Pain Management.
- pathology : Fabry Disease, Ganglia, Spinal.
- therapy : Fabry Disease.
- Diagnosis, Differential, Enzyme Replacement Therapy, Female, Humans, Life Style, Male, Pain Measurement, Surveys and Questionnaires.

Abstract

Patients with Fabry disease (FD) characteristically develop peripheral neuropathy at an early age, with pain being a crucial symptom of underlying pathology. However, the diagnosis of pain is challenging due to the heterogeneous and nonspecific symptoms. Practical guidance on the diagnosis and management of pain in FD is needed.

DOI: 10.1111/cns.12542
PubMed: 27297686

Links to Exploration step

pubmed:27297686

Le document en format XML

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<author><name sortKey="Bouhassira, Didier" sort="Bouhassira, Didier" uniqKey="Bouhassira D" first="Didier" last="Bouhassira">Didier Bouhassira</name>
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<author><name sortKey="Germain, Dominique P" sort="Germain, Dominique P" uniqKey="Germain D" first="Dominique P" last="Germain">Dominique P. Germain</name>
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<author><name sortKey="Guerrero Sola, Antonio" sort="Guerrero Sola, Antonio" uniqKey="Guerrero Sola A" first="Antonio" last="Guerrero-Sola">Antonio Guerrero-Sola</name>
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<author><name sortKey="Hilz, Max J" sort="Hilz, Max J" uniqKey="Hilz M" first="Max J" last="Hilz">Max J. Hilz</name>
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<author><name sortKey="Hutton, Elspeth J" sort="Hutton, Elspeth J" uniqKey="Hutton E" first="Elspeth J" last="Hutton">Elspeth J. Hutton</name>
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<author><name sortKey="Liguori, Rocco" sort="Liguori, Rocco" uniqKey="Liguori R" first="Rocco" last="Liguori">Rocco Liguori</name>
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<author><name sortKey="Uceyler, Nurcan" sort="Uceyler, Nurcan" uniqKey="Uceyler N" first="Nurcan" last="Üçeyler">Nurcan Üçeyler</name>
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</affiliation>
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<author><name sortKey="Zeltzer, Lonnie K" sort="Zeltzer, Lonnie K" uniqKey="Zeltzer L" first="Lonnie K" last="Zeltzer">Lonnie K. Zeltzer</name>
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</affiliation>
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<author><name sortKey="Burlina, Alessandro" sort="Burlina, Alessandro" uniqKey="Burlina A" first="Alessandro" last="Burlina">Alessandro Burlina</name>
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<author><name sortKey="Germain, Dominique P" sort="Germain, Dominique P" uniqKey="Germain D" first="Dominique P" last="Germain">Dominique P. Germain</name>
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</affiliation>
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<author><name sortKey="Hilz, Max J" sort="Hilz, Max J" uniqKey="Hilz M" first="Max J" last="Hilz">Max J. Hilz</name>
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</affiliation>
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<author><name sortKey="Hutton, Elspeth J" sort="Hutton, Elspeth J" uniqKey="Hutton E" first="Elspeth J" last="Hutton">Elspeth J. Hutton</name>
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</affiliation>
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<author><name sortKey="Liguori, Rocco" sort="Liguori, Rocco" uniqKey="Liguori R" first="Rocco" last="Liguori">Rocco Liguori</name>
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</affiliation>
</author>
<author><name sortKey="Uceyler, Nurcan" sort="Uceyler, Nurcan" uniqKey="Uceyler N" first="Nurcan" last="Üçeyler">Nurcan Üçeyler</name>
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</affiliation>
</author>
<author><name sortKey="Zeltzer, Lonnie K" sort="Zeltzer, Lonnie K" uniqKey="Zeltzer L" first="Lonnie K" last="Zeltzer">Lonnie K. Zeltzer</name>
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</affiliation>
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<author><name sortKey="Burlina, Alessandro" sort="Burlina, Alessandro" uniqKey="Burlina A" first="Alessandro" last="Burlina">Alessandro Burlina</name>
<affiliation><nlm:affiliation>Neurological Unit, St Bassiano Hospital, Bassano del Grappa, Italy.</nlm:affiliation>
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<term>Diagnosis, Differential</term>
<term>Enzyme Replacement Therapy</term>
<term>Fabry Disease (complications)</term>
<term>Fabry Disease (pathology)</term>
<term>Fabry Disease (therapy)</term>
<term>Female</term>
<term>Ganglia, Spinal (pathology)</term>
<term>Humans</term>
<term>Life Style</term>
<term>Male</term>
<term>Pain (diagnosis)</term>
<term>Pain (etiology)</term>
<term>Pain Management (methods)</term>
<term>Pain Measurement</term>
<term>Surveys and Questionnaires</term>
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<term>Anti-Inflammatory Agents, Non-Steroidal</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Fabry Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Pain</term>
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<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Pain</term>
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<term>Ganglia, Spinal</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Fabry Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Diagnosis, Differential</term>
<term>Enzyme Replacement Therapy</term>
<term>Female</term>
<term>Humans</term>
<term>Life Style</term>
<term>Male</term>
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<front><div type="abstract" xml:lang="en">Patients with Fabry disease (FD) characteristically develop peripheral neuropathy at an early age, with pain being a crucial symptom of underlying pathology. However, the diagnosis of pain is challenging due to the heterogeneous and nonspecific symptoms. Practical guidance on the diagnosis and management of pain in FD is needed.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">27297686</PMID>
<DateCreated><Year>2016</Year>
<Month>06</Month>
<Day>14</Day>
</DateCreated>
<DateCompleted><Year>2017</Year>
<Month>04</Month>
<Day>17</Day>
</DateCompleted>
<DateRevised><Year>2017</Year>
<Month>04</Month>
<Day>17</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1755-5949</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>22</Volume>
<Issue>7</Issue>
<PubDate><Year>2016</Year>
<Month>07</Month>
</PubDate>
</JournalIssue>
<Title>CNS neuroscience & therapeutics</Title>
<ISOAbbreviation>CNS Neurosci Ther</ISOAbbreviation>
</Journal>
<ArticleTitle>Pain in Fabry Disease: Practical Recommendations for Diagnosis and Treatment.</ArticleTitle>
<Pagination><MedlinePgn>568-76</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/cns.12542</ELocationID>
<Abstract><AbstractText Label="AIMS">Patients with Fabry disease (FD) characteristically develop peripheral neuropathy at an early age, with pain being a crucial symptom of underlying pathology. However, the diagnosis of pain is challenging due to the heterogeneous and nonspecific symptoms. Practical guidance on the diagnosis and management of pain in FD is needed.</AbstractText>
<AbstractText Label="METHODS">In 2014, experts met to discuss recent advances on this topic and update clinical guidance.</AbstractText>
<AbstractText Label="RESULTS">Emerging disease-specific tools, including FabryScan, Fabry-specific Pediatric Health and Pain Questionnaire, and Würzburg Fabry Pain Questionnaire, and more general tools like the Total Symptom Score can aid diagnosis, characterization, and monitoring of pain in patients with FD. These tools can be complemented by more objective and quantifiable sensory testing. In male and female patients of any age, pain related to FD can be an early indication to start disease-specific enzyme replacement therapy before potentially irreversible organ damage to the kidneys, heart, or brain occurs.</AbstractText>
<AbstractText Label="CONCLUSION">To improve treatment outcomes, pain should be diagnosed early in unrecognized or newly identified FD patients. Treatment should include: (a) enzyme replacement therapy controlling the progression of underlying pathology; (b) adjunctive, symptomatic pain management with analgesics for chronic neuropathic and acute nociceptive, and inflammatory or mixed pain; and (c) lifestyle modifications.</AbstractText>
<CopyrightInformation>© 2016 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Politei</LastName>
<ForeName>Juan M</ForeName>
<Initials>JM</Initials>
<AffiliationInfo><Affiliation>Fundación para el Estudio de las Enfermedades Neurometabólicas (FESEN), Buenos Aires, Argentina.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bouhassira</LastName>
<ForeName>Didier</ForeName>
<Initials>D</Initials>
<AffiliationInfo><Affiliation>INSERM U-987, Centre d'Evaluation et de Traitement de la Douleur, Hôpital Ambroise Paré, Boulogne, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Germain</LastName>
<ForeName>Dominique P</ForeName>
<Initials>DP</Initials>
<AffiliationInfo><Affiliation>Division of Medical Genetics, University of Versailles - St Quentin en Yvelines, Paris-Saclay University, Montigny, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Goizet</LastName>
<ForeName>Cyril</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>CHU Bordeaux, Hôpital Pellegrin, Service de Génétique Médicale and Université Bordeaux, Laboratoire Maladies Rares: Génétique et Métabolisme (MRGM) EA4576, Bordeaux, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Guerrero-Sola</LastName>
<ForeName>Antonio</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Neuromuscular Unit, Neurology Department, Hospital Clínico San Carlos, Madrid, Spain.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hilz</LastName>
<ForeName>Max J</ForeName>
<Initials>MJ</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, University of Erlangen-Nuremberg, Erlangen, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hutton</LastName>
<ForeName>Elspeth J</ForeName>
<Initials>EJ</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, The Alfred Hospital, Melbourne, Vic., Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Karaa</LastName>
<ForeName>Amel</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Liguori</LastName>
<ForeName>Rocco</ForeName>
<Initials>R</Initials>
<AffiliationInfo><Affiliation>Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>IRCCS Institute of Neurological Sciences, Bologna, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Üçeyler</LastName>
<ForeName>Nurcan</ForeName>
<Initials>N</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, University of Würzburg, Würzburg, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Zeltzer</LastName>
<ForeName>Lonnie K</ForeName>
<Initials>LK</Initials>
<AffiliationInfo><Affiliation>Pediatric Pain and Palliative Care Program, Department of Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Burlina</LastName>
<ForeName>Alessandro</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Neurological Unit, St Bassiano Hospital, Bassano del Grappa, Italy.</Affiliation>
</AffiliationInfo>
</Author>
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<Language>eng</Language>
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<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<Month>03</Month>
<Day>28</Day>
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<Month>02</Month>
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	Serveur d'exploration sur les relations entre la France et l'Australie
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Pain in Fabry Disease: Practical Recommendations for Diagnosis and Treatment.

Pain in Fabry Disease: Practical Recommendations for Diagnosis and Treatment.

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