European Headache Federation guideline on idiopathic intracranial hypertension

Background Idiopathic Intracranial Hypertension (IIH) is characterized by an elevation of intracranial pressure (ICP no identifiable cause. The aetiology remains largely unknown, however observations made in a number of recent clinical studies are increasing the understanding of the disease and now...

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Published inJournal of headache and pain Vol. 19; no. 1; pp. 93 - 15
Main Authors Hoffmann, Jan, Mollan, Susan P, Paemeleire, Koen, Lampl, Christian, Jensen, Rigmor H, Sinclair, Alexandra J
Format Journal Article
LanguageEnglish
Published Milan Springer Milan 08.10.2018
BMC
Subjects
Consensus
Consensus Article
Headache - etiology
Headache - therapy
Humans
Internal Medicine
Medicine
Medicine & Public Health
Neurology
Pain Medicine
Pseudotumor Cerebri - etiology
Pseudotumor Cerebri - therapy
Randomized Controlled Trials as Topic
Idiopathic Intracranial Hypertension
European Headache Federation
Evidence-based Treatment Strategies
Bilateral Sixth Nerve Palsy
Optic Nerve Sheath Fenestration (ONSF)
Online AccessGet full text

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Abstract Background Idiopathic Intracranial Hypertension (IIH) is characterized by an elevation of intracranial pressure (ICP no identifiable cause. The aetiology remains largely unknown, however observations made in a number of recent clinical studies are increasing the understanding of the disease and now provide the basis for evidence-based treatment strategies. Methods The Embase, CDSR, CENTRAL, DARE and MEDLINE databases were searched up to 1st June 2018. We analyzed randomized controlled trials and systematic reviews that investigate IIH. Results Diagnostic uncertainty, headache morbidity and visual loss are among the highest concerns of clinicians and patients in this disease area. Research in this field is infrequent due to the rarity of the disease and the lack of understanding of the underlying pathology. Conclusions This European Headache Federation consensus paper provides evidence-based recommendations and practical advice on the investigation and management of IIH.
AbstractList Background Idiopathic Intracranial Hypertension (IIH) is characterized by an elevation of intracranial pressure (ICP no identifiable cause. The aetiology remains largely unknown, however observations made in a number of recent clinical studies are increasing the understanding of the disease and now provide the basis for evidence-based treatment strategies. Methods The Embase, CDSR, CENTRAL, DARE and MEDLINE databases were searched up to 1st June 2018. We analyzed randomized controlled trials and systematic reviews that investigate IIH. Results Diagnostic uncertainty, headache morbidity and visual loss are among the highest concerns of clinicians and patients in this disease area. Research in this field is infrequent due to the rarity of the disease and the lack of understanding of the underlying pathology. Conclusions This European Headache Federation consensus paper provides evidence-based recommendations and practical advice on the investigation and management of IIH.
Idiopathic Intracranial Hypertension (IIH) is characterized by an elevation of intracranial pressure (ICP no identifiable cause. The aetiology remains largely unknown, however observations made in a number of recent clinical studies are increasing the understanding of the disease and now provide the basis for evidence-based treatment strategies.BACKGROUNDIdiopathic Intracranial Hypertension (IIH) is characterized by an elevation of intracranial pressure (ICP no identifiable cause. The aetiology remains largely unknown, however observations made in a number of recent clinical studies are increasing the understanding of the disease and now provide the basis for evidence-based treatment strategies.The Embase, CDSR, CENTRAL, DARE and MEDLINE databases were searched up to 1st June 2018. We analyzed randomized controlled trials and systematic reviews that investigate IIH.METHODSThe Embase, CDSR, CENTRAL, DARE and MEDLINE databases were searched up to 1st June 2018. We analyzed randomized controlled trials and systematic reviews that investigate IIH.Diagnostic uncertainty, headache morbidity and visual loss are among the highest concerns of clinicians and patients in this disease area. Research in this field is infrequent due to the rarity of the disease and the lack of understanding of the underlying pathology.RESULTSDiagnostic uncertainty, headache morbidity and visual loss are among the highest concerns of clinicians and patients in this disease area. Research in this field is infrequent due to the rarity of the disease and the lack of understanding of the underlying pathology.This European Headache Federation consensus paper provides evidence-based recommendations and practical advice on the investigation and management of IIH.CONCLUSIONSThis European Headache Federation consensus paper provides evidence-based recommendations and practical advice on the investigation and management of IIH.
Abstract Background Idiopathic Intracranial Hypertension (IIH) is characterized by an elevation of intracranial pressure (ICP no identifiable cause. The aetiology remains largely unknown, however observations made in a number of recent clinical studies are increasing the understanding of the disease and now provide the basis for evidence-based treatment strategies. Methods The Embase, CDSR, CENTRAL, DARE and MEDLINE databases were searched up to 1st June 2018. We analyzed randomized controlled trials and systematic reviews that investigate IIH. Results Diagnostic uncertainty, headache morbidity and visual loss are among the highest concerns of clinicians and patients in this disease area. Research in this field is infrequent due to the rarity of the disease and the lack of understanding of the underlying pathology. Conclusions This European Headache Federation consensus paper provides evidence-based recommendations and practical advice on the investigation and management of IIH.
Idiopathic Intracranial Hypertension (IIH) is characterized by an elevation of intracranial pressure (ICP no identifiable cause. The aetiology remains largely unknown, however observations made in a number of recent clinical studies are increasing the understanding of the disease and now provide the basis for evidence-based treatment strategies. The Embase, CDSR, CENTRAL, DARE and MEDLINE databases were searched up to 1st June 2018. We analyzed randomized controlled trials and systematic reviews that investigate IIH. Diagnostic uncertainty, headache morbidity and visual loss are among the highest concerns of clinicians and patients in this disease area. Research in this field is infrequent due to the rarity of the disease and the lack of understanding of the underlying pathology. This European Headache Federation consensus paper provides evidence-based recommendations and practical advice on the investigation and management of IIH.
ArticleNumber 93
Author Sinclair, Alexandra J
Lampl, Christian
Mollan, Susan P
Jensen, Rigmor H
Hoffmann, Jan
Paemeleire, Koen
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  givenname: Jan
  orcidid: 0000-0002-2103-9081
  surname: Hoffmann
  fullname: Hoffmann, Jan
  email: jan.hoffmann@kcl.ac.uk
  organization: Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, Wellcome Foundation Building, Denmark Hill Campus, King’s College London
– sequence: 2
  givenname: Susan P
  surname: Mollan
  fullname: Mollan, Susan P
  organization: Birmingham Neuro-Ophthalmology, University Hospitals Birmingham NHS Foundation Trust, Queen Elizabeth Hospital
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  givenname: Koen
  surname: Paemeleire
  fullname: Paemeleire, Koen
  organization: Department of Neurology, Ghent University Hospital
– sequence: 4
  givenname: Christian
  surname: Lampl
  fullname: Lampl, Christian
  organization: Headache Medical Centre, Seilerstaette Linz, Ordensklinikum Linz
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  givenname: Alexandra J
  surname: Sinclair
  fullname: Sinclair, Alexandra J
  organization: Metabolic Neurology, Institute of Metabolism and Systems Research, University of Birmingham
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30298346$$D View this record in MEDLINE/PubMed
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ISSN 1129-2369
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Issue 1
Keywords Idiopathic Intracranial Hypertension
European Headache Federation
Evidence-based Treatment Strategies
Bilateral Sixth Nerve Palsy
Optic Nerve Sheath Fenestration (ONSF)
Language English
License Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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ORCID 0000-0002-2103-9081
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.1186/s10194-018-0919-2
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PublicationDate 2018-10-08
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  year: 2018
  text: 2018-10-08
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PublicationSubtitle Official Journal of the "European Headache Federation" and of "Lifting The Burden - The Global Campaign against Headache"
PublicationTitle Journal of headache and pain
PublicationTitleAbbrev J Headache Pain
PublicationTitleAlternate J Headache Pain
PublicationYear 2018
Publisher Springer Milan
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SSID ssj0020385
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Snippet Background Idiopathic Intracranial Hypertension (IIH) is characterized by an elevation of intracranial pressure (ICP no identifiable cause. The aetiology...
Idiopathic Intracranial Hypertension (IIH) is characterized by an elevation of intracranial pressure (ICP no identifiable cause. The aetiology remains largely...
Abstract Background Idiopathic Intracranial Hypertension (IIH) is characterized by an elevation of intracranial pressure (ICP no identifiable cause. The...
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StartPage 93
SubjectTerms Consensus
Consensus Article
Headache - etiology
Headache - therapy
Humans
Internal Medicine
Medicine
Medicine & Public Health
Neurology
Pain Medicine
Pseudotumor Cerebri - etiology
Pseudotumor Cerebri - therapy
Randomized Controlled Trials as Topic
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Title European Headache Federation guideline on idiopathic intracranial hypertension
URI https://link.springer.com/article/10.1186/s10194-018-0919-2
https://www.ncbi.nlm.nih.gov/pubmed/30298346
https://www.proquest.com/docview/2117387595
https://pubmed.ncbi.nlm.nih.gov/PMC6755569
https://doaj.org/article/0f8c9b50e7884aabb32cee619f383188
Volume 19
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