Evidence map›Paper›PMID 38197939›Full record

ReviewSchmerz (Berlin, Germany)2024

[Neuropathic pain as a symptom in autonomic neuropathies and other rare diseases : Small fiber neuropathy: its recognition, diagnosis, and treatment].

Fiona Fischer, Maike F Dohrn, Romina Kapfenberger, Denver Igharo, Diana Seeber, Elena de Moya Rubio, Kalliopi Pitarokoili, Natalie Börsch, Martin Mücke, Roman Rolke and 2 more

Abstract readEnglish AbstractReview
PubMed Publisher
In one paragraph

Review in Schmerz (Berlin, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 100% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 2 countries.

Fiona FischerKlinik für Neurologie, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland.
Maike F DohrnKlinik für Neurologie, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland.
Romina KapfenbergerKlinik für Neurologie, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland.
Denver IgharoKlinik für Neurologie, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland.
Diana SeeberKlinik für Neurologie, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland.
Elena de Moya RubioPOTS und andere Dysautonomien e. V., Bochum, Deutschland.
Kalliopi PitarokoiliNeurologische Universitätsklinik am St. Josef Hospital Katholisches Klinikum Bochum, Bochum, Deutschland.
Natalie BörschInstitut für Digitale Allgemeinmedizin, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland.
Martin MückeInstitut für Digitale Allgemeinmedizin, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland.
Roman RolkeKlinik für Palliativmedizin, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland.
Jörg B SchulzKlinik für Neurologie, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland.
Andrea MaierKlinik für Neurologie, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland. amaier@ukaachen.de.ORCID http://orcid.org/0000-0002-3427-4806
RWTH Aachen University · DEHelios Klinikum Krefeld · DEJülich Aachen Research Alliance · DESt. Josef-Hospital · DEUniversitätsklinikum Aachen · DEUniversity Hospitals of the Ruhr-University of Bochum · DEVolga State University of Technology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeuropathic pain is difficult to diagnose and treat. Small fiber neuropathy (SFN) flies under the radar of nerve conduction studies.

objectivesThe importance of a structured patient history and physical examination in the context of neuropathic pain is emphasized. Describing SFN as an important cause, the authors consider rare but partially treatable differential diagnoses. They conclude that autonomic symptoms are frequently associated, often presenting with diverse symptoms.

methodsA selective literature research to present SFN symptoms as well as differential diagnostic and therapeutic steps in the context of SFN and rare diseases focusing on the autonomic nervous system.

resultsNeuropathic pain significantly reduces quality of life. To shorten the time until diagnosis and to initiate therapy, the authors recommend a structured patient history including sensory plus and minus symptoms and non-specific autonomic signs. If the initial search for the cause is not successful, rare causes such as treatable transthyretin (ATTR) amyloidosis and Fabry's disease or autoimmune causes should be considered, particularly in the case of progressive and/or autonomic symptoms.

conclusionThe diagnosis and therapy of rare SFN requires interdisciplinary collaboration and, in many cases, a referral to specialized centers to achieve the best patient care.

Indexed as

NeuralgiaSmall Fiber NeuropathyAutonomic Nervous SystemHumansQuality of LifeRare DiseasesAutonomic nervous systemBiopsy/skinFunctional diagnosticsQuantitative sensory testingSmall fiber neuropathy/genetics

Identifiers

PMID38197939
OpenAlexW4390702581

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.