Evidence map›Paper›PMID 31177398›Full record

Observational studyClinical rheumatology2019

Vascular acrosyndromes in young adult population. Definition of clinical symptoms and connections to joint hypermobility.

Periklis Vounotrypidis, Athina Pyrpasopoulou, Grigorios T Sakellariou, Dimitrios Zisopoulos, Nikoleta Kefala, Dimitrios I Oikonomou, Constantinos Stefanis, Spyros Aslanidis, Charalambos Bermperidis, Periklis Pappas

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Clinical rheumatology, 2019. 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
0.2field-weighted citation impact, top 37% 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, 3 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

10 authors at 2 institutions in 1 country.

Periklis VounotrypidisRheumatology Department, 424 General Military Hospital, Nea Efkarpia, 56249, Thessaloniki, Greece. perivoun@email.com.
Athina Pyrpasopoulou2nd Propaedeutic Clinic, Department of Internal Medicine, "Ippokration" Hospital, Thessaloniki, Greece.
Grigorios T SakellariouRheumatology Department, 424 General Military Hospital, Nea Efkarpia, 56249, Thessaloniki, Greece.
Dimitrios ZisopoulosRheumatology Department, 424 General Military Hospital, Nea Efkarpia, 56249, Thessaloniki, Greece.
Nikoleta KefalaRheumatology Department, 424 General Military Hospital, Nea Efkarpia, 56249, Thessaloniki, Greece.
Dimitrios I OikonomouDepartment of Immunology and Microbiology, 424 General Military Hospital, Thessaloniki, Greece.
Constantinos StefanisCardiology Department, 424 General Military Hospital, Thessaloniki, Greece.
Spyros Aslanidis2nd Propaedeutic Clinic, Department of Internal Medicine, "Ippokration" Hospital, Thessaloniki, Greece.
Charalambos BermperidisRheumatology Department, 424 General Military Hospital, Nea Efkarpia, 56249, Thessaloniki, Greece.
Periklis PappasVascular Surgery Department, 424 General Military Hospital, Thessaloniki, Greece.
424 General Military Hospital · GRIppokrateio General Hospital of Thessaloniki · GR

Funding

Hellenic Rheumatology Society A68/25-7-2011
6 · The paper itself

Abstract

objectivesClinical recognition of vascular acrosyndromes is often challenging. The term Raynaud's phenomenon (RP) is commonly overused to describe any form of cold-related disorder. This study aims to formally evaluate peripheral vascular symptoms affecting the population, aged ≤ 40 years, and identify any correlations to joint hypermobility (JH). PATIENTS AND

methodsFifty patients (31 males, 19 females) with vasomotor symptoms enrolled in this five-year prospective observational study. Clinical examination by a rheumatologist and a vascular surgeon was performed along with cardiology, echocardiographic and Doppler evaluation. Patients underwent blood cell count, biochemistry, thyroid and selectively immunologic testing. Twenty-four (48%) of them performed nailfold capillaroscopy. The SPSS for Windows, v.17.0, Chicago, USA, was used for the statistical analyses.

resultsTwenty-eight patients (56%) presented with erythromelalgia (EM), 6 (12%) with acrocyanosis (AC) and 9 (18%) as a combination of the above disorder. RP diagnosed in five (10%) while two patients (4%) presented as a mix of EM-RP. There was no correlation with abnormal laboratory tests. Increased incidence of JH was found in EM and AC patients. Among those who were tested with nailfold capillaroscopy, 75% had abnormalities ranged from mild to autoimmune-like diseases.

conclusionsErythromelalgia is the commonest functional vasculopathy in young population followed by acrocyanosis and a combination of these conditions. Joint hypermobility is markedly increased, indicating that dysautonomy may be considered the causative factor following a trigger event. Overall, RP was observed in 14% of patients. Clinical recognition of these disorders avoids unnecessary investigation. Key Points • Vascular acrosyndromes in young adults are commonly functional disorders resembling vascular algodystrophy induced by thermic stress. • Dysautonomy of joint hypermobility is the co-factor influencing the appearance of the vascular disorders. • Raynaud's phenomenon accounts to approximately 14% of vascular acrosyndromes presented in the young adult population.

Indexed as

AdolescentAdultCyanosisErythromelalgiaFemaleHumansIncidenceJoint InstabilityMaleMicroscopic AngioscopyMiddle AgedProspective StudiesRaynaud DiseaseVascular DiseasesYoung AdultAcrocyanosisCapillaroscopyDysautonomyErythromelalgiaRaynaud’s phenomenon

Identifiers

PMID31177398
OpenAlexW2953793474

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.