Evidence map›Paper›PMID 32892539›Full record

ArticleTurkish journal of medical sciences2021

A survey of bullous diseases in a Turkish university hospital: clinicoepidemiological characteristics and follow-up

Zekayi Kutlubay, Ayşegül Sevim Keçici, Uğur Çelik, Mehmet Cem Mat

Open access · greenAbstract read
In one paragraph

Article in Turkish journal of medical sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. A Global View of Pemphigus: Geographical Variations.Clinical reviews in allergy & immunology · 2024
    Review
  2. Burden of pemphigus vulgaris with a particular focus on women: A review.International journal of women's dermatology · 2022
    Review
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

4 authors at 4 institutions in 1 country.

Zekayi KutlubayDepartment of Dermatology, İstanbul University-Cerrahpaşa, Cerrahpaşa Medical Faculty, İstanbul, TurkeyORCID 0000-0003-0809-1624
Ayşegül Sevim KeçiciDepartment of Dermatology, University of Medical Sciences, Haydarpaşa Numune Training and Research Hospital, İstanbul, TurkeyORCID 0000-0001-5505-6624
Uğur ÇelikDepartment of Dermatology, Medipol University, İstanbul, TurkeyORCID 0000-0003-0338-8111
Mehmet Cem MatDepartment of Dermatology, Private Practice, İstanbul, TurkeyORCID 0000-0002-5738-336X
Haydarpaşa Numune Eğitim ve Araştırma Hastanesi · TRIstanbul Medipol University · TRIstanbul University-Cerrahpaşa · TRTurkish Society of Hematology · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: Autoimmune bullous diseases, if left untreated, are life-threatening conditions affecting primarily skin and mucous membranes. These blistering disorders are characterized by epidermal or subepidermal detachment. Autoimmunity plays a key role in pathogenesis; therefore, immunosuppressive agents are the treatment of choice. The aim of this study is to document relative frequencies of different autoimmune bullous diseases, patient characteristics, treatment options, and side effects in patients presenting to our bullous skin disease center at İstanbul University, Cerrahpaşa, Cerrahpaşa Medical Faculty. Materials and methods: Medical files were examined retrospectively for all patients with autoimmune bullous diseases who were followed up between 2003 and 2019 at the Bullous Skin Disease Center at İstanbul University, Cerrahpaşa. Results: A total of 346 patient files were examined. Pemphigus vulgaris was the most frequent autoimmune bullous disease, followed by bullous pemphigoid and pemphigus foliaceus, according to our study. There is a general female predominancy for all autoimmune bullous diseases. The most commonly preferred treatment options were high-dose daily corticosteroids. Conclusion: This retrospective study summarizes the patient characteristics, comorbidities, treatment choices, and side effects during 16 years of clinical practice.

Indexed as

Autoimmune DiseasesSkin Diseases, VesiculobullousAdrenal Cortex HormonesAdultAgedFemaleFollow-Up StudiesHospitals, UniversityHumansMaleMiddle AgedPemphigoid, BullousPemphigusRetrospective StudiesSex FactorsSkinAdrenal Cortex HormonesBullous diseases epidemiologybullous pemphigoidpemphigus vulgaris

Identifiers

PMID32892539
PMCPMC7991873
OpenAlexW3084102854

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.