Evidence map›Paper›PMID 31058156›Full record

ArticleFrontiers in medicine2019

Hereditary Angioedema-Associated Acute Pancreatitis in C1-Inhibitor Deficient and Normal C1-Inhibitor Patients: Case Reports and Literature Review.

Camila Lopes Veronez, Régis Albuquerque Campos, Rosemeire Navickas Constantino-Silva, Priscila Nicolicht, João Bosco Pesquero, Anete Sevciovic Grumach

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Idiopathic Angioedema: Current Challenges.Journal of asthma and allergy · 2020
    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

6 authors at 3 institutions in 1 country.

Camila Lopes VeronezDepartment of Biophysics, Universidade Federal de São Paulo, São Paulo, Brazil.
Régis Albuquerque CamposDepartment of Clinical Immunology, Universidade Federal da Bahia, Salvador, Brazil.
Rosemeire Navickas Constantino-SilvaDepartment of Clinical Immunology, Faculdade de Medicina ABC, Santo André, Brazil.
Priscila NicolichtDepartment of Biophysics, Universidade Federal de São Paulo, São Paulo, Brazil.
João Bosco PesqueroDepartment of Biophysics, Universidade Federal de São Paulo, São Paulo, Brazil.
Anete Sevciovic GrumachDepartment of Clinical Immunology, Faculdade de Medicina ABC, Santo André, Brazil.
Universidade Federal de São Paulo · BRFaculdade de Medicina do ABC · BRUniversidade Federal da Bahia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abdominal pain due to intestinal swellings is one of the most common manifestations in hereditary angioedema (HAE). Bowel swellings can cause severe abdominal pain, nausea, vomiting, and diarrhea, which may lead to misdiagnosis of gastrointestinal disorders. In rare cases, HAE abdominal attacks can be accompanied by acute pancreatitis. Here, we report 3 patients with HAE and acute pancreatitis and present a literature review of similar cases. Patients with confirmed diagnosis of HAE secondary to C1-inhibitor (C1-INH) deficiency (

Indexed as

abdominal swellingacute pancreatitisC1-inhibitor deficiencyF12 mutationhereditary angioedema

Identifiers

PMID31058156
PMCPMC6478673
OpenAlexW2937450775

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.