Evidence map›Paper›PMID 34565130›Full record

ArticleJournal of clinical research in pediatric endocrinology2023

A Potentially Fatal Outcome of Oral Contraceptive Therapy: Estrogen-Triggered Hereditary Angioedema in an Adolescent

Uğur Berkay Balkancı, Demet Demirkol, Gül Yeşiltepe Mutlu, Esra Birben, Özge Soyer, Özlem Yılmaz, Cansın Saçkesen

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

7 authors at 3 institutions in 1 country.

Uğur Berkay BalkancıKoç University Faculty of Medicine, İstanbul, TurkeyORCID 0000-0003-1377-8332
Demet DemirkolKoç University Faculty of Medicine, Department of Pediatric Intensive Care; İstanbul University, İstanbul Faculty of Medicine, Department of Pediatric Intensive Care, İstanbul, TurkeyORCID 0000-0001-9578-9267
Gül Yeşiltepe MutluKoç University Faculty of Medicine, Department of Pediatric Endocrinology, İstanbul, TurkeyORCID 0000-0003-3919-7763
Esra BirbenHacettepe University Faculty of Medicine, Department of Pediatric Allergy, Ankara, TurkeyORCID 0000-0003-1192-309X
Özge SoyerHacettepe University Faculty of Medicine, Department of Pediatric Allergy, Ankara, TurkeyORCID 0000-0002-7444-251X
Özlem YılmazKoç University Faculty of Medicine, Department of Pediatric Allergy, İstanbul, TurkeyORCID 0000-0003-2971-283X
Cansın SaçkesenKoç University Faculty of Medicine, Department of Pediatric Allergy, İstanbul, TurkeyORCID 0000-0002-1115-9805
Koç University · TRHacettepe University · TRIstanbul University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary angioedema (HAE) is characterized by recurrent angioedema attacks with no urticaria. This disease has a high mortality due to asphyxia. Level of complement component 4 (C4), C1 esterase inhibitor (C1-INH) level and function, and genetic mutations determine different endotypes of HAE. Clinical presentation and the triggers of vasogenic edema may change according to the endotypes. An adolescent girl with oligomenorrhea, obesity, hirsutism, and acanthosis nigricans was diagnosed with polycystic ovary syndrome and prescribed ethinyl estradiol and cyproterone acetate containing oral contraceptive (OC). On the sixteenth day of treatment, she developed angioedema of the face, neck, and chest leading to dyspnea. Adrenaline, antihistamine, and corticosteroid treatments were ineffective. In the family history, the patient’s mother and two cousins had a history of angioedema. C1-INH concentrate was administered with a diagnosis of HAE. C4 and C1-INH level and activity were normal. Genetic analysis identified a mutation in the factor 12 (

Indexed as

angioedemafactor 12hereditary angioedemaHereditary angioedema type 3polycystic ovary syndrome

Identifiers

PMID34565130
PMCPMC10234060
OpenAlexW3204301864

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.