Evidence map›Paper›PMID 24362722›Full record

ArticlePediatric radiology2014

C1-esterase inhibitor deficiency in pediatric heart transplant recipients: incidence and findings on ultrasound.

Sabine Pabst, Nadja Hamscho, Fritz Roller, Holger Stracke, Dietmar Schranz, Claudia Lämmler, Gerhard Alzen, Gabriele A Krombach

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Article in Pediatric radiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Sabine PabstDepartment of Pediatric Radiology, University Hospital Giessen, Justus Liebig University Giessen, Klinikstrasse 33, 35392, Giessen, Germany.
Nadja Hamscho
Fritz Roller
Holger Stracke
Dietmar Schranz
Claudia Lämmler
Gerhard Alzen
Gabriele A Krombach
University of Giessen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcquired angioedema of the bowel caused by a deficiency of C1-esterase inhibitor can lead to severe abdominal pain with sudden onset, mimicking an acute surgical abdomen. In contrast to hereditary angioedema, which usually manifests in childhood, acquired angioedema is broadly recognized to affect people older than 40 years.

objectiveTo determine the incidence of acquired angioedema in a cohort of pediatric heart transplant recipients and assess imaging findings on ultrasonography. MATERIALS AND

methodsA cohort of 207 children and adolescents who had undergone heart transplantation were assessed at regular follow-up examinations for incidence of acquired angioedema. All patients received ACE inhibitors and immune inhibitors. Control examinations carried out in 3-month intervals included history, assessment of clinical symptoms, physical examination, US of the abdomen and laboratory blood analysis. In addition, if clinical symptoms were newly encountered, children were admitted between regularly scheduled intervals. We analyzed results of abdominal US for pathological findings of the bowel, and we assessed imaging findings in children diagnosed with acquired angioedema.

resultsAcquired angioedema was diagnosed in 3/207 patients (2 girls ages 16 and 17 years and 1 boy age 9 months). These children presented with sudden onset of severe abdominal pain. The bowel wall was thickened in the presence of ascites. After a mean of 72 h, abdominal pains resolved. Thickening of bowel loops dissolved and ascites disappeared.

conclusionSingle episodes of acquired angioedema were encountered in 1.4% of our series of pediatric heart transplant recipients. Radiologists should be familiar with this disease so they can diagnose it on US imaging.

Indexed as

Abdomen, AcuteAdolescentAngioedemas, HereditaryCausalityChildChild, PreschoolComorbidityDiagnosis, DifferentialFemaleGermanyHeart TransplantationHumansIncidenceInfantInfant, NewbornIntestinal Diseases

Identifiers

PMID24362722
OpenAlexW2094468885

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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.