Evidence map›Paper›PMID 34917969›Full record

ArticleJACC. Case reports2021

Severe Hypoxemia Caused by High-Output Heart Failure and Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia.

Hiroaki Yamamoto, Chieko Itamoto, Tomomi Yamaguchi, Tomoki Koshyo

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

Article in JACC. Case reports, 2021. 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
0.1field-weighted citation impact, top 47% 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, 1 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

4 authors at 2 institutions in 3 countries.

Hiroaki YamamotoDepartment of Cardiology, Nagano Chuo Hospital, Nagano, Japan.
Chieko ItamotoDepartment of Cardiology, Nagano Chuo Hospital, Nagano, Japan.
Tomomi YamaguchiDepartment of Genetic Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
Tomoki KoshyoDepartment of Genetic Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
Medical Genetics Center · DENagano Municipal Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A man affected by hereditary hemorrhagic telangiectasia who had chronic severe hypoxemia is presented. This hypoxemia was synergistically caused by high-output heart failure due to severe hepatic shunts and multiple pulmonary arteriovenous shunts. The symptomatic combination is rare, and genetic testing showed a novel endoglin mutation. (

Indexed as

AVM, arteriovenous malformationchronic heart failureCT, computed tomographygenetic disordersgenotypeHAVM, hepatic arteriovenous malformationHF, heart failureHHT, hereditary hemorrhagic telangiectasiaPAVM, pulmonary arteriovenous malformationphenotyperight-sided catheterization

Identifiers

PMID34917969
PMCPMC8642735
OpenAlexW3217207557

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.