Evidence map›Paper›PMID 33294357›Full record

ArticleRespiratory medicine case reports2020

Pulmonary hypertension associated with congenital heart disease; clinical decision scenario.

Ali A Alakhfash, Abdullah Alqwaiee, Ghadeer Ali Alakhfash, Athkar Alhajjaj, Abdulrahman A Almesned

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

Article in Respiratory medicine case reports, 2020. 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 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

5 authors at 1 institution in 1 country.

Ali A AlakhfashConsultant Pediatric Cardiologist, Prince Sultan Cardiac Center-Qassim, Saudi Arabia.
Abdullah AlqwaieeConsultant Pediatric Cardiologist, Prince Sultan Cardiac Center-Qassim, Saudi Arabia.
Ghadeer Ali AlakhfashAlrajehi University, Saudi Arabia.
Athkar AlhajjajPSCC-Qassim, Saudi Arabia.
Abdulrahman A AlmesnedConsultant Pediatric Cardiologist, Prince Sultan Cardiac Center-Qassim, Saudi Arabia.
Saud Al-babtain Cardiac Centre · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary arterial hypertension associated with congenital heart disease (PAH-CHD) is one type under group 1 PH. Undiagnosed or delayed diagnosis of significant CHD might lead to significant PAH and at the end might lead to Eisenmenger syndrome. We could expect the degree of PAH in patients with CHD by proper clinical assessment as well as by the basic assessment tools including the chest x-ray (CXR), ECG, and transthoracic echocardiography (TTE). We are presenting a three and half years old child with a delayed/missed diagnosis of large patent ductus arteries (PDA) who present with significant PAH. Clinical evaluation, CXR, ECG, TTE, as well as cardiac catheterization data are presented, with a review of the current guidelines regarding the management of pediatric patients with PAH-CHD.

Indexed as

APW, Aortopulmonary windowBPD, Bronchopulmonary dysplasiaCHD, Congenital Heart DiseaseCongenital heart defectsPAH, Pulmonary arterial hypertensionPCW, pulmonary capillary wedgePDA closurePDA, Patent ductus arteriosusPH, Pulmonary hypertensionPulmonary arterial hypertensionPVR, pulmonary vascular resistanceQp, pulmonary blood flowQs, Systemic blood flowSVR, Systemic vascular resistanceVSD, Ventricular septal defect

Identifiers

PMID33294357
PMCPMC7683341
OpenAlexW3099713821

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.