Evidence map›Paper›PMID 30961612›Full record

ArticleOrphanet journal of rare diseases2019

Tetralogy of Fallot in Spain: a nationwide registry-based mortality study across 36 years.

Laura Llamosas-Falcón, Eva Bermejo-Sánchez, Germán Sánchez-Díaz, Ana Villaverde-Hueso, Manuel Posada de la Paz, Verónica Alonso-Ferreira

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Observational
  6. 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

6 authors.

Laura Llamosas-FalcónPreventive Medicine and Public Health, Hospital Universitario 12 de Octubre, 28041, Madrid, Spain.
Eva Bermejo-SánchezInstitute of Rare Diseases Research (IIER), Instituto de Salud Carlos III, 28029, Madrid, Spain.
Germán Sánchez-DíazInstitute of Rare Diseases Research (IIER), Instituto de Salud Carlos III, 28029, Madrid, Spain.
Ana Villaverde-HuesoInstitute of Rare Diseases Research (IIER), Instituto de Salud Carlos III, 28029, Madrid, Spain.
Manuel Posada de la PazInstitute of Rare Diseases Research (IIER), Instituto de Salud Carlos III, 28029, Madrid, Spain.
Verónica Alonso-FerreiraInstitute of Rare Diseases Research (IIER), Instituto de Salud Carlos III, 28029, Madrid, Spain. valonso@isciii.es.

Funding

Instituto de Salud Carlos III TPY1238/15Ministerio de Educación, Cultura y Deporte FPU14/03914
6 · The paper itself

Abstract

backgroundTetralogy of Fallot (TOF) is the most frequent cyanotic congenital heart defect. TOF mortality has fallen remarkably in recent years due to therapeutic advances. Accordingly, the aim of this study was to assess temporal and spatial variability in TOF-related mortality in Spain across the period 1981-2016, using data drawn from the nationwide population-based registry.

methodsAnnual deaths due to TOF were sourced from the Spanish National Institute of Statistics database by reference to International Classification of Diseases (ICD), 9th and 10th Revision codes, namely, ICD-9 code 745.2 (period 1981-1998) and ICD-10 code Q21.3 (period 1999-2016). Age-specific and age-adjusted mortality rates were calculated, as were standardised mortality ratios (SMRs) by province, district and municipality for the period 1999-2016.

resultsA total of 1035 deaths were attributed to TOF (57.78% of them were men and 42.22% were women). The age-adjusted mortality rate ranged from 0.75 per 1,000,000 inhabitants (95% confidence interval [CI]: 0-1.36) in 1981 to 0.03 per 1,000,000 (95% CI: 0.01-0.06) in 2016 for both sexes. In 2011, there was a change in the mortality trend, with a significant decrease of 49.22% per year (p < 0.001). In terms of geographical analysis, some areas with a significantly higher risk of TOF mortality were identified in the south of Spain, though no specific spatial pattern was in evidence.

conclusionThe decrease in TOF mortality may be related to improvements in diagnostic and treatment techniques. More studies are needed to analyse regions with a higher mortality risk, in order to improve medical planning and resource allocation, and identify risk factors and preventive measures.

Indexed as

AdolescentAdultChildChild, PreschoolFemaleHeart Defects, CongenitalHumansInfantInfant, NewbornInternational Classification of DiseasesMaleRegistriesRetrospective StudiesRisk FactorsSpainTetralogy of FallotCongenital heart defectMortalitySpainSpatial-analysisTemporal-analysisTetralogy of Fallot

Identifiers

PMID30961612
PMCPMC6454694

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.