Evidence map›Paper›PMID 36455994›Full record

ArticleOpen heart2022

Comparison of approaches to determine echocardiographic outcomes for children with latent rheumatic heart disease.

Joselyn Rwebembera, Andrea Beaton, Emmy Okello, Daniel Engelman, Ndate Fall, Mariana Mirabel, Miriam Nakitto, Maria Carmo Pereira Nunes, Jafesi Pulle, Rachel Sarnacki and 5 more

Abstract read
In one paragraph

Article in Open heart, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

15 authors.

Joselyn RwebemberaCardiology, Uganda Heart Institute Ltd, Kampala, Uganda.
Andrea BeatonCincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Emmy OkelloCardiology, Uganda Heart Institute Ltd, Kampala, Uganda.ORCID 0000-0002-6109-0092
Daniel EngelmanCentre for International Child Heath, The Royal Children's Hospital Melbourne, Parkville, Victoria, Australia.
Ndate FallCincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Mariana MirabelCardiovascular Research Center PARCC, Université de Paris 1, Paris, France.
Miriam NakittoUganda Heart Institute Ltd, Kampala, Uganda.
Maria Carmo Pereira NunesInternal Medicine, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Jafesi PulleCardiology, Uganda Heart Institute Ltd, Kampala, Uganda.ORCID 0000-0001-7955-3481
Rachel SarnackiChildren's National Medical Center, Washington, District of Columbia, USA.
Amy ScheelChildren's Hospital of Philadelphia Pediatrics Residency Program, Philadelphia, Pennsylvania, USA.
Liesl ZuhlkePaediatric Cardiology, University of Cape Town, Rondebosch, South Africa.
Anneke GroblerMurdoch Children's Research Institute, Parkville, Victoria, Australia.
Andrew Craig SteerGroup A Streptococcal Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Craig SablePediatric Cardiology, Children's National Hospital, Washington, District of Columbia, USA CSABLE@childrensnational.org.ORCID 0000-0002-6798-2737

Funding

Medical Research Council MR/S005242/1
6 · The paper itself

Abstract

backgroundScreening programmes using echocardiography offer opportunity for intervention through identification and treatment of early (latent) rheumatic heart disease (RHD). We aimed to compare two methods for classifying progression or regression of latent RHD: serial review method and blinded, side-by-side review.

methodsA four-member expert panel reviewed 799 enrolment (in 2018) and completion (in 2020) echocardiograms from the GOAL Trial of latent RHD in Uganda to make consensus determination of normal, borderline RHD or definite RHD. Serial interpretations (enrolment and completion echocardiograms read at two different time points, 2 years apart, not beside one another) were compared with blinded side-by-side comparisons (enrolment and completion echocardiograms displayed beside one another in random order on same screen) to determine outcomes according to prespecified definitions of disease progression (worsening), regression (improving) or no change. We calculated inter-rater agreement using Cohen's kappa.

resultsThere were 799 pairs of echocardiogram assessments included. A higher number, 54 vs 38 (6.8% vs 4.5%), were deemed as progression by serial interpretation compared with side-by-side comparison. There was good inter-rater agreement between the serial interpretation and side-by-side comparison methods (kappa 0.89). Disagreement was most often a result of the difference in classification between borderline RHD and mild definite RHD. Most discrepancies between interpretation methods (46 of 47, 98%) resulted from differences in valvular morphological evaluation, with valves judged to be morphologically similar between enrolment and final echocardiograms when compared side by side but classified differently on serial interpretation.

conclusionsThere was good agreement between the methods of serial and side-by-side interpretation of echocardiograms for change over time, using the World Heart Federation criteria. Side-by-side interpretation has higher specificity for change, with fewer differences in the interpretation of valvular morphology, as compared with serial interpretation.

Indexed as

Rheumatic Heart DiseaseChildConsensusEchocardiographyHeartHumansEchocardiographyGlobal HealthHeart Valve Diseases

Identifiers

PMID36455994
PMCPMC9716950

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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.