Evidence map›Paper›PMID 39213445›Full record

ArticlePLoS neglected tropical diseases2024

Living with rheumatic fever and rheumatic heart disease in Victoria, Australia: A qualitative study.

Jane Oliver, Loudeen Fualautoalasi-Lam, Angeline Ferdinand, Ramona Tiatia, Bryn Jones, Daniel Engelman, Katherine B Gibney, Andrew C Steer

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

8 authors.

Jane OliverMurdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Australia.ORCID 0000-0001-5548-7512
Loudeen Fualautoalasi-LamMurdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Australia.
Angeline FerdinandCentre for Health Policy, Melbourne School of Population and Global Health, University of Melbourne, Victoria, Australia.
Ramona TiatiaDepartment of Public Health, University of Otago Wellington, Wellington, New Zealand.
Bryn JonesMurdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Australia.
Daniel EngelmanMurdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Australia.
Katherine B GibneyDepartment of Infectious Diseases, University of Melbourne, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
Andrew C SteerMurdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Australia.

Funding

Murdoch Children's Research Institute 2022 Stimulus AwardNational Health and Medical Research Council of Australia 2009798
6 · The paper itself

Abstract

backgroundIn Victoria, Australia, children with Pacific Islander ('Pacific') ethnicities are overrepresented in acute rheumatic fever (ARF) and rheumatic heart disease (RHD). In June 2023, ARF and RHD became notifiable in Victoria. To inform public health and clinical practice, we described young Pacific patients' and their caregivers' understandings and experiences of ARF/RHD, and identified possible ways to improve the delivery of clinical care.

methodsWe established a project reference group including local Pacific people to guide this research. Pacific patients who attended an ARF/RHD clinic at The Royal Children's Hospital, Melbourne, were invited to participate, as were their caregivers. A Samoan researcher conducted qualitative 'talanoa' (conversational) interviews with patients and caregivers. A second researcher conducted semi-structured interviews with treating clinicians and other stakeholders. Interview transcripts underwent thematic analysis guided by the Tuilaepa Youth Mentoring Services Pacific Youth Wellbeing Framework.

resultsWe interviewed 27 participants. This included nine patients and nine caregivers, all of whom were Samoan. These 18 participants expressed a desire to learn more about ARF/RHD and connect with other affected people. While some shared their experiences of having well-liked and trusted healthcare providers, patients often struggled to have two-way clinical conversations. The need to support clinicians working with high-risk populations to improve their awareness of ARF was identified. Receiving treatment on time was a top priority for affected families, despite injection pain, inconvenience and financial costs. The need to support continuity of care for young adult patients was raised by participants.

conclusionsPacific people living with ARF/RHD and their families require additional support to receive high quality management in Victoria. Introducing a patient register and a specialist RHD nurse would enhance access to treatment, as would removing cost barriers, improving clinical awareness of ARF/RHD and creating Victoria-specific patient resources.

Indexed as

CaregiversQualitative ResearchRheumatic FeverRheumatic Heart DiseaseAdolescentAdultChildFemaleHumansMaleMiddle AgedPacific Island PeopleVictoriaYoung Adult

Identifiers

PMID39213445
PMCPMC11392276

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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.