Evidence map›Paper›PMID 41787485›Full record

ArticleBMC health services research2026

Bridging communication gaps to improve adult congenital heart disease care: patient perspectives from a qualitative study.

Sasha Ruban, Larissa Lloyd, Tanya Badal, Geoff Strange, David S Celermajer, Carissa Bonner

Abstract read
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Article in BMC health services research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Sasha RubanClinical Research Group, Heart Research Institute, Sydney, NSW, Australia.
Larissa LloydClinical Research Group, Heart Research Institute, Sydney, NSW, Australia.
Tanya BadalClinical Research Group, Heart Research Institute, Sydney, NSW, Australia.
Geoff StrangeClinical Research Group, Heart Research Institute, Sydney, NSW, Australia.
David S CelermajerClinical Research Group, Heart Research Institute, Sydney, NSW, Australia.
Carissa BonnerFaculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia. carissa.bonner@sydney.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdults with Congenital Heart Disease (CHD) require lifelong specialist care, yet many report communication challenges that undermine health understanding, managing their condition and their overall wellbeing. Effective specialist-patient communication is associated with better outcomes, but little research has explored adult CHD (ACHD) patients’ perspectives on these interactions.

methodsThis qualitative study was conducted as part of a larger investigation of ACHD care in Australia. Using purposive sampling, 43 adults aged 20–54 years with mild, moderate, or severe CHD were recruited from four hospitals. Semi-structured interviews were conducted via video conferencing, transcribed, and analysed using Framework Analysis. Rigour was maintained through double coding, iterative refinement of the thematic framework, and multidisciplinary team review.

resultsFour themes shaped patient experiences of communication: (1) fragmented communication between providers; (2) inadequate patient-facing communication; (3) gaps in understanding of condition; and (4) emotional impacts of suboptimal communication. Conversely, clear, respectful, and empathic communication fostered trust, confidence, and adherence. Participants recommended structured handovers, accessible records, plain-language explanations, visual and written aids, and routine psychosocial support.

conclusionsThis study demonstrates that communication in ACHD care is not merely an aide to clinical management but a defining element of quality, continuity, and patient wellbeing. Participants’ experiences revealed that fragmented inter-specialist communication and limited patient-facing explanations contribute to confusion, care discontinuity, and emotional distress. These findings highlight that improving communication practices is essential to strengthening patient autonomy, mitigating psychosocial burden, and sustaining engagement in lifelong specialist care. PRACTICE IMPLICATIONS: ACHD services should establish structured handover pathways, shared records, and designated care coordinators to minimise fragmentation. Specialists could engage patients more directly with age-appropriate, plain-language discussions, progressive transfer of responsibility during adolescence, and revisiting knowledge in adulthood. Incorporating visual aids, written summaries, and psychosocial screening into routine practice, alongside training specialists in empathic, patient-centred communication, could strengthen trust, improve adherence, and enhance long-term outcomes.

Indexed as

CommunicationHeart Defects, CongenitalPhysician-Patient RelationsAdultAustraliaFemaleHumansInterviews as TopicMaleMiddle AgedQualitative ResearchYoung AdultAdult Congenital Heart Disease (ACHD)Continuity of careHealth communicationPatient-centred carePatient educationPsychosocial wellbeingTransition of care

Identifiers

PMID41787485
PMCPMC13072496

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LicenceCC BY-NC-ND
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Registered trials

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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.