Evidence map›Paper›PMID 35698902›Full record

ReviewJournal of intellectual disabilities : JOID2023

Down syndrome: Parental experiences of a postnatal diagnosis.

Fiona Mc Grane, Fiona Lynn, Joanne Balfe, Eleanor Molloy, Lynne Marsh

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of intellectual disabilities : JOID, 2023. 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
3.8field-weighted citation impact, top 7% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Fiona Mc GraneSchool of Nursing and Midwifery, Queens University, Belfast, Ireland; Department of Paediatrics, Trinity College, Dublin, Ireland; Department of Neurodisability and Developmental Paediatrics, Children's Health Ireland at Tallaght, Dublin, Ireland.ORCID 0000-0002-9244-5992
Fiona LynnSchool of Nursing and Midwifery, Queens University, Belfast, Ireland.
Joanne BalfeDepartment of Paediatrics, Trinity College, Dublin, Ireland; Department of Neurodisability and Developmental Paediatrics, Children's Health Ireland at Tallaght, Dublin, Ireland; Neonatology, Children's Health Ireland at Crumlin, Ireland; LauraLynn Ireland's Children's Hospice, Ireland.
Eleanor MolloyDepartment of Paediatrics, Trinity College, Dublin, Ireland; Department of Neurodisability and Developmental, Paediatrics, Children's Health Ireland at Tallaght, Dublin, Ireland; Neonatology, Coombe Women's and Infant University Hospital, Ireland; Neonatology, Children's Health Ireland at Crumlin, Ireland.
Lynne MarshSchool of Nursing and Midwifery, Queens University, Belfast, Ireland.
Trinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Globally it is estimated that Down syndrome occurs in 1 in 800 live births (Bull 2020). It has also been estimated that the incidence of Down syndrome occurs in 1/444 live births in the Republic of Ireland. Given the prevalence of Down syndrome births in Ireland and the fact that care is provided by the majority of parents at home, this qualitative study aimed to explore the experiences of Irish parents receiving a postnatal diagnosis of Down syndrome. A qualitative research approach was used through semi structured interviews. Eight parents of a baby diagnosed postnatally with Down syndrome participated in this study sharing their stories of their postnatal diagnosis experiences. Five overarching themes emerged using a descriptive thematic analysis; 1. prenatal screening, pregnancy and delivery; 2. how the diagnosis was delivered; 3. setting and emotional experiences; 4. moving on with the postnatal diagnosis and 5. Future recommendations from parents' perspectives. This study highlighted the importance of the need for clinicians to ensure that partners are present at the time of the disclosure, that ample time is allocated and that verbal and written communications are provided to parents using less medical jargon when delivering the postnatal diagnosis of Down syndrome. These reasonable adjustments could alleviate parental anxiety at this critical juncture in their lives. Online resources and support forums were also identified as an integral support for families on discharge from the maternity centres and in the early months and years.

Indexed as

Down SyndromeIntellectual DisabilityAnimalsCattleFemaleHumansInfantMaleParentsPregnancyPrenatal DiagnosisQualitative ResearchDown syndromeintellectual disabilityparentspostnatal diagnosis

Identifiers

PMID35698902
PMCPMC10647884
OpenAlexW4282840492

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.