Evidence map›Paper›PMID 28952009›Full record

Trial reportJournal of genetic counseling2018

Psychosocial Distress and Knowledge Deficiencies in Parents of Children in Ireland Who Carry an Altered Cystic Fibrosis Gene.

S J Quigley, B Linnane, S Connellan, A Ward, P Ryan

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Journal of genetic counseling, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 2 pooled it
0.2field-weighted citation impact, top 40% 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

5 citing papers in PubMed, 2 syntheses or guidelines pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Review
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 3 institutions in 1 country.

S J QuigleyDepartment of Psychology, University of Limerick, Limerick, Ireland. stephenjamesquigley@gmail.com.
B LinnaneGraduate Entry Medical School and Centre for Interventions, Infection, Inflammation and Immunity (4i), University Hospital Limerick, Dooradoyle, Limerick, Ireland.
S ConnellanCystic Fibrosis Psychology Service, University Hospital Limerick, Dooradoyle, Limerick, Ireland.
A WardNational Centre for Medical Genetics, Our Lady's Hospital for Sick Children, Dublin, Ireland.
P RyanDepartment of Psychology, University of Limerick, Limerick, Ireland.
University Hospital Limerick · IEUniversity of Limerick · IEOur Lady's Hospital · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significant gaps have been identified in parental understanding of CF newborn screening and the consequences of carrying an altered CF gene. Seven potential causes of psychosocial adversity arising from false positive newborn screening for CF have been identified. The current study aimed to increase parents understanding of CF, reduce their levels of stress, and investigate psychosocial adversity arising from false-positive screening. This national study was run over one year in the Republic of Ireland. Parents were recruited for the study following a diagnostic sweat test confirming their child carried a single altered CF gene. Parents were randomly assigned into a control and intervention group, with those in the intervention group receiving a carefully designed information pack. All parents took part in semi-structured interviews. Parents (n = 16) who received an information pack had significantly higher CF knowledge scores than parents (n = 16) in the control group. 66% of parents in the control group misunderstood the health implications of carrying an altered CF gene, no parents in the intervention group had the same misunderstanding. There was no significant difference in stress scores between the groups. Parents of infants who had more than one sweat test due to insufficient sweat quantity had higher overall stress percentiles (50%), than parents of infants who had one sweat test (30%), indicating greater parental stress. The combination of written and audio-visual information contained in the information pack successfully increased parents comprehension of CF. The study also evaluates the potential for psychosocial adversity following false positive newborn screening for CF.

Indexed as

Health Knowledge, Attitudes, PracticeAdaptation, PsychologicalChildCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorFemaleGenetic Carrier ScreeningGenetic CounselingHumansInfantInfant, NewbornIrelandMaleNeonatal ScreeningParentsSweatCystic Fibrosis Transmembrane Conductance RegulatorCarrierCystic fibrosisNewborn screeningRepeat testing

Identifiers

PMID28952009
OpenAlexW2756506282

What OpenQuestion holds

Textmetadata
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.