Evidence map›Paper›PMID 23949628›Full record

ArticlePediatric nephrology (Berlin, Germany)2013

Psychosocial aspects of children and families of children treated with automated peritoneal dialysis.

Katarzyna Kiliś-Pstrusińska, Anna Wasilewska, Anna Medyńska, Irena Bałasz-Chmielewska, Ryszard Grenda, Agnieszka Kluska-Jóźwiak, Beata Leszczyńska, Ilona Olszak-Szot, Monika Miklaszewska, Maria Szczepańska and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Care of the pediatric patient on chronic peritoneal dialysis.Pediatric nephrology (Berlin, Germany) · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Caregiver burden in pediatric dialysis.Pediatric nephrology (Berlin, Germany) · 2020
    Review
  13. Review
  14. Article
  15. Observational
  16. 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

17 authors at 9 institutions in 1 country.

Katarzyna Kiliś-PstrusińskaDepartment of Paediatric Nephrology, Wrocław Medical University, ul. Borowska 213, 50-556, Wrocław, Poland, katarzyna.kilis-pstrusinska@am.wroc.pl.
Anna Wasilewska
Anna Medyńska
Irena Bałasz-Chmielewska
Ryszard Grenda
Agnieszka Kluska-Jóźwiak
Beata Leszczyńska
Ilona Olszak-Szot
Monika Miklaszewska
Maria Szczepańska
Marcin Tkaczyk
Agnieszka Urzykowska
Katarzyna Zachwieja
Maria Zajączkowska
Helena Ziółkowska
Ilona Zagożdżon
Danuta Zwolińska
Wroclaw Medical University · PLChildren's Memorial Health Institute · PLGdańsk Medical University · PLJagiellonian University · PLMedical University of Warsaw · PLMedical University of Białystok · PLMedical University of Lublin · PLPolish Mother’s Memorial Hospital Research Institute · PLPoznan University of Medical Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this study was to analyze psychosocial aspects of chronic kidney disease (CKD) in children treated with automated peritoneal dialysis (APD).

methodsThe study assessed 41 children > 2 (range 2.1-18) years of age and their parents. Data concerning the illness and sociodemographic parameters were collected. Patients completed the Paediatric Quality of Life Inventory (PedsQL) and their parents the PedsQL-proxy version, General Health Questionnaire (GHQ-12), Berlin Social Support Scales (BSSS), and Caregiver's Burden Scale (CBS).

resultsParents rated their children's overall health-related quality of life (QoL) as well as their physical and emotional functioning lower than the patients themselves. The majority of primary caregivers had a medium level of the total burden index in the CBS and higher values in the scales need for support and perceived available support than in the received support (BSSS). In the GHQ-12, 51.2% of primary caregivers had scores >2 points, which indicated the possible occurrence of abnormal mental functioning.

conclusionsFinancial support for patients' families is necessary. Parents who provide primary care to children on PD require, above all, emotional support and assistance in self-fulfilment. More than half of them may have impaired mental function. There is the strong need to provide continuous psychological care for caregivers. Differences in perception of the children's activity in varied areas by the patients themselves and their caregivers may contribute to further problems within families.

Indexed as

AdolescentAutomationCaregiversChildChild, PreschoolCost of IllnessCross-Sectional StudiesEducational StatusEmotionsFamilyFemaleHealth StatusHealth SurveysHumansMaleParents

Identifiers

PMID23949628
PMCPMC3824203
OpenAlexW2156194589

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.