Evidence map›Paper›PMID 29173030›Full record

ArticleJournal of palliative medicine2018

A Summary of Pediatric Palliative Care Team Structure and Services as Reported by Centers Caring for Children with Cancer.

Meaghann S Weaver, Abby R Rosenberg, Julia Tager, Christopher S Wichman, Lori Wiener

Abstract read
In one paragraph

Article in Journal of palliative medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 2 pooled it
13.4field-weighted citation impact, top 1% 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

43 citing papers in PubMed, 2 syntheses or guidelines pooled it, 89 citations in OpenAlex.

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  13. Paediatric palliative care in cancer.Ecancermedicalscience · 2024
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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 4 institutions in 1 country.

Meaghann S Weaver1 Divisions of Palliative Care and Oncology, Department of Pediatrics, Children's Hospital and Medical Center , Omaha, Nebraska.
Abby R Rosenberg2 Center for Clinical and Translational Research and Treuman Katz Center for Pediatric Bioethics, Seattle Children's Research Institute , Seattle, Washington.
Julia Tager4 National Institutes of Health, National Cancer Institute , Center for Cancer Research, Bethesda, Maryland.
Christopher S Wichman5 Division of Biostatistics, University of Nebraska Medical Center , Omaha, Nebraska.
Lori Wiener4 National Institutes of Health, National Cancer Institute , Center for Cancer Research, Bethesda, Maryland.
Children's Hospital & Medical Center · USNational Cancer Institute · USNational Institutes of Health · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLittle is known about the composition, availability, integration, communication, perceived barriers, and work load of pediatric palliative care (PPC) providers serving children and adolescents with cancer.

objectiveTo summarize the structure and services of programs to better understand successes and gaps in implementing palliative care as a standard of care.

methodsCross-sectional online survey about the palliative care domains determined by the Psychosocial Care of Children with Cancer and Their Families Workgroup. SUBJECTS: A total of 142 surveys were completed with representation from 18 countries and 39 states.

resultsThree-fourths of sites reported having a PPC program available for the pediatric cancer population at their center. Over one-fourth (28%) have been in existence less than five years. Fewer than half of sites (44%) offered 24/7 access to palliative care consultations. Neither hospital-based nor local community hospice services were available for pediatric patients at 24% of responding sites. A specific inpatient PPC unit was available at 8% of sites. Criteria for automatic palliative referrals ("trigger" diagnoses) were reported by 44% respondents. The presence of such "triggers" increased the likelihood of palliative principle introduction 3.41 times (p < 0.003). Six percent of respondents perceived pediatric oncology patients and their families "always" were introduced to palliative care concepts and 17% reported children and families "always" received communication about palliative principles. The most prevalent barriers to palliative care were at the provider level. DISCUSSION: Children and adolescents with cancer do not yet receive concurrent palliative care as a universal standard.

Indexed as

Cross-Sectional StudiesHumansNeoplasmsPalliative CarePatient Care TeamPediatricsSurveys and Questionnairespediatric cancerpediatric oncologypediatric palliative care

Identifiers

PMID29173030
PMCPMC5915222
OpenAlexW2769195488

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.