Evidence map›Paper›PMID 33469741›Full record

ArticleJournal of general internal medicine2021

Hospice Care Experiences Among Cancer Patients and Their Caregivers.

Layla Parast, Anagha A Tolpadi, Joan M Teno, Marc N Elliott, Rebecca Anhang Price

Open access · bronzeAbstract read
In one paragraph

Article in Journal of general internal medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. TheWestern journal of nursing research · 2025
    Trial
  2. Article
  3. Article
  4. Article
  5. e-PainSupport: A Digital Pain Management Application for Home Hospice Care.The American journal of hospice & palliative care · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Variation in Hospice Experiences by Care Setting for Patients With Dementia.Journal of the American Medical Directors Association · 2022
    Article
  10. 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

5 authors at 2 institutions in 1 country.

Layla ParastRAND Corporation, Santa Monica, CA, USA. parast@rand.org.ORCID 0000-0002-7288-1009
Anagha A TolpadiRAND Corporation, Santa Monica, CA, USA.
Joan M TenoOregon Health & Science University, Portland, OR, USA.
Marc N ElliottRAND Corporation, Santa Monica, CA, USA.
Rebecca Anhang PriceRAND Corporation, Arlington, VA, USA.
RAND Corporation · USOregon Health & Science University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLittle is known about the current quality of care for hospice cancer patients and how it varies across hospice programs in the USA.

objectiveTo examine hospice care experiences among decedents with a primary cancer diagnosis and their family caregivers, comparing quality across settings of hospice care.

designWe analyzed data from the Consumer Assessment of Healthcare Providers and Systems Hospice Survey (32% response rate). Top-box outcomes (0-100) were calculated overall and by care setting, adjusting for survey mode and patient case mix.

participantsTwo hundred seventeen thousand five hundred ninety-six caregiver respondents whose family member had a primary cancer diagnosis and died in 2017 or 2018 while receiving hospice care from 2,890 hospices nationwide. MAIN MEASURES: Outcomes (0-100 scale) included 8 National Quality Forum-endorsed quality measures, as well as responses to 4 survey questions assessing whether needs were met for specific symptoms (pain, dyspnea, constipation, anxiety/sadness). KEY

resultsQuality measure scores ranged from 74.9 (Getting Hospice Care Training measure) to 89.5 (Treating Family Member with Respect measure). The overall score for Getting Help for Symptoms was 75.1 with item scores within this measure ranging from 60.6 (getting needed help for feelings of anxiety or sadness) to 84.5 (getting needed help for pain). Measure scores varied significantly across settings and differences were large in magnitude, with caregivers of decedents who received care in a nursing home (NH) or assisted living facility (ALF) setting consistently reporting poorer quality of care.

conclusionsImportant opportunities exist to improve hospice care for symptom palliation and providing training for caregivers when their family members are at home or in an ALF setting. Efforts to improve care for cancer patients in the NH and ALF setting are especially needed.

Indexed as

Hospice CareNeoplasmsCaregiversFamilyHumansPalliative Carecancerhospice carepainpatient experience

Identifiers

PMID33469741
PMCPMC8042100
OpenAlexW3122268948

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.