Evidence map›Paper›PMID 41448373›Full record

ArticleJournal of pain and symptom management2026

Unseen, Unrelenting, and Uncertain: Caregiver-Identified Targets For Pediatric Palliative Care.

Amy S Porter, Mikhaila Layshock, Jori Bogetz, Lydia McLachlan, Sydney Weill, Jennifer M Snaman, Amy Houtrow, Robert Noll, Abby R Rosenberg, Yael Schenker and 1 more

Abstract read
In one paragraph

Article in Journal of pain and symptom management, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Amy S PorterDivision of Supportive and Palliative Care, Department of Pediatrics, Mass General for Children (A.S.P.), Massachusetts General Hospital, Boston, Massachusetts, USA; Department of Pediatrics (A.S.P., J.M.S., A.R.R.), Harvard Medical School, Boston, Massachusetts, USA.
Mikhaila LayshockNationwide Children's Hospital (M.L.), Columbus, Ohio, USA.
Jori BogetzDepartment of Pediatrics, Division of Bioethics and Palliative Care (J.B.), University of Washington School of Medicine, Seattle, Washington, USA; Treuman Katz Center for Pediatric Bioethics and Palliative Care, Center for Clinical and Translational Research (J.B.), Seattle Children's Research Institute, Seattle, Washington, USA.
Lydia McLachlanCase Western Reserve University School of Medicine (L.M.), Cleveland, Ohio, USA.
Sydney WeillDepartment of Medicine (S.W.), University of Pittsburgh Medical Center (UPMC), Pittsburgh, Pennsylvania, USA.
Jennifer M SnamanDepartment of Pediatrics (A.S.P., J.M.S., A.R.R.), Harvard Medical School, Boston, Massachusetts, USA; Department of Supportive Oncology (J.M.S., A.R.R.), Dana Farber Cancer Institute, Boston, MA; Department of Pediatrics (J.M.S., A.R.R.), Boston Children's Hospital, Boston, MA.
Amy HoutrowDepartment of Physical Medicine & Rehabilitation (A.H.), University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Robert NollUniversity of Pittsburgh School of Medicine (R.N.), Pittsburgh, Pennsylvania, USA.
Abby R RosenbergDepartment of Pediatrics (A.S.P., J.M.S., A.R.R.), Harvard Medical School, Boston, Massachusetts, USA; Department of Supportive Oncology (J.M.S., A.R.R.), Dana Farber Cancer Institute, Boston, MA; Department of Pediatrics (J.M.S., A.R.R.), Boston Children's Hospital, Boston, MA.
Yael SchenkerDivision of General Internal Medicine, Department of Medicine (Y.S.), University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA; Palliative Research Center (PaRC) (Y.S.), Division of Palliative and Supportive Care, Section of Palliative Care and Medical Ethics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Justin A YuUPMC Children's Hospital (J.A.Y.), Pittsburgh, Pennsylvania, USA; Department of Pediatrics (J.A.Y.), University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA. Electronic address: yuja@upmc.edu.

Funding

Refining and Pilot Testing a Meaning-Centered and Cognitive-Behavioral Intervention to Improve the Emotional Well-Being of Family Caregivers of Children with Medical ComplexityK23HD115947 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Justin Anthony Yu · 2025 to 2026
$323k
NICHD NIH HHS K23 HD115947
6 · The paper itself

Abstract

BACKGROUND &

objectiveParent caregivers of children with medical complexity (CMC) provide continuous, multidimensional care over decades. Given that the growing CMC population now comprises most of pediatric palliative care (PPC) patients, palliative care clinicians are positioned to support parents in discipline- and expertise-specific ways distinct from pediatric complex care and other subspecialties. This study aimed to identify CMC parent caregiver challenges that can be optimally addressed using PPC expertise.

methodsThis secondary qualitative analysis of semi-structured interviews with CMC parents explored caregiving challenges, using thematic analysis to identify themes. Themes were synthesized to identify potential levers for subspecialty palliative care-specific interventions and drive design of a conceptual framework to inform the ongoing development and implementation of PPC services for CMC parent caregivers.

resultsNineteen CMC parent caregivers participated in interviews, most of whose children had chronic health conditions affecting primarily the neurologic/neuromuscular, gastrointestinal, and respiratory systems. Almost all represented children were supported by medical technology and relied on Medicaid for primary insurance coverage. Parent report of challenges that may be addressed by PPC highlighted three themes: being unseen in their care work, tackling unrelenting caregiving responsibilities, and facing uncertainty-henceforth referred to as "the 3U's." Each of these themes presented at three levels-the personal, the healthcare system, and the community.

conclusionCMC parents' distressing caregiving challenges fall into three themes, which suggest key levers for clinicians aiming to support parent caregivers. This qualitative analysis offers guidance on how to optimally use a PPC-specific skillset for parent caregiver support.

Indexed as

CaregiversPalliative CareParentsAdolescentAdultChildChild, PreschoolChronic DiseaseFemaleHumansInfantInterviews as TopicMaleMiddle AgedPediatricsQualitative ResearchCaregiversPalliative carePediatricsPsychosocial support

Identifiers

PMID41448373
PMCPMC13343760

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.