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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Instruments to Measure Outcomes in Pediatric Palliative Care: A Systematic Review
Marie Friedel, Isabelle Aujoulat, A Dubois, et al.
PEDIATRICS (2018) Vol. 143, Iss. 1
Open Access | Times Cited: 58

Showing 1-25 of 58 citing articles:

International Standards for Pediatric Palliative Care: From IMPaCCT to GO-PPaCS
Franca Benini, Danai Papadatou, Mercedes Bernadá, et al.
Journal of Pain and Symptom Management (2022) Vol. 63, Iss. 5, pp. e529-e543
Open Access | Times Cited: 131
Response to Suffering of the Seriously Ill Child: A History of Palliative Care for Children
Bryan A. Sisk, Chris Feudtner, Myra Bluebond‐Langner, et al.
PEDIATRICS (2019) Vol. 145, Iss. 1
Open Access | Times Cited: 62
Impact of Specialized Pediatric Palliative Care: A Systematic Review
Katherine L. Marcus, Gisella Santos, Agustín Ciapponi, et al.
Journal of Pain and Symptom Management (2019) Vol. 59, Iss. 2, pp. 339-364.e10
Open Access | Times Cited: 61
Achieving child-centred care for children and young people with life-limiting and life-threatening conditions—a qualitative interview study
Lucy Coombes, Debbie Braybrook, Anna Roach, et al.
European Journal of Pediatrics (2022) Vol. 181, Iss. 10, pp. 3739-3752
Open Access | Times Cited: 32
Integration of Pediatric Palliative Care Into Cardiac Intensive Care: A Champion-Based Model
Katie M. Moynihan, Jennifer M. Snaman, Erica C. Kaye, et al.
PEDIATRICS (2019) Vol. 144, Iss. 2
Open Access | Times Cited: 51
The support needs of parent caregivers of children with a life-limiting illness and approaches used to meet their needs: A scoping review
Fenella J. Gill, Zahraa Hashem, Roswitha Stegmann, et al.
Palliative Medicine (2020) Vol. 35, Iss. 1, pp. 76-96
Closed Access | Times Cited: 46
Quality Measure Considerations for Pediatric Palliative and End-of-Life Care
Hannah Hommes, Diane McNally Forsyth, April Rowe Neal
American Journal of Hospice and Palliative Medicine® (2025)
Closed Access
Effectiveness of complementary therapies for the management of symptom clusters in palliative care in pediatric oncology: a systematic review
Luí­s Carlos Lopes-Júnior, Isadora Rangel Urbano, Sara Isabel Pimentel de Carvalho Schuab, et al.
Revista da Escola de Enfermagem da USP (2021) Vol. 55
Open Access | Times Cited: 25
What are the anticipated benefits, risks, barriers and facilitators to implementing person-centred outcome measures into routine care for children and young people with life-limiting and life-threatening conditions? A qualitative interview study with key stakeholders
Hannah May Scott, Lucy Coombes, Debbie Braybrook, et al.
Palliative Medicine (2024) Vol. 38, Iss. 4, pp. 471-484
Open Access | Times Cited: 3
Quality of Life in Palliative Care: A Systematic Meta-Review of Reviews and Meta-Analyses
Mauro Demuro, Elisa Bratzu, Stefano Lorrai, et al.
Clinical Practice and Epidemiology in Mental Health (2024) Vol. 20, Iss. 1
Open Access | Times Cited: 3
Parent-Reported Symptoms and Medications Used Among Children With Severe Neurological Impairment
James A. Feinstein, Chris Feudtner, Allison B. Blackmer, et al.
JAMA Network Open (2020) Vol. 3, Iss. 12, pp. e2029082-e2029082
Open Access | Times Cited: 26
Towards person-centred quality care for children with life-limiting and life-threatening illness: Self-reported symptoms, concerns and priority outcomes from a multi-country qualitative study
Eve Namisango, Katherine Bristowe, Fliss EM Murtagh, et al.
Palliative Medicine (2020) Vol. 34, Iss. 3, pp. 319-335
Open Access | Times Cited: 24
“It Is a Whole Different Life from the Life I Used to Live”: Assessing Parents’ Support Needs in Paediatric Palliative Care
Samar Aoun, Roswitha Stegmann, Renee Deleuil, et al.
Children (2022) Vol. 9, Iss. 3, pp. 322-322
Open Access | Times Cited: 14
Measuring Pediatric Palliative Care Quality: Challenges and Opportunities
Jackelyn Y. Boyden, Jori F. Bogetz, Emily E. Johnston, et al.
Journal of Pain and Symptom Management (2023) Vol. 65, Iss. 5, pp. e483-e495
Open Access | Times Cited: 7
The Quality of Life of Children Facing Life-Limiting Conditions and That of Their Parents in Belgium: A Cross-Sectional Study
Marie Friedel, Isabelle Aujoulat, Bénédicte Brichard, et al.
Children (2023) Vol. 10, Iss. 7, pp. 1167-1167
Open Access | Times Cited: 7
Pediatric Palliative Care: Insights into Assessment Tools and Review Instruments
Simonetta Papa, Anna Mercante, Luca Giacomelli, et al.
Children (2023) Vol. 10, Iss. 8, pp. 1406-1406
Open Access | Times Cited: 7
Patient-reported outcome measures in children, adolescents, and young adults with palliative care needs—a scoping review
Heidi Holmen, Anette Winger, Simen A. Steindal, et al.
BMC Palliative Care (2023) Vol. 22, Iss. 1
Open Access | Times Cited: 7
Exploring critical factors in pediatric palliative care in Latin America: A scoping review
Laia Riera-Negre, Paula Hidalgo-Andrade, María Rosa Rosselló Ramon, et al.
Global Public Health (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 2
Who, What, Where, and How? The State of Family Science in Pediatric Palliative Care
Elizabeth G. Broden, Jackelyn Y. Boyden, Susan Keller, et al.
Journal of Pain and Symptom Management (2024) Vol. 68, Iss. 4, pp. e254-e279
Closed Access | Times Cited: 2
Caregiver Perspectives on Provider Continuity During Prolonged PICU Hospitalizations: A Single-Center Qualitative Study, 2021–2022
Patricia Peña Jiménez, Wendy Leatherman Phipps, Elizabeth Jacob‐Files, et al.
Pediatric Critical Care Medicine (2024) Vol. 25, Iss. 12, pp. 1159-1167
Closed Access | Times Cited: 2
Assessment of an Instrument to Measure Interdisciplinary Staff Perceptions of Quality of Dying and Death in a Pediatric Cardiac Intensive Care Unit
Valerie Bailey, Dorothy M. Beke, Jennifer M. Snaman, et al.
JAMA Network Open (2022) Vol. 5, Iss. 5, pp. e2210762-e2210762
Open Access | Times Cited: 10
Quality Indicators in Pediatric Palliative Care: Considerations for Latin America
Gregorio Zúñiga-Villanueva, Jorge Alberto Ramos-Guerrero, Mónica Osio-Saldaña, et al.
Children (2021) Vol. 8, Iss. 3, pp. 250-250
Open Access | Times Cited: 13
State of the science and future research directions in palliative and end-of-life care in paediatric cardiology: a report from the Harvard Radcliffe Accelerator Workshop
Melissa K. Cousino, Blyth Lord, Elizabeth D. Blume
Cardiology in the Young (2021) Vol. 32, Iss. 3, pp. 431-436
Open Access | Times Cited: 12
Quality of life in childhood advanced cancer: from conceptualization to assessment with the Advance QoL tool
Josianne Avoine-Blondin, Émilie Dumont, Marc-Antoine Marquis, et al.
BMC Palliative Care (2022) Vol. 21, Iss. 1
Open Access | Times Cited: 8
Processus pour le développement d’une stratégie d’évaluation de la qualité de vie en cancer avancé pédiatrique
Lye-Ann Robichaud, Marianne Olivier-d’Avignon, Julie Felipe, et al.
Psycho-Oncologie (2024) Vol. 18, Iss. 2, pp. 127-135
Open Access | Times Cited: 1
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