The NeoPACE study: study protocol for the development of a core outcome set for neonatal palliative care

被引:2
作者
Gallagher, Katie [1 ]
Chant, Kathy [1 ]
Mancini, Alex [2 ]
Bluebond-Langner, Myra [3 ]
Marlow, Neil [1 ]
机构
[1] UCL, UCL Elizabeth Garrett Anderson Inst Womens Hlth, 74 Huntley St, London WC1E 6AU, England
[2] Chelsea & Westminster Hosp NHS Fdn Trust, London, England
[3] UCL, UCL Inst Child Hlth, London, England
关键词
Neonatal intensive care; Palliative care; Outcome studies; INFANTS; LIFE; END;
D O I
10.1186/s12904-023-01326-x
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
BackgroundNeonatal death is the leading category of death in children under the age of 5 in the UK. Many babies die following decisions between parents and the neonatal team; when a baby is critically unwell, with the support of healthcare professionals, parents may make the decision to stop active treatment and focus on ensuring their baby has a 'good' death. There is very little evidence to support the clinical application of neonatal palliative care and/or end-of-life care, resulting in variation in clinical provision between neonatal units. Developing core outcomes for neonatal palliative care would enable the development of measures of good practice and enhance our care of families. The aim of this study is to develop a core outcome set with associated tools for measuring neonatal palliative care.MethodThis study has four phases: (1) identification of potential outcomes through systematic review and qualitative interviews with key stakeholders, including parents and healthcare professionals (2) an online Delphi process with key stakeholders to determine core outcomes (3) identification of outcome measures to support clinical application of outcome use (4) dissemination of the core outcome set for use across neonatal units in the UK. Key stakeholders include parents, healthcare professionals, and researchers with a background in neonatal palliative care.DiscussionDeveloping a core outcome set will standardise minimum reported outcomes for future research and quality improvement projects designed to determine the effectiveness of interventions and clinical care during neonatal palliative and/or end-of-life care. The core outcome set will provide healthcare professionals working in neonatal palliative and/or end-of-life support with an increased and consistent evidence base to enhance practice in this area.Trial registrationThe study has been registered with the COMET initiative (https://www.comet-initiative.org/Studies/Details/1470) and the systematic review is registered with the International Prospective Register of Systematic Reviews (PROSPERO) (CRD42023451068).
引用
收藏
页数:8
相关论文
共 50 条
  • [31] Qualitative Study of Nurses ' Experiences as They Learned to Provide Neonatal Palliative Care
    St Louis, Julia
    Raffin-Bouchal, Shelley
    Benzies, Karen
    Sinclair, Shane
    JOGNN-JOURNAL OF OBSTETRIC GYNECOLOGIC AND NEONATAL NURSING, 2024, 53 (03): : 264 - 271
  • [32] Core outcome domains of pediatric palliative care for children with severe neurological impairment and their families: A qualitative interview study
    Ribbers, Sophie
    Wager, Julia
    Hartenstein-Pinter, Almut
    Zernikow, Boris
    Reuther, Mandira
    PALLIATIVE MEDICINE, 2020, 34 (03) : 309 - 318
  • [33] Development, implementation and evaluation a palliative care program for colorectal cancer patients: a mixed methods protocol study
    Bahrami, Masoud
    Masoumy, Masoumeh
    Sadeghi, Alireza
    Mosavizadeh, Rohallah
    BMC CANCER, 2022, 22 (01)
  • [34] Development, implementation and evaluation a palliative care program for colorectal cancer patients: a mixed methods protocol study
    Masoud Bahrami
    Masoumeh Masoumy
    Alireza Sadeghi
    Rohallah Mosavizadeh
    BMC Cancer, 22
  • [35] Monitoring of Palliative Care Symptoms and Concerns in Specialized Palliative Home Care Using an Electronic Version of the Integrated Palliative care Outcome Scale (Palli-MONITOR): protocol for a mixed-methods study
    Bolzani, Anna
    Ramsenthaler, Christina
    Hodiamont, Farina
    Burner-Fritsch, Isabel Sophie
    Bausewein, Claudia
    BMJ OPEN, 2021, 11 (06):
  • [36] Continuous palliative sedation until death: a qualitative study of palliative care clinicians' experiences
    Guite-Verret, Alexandra
    Boivin, Jessica
    Hanna, Andrew M. R.
    Downar, James
    Bush, Shirley H.
    Marcoux, Isabelle
    Guay, Diane
    Tapp, Diane
    Lapenskie, Julie
    Gagnon, Bruno
    BMC PALLIATIVE CARE, 2024, 23 (01)
  • [37] Care plus study: a multi-site implementation of early palliative care in routine practice to improve health outcomes and reduce hospital admissions for people with advanced cancer: a study protocol
    Philip, Jennifer
    Le Gautier, Roslyn
    Collins, Anna
    Nowak, Anna K.
    Le, Brian
    Crawford, Gregory B.
    Rankin, Nicole
    Krishnasamy, Meinir
    Mitchell, Geoff
    McLachlan, Sue-Anne
    IJzerman, Maarten
    Hudson, Robyn
    Rischin, Danny
    Sousa, Tanara Vieira
    Sundararajan, Vijaya
    BMC HEALTH SERVICES RESEARCH, 2021, 21 (01)
  • [38] Improvement and implementation of a national individual care plan in paediatric palliative care: a study protocol
    Joren, Chantal Y.
    Kars, Marijke C.
    Kremer, Leontien C. M.
    Rippen, Hester
    Verhagen, A. A. Eduard
    Aris-Meijer, Judith L.
    BMJ PAEDIATRICS OPEN, 2023, 7 (01)
  • [39] Leadership Core Competencies in Palliative Care-Recommendations from the European Association for Palliative Care: Delphi Study
    Parczyk, Olivia
    Frerich, Gerrit
    Loucka, Martin
    Voltz, Raymond
    Payne, Sheila
    JOURNAL OF PALLIATIVE MEDICINE, 2024, 27 (03) : 345 - 357
  • [40] A Survey of Attitudes and Beliefs about Care, Compassion and Communities Networks in Palliative Care. A Preliminary Study for the Development of a Compassionate University
    Librada Flores, Silvia
    Roa Trujillo, Sonia Herminia
    Torrejano Gonzalex, Nurlian
    Garcia Buitrago, Maria del Pilar
    Lucas Diaz, Miguel Angel
    HEALTHCARE, 2021, 9 (08)