[1] |
World Heath Organization. Palliative care for children[EB/OL]. (2023-06-01)[2024-05-10]. https://www.who.int/europe/news-room/fact-sheets/item/palliative-care-for-children.
|
[2] |
Ortiz R, Vásquez L, Giri B, et al. Developing and sustaining high-quality care for children with cancer:the WHO global initia-tive for childhood cancer[J]. Rev Panam Salud Publica, 2023, 47:e164.
|
[3] |
Vanbutsele G, van Belle S, Surmont V, et al. The effect of early and systematic integration of palliative care in oncology on quality of life and health care use near the end of life:a randomised controlled trial[J]. Eur J Cancer, 2020,124:186-193.
|
[4] |
Ananth P, Lindsay M, Nye R, et al. End-of-life care quality for children with cancer who receive palliative care[J]. Pediatr Blood Cancer, 2022, 69(9):e29841.
|
[5] |
褚云怡, 江子芳, 贺泽翻, 等. 基于癌症患者体验的安宁疗护质量评估工具的系统评价[J]. 中华护理杂志, 2024, 59(13):1657-1665.
DOI
|
|
Chu YY, Jiang ZF, He ZF, et al. Palliative care quality assess-ment tools based on the cancer patient experience:a systema-tic review[J]. Chin J Nurs, 2024, 59(13):1657-1665.
|
[6] |
Prinsen CAC, Mokkink LB, Bouter LM, et al. COSMIN guideline for systematic reviews of patient-reported outcome measures[J]. Qual Life Res, 2018, 27(5):1147-1157.
DOI
PMID
|
[7] |
Lindley LC, Edwards SL. Geographic access to hospice care for children with cancer in Tennessee,2009 to 2011[J]. Am J Hosp Palliat Care, 2015, 32(8):849-854.
DOI
PMID
|
[8] |
Mokkink LB, de Vet HCW, Prinsen CAC, et al. COSMIN risk of bias checklist for systematic reviews of patient-reported outcome measures[J]. Qual Life Res, 2018, 27(5):1171-1179.
DOI
PMID
|
[9] |
Alhazzani W, Guyatt G. An overview of the GRADE approach and a peek at the future[J]. Med J Aust, 2018, 209(7):291-292.
PMID
|
[10] |
Mokkink LB, de Vet HCW, Prinsen CAC, et al. COSMIN risk of bias checklist for systematic reviews of patient-reported outcome measures[J]. Qual Life Res, 2018, 27(5):1171-1179.
DOI
PMID
|
[11] |
Sellers DE, Dawson R, Cohen-Bearak A, et al. Measuring the quality of dying and death in the pediatric intensive care setting:the clinician PICU-QODD[J]. J Pain Symptom Manage, 2015, 49(1):66-78.
|
[12] |
Nagoya Y, Miyashita M, Shiwaku H. Pediatric cancer patients’ important end-of-life issues,including quality of life:a survey of pediatric oncologists and nurses in Japan[J]. J Palliat Med, 2017, 20(5):487-493.
DOI
PMID
|
[13] |
Kim JY, Park BK. The most important aspects for a good death:perspectives from parents of children with cancer[J]. Inquiry, 2021,58:469580211028580.
|
[14] |
Zimmermann K, Cignacco E, Eskola K, et al. Development and initial validation of the Parental PELICAN Questionnaire(PaPEQu):an instrument to assess parental experiences and needs during their child’s end-of-life care[J]. J Adv Nurs, 2015, 71(12):3006-3017.
DOI
PMID
|
[15] |
Boyden JY, Feudtner C, Deatrick JA, et al. Developing a family-reported measure of experiences with home-based pediatric palliative and hospice care:a multi-method,multi-stakeholder approach[J]. BMC Palliat Care, 2021, 20(1):17.
|
[16] |
Widger K, Tourangeau AE, Steele R, et al. Initial development and psychometric testing of an instrument to measure the quality of children’s end-of-life care[J]. BMC Palliat Care, 2015, 14(1):1.
|
[17] |
Kristjanson LJ. Validity and reliability testing of the FAM-CARE Scale:measuring family satisfaction with advanced cancer care[J]. Soc Sci Med, 1993, 36(5):693-701.
DOI
PMID
|
[18] |
Chattat R, Ottoboni G, Zeneli A, et al. The Italian version of the FAMCARE Scale:a validation study[J]. Support Care Cancer, 2016, 24(9):3821-3830.
DOI
PMID
|
[19] |
Coombes L, Hareardóttir D, Braybrook D, et al. Achieving con-sensus on priority items for paediatric palliative care outcome measurement:results from a modified Delphi survey,engage-ment with a children’s research involvement group and expert item generation[J]. Palliat Med, 2023, 37(10):1509-1519.
DOI
PMID
|
[20] |
Friedel M, Brichard B, Boonen S, et al. Face and content vali-dity,acceptability,and feasibility of the adapted version of the Children’s Palliative Outcome Scale:a qualitative pilot study[J]. J Palliat Med, 2021, 24(2):181-188.
|
[21] |
Namisango E, Bristowe K, Murtagh FE, et al. Face and content validity,acceptability,feasibility,and implementability of a novel outcome measure for children with life-limiting or life-threa-tening illness in three sub-Saharan African countries[J]. Palliat Med, 2022, 36(7):1140-1153.
DOI
PMID
|
[22] |
Williams C, Cairnie J, Fines V, et al. Construction of a parent-derived questionnaire to measure end-of-life care after with-drawal of life-sustaining treatment in the neonatal intensive care unit[J]. Pediatrics, 2009, 123(1):e87-e95.
|
[23] |
Lykke C, Ekholm O, Olsen M, et al. Paediatric End-of-Life Care-Symptoms and Problems:parent assessment[J]. BMJ Support Palliat Care, 2023, 13(e2):e327-e333.
|
[24] |
刘素香, 边莉, 张叶群, 等. 基于COSMIN指南对糖尿病患者健康素养评估工具的系统评价[J]. 中华护理杂志, 2023, 58(21):2670-2677.
DOI
|
|
Liu SX, Bian L, Zhang YQ, et al. A systematic review of health literacy assessment tools for diabetic patients based on COSMIN guidelines[J]. Chin J Nurs, 2023, 58(21):2670-2677.
DOI
|
[25] |
Terwee CB, Prinsen CAC, Ricci Garotti MG, et al. The quality of systematic reviews of health-related outcome measurement instruments[J]. Qual Life Res, 2016, 25(4):767-779.
DOI
PMID
|
[26] |
Lee EH, Kim CJ, Lee J, et al. Self-administered health literacy instruments for people with diabetes:systematic review of measurement properties[J]. J Adv Nurs, 2017, 73(9):2035-2048.
|
[27] |
陈丽霞, 施慧, 朱德政, 等. 成人低血糖恐惧评估工具的质量评价[J]. 中华护理杂志, 2024, 59(9):1072-1079.
|
|
Chen LX, Shi H, Zhu DZ, et al. Quality appraisal of hypogly-cemia fear assessment tools for adults[J]. Chin J Nurs, 2024, 59(9):1072-1079.
|