Differences in Inpatient Palliative Care Consultation During the Terminal Admission for Pediatric Neuro-Oncology Patients.

Chinwe S Udemgba, Brett K Palama, Wendy Darlington, K Sarah Hoehn
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Abstract

Pediatric neuro-oncology patients have one of the highest mortality rates among all children with cancer. Our study examines the potential relationship between palliative care consultation and intensity of in-hospital care and determines if racial and ethnic differences are associated with palliative care consultations during their terminal admission. Retrospective observational study using the Pediatric Health Information System (PHIS) database with data from U.S. children's hospitals. PHIS was queried for patients under 18 years of age who received a diagnosis of brain tumor and had their terminal admission between January 1, 2017 and December 31, 2021. Of the 567 patients who fit the inclusion criteria, 359 (63%) patients had an inpatient palliative care consultation during their terminal hospital stay. There were no statistically significant differences seen when comparing palliative care consultation rates among racial groups. When comparing the ethnicity variables, patients in the Hispanic group had approximately a 10% higher rate of palliative care consultations than their non-Hispanic counterpart. Patients with palliative care consultations had a lower percentage of PICU admission (64.9 vs 83.2), mechanical ventilation (51.0 vs 76.0), and TPN use (18.1 vs 25.5) despite having similar lengths of stay. Pediatric neuro-oncology patients who received a palliative care consultation during their terminal hospital stay had lower intensity care (lower rates PICU admission, mechanical ventilation use, and TPN use) despite having similar lengths of stay. This may reflect the enhanced decision-making support for the patients and their families so that they may consider all options. Children facing a terminal illness and their families deserve access to optimal supportive services. This study highlights the importance of integrating palliative care in hospital admissions of terminally ill children with neuro-oncological diagnoses.

小儿神经肿瘤患者临终住院期间姑息治疗咨询的差异。
小儿神经肿瘤患者是所有癌症儿童中死亡率最高的患者之一。我们的研究考察了姑息治疗咨询与院内护理强度之间的潜在关系,并确定种族和民族差异是否与临终住院期间的姑息治疗咨询有关。回顾性观察研究使用儿童健康信息系统(PHIS)数据库的数据来自美国儿童医院。对2017年1月1日至2021年12月31日期间被诊断为脑肿瘤并最终入院的18岁以下患者进行了PHIS查询。在符合纳入标准的567例患者中,359例(63%)患者在临终住院期间进行了住院姑息治疗咨询。当比较不同种族的姑息治疗咨询率时,没有统计学上的显著差异。当比较种族变量时,西班牙裔组患者的姑息治疗咨询率比非西班牙裔患者高约10%。尽管住院时间相似,但接受姑息治疗咨询的患者PICU入院率(64.9比83.2)、机械通气率(51.0比76.0)和TPN使用率(18.1比25.5)较低。在终末住院期间接受姑息治疗咨询的儿科神经肿瘤患者,尽管住院时间相似,但其护理强度较低(PICU入院率较低,机械通气率较低,TPN使用率较低)。这可能反映了对患者及其家属的决策支持的增强,以便他们可以考虑所有的选择。面临绝症的儿童及其家人应该获得最佳的支持性服务。本研究强调了将姑息治疗纳入患有神经肿瘤诊断的绝症儿童住院治疗的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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