Manikowski Alison, Williamson Lewis Rebecca, Bennett Tonya, Miller Heather, Mertens Ann, Wasilewski-Masker Karen, Escoffery Cam, Gilleland Marchak Jordan
Emory University School of Medicine, Atlanta, GA.
Aflac Cancer and Blood Disorders Center, Atlanta, GA.
JCO Oncol Pract. 2022 Jul;18(7):e1198-e1208. doi: 10.1200/OP.21.00836. Epub 2022 Apr 20.
This study aimed to evaluate the reach and implementation of an electronic psychosocial screening program among caregivers of pediatric oncology patients, as well as characterize caregiver distress.
Participants (N = 2,013) included caregivers of patients age 0-17.99 years presenting across 9,280 outpatient oncology visits (median = 2; range = 1-52) from September 2018 to June 2019. At check-ins, caregivers electronically completed the pediatric distress thermometer via a patient-facing electronic health record (EHR) application. Caregiver distress ratings ≥ 8 triggered electronic alerts to medical teams to refer for social work support at point of care. Patient clinical and demographic differences in reach and fidelity were evaluated using univariate chi-square and t-tests. Caregivers reporting high distress were compared with caregivers without reports of high distress using univariate and multivariable logistic regression.
The e-screening program was able to reach a caregiver for nearly all children seen during the study period, with 95.5% (1,923/2,013) of patients having a caregiver-completed pediatric distress thermometer. On screeners where caregivers reported high distress, medical teams made appropriate referrals to social work 95.5% (471/493) of the time. Overall, 16.9% (325/1,923) of caregivers ever indicated high distress (score ≥ 8), with caregivers of newly diagnosed (odds ratio = 3.16; 95% CI, 2.12 to 4.71) and on-therapy (odds ratio = 2.81; 95% CI, 2.11 to 3.76) patients being more likely to report high distress, compared with those who were off-treatment for the entire study.
Leveraging EHR technology to provide evidence-based psychosocial screening can aid in successfully reaching a significant proportion of caregivers of pediatric oncology patients to identify and respond to ongoing psychosocial distress.
本研究旨在评估电子心理社会筛查项目在儿科肿瘤患者照料者中的覆盖范围和实施情况,并对照料者的痛苦程度进行特征描述。
参与者(N = 2013)包括0至17.99岁患者的照料者,这些患者在2018年9月至2019年6月期间进行了9280次门诊肿瘤就诊(中位数 = 2;范围 = 1至52)。在登记时,照料者通过面向患者的电子健康记录(EHR)应用程序以电子方式完成儿科痛苦温度计评估。照料者痛苦评分≥8会触发电子警报,提示医疗团队在护理点转介以获得社会工作支持。使用单因素卡方检验和t检验评估患者在覆盖范围和依从性方面的临床和人口统计学差异。使用单因素和多变量逻辑回归将报告高度痛苦的照料者与未报告高度痛苦的照料者进行比较。
电子筛查项目能够覆盖研究期间几乎所有就诊儿童的照料者,95.5%(1923/2013)的患者有照料者完成的儿科痛苦温度计评估。在照料者报告高度痛苦的筛查中,医疗团队在95.5%(471/493)的情况下适当转介给了社会工作。总体而言,16.9%(325/1923)的照料者曾表示高度痛苦(评分≥8),与整个研究期间未接受治疗的患者照料者相比,新诊断患者的照料者(优势比 = 3.16;95% CI,2.12至4.71)和正在接受治疗的患者照料者(优势比 = 2.81;95% CI,2.11至3.76)更有可能报告高度痛苦。
利用电子健康记录技术提供基于证据的心理社会筛查有助于成功覆盖很大一部分儿科肿瘤患者的照料者,以识别并应对持续存在的心理社会痛苦。