Rachel C Ashworth, Jay R Malone, Dana Franklin, Lauren R Sorce, Marla L Clayman, Joel Frader, Douglas B White, Kelly N Michelson
{"title":"患者和家长特征与 PICU 中家长决定后悔的关系:2015-2017年 \"导航 \"随机比较试验的二次分析。","authors":"Rachel C Ashworth, Jay R Malone, Dana Franklin, Lauren R Sorce, Marla L Clayman, Joel Frader, Douglas B White, Kelly N Michelson","doi":"10.1097/PCC.0000000000003534","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>To identify self-reported meaningful decisions made by parents in the PICU and to determine patient and parent characteristics associated with the development of parental decision regret, a measurable, self-reported outcome associated with psychologic morbidity.</p><p><strong>Design: </strong>Secondary analysis of the Navigate randomized comparative trial (NCT02333396).</p><p><strong>Setting: </strong>Two tertiary, academic PICUs.</p><p><strong>Patients: </strong>Spanish- or English-speaking parents of PICU patients aged less than 18 years who were expected to remain in the PICU for greater than 24 hours from time of enrollment or who had a risk of mortality greater than 4% based on Pediatric Index of Mortality 2 score.</p><p><strong>Interventions: </strong>None.</p><p><strong>Measurements and main results: </strong>Between April 2015 and March 2017, 233 parents of 209 patients completed a survey 3-5 weeks post-PICU discharge which included the Decision Regret Scale (DRS), a 5-item, 5-point Likert scale tool scored from 0 (no regret) to 100 (maximum regret). Two hundred nine patient/parent dyads were analyzed. The decisions parents reported as most important were categorized as: procedure, respiratory support, medical management, parent-staff interactions and communication, symptom management, fluid/electrolytes/nutrition, and no decision. Fifty-one percent of parents had some decision regret (DRS > 0) with 19% scoring in the moderate-severe range (DRS 26-100). The mean DRS score was 12.7 ( sd 18.1). Multivariable analysis showed that parental Hispanic ethnicity was associated with greater odds ratio (OR 3.12 [95% CI, 1.36-7.13]; p = 0.007) of mild regret. Being parents of a patient with an increased PICU length of stay (LOS) or underlying respiratory disease was associated with greater odds of moderate-severe regret (OR 1.03 [95% CI, 1.009-1.049]; p = 0.004 and OR 2.91 [95% CI, 1.22-6.94]; p = 0.02, respectively).</p><p><strong>Conclusions: </strong>Decision regret was experienced by half of PICU parents in the 2015-2017 Navigate study. The characteristics associated with decision regret (parental ethnicity, PICU LOS, and respiratory disease) are easily identifiable. Further study is needed to understand what contributes to regret in this population and what interventions could provide support and minimize the development of regret.</p>","PeriodicalId":19760,"journal":{"name":"Pediatric Critical Care Medicine","volume":" ","pages":"795-803"},"PeriodicalIF":4.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Associations of Patient and Parent Characteristics With Parental Decision Regret in the PICU: A Secondary Analysis of the 2015-2017 Navigate Randomized Comparative Trial.\",\"authors\":\"Rachel C Ashworth, Jay R Malone, Dana Franklin, Lauren R Sorce, Marla L Clayman, Joel Frader, Douglas B White, Kelly N Michelson\",\"doi\":\"10.1097/PCC.0000000000003534\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>To identify self-reported meaningful decisions made by parents in the PICU and to determine patient and parent characteristics associated with the development of parental decision regret, a measurable, self-reported outcome associated with psychologic morbidity.</p><p><strong>Design: </strong>Secondary analysis of the Navigate randomized comparative trial (NCT02333396).</p><p><strong>Setting: </strong>Two tertiary, academic PICUs.</p><p><strong>Patients: </strong>Spanish- or English-speaking parents of PICU patients aged less than 18 years who were expected to remain in the PICU for greater than 24 hours from time of enrollment or who had a risk of mortality greater than 4% based on Pediatric Index of Mortality 2 score.</p><p><strong>Interventions: </strong>None.</p><p><strong>Measurements and main results: </strong>Between April 2015 and March 2017, 233 parents of 209 patients completed a survey 3-5 weeks post-PICU discharge which included the Decision Regret Scale (DRS), a 5-item, 5-point Likert scale tool scored from 0 (no regret) to 100 (maximum regret). Two hundred nine patient/parent dyads were analyzed. The decisions parents reported as most important were categorized as: procedure, respiratory support, medical management, parent-staff interactions and communication, symptom management, fluid/electrolytes/nutrition, and no decision. Fifty-one percent of parents had some decision regret (DRS > 0) with 19% scoring in the moderate-severe range (DRS 26-100). The mean DRS score was 12.7 ( sd 18.1). Multivariable analysis showed that parental Hispanic ethnicity was associated with greater odds ratio (OR 3.12 [95% CI, 1.36-7.13]; p = 0.007) of mild regret. Being parents of a patient with an increased PICU length of stay (LOS) or underlying respiratory disease was associated with greater odds of moderate-severe regret (OR 1.03 [95% CI, 1.009-1.049]; p = 0.004 and OR 2.91 [95% CI, 1.22-6.94]; p = 0.02, respectively).</p><p><strong>Conclusions: </strong>Decision regret was experienced by half of PICU parents in the 2015-2017 Navigate study. The characteristics associated with decision regret (parental ethnicity, PICU LOS, and respiratory disease) are easily identifiable. Further study is needed to understand what contributes to regret in this population and what interventions could provide support and minimize the development of regret.</p>\",\"PeriodicalId\":19760,\"journal\":{\"name\":\"Pediatric Critical Care Medicine\",\"volume\":\" \",\"pages\":\"795-803\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pediatric Critical Care Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1097/PCC.0000000000003534\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/5/10 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CRITICAL CARE MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Critical Care Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/PCC.0000000000003534","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/5/10 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CRITICAL CARE MEDICINE","Score":null,"Total":0}
引用次数: 0
摘要
目的:确定重症监护病房中父母自我报告的有意义决定,并确定与父母决定后悔相关的患者和父母特征:确定PICU中父母自我报告的有意义决定,并确定与父母决定后悔相关的患者和父母特征,这是一种可测量的、自我报告的与心理发病率相关的结果:设计:Navigate随机对比试验(NCT02333396)的二次分析:两所三级学术性 PICU:患者:年龄小于 18 岁的 PICU 患者的西班牙语或英语父母,这些患者自注册时起预计将在 PICU 留院超过 24 小时,或根据儿科死亡率指数 2 评分,其死亡风险超过 4%:无:2015年4月至2017年3月期间,209名患者的233名家长完成了PICU出院后3-5周的调查,其中包括决定后悔量表(DRS),这是一种5项5分的李克特量表工具,评分范围从0(无后悔)到100(最大后悔)。共对 29 个患者/家长二元组进行了分析。家长认为最重要的决定分为以下几类:手术、呼吸支持、医疗管理、家长与医护人员的互动和沟通、症状管理、输液/电解质/营养以及不做决定。51%的家长对做出决定有些后悔(DRS > 0),19%的家长评分在中度-重度范围内(DRS 26-100)。DRS 平均得分为 12.7(sd 18.1)。多变量分析显示,父母为西班牙裔与轻度遗憾的几率比较大(OR 3.12 [95% CI, 1.36-7.13]; p = 0.007)有关。PICU住院时间(LOS)延长或患有呼吸系统疾病的患者的父母与中度-重度后悔的几率较大相关(OR 1.03 [95% CI, 1.009-1.049]; p = 0.004 和 OR 2.91 [95% CI, 1.22-6.94]; p = 0.02):在2015-2017年的 "导航 "研究中,有一半的PICU家长经历过决策后悔。与决定后悔相关的特征(父母种族、PICU LOS 和呼吸系统疾病)很容易识别。还需要进一步研究,以了解是什么导致了这一人群的后悔,以及哪些干预措施可以提供支持并最大限度地减少后悔的发生。
Associations of Patient and Parent Characteristics With Parental Decision Regret in the PICU: A Secondary Analysis of the 2015-2017 Navigate Randomized Comparative Trial.
Objectives: To identify self-reported meaningful decisions made by parents in the PICU and to determine patient and parent characteristics associated with the development of parental decision regret, a measurable, self-reported outcome associated with psychologic morbidity.
Design: Secondary analysis of the Navigate randomized comparative trial (NCT02333396).
Setting: Two tertiary, academic PICUs.
Patients: Spanish- or English-speaking parents of PICU patients aged less than 18 years who were expected to remain in the PICU for greater than 24 hours from time of enrollment or who had a risk of mortality greater than 4% based on Pediatric Index of Mortality 2 score.
Interventions: None.
Measurements and main results: Between April 2015 and March 2017, 233 parents of 209 patients completed a survey 3-5 weeks post-PICU discharge which included the Decision Regret Scale (DRS), a 5-item, 5-point Likert scale tool scored from 0 (no regret) to 100 (maximum regret). Two hundred nine patient/parent dyads were analyzed. The decisions parents reported as most important were categorized as: procedure, respiratory support, medical management, parent-staff interactions and communication, symptom management, fluid/electrolytes/nutrition, and no decision. Fifty-one percent of parents had some decision regret (DRS > 0) with 19% scoring in the moderate-severe range (DRS 26-100). The mean DRS score was 12.7 ( sd 18.1). Multivariable analysis showed that parental Hispanic ethnicity was associated with greater odds ratio (OR 3.12 [95% CI, 1.36-7.13]; p = 0.007) of mild regret. Being parents of a patient with an increased PICU length of stay (LOS) or underlying respiratory disease was associated with greater odds of moderate-severe regret (OR 1.03 [95% CI, 1.009-1.049]; p = 0.004 and OR 2.91 [95% CI, 1.22-6.94]; p = 0.02, respectively).
Conclusions: Decision regret was experienced by half of PICU parents in the 2015-2017 Navigate study. The characteristics associated with decision regret (parental ethnicity, PICU LOS, and respiratory disease) are easily identifiable. Further study is needed to understand what contributes to regret in this population and what interventions could provide support and minimize the development of regret.
期刊介绍:
Pediatric Critical Care Medicine is written for the entire critical care team: pediatricians, neonatologists, respiratory therapists, nurses, and others who deal with pediatric patients who are critically ill or injured. International in scope, with editorial board members and contributors from around the world, the Journal includes a full range of scientific content, including clinical articles, scientific investigations, solicited reviews, and abstracts from pediatric critical care meetings. Additionally, the Journal includes abstracts of selected articles published in Chinese, French, Italian, Japanese, Portuguese, and Spanish translations - making news of advances in the field available to pediatric and neonatal intensive care practitioners worldwide.