Division of Cardiology Department of Pediatrics Children's Hospital Los Angeles Los Angeles CA.
Department of Cardiology Boston Children's Hospital Boston MA.
J Am Heart Assoc. 2021 Jan 19;10(2):e018488. doi: 10.1161/JAHA.120.018488. Epub 2021 Jan 14.
Background The unpredictable trajectory of pediatric advanced heart disease makes prognostication difficult for physicians and informed decision-making challenging for families. This study evaluated parent and physician understanding of disease burden and prognosis in hospitalized children with advanced heart disease. Methods and Results A longitudinal survey study of parents and physicians caring for patients with advanced heart disease age 30 days to 19 years admitted for ≥7 days was performed over a 1-year period (n=160 pairs). Percentage agreement and weighted kappa statistics were used to assess agreement. Median patient age was 1 year (interquartile range, 1-5), 39% had single-ventricle lesions, and 37% were in the cardiac intensive care unit. Although 92% of parents reported understanding their child's prognosis "extremely well" or "well," 28% of physicians thought parents understood the prognosis only "a little," "somewhat," or "not at all." Better parent-reported prognostic understanding was associated with greater preparedness for their child's medical problems (odds ratio, 4.7; 95% CI, 1.4-21.7, =0.02). There was poor parent-physician agreement in assessing functional class, symptom burden, and likelihood of limitations in physical activity and learning/behavior; on average, parents were more optimistic. Many parents (47%) but few physicians (6%) expected the child to have normal life expectancy. Conclusions Parents and physicians caring for children with advanced heart disease differed in their perspectives regarding prognosis and disease burden. Physicians tended to underestimate the degree of parent-reported symptom burden. Parents were less likely to expect limitations in physical activity, learning/behavior, and life expectancy. Combined interventions involving patient-reported outcomes, parent education, and physician communication tools may be beneficial.
背景 儿科晚期心脏病的不可预测轨迹使得医生难以预测,家庭也难以做出明智决策。本研究评估了住院患有晚期心脏病的儿童的父母和医生对疾病负担和预后的理解。
方法和结果 在为期 1 年的时间内(n=160 对),对 30 天至 19 岁的患有晚期心脏病且住院时间≥7 天的患儿的父母和医生进行了一项前瞻性纵向调查研究。使用百分比一致性和加权 kappa 统计来评估一致性。患者的中位年龄为 1 岁(四分位间距,1-5 岁),39%有单心室病变,37%在心脏重症监护病房。尽管 92%的父母报告说他们“非常”或“很好”地了解他们孩子的预后,但 28%的医生认为父母仅“有点”、“有些”或“根本不了解”预后。父母报告的预后理解程度更好与他们对孩子医疗问题的准备程度更高相关(优势比,4.7;95%CI,1.4-21.7,=0.02)。在评估功能分级、症状负担以及身体活动和学习/行为受限的可能性方面,父母和医生之间的意见存在差异;平均而言,父母更为乐观。许多父母(47%)而很少有医生(6%)期望孩子具有正常的预期寿命。
结论 照顾患有晚期心脏病的儿童的父母和医生在预后和疾病负担方面的观点存在差异。医生往往低估了父母报告的症状负担程度。父母不太可能期望身体活动、学习/行为和预期寿命受限。涉及患者报告结果、父母教育和医生沟通工具的综合干预措施可能是有益的。