Early assessment of clinical complexity and home care in patients affected by trisomy 13 and 18.

IF 2.6 3区 医学 Q1 PEDIATRICS European Journal of Pediatrics Pub Date : 2025-02-12 DOI:10.1007/s00431-025-06020-z
Anna Zanin, Matteo Patti, Isabella Rosato, Antuan Divisic, Francesca Rusalen, Irene Maghini, Caterina Agosto, Franca Benini
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Abstract

Purpose: Trisomy 13 and 18 consist of a recurrent pattern of multiple congenital anomalies. The aim of this study was to analyze the clinical characteristics and disease trajectory of a cohort of children with trisomy 13 and 18 followed up by an Italian pediatric palliative care service.

Methods: A single-center retrospective observational study was conducted examining the medical records of patients with trisomy 13 and 18 seen in the Pediatric Palliatives Care (PPC) center of the University Hospital of Padua from 2007 to 2022.

Results: Seventeen patients were included in the analysis. All were born alive; four children are still alive and only three (23%) died at home. All presented high care complexity, as estimated by ACCAPED index (median 86, range 38-129). The median time to receive care from PPC was 3 months (0-108). All patients' parents shared an advance care plan with the PPC team: 13/17 patients (76%) accepted a do not resuscitate (DNR) order. Approximately 12% of patients received at least one surgery. The trend of survival compared with other cohorts reported in the literature does not appear to differ significantly after the initial stages.

Conclusions: The possible recognition of an early evolution toward medical complexity and the availability of home care resources and programs are crucial factors in the management of these children. These indices could become a driving factor in the definition of new outcomes that are more patient-oriented, in addition to mortality.

What is known: • Trisomy 13 and 18 are serious genetic conditions with high mortality rates. In the last years medical interventions including surgery are being offered more frequently, though the appropriateness of these interventions is still debated.

What is new: • The study emphasizes the crucial role of early referral to specialized pediatric palliative care teams and the coordination they provide enabling families to care for their children at home, even with complex medical needs.

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13和18三体患者临床复杂性和家庭护理的早期评估。
目的:13和18三体是一种复发型的多发性先天性异常。本研究的目的是分析意大利儿科姑息治疗服务随访的13和18三体患儿队列的临床特征和疾病轨迹。方法:采用单中心回顾性观察研究,对2007年至2022年在帕多瓦大学医院儿科姑息治疗(PPC)中心就诊的13和18三体患者的病历进行分析。结果:17例患者纳入分析。所有人出生时都是活着的;4名儿童仍然活着,只有3名(23%)在家中死亡。根据accap指数(中位数86,范围38-129),所有患者均表现出较高的护理复杂性。接受PPC治疗的中位时间为3个月(0-108)。所有患者的父母都与PPC团队分享了一份预先护理计划:13/17名患者(76%)接受了不复苏(DNR)命令。大约12%的患者接受了至少一次手术。与文献中报道的其他队列相比,生存趋势在初始阶段后似乎没有显着差异。结论:可能认识到医疗复杂性的早期演变以及家庭护理资源和方案的可用性是这些儿童管理的关键因素。除了死亡率之外,这些指标可能成为定义更以患者为导向的新结果的驱动因素。已知情况:•13和18三体是死亡率高的严重遗传病。在过去几年中,包括手术在内的医疗干预措施越来越频繁,尽管这些干预措施的适当性仍存在争议。新发现:•该研究强调了早期转诊到专门的儿科姑息治疗团队的关键作用,以及他们提供的协调,使家庭能够在家照顾孩子,即使有复杂的医疗需求。
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来源期刊
CiteScore
5.90
自引率
2.80%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The European Journal of Pediatrics (EJPE) is a leading peer-reviewed medical journal which covers the entire field of pediatrics. The editors encourage authors to submit original articles, reviews, short communications, and correspondence on all relevant themes and topics. EJPE is particularly committed to the publication of articles on important new clinical research that will have an immediate impact on clinical pediatric practice. The editorial office very much welcomes ideas for publications, whether individual articles or article series, that fit this goal and is always willing to address inquiries from authors regarding potential submissions. Invited review articles on clinical pediatrics that provide comprehensive coverage of a subject of importance are also regularly commissioned. The short publication time reflects both the commitment of the editors and publishers and their passion for new developments in the field of pediatrics. EJPE is active on social media (@EurJPediatrics) and we invite you to participate. EJPE is the official journal of the European Academy of Paediatrics (EAP) and publishes guidelines and statements in cooperation with the EAP.
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