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解决胱氨酸病患者向成人护理过渡的心理社会方面问题。

Addressing the psychosocial aspects of transition to adult care in patients with cystinosis.

机构信息

1st Department of Pediatrics, Aristotle University Thessaloniki, Hippokratio Hospital, 49 Konstantinoupoleos Str, 54642, Thessaloniki, Greece.

Department of Pediatric Nephrology, University Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Pediatr Nephrol. 2024 Oct;39(10):2861-2874. doi: 10.1007/s00467-024-06345-1. Epub 2024 Mar 22.

Abstract

Cystinosis is a rare autosomal-recessive lysosomal storage disease that progressively affects multiple organs beginning with the kidneys. Patients require lifelong multidisciplinary care for the management of kidney disease and progressive extra-renal manifestations, and thus, they are especially fragile and vulnerable during transition from pediatric to adult care. Previous documents have provided guidance to help the medical transition of these highly burdened patients. Patients and their families often experience great psychological distress and face significant social challenges; for these reasons, they often need help from psychologists, social workers, and other psychosocial professionals. Due to the rarity of the disease, most psychosocial professionals have no expertise in this disorder and require advice. To this end, a steering committee (SC) composed of six experts, including pediatric nephrologists, psychologists, and social workers with experience in the care for patients with cystinosis, have identified and addressed seven key questions related to psychosocial challenges of the disease and the burden of treatment. Ten additional international experts (the extended faculty, EF) were invited to answer these questions. Since robust evidence is lacking, as in many rare diseases, conclusions were based on collective agreement between members of the SC and the EF, and the consolidated answers were summarized into expert opinion statements. The present document contains information on the concerns and psychosocial burden of patients with cystinosis and of their caregivers, and provides practical advice for timely and appropriate support to facilitate the transition to adult care.

摘要

胱氨酸病是一种罕见的常染色体隐性溶酶体贮积病,它从肾脏开始逐渐影响多个器官。患者需要终身接受多学科护理,以管理肾脏疾病和进行性的肾脏外表现,因此,在从儿科护理向成人护理过渡期间,他们尤其脆弱和易受影响。之前的文件提供了指导,以帮助这些负担沉重的患者进行医学过渡。患者及其家属经常经历巨大的心理困扰,并面临重大的社会挑战;因此,他们通常需要心理学家、社会工作者和其他社会心理专业人员的帮助。由于该疾病罕见,大多数社会心理专业人员对这种疾病没有专业知识,因此需要提供建议。为此,一个由六名专家组成的指导委员会 (SC),包括儿科肾脏病学家、心理学家和有胱氨酸病患者护理经验的社会工作者,确定并解决了与疾病的社会心理挑战和治疗负担有关的七个关键问题。还邀请了另外 10 名国际专家(扩展教师,EF)来回答这些问题。由于缺乏强有力的证据,就像许多罕见疾病一样,结论是基于 SC 和 EF 成员之间的集体协议,总结出的综合答案被概括为专家意见声明。本文件包含了关于胱氨酸病患者及其照顾者的关注点和社会心理负担的信息,并为及时和适当的支持提供了实用建议,以促进向成人护理的过渡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee38/11349776/a603df7c81d1/467_2024_6345_Figa_HTML.jpg

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