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1型戈谢病患者从儿科护理向成人护理的过渡:两项针对患者和医疗保健专业人员的国际调查结果

Transition of patients with Gaucher disease type 1 from pediatric to adult care: results from two international surveys of patients and health care professionals.

作者信息

Stepien Karolina M, Žnidar Irena, Kieć-Wilk Beata, Jones Angel, Castillo-García Daniela, Abdelwahab Magy, Revel-Vilk Shoshana, Lineham Ella, Hughes Derralynn, Ramaswami Uma, Collin-Histed Tanya

机构信息

Adult Inherited Metabolic Diseases, Salford Royal Organization, Northern Care Alliance NHS Foundation Trust, Salford, United Kingdom.

International Gaucher Alliance (IGA), London, United Kingdom.

出版信息

Front Pediatr. 2024 Aug 27;12:1439236. doi: 10.3389/fped.2024.1439236. eCollection 2024.

Abstract

INTRODUCTION

Gaucher disease (GD) is a rare, autosomal recessive lysosomal storage disorder caused by a deficiency in the enzyme glucocerebrosidase. The most common subtype in Europe and the USA, type 1 (GD1), is characterized by fatigue, cytopenia, splenomegaly, hepatomegaly, bone disease, and rarely pulmonary disease. Increased life expectancy brought about by improved treatments has led to new challenges for adolescents and their transition to adult care. Efficient healthcare transition to adult care is essential to manage the long-term age-related complications of the disease.

METHODS

This international study consisted of two online surveys: one survey for patients with GD1 and one survey for healthcare professionals (HCPs) involved in treatment of patients with GD1. The aims of this international, multi-center project were to evaluate the current transition process in various countries and to understand the challenges that both HCPs and patients experience.

RESULTS

A total of 45 patients and 26 HCPs took part in the survey, representing 26 countries. Our data showed that a third (11/33) of patients were aware of transition clinics and most stated that the clinic involved patients with metabolic diseases or with GD. Seven patients attended a transition clinic, where most patients (5/7) received an explanation of the transition process. Approximately half of HCPs (46%; 12/26) had a transition clinic coordinator in their healthcare center, and 10 of HCPs had a transition clinic for patients with metabolic diseases in their healthcare center. HCPs reported that transition clinics were comprised of multi-disciplinary teams, with most patients over the age of 18 years old managed by hematology specialists. The main challenges of the transition process reported by HCPs included limited funding, lack of expertise and difficulty coordinating care amongst different specialties.

DISCUSSION

Our study demonstrates the lack of a standardized process, the need to raise awareness of transition clinics amongst patients and the differences between the transition process in different countries. Both patients and HCPs expressed the need for a specialist individual responsible for transition, efficient coordination between pediatricians and adult specialists and for patient visits to the adult center prior to final transition of care.

摘要

引言

戈谢病(GD)是一种罕见的常染色体隐性溶酶体贮积症,由葡萄糖脑苷脂酶缺乏引起。在欧洲和美国最常见的亚型1型(GD1),其特征为疲劳、血细胞减少、脾肿大、肝肿大、骨病,且很少出现肺部疾病。治疗改善带来的预期寿命延长给青少年及其向成人护理过渡带来了新挑战。高效的医疗护理过渡到成人护理对于管理该疾病与年龄相关的长期并发症至关重要。

方法

这项国际研究包括两项在线调查:一项针对GD1患者的调查,另一项针对参与GD1患者治疗的医疗保健专业人员(HCP)的调查。这个国际多中心项目的目的是评估各国当前的过渡过程,并了解HCP和患者所面临的挑战。

结果

共有45名患者和26名HCP参与了调查,代表26个国家。我们的数据显示,三分之一(11/33)的患者知晓过渡诊所,且大多数表示该诊所涉及患有代谢疾病或GD的患者。7名患者参加了过渡诊所,其中大多数患者(5/7)收到了关于过渡过程的解释。约一半的HCP(46%;12/26)所在的医疗保健中心有过渡诊所协调员,10名HCP所在的医疗保健中心有为患有代谢疾病的患者设立的过渡诊所。HCP报告称,过渡诊所由多学科团队组成,大多数18岁以上的患者由血液学专家管理。HCP报告的过渡过程中的主要挑战包括资金有限、缺乏专业知识以及不同专科之间协调护理困难。

讨论

我们的研究表明缺乏标准化流程,需要提高患者对过渡诊所的认识,以及不同国家过渡过程存在差异。患者和HCP都表示需要有一名负责过渡的专科人员、儿科医生和成人专科医生之间进行高效协调,以及患者在最终护理过渡前到成人中心就诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b300/11430091/22418ed91459/fped-12-1439236-g001.jpg

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