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

被引:0
作者
Stepien, Karolina M. [1 ]
Znidar, Irena [2 ]
Kiec-Wilk, Beata [3 ,4 ]
Jones, Angel [2 ]
Castillo-Garcia, Daniela [5 ]
Abdelwahab, Magy [6 ,7 ]
Revel-Vilk, Shoshana [8 ,9 ]
Lineham, Ella [10 ]
Hughes, Derralynn [11 ,12 ]
Ramaswami, Uma [13 ]
Collin-Histed, Tanya [2 ]
机构
[1] Salford Royal Org, Northern Care Alliance NHS Fdn Trust, Adult Inherited Metab Dis, Salford, England
[2] Int Gaucher Alliance IGA, London, England
[3] Krakow Specialist Hosp St John Paul II, Metab Dis Off, Krakow, Poland
[4] Jagiellonian Univ, Med Coll, Unit Rare Metab Dis, Krakow, Poland
[5] Hosp Infantil Mexico Federico Gomez Inst Nacl Salu, Dept Pediat, Mexico City, Mexico
[6] Cairo Univ Pediat Hosp, Fac Med, Pediat Hematol BMT Unit, Cairo, Egypt
[7] Cairo Univ Pediat Hosp, KasrAlainy Hosp, Social & Prevent Ctr, Fac Med, Cairo, Egypt
[8] Shaare Zedek Med Ctr, Eisenberg R&D Author, Gaucher Unit, Pediat Hematol Oncol Unit, Jerusalem, Israel
[9] Hebrew Univ Jerusalem, Fac Med, Jerusalem, Israel
[10] Rare Dis Res Partners RDRP, MPS House, Amersham, England
[11] UCL, Lysosomal Disorders Unit, London, England
[12] Royal Free London NHS Fdn Trust, London, England
[13] Royal Free London NHS Fdn Trust, Dept Infect Immun & Rare Dis, Lysosomal Disorders Unit, London, England
来源
FRONTIERS IN PEDIATRICS | 2024年 / 12卷
关键词
healthcare transition; Gaucher; child and adolescent health; transition clinic; transfer of care; ENZYME REPLACEMENT THERAPY; CONGENITAL HEART-DISEASE; YOUNG-ADULTS; MANIFESTATIONS; ADOLESCENTS; MANAGEMENT; DIAGNOSIS; PROGRAM;
D O I
10.3389/fped.2024.1439236
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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.
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共 53 条
  • [1] Abdelwahab M., 2023, Transition Care in Gaucher Disease
  • [2] Age of Transition Readiness of Adolescents and Young Adults With Chronic Diseases in Oman: Need an Urgent Revisit
    Abdwani, Reem
    al Saadoon, Muna
    Jaju, Sanjay
    Elshinawy, Mohamed
    Almaimani, Asmaa
    Wali, Yasser
    Khater, Doaa
    [J]. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2022, 44 (04) : E826 - E832
  • [3] Macrophage Models of Gaucher Disease for Evaluating Disease Pathogenesis and Candidate Drugs
    Aflaki, Elma
    Stubblefield, Barbara K.
    Maniwang, Emerson
    Lopez, Grisel
    Moaven, Nima
    Goldin, Ehud
    Marugan, Juan
    Patnaik, Samarjit
    Dutra, Amalia
    Southall, Noel
    Zheng, Wei
    Tayebi, Nahid
    Sidransky, Ellen
    [J]. SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (240)
  • [4] Clinical Report-Supporting the Health Care Transition From Adolescence to Adulthood in the Medical Home
    Cooley W.C.
    Sagerman P.J.
    Barr M.S.
    Ciccarelli M.
    Hergenroeder A.C.
    Klitzner T.S.
    Mann M.
    Pickler L.
    Strickland B.
    Thompson B.
    Weinberg S.T.
    White P.H.
    Wilkie N.C.
    Skipper S.M.
    Brin A.
    Flinn S.K.
    [J]. PEDIATRICS, 2011, 128 (01) : 182 - +
  • [5] [Anonymous], 2016, Transition from children's to adults' services for young people using health or social care services (NICE Guideline NG 43)
  • [6] Baris HN, 2014, PEDIATR ENDOCR REV P, V12, P72
  • [7] Global Incidence and Prevalence of Gaucher Disease: A Targeted Literature Review
    Castillon, Genaro
    Chang, Shun-Chiao
    Moride, Yola
    [J]. JOURNAL OF CLINICAL MEDICINE, 2023, 12 (01)
  • [8] Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M)
    Chabrol, B.
    Jacquin, P.
    Francois, L.
    Broue, P.
    Dobbelaere, D.
    Douillard, C.
    Dubois, S.
    Feillet, F.
    Perrier, A.
    Fouilhoux, A.
    Labarthe, F.
    Lamireau, D.
    Mazodier, K.
    Maillot, F.
    Mochel, F.
    Schiff, M.
    Belmatoug, N.
    [J]. ARCHIVES DE PEDIATRIE, 2018, 25 (05): : 344 - 349
  • [9] The effect of enzyme replacement therapy on bone crisis and bone pain in patients with type 1 Gaucher disease
    Charrow, J.
    Dulisse, B.
    Grabowski, G. A.
    Weinreb, N. J.
    [J]. CLINICAL GENETICS, 2007, 71 (03) : 205 - 211
  • [10] The Gaucher registry -: Demographics and disease characteristics of 1698 patients with Gaucher disease
    Charrow, J
    Andersson, HC
    Kaplan, P
    Kolodny, EH
    Mistry, P
    Pastores, G
    Rosenbloom, BE
    Scott, CR
    Wappner, RS
    Weinreb, NJ
    Zimran, A
    [J]. ARCHIVES OF INTERNAL MEDICINE, 2000, 160 (18) : 2835 - 2843