Transition from child to adult health care for patients with lysosomal storage diseases in France: current status and priorities-the TENALYS study, a patient perspective survey

被引:8
作者
Genevaz, Delphine [1 ]
Arnoux, Armelle [2 ,3 ,4 ]
Marcel, Catherine [5 ]
Brassier, Anais [6 ]
Pichard, Samia [6 ]
Feillet, Francois [7 ]
Labarthe, Francois [8 ]
Chabrol, Brigitte [9 ]
Berger, Marc [10 ]
Lapointe, Anne-Sophie [1 ]
Frigout, Yvann [2 ,3 ,4 ]
Heron, Benedicte [11 ]
Chatellier, Gilles [2 ,3 ,4 ]
Belmatoug, Nadia [5 ]
机构
[1] Vaincre Malad Lysosomales VML, Massy, France
[2] Paris Univ, Assistance Publ Hop Paris Ctr, Clin Invest Ctr 14 18, Clin Epidemiol INSERM, Paris, France
[3] Paris Univ, Assistance Publ Hop Paris Ctr, Clin Res Unit, Paris, France
[4] Hop Europeen Georges Pompidou, Paris, France
[5] Paris Univ, Beaujon Hosp, AP HP, Reference Ctr Lysosomal Dis, Paris, France
[6] Paris Univ, Necker Hosp, AP HP, Reference Ctr Inherited Metab Dis, Paris, France
[7] Nancy Univ Hosp, Reference Ctr Inherited Metab Dis, Vandoeuvre Les Nancy, France
[8] Univ Hosp, Clocheville Hosp, Reference Ctr Inherited Metab Dis, Tours, France
[9] Univ Hosp Marseille, Reference Ctr Inherited Metab Dis, AP HM, Marseille, France
[10] Estaing Univ Hosp, Reference Ctr Lysosomal Dis, Clermont Ferrand, France
[11] Sorbonne Univ, Trousseau Hosp, AP HP, Reference Ctr Lysosomal Dis, Paris, France
关键词
Lysosomal diseases; Transition from childhood to adulthood; Patient survey; Patient opinion; YOUNG-ADULTS; PROGRAM;
D O I
10.1186/s13023-022-02232-w
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Transition from childhood to adulthood (TCA) is usually difficult in rare, progressive and multisystemic diseases. New treatments and modalities of care for many lysosomal diseases (LD) can increase life expectancy, and a successful TCA can help patient who reach adulthood to avoid disruption to health care. In France, some TCA initiatives have been taken by referral centers but in view of the problems encountered by Vaincre les Maladies Lysosomales (VML), the LD patient association, they seem to be insufficient. The aim of this study is to determine the current state of the TCA process and to identify actions to improve it through interviews with patient families and physicians in LD referral centers. The study is based upon an observational, non-interventional, cross-sectional, national survey which used two anonymous questionnaires. These questionnaires, developed by a scientific committee including representatives from VML and medical specialists in LD, were sent to patients who were receiving care in pediatric departments at age 15 years or older. Questionnaires were also sent to their referral pediatricians. Results Fifty-four patients were included. Forty-two questionnaires were completed by patients and their corresponding physicians and 12 were completed by physicians only. The majority of the patients (80%) were informed that transfer to adult healthcare would occur, but 52% were informed after their eighteenth birthday. Forty-eight percent indicated that they were informed that a TCA coordinator would be appointed; for 39% the time frame for the transfer was communicated, and 31% were informed of the composition of the adult medical team. Among the actions that patients rated as "important/very important", and considered to be a priority in their comments, the most frequently cited were the provision of explanatory documents on the TCA (94%), the transmission of the medical file from the pediatric sector to the adult sector (94%) and a joint consultation with both pediatrician and adult unit physician (91%). Physicians were in agreement concerning the primary importance of the last two actions. Conclusion This study provides a basis for the deployment, on the national level, of transition programs which include specific actions that patients view as priorities.
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页数:9
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共 16 条
  • [1] [Anonymous], Resultats de l'etat des lieux transition au sein du reseau des FSMR-2017/2018
  • [2] Optimization of the transition process of youth with liver disease in adulthood: A position paper from FILFOIE, the French network for paediatric and adult rare liver diseases
    Antonini, Teresa Maria
    Girard, Muriel
    Habes, Dalila
    Goria, Odile
    Debray, Dominique
    [J]. CLINICS AND RESEARCH IN HEPATOLOGY AND GASTROENTEROLOGY, 2020, 44 (02) : 135 - 141
  • [3] "Thrust into adulthood": Transition experiences of young adults with cerebral palsy
    Bagatell, Nancy
    Chan, Dara
    Rauch, Kimberly Karrat
    Thorpe, Deborah
    [J]. DISABILITY AND HEALTH JOURNAL, 2017, 10 (01) : 80 - 86
  • [4] Experiences of patients with Poland syndrome of diagnosis and care in Italy: a pilot survey
    Baldelli, Ilaria
    Gallo, Fabio
    Crimi, Marco
    Fregatti, Piero
    Mellini, Lorenzo
    Santi, Pierluigi
    Ciliberti, Rosagemma
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2019, 14 (01)
  • [5] 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
  • [6] Evaluation of a cystic fibrosis transition program from pediatric to adult care
    Chaudhry, Sarah R.
    Keaton, Meghan
    Nasr, Samya Z.
    [J]. PEDIATRIC PULMONOLOGY, 2013, 48 (07) : 658 - 665
  • [7] Ready, Steady, Go - Achieving successful transition in cystic fibrosis
    Connett, Gary James
    Nagra, Arvind
    [J]. PAEDIATRIC RESPIRATORY REVIEWS, 2018, 27 : 13 - 15
  • [8] From pediatric to adult care: strategic evaluation of a transition program for patients with osteogenesis imperfecta
    Dogba, Maman Joyce
    Rauch, Frank
    Wong, Trudy
    Ruck, Joanne
    Glorieux, Francis H.
    Bedos, Christophe
    [J]. BMC HEALTH SERVICES RESEARCH, 2014, 14
  • [9] An Exploratory Study: Transition to Adulthood for College Students with Type 1 Diabetes and Their Parents
    Ersig, Anne L.
    [J]. JOURNAL OF PEDIATRIC NURSING-NURSING CARE OF CHILDREN & FAMILIES, 2019, 46 : 12 - 17
  • [10] Factors impacting the transition to adulthood of youth with fragile X syndrome and their families: Facilitators, obstacles and needs
    Gauthier-Boudreault, Camille
    Gallagher, Frances
    Trepanier, Jordane
    Corbin, Francois
    Couture, Melanie
    [J]. RESEARCH IN DEVELOPMENTAL DISABILITIES, 2020, 103