Clinicians' Experiences with the Fragile X Clinical and Research Consortium

被引:6
|
作者
Liu, Jessica A. [1 ,10 ]
Hagerman, Randi J. [2 ,3 ]
Miller, Robert M. [4 ]
Craft, Lisa T. [5 ]
Finucane, Brenda [6 ]
Tartaglia, Nicole [7 ]
Berry-Kravis, Elizabeth M. [8 ]
Sherman, Stephanie L. [9 ]
Kidd, Sharon A. [1 ,11 ]
Cohen, Jeffrey [1 ]
机构
[1] Natl Fragile X Fdn, Washington, DC USA
[2] Univ Calif Davis, MIND Inst, Sacramento, CA 95817 USA
[3] Univ Calif Davis Hlth Syst, Dept Pediat, Sacramento, CA USA
[4] Rob Miller Human Serv Consulting, Pleasant Hill, CA USA
[5] Univ Louisville, Dept Pediat, Weisskopf Child Evaluat Ctr, Louisville, KY 40292 USA
[6] Geisinger Hlth Syst, Autism & Dev Med Inst, Lewisburg, PA USA
[7] Univ Colorado, Dept Pediat, Sch Med, Aurora, CO USA
[8] Rush Univ, Med Ctr, Dept Pediat, Neurol Sci,Biochem, Chicago, IL 60612 USA
[9] Emory Univ, Dept Human Genet, Atlanta, GA 30322 USA
[10] Sutter Hlth Syst, Walnut Creek, CA USA
[11] Univ Calif San Francisco, San Francisco, CA 94143 USA
关键词
fragile X syndrome; consortium; intellectual and developmental disabilities; survey; TREMOR/ATAXIA SYNDROME; FMR1; PREMUTATION; GENETICS; AUTISM; FEATURES; CHILDREN; NETWORK;
D O I
10.1002/ajmg.a.37948
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The objectives of the study were to assess the attitudes and experiences of clinicians involved in a consortium of clinics serving people with fragile X-associated disorders to gauge satisfaction with the consortium and its efforts to improve quality of life for patients and the community. An internet survey was sent to 26 fragile X (FX) clinic directors participating in the Fragile X Clinical and Research Consortium (FXCRC). Respondents were asked to complete 19 questions on consortium performance and outcomes relevant for their own clinic. The response rate was 84% (22/26), with two surveys providing incomplete data. Assistance with clinic establishment, opportunities for research collaborations, and access to colleagues and information were highly valued. Approximately 76% of clinicians reported improvements in patient care and 60% reported an increase in patient services. There was a 57% increase in participation in a FX-related clinical trial among clinics since joining the FXCRC (24% vs. 81%). Overall, respondents reported primarily positive experiences from participation in the FXCRC. Common suggestions for improvement included additional financial support and increased utilization of collected patient data for research purposes. Additionally, a Clinic Services Checklist was administered annually to examine changes in services offered over time. There were several important changes regarding the provision of services by clinics, often with multiple clinics changing with respect to a service. In conclusion, the FXCRC has led to the establishment and sustainment of fragile X clinics in the U.S., fostered cooperation among fragile X clinicians, and provided clinics with a platform to share recommendations and best practices to maximize quality of life for their patients and the overall fragile X community. The results from the survey and checklist also provide suggestions to strengthen the FXCRC and enhance future collaborations among FXCRC members. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:3138 / 3143
页数:6
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