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Diagnostic Value of a Multidisciplinary Clinic for Intellectual Disability
被引:10
|作者:
van Karnebeek, Clara
[4
]
Murphy, Tyler
[1
]
Giannasi, Wynona
[2
]
Thomas, Marion
[3
]
Connolly, Mary
[1
]
Stockler-Ipsiroglu, Sylvia
[4
]
机构:
[1] Univ British Columbia, BC Childrens Hosp, TIDE BC, Div Pediat Neurol, Vancouver, BC V6H 3V4, Canada
[2] Univ British Columbia, BC Childrens Hosp, TIDE BC, Howe Consulting Grp, Vancouver, BC V6H 3V4, Canada
[3] Univ British Columbia, BC Childrens Hosp, TIDE BC, Dept Med Genet, Vancouver, BC V6H 3V4, Canada
[4] Univ British Columbia, BC Childrens Hosp, TIDE BC, Div Biochem Dis, Vancouver, BC V6H 3V4, Canada
关键词:
GLOBAL DEVELOPMENTAL DELAY;
MENTAL-RETARDATION;
CHILDREN;
ETIOLOGY;
YIELD;
CARE;
D O I:
10.1017/S0317167100017273
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Background: Identification of the underlying cause of intellectual disability (ID) is important as it improves genetic counselling, management, adaptation; yet its etiologic heterogeneity is challenging and often leads to an expensive work-up. Methods: To improve this diagnostic trajectory, the multidisciplinary Complex Diagnostic Clinic (CDC) was established for ID patients with unexplained complex systemic and/or neurologic features that were referred to the CDC and evaluated by three medical specialists followed by multi-disciplinary rounds. Analyses included surveys and interviews, (retrospective) chart review, costs calculations and comparison. Results: 24 children (9 male) were evaluated during seven clinics held over 16 months. The average patient age was 7 years 11 months (range 9 months-18 years). All the children had previously been seen by 2-10 specialist services. The diagnostic yield of the CDC was higher than expected with confirmed and working diagnoses in 11(46%) and 9 (38%) children respectively. Cost-savings included fewer trips to hospital and fewer tests via more streamlined evaluations. Positive feedback was received from both families and medical professionals. Conclusions: The CDC represents an innovative model of personalized care. Specialist collaboration in the interpretation of relevant clinical, biochemical and genomic data resulted in diagnoses, where none had previously been possible.
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页码:333 / 345
页数:13
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