Achieving the "triple aim" for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence framework

被引:27
作者
Potter, Beth K. [1 ]
Chakraborty, Pranesh [2 ,3 ,4 ]
Kronick, Jonathan B. [5 ,6 ]
Wilson, Kumanan [7 ,8 ]
Coyle, Doug [1 ]
Feigenbaum, Annette [5 ,6 ]
Geraghty, Michael T. [2 ,3 ,4 ]
Karaceper, Maria D. [1 ]
Little, Julian [1 ]
Mhanni, Aizeddin [9 ,10 ]
Mitchell, John J. [9 ,11 ]
Siriwardena, Komudi [5 ,6 ]
Wilson, Brenda J. [1 ]
Syrowatka, Ania [1 ]
机构
[1] Univ Ottawa, Dept Epidemiol & Community Med, Ottawa, ON, Canada
[2] Childrens Hosp Eastern Ontario, Dept Pediat, Ottawa, ON K1H 8L1, Canada
[3] Univ Ottawa, Dept Pediat, Ottawa, ON K1N 6N5, Canada
[4] Childrens Hosp Eastern Ontario, Newborn Screening Ontario, Ottawa, ON K1H 8L1, Canada
[5] Hosp Sick Children, Div Clin & Metab Genet, Toronto, ON M5G 1X8, Canada
[6] Univ Toronto, Dept Paediat, Toronto, ON M5S 1A1, Canada
[7] Univ Ottawa, Ottawa Hosp Res Inst, Ottawa, ON, Canada
[8] Univ Ottawa, Dept Med, Ottawa, ON, Canada
[9] Univ Manitoba, Dept Pediat & Child Hlth, Winnipeg, MB R3T 2N2, Canada
[10] Univ Manitoba, Dept Biochem & Med Genet, Winnipeg, MB, Canada
[11] Montreal Childrens Hosp, Dept Pediat, Montreal, PQ H3H 1P3, Canada
关键词
inborn errors of metabolism; practice-based evidence; rare diseases; research network; STEM-CELL TRANSPLANTATION; UREA CYCLE DISORDERS; PHENYLALANINE-HYDROXYLASE DEFICIENCY; COA DEHYDROGENASE-DEFICIENCY; ACID OXIDATION DISORDERS; EVIDENCE-BASED MEDICINE; SYRUP-URINE-DISEASE; SAPROPTERIN DIHYDROCHLORIDE; CLINICAL-TRIALS; RARE DISEASES;
D O I
10.1038/gim.2012.153
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Across all areas of health care, decision makers are in pursuit of what Berwick and colleagues have called the "triple aim": improving patient experiences with care, improving health outcomes, and managing health system impacts. This is challenging in a rare disease context, as exemplified by inborn errors of metabolism. There is a need for evaluative outcomes research to support effective and appropriate care for inborn errors of metabolism. We suggest that such research should consider interventions at both the level of the health system (e.g., early detection through newborn screening, programs to provide access to treatments) and the level of individual patient care (e.g., orphan drugs, medical foods). We have developed a -practice-based evidence framework to guide outcomes research for inborn errors of m-etabolism. Focusing on outcomes across the triple aim, this framework integrates three priority themes: tailoring care in the context of clinical heterogeneity; a shift from "urgent care" to "opportunity for improvement"; and the need to evaluate the comparative effectiveness of emerging and established therapies. Guided by the framework, a new Canadian research network has been established to generate knowledge that will inform the design and delivery of health services for patients with inborn errors of metabolism and other rare diseases.
引用
收藏
页码:415 / 422
页数:8
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