Journal article
The time consuming nature of phenylketonuria: A cross-sectional study investigating time burden and costs of phenylketonuria in the Netherlands
Indra Eijgelshoven, Serwet Demirdas, T Alexander Smith, Jeanni MT van Loon, Sabine Latour, Annet M Bosch
MOLECULAR GENETICS AND METABOLISM | ACADEMIC PRESS INC ELSEVIER SCIENCE | Published : 2013
Abstract
BACKGROUND: Phenylketonuria (PKU) is a rare inborn error of metabolism that affects the ability of patients to metabolise phenylalanine (Phe). Lifelong management of blood Phe levels is required in order to avoid the complications associated with PKU. This constitutes a severely protein restricted diet, and regular monitoring of Phe levels. Management of PKU may be costly and time-consuming for adult patients or caregivers of PKU-affected children. A cross-sectional study was performed with patients or their caregivers in the Netherlands to gain insight into the personal time burden and cost of living with PKU. METHODS: A systematic literature review was performed to identify all aspects of ..
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Funding Acknowledgements
IE, TAS, and JVL are employed by MAPI Consultancy. MAPI Consultancy received funding of the study from Merck Serono S.A., Geneva, Switzerland. SL is employed by Merck Serono S.A., Geneva, Switzerland. SD and AB did not receive funding. AB is a member of advisory boards for Merck Serono and for Danone.