Literature DB >> 16961684

Home delivery of dietary products in inherited metabolic disorders reduces prescription and dispensing errors.

A MacDonald1, N Manji, S Evans, P Davies, A Daly, C Hendriksz, A Chakrapani.   

Abstract

UNLABELLED: In the UK, for patients with inherited metabolic disorders (IMD) the traditional system for acquiring essential dietary products [patient prompted prescriptions generated by a medical general practitioner (GP) and dispensed by a chemist] is problematic.
OBJECTIVE: To investigate the efficacy of a home delivery service (HDS) for essential dietary products (EDP) (i.e. protein substitutes, milk replacements, energy and vitamin and mineral supplements) for subjects with IMD, particularly examining any prescription and dispensing errors, metabolic control and consumer satisfaction.
METHODS: A prospective, controlled, home delivery trial for EDP was conducted in patients with IMD for 12 months. Sixty-two patients with IMD [50 with phenylketonuria (PKU); 12 with other IMD: aged 6 months-30 years] were recruited. Thirty subjects used a monthly HDS (Homeward: Nutricia) to receive EDP, 32 remained on the traditional system. Each month, the HDS checked home stock levels of EDP, obtained their prescriptions directly from GP's, and then delivered them to the subjects' homes. An independent researcher completed monthly telephone interviews with patients/parents about any EDP prescription errors or delay in receipt.
RESULTS: Incorrect protein substitute was dispensed once by the HDS compared with nine subjects who had 12 errors in the control group (P = 0.01); incorrect flavours of protein substitute were dispensed to the home delivery group once compared with eight subjects getting 11 errors via the chemist (P = 0.03). The HDS delayed delivery of protein substitute for one subject on three occasions compared with 39 occasions in 16 subjects via the chemist (P = 0.001). In patients with PKU, plasma phenylalanine control deteriorated in the control group (P < 0.05) but not in the HDS group.
CONCLUSIONS: The long-term use of a HDS for EDP in IMD is safer, effective and more reliable than conventional systems.

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Mesh:

Year:  2006        PMID: 16961684     DOI: 10.1111/j.1365-277X.2006.00717.x

Source DB:  PubMed          Journal:  J Hum Nutr Diet        ISSN: 0952-3871            Impact factor:   3.089


  5 in total

Review 1.  The reality of dietary compliance in the management of phenylketonuria.

Authors:  Anita MacDonald; Hulya Gokmen-Ozel; Margreet van Rijn; Peter Burgard
Journal:  J Inherit Metab Dis       Date:  2010-04-07       Impact factor: 4.982

2.  Clinical significance of medication reconciliation in children admitted to a UK pediatric hospital: observational study of neurosurgical patients.

Authors:  David R P Terry; Guirish A Solanki; Anthony G Sinclair; John F Marriott; Keith A Wilson
Journal:  Paediatr Drugs       Date:  2010-10-01       Impact factor: 3.022

3.  Home delivery service of low protein foods in inherited metabolic disorders: Does it help?

Authors:  A MacDonald; A Pinto; S Evans; C Ashmore; J MacDonald; A Daly
Journal:  Mol Genet Metab Rep       Date:  2019-03-22

4.  Prescribing issues experienced by people living with phenylketonuria in the UK.

Authors:  Suzanne Ford; Mike O'Driscoll; Anita MacDonald
Journal:  Mol Genet Metab Rep       Date:  2019-10-25

Review 5.  Organising healthcare services for persons with an intellectual disability.

Authors:  Robert Balogh; Carly A McMorris; Yona Lunsky; Helene Ouellette-Kuntz; Laurie Bourne; Angela Colantonio; Daniela C Gonçalves-Bradley
Journal:  Cochrane Database Syst Rev       Date:  2016-04-11
  5 in total

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