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Nutritional outcomes from a randomised investigation of intradialytic oral nutritional supplements in patients receiving haemodialysis, (NOURISH): a protocol for a pilot randomised controlled trial

Overview of attention for article published in SpringerPlus, October 2013
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Title
Nutritional outcomes from a randomised investigation of intradialytic oral nutritional supplements in patients receiving haemodialysis, (NOURISH): a protocol for a pilot randomised controlled trial
Published in
SpringerPlus, October 2013
DOI 10.1186/2193-1801-2-515
Pubmed ID
Authors

Louise Jackson, Benjamin Sully, Judith Cohen, Steven Julious

Abstract

Haemodialysis is a form of renal replacement therapy but is a catabolic process that not only filters toxins but is also known to lead to amino acid losses. Patients with chronic kidney disease often have a poor appetite and this in combination with limited dietary intake and the detrimental effects of haemodialysis can lead to the development of malnutrition. Between 20% and 50% of haemodialysis patients are thought to be malnourished. Malnutrition can worsen clinical outcomes and increase the risk of hospitalisation. We hypothesise that a nutritional supplement taken during haemodialysis may help to improve nutritional status. The aim of this study is to conduct a pilot randomised controlled trial to assess the use of an intradialytic nutritional supplement on nutritional status. The objectives are to assess the feasibility of the trial including: recruitment and retention of participants; preference of nutritional supplements; compliance with the intervention; ease of completion of the questionnaires and appropriateness of the tools used. Secondary outcomes include clinical outcomes to obtain variance in the patient population and estimates of effect size to inform the sample size for a future definitive trial. The trial is a single centre, randomised, parallel-group, two armed external pilot with an intervention and control group. The intervention group will take a nutritional supplement each dialysis session from a choice of prescribable drink or pudding style supplements. The control group will receive standard care. Recruitment and feasibility elements are the primary outcomes. Recruitment will be to time (t = 6 weeks). In order to collect sufficient data to inform a future sample size calculation, we will aim to recruit 30 participants to obtain 12 evaluable per arm anticipating some drop out. Secondary outcome measures include clinical variables; hand grip strength, quality of life, weight and biochemistry completed at baseline, 1 and 2 months. Descriptive statistics will be used to analyse the baseline characteristics of the recruited participants. Means, confidence intervals and standard deviations will be reported for the outcome measures of handgrip strength, dietary intake, quality of life and weight.

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Mendeley readers

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Geographical breakdown

Country Count As %
Spain 1 2%
Unknown 49 98%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 16%
Student > Master 7 14%
Student > Bachelor 5 10%
Other 4 8%
Student > Ph. D. Student 4 8%
Other 9 18%
Unknown 13 26%
Readers by discipline Count As %
Medicine and Dentistry 23 46%
Nursing and Health Professions 5 10%
Social Sciences 3 6%
Biochemistry, Genetics and Molecular Biology 1 2%
Environmental Science 1 2%
Other 2 4%
Unknown 15 30%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 25 October 2013.
All research outputs
#20,207,295
of 22,727,570 outputs
Outputs from SpringerPlus
#1,462
of 1,853 outputs
Outputs of similar age
#182,908
of 209,119 outputs
Outputs of similar age from SpringerPlus
#99
of 105 outputs
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