The effects of the administration of oral nutritional supplementation with medication rounds on the achievement of nutritional goals: a randomized controlled trial
| Autor: | Robert Lindeboom, Gerda H. van den Berg, Wil C. van der Zwet |
|---|---|
| Přispěvatelé: | Amsterdam Public Health, Master Evidence Based Practice |
| Jazyk: | angličtina |
| Rok vydání: | 2015 |
| Předmět: |
Male
Pediatrics medicine.medical_specialty Nutritional Supplementation Hospitalized patients Administration Oral Intervention group Critical Care and Intensive Care Medicine Drug Administration Schedule law.invention Primary outcome Randomized controlled trial law Medicine Humans Aged Aged 80 and over Nutrition and Dietetics business.industry Malnutrition Absolute risk reduction Middle Aged Clinical trial Hospitalization Dietary Supplements Patient Compliance Female Dietary Proteins business Usual care group |
| Zdroj: | Clinical nutrition (Edinburgh, Scotland), 34(1), 15-19. Churchill Livingstone |
| ISSN: | 0261-5614 |
| Popis: | Summary Background & aims Oral nutritional supplements (ONS) are often considered for hospitalized patients with acute severe malnutrition, however the compliance to the supplements is known to be variable. The aim of our study was to investigate whether providing a lower volume of ONS at a higher frequency during medication rounds would improve the intake of the supplements. Methods In this randomized controlled trial, 234 malnourished inpatients (mean age 71.2 years, 55% male, median LOS 10 days) were randomized to receive ONS (300 kcal and 12 g Protein per 125 ml serving) in one of three different schemes. The usual care group ( n = 88) was offered ONS 125 ml twice per day in between meals. This was compared to two intervention groups that were offered ONS during medication rounds: intervention group 1 ( n = 66) received 125 ml of ONS twice per day, at 12 and 17 o'clock, and intervention group 2 ( n = 80) received 62 ml of ONS four times a day, at 8, 12, 17 and 20 o'clock. Follow-up was performed until discharge or until ONS was no longer needed, with a maximum follow-up period of 30 days. The primary outcome measure was the percentage of patients who consumed at least 75% of the prescribed volume of ONS. Results No significant differences were observed between the control groups and intervention group 1 (risk difference of −16.0% (95% CI −33.2–1.2). However, the percentage of patients consuming at least 75% of the prescribed ONS was higher in intervention group 2, with a risk difference 23.4% (95% CI 7.8–39.0%) and a mean increased intake of 35 ml (84 kcal) per day, p Conclusion A higher frequency of a lower volume of ONS during medication rounds increased the compliance of patients needing ONS. Clinical trial registration number NTR2535; www.trialregister.nl. |
| Databáze: | OpenAIRE |
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