PP62 Assessment Of Evidence On The Efficacy And Safety Of Oral Nutritional Supplements For Malnutrition In Hospitals

Introduction Hospital malnutrition is caused by metabolic imbalance and is associated with increased rates of morbidity and mortality and unfavorable prognosis for hospitalized patients. In 2001, severe malnutrition was detected in 12.5 percent of hospitalized patients in Brazil. The aim of this study was to evaluate evidence on the efficacy and safety of oral nutritional supplements for malnutrition in hospitalized patients. Methods Search strategies developed for the PubMed, Embase, LILACS and Cochrane Library databases were used to search and select the available evidence. The included evidence compared oral nutritional supplementation with standard hospital care or placebo. A total of 47 clinical trials were selected. For mortality, a meta-analysis was performed combining the effect measures of 40 clinical trials. R software was used with the meta package installed. The revised Cochrane risk-of-bias tool was used to assess the risk of bias. Results For the primary outcomes of mortality (relative risk [RR] 0.94, 95% CI: 0.77, 1.15), length of hospital stay, and number of hospital readmissions (RR 0.97, 95% CI: 0.74, 1.28), oral supplementation offered no benefit, compared with the control group. Regarding infectious and non-infectious complications, there was a significant reduction in the number of patients with complications in the supplemented group, compared with the control group (RR 0.71, 95% CI: 0.59, 0.86). Regarding the risk-of-bias assessment, most of the studies had a high risk of bias and limitations in almost all areas. Conclusions The designs of the selected studies were quite heterogeneous in terms of follow-up time, population, and sampling, among others, and several doubts were raised about the methodology used in the clinical trials. These aspects were reflected in the low quality and high risk of bias of the primary studies, which proved to be an important limitation.

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Publication Details

Journal
International Journal of Technology Assessment in Health Care
Published
2025-12-01
DOI
https://doi.org/10.1017/s026646232510281x
Primary Topic
Nutrition and Health in Aging
Type
article
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article

PP62 Assessment Of Evidence On The Efficacy And Safety Of Oral Nutritional Supplements For Malnutrition In Hospitals

Larissa Silva, Everton Macêdo Silva, Juliana Girardi, Keyla Caroline Almeida
International Journal of Technology Assessment in Health Care
Nutrition and Health in Aging
article

PP62 Assessment Of Evidence On The Efficacy And Safety Of Oral Nutritional Supplements For Malnutrition In Hospitals

Larissa Silva, Everton Macêdo Silva, Juliana Girardi, Keyla Caroline Almeida
article en

Abstract

Introduction Hospital malnutrition is caused by metabolic imbalance and is associated with increased rates of morbidity and mortality and unfavorable prognosis for hospitalized patients. In 2001, severe malnutrition was detected in 12.5 percent of hospitalized patients in Brazil. The aim of this study was to evaluate evidence on the efficacy and safety of oral nutritional supplements for malnutrition in hospitalized patients. Methods Search strategies developed for the PubMed, Embase, LILACS and Cochrane Library databases were used to search and select the available evidence. The included evidence compared oral nutritional supplementation with standard hospital care or placebo. A total of 47 clinical trials were selected. For mortality, a meta-analysis was performed combining the effect measures of 40 clinical trials. R software was used with the meta package installed. The revised Cochrane risk-of-bias tool was used to assess the risk of bias. Results For the primary outcomes of mortality (relative risk [RR] 0.94, 95% CI: 0.77, 1.15), length of hospital stay, and number of hospital readmissions (RR 0.97, 95% CI: 0.74, 1.28), oral supplementation offered no benefit, compared with the control group. Regarding infectious and non-infectious complications, there was a significant reduction in the number of patients with complications in the supplemented group, compared with the control group (RR 0.71, 95% CI: 0.59, 0.86). Regarding the risk-of-bias assessment, most of the studies had a high risk of bias and limitations in almost all areas. Conclusions The designs of the selected studies were quite heterogeneous in terms of follow-up time, population, and sampling, among others, and several doubts were raised about the methodology used in the clinical trials. These aspects were reflected in the low quality and high risk of bias of the primary studies, which proved to be an important limitation.

International Journal of Technology Assessment in Health CareVol. 41(S1)
Zero hunger
Openalex Percentile: Top 32%
Nutrition and Health in Aging
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