ESPGHAN/ESPEN/ESPR/CSPEN guidelines on pediatric parenteral nutrition: Standard versus individualized parenteral nutrition

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F18%3A10387106" target="_blank" >RIV/00216208:11110/18:10387106 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00216208:11130/18:10387106 RIV/00064203:_____/18:10387106 RIV/00064165:_____/18:10387106

Výsledek na webu

<a href="https://doi.org/10.1016/j.clnu.2018.06.955" target="_blank" >https://doi.org/10.1016/j.clnu.2018.06.955</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.clnu.2018.06.955" target="_blank" >10.1016/j.clnu.2018.06.955</a>

Jazyk výsledku

angličtina

Název v původním jazyce

ESPGHAN/ESPEN/ESPR/CSPEN guidelines on pediatric parenteral nutrition: Standard versus individualized parenteral nutrition

Popis výsledku v původním jazyce

PN can be provided as a standard, usually commercial, formulation that is designed to meet the nutritional needs of most patients of the same age group with a similar condition. The aim of standardizing parenteral nutrition (PN) is to improve patient safety (minimize procedural incidents) and optimize resource efficiency at the same time as providing clinically appropriate nutrition (meeting individual patient requirements). Alternatively, an individually tailored PN formulation, adapted to the individual patient&apos;s nutritional needs, can be prescribed. Both types of PN preparations have advantages and disadvantages. Stability of the final product, time pressures on the pharmacy, quality control and cost benefit considerations make the use of standard solutions an attractive option. These standard formulas do not necessarily meet all the requirements of newborns, infants and children, although even in those units that rely on individualized prescribing, there is some scope for their use in stable patients.

Název v anglickém jazyce

ESPGHAN/ESPEN/ESPR/CSPEN guidelines on pediatric parenteral nutrition: Standard versus individualized parenteral nutrition

Popis výsledku anglicky

PN can be provided as a standard, usually commercial, formulation that is designed to meet the nutritional needs of most patients of the same age group with a similar condition. The aim of standardizing parenteral nutrition (PN) is to improve patient safety (minimize procedural incidents) and optimize resource efficiency at the same time as providing clinically appropriate nutrition (meeting individual patient requirements). Alternatively, an individually tailored PN formulation, adapted to the individual patient&apos;s nutritional needs, can be prescribed. Both types of PN preparations have advantages and disadvantages. Stability of the final product, time pressures on the pharmacy, quality control and cost benefit considerations make the use of standard solutions an attractive option. These standard formulas do not necessarily meet all the requirements of newborns, infants and children, although even in those units that rely on individualized prescribing, there is some scope for their use in stable patients.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

30308 - Nutrition, Dietetics

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2018

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Clinical Nutrition

ISSN

0261-5614

e-ISSN

—

Svazek periodika

37

Číslo periodika v rámci svazku

6

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

9

Strana od-do

2409-2417

Kód UT WoS článku

000454376500014

EID výsledku v databázi Scopus

2-s2.0-85050362305