Fluid management guided by a continuous non-invasive arterial pressure device is associated with decreased postoperative morbidity after total knee and hip replacement

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F15%3A10301840" target="_blank" >RIV/00216208:11140/15:10301840 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00669806:_____/15:10301840

Výsledek na webu

<a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608292/" target="_blank" >http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608292/</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1186/s12871-015-0131-8" target="_blank" >10.1186/s12871-015-0131-8</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Fluid management guided by a continuous non-invasive arterial pressure device is associated with decreased postoperative morbidity after total knee and hip replacement

Popis výsledku v původním jazyce

Background: The use of goal directed fluid protocols in intermediate risk patients undergoing hip or knee replacement was studied in few trials using invasive monitoring. For this reason we have implemented two different fluid management protocols, bothbased on a novel totally non-invasive arterial pressure monitoring device and compared them to the standard (no-protocol) treatment applied before the transition in our academic institution. Methods: Three treatment groups were compared in this prospective study: the observational (CONTROL, N=40) group before adoption of fluid protocols and two randomized groups after the transition to protocol fluid management with the use of the continuous non-invasive blood pressure monitoring (CNAP(R)) device. In the PRESSURE group (N=40) standard variables were used for restrictive fluid therapy. Goal directed fluid therapy using pulse pressure variation was used in the GDFT arm (N=40). The influence on the rate of postoperative complications, on t

Název v anglickém jazyce

Fluid management guided by a continuous non-invasive arterial pressure device is associated with decreased postoperative morbidity after total knee and hip replacement

Popis výsledku anglicky

Background: The use of goal directed fluid protocols in intermediate risk patients undergoing hip or knee replacement was studied in few trials using invasive monitoring. For this reason we have implemented two different fluid management protocols, bothbased on a novel totally non-invasive arterial pressure monitoring device and compared them to the standard (no-protocol) treatment applied before the transition in our academic institution. Methods: Three treatment groups were compared in this prospective study: the observational (CONTROL, N=40) group before adoption of fluid protocols and two randomized groups after the transition to protocol fluid management with the use of the continuous non-invasive blood pressure monitoring (CNAP(R)) device. In the PRESSURE group (N=40) standard variables were used for restrictive fluid therapy. Goal directed fluid therapy using pulse pressure variation was used in the GDFT arm (N=40). The influence on the rate of postoperative complications, on t

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FP - Ostatní lékařské obory

OECD FORD obor

—

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2015

Kód důvěrnosti údajů

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

Název periodika

BMC Anesthesiology

ISSN

1471-2253

e-ISSN

—

Svazek periodika

15

Číslo periodika v rámci svazku

1

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

10

Strana od-do

—

Kód UT WoS článku

000362807400002

EID výsledku v databázi Scopus

2-s2.0-84944890296