Maastricht criteria III in the global context: a systematic review of development and implementation
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60076658%3A12110%2F25%3A43911068" target="_blank" >RIV/60076658:12110/25:43911068 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11140/25:10507172
Výsledek na webu
<a href="https://czasopisma.umlub.pl/piel21w/article/view/3170/3149" target="_blank" >https://czasopisma.umlub.pl/piel21w/article/view/3170/3149</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.12923/pielxxiw-2025-0039" target="_blank" >10.12923/pielxxiw-2025-0039</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Maastricht criteria III in the global context: a systematic review of development and implementation
Popis výsledku v původním jazyce
This review examines the development and implementation of the Maastricht Criteria III in controlled (cDCD) and uncontrolled (uDCD) Donation after Circulatory Death in various healthcare systems, evaluates compliance with the no-touch interval, and the influence of opt-in versus opt-out consent models on the availability and use of donor organs. Material and methods. Following Evidence-Based Practice principles, a systematic search was performed in full-text electronic databases covering healthcare, bioethics, and transplantation sciences. Peer-reviewed, full-text studies relevant to DCD classification and clinical application were included. Additionally, a critical methodological quality appraisal of all included studies was conducted using a standardised tool, thereby enhancing the robustness of our conclusions. Results. Eleven studies met inclusion criteria, addressing DCD classification, consent frameworks, no-touch interval adherence, and organ procurement impact. Substantial international variability emerged: presumed consent (opt-out) systems achieved higher donor conversion rates, whereas extended no-touch intervals detrimentally affected organ viability. Conclusions. This review presents a structured analysis of Maastricht Criteria III application, particularly in Europe. cDCD follows increasingly standardised protocols, while uDCD remains inconsistently implemented due to ethical and logistical challenges. To enhance donor identification, organ utilisation, and transplantation outcomes, it is essential to standardise protocols, refine ischemia-mitigation techniques, and strengthen international collaboration.
Název v anglickém jazyce
Maastricht criteria III in the global context: a systematic review of development and implementation
Popis výsledku anglicky
This review examines the development and implementation of the Maastricht Criteria III in controlled (cDCD) and uncontrolled (uDCD) Donation after Circulatory Death in various healthcare systems, evaluates compliance with the no-touch interval, and the influence of opt-in versus opt-out consent models on the availability and use of donor organs. Material and methods. Following Evidence-Based Practice principles, a systematic search was performed in full-text electronic databases covering healthcare, bioethics, and transplantation sciences. Peer-reviewed, full-text studies relevant to DCD classification and clinical application were included. Additionally, a critical methodological quality appraisal of all included studies was conducted using a standardised tool, thereby enhancing the robustness of our conclusions. Results. Eleven studies met inclusion criteria, addressing DCD classification, consent frameworks, no-touch interval adherence, and organ procurement impact. Substantial international variability emerged: presumed consent (opt-out) systems achieved higher donor conversion rates, whereas extended no-touch intervals detrimentally affected organ viability. Conclusions. This review presents a structured analysis of Maastricht Criteria III application, particularly in Europe. cDCD follows increasingly standardised protocols, while uDCD remains inconsistently implemented due to ethical and logistical challenges. To enhance donor identification, organ utilisation, and transplantation outcomes, it is essential to standardise protocols, refine ischemia-mitigation techniques, and strengthen international collaboration.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30307 - Nursing
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Pielegniarstwo XXI Wieku-Nursing in the 21 Century
ISSN
1730-1912
e-ISSN
2450-646X
Svazek periodika
24
Číslo periodika v rámci svazku
4
Stát vydavatele periodika
PL - Polská republika
Počet stran výsledku
7
Strana od-do
332-338
Kód UT WoS článku
001687116700007
EID výsledku v databázi Scopus
2-s2.0-105028402463