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Trials / Completed

CompletedNCT07532772

Transfusion Practices in Intensive Care Units: a Hungarian Nationwide Survey

Status
Completed
Phase
Study type
Observational
Enrollment
97 (actual)
Sponsor
Pest County Flór Ferenc Hospital · Academic / Other
Sex
All
Age
24 Years
Healthy volunteers
Accepted

Summary

The aim of our data analysis-based questionnaire study is to assess the daily transfusion practices used in the care of critically ill patients in intensive care units in Hungary. The rate and frequency of the application of physiological parameters (serum lactate level, central venous oxygen saturation and arteriovenous carbon dioxide difference, arteriovenous oxygen content difference) recommended as transfusion triggers in the international literature in daily practice will be assessed. The aim of our survey is not only to collect statistical data, but also to map practical experiences, knowledge, opinions and possible institutional differences. Our aim is to obtain a more comprehensive picture of the operation of the care system, including transfusion activities, and any possible different practices applied in individual institutions, based on the experiences and observations of colleagues directly involved in patient care.

Detailed description

The aim of our study is to assess the transfusion practice applied in the care of anemic, critically ill patients in intensive care units in Hungary. In this study, we examine the rate and frequency of the application of physiological parameters (serum lactate level, central venous oxygen saturation and arteriovenous carbon dioxide difference, arteriovenous oxygen content difference) recommended as transfusion triggers in the international literature in everyday practice. This is a non-interventional, cross-sectional observational survey study. We use a descriptive, Hungarian-language online questionnaire (Google Forms, Google Inc., Mountain View, CA) survey regarding the transfusion practice of intensive care units in Hungary is based on 15 mandatory and 1 optional question. Participation in the study is completely voluntary and anonymous. No personal or other sensitive data is recorded or stored during the data collection process, so respondents cannot be identified. The names of the responding institutions are registered solely for the purpose of geographical distribution of responses. The MedCalc statistical analysis software (MedCalc Software bvba, Ostend, Belgium) was used to evaluate the questionnaires, and the results were expressed as a percentage of the number of respondents, using a 95% confidence interval. The normality of the data was checked using the Kolmogorov-Smirnov test. The data were presented as mean ± standard deviation in the case of normal distribution, and median (interquartile range) in the case of non-normal distribution. The relationship between the different subgroups (specialist trainees vs. specialists; university centers vs. public hospitals) was examined using Pearson's correlation. The analysis between the groups was performed using the chi-square test, and the relationship between the use of the PBM program and transfusion triggers was examined using a two-way repeated measures analysis of variance (2-way RM ANOVA). A p\<0.05 was considered statistically significant.

Conditions

Interventions

TypeNameDescription
OTHERSurvey using a questionnaire.The questionnaire consists of 15 mandatory and 1 optional question.

Timeline

Start date
2025-07-01
Primary completion
2025-09-30
Completion
2025-09-30
First posted
2026-04-16
Last updated
2026-04-16

Locations

1 site across 1 country: Hungary

Source: ClinicalTrials.gov record NCT07532772. Inclusion in this directory is not an endorsement.