Slagelse Hospital
Slagelse, Region Sjælland, 4200, Denmark
NCT Number: NCT04514575
BACKGROUND
* Major blood loss is frequent in open repair of ruptured and intact abdominal aortic aneurysm (AAA) as well as in aorto-bifurcated prosthesis insertion due to aortoiliac occlusive disease. * Major blood loss is associated with death, post-operative complications and coagulopathy. * Data from randomized trials in trauma patients indicate that a high plasma to red blood cell (RBC) transfusion ratio reduces 30-day mortality. * No randomized trial data are available for the AAA population. * Observational data demonstrate, that a high plasma:RBC transfusion ratio associates to a lower 30 day mortality. However, the reports are based on small cohorts of 78-165 patients, short term outcomes and lack information on major adverse events such as cardiac and respiratory. * The Danish Vascular Registry (DVR), covering 1996-2018, contains data on approx. 4,400 ruptured and 8,200 intact (elective/symptomatic) AAA repairs, and 5,400 open aortoiliac repairs due to occlusive disease. Expected total count 1997-2018: 17,000. * The Danish Transfusion Database (DTDB), covering approx. 1997-2018, contains information on units of RBCs, plasma and platelets transfused. A unique patient identification number (CPR) allows merging of all data set.
OBJECTIVE
To identify whether resuscitation with a high plasma to RBC ratio associates to improves survival in open abdominal aortic surgery as compared to a low plasma to RBC-ratio.
PICO
* Population: Open abdominal aortic surgery * Intervention: "High FFP": FFP to RBC unit ratio of 2:3 to 3:3 (0.7 - 1.0) * Comparison: "Low FFP": FFP to RBC unit ratio of 0:3 to 1:3 (0.0 - 0.3) * Outcome: All-cause mortality 90 days following surgery.
DATA SOURCES
CPR, Danish Civil Registration System. DNPR, Danish National Patient registry. DVR, Danish Vascular registry. DPDB, The Danish national Prescription DataBase.
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Notify Me41 year–99 year
All sexes
Observational
Slagelse, Region Sjælland, 4200, Denmark
STATISTICAL ANALYSIS PLAN
The primary analysis will be a stratified cox regression model.
STRATIFICATION:
COVARIATE ADJUSTMENT:
ADDITIONAL ANALYSES:
MISSING DATA
Missing data will not be an issue for the number of blood transfusions because units of blood products transfused are used as an inclusion criterion. All remaining covariates are discrete, and missing data for each of those will be included as separate parameters (factor level).
STATISTICAL SIGNIFICANCE LEVEL
Bonferroni adjustment of the significance level will be applied to control for multiple testing.
With one primary and four secondary outcomes, only a P-value below 0.01 (0.05/5) will be considered statistically significant. A P-value between 0.01 and 0.05 will be considered borderline significant.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
(*) = Allogeneic packed RBCs, FFP, cryoprecipitate, or platelets. Cryoprecipitate will account for 4 units of FFP in the FFP:RBC ratio.
Exclusion criteria
Excluding patients with surgery time less than 50 minutes or cases where no prosthesis has been inserted is expected to minimize survival bias from patients exsanguinating in the operation theater before blood products can be delivered. Intentionally, it may also exclude cases where surgery was considered futile and halted.
Transfusion of allogeneic fresh frozen plasma or cryoprecipitate
Time frame: First 90 days after index surgery
Survival data. Source: CPR
Time frame: First 30 days after index surgery
Survival data. Source: CPR
Time frame: 1 year after index surgery
Survival data. Source: CPR
Time frame: First 90 days after index surgery
Dichotomous outcome. Source: DNPR and DVR.
A. Major adverse cardiovascular events "MACE" [ICD10-codes]
B. Major adverse respiratory events
C. Major adverse vascular event
D. Other
Time frame: Day 90 after index surgery
Count data. Source: DNPR and CPR
Naestved Hospital
Other
Plasma Transfusion in Major Vascular Surgery: a Danish Nationwide Registry Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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