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Investigation of the Transfusion Practices in Surgical Patients in Turkey

Investigation of the Transfusion Practices in Surgical Patients in Turkey

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03468738
Acronym
CeKATU
Enrollment
6481
Registered
2018-03-19
Start date
2018-04-02
Completion date
2019-02-01
Last updated
2019-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anemia, Blood Loss Anemia, Blood Loss, Surgical, Blood Transfusion, Coagulation Disorder, Surgery

Brief summary

The aim of this study is to describe the transfusion practices in patients undergoing major surgery in Turkey. The transfusion rates of red blood cells (RBC), fresh frozen plasma (FFP) and platelets; the transfusion predictors and transfusion related patient outcomes are investigated.

Detailed description

Patient Blood Management (PBM) is an evidence based multidisciplinary approach for the care of patients who may need blood transfusion. The aim of PBM is achieving better patient outcomes by focusing on the patients' own blood as a source. To date PBM is considered good transfusion practice and is being implemented in a growing number of countries. The Turkish Society of Anesthesiologists PBM Task Force is working on this subject since 4 years and decided to conduct a study. Before starting a PBM program, the transfusion practices of clinicians working at diverse surgical fields; differences between current transfusion practices and PBM strategies; the areas for improvement and the obstacles that could prevent change could be identified with this study. Data collection will also serve to identify the current situation as a reference and to control the achievement of the PBM's aim: improving clinical outcomes. These data will be refered as The Turkish National Perioperative Transfusion Study (TULIP TS) data. The aim of this study is to describe the transfusion practices in patients undergoing major surgery in Turkey. The study evaluates i. The perioperative transfusion rates of RBCs, FFP and platelets. ii. With which reasons the anesthesiologists decide to transfuse a patient (co morbidities of the patients, physiologic transfusion triggers, hemoglobin trigger, uncontrolled bleeding, on request from surgeon etc.). iii. The relation of transfusion and the patients co-morbidity index, the P POSSUM score and SORT score; anesthesia methods; monitorisation methods (hemodynamic, coagulation); amount of bleeding; type of surgery; type of hospital. iv. The relation of transfusion and patient outcomes (unanticipated ICU admission, prolonged ICU stay, acute renal failure, thromboembolic events, ischemic events, pulmonary complications, cardiac advers events, infections, acute respiratory distress, infection, all-cause mortality).

Interventions

OTHERBlood transfusion

Transfusion of blood products in the perioperative period in patients undergoing major surgery

Sponsors

Turkish Society of Anesthesiology and Reanimation
CollaboratorOTHER
Diskapi Teaching and Research Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Patients undergoing major elective surgery

Exclusion criteria

Trauma patients, emergency surgery

Design outcomes

Primary

MeasureTime frameDescription
Preoperative amount of blood products transfusedBefore surgery at day 0Preoperative amount of blood products: RBCs,FFP and platelets transfused
Intraoperative amount of blood products transfusedDuring surgery at day 0Intraoperative amount of blood products: RBC's,FFP and platelets transfused
Postoperative amount of blood products transfused24 hours after surgeryPostoperative amount of blood products: RBCs,FFP and platelets transfused

Secondary

MeasureTime frameDescription
Unanticipated ICU admissionAfter surgery at day 1Whether the patient had an unanticipated ICU admission
Prolonged length of stay in ICUAfter surgery at day 2Whether the patient had a prolonged length of stay in ICU
Acute renal failureAfter surgery at day 2Whether the patient had acute renal failure
Thromboembolic eventAfter surgery at day 2Whether the patient had a thromboembolic event concerning lungs (pulmonary embolism), brain (stroke), gastrointestinal tract, kidneys, or extremities etc.
Ischemic eventAfter surgery at day 2Whether the patient had an ischemic event concerning heart, nervous system,limb, gastrointestinal tract etc.
InfectionAfter surgery at day 2Whether the patient had infection: wound, pneumonia, urinary, sepsis etc.
Postoperative transfusion indications24 hours after surgeryThe reasons to decide to transfuse (factors determining transfusion) blood products
Mortalityafter surgery at day 30Whether the patient died: all cause mortality
Preoperative anemiaBefore surgery at day 0Whether the patient had anemia (Hemoglobin male \< 13 female \< 12 g/dL)
Preoperative coagulopathyBefore surgery at day 0Whether the patient had coagulopathy due to disease or drugs
Pretransfusion hemoglobin valuesBefore surgery at day 0The hemoglobin concentration before transfusion
Advers cardiac eventsAfter surgery at day 30Whether the patient had an advers cardiac event: myocardial infaction; non fatal cardiac arest; arrhytmia; cardiogenic pulmonary edema etc
Acute respiratory distressAfter surgery at day 2Whether the patient had acute respiratory distress
Preoperative transfusion indicationsBefore surgery at day 0The reasons to decide to transfuse (factors determining transfusion) blood products
Intraoperative transfusion indicationsDuring surgery at day 1The reasons to decide to transfuse (factors determining transfusion) blood products

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026