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Predicting CSA-AKI With ACTA-PORT Score

Predictive Power of the ACTA-PORT Score for Cardiac Surgery-Associated Acute Kidney Injury: A Prospective Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06484907
Enrollment
467
Registered
2024-07-03
Start date
2024-07-01
Completion date
2024-12-01
Last updated
2025-06-26

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

Conditions

Acute Kidney Injury, Blood Transfusion, Cardiac Disease

Keywords

Cardiopulmonary Bypass, Cardiac Surgery, Transfusion, Acute Kidney Injury, ACTA PORT

Brief summary

In the scope of this study, it will be determined whether the ACTA-PORT (Association of Cardiothoracic Anesthetists perioperative risk of blood transfusion) scoring system can predict the incidence of events in other organ systems, and the feasibility of conducting multiple assessments using a single simple score will be investigated.

Detailed description

ACTA-PORT (Association of Cardiothoracic Anesthetists perioperative risk of blood transfusion) score is a simple, reliable, and validated tool used to predict the risk of transfusion in patients undergoing heart surgery. In calculating ACTA-PORT score, age, gender, hemoglobin, body surface area, EuroSCORE, creatinine, and type of operation are used. In this study, it will be determined whether the ACTA-PORT (Association of Cardiothoracic Anesthetists perioperative risk of blood transfusion) scoring system can predict the incidence of events in other organ systems, and the feasibility of conducting multiple assessments using a single simple score will be investigated. The files of patients undergoing open heart surgery in the cardiovascular surgical operating rooms of Ankara Bilkent City Hospital, along with anesthesia records, transfusion records, and test results identified through the Hospital Information Management System, will be prospectively evaluated. Data will be collected after patients are admitted to the intraoperative and postoperative intensive care unit.

Interventions

None listed

Sponsors

Ankara City Hospital Bilkent
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients over 18 years old * Patients having open heart surgery * Patients undergoing surgery by using cardiopulmonary bypass pump

Exclusion criteria

* Patients under 18 years old * Patients diagnosed with kidney disease

Design outcomes

Primary

MeasureTime frameDescription
KDIGO AKI StagingPreoperative (last week before operation) and daily after the operation for 7 daysKDIGO is in the process of developing the Clinical Practice Guideline for Acute Kidney Injury (AKI) and Acute Kidney Disease (AKD). ///// Stage 1: Serum creatinine 1.5-1.9 times baseline or ≥0.3 mg/dl (≥26.5 mmol/l) increase or Urine output \<0.5 ml/kg/h for 6-12 hours ////// Stage 2: Serum creatinine 2.0-2.9 times baseline or \<0.5 ml/kg/h for ≥12 hours /////// Stage 3: Serum creatinine 3.0 times baseline or Increase in serum creatinine to ≥4.0 mg/dl (≥353.6 mmol/l) or Initiation of renal replacement therapy or in patients \<18 years, decrease in eGFR to \<35 ml/min per 1.73 m² or Urine output \<0.3 ml/kg/h for ≥24 hours or anuria for ≥12 hours

Secondary

MeasureTime frameDescription
Intensive Care Durationthe duration after surgery up to a monthThe duration the patient remains in intensive care unit after surgery
Hospital Stay Durationthe duration after surgery up to a monthThe duration the patient stays in the hospital after surgery until discharge
Mechanical Ventilation Durationthe duration after surgery up to a monthThe duration the patient remains intubated from surgery to extubation
Complicationsthe duration after surgery up to a monthCardiac, Pulmonary, Neurological, Infectious, Thrombotic complications and Presence of MODS (Multiple Organ Dysfunction Syndrome) / SIRS (Systemic Inflammatory Response Syndrome)
Reoperation Necessitythe duration after surgery up to a monthThe need for reoperation due to bleeding
Mortalitythe duration after surgery up to a monthIf the patient dies within 1 month or not

Countries

Turkey (Türkiye)

Outcome results

None listed

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