Prognostic Value of NLR, TLR, and ALC in Predicting ToF Primary Repair Outcome

Sponsor
National Cardiovascular Center Harapan Kita Hospital Indonesia (Other)
Overall Status
Completed
CT.gov ID
NCT05976204
Collaborator
(none)
501
1
41.9
12

Study Details

Study Description

Brief Summary

Tetralogy of Fallot (ToF) were cyanotic congenital heart disease with chronic hypoxia which increases the risk of exacerbated inflammatory response in ToF primary repair. Various studies have recently shown inflammatory biomarkers to predict morbidity and mortality in hypoxemic patients, but they are not readily available and expensive.This study aims to compare the prognostic value of neutrophil-lymphocyte ratio (NLR), absolute lymphocyte count (ALC), and thrombocyte-lymphocyte ratio (TLR) in predicting ToF primary repair outcomes. This was a retrospective observational study on ToF primary repair in National Cardiovascular Center Harapan Kita between Januari 2020 until December 2022. Preoperative NLR, ALC, and TLR were derived from blood test obtained <14 days before surgery. The primary endpoints were redo surgery, 30-day mortality, and complications. The secondary endpoints were hospital length of stay (HLOS) and postoperative LOS.

Detailed Description

This was a retrospective observational study on tetralogy of Fallot (ToF) primary repair in National Cardiovascular Center Harapan Kita between Januari 2020 until December 2022. The preoperative demographic data included were patients' gender, age, weight, oxygen saturation, and associated diagnosis other than ToF. The preoperative data of complete blood count and differential count must be tested from the most recent peripheral blood samples taken no later than 14 days before the surgery. The data obtained were the number of days of the most recent blood test including the leukocyte count, percentage neutrophil, percentage and absolute lymphocyte count, thrombocyte count, as well as the derived variables such as neutrophil lymphocyte ratio (NLR) ratio and thrombocyte lymphocyte ratio (TLR). The intraoperative data included were the use of cardiopulmonary bypass (CPB), CPB time, aortic cross-clamp (AOX) time, and the total duration of surgery. Patients were evaluated and followed-up for any complications and postoperative mortality during the same hospital stay until discharge. Patients were then followed up for any cause of mortality within 30 days postoperative.

Study Design

Study Type:
Observational
Actual Enrollment :
501 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Prognostic Value of Neutrophil-Lymphocyte Ratio (NLR), Absolute Lymphocyte Count (ALC), and Thrombocyte-Lymphocyte Ratio (TLR) in Predicting the Outcomes of Tetralogy of Fallot Primary Repair
Actual Study Start Date :
Jan 1, 2020
Actual Primary Completion Date :
Dec 31, 2022
Actual Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
ToF primary repair

Patients who underwent ToF primary repair from January 2020 until December 2022

Procedure: ToF primary repair
ToF primary repair for patients with ToF

Outcome Measures

Primary Outcome Measures

  1. Number of Patients Requiring Redo surgery [From the initial primary ToF until the discharge of the patients or until 2 weeks after the operation, whichever came first]

    Redo surgery was defined as additional or corrective surgery after the initial primary ToF repair within the same hospital admission.

  2. Mortality [Until 30 days postoperative]

    Mortality intraoperative or postoperative

  3. Complications (categorized as mild, moderate, severe) [From the initial primary ToF until the discharge of the patients or until 2 weeks after the operation, whichever came first]

    Complication was defined as any adverse events that arised during the operation or postoperative until the discharge of the patient.

Secondary Outcome Measures

  1. Hospital Length of Stay [From the initial primary ToF until the discharge of the patients or until 12 weeks after the operation, whichever came first]

    Hospital length of stay (HLOS) was defined as the duration of stay in the hospital from the initial admission to discharge.

  2. Postoperative Length of Stay [From the initial primary ToF until the discharge of the patients or until 12 weeks after the operation, whichever came first]

    Longer postoperative LOS was defined as hospitalization of more than 5 days from the period of surgery until postoperative discharge (based on our center).

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 18 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • All patients with ToF and any other associated cardiac anomalies, who underwent ToF primary repair and had a complete blood cell count with differential count available preoperatively
Exclusion Criteria:
  • Surgery other than ToF primary repair

  • Association with other procedures (except patent ductus arteriosus/PDA ligation, patent foramen ovale/PFO or atrial septal defect/ASD closure, or pulmonary arteries enlargement)

  • Preoperative hemodynamic instability

  • Suspected or confirmed infection with prior antibiotic administration during the same hospital admission

  • Absence of complete blood count with differential count

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Cardiovascular Center Harapan Kita Jakarta Indonesia Jakarta Indonesia

Sponsors and Collaborators

  • National Cardiovascular Center Harapan Kita Hospital Indonesia

Investigators

  • Principal Investigator: Sisca N Siagian, MD, National CCHK

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sisca Natalia Siagian, Principal Investigator, National Cardiovascular Center Harapan Kita Hospital Indonesia
ClinicalTrials.gov Identifier:
NCT05976204
Other Study ID Numbers:
  • LB.02.01/VII/2023/NLR
First Posted:
Aug 4, 2023
Last Update Posted:
Aug 8, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sisca Natalia Siagian, Principal Investigator, National Cardiovascular Center Harapan Kita Hospital Indonesia
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 8, 2023