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Peer-reviewedCC BY-NCZagazig University Medical Journal

Autologous blood transfusion in Coronary Artery Bypass Graft Surgery.

  1. 1Cardio thoracic surgery department, faculty of medicine, menofia university , shebin elkom , menofia, Egypt
  2. 2department of general surgery , faculty of medicine , menofia universty ,shebin Elkom , eypt

Abstract

Background: Coronary artery bypass grafting (CABG) is frequently related to significant blood loss and allogeneic transfusion, which carries risks of infection, immunomodulation, and increased morbidity. Intraoperative autologous blood transfusion is a potential blood-conservation strategy. Aim: To estimate feasibility, safety and effectiveness of intraoperative autologous blood transfusion as an approach for blood conservation in cases having elective coronary artery bypass graft surgery. Patients and methods: This prospective cohort research has been done at the Cardiothoracic Surgery Department, Menoufia University Hospitals, Egypt, included 52 adult cases admitted for elective isolated CABG surgery, patients have been allocated into two equal groups: Group A (Autologous Blood Group). Group B (Control Group) Results: Baseline characteristics were largely comparable. Hematocrit on the second postoperative day was significantly greater in the autologous group (30.8 ± 3.3% vs 28.6 ± 3.1%, p=0.009). Early chest-tube drainage (first 12 hours) was significantly lower (327 ± 139 vs 427 ± 119 mL, p=0.008). Postoperative transfusion rates (50% vs 61.5%) and complications showed no significant differences. Conclusion: Intraoperative autologous blood transfusion is a feasible and safe technique that reduces early postoperative bleeding and improves hematocrit recovery by the second postoperative day, although it did not significantly decrease allogeneic transfusion rates in this cohort.

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BibTeX
@article{ayanah2026autologous,
  title = {{Autologous blood transfusion in Coronary Artery Bypass Graft Surgery.}},
  author = {Ahmad Ayanah and Abdelaziz Taalab and Mostafa Aboollo and Montaser Abdelaziz and Eman Moatty},
  journal = {Zagazig University Medical Journal},
  year = {2026},
  month = oct,
  doi = {10.21608/zumj.2026.523830.4787},
  url = {https://doi.org/10.21608/zumj.2026.523830.4787},
  note = {CC BY-NC},
}
RIS
TY  - JOUR
TI  - Autologous blood transfusion in Coronary Artery Bypass Graft Surgery.
AU  - Ahmad Ayanah
AU  - Abdelaziz Taalab
AU  - Mostafa Aboollo
AU  - Montaser Abdelaziz
AU  - Eman Moatty
PY  - 2026
DA  - 2026/10/25
JO  - Zagazig University Medical Journal
DO  - 10.21608/zumj.2026.523830.4787
UR  - https://doi.org/10.21608/zumj.2026.523830.4787
AB  - Background: Coronary artery bypass grafting (CABG) is frequently related to significant blood loss and allogeneic transfusion, which carries risks of infection, immunomodulation, and increased morbidity. Intraoperative autologous blood transfusion is a potential blood-conservation strategy. Aim: To estimate feasibility, safety and effectiveness of intraoperative autologous blood transfusion as an approach for blood conservation in cases having elective coronary artery bypass graft surgery. Patients and methods: This prospective cohort research has been done at the Cardiothoracic Surgery Department, Menoufia University Hospitals, Egypt, included 52 adult cases admitted for elective isolated CABG surgery, patients have been allocated into two equal groups: Group A (Autologous Blood Group). Group B (Control Group) Results: Baseline characteristics were largely comparable. Hematocrit on the second postoperative day was significantly greater in the autologous group (30.8 ± 3.3% vs 28.6 ± 3.1%, p=0.009). Early chest-tube drainage (first 12 hours) was significantly lower (327 ± 139 vs 427 ± 119 mL, p=0.008). Postoperative transfusion rates (50% vs 61.5%) and complications showed no significant differences. Conclusion: Intraoperative autologous blood transfusion is a feasible and safe technique that reduces early postoperative bleeding and improves hematocrit recovery by the second postoperative day, although it did not significantly decrease allogeneic transfusion rates in this cohort.
SN  - 2357-0717
SN  - 1110-1431
ER  -