The Algerian Cardiac Surgeon
Volume 1, Numéro 1, Pages 67-73
2025-02-01
Auteurs : Haneche Hynda . Boukhmis Abdelkader . Allaoui Atika . Aitmohand Rachid . Bekai Yacine . Khichane Malika . Hamzaoui Azzedine . Djafer Boulanouar .
Sickle cell disease is a genetic hemoglobinopathy characterized by a pathological hemoglobin Hb S responsible for a process of polymerization under conditions of deoxygenation. It is manifested by anemic episodes, vaso-occlusive crises, severe infectious syndromes and multiple functional degenerations. Surgery exposes these patients to a relatively higher risk of perioperative mortality. The cardiac surgery is particularly high-risk, as extracorporeal circulation is a major factor in falciformation. Perioperative management requires multidisciplinary consultation and the development of transfusion or exchange transfusion protocols to reduce the concentration of Hemoglobin S concentration below the threshold.
Sickle Cell Disease, Cardiopulmonary Bypass, Anesthesia, Cardiac Surgical Procedures
Leklou H.
.
pages 39-44.
Zahi Chahrazade
.
Toumi Samira
.
Amrane Hacène
.
ص 33-63.
Lassoued Rim
.
pages 83-102.
Fellague Chebra Yassine
.
Boukhmis Abdelkader
.
Haddad Assia
.
Halimi Djamila
.
Medjber Nabil
.
Ziari Radja
.
Karcouche Mohamed El Hadi
.
Djafer Boulanouar
.
pages 80-83.
Lakehal Rédha
.
Boukarroucha Radouane
.
pages 602-605.