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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Sickle cell disease and the general surgeon
1Department of Surgery, Dammam Central Hospital, Eastern Province, Saudi Arabia.
Insights
Sickle cell disease (SCD) is a genetic disorder causing anemia and pain crises. Recognizing and managing surgical issues in SCD patients is crucial due to high risks, requiring medical and surgical team collaboration.
Area of Science:
- Hematology
- Genetics
- Vascular Biology
Background:
- Sickle cell disease (SCD) is a prevalent genetic disorder with significant global health implications.
- Characterized by chronic hemolytic anemia and vaso-occlusive crises, SCD leads to organ damage via vascular occlusion by sickled red blood cells.
- SCD presents as a multisystem disease, posing diverse surgical challenges across various surgical specialties.
Purpose of the Study:
- To review the spectrum of surgical problems encountered in patients with sickle cell disease.
- To discuss the management strategies for these surgical complications in the context of SCD.
- To emphasize the importance of recognizing surgical implications of SCD for general surgeons.
Main Methods:
- Literature review of surgical complications in sickle cell disease patients.
- Analysis of case studies and management approaches.
- Synthesis of current recommendations for surgical care in SCD.
Main Results:
- SCD patients face a wide array of surgical ailments due to the disease's multisystemic nature.
- Surgical interventions in SCD are associated with elevated rates of morbidity and mortality.
- Effective management necessitates close interdisciplinary collaboration between medical and surgical teams.
Conclusions:
- The surgical management of sickle cell disease patients requires careful consideration and planning.
- Enhanced awareness and understanding of surgical implications are vital for surgeons managing these patients.
- Integrated care models are essential to improve outcomes for SCD patients requiring surgical intervention.
Abstract:
Sickle cell disease (SCD) is a common genetic disorder which represents a major medical problem in certain parts of the world. It is characterized by chronic haemolytic anaemia and vaso-occlusive crises, which can lead to widespread vascular occlusion by sickled red blood cells leading to multiple organ infarctions. In this respect, SCD can be considered as a multisystem disease presenting, to various surgical disciplines, a wide variety of surgical ailments. As surgical management of these patients is associated with high morbidity and mortality, close collaboration between medical and surgical services is essential. Greater population mobility makes recognition of the surgical implications of this disease of paramount importance in surgical practice. This article reviews surgical problems with which SCD patients may present to general surgeons and discusses their management.
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