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Functional hyposplenism following allogeneic bone marrow transplantation
R J Cuthbert1, A Iqbal, A Gates
1Department of Haematology, City Hospital, Nottingham.
Journal of Clinical Pathology
|March 1, 1995
Summary
Functional hyposplenism occurs in 15% of patients after allogeneic bone marrow transplantation (BMT). This condition, linked to graft-versus-host disease (GvHD), may increase infection risk.
Area of Science:
- Hematology
- Immunology
- Transplantation Medicine
Background:
- Allogeneic bone marrow transplantation (BMT) can lead to complications affecting immune function.
- Hyposplenism, a reduced spleen function, increases susceptibility to encapsulated bacterial infections.
- Assessing splenic function post-BMT is crucial for understanding infection risks.
Purpose of the Study:
- To determine the incidence of functional hyposplenism in patients following allogeneic BMT.
- To explore the association between functional hyposplenism and graft-versus-host disease (GvHD) post-BMT.
Main Methods:
- Splenic function was evaluated by quantifying pitted red blood cells using interference phase microscopy.
- Pitted red blood cell counts exceeding 2% indicate hyposplenism, with 25-40% seen in splenectomy patients.
- The study compared 28 BMT recipients with healthy volunteers and patients with splenic atrophy.
Main Results:
- Fifteen percent (4 of 27) of BMT recipients exhibited functional hyposplenism, with pitted red blood cell counts ranging from 5.0% to 34.0%.
- One patient with active chronic GvHD showed evidence of hyposplenism.
- Only one patient displayed typical peripheral blood red cell changes associated with hyposplenism.
Conclusions:
- Extensive chronic GvHD is confirmed as a significant factor associated with hyposplenism post-BMT.
- Functional hyposplenism can occur after BMT even without chronic GvHD or typical blood film findings.
- The presence of hyposplenism post-BMT may contribute to increased susceptibility to infections by encapsulated bacteria.