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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
Experience with the Port-A-Cath in sickle cell disease
C E McCready1, H A Doughty, T C Pearson
1Department of Haematology, St Thomas' Hospital, London, UK.
Insights
Totally implantable venous access devices (TIVADs) pose a high risk of infection in sickle cell disease (SCD) patients. Complications like SBE and thrombosis led to device removal, suggesting TIVADs are unsuitable for SCD patients.
Area of Science:
- Hematology
- Vascular Surgery
- Infectious Diseases
Background:
- Peripheral venous access is challenging in sickle cell disease (SCD) patients.
- Totally implantable venous access devices (TIVADs) are used for long-term venous access in other patient groups.
Observation:
- A Port-A-Cath TIVAD was used in five SCD patients undergoing exchange transfusion.
- All five TIVADs were removed due to complications including infection (SBE, septic arthritis), pulmonary embolism, and axillary vein thrombosis.
Findings:
- Infective complications occurred at a rate of 0.4 per 100 patient days, significantly higher than in HIV or malignancy patients.
- Common pathogens included Staphylococcus aureus, Staphylococcus epidermidis, and Streptococcus sp.
- Bone infection was more prevalent in patients with pre-existing infarcted tissue.
Implications:
- The incidence of Port-A-Cath associated infections in SCD patients is unacceptably high.
- TIVADs may not be a suitable long-term venous access solution for patients with SCD.
- Further research is needed to explore safer venous access methods for this population.
Abstract:
Peripheral vein access is often a problem in patients with sickle cell disease (SCD). Totally implantable venous access devices (TIVAD) have offered other groups of patients safe long-term venous access. We reviewed our own experience with the use of a Port-A-Cath device in five patients with SCD undergoing exchange transfusion programmes. All five lines required removal due to infection associated with SBE, septic arthritis, pulmonary embolus and axillary vein thrombosis. The organisms involved were Staphylococcus aureus (3), Staphylococcus epidermidis (1) and Streptococcus sp. (1). The median working life of the catheters was 240 days (range 61-428). The median length of time from presentation to the diagnosis of a line-associated infection was 29 days (range 1-58). The rate of complications (0.4 per 100 patient days) in this small group of patients contrasts with the lower rates in patients with HIV and malignancy (0-0.1 per 100 patient days). Our results suggest that patients with SCD suffer an unacceptable incidence of infective complications associated with the Port-A-Cath. Bone infection is more common where there is pre-existing infarcted tissue. While these systems provide a valuable tool, our experience has led us to discontinue the use of TIVADs in SCD.
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