Transfusion-related exposure to the plasticizer di(2-ethylhexyl)phthalate in patients receiving plateletpheresis concentrates

• Published in: Transfusion (Philadelphia, Pa.) Pa.), 2005-05, Vol.45 (5), p.798-802
• Main Authors: Buchta, Christoph, Bittner, Claudia, Heinzl, Harald, Höcker, Paul, Macher, Maria, Mayerhofer, Matthias, Schmid, Rainer, Seger, Christoph, Dettke, Markus
• Format: Article
• Language: English
• Subjects: Adult; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy; Biological and medical sciences; Blood Component Removal - instrumentation; Blood Preservation - instrumentation; Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis; Clinical death. Palliative care. Organ gift and preservation; Diethylhexyl Phthalate - blood; Diethylhexyl Phthalate - pharmacokinetics; Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care; Female; Humans; Intensive care medicine; Male; Medical sciences; Plasticizers - pharmacokinetics; Platelet Transfusion; Plateletpheresis - instrumentation; Thrombocytopenia - therapy; Transfusions. Complications. Transfusion reactions. Cell and gene therapy
• ISSN: 0041-1132; 1537-2995
• DOI: 10.1111/j.1537-2995.2005.04380.x

BACKGROUND: Di(2‐ethylhexyl)phthalate (DEHP) is a plasticizer that can leach from medical devices including storage bags for plateletpheresis concentrates (PCs). In this study, the DEHP exposure to patients receiving PCs was determined and several variables were evaluated to reduce DEHP load to PC recipients. STUDY DESIGN AND METHODS: In 12 patients, serum DEHP was assessed before and after PC transfusion. For in vitro investigations, PCs were produced either with donor plasma or with 65 percent additive solution (AS; T‐Sol) and stored for 5 days. Washing of PCs was performed according to AABB standards. DEHP levels were determined by gas chromatography‐mass spectrometry. RESULTS: Transfusion of PCs led to a significant increase in serum DEHP. DEHP levels in the PCs continuously increased during storage, although the accumulation of DEHP was less in PCs stored in the AS, T‐Sol, than when stored in plasma. Storage‐related accumulation of DEHP contributed to a major part of the total DEHP load in PCs stored for 5 days. Washing of PCs led to a reduction of DEHP load. CONCLUSION: Recipients of PCs are exposed to DEHP, although the total amount represents only a small percentage of the defined tolerable intake. Reduction of storage time, the storage of PC in T‐Sol, or the exchange of the storage medium before transfusion are practicable means to reduce the DEHP load in PC.