D. Comas et J. Mateu, TREATMENT OF EXTRAVASATION OF BOTH DOXORUBICIN AND VINCRISTINE ADMINISTRATION IN A Y-SITE INFUSION, The Annals of pharmacotherapy, 30(3), 1996, pp. 244-246
OBJECTIVE: To describe a patient treated with vincristine, doxorubicin
, and dexamethasone who experienced extravasation of both doxorubicin
and vincristine during a Y-site infusion. CASE SUMMARY: A 74-year-old
white woman was diagnosed with multiple myeloma IgA kappa in stage ITA
. One year after a complete remission she relapsed. Her treatment incl
uded daily doxorubicin 16 mg in 500 mt of dextrose 5% and vincristine
0.4 mg in 500 mt of dextrose 5% administered in a Y-site continuous in
fusion into a peripheral vein of her left forearm. Extravasation occur
red during administration of these drugs. Immediately, chondroitinsulf
atase, a mucopolysaccharidase similar to hyaluronidase, was administer
ed subcutaneously around the extravasation area and repeated 24 hours
later. Furthermore, dimethyl sulfoxide 90% v/v was applied topically o
n the area four times daily for 2 weeks. All inflammatory signs resolv
ed and no necrosis developed. DISCUSSION: This is the first report of
an extravasation of two cytotoxic drugs. Doxorubicin and vincristine h
ave different antidotes and opposite physical treatments for their ext
ravasation. The antidotes dimethyl sulfoxide and chondroitinsulfatase
have different mechanisms of action, but both cause uptake of the cyto
toxic agent from the tissue and are likely to be administered together
. No warming or cooling was performed. CONCLUSIONS: Topical dimethyl s
ulfoxide four times daily for 14 days plus subcutaneous chondroitinsul
fatase in one or two applications effectively treated an extravasation
of both doxorubicin and vincristine in our patient.