TY - JOUR
T1 - Use of a eutectic mixture of local anesthetics for prolonged subcutaneous drug administration
AU - Berkovitch, M.
AU - Davis, S.
AU - Matsui, D.
AU - Donsky, J.
AU - Koren, G.
AU - Olivieri, N. F.
PY - 1995
Y1 - 1995
N2 - The efficacy of a eutectic mixture of local anesthetics (EMLA) in alleviating the pain associated with subcutaneous needle insertion for infusion of the iron-chelating agent, deferoxamine, was examined in 12 patients with homozygous β-thalassemia. As reported by the patient using a 100-mm visual analogue scale, the pain of insertion was rated as significantly less after application of EMLA (mean ± SD, 1.5 ± 2.2 mm) than the pain associated with needle insertion without EMLA (34.8 ± 33.5 mm, P = .005). Subsequently, in a double-blind randomized trial of 10 β-thalassemia patients. EMLA was significantly better (5.7 ± 8.2 mm) than placebo (27.0 ± 22.8 mm, P = .01) in reducing the pain of needle insertion for deferoxamine infusion. No adverse effects were reported with the use of EMLA cream. These results suggest that EMLA may be effective in reducing the pain associated with needle insertion for subcutaneous deferoxamine infusion in β- thalassemia patients, which may lead to improved compliance with this irritating, prolonged therapy. The safety of EMLA use in these patients, and others receiving regular parenteral therapy, should now be examined.
AB - The efficacy of a eutectic mixture of local anesthetics (EMLA) in alleviating the pain associated with subcutaneous needle insertion for infusion of the iron-chelating agent, deferoxamine, was examined in 12 patients with homozygous β-thalassemia. As reported by the patient using a 100-mm visual analogue scale, the pain of insertion was rated as significantly less after application of EMLA (mean ± SD, 1.5 ± 2.2 mm) than the pain associated with needle insertion without EMLA (34.8 ± 33.5 mm, P = .005). Subsequently, in a double-blind randomized trial of 10 β-thalassemia patients. EMLA was significantly better (5.7 ± 8.2 mm) than placebo (27.0 ± 22.8 mm, P = .01) in reducing the pain of needle insertion for deferoxamine infusion. No adverse effects were reported with the use of EMLA cream. These results suggest that EMLA may be effective in reducing the pain associated with needle insertion for subcutaneous deferoxamine infusion in β- thalassemia patients, which may lead to improved compliance with this irritating, prolonged therapy. The safety of EMLA use in these patients, and others receiving regular parenteral therapy, should now be examined.
UR - http://www.scopus.com/inward/record.url?scp=0028911752&partnerID=8YFLogxK
U2 - 10.1002/j.1552-4604.1995.tb04062.x
DO - 10.1002/j.1552-4604.1995.tb04062.x
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C2 - 7608320
AN - SCOPUS:0028911752
SN - 0091-2700
VL - 35
SP - 295
EP - 297
JO - Journal of Clinical Pharmacology
JF - Journal of Clinical Pharmacology
IS - 3
ER -