Assessing the impact of heat on the systemic delivery of fentanyl through the transdermal fentanyl delivery system
被引:43
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作者:
Shomaker, TS
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机构:
Univ Utah, Sch Med, Dept Anesthesiol, Off Dean, Salt Lake City, UT 84132 USAUniv Utah, Sch Med, Dept Anesthesiol, Off Dean, Salt Lake City, UT 84132 USA
Shomaker, TS
[1
]
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机构:
Zhang, J
[1
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Ashburn, MA
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机构:
Univ Utah, Sch Med, Dept Anesthesiol, Off Dean, Salt Lake City, UT 84132 USAUniv Utah, Sch Med, Dept Anesthesiol, Off Dean, Salt Lake City, UT 84132 USA
Ashburn, MA
[1
]
机构:
[1] Univ Utah, Sch Med, Dept Anesthesiol, Off Dean, Salt Lake City, UT 84132 USA
opioid analgesic;
fentanyl;
transdermal drug delivery;
cancer pain;
D O I:
10.1046/j.1526-4637.2000.00030.x
中图分类号:
R614 [麻醉学];
学科分类号:
100217 ;
摘要:
Objectives. To examine the effects of locally applied heat on the systemic delivery of fentanyl through the Transdermal Fentanyl Delivery System. Design. Open, 2-period crossover randomized study conducted in the anesthesia department of a university teaching hospital. Method. Six healthy adult volunteers received a fentanyl 25-mug/h patch with and without local heat for 240 minutes followed by administration without heat for an additional 20 hours. Participants then crossed over. Venous blood was drawn at baseline and hourly for 24 hours. Peak plasma concentration (CMax) of fentanyl was measured and the area under the curve (AUC) of the plasma fentanyl concentration versus time post administration graph was evaluated. Results. Difference in CMax and AUC were not statistically significant over the entire 24-hour study period. However, for the 4-hour period of heat application statistically significant differences were seen in both mean CMax (heat, 0.4 ng/mL versus no heat, 0.1 ng/mL (P =.030)) and mean AUC (heat, 10 ng/mL min versus no heat, 10 ng/mL min (P =.010)). Conclusion. Local heat can speed the onset of steady state fentanyl concentration in the Fentanyl Transdermal Drug Delivery System(TM) thus limiting the delay in onset of analgesia and allowing earlier identification and treatment of side effects.
机构:
Division of Emergency Medicine, Weill Cornell Medical College, New York Presbyterian Hospital, New York, NY 10065Division of Emergency Medicine, Weill Cornell Medical College, New York Presbyterian Hospital, New York, NY 10065
Prosser J.M.
Jones B.E.
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New York University School of Medicine, New York City Poison Center, New York, NY 10016Division of Emergency Medicine, Weill Cornell Medical College, New York Presbyterian Hospital, New York, NY 10065
Jones B.E.
Nelson L.
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机构:
Department of Emergency Medicine and Fellowship in Medical Toxicology, New York City Poison Center, New York University School of Medicine, New York, NY 10016Division of Emergency Medicine, Weill Cornell Medical College, New York Presbyterian Hospital, New York, NY 10065
机构:
Swedish Univ Agr Sci, Fac Vet Med & Anim Sci, Dept Clin Sci, S-75007 Uppsala, SwedenSwedish Univ Agr Sci, Fac Vet Med & Anim Sci, Dept Clin Sci, S-75007 Uppsala, Sweden
Malavasi, LM
Augustsson, H
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Swedish Univ Agr Sci, Fac Vet Med & Anim Sci, Dept Clin Sci, S-75007 Uppsala, SwedenSwedish Univ Agr Sci, Fac Vet Med & Anim Sci, Dept Clin Sci, S-75007 Uppsala, Sweden
Augustsson, H
Jensen-Waern, M
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Swedish Univ Agr Sci, Fac Vet Med & Anim Sci, Dept Clin Sci, S-75007 Uppsala, SwedenSwedish Univ Agr Sci, Fac Vet Med & Anim Sci, Dept Clin Sci, S-75007 Uppsala, Sweden
Jensen-Waern, M
Nyman, G
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机构:
Swedish Univ Agr Sci, Fac Vet Med & Anim Sci, Dept Clin Sci, S-75007 Uppsala, SwedenSwedish Univ Agr Sci, Fac Vet Med & Anim Sci, Dept Clin Sci, S-75007 Uppsala, Sweden