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Skaer TL. Transdermal opioids for cancer pain. Health Qual Life Outcomes. 2006 Mar 31, 4 :24. [PMC free article : PMC1526423 ] [PubMed : 16573839 ]
Dowell D, Haegerich TM, Chou R. CDC Guideline for Prescribing Opioids for Chronic Pain - United States, 2016. MMWR Recomm Rep. 2016 Mar 18, 65 (1):1-49. [PubMed : 26987082 ]
Gulur P, Williams L, Chaudhary S, Koury K, Jaff M. Opioid tolerance--a predictor of increased length of stay and higher readmission rates. Pain Physician. 2014 Jul-Aug, 17 (4):E503-7. [PubMed : 25054400 ]
Ramos-Matos CF, Bistas KG, Lopez-Ojeda W. StatPearls [Internet]. StatPearls Publishing, Treasure Island (FL): May 29, 2023. Fentanyl. [PubMed : 29083586 ]
Nelson L, Schwaner R. Transdermal fentanyl: pharmacology and toxicology. J Med Toxicol. 2009 Dec, 5 (4):230-41. [PMC free article : PMC3550407 ] [PubMed : 19876859 ]
Ziesenitz VC, Vaughns JD, Koch G, Mikus G, van den Anker JN. Pharmacokinetics of Fentanyl and Its Derivatives in Children: A Comprehensive Review. Clin Pharmacokinet. 2018 Feb, 57 (2):125-149. [PMC free article : PMC5756700 ] [PubMed : 28688027 ]
Peng PW, Sandler AN. A review of the use of fentanyl analgesia in the management of acute pain in adults. Anesthesiology. 1999 Feb, 90 (2):576-99. [PubMed : 9952166 ]
LoVecchio F, Ramos L. Suicide by Duragesic transdermal fentanyl patch toxicity. Am J Emerg Med. 2011 Jan, 29 (1):131.e1-2. [PubMed : 20825866 ]
Prosser JM, Jones BE, Nelson L. Complications of oral exposure to fentanyl transdermal delivery system patches. J Med Toxicol. 2010 Dec, 6 (4):443-7. [PMC free article : PMC3550454 ] [PubMed : 20532845 ]
Mystakidou K, Katsouda E, Tsilika E, Parpa E, Vlahos L. Transdermal therapeutic fentanyl-system (TTS-F). In Vivo. 2004 Sep-Oct, 18 (5):633-42. [PubMed : 15523905 ]
Jeal W, Benfield P. Transdermal fentanyl. A review of its pharmacological properties and therapeutic efficacy in pain control. Drugs. 1997 Jan, 53 (1):109-38. [PubMed : 9010652 ]
Contraindications of transdermal fentanyl include use during the acute postoperative pain period for short term pain control, intermittent pain control, or mild pain.[10][11][12] Patients who experience hypoventilation, respiratory compromise (including acute or severe asthma) or respiratory depression may not take transdermal fentanyl.[10][11] Children under the age of 12 or children with a weight of under 50 kgs and who are over 18 should not use this drug.[13] Additionally, patients who are sensitive to fentanyl or other opiates or non-tolerant to opioids should not receive transdermal fentanyl. Due to the administration mechanism, patients who experience sensitivity to adhesive should not use transdermally administered fentanyl and consider other forms of administration.[11]
Fentanyl is an extremely potent opioid and requires monitoring due to the low therapeutic drug concentration. A blood concentration of 0.6 ng/ml to 3.0 ng/ml is appropriate for analgesia. The gold standard method of determining fentanyl concentration for monitoring is Liquid chromatography-mass spectrometry. Alternative methods of monitoring included radioimmunoassay. However, it is known to overestimate concentrations of fentanyl by 29 to 100%. Monitoring Fentanyl is increasingly important when the patient is subject to polypharmacy. Notable drugs to pay special attention to are those which inhibit CYP3A4 metabolism and cause an increase in Fentanyl concentration leading to toxicity. Examples of such medications include azole class antifungals as well as macrolide antibiotics.[13]
CYP3A4 inducers may also reduce the level of fentanyl to a non-therapeutic level causing the patient inadequate analgesia and distress. Such drugs include rifampin, phenytoin, and carbamazepine.[13] Other medications such as those that fully or partially block Mu opioid receptors (Naloxone and Buprenorphine, respectively) will induce withdrawal as transdermal fentanyl will not be able to exert its effect on Mu opioid receptors.[7] Monitoring proper disposal and screening for misuse within the healthcare industry is especially important for this drug. Fully used transdermal fentanyl patches contain up to 84% of the original dose within the adhesive gel and may be misused by healthcare personnel.[5]
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