The Studies on the Concomitant Diseases and Combined Medication in Patients with Onychomycosis
Abstract
Background: Oral terbinafine, itraconazole and fluconazole are the most common agents used for the treatment of toenail onychomycosis. However, these agents differ markedly in their potential to cause clinically significant drug interactions. Triazoles such as fluconazole and itraconazole have been responsible for a greater number of clinically significant drug interactions than terbinafine.
Objective: We performed this survey to provide the information about how many patients with onychomycosis have concomitant diseases and combined medication and to gauge about the drug interaction risk of antifungal agent.
Method: The findings presented in this report are based on total 569 onychomycosis patients, with KOH positive, who visited 6 university hospitals from February 2007 to March 2007.
Result: The patients with onychomycosis had concomitant diseases (43.1%) and used combination medication (36.4%). The majority of the patient have concomitant diseases, such as hypertension (12.2%), diabetic melitus (9.5%) and hyperlipidemia (4.1%), more frequent in elderly patients. Main factor to choose antifungal agent for the cure of onychomycosis is the efficacy of the medication (55%), as well as, the safety and drug interaction risk of antifungal agent, more important in case of the patient taking a variety of concomitant drugs.
Conclusion: It is concluded that physicians should be aware of the potential interaction of the medications in order to prevent or reduce the burden of adverse events. It is required to have more cautious choice of oral antifungal agent in those patients who are taking combined medications in patients with onycomycosis.
Keywords
Combined medication Concomitant disease Fluconazole Itraconazole Onychomycosis Terbinafine
KJMM
2007 September;12(3):163-172(10). Epub 2016 February 22
Copyright © 2007 by Korean Journal of Medical Mycology
Language
Korean/English
Author
Young Chan Song; Department of Dermatology, Konkuk University School of Medicine, Seoul, Korea
Kyu Joong Ahn; Department of Dermatology, Konkuk University School of Medicine, Seoul, Korea
Hyung Ok Kim; Department of Dermatology, The Catholic University College of Medicine, Seoul, Korea
Young Chul Kye; Department of Dermatology, Korea University College of Medicine, Seoul, Korea
Jee Ho Choi; Department of Dermatology, Ulsan University College of Medicine, Seoul, Korea
Chun Wook Park; Department of Dermatology, Hallym University College of Medicine, Anyang, Korea
Kwang Joong Kim; Department of Dermatology, Hallym University College of Medicine, Anyang, Korea
Corresponding
Kyu Joong Ahn, Department of Dermatology, Konkuk University School of Medicine, Seoul, Korea. Tel: (02) 2030-5170, Fax: (02) 2030-5179, e-mail: kjahn@kuh.ac.kr
Publication history
Acknowledgements
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Young Chan Song
Department of Dermatology, Konkuk University School of Medicine, Seoul, Korea
Kyu Joong Ahn
Department of Dermatology, Konkuk University School of Medicine, Seoul, Korea
Hyung Ok Kim
Department of Dermatology, The Catholic University College of Medicine, Seoul, Korea
Young Chul Kye
Department of Dermatology, Korea University College of Medicine, Seoul, Korea
Jee Ho Choi
Department of Dermatology, Ulsan University College of Medicine, Seoul, Korea
Chun Wook Park
Department of Dermatology, Hallym University College of Medicine, Anyang, Korea
Kwang Joong Kim
Department of Dermatology, Hallym University College of Medicine, Anyang, Korea
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