Vadiei Nina, Smith Tawny L, Garcia-Pittman Erica C
(Corresponding author) Assistant Professor, The University of Arizona, College of Pharmacy Practice and Science, Tucson, Arizona,
Associate Professor, Dell Medical School at The University of Texas at Austin, Department of Psychiatry, Austin, Texas.
Ment Health Clin. 2018 Jun 29;8(4):188-190. doi: 10.9740/mhc.2018.07.188. eCollection 2018 Jul.
To report a case of oral candidiasis that developed in a 70-year-old white female both upon initiation and rechallenge of extended-release bupropion therapy.
A 70-year-old female with a past medical history of osteoarthritis, degenerative joint disease, and polycythemia vera developed oral candidiasis on 2 occasions following initiation of extended-release bupropion for the treatment of recurrent depression. During both instances, the reaction occurred with an increased dose of the medication, suggesting the adverse event may have been dose-related. The patient had no risk factors for oral candidiasis aside from dry mouth at baseline that reportedly worsened on bupropion.
Though there are no other reports to our knowledge describing the development of oral candidiasis with bupropion, the likelihood of this having been an adverse reaction in this patient is probable as indicated by a calculated score of 8 from the Naranjo Algorithm. The adverse event appeared following bupropion administration and improved over time following its discontinuation. The adverse event reappeared following readministration of the agent, and no alternative causes were able to be identified. Additionally, the reaction occurred following an increase in the dose on both occasions, with the lower dose having only resulted in worsening dry mouth.
This case demonstrates that an additional adverse event to screen for with bupropion treatment is the development of oral candidiasis. This adverse event may be more likely to occur in the older adult population.
报告一例70岁白人女性在开始及再次使用缓释安非他酮治疗时发生口腔念珠菌病的病例。
一名70岁女性,有骨关节炎、退行性关节病和真性红细胞增多症病史,在开始使用缓释安非他酮治疗复发性抑郁症后两次发生口腔念珠菌病。在这两种情况下,反应均在药物剂量增加时出现,提示该不良事件可能与剂量相关。除了据报道在服用安非他酮后加重的基线口干外,患者没有口腔念珠菌病的危险因素。
据我们所知,虽然没有其他关于安非他酮导致口腔念珠菌病的报道,但根据Naranjo算法计算得分为8,表明该患者发生不良反应的可能性很大。不良事件在服用安非他酮后出现,并在停药后随时间改善。再次给药后不良事件再次出现,且未发现其他原因。此外,两次反应均在剂量增加后发生,较低剂量仅导致口干加重。
本病例表明,安非他酮治疗时需要筛查的另一种不良事件是口腔念珠菌病的发生。这种不良事件在老年人群中可能更易发生。