Nguyen Joanne, Chin Justin J, Blalock Meredith
Healthcare Operations Squadron, 78th Medical Group, United States Air Force, Robins Air Force Base, GA, and Detachment-1, 116th Medical Group, Georgia Air National Guard, Robins Air Force Base, GA, USA.
Operational Medical Readiness Squadron, 78th Medical Group, United States Air Force, Robins Air Force Base, GA, USA.
Am J Health Syst Pharm. 2023 Jan 1;80(1):e14-e17. doi: 10.1093/ajhp/zxac257.
The following case report discusses probable clitoral priapism secondary to duloxetine and pregabalin. While this is a rare adverse effect, it is possible given the mechanism of action and potentiating effects of the combined therapy. This adverse drug reaction was reported to MedWatch and shows that additional research into the physiology of clitoral erection is warranted given the scarcity of information on how drugs influence this reaction.
A 53-year-old African American female with uncontrolled anxiety was started on duloxetine. Pregabalin was added 1 month later due to continued feelings of anxiety. Three weeks later, the patient reported symptoms of clitoral pain, as well as a swollen, tender, and erect clitoris. These adverse effects remained for 4 days, prompting the patient to present to the emergency department where a physical exam was completed with no significant finding except as noted above. Pregabalin was immediately discontinued by the attending physician based on the probability that the swelling was likely drug-induced clitoral priapism. During follow-up, the patient continued to note clitoral erection and pain. The psychiatric pharmacist tapered off duloxetine over 2 weeks with resolution of symptoms. In an examination of the mechanism of action of both drugs, pregabalin can amplify duloxetine's inhibitory effects on voltage-dependent calcium channels. It is likely this mechanism that causes smooth muscle relaxation and led to clitoral priapism.
This case suggests that pharmacological agents affecting vasoconstriction through serotonergic receptors or calcium-dependent channels can also influence clitoral erection.
以下病例报告讨论了度洛西汀和普瑞巴林继发的可能的阴蒂异常勃起。虽然这是一种罕见的不良反应,但鉴于联合治疗的作用机制和增强效应,这种情况是有可能发生的。该药物不良反应已报告给美国食品药品监督管理局的药品不良事件监测系统(MedWatch),鉴于关于药物如何影响这种反应的信息匮乏,有必要对阴蒂勃起的生理学进行更多研究。
一名53岁的非洲裔美国女性,患有无法控制的焦虑症,开始服用度洛西汀。1个月后,由于焦虑情绪持续存在,加用了普瑞巴林。三周后,患者报告出现阴蒂疼痛症状,以及阴蒂肿胀、触痛和勃起。这些不良反应持续了4天,促使患者前往急诊科就诊,在那里进行了体格检查,除上述情况外未发现明显异常。主治医生基于肿胀可能是药物引起的阴蒂异常勃起这一可能性,立即停用了普瑞巴林。在随访期间,患者仍持续出现阴蒂勃起和疼痛。精神科药剂师在2周内逐渐减少度洛西汀用量,症状得以缓解。在研究这两种药物的作用机制时发现,普瑞巴林可增强度洛西汀对电压依赖性钙通道的抑制作用。很可能正是这种机制导致平滑肌松弛并引发了阴蒂异常勃起。
该病例表明,通过血清素能受体或钙依赖性通道影响血管收缩的药物制剂也可影响阴蒂勃起。