1 Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, Ohio, USA.
2 Cleveland Clinic Lerner Research Institute, Cleveland, Ohio, USA.
Otolaryngol Head Neck Surg. 2018 Sep;159(3):508-515. doi: 10.1177/0194599818768517. Epub 2018 Apr 10.
Objective To evaluate the short- and long-term effects of tricyclic antidepressants (TCAs) and gabapentin in the treatment of unexplained chronic cough (UCC). Study Design Prospective cohort. Setting Tertiary care hospital. Subjects and Methods Patients seen between July 2016 and March 2017 were included following a formal workup and clinical evaluation indicative of UCC. Patients were placed on either a TCA (amitriptyline or nortriptyline) or gabapentin. Leicester Cough Questionnaire (LCQ) and percentage improvement scores were obtained prior to treatment initiation and at 2 and 6 months of neuromodulator treatment. A linear mixed model assessed the change in LCQ score between the 2 treatment time points and baseline scores. Results Twenty-eight patients completed a total of 37 neuromodulator trials. Gabapentin demonstrated statistically significant improvement in LCQ scores at 2 months (2.48 points, P≤ .01) and 6 months (5.40 points, P = .01) of treatment as compared with baseline. Patients taking TCAs demonstrated statistically significant improvement of LCQ scores at 2 months of treatment (3.46 points, P≤ .01). However, the majority of patients discontinued treatment, most commonly secondary to the development of tachyphylaxis after 2 months, precluding analysis at 6 months. Conclusion While both neuromodulator classes demonstrated short-term benefit, the majority of patients discontinue treatment prior to 6 months, with patients taking TCAs discontinuing more frequently than patients on gabapentin. Future investigations are warranted evaluating tachyphylaxis and the utility of dual treatment therapies designed to address peripheral and central sensory pathways involved in UCC.
评估三环类抗抑郁药(TCAs)和加巴喷丁治疗不明原因慢性咳嗽(UCC)的短期和长期疗效。
前瞻性队列研究。
三级保健医院。
2016 年 7 月至 2017 年 3 月间,对经过正规检查和临床评估提示为 UCC 的患者进行了前瞻性队列研究。将患者分为 TCA(阿米替林或去甲替林)或加巴喷丁治疗组。在开始神经调节剂治疗前、治疗后 2 个月和 6 个月时,采用莱斯特咳嗽问卷(LCQ)和改善百分比评分进行评估。采用线性混合模型评估 2 个治疗时间点与基线之间 LCQ 评分的变化。
28 例患者共完成了 37 次神经调节剂试验。与基线相比,加巴喷丁治疗 2 个月(2.48 分,P≤.01)和 6 个月(5.40 分,P =.01)时 LCQ 评分有统计学显著改善。服用 TCA 的患者在治疗 2 个月时 LCQ 评分有统计学显著改善(3.46 分,P≤.01)。然而,大多数患者停药,最常见的原因是在 2 个月后出现快速耐受,因此无法在 6 个月时进行分析。
虽然两种神经调节剂都显示出短期疗效,但大多数患者在 6 个月前停药,服用 TCA 的患者比服用加巴喷丁的患者停药更频繁。未来需要进一步研究快速耐受以及设计用于治疗涉及 UCC 的外周和中枢感觉途径的双重治疗疗法的实用性。