Zhang Mengru, Chen Qiang, Dong Ran, Yu Li, Ai Zisheng, Xu Xianghuai, Qiu Zhongmin
Department of Pulmonary and Critical Care Medicine, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Department of Preventive Medicine, Tongji University School of Medicine, Shanghai, China.
Ther Adv Chronic Dis. 2020 Dec 26;11:2040622320982463. doi: 10.1177/2040622320982463. eCollection 2020.
BACKGROUND: Gabapentin is recommended for the treatment of chronic refractory cough (CRC). This study aims to identify its therapeutic predictors in a prospective clinical study. METHODS: A total of 179 patients with CRC were treated with gabapentin. Prior to the therapy, all patients were assessed by Hull Airway Reflux Questionnaire (HARQ) and inhaled capsaicin challenge. When the treatment ended and cough resolution was confirmed, a stepwise logistic regression analysis was performed to identify the therapeutic predictors for gabapentin and to establish the prediction equation. RESULTS: Gabapentin treatment achieved a therapeutic success rate of 66.48%. HARQ scores were significantly higher in responders than non-responders to gabapentin (29.79 ± 9.58 21.95 ± 7.83, = -3.685, <0.001), which were positively related to the therapeutic efficacy of gabapentin ( = 0.433, <0.001). The optimal cutoff point of 21.50 in HARQ presented with a moderate ability to predict gabapentin efficacy, with a sensitivity of 84.60% and specificity of 63.60%. Multiple logistic regression identified items of "A tickle in your throat, or a lump in your throat" (OR = 7.927, = 0.005), "Cough when you get out of bed in the morning" (OR = 7.016, = 0.045), and "Cough with eating" (OR = 6.689, = 0.011) as independent predictors. The established logistic regression equation predicted 83.72% of the treatment success rate of gabapentin, which was verified by consequent preliminary revalidating study in 59 patients. CONCLUSION: HARQ may be useful to screen patients with CRC most likely responsive to gabapentin, and help improve the therapeutic success. TRIAL REGISTRATION: http://www.chictr.org/; No.: ChiCTR-ONC-13003123.
背景:加巴喷丁被推荐用于治疗慢性难治性咳嗽(CRC)。本研究旨在通过一项前瞻性临床研究确定其治疗预测因素。 方法:共有179例CRC患者接受加巴喷丁治疗。治疗前,所有患者均通过赫尔气道反流问卷(HARQ)和吸入辣椒素激发试验进行评估。治疗结束并确认咳嗽缓解后,进行逐步逻辑回归分析以确定加巴喷丁的治疗预测因素并建立预测方程。 结果:加巴喷丁治疗的有效率为66.48%。加巴喷丁治疗有反应者的HARQ评分显著高于无反应者(29.79±9.58对21.95±7.83,t=-3.685,P<0.001),且与加巴喷丁的治疗效果呈正相关(r=0.433,P<0.001)。HARQ中21.50的最佳截断点对加巴喷丁疗效的预测能力中等,敏感性为84.60%,特异性为63.60%。多因素逻辑回归确定“喉咙发痒或有异物感”(OR=7.927,P=0.005)、“早晨起床时咳嗽”(OR=7.016,P=0.045)和“进食时咳嗽”(OR=6.689,P=0.011)为独立预测因素。建立的逻辑回归方程预测加巴喷丁治疗成功率为83.72%,随后在59例患者中进行的初步再验证研究证实了这一点。 结论:HARQ可能有助于筛选出最可能对加巴喷丁有反应的CRC患者,并有助于提高治疗成功率。 试验注册:http://www.chictr.org/;编号:ChiCTR-ONC-13003123 。
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