Table 1. Characteristics of included studies.
Study | Age, y, mean (range) | Type of study | Location | Patients | Num | Type of outcome | Control group or arm | Medicine dose/day | Therapy duration | Side effects |
---|---|---|---|---|---|---|---|---|---|---|
Ryan 2012 | 61–63 | Randomized double-blind placebo-controlled | Australia | refractory chronic cough | 62 (52 completed) | +clinical improvement in LCQ score =20:12 mean VAS score (cm) =36:42 | Placebo (n=26) | Gabapentin in maximum tolerable of 1,800 mg (n=26) | 12 weeks | Nausea, stomach pain, fatigue, dizziness, dry mouth |
Jeyakumar 2006 | 55 | Randomized | USA | chronic cough resulting from postviral vagal neuropathy | 28 | # Patients’ subjective cough responses: complete response =11:0 partial response =3:3 no response =1:10 QOL data correlated strongly with the patients’ subjective responses | Codeine/guaifenesin (n=13) | Amitriptyline 10 mg qn (n=15) | 10 days | No |
Dicpinigaitis 1998 | 37–69 | Randomized double-blind placebo-controlled, cross-over | USA | refractory cough | 2 | Cough episodes per 24 hours by diaries documenting 2:0 | Placebo (n=2) | Baclofen 10 mg tid (n=2) | 28 days | No |
#, those patients experiencing a 75% to 100% cough reduction were recorded as having a complete response, 25% to 50% a partial response, and 0% as having no response; LCQ, Leicester cough questionnaire; QOL, quality-of-life; +, a clinical improvement in LCQ score of greater than 1∙3 the smallest change in score regarded as clinically meaningful; VAS, visual analogue scale.