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Expectorants

	

Guaiphenesin

	

Mechanism of action:

As an expectorant, Guaiphenesin is used to promote the expectoration of bronchial secretions (AMH, 2004) by decreasing sputum viscosity, and hence facilitating its removal It also increases the amount of respiratory tract fluid thereby having a demulcent action on the mucosal lining. (Merck Manual). Dicpinigaitis and Galye (2003) proposed that guaiphenesin inhibits the cough reflex sensitivity in patients with a URTI, whereby these patients have cough receptors that are transiently hypersensitive. Inhibition of the cough reflex was postulated to have been achieved by guaiphenesin having either a central anti-tussive effect or a peripheral effect. If it is indeed the later, then Dicpinigaitis and Galye thought that guaiphenesin increased sputum volume as a barrier to shield the cough receptors within the respiratory epithelium from tussive stimulus

Contra-indications:

There has been no evidence to show that Guaiphenesin is contra-indicated in any disease state, and subsequently can be used in combination with any drug.

Disease state information:

All evidence indicates that Guaiphenesin should be only be used for the treatment of an acute cough of unknown or URTI cause, and only after all other possible conditions (asthma, COPD, etc) have been excluded. Parvez et al. (1996), however, looked at the effects Guaiphenesin had on a chronic cough.

Protocols for the use of Guaiphenesin:

Within the Cochrane Database of Systematic Reviews, Schroeder and Fahey (2004) reviewed the use of OTC medications for acute cough in children and adults in ambulatory settings. Schroeder and Fahey found that guaiphenesin had been included in two trials, both performed in adults only. The first trial was performed by Robinson (1977) and was a random controlled trial (RCT) with n=239 participants. Each participant was given a dose of either guaiphenesin 200mg/10ml qid 3/7 or a placebo. Of those patients, 75% (79/105) stated that guaiphenesin was helpful after 72hrs in reducing cough frequency and intensity compared with 31% (33/106) in the placebo group. The outcomes in this study were reported based on a patient questionnaire and a cough score of 0-3. The only adverse drug reactions that were reported in this trial were from 4 participants; 2 receiving guaiphenesin reported nausea and urticaria, 2 receiving placebo reported headaches, drowsiness and excessive perspiration. A conclusion that could be drawn from this study is that guaiphenesin is effective in reducing a coughs frequency and intensity. The second trial was performed by Kuhn (1982) and was also a RCT with n=65 participants. Unlike Robinson, Kuhn looked at the anti-tussive effect of guaiphenesin. Each participant was given a dose of either 480mg/30ml q6h for 30hrs or a placebo. Of those patients, 100% (33/33) of patients receiving guaiphenesin reported improvements after 36hrs in cough frequency and severity compared with 94% (30/32) and 91% (29/32) respectively in those patients receiving the placebo. 96% of the guaiphenesin users reported reduced sputum thickness compared with 54% of the placebo users. The outcomes in this study were reported based on tape recordings of cough frequency as well as a patient questionnaire on 6 symptoms. A conclusion that could be drawn from this study is that guaiphenesin is not effective in cough frequency and intensity, but is effective in reducing sputum thickness. Schroeder and Fahey concluded that there was no good evidence for or against the effectiveness of OTC medications in the treatment of an acute cough. This was possibly due to the limited number of patients involved in each trail.