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Deborah Gore
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[DYSPHAGIA] drooling & medication



The following is a review of some recent literature on the use of medication to control drooling:

Drugs have been used to block either the sympathetic or parasympathetic innervation of saliva production. Drugs that block sympathetic innervation tend to alter the consistency of saliva produced while drugs blocking the parasympathetic innervation tend to alter the quantity of saliva produced (Johnson & Scott, 1993). The most commonly used drugs reported in the drooling literature are Transdermal Scopolamine (Dreyfuss, Vogel, & Walsh, 1991; Good & Crain, 1996; Lewis et al., 1994; Siegel & Klingbeil, 1991), Glycopyrrolate (Blasco & Stansbury, 1996; Stern, 1997), Benztropine (Owen & Stern, 1992), and Benzhexol Hydrochloride (Reddihough et al., 1990).

Transdermal Scopolamine blocks parasympathetic innervation to the salivary glands and has been reported to be successful in reducing saliva flow (Siegel & Klingbeil, 1991). Lewis et al. (1994) reported that over half of the subjects in their study had at least a two-fold reduction in drooling and in a third of the subjects drooling was eliminated. Side effects reported included irritation around the patch site, pupillary dilation (Lewis et al., 1994) and esotropia (Good & Crain, 1996), although in a few cases where the medication has been used to prevent motion sickness, hallucinations have been reported (Wilkinsoin, 1987; Zisking, 1988). Glycopyrrolate is a drug with anticholinergic properties that has been used as a preanasthetic agent. Stern (1997) reported the majority of subjects demonstrating a reduction in drooling while taking glycopyrrolate. Blasco & Stansbury (1996) also found that glycopyrrolate reduced drooling, but rarely eliminated the problem. A common side effect of the drug included problems with constipation (Blasco & Stansbury, 1996; Stern, 1997) but other side effects were noted including thirst in hot weather, dilated pupils, and dry lips (Stern, 1997). Reddihough et al. (1990) reported reduction in drooling with Benzhexol Hydrochloride in 17 of 20 subjects. Side effects included behavioral changes (restlessness and overactivity). Benztropine has also been reported to significantly reduce drooling (Owen & Stern, 1992). Aside from side-effects, it has been suggested that a disadvantage of pharmacological treatment is the possibility of adaption in which the salivary glands adapt to a reduced level of stimulation and become hypersensitive. If adaption occurs, saliva production can return to pre-medication levels over the course of treatment (Johnson & Scott, 1993).

References:

Blasco, P. A., & Stansbury, J. C. K. (1996). Glycopyrrolate treatment of chronic drooling. Archives of Pediatric and Adolescent Medicine, 150, 932-935.

Dreyfuss, P., Vogel, D., & Walsh, N. (1991). The use of transdermal scopolamine to control drooling. American Journal of Physical Medicine and Rehabilitation, 70, 220-222.

Good, W. V., & Crain, L. S. (1996). Esotropia in a child treated with a scopolamine patch for drooling. Pediatrics, 126-127.

Johnson, H., & Scott, A. (1993). A Practical Approach to Saliva Control. Tuscon, AZ: Communication Skill Builders.


Lewis, D. W., Fontana, C., Mehallick, L., K., & Everett, Y. (1994). Transdermal scopolamine for reduction of drooling in developmentally delayed children. Developmental Medicine and Child Neurology, 36, 484-486.

Owen, S. E., & Stern, L. M. (1992). Management of drooling in cerebral palsy: three single case studies. International Journal of Rehabilitation Research, 15(2), 166-169.

Reddihough, D., Johnson, H., Staples, M., Hudson, I., & Exarchos, H. (1990). Use of Benzhexol Hydrochloride to control drooling of children with cerebral palsy. Developmental Medicine & Child Neurology, 32, 985-989.

Siegel, L. K., & Klingbeil, M. A. (1991). Control of drooling with transdermal scopolamine in a child with cerebral palsy. Developmental Medicine and Child Neurology, 33(11), 1013-1014.

Stern, L. M. (1997). Preliminary study of glycopyrrolate in the management of drooling. Journal of Paediatric and Child Health, 33, 52-54.