Efficacy and safety of orally administered pilocarpine hydrochloride for patients with juvenile-onset Sj?gren’s syndrome
Minako Tomiita1 , Syuji Takei2 , Naomi Kuwada2 , Yukiko Nonaka2 , Kimiyuki Saito3 , Naoki Shimojo1 , Yoichi Kohno1
12 February 2010
20 April 2010
3 June 2010
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The number of patients with juvenile-onset Sj?gren’s syndrome (SS) has recently increased. However, there is no drug that is safe and effective for the xerostomia that occurs in patients of this age group. We evaluated the efficacy and safety of orally administered pilocarpine hydrochloride for juvenile-onset SS patients. Five female patients, aged from 9 to 16 years, received 5?10 mg/day for 4 weeks. On days 1 and 28, salivary production was measured by the Saxon test, and patients completed subjective self-evaluations of xerostomia symptoms and were asked about changes in water intake and overall improvement of dry mouth on day 28. After 4 weeks of pilocarpine administration, salivary production increased significantly in all patients, and overall status was assessed as “improved” in all patients. One patient had excessive sweating. No serious adverse events or laboratory examination abnormalities correlated with pilocarpine administration were found. In conclusion, the results of this study suggest that orally administered pilocarpine is safe and effective for treating xerostomia in juvenile-onset SS patients. This is the first report of the efficacy of pilocarpine for juvenile SS patients; further evaluations are needed to confirm our result.
Juvenile onset - Pilocarpine - Salivary glands - Sj?gren’s syndrome - Xerostomia