کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4162564 | 1274284 | 2012 | 5 صفحه PDF | دانلود رایگان |

ObjectiveTo determine whether safety warnings issued by health regulatory agencies regarding desmopressin treatment influenced treatment rates among children.Patient population and methodsWe conducted a time-series analysis using health administrative data from Ontario, Canada, between January 1, 2003 and March 31, 2010. We examined desmopressin prescribing rates among children (<13 years) and investigated the impact of a United States Food and Drug Administration warning (December 2007) and a subsequent Health Canada warning (July 2008) on these rates. A secondary analysis stratified rates according to route of administration.ResultsOn average, quarterly desmopressin treatment rates were 29.8% lower following the two warnings (4.7 per 1000 population) compared with the period prior to warnings being issued (6.7 per 1000 population). Structural break analyses identified a significant decrease in overall desmopressin prescribing rates in Q3 2008, with the 95% confidence interval (CI) spanning both safety warnings (Q4 2007 to Q1 2009). A secondary analysis of prescribing rates for oral formulations found consistent results (structural break Q4 2008, 95% CI Q2 2007 to Q2 2009). The average quarterly prescribing rate of intranasal formulations declined by 73.1% following the warnings compared with the period preceding the warnings.ConclusionSafety warnings issued by regulatory agencies dramatically influenced desmopressin use among Ontario’s children.
► Desmopressin use can lead to serious adverse events, including hyponatremia.
► This study investigates the impact of safety warnings on desmopressin use.
► Safety warnings led to a reduction in desmopressin prescribing in children.
► Warnings from regulatory agencies can influence physician prescribing behavior.
Journal: Journal of Pediatric Urology - Volume 8, Issue 3, June 2012, Pages 249–253