Utilization of Acid Suppressants After Withdrawal of Ranitidine in Korea: An Interrupted Time Series Analysis.

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Tác giả: Jeong Pil Choi, Nam-Kyong Choi, Mi-Sook Kim, Sangwan Kim, Joongyub Lee, Jung Su Park, Cheol Min Shin

Ngôn ngữ: eng

Ký hiệu phân loại: 781.726 *Holy Week

Thông tin xuất bản: Korea (South) : Journal of preventive medicine and public health = Yebang Uihakhoe chi , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 60363

 OBJECTIVES: This study was performed to evaluate the utilization patterns of acid suppressants following the withdrawal of ranitidine in Korea. METHODS: Health Insurance Review &
  Assessment Service (HIRA) data from January 2016 to May 2023 were utilized to assess the usage of histamine H2 receptor antagonists (H2RAs) and proton pump inhibitors (PPIs) for acid-related diseases. Drug utilization was calculated for each agent based on the defined daily dose (DDD). To evaluate changes in utilization following the ranitidine recall, an interrupted time series analysis was conducted using segmented linear regression and an autoregressive integrated moving average model. RESULTS: Before the withdrawal of ranitidine, the DDD per 100 000 inhabitants per day was increasing by 6.9 (95% confidence interval [CI], 4.7 to 9.0) for H2RAs and by 19.3 (95% CI, 16.9 to 21.8) for PPIs each month. After the recall, H2RA utilization immediately declined by -1041.7 (95% CI, -1115.8 to -967.7), followed by a monthly increase of 6.6 (95% CI, 3.7 to 9.6) above the previous trend. PPI utilization temporarily surged by 235.2 (95% CI, 149.1 to 321.3), then displayed a monthly increase of 4.1 (95% CI, 0.7 to 7.6) on top of the pre-recall trend. Among PPIs, esomeprazole and rabeprazole demonstrated notable increases, representing the most commonly used acid suppressants in 2023. CONCLUSIONS: PPI usage rose prominently following the withdrawal of ranitidine from the market. Considering the potential adverse effects of PPIs, further research is necessary to evaluate the public health implications of shifts in the utilization of acid suppressants.
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