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首页> 外文期刊>The Journal of dermatology >Treatment patterns of postherpetic neuralgia patients before and after the launch of pregabalin and its effect on medical costs: Analysis of Japanese claims data provided by Japan Medical Data Center
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Treatment patterns of postherpetic neuralgia patients before and after the launch of pregabalin and its effect on medical costs: Analysis of Japanese claims data provided by Japan Medical Data Center

机译:PREGABALIN发射前后POSTHERPETICGIA患者的治疗模式及其对医疗成本的影响:日本医学数据中心提供的日本声称数据分析

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摘要

Except for neurotrophin, no drug had an indication for postherpetic neuralgia (PHN) in Japan prior to pregabalin approval. This approval might have changed PHN treatment patterns. This study aimed to compare PHN treatment patterns and medical costs between patients who started treatment before and after pregabalin approval. Japanese claims data were used to identify patients aged 18 years or more with PHN, postherpetic trigeminal neuralgia or postherpetic polyneuropathy who were initiated on their first PHN-associated prescription through May 2010 (before approval) or from June 2010 (after approval). From these claims, 6-month treatment patterns from first prescription were compared for the periods before and after approval. These patterns included pain-related medications and the frequency of pain-relief procedures. All-cause and pain-related medical costs were also compared for these periods. The number of PHN patients who were initiated on treatment before and after approval were 107 (mean age, 47.4 +/- 13.0 years) and 505 (45.9 +/- 13.0), respectively. Post-approval, significant reductions were observed for prescription of non-steroidal anti-inflammatory drugs, tricyclic antidepressants and neurotrophin relative to before approval. Excluding pregabalin acquisition costs, mean costs per patient for medications associated with PHN for 6 months from the first prescription were significantly lower after approval, yen2882 vs yen4185. Total medical costs were similar in both periods. Approval of pregabalin appeared to result in a treatment paradigm toward use of an approved therapy with demonstrated efficacy.
机译:除神经营养蛋白外,在普罗那巴林批准之前,没有药物在日本的Postherpetic Geatergia(PHN)有迹象表明。此批准可能改变了PHN治疗模式。本研究旨在比较普瑞巴林批准之前和之后开始治疗的患者的PHN治疗模式和医疗费用。日本声称数据用于鉴定18岁以上的患者,用PHN,POSTherpetic Trigleminal Gerultgia或Postherpeticocathy或Postherpeticocathy通过2010年5月(在批准之前)或2010年6月(批准后)开始。根据这些权利要求,比较了第一次处方的6个月治疗模式,以便在批准之前和之后进行比较。这些模式包括疼痛相关的药物和疼痛缓解程序的频率。这些时期还比较了全原因和与疼痛相关的医疗费用。在批准前后进行治疗的PHN患者的数量分别为107(平均年龄,47.4 +/- 13.0岁)和505(45.9 +/- 13.0)。批准后,观察到非甾体抗炎药,三环抗抑郁药和神经营养蛋白相对于批准之前的批准。不包括普瑞巴林习得成本,在批准后,与第一个处方有6个月的患者的每位患者的每位患者的费用显着降低,YEN2882 VS YEN4185。两期都有总医疗费用。普瑞巴林的批准似乎导致治疗范例用于使用经批准的治疗,具有证明的疗效。

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