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首页> 外文期刊>Therapeutic innovation & regulatory science. >Age-Appropriate Pediatric Dosage Forms in Japan: Insights into End-User Perceptions From an Observational Cross-Sectional Survey Assessing the Acceptability of Oral Formulation
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Age-Appropriate Pediatric Dosage Forms in Japan: Insights into End-User Perceptions From an Observational Cross-Sectional Survey Assessing the Acceptability of Oral Formulation

机译:日本的适当儿科剂型:从观察横断面调查评估口腔制剂的可接受性的观察横断面调查中的最终用户看法

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Background: The lack of appropriate pediatric formulations is a global issue and information on acceptability is urgently needed to develop standard pediatric formulations. This study aimed to assess perceptions of acceptability of several oral dosage forms among pediatric patients at a community and a pediatric hospital in Japan and collected information about age-appropriate pediatric formulations, aiming to contribute to drug development promotion worldwide. Methods: A cross-sectional observational study was performed. A convenience sample of caregivers was recruited from available chain-owned retail pharmacies and inpatient pediatric units. The questionnaire was composed of 3 parts: (1) acceptability of the 5 dosage forms (tablets, capsules, powders, liquids, and orally disintegrating tablet) by age; (2) acceptability of dosage size, amount, and volume by age; and (3) the actual method of administration. Face-to-face interviews were conducted at 3 independent community pharmacies (324 parents) and tertiary care pediatric hospital wards (112 nursing staff). Acceptability scores and acceptable dosages were then determined. The survey was conducted from October 1 to December 1, 2017, for the hospital setting and November 1 to 30, 2017, for the outpatient setting. Results: The acceptability of oral dosage forms was roughly similar to the matrix drafted by the European Medical Agency. Differences in perception of the powder forms between communities and hospitals were also observed, with the nursing staff perceiving powder as being acceptable from the neonatal period. Conclusions: The difference in caregivers' perception of the acceptability of oral formulations between Japan and Europe was small. The powder form was found to be more acceptable in Japan. Further intervention studies are needed to assess the preferred pediatric formulation worldwide.
机译:背景:缺乏适当的儿科制剂是全球问题,迫切需要有关可接受性的信息来制定标准的儿科制剂。本研究旨在评估社区儿科患者和日本儿科医院的几种口服剂型的可接受性的看法,并收集了有关年龄适当的儿科制剂的信息,旨在为全世界的毒品开发促进提供促进。方法:进行横截面观察研究。从可用的连锁公司零售药房和住院儿科单位招募了可怜的护理人员样本。调查问卷由3份组成:(1)按年龄为5份(1)份5剂型(片剂,胶囊,粉末,液体和口服崩解片)的可接受性; (2)按年龄的剂量尺寸,量和体积的可接受性; (3)实际的管理方法。面对面采访是在3名独立社区药房(324名家长)和第三级护理儿科医院病房(112名护理人员)进行的面试。然后测定可接受性评分和可接受的剂量。该调查是从2017年10月1日至12月1日进行的,为住院环境和2017年11月1日至30日,为期间设定。结果:口腔剂型的可接受性大致相似,欧洲医疗机构起草的矩阵。还观察到社区与医院之间粉末形式感知的差异,护理人员感知粉末作为新生儿期可接受的粉末。结论:护理人员对日本和欧洲口腔配方的可接受性的看法很小。发现粉末形式在日本更加接受。需要进一步的干预研究来评估全世界优选的儿科制剂。

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