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一项关于阿奇霉素单剂量缓释制剂所致腹泻及服用便利性的调查。

A survey on diarrhea and convenience of intake associated with a single-dose extended release formulation of azithromycin.

作者信息

Okayasu S, Matsuura K, Kondoh Y, Tsuruta E, Takashima E, Suzuki M, Nagai T, Yasuda K, Itoh Y

机构信息

Department of Pharmacy, Gifu University Hospital, Gifu, Japan.

出版信息

Pharmazie. 2011 Mar;66(3):226-9.

Abstract

The development of a single-dose extended release formulation of azithromycin (AZ-SR) improves the adherence. However, gastrointestinal side effects such as diarrhea are frequent adverse drug reactions. The aim of the present study was to investigate the incidence of patient-reported in a diarrhea and the convenience of intake of AZ-SR in an Asian population. To assess the incidence of diarrhea and convenience of intake, patient-reported in a questionnaire about the incidence, onset, duration and severity of diarrhea, shape of stool, and patients' impression on taste. The drug was prepared and used in common with the hospital pharmacy and the community pharmacy. AZ-SR was prescribed in 96 outpatients, among whom 81 patients received the medicine and the questionnaire at the hospital pharmacy or one of five neighboring community pharmacies. The recovery of the questionnaire was 40.7%. Diarrhea occurred in 18 of 33 patients (54.5%), which was more frequent than in earlier reports, although the symptom was mild (grade 1-2) and occurred in most cases within 2 days. Approximately one third of patients reported inconvenience in taking the formulation in respect of the ease (36.4%), amount (42.4%), and unpleasant bitter taste (36.4%). We report here the importance of collaboration between hospital pharmacists and community pharmacists in providing accurate drug information, including the incidence of diarrhea, to patients receiving AZ-SR.

摘要

阿奇霉素单剂量缓释制剂(AZ-SR)的研发提高了患者的依从性。然而,腹泻等胃肠道副作用是常见的药物不良反应。本研究的目的是调查亚洲人群中患者报告的腹泻发生率以及AZ-SR的服用便利性。为评估腹泻发生率和服用便利性,通过问卷调查患者关于腹泻的发生率、发作时间、持续时间和严重程度、粪便形状以及患者对味道的印象。该药物由医院药房和社区药房共同配制和使用。96名门诊患者被开具了AZ-SR,其中81名患者在医院药房或五家邻近社区药房之一领取了药物并填写了问卷。问卷回收率为40.7%。33名患者中有18名(54.5%)出现腹泻,虽然症状较轻(1-2级)且大多在2天内出现,但腹泻发生率高于早期报告。约三分之一的患者表示在服用该制剂时在服用 ease(36.4%)、剂量(42.4%)和苦味不适(36.4%)方面存在不便。我们在此报告医院药剂师和社区药剂师之间合作的重要性,即在向接受AZ-SR治疗的患者提供准确的药物信息(包括腹泻发生率)方面。 (注:原文中“ease”此处可能有误,结合语境推测可能是“服用便利性”之类的意思,但按要求未做修改)

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