Montelukast deprescribing in outpatient specialty clinics: A single center cross-sectional study

IF 1.8 Q3 PHARMACOLOGY & PHARMACY Exploratory research in clinical and social pharmacy Pub Date : 2024-12-01 Epub Date: 2024-09-17 DOI:10.1016/j.rcsop.2024.100509
David C. Foote , Jamie L. Miller , Grant H. Skrepnek , Stephen Neely , Kiya Bennett , Paul M. Boylan
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Abstract

Objective

To identify and evaluate montelukast deprescribing in outpatient specialty clinics.

Methods

This was a single-center, retrospective, cross-sectional study conducted at an academic health system in the southern US including 21 specialty clinics. Subjects included adults ≥18 years with an active prescription for montelukast who attended at least one appointment in pulmonology, otolaryngology, or neurology outpatient specialty clinics between January 1, 2021 to December 31, 2022. Patients <18 years and those with diagnoses of uncontrolled asthma or allergic rhinitis were excluded. Outcomes assessed included the frequency and period prevalence of montelukast deprescribing, defined by a documented montelukast discontinuation within the medical record, and evaluation of reasoning for discontinuation mentioned in visit notes.

Results

There were 1152 patients who met inclusion criteria. Of these, 43 (3.7 %) experienced a montelukast deprescribing event: 18 (41.9 %) in neurology, 13 (30.2 %) in otolaryngology, and 12 (27.9 %) in pulmonology. Documented reasons for deprescribing were only available for 11 patients (25.6 %); reasons for deprescribing included patient-provider shared decision-making regarding the Black Box Warning [n = 5 (11.6 %)], inadequate treatment response [n = 3 (7.0 %)], suicidal thought development [n = 1 (2.3 %)], adverse drug event [n = 1 (2.3 %)], and pregnancy planning [n = 1 (2.3 %)].

Conclusion

Montelukast deprescribing rates were less than 5 % in outpatient specialty clinics. Factors associated with montelukast deprescribing beget further investigation.

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门诊专科诊所的孟鲁司特去势:单中心横断面研究
方法 这是一项单中心、回顾性、横断面研究,在美国南部的一个学术医疗系统进行,包括 21 个专科门诊。研究对象包括 2021 年 1 月 1 日至 2022 年 12 月 31 日期间在肺科、耳鼻喉科或神经内科专科门诊至少就诊过一次、持有孟鲁司特有效处方、年龄≥18 岁的成人。18岁及诊断为哮喘或过敏性鼻炎未得到控制的患者除外。评估的结果包括停用孟鲁司特的频率和时期流行率(定义为病历中记录的孟鲁司特停药情况),以及对就诊记录中提到的停药原因进行评估。其中,43 例(3.7%)发生了孟鲁司特停药事件:神经内科 18 例(41.9%),耳鼻喉科 13 例(30.2%),肺科 12 例(27.9%)。仅有 11 名患者(25.6%)提供了有记录的停药原因;停药原因包括:患者与医护人员共同决定黑框警告 [n = 5 (11.6%)]、治疗反应不充分 [n = 3 (7.0%)]、有自杀倾向 [n = 3 (7.0%)]。结论孟鲁司特在专科门诊的停药率低于 5%。与停用孟鲁司特相关的因素有待进一步调查。
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CiteScore
1.60
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0.00%
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审稿时长
103 days
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