The Requirement to Monitor Low-dose Oral Minoxidil in the Management of Hair Loss.

Q2 Medicine
International Journal of Trichology Pub Date : 2025-05-01 Epub Date: 2025-11-19 DOI:10.4103/ijt.ijt_8_24
Donna M Cummins, Anwar Alramthan, Hussain Raja, Calvin Heal, Sona Mistry, Caroline White, Nuala O'Donoghue, Matthew Harries
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Abstract

Context: Low-dose oral minoxidil (LDOM) can safely and effectively treat numerous hair disorders. Reported doses range from 0.25 mg to 5 mg daily titrated against clinical effectiveness and adverse events. Some clinicians advocate routine monitoring of patients treated with LDOM. However, there is limited evidence on whether minoxidil in such small doses adversely impacts patients with normal hemodynamic and biochemical baseline profiles.

Aims: The aim of the study is to evaluate the need for regular monitoring of patients treated with LDOM.

Subjects and methods: This is a retrospective analysis of patients treated with LDOM in a tertiary hair clinic between April 2017 and June 2020. The clinical and laboratory parameters were assessed every 6 months. On commencing LDOM, baseline blood pressure, heart rate, and weight were recorded, and renal and liver function tests were performed.

Statistical analysis: The data were analyzed using graphical exploration.

Results: The heart rate, weight, renal function, and liver function appeared stable throughout the treatment course. The weight and estimated glomerular filtration rate showed a trend to increase over time, but these findings were not statistically significant for any of the outcomes.

Conclusions: The data support the position that routine monitoring is not required during treatment in asymptomatic patients with normal baseline values. Regular monitoring of blood pressure, heart rate, weight as well as liver and kidney function is not required during treatment with LDOM in patients with normal hemodynamic and biochemical baseline profiles. Patients with preexisting renal impairment can be prescribed oral minoxidil; however, we advocate ongoing monitoring in this subgroup, especially those with moderate-to-advanced disease. To the best of our knowledge, this is the first study that provides longitudinal monitoring data for LDOM with a follow-up period beyond 6 months and up to 36 months on treatment.

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Abstract Image

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监测低剂量口服米诺地尔治疗脱发的要求。
背景:低剂量口服米诺地尔(LDOM)可以安全有效地治疗多种头发疾病。报告的剂量范围为每日0.25毫克至5毫克,根据临床疗效和不良事件进行滴定。一些临床医生提倡对接受LDOM治疗的患者进行常规监测。然而,关于如此小剂量的米诺地尔是否会对血液动力学和生化基线正常的患者产生不利影响的证据有限。目的:本研究的目的是评估对LDOM治疗患者进行定期监测的必要性。对象和方法:这是对2017年4月至2020年6月在三级美发诊所接受LDOM治疗的患者的回顾性分析。每6个月评估一次临床和实验室参数。开始LDOM时,记录基线血压、心率和体重,并进行肾功能和肝功能检查。统计分析:采用图形化方法对数据进行分析。结果:在整个治疗过程中,心率、体重、肾功能、肝功能均保持稳定。体重和估计的肾小球滤过率随时间的推移呈增加趋势,但这些发现对任何结果都没有统计学意义。结论:数据支持无症状且基线值正常的患者在治疗期间不需要常规监测的立场。血液动力学和生化基线情况正常的患者在LDOM治疗期间不需要定期监测血压、心率、体重以及肝肾功能。既往存在肾脏损害的患者可以口服米诺地尔;然而,我们提倡对这一亚组进行持续监测,特别是那些患有中晚期疾病的患者。据我们所知,这是第一个提供LDOM纵向监测数据的研究,随访期超过6个月,治疗后长达36个月。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
38
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