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Time until Need for Levodopa among New Users of Dopamine Agonists or MAO-B Inhibitors.

作者信息

Binde Caroline D, Tvete Ingunn F, Klemp Marianne

机构信息

Department of Pharmacology, University of Oslo, Oslo, Norway.

Norwegian Computing Center, Oslo, Norway.

出版信息

Parkinsons Dis. 2021 Jul 1;2021:9952743. doi: 10.1155/2021/9952743. eCollection 2021.


DOI:10.1155/2021/9952743
PMID:34306611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8270692/
Abstract

OBJECTIVE: To investigate the use of dopamine agonists and monoamine oxidase type B (MAO-B) inhibitors in the Norwegian population, between 1 July 2006 and 31 December 2016. Our primary endpoint was time until need for levodopa among new monotherapy users of dopamine agonists and MAO-B inhibitors. METHODS: A prospective cohort study including all patients, aged 50 years or above, who had at least one prescription for a dopamine agonist or a MAO-B inhibitor dispensed in the study period. We used data from the Norwegian Prescription Database (NorPD). As we wished to focus on new Parkinson patients, we excluded patients who had levodopa dispensed less than 180 days prior to their first dopamine agonist or MAO-B inhibitor redemption. We explored the demographics and the time until monotherapy was insufficient treatment (defined as need for levodopa prescription). RESULTS: We included 22958 new monotherapy users. Of these, 22108 used dopamine agonists and 850 used MAO-B inhibitors. The mean number of days until the first prescription of levodopa was dispensed was higher among the dopamine agonist users (621 days) compared to the MAO-B inhibitor users (352 days). The proportion of dopamine agonist users who started levodopa treatment during the study period was less than 7%, while the corresponding proportion of MAO-B inhibitor users was almost 59%. CONCLUSIONS: We found that new dopamine agonist users had a much greater delay in the need for levodopa than new MAO-B inhibitor users. It seems to be beneficial to initiate treatment with dopamine agonists when starting pharmacological treatment for new Parkinson patients.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e182/8270692/515149cfae8c/PD2021-9952743.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e182/8270692/e2863614eac0/PD2021-9952743.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e182/8270692/515149cfae8c/PD2021-9952743.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e182/8270692/e2863614eac0/PD2021-9952743.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e182/8270692/515149cfae8c/PD2021-9952743.002.jpg

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本文引用的文献

[1]
Therapeutic strategies for Parkinson's disease: promising agents in early clinical development.

Expert Opin Investig Drugs. 2020-11

[2]
Comparative effectiveness of dopamine agonists and monoamine oxidase type-B inhibitors for Parkinson's disease: a multiple treatment comparison meta-analysis.

Eur J Clin Pharmacol. 2020-12

[3]
Pharmacokinetics and pharmacodynamics of levodopa/carbidopa cotherapies for Parkinson's disease.

Expert Opin Drug Metab Toxicol. 2020-5

[4]
A multiple treatment comparison meta-analysis of monoamine oxidase type B inhibitors for Parkinson's disease.

Br J Clin Pharmacol. 2018-6-25

[5]
International Parkinson and movement disorder society evidence-based medicine review: Update on treatments for the motor symptoms of Parkinson's disease.

Mov Disord. 2018-3-23

[6]
An observational study of rotigotine transdermal patch and other currently prescribed therapies in patients with Parkinson's disease.

J Neural Transm (Vienna). 2018-2-26

[7]
Trends in inpatient antiparkinson drug use in the USA, 2001-2012.

Eur J Clin Pharmacol. 2015-8

[8]
Initial management of Parkinson's disease.

BMJ. 2014-12-19

[9]
The Nordic prescription databases as a resource for pharmacoepidemiological research--a literature review.

Pharmacoepidemiol Drug Saf. 2013-5-23

[10]
Milestones in Parkinson's disease therapeutics.

Mov Disord. 2011-5

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