Why the study?
Real-world data were needed to describe first antiparkinsonian drug prescription patterns and evaluate disease duration until levodopa treatment and death by age group.
Does the choice of first antiparkinsonian drug affect time to levodopa initiation and survival in patients with Parkinson disease?
Cohort (n=6,243)
Does the choice of first antiparkinsonian drug affect time to levodopa initiation and survival in patients with Parkinson disease?
Hazard Ratio: 0.41 (95% CI 0.31–0.55)
The choice of first antiparkinsonian drug is age and sex dependent and is associated with time to levodopa initiation and survival, though this may reflect baseline disease severity.
OBJECTIVES: Real-world data were used to describe first antiparkinsonian drug (FAPD) prescription patterns among Parkinson disease (PD) patients and to evaluate disease duration until levodopa (l-DOPA) treatment and until death, as related to FAPD, by age group. METHODS: The community-based cohort (2000-2012) included 6243 patients, members of an Israeli Health Maintenance Organizations. Time from FAPD purchase to 2 end points (l-DOPA purchase and death) was calculated. Cox regressions were used to estimate adjusted heart rate (HR) to either end point as related to FAPD type, by age group. RESULTS: During a mean follow-up of 4.8 ± 3.2 years, one third of the cohort died. The percent of l-DOPA use as a start drug increased with age, whereas the percent of dopamine agonists (DAs) and monoamine oxidase inhibitor B inhibitor (MAO-BI) decreased with age. Younger women were treated more often with DA as a start drug compared with younger men. In ages of younger than 50 years, time to l-DOPA start in the initial DA-group was 4 times longer than in the initial MAO-BI group (HR, 0.23; 95% confidence interval, 0.08-0.43; 1/0.23, 4.35). All age groups exhibited a similar survival time trend associated with initial drug type. An age-pooled HR with initial l-DOPA-group as a reference group yielded that survival time was 2.4 times longer for the initial DA group (HR, 0.41; 95% confidence interval, 0.31-0.55; 1/0.41, 2.44), 1.9 times and 1.4 times for initial MAO-BI or amantadine, respectively. CONCLUSIONS: First antiparkinsonian drug choice might be associated with time until l-DOPA initiation but may represent disease severity at the time of prescription, thus also affecting survival time as well. Real-world data illustrated that this choice is also age and sex dependent.
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Faust‐Socher et al. (2021) conducted a cohort in Parkinson disease (n=6,243). Dopamine agonists (initial treatment) vs. Levodopa (initial treatment) was evaluated on Survival time (death) (HR 0.41, 95% CI 0.31-0.55).
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