TY - JOUR
T1 - Real World Pharmacological First Treatment Patterns of Patients with Parkinson Disease and Disease Duration
T2 - A Large-Scale Cohort Study Using an Health Maintenance Organization Database
AU - Faust-Socher, Achinoam
AU - Gurevich, Tanya
AU - Rozani, Violetta
AU - Giladi, Nir
AU - Hemo, Beatriz
AU - Peretz, Chava
N1 - Funding Information:
Conflicts of Interest and Source of Funding: T.G. reports advisory board membership with honoraria to her and to her Institution AbbVie Israel, Neuroderm, Ltd, and Allergan and research support from Phonetica, Ltd, Israeli Innovation Authority, Sagol School of Neuroscience (Brain Boost) and Parkinson's Foundation. N.G. reports that he is a consultant for Neuroderm, Intec Pharma, Teva, Genzyme-Sanofi, Biogen, Lysosomal Therapeutics, Denali, Cellanis, GaitBetter, Vibrant, and Sionara; that he holds shares or options in Lysosomal Therapeutics, Cellanis, GaitBetter, and Vibrant; that he has received royalties from Lysosomal Therapeutics; that he received honorarium from UCB, Teva, Novartis, AbbVie, Genzyme-Sanofie, Neuroderm, Bial, Shire, and MDS; that he has chaired the DSMBs for Teva and Pharma2B; that he is a Principal Investigator on a Center Grant given by Biogen to TLVMC; that he has submitted a patent application on the use of body-fixed sensors for assessing PD symptoms, the intellectual property rights for which are held by the Tel Aviv Medical Center; and that he received grants from Teva, Biogen, LTI, ISF, EU, National Institutes of Health, MJFF, Parkinson Foundation, and Pfizer. The other authors have no conflicts of interest to declare.
Publisher Copyright:
© Wolters Kluwer Health, Inc. All rights reserved.
PY - 2021/9/1
Y1 - 2021/9/1
N2 - 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.
AB - 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.
KW - Parkinson disease
KW - drug purchase
KW - hazard ratio
KW - levodopa
KW - mortality
UR - http://www.scopus.com/inward/record.url?scp=85116632404&partnerID=8YFLogxK
U2 - 10.1097/WNF.0000000000000461
DO - 10.1097/WNF.0000000000000461
M3 - Article
C2 - 34238785
AN - SCOPUS:85116632404
SN - 0362-5664
VL - 44
SP - 169
EP - 174
JO - Clinical Neuropharmacology
JF - Clinical Neuropharmacology
IS - 5
ER -