GASTROINTESTINAL DISORDERS IN PATIENTS WITH PARKINSON'S DISEASE- A DOUBLE-EDGED SWORD

Author(s)

Richy F1, Gunn A1, Makaroff L2, Gervasoni C3, Helmers S41UCB Pharma S.A., Brussels, Belgium, 2Business & Decision, Brussels, Belgium, 3Keyrus, Waterloo, Belgium, 4Emory School of Medicine, Atlanta, GA, USA

OBJECTIVES: A majority of patients with Parkinson's disease (PD) eventually develop gastrointestinal disorders (GID), which can impair the onset of symptom relief by PD drugs. There was a need to better understand the rate and consequences of GID amongst patients diagnosed with PD. METHODS: A two years matched retrospective cohort study was performed in a registered Pharmetrics® datacut, a US claims database containing records on demographics, diagnoses, procedures, provider, prescriptions and claims that span from 2000 to 2008. Patients with at least two prior diagnoses of Parkinson’s Disease, with continuous prescriptions of levodopa or dopamine agonists between September 1, 2005 and September 1, 2006 were selected. Patients with and without GID were matched by age, gender, comorbidities, and treatment regime. Their respective emerging health outcomes were followed-up for two years. Outcomes were defined on the basis of a literature review and included neuropsychiatric, motor, urogenital disturbances, healthcare utilization and related costs. RESULTS: In the datacut, GID incidence among patients with PD increased over time to stabilize at 75% at 92 months. 485 patients with PD and GID were matched to 485 controls with PD but without GID. GID was associated with significantly higher rates of neuropsychiatric and motor disorders, including psychosexual dysfunction (RR=8, p=0.05), anxiety (RR=1.61, p<0.01), depression (RR=1.28, p=0.03), ataxia (RR=1.24, p=0.03), pain (RR=1.28, p<0.01), movement disorders (RR=1.39, p<0.01), urinary incontinence (RR=1.43, p=0.02), and risk of fall (RR=1.44, p=0.04). ER admissions (ratio=1.42, p<0.01), number of concurrent drugs (ratio=1.06, p=0.04) and PD and non-PD healthcare costs (ratios= 1.13 and 1.12, p<0.01 respectively) increased during the observation period in the GID patients. CONCLUSIONS: GID have a substantial deleterious effect on major PD-related clinical and societal outcomes. Non oral formulations of PD drugs (apomorphine or L-dopa pumps or rotigotine)  may offer a good opportunity to bypass gastrointestinal tract, and accordingly maximize patient response to treatment.

Conference/Value in Health Info

2010-05, ISPOR 2010, Atlanta, GA, USA

Value in Health, Vol. 13, No. 3 (May 2010)

Code

PND3

Topic

Epidemiology & Public Health

Topic Subcategory

Safety & Pharmacoepidemiology

Disease

Neurological Disorders

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