NICE guidance suggests (1)
First-line treatment (1)
- levodopa should be offered to people in the early stages of Parkinson's disease whose motor symptoms impact on their quality of life
- for people in the early stages of Parkinson's disease whose motor symptoms do not impact on their quality of life
- consider a choice of dopamine agonists, levodopa or monoamine oxidase B (MAO-B) inhibitors
- do not offer ergot-derived dopamine agonists as first-line treatment for Parkinson's disease
Adjuvant treatment of motor symptoms
- if a person with Parkinson's disease has developed dyskinesia and/or motor fluctuations, including medicines 'wearing off', seek advice from a healthcare professional with specialist expertise in Parkinson's disease before modifying therapy
- a choice of dopamine agonists, MAO-B inhibitors or catechol-O-methyl transferase (COMT) inhibitors should be offered as an adjunct to levodopa for people with Parkinson's disease who have developed dyskinesia or motor fluctuations despite optimal levodopa therapy, after discussing:
- person's individual clinical circumstances, for example, their Parkinson's disease symptoms, comorbidities and risks from polypharmacy
- person's individual lifestyle circumstances, preferences, needs and goals
- potential benefits and harms of the different drug classes
| | | | |
| amelioration in motor symptoms | amelioration in motor symptoms | amelioration in motor symptoms | No evidence of amelioration in motor symptoms |
Activities of daily living | amelioration in activities of daily living | amelioration in activities of daily living | amelioration in activities of daily living | No evidence of amelioration in activities of daily living |
| | | | No studies reporting this outcome |
| Intermediate risk of adverse events | | | No studies reporting this outcome |
| More risk of hallucinations | Lower risk of hallucinations | Lower risk of hallucinations | No studies reporting this outcome |
- in most cases a non-ergot-derived dopamine agonist in most cases, because of the monitoring that is needed with ergot-derived dopamine agonists
- an ergot-derived dopamine agonist should only be chosesn as an adjunct to levodopa for people with Parkinson's disease:
- who have developed dyskinesia or motor fluctuations despite optimal levodopa therapy and
- whose symptoms are not adequately controlled with a non-ergot-derived dopamine agonist
- amantadine should be considered if dyskinesia is not adequately managed by modifying existing therapy
The commonly used drugs in the management of Parkinson's disease are listed below:
- L-dopa:
- levodopa may be used as a symptomatic treatment for people with early PD (1)
- first line treatment for most patients
- offer levodopa to people in the early stages of Parkinson's disease whose motor symptoms impact on their quality of life (1)
- usually combined with an inhibitor of peripheral dopa decarboxylase
- slow-release preparations may reduce side-effects
- the dose of levodopa should be kept as low as possible to maintain good function in
order to reduce the development of motor complications (1) - a newer preparation of the drug has been licensed for the treatment of severe motor complications - a levedopa gel (Duodopa) used as a continuous infusion directly into the jejunum (2)
- dopamine receptor (D2) agonists:
- Dopamine agonists may be used as a symptomatic treatment for people with early PD (1)
- considered a possible first line treatment (1)
- in advanced disease used in conjunction with L-dopa to control fluctuations in response and required levadopa dose (2)
- may be used as monotherapy in early disease - it has been hypothesised that introducing dopamine agonists in the early stages of disease, before L-dopa
- is useful in controlling the motor symptoms (although less effective than levadopa)
- is associated with fewer motor complications compared to levadopa (2)
- there are 2 groups
- ergot-related - bromocriptine, cabergoline, lisuride and pergolide
- non-ergot-related - ropinirole, pramipexole and rotigotine (2)
- non ergot related drugs are used as first line treatment due to the associated risk of severe fibrotic and serosal inflammatory disorders seen with the ergot related preparations (2).
- if an ergot-derived dopamine agonist is used, the patient should have a minimum of renal function tests, erythrocyte sedimentation rate (ESR) and chest radiograph performed before starting treatment, and annually thereafter (1)
- ropinirole XL (once-daily) can be used in both the early and advanced disease (2)
- MAOB (monamine oxidase type B) inhibitors e.g. selegiline, rasagiline:
- inhibitors may be used as a symptomatic treatment for people with early PD (1)
- the use of this drug class is controversial
- may be used in advanced Parkinson's to reduce motor fluctuations (2)
- considered a possible first-line therapy (1)
- COMT-inhibition: e.g.- entacapone, tolcapone:
- second line treatment
- used as an adjunct to L-dopa (increases half life of the drug)
- anticholinergic agents:
- occasionally used especially when tremor predominates
- may be used as a symptomatic treatment typically in young people with early PD and severe tremor
- should not be drugs of first choice due to limited efficacy and the propensity to cause neuropsychiatric side effects
- amantadine:
- response rate is low and tolerance occurs
- may be used as a treatment for people with early PD but should not be a drug of first choice
- beta blockers
- may be used in the symptomatic treatment of selected people with postural tremor in PD, but should not be drugs of first choice (1)
- apomorphine
- a potent dopamine agonist
- useful in patients with severe motor complications to decrease 'off' periods and dyskinesia
- currently two treatment approaches are used
- in patients with less than six 'off' periods per day - intermittent subcutaneous rescue injections
- in patients with more frequent episodes - continuous infusion (2)
Reference:
- NICE (July 2017). Parkinson's disease in adults
- Turnbull C, Fitzsimmons P. Advances in the treatment of the motor symptoms of Parkinson's disease. J R Coll Physicians Edinb 2009; 39:29-31
- MeReC Bulletin 1999;10 (10): 37-40.
- Parkinson's disease Research Group of the United Kingdom. Comparison of therapeutic effects and mortality data of levodopa and levodopa commbined with selegiline in patients with early, mild Parkinson's disease. BMJ 1995; 311: 1602-7.