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.