Multiple system atrophy
ICD-10 G23.2; G23.3 · ICD-11 8D87.0

Treatment of Multiple System Atrophy with Parkinsonism: Bradykinesia with Resting Tremor or Rigidity (MSA-P)

Clinical Scenario

This protocol targets the parkinsonian type of multiple system atrophy (MSA-P), where the primary motor presentation is parkinsonism — bradykinesia accompanied by resting tremor, rigidity, or both, with or without postural instability.

Presentation

Parkinsonism is the defining motor constellation of MSA-P. Bradykinesia is the core feature, combined with either a resting tremor or rigidity (or both); postural instability may also be present. Recognition of this specific motor pattern within the MSA-P subtype is essential for selecting the appropriate management strategy.

Treatment Approach (overview)

First-line management is built around a specific dopaminergic agent, administered with careful attention to autonomic tolerability — particularly orthostatic effects. An alternative dopaminergic class may also be considered, though it generally carries a less favourable efficacy and side-effect profile compared to the first-line option.

The complete first-line regimen, titration approach, monitoring parameters, and decision pathway are available in the full protocol below.

Instant Access to Structured Evidence-Based Regimens
References

DOI: 10.1212/cont.0000000000001598

Parkinsonism is the major motor constellation of the parkinsonian type of multiple system atrophy, which consists of bradykinesia, with either resting tremor or rigidity or both, with or without postural instability.

Hence, levodopa therapy was usually recommended as the first-line treatment for parkinsonism, although levodopa may cause orofacial or facial cervical dystonia.

Dopamine agonists usually have lower therapeutic efficacy and more side effects than levodopa.

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