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. Author manuscript; available in PMC: 2019 Apr 1.
Published in final edited form as: Parkinsonism Relat Disord. 2017 Dec 29;49:9–16. doi: 10.1016/j.parkreldis.2017.12.030

Table 3.

Updated diagnostic approach VaPark subtypes

Acute/subacute Post-stroke VaPark Insidious VaPark Mixed neurodegenerative parkinsonism and CVD (mixed PD/CVD)
Obligatory
  • Acute/subacute onset of parkinsonism (typically) asymmetric

  • Imaging evidence of stroke in the nigrostriatal pathway

  • Progressive disease (insidious or stepwise)

  • Mixed shuffling/ataxic gait

  • Postural instability

  • Imaging evidence of cerebrovascular small vessel disease beyond the nigrostriatal pathway

  • Patients meeting clinical diagnostic criteria for probable neurodegenerative parkinsonism (PD, DLB, PSP, MSA, CBS, non-tau FTD parkinsonism)

    and

  • Imaging evidence of cerebrovascular disease in location(s) that is/are spatially congruent with presenting parkinsonism, in particular postural instability and gait difficulties, upper motor neuron signs or incontinence.

Supportive
  • Presynaptic striatal dopamine transporter deficiency congruent with the stroke

  • Preserved levodopa responsiveness

  • Freezing of gait

  • Pyramidal signs

  • Cognitive decline

  • Urinary urgency/incontinence

  • Pseudobulbar symptoms

  • Absence of significant levodopa responsiveness

  • Abnormal striatal dopamine transporter imaging findings not explained by vascular lesions

  • Abnormal cardiac sympathetic nerve terminal imaging findings

Non-supportive
  • Abnormal striatal dopamine transporter imaging findings not explained by nigrostriatal pathway vascular lesions

  • Abnormal cardiac sympathetic nerve terminal imaging

  • Abnormal striatal dopamine transporter imaging findings not explained by striatal vascular lesions

  • Abnormal cardiac sympathetic nerve terminal imaging findings

  • Normal striatal dopamine transporter imaging

Legend: CBS, corticobasal syndrome; CVD, cerebrovascular disease; DLB, dementia with Lewy bodies; FTD, frontotemporal dementia; MSA, multiple system atrophy; PD, Parkinson disease; PSP, progressive supranuclear palsy.