Table 1.
Supportive criteria |
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|
Absolute exclusion criteria: the presence of any of these features rules out PD |
Unequivocal cerebellar abnormalities, such as cerebellar gait, limb ataxia, or cerebellar oculomotor abnormalities (e.g., sustained gaze evoked nystagmus, macro square wave jerks, hypermetric saccades) |
Downward vertical supranuclear gaze palsy or selective slowing of downward vertical saccades |
Diagnosis of probable behavioral variant frontotemporal dementia or primary progressive aphasia, defined according to consensus criteria within the first 5 years of disease |
Parkinsonian features restricted to the lower limbs for more than 3 years |
Treatment with a dopamine receptor blocker or a dopamine-depleting agent in a dose/time-course consistent with drug-induced parkinsonism |
Absence of observable response to high-dose levodopa despite at least moderate severity of disease |
Unequivocal cortical sensory loss (graphesthesia, stereognosis with intact primary sensory modalities), clear limb ideomotor apraxia, or progressive aphasia |
Normal functional neuroimaging of the presynaptic dopaminergic system |
Documentation of an alternative condition known to produce parkinsonism and plausibly connected to the patient’s symptoms, or, the expert evaluating physician, based on the full diagnostic assessment feels that an alternative syndrome is more likely than PD |
Red flags |
Rapid progression of gait impairment requiring regular use of wheelchair within 5 years of onset |
A complete absence of progression of motor symptoms or signs over 5 or more years unless stability is related to treatment |
Early bulbar dysfunction: severe dysphonia or dysarthria (speech unintelligible most of the time) or severe dysphagia (requiring soft food, NG tube, or gastrostomy) within first 5 years |
Inspiratory respiratory dysfunction: either diurnal or nocturnal inspiratory stridor or frequent inspiratory sighs |
Severe autonomic failure in the first 5 years of disease. This can include:
|
Red flags |
Recurrent (>1/year) falls because of impaired balance within 3 years of onset |
Disproportionate anterocollis (dystonic) or contractures of hand or feet within the first 10 years |
Absence of any of the common non-motor features of disease despite 5 years disease duration. These include sleep dysfunction (sleep-maintenance insomnia, excessive daytime somnolence, symptoms of REM sleep behavior disorder), autonomic dysfunction (constipation, daytime urinary urgency, symptomatic orthostasis), hyposmia, or psychiatric dysfunction (depression, anxiety, or hallucinations) |
Otherwise-unexplained pyramidal tract signs, defined as pyramidal weakness or clear pathologic hyperreflexia (excluding mild reflex asymmetry and isolated extensor plantar response) |
Bilateral symmetric parkinsonism. The patient or caregiver reports bilateral symptom onset with no side predominance, and no side predominance is observed on objective examination |
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