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MDS Clinical Diagnostic Criteria for Parkinson's Disease

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(1)MDS Clinical Diagnostic Criteria for Parkinson‘s Disease Part 2.

(2) Diagnostic Criteria For PD.

(3) Diagnosis of clinically “ESTABLISHED” PD. At least 2 supportive criteria. Absence of absolute exclusion criteria No red flags.

(4) Diagnosis of clinically “PROBABLE” PD. Numbers of supportive criteria = red flags (but no more than 2 red flags) Absence of absolute exclusion criteria.

(5) Supportive Criteria.

(6) 1..  Clear and dramatic beneficial response to dopaminergic therapy  Note  Initial treatment: patient retuned to normal or near-normal function.  Marked improvement with dose increases (>30% in UPDRS III 或 subjectively with a clear history)  Marked on/off fluctuations + predictable end-of-dose wearing off  Can be from retrospective history (不用再特地調整藥物讓病患fluctuations).

(7) 2..  Presence of levodopa-induced dyskinesia.

(8) 3..  Rest tremor of a limb  Note  Documented in the past, or on current examination  Included because ……  Less common in alternate conditions  Rest tremor occasionally less responsive to therapy  if so, criterion 1 may be harder to meet.

(9) 4..  At least one ancillary diagnostic test (specificity > 80%)  Note  Olfactory loss (anosmia by age and sex)  Metaiodobenzylguanidine scintigraphy  cardiac sympathetic denervation.

(10) Absolute Exclusion Criteria.

(11)  For all other criteria with a time component.  Waiting until the duration before the criterion is considered as not met is. necessary. not.

(12) 1..  Unequivocal cerebellar abnormalities on examination  Note  Cerebellar gait  Limb ataxia  Cerebellar oculomotor abnormalities (sustained gaze-evoked nystagmus, macro square wave jerks, hypermetric saccades).

(13) 2..  Downward vertical supranuclear gaze palsy  Selective slowing of downward vertical saccades.

(14) 3..  Diagnosis of probable behavioral variant frontotemporal dementia 或 primary progressive aphasia. within the first 5 y of disease.  Note  Other forms of dementia are not exclusion.

(15) 4..  Parkinsonian features restricted to lower limbs for more than 3 y.

(16) 5..  Dopamine receptor blocker/ dopamine-depleting agent (dose and time course) consistent with drug-induced parkinsonism.

(17) 6.  Absence of observable response to high-dose levodopa despite at least moderate severity of disease  Note  High dose of levodopa daily = 600 mg/d  Moderate severity parkinsonism = MDS-UPDRS score >2 (one measure of rigidity or bradykinesia)  Absence of response  Reported by patient (or reliable witness)  Sequential examinations = improvement ≦ 3 points on the MDS-UPDRS Part III.

(18) 7..  Unequivocal cortical sensory loss (ie, graphesthesia, stereognosis with intact primary sensory modalities), clear limb ideomotor apraxia, or progressive aphasia.

(19) 8..  Normal functional neuroimaging of the presynaptic dopaminergic system  Note. NOT imply that dopaminergic functional imaging is required for diagnosis.

(20) 9..  Documentation of an alternative condition known to produce parkinsonism and plausibly connected to the patient’s symptoms  Note  Dementia with Lewy Bodies is not considered an alternative parkinsonian syndrome.

(21) Red Flags.

(22) 1..  Rapid progression of gait impairment requiring regular use of wheelchair within 5 y of onset.

(23) 2..  Complete absence of progression of motor s/s over 5 or more years (unless stability is related to treatment)  Note  Targeted at patients who may have been misdiagnosed with parkinsonism.

(24) 3..  Early bulbar dysfunction (within the first 5 y of disease)  Severe dysphonia  Dysarthria  Severe dysphagia  Note  MDS-UPDRS: 4 for dysarthria, 3 for dysphagia.

(25) 4..  Inspiratory respiratory dysfunction  Diurnal or nocturnal inspiratory stridor  Frequent inspiratory sighs.

(26) 5.  Severe autonomic failure in the first 5y of disease  Orthostatic hypotension  Decrease of BP within 3 min of standing (at least 30 mm Hg SBP or 15 mm Hg DBP)  Absence of dehydration, medication, or other diseases.  Severe urinary incontinence/ retention  Excluding longstanding low-volume stress incontinence (in women).  Must be associated with erectile dysfunction; Not be caused by prostate disease (in men)  Not functional incontinence.  Note  To identify the severe autonomic dysfunction associated with MSA.

(27) 6..  Recurrent (>1/y) falls because of impaired balance within 3 y of. onset.  Note  Be attributable to impaired balance  暈厥,癲癇,正常人也會跌倒的活動不算.

(28) 7..  Disproportionate anterocollis (dystonic in nature) or contractures of hand or feet within the first 10 y.

(29) 8.  Absence of common nonmotor features of disease despite 5 y. disease duration  Sleep dysfunction.  Autonomic dysfunction  Hyposmia  Psychiatric dysfunction  Note  To detect non-parkinsonian conditions mimicking PD (dystonic tremor, essential tremor).

(30) 9..  Unexplained pyramidal tract signs  = pyramidal weakness 或 pathologic hyperreflexia.  Note  Mild reflex asymmetry is excluded (commonly be seen in PD)  Isolated extensor plantar response is excluded (difficulty in differentiating from a “striatal toe”).

(31) 10.. Bilateral symmetric parkinsonism  Bilateral symptom onset  No side predominance.

(32) Conclusion.

(33)  要臨床確診 = 至少兩個支持條件,不能有排除條件,不能亮紅旗  支持條件  藥物有明顯效果,或有明顯停電來電現象  藥物造成的異動  靜止性顫抖  嗅覺測試或MIBG有發現.

(34)  排除條件  中等嚴重症狀,但高劑量藥物無效  突觸前多巴胺功能性影像正常.  症狀局限於下肢超過三年  垂直眼球運動受限  小腦症狀  五年內出現額葉顳葉失智或漸進性失語症  皮質症狀 (皮質感覺缺損,失用,漸進失語)  藥物造成的的類巴金森症狀  有其他可能造成類巴金森症狀. +syndrome.

(35)  紅旗  進展太快,五年內很快坐輪椅  進展太慢,五年後動作症狀沒惡化.  一開始就是雙側性症狀  口咽五年內受影響  呼吸功能異常  無法解釋的錐體路徑症狀.  十年內太過度的頸項前屈,或肢體蜷曲  三年內平衡不好太常跌倒  五年內出現自主神經異常  五年後沒出現非運動症狀(睡眠,自主神經,嗅覺喪失,精神症狀).

(36)

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