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パーキンソン病のすくみ足治療アルゴリズム

出典
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1: Freezing of gait: a practical approach to management.
Lancet Neurol. 2015 Jul;14(7):768-78. doi: 10.1016/S1474-4422(15)00041-1. Epub 2015 May 24.

さまざまな歩行障害とその特徴的な歩行

a:痙性片麻痺歩行(円描き歩行、ぶん回し歩行)
b:痙性対麻痺歩行(内反尖足、はさみ足歩行)
c:失調性歩行(酩酊性歩行)
d:脊髄後索性歩行(踵打ち歩行、竹馬徴候)
e:両側の垂れ足歩行(鶏歩)
f:動揺性歩行(waddling gait)
g:パーキンソン歩行(小きざみ・突進歩行)

進行期パーキンソン病の姿勢異常

パーキンソン病のすくみ足に対する薬剤の推奨度

各種抗パーキンソン病薬のすくみ足に対する効果
出典
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1: Medical treatment of freezing of gait.
著者: Nir Giladi
雑誌名: Mov Disord. 2008;23 Suppl 2:S482-8. doi: 10.1002/mds.21914.
Abstract/Text: Freezing of gait (FOG) is frequently considered as one of the dopamine-resistant motor symptoms of Parkinsonism. Recent studies have clearly demonstrated that the Off-related FOG is improved by levodopa (L-dopa) or entacapone treatment. L-dopa can decrease duration of each FOG episode as well as its frequency. On-related FOGs are not common and difficult to diagnose. Only in the most advanced stages of the disease, FOGs are resistant to treatment as many other symptoms. Off-related FOGs are likely to be improved by dopamine agonists (DAs), but this has never been looked at systematically. In contrast, DA treatment might provoke FOG, and in two pivotal studies when DAs were compared to L-dopa in early stages of Parkinson's disease, the DA-treated arms experienced more FOGs. MAO-B inhibitors (selegiline and rasagiline) can decrease FOG frequency or severity, but its clinical significance is still unknown. L-Threo-DOPS has been reported to have a symptomatic beneficial effect in patients with pure freezing syndrome, but small-scale, controlled trials in Parkinson's disease could not support those early observations. Botulinum toxin injected into the calf muscles has been suggested to have a symptomatic benefit. However, double-blind, prospective studies could not support that early observation and increased fall risk in the injected patients has put this direction of treatment on hold. The potential benefit of amantadine, antidepressive drugs, acetylcholine esterase inhibitors, and methylphenidate on FOG has been studied in small-scale studies, and there is a need for prospective studies to understand the future role of those drugs.

(c) 2008 Movement Disorder Society.
Mov Disord. 2008;23 Suppl 2:S482-8. doi: 10.1002/mds.21914.

Freezing of gait questionnaire; FOG-Q

すくみ足は診察室では目立たないことがあり、どのように検出するかが大切である。すくみ足検出のための質問用紙(Freezing of gait questionnaire; FOG-Q)が有用である。
出典
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1: Validation of the freezing of gait questionnaire in patients with Parkinson's disease.
著者: Nir Giladi, Joseph Tal, Tali Azulay, Oliver Rascol, David J Brooks, Eldad Melamed, Wolfgang Oertel, Werner H Poewe, Fabrizio Stocchi, Eduardo Tolosa
雑誌名: Mov Disord. 2009 Apr 15;24(5):655-61. doi: 10.1002/mds.21745.
Abstract/Text: To revalidate the Freezing of Gait Questionnaire (FOG-Q), patients with Parkinson's disease (PD) were randomly assigned to receive rasagiline (1 mg/day) (n = 150), entacapone (200 mg with each dose of levodopa) (n = 150), or placebo (n = 154). Patients were assessed at baseline and after 10 weeks using the FOG-Q, Unified Parkinson's Disease Rating Scale (UPDRS), Beck Depression Inventory (BDI), and Parkinson's Disease Questionnaire (PDQ-39). FOG-Q dimensionality, test-retest reliability, and internal reliability were examined. Convergent and divergent validities were assessed by correlating FOG-Q with UPDRS, BDI, and PDQ-39. Comparisons between FOG-Q item 3 and UPDRS item 14 were also made. Principal component analysis indicated that FOG-Q measures a single dimension. Test-retest reliability and internal reliability of FOG-Q score was high. FOG-Q was best correlated to items of the UPDRS relating to walking, general motor issues, and mobility. Correlations between baseline and endpoint suggested that FOG-Q item 3 is at least as reliable as UPDRS item 14. At baseline, 85.9% of patients were identified as "Freezers" using FOG-Q item 3 (> or =1) and 44.1% using UPDRS item 14 (> or =1) (P < 0.001). FOG-Q was a reliable tool for the assessment of treatment intervention. FOG-Q item 3 was effective as a screening question for the presence of FOG.
Mov Disord. 2009 Apr 15;24(5):655-61. doi: 10.1002/mds.21745.

歩行障害の病態別分類

神経系の障害部位による歩行障害の原因疾患
参考文献:
  1. Manek S, Lew MF. Gait and Balance Dysfunction in Adults. Curr Treat Options Neurol. 2003 Mar;5(2):177-185. PMID: 12628066.
  1. Jankovic J, Nutt JG, Sudarsky L. Classification, diagnosis, and etiology of gait disorders. Adv Neurol. 2001;87:119-33. PMID: 11347215.
出典
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1: 著者提供

すくみ足の治療アルゴリズム

パーキンソン病のすくみ足に対する対策についての有用な指針
出典
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1: 日本神経学会監修.パーキンソン病治療ガイドライン2018.医学書院,p188-191, 2018

転倒のパターン

転倒の仕方による疾患の鑑別
参考文献:
  1. Manek S, Lew MF. Gait and Balance Dysfunction in Adults. Curr Treat Options Neurol. 2003; 5(2): 177-185. PMID: 12628066.
  1. Nutt JG. Classification of gait and balance disorders. Adv Neurol. 2001; 87: 135-41. PMID: 11347216.
出典
img
1: 著者提供

パーキンソン病のすくみ足治療アルゴリズム

出典
imgimg
1: Freezing of gait: a practical approach to management.
Lancet Neurol. 2015 Jul;14(7):768-78. doi: 10.1016/S1474-4422(15)00041-1. Epub 2015 May 24.

さまざまな歩行障害とその特徴的な歩行

a:痙性片麻痺歩行(円描き歩行、ぶん回し歩行)
b:痙性対麻痺歩行(内反尖足、はさみ足歩行)
c:失調性歩行(酩酊性歩行)
d:脊髄後索性歩行(踵打ち歩行、竹馬徴候)
e:両側の垂れ足歩行(鶏歩)
f:動揺性歩行(waddling gait)
g:パーキンソン歩行(小きざみ・突進歩行)