scholarly journals The Experience of Caregiving: Differences Between Behavioral Variant of Frontotemporal Dementia and Alzheimer Disease

2012 ◽  
Vol 20 (8) ◽  
pp. 724-728 ◽  
Author(s):  
Cindy Wong ◽  
Jennifer Merrilees ◽  
Robin Ketelle ◽  
Cynthia Barton ◽  
Margaret Wallhagen ◽  
...  
2004 ◽  
Vol 25 ◽  
pp. S87
Author(s):  
Julene K. Johnson ◽  
Anne Lipton ◽  
Stephen Allison ◽  
Kristin Martin-Cook ◽  
Jennifer Merrilees ◽  
...  

2013 ◽  
Vol 27 (1) ◽  
pp. 68-73 ◽  
Author(s):  
Eneida Mioshi ◽  
David Foxe ◽  
Felicity Leslie ◽  
Sharon Savage ◽  
Sharpley Hsieh ◽  
...  

2020 ◽  
pp. 089198872094423
Author(s):  
Thaís Bento Lima-Silva ◽  
Eneida Mioshi ◽  
Valéria Santoro Bahia ◽  
Mário Amore Cecchini ◽  
Luciana Cassimiro ◽  
...  

Introduction: There is a shortage of validated instruments to estimate disease progression in frontotemporal dementia (FTD). Objectives: To evaluate the ability of the FTD Rating Scale (FTD-FRS) to detect functional and behavioral changes in patients diagnosed with the behavioral variant of FTD (bvFTD), primary progressive aphasia (PPA), and Alzheimer disease (AD) after 12 months of the initial evaluation, compared to the Clinical Dementia Rating scale−frontotemporal lobar degeneration (CDR-FTLD) and the original Clinical Dementia Rating scale (CDR). Methods: The sample consisted of 70 individuals, aged 40+ years, with at least 2 years of schooling, 31 with the diagnosis of bvFTD, 12 with PPA (8 with semantic variant and 4 with non-fluent variant), and 27 with AD. The FTD-FRS, the CDR, and the 2 additional CDR-FTLD items were completed by a clinician, based on the information provided by the caregiver with frequent contact with the patient. The Addenbrooke Cognitive Examination-Revised was completed by patients. After 12 months, the same protocol was applied. Results: The FTD-FRS, CDR-FTLD, and CDR detected significant decline after 12 months in the 3 clinical groups (exception: FTD-FRS for PPA). The CDR was less sensitive to severe disease stages. Conclusions: The FTD-FRS and the CDR-FTLD are especially useful tools for dementia staging in AD and in the FTD spectrum.


2004 ◽  
Vol 128 (1) ◽  
pp. 32-38 ◽  
Author(s):  
Catherina Fu ◽  
Dennis J. Chute ◽  
Emad S. Farag ◽  
Justine Garakian ◽  
Jeffrey L. Cummings ◽  
...  

Abstract Context.—There is a paucity of accurate postmortem data pertinent to comorbid medical conditions in patients with dementia, including Alzheimer disease. Objectives.—The purposes of this study were (a) to examine general autopsy findings in patients with a dementia syndrome and (b) to establish patterns of central nervous system comorbidity in these patients. Design.—Review of autopsy reports and selected case material from 202 demented patients who had “brain-only” autopsies during a 17-year period (1984–2000) and from 52 demented patients who had general autopsies during a 6-year period (1995–2000). Setting.—Large academic medical center performing approximately 200 autopsies per year. Results.—Among the 52 patients who underwent complete autopsy, the most common cause of death was bronchopneumonia, which was found in 24 cases (46.1%). Other respiratory problems included emphysema, found in 19 (36.5%) of 52 patients, and pulmonary thromboembolism, found in 9 (17.3%) of 52 patients. In 6 cases, pulmonary thromboembolism was the proximate cause of death. Twenty-one (40.3%) of the 52 patients had evidence of a myocardial infarct (varying ages) and 38 (73.1%) had atherosclerotic cardiovascular disease, 27 of a moderate to severe degree. Four clinically unsuspected malignancies were found: 1 each of glioblastoma multiforme, diffusely infiltrative central nervous system lymphoma, pancreatic adenocarcinoma, and adenocarcinoma of the lung. One patient with frontotemporal dementia and amyotrophic lateral sclerosis died of severe meningoencephalitis/ventriculitis, probably secondary to seeding of the central nervous system by an infected cardiac valve. Of the 202 demented patients who underwent brain-only autopsies, the following types of dementia were found: 129 (63.8%) cases showed changes of severe Alzheimer disease, 21 (10.4%) showed combined neuropathologic abnormalities (Alzheimer disease plus another type of lesion, such as significant ischemic infarcts or diffuse Lewy body disease), 12 (5.9%) cases of relatively pure ischemic vascular dementia, 13 (6.4%) cases of diffuse Lewy body disease, and 8 (4.0%) cases of frontotemporal dementia. The remaining 19 (9.4%) patients showed miscellaneous neuropathologic diagnoses, including normal pressure hydrocephalus and progressive supranuclear palsy. Among the demented patients, 92 (45.5%) had cerebral atherosclerosis, which was moderate to severe in 65 patients (32.2%). Conclusions.—Some of the conditions found at autopsy, had they been known antemortem, would likely have affected clinical management of the patients. Autopsy findings may be used as a quality-of-care measure in patients who have been hospitalized in chronic care facilities for a neurodegenerative disorder.


Author(s):  
Mark Hallett

Apraxia is the inability to perform skilled and/or learned movements, not explainable on the basis of more elemental abnormalities. There are several types of apraxia of which the most commonly recognized are (1) limb kinetic apraxia, the loss of hand and finger dexterity; (2) ideomotor apraxia, deficits in pantomiming tool use and gestures with temporal and spatial errors, but with knowledge of the tasks still present; (3) ideational apraxia, the failure to carry out a series of tasks using multiple objects for an intended purpose; and (4) conceptual apraxia, loss of tool knowledge, when tools and objects are used inappropriately. Apraxia can be a feature of both frontotemporal dementia and Alzheimer disease, and even a rare presenting manifestation of both. How sensitive apraxia measures would be in early detection is not well known.


Neurology ◽  
2006 ◽  
Vol 67 (7) ◽  
pp. 1215-1220 ◽  
Author(s):  
A. T. Du ◽  
G. H. Jahng ◽  
S. Hayasaka ◽  
J. H. Kramer ◽  
H. J. Rosen ◽  
...  

2010 ◽  
Vol 23 (3) ◽  
pp. 159-164 ◽  
Author(s):  
John M. Ringman ◽  
Eunice Kwon ◽  
Deborah L. Flores ◽  
Carol Rotko ◽  
Mario F. Mendez ◽  
...  

2011 ◽  
Vol 2 (2) ◽  
pp. a006254-a006254 ◽  
Author(s):  
M. Goedert ◽  
B. Ghetti ◽  
M. G. Spillantini

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