Memantine in moderate to severe Alzheimer’s disease: an observational post-marketing study
Abstract Memantine is an N-methyl-d-aspartate (NMDA) receptor antagonist, approved for the treatment of moderate to severe Alzheimer’s disease (AD). We conducted a 4-month observational, post-marketing, Austrian study of memantine in 377 outpatients with moderate to severe AD. In this ‘real-life’ se...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Rainer, Michael [verfasserIn] Wuschitz, A. [verfasserIn] Jagsch, C. [verfasserIn] Erb, C. [verfasserIn] Chirikdjian, J.-J. [verfasserIn] Mucke, H. A. M. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2011 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Journal of neural transmission - Wien [u.a.] : Springer, 1950, 118(2011), 8 vom: 02. Apr. |
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| Übergeordnetes Werk: |
volume:118 ; year:2011 ; number:8 ; day:02 ; month:04 |
| Links: |
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| DOI / URN: |
10.1007/s00702-011-0623-8 |
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| Katalog-ID: |
SPR007677804 |
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| 520 | |a Abstract Memantine is an N-methyl-d-aspartate (NMDA) receptor antagonist, approved for the treatment of moderate to severe Alzheimer’s disease (AD). We conducted a 4-month observational, post-marketing, Austrian study of memantine in 377 outpatients with moderate to severe AD. In this ‘real-life’ setting, memantine was well-tolerated, and produced benefits in cognition (Mini-Mental State Examination), activities of daily living (Activities of Daily Living score), and global function (Clinical Global Impression scale). Treatment effects were apparent in both pre-treated and treatment-naïve patient subgroups. | ||
| 650 | 4 | |a Alzheimer’s disease |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Dementia |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Memantine |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Activities of daily living |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Post-marketing |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a ‘Real-life’ setting |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Wuschitz, A. |e verfasserin |4 aut | |
| 700 | 1 | |a Jagsch, C. |e verfasserin |4 aut | |
| 700 | 1 | |a Erb, C. |e verfasserin |4 aut | |
| 700 | 1 | |a Chirikdjian, J.-J. |e verfasserin |4 aut | |
| 700 | 1 | |a Mucke, H. A. M. |e verfasserin |4 aut | |
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10.1007/s00702-011-0623-8 doi (DE-627)SPR007677804 (SPR)s00702-011-0623-8-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Rainer, Michael verfasserin aut Memantine in moderate to severe Alzheimer’s disease: an observational post-marketing study 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Memantine is an N-methyl-d-aspartate (NMDA) receptor antagonist, approved for the treatment of moderate to severe Alzheimer’s disease (AD). We conducted a 4-month observational, post-marketing, Austrian study of memantine in 377 outpatients with moderate to severe AD. In this ‘real-life’ setting, memantine was well-tolerated, and produced benefits in cognition (Mini-Mental State Examination), activities of daily living (Activities of Daily Living score), and global function (Clinical Global Impression scale). Treatment effects were apparent in both pre-treated and treatment-naïve patient subgroups. Alzheimer’s disease (dpeaa)DE-He213 Dementia (dpeaa)DE-He213 Memantine (dpeaa)DE-He213 Activities of daily living (dpeaa)DE-He213 Post-marketing (dpeaa)DE-He213 ‘Real-life’ setting (dpeaa)DE-He213 Wuschitz, A. verfasserin aut Jagsch, C. verfasserin aut Erb, C. verfasserin aut Chirikdjian, J.-J. verfasserin aut Mucke, H. A. M. verfasserin aut Enthalten in Journal of neural transmission Wien [u.a.] : Springer, 1950 118(2011), 8 vom: 02. Apr. (DE-627)300185901 (DE-600)1481655-6 1435-1463 nnns volume:118 year:2011 number:8 day:02 month:04 https://dx.doi.org/10.1007/s00702-011-0623-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 118 2011 8 02 04 |
| spelling |
10.1007/s00702-011-0623-8 doi (DE-627)SPR007677804 (SPR)s00702-011-0623-8-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Rainer, Michael verfasserin aut Memantine in moderate to severe Alzheimer’s disease: an observational post-marketing study 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Memantine is an N-methyl-d-aspartate (NMDA) receptor antagonist, approved for the treatment of moderate to severe Alzheimer’s disease (AD). We conducted a 4-month observational, post-marketing, Austrian study of memantine in 377 outpatients with moderate to severe AD. In this ‘real-life’ setting, memantine was well-tolerated, and produced benefits in cognition (Mini-Mental State Examination), activities of daily living (Activities of Daily Living score), and global function (Clinical Global Impression scale). Treatment effects were apparent in both pre-treated and treatment-naïve patient subgroups. Alzheimer’s disease (dpeaa)DE-He213 Dementia (dpeaa)DE-He213 Memantine (dpeaa)DE-He213 Activities of daily living (dpeaa)DE-He213 Post-marketing (dpeaa)DE-He213 ‘Real-life’ setting (dpeaa)DE-He213 Wuschitz, A. verfasserin aut Jagsch, C. verfasserin aut Erb, C. verfasserin aut Chirikdjian, J.-J. verfasserin aut Mucke, H. A. M. verfasserin aut Enthalten in Journal of neural transmission Wien [u.a.] : Springer, 1950 118(2011), 8 vom: 02. Apr. (DE-627)300185901 (DE-600)1481655-6 1435-1463 nnns volume:118 year:2011 number:8 day:02 month:04 https://dx.doi.org/10.1007/s00702-011-0623-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 118 2011 8 02 04 |
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10.1007/s00702-011-0623-8 doi (DE-627)SPR007677804 (SPR)s00702-011-0623-8-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Rainer, Michael verfasserin aut Memantine in moderate to severe Alzheimer’s disease: an observational post-marketing study 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Memantine is an N-methyl-d-aspartate (NMDA) receptor antagonist, approved for the treatment of moderate to severe Alzheimer’s disease (AD). We conducted a 4-month observational, post-marketing, Austrian study of memantine in 377 outpatients with moderate to severe AD. In this ‘real-life’ setting, memantine was well-tolerated, and produced benefits in cognition (Mini-Mental State Examination), activities of daily living (Activities of Daily Living score), and global function (Clinical Global Impression scale). Treatment effects were apparent in both pre-treated and treatment-naïve patient subgroups. Alzheimer’s disease (dpeaa)DE-He213 Dementia (dpeaa)DE-He213 Memantine (dpeaa)DE-He213 Activities of daily living (dpeaa)DE-He213 Post-marketing (dpeaa)DE-He213 ‘Real-life’ setting (dpeaa)DE-He213 Wuschitz, A. verfasserin aut Jagsch, C. verfasserin aut Erb, C. verfasserin aut Chirikdjian, J.-J. verfasserin aut Mucke, H. A. M. verfasserin aut Enthalten in Journal of neural transmission Wien [u.a.] : Springer, 1950 118(2011), 8 vom: 02. Apr. (DE-627)300185901 (DE-600)1481655-6 1435-1463 nnns volume:118 year:2011 number:8 day:02 month:04 https://dx.doi.org/10.1007/s00702-011-0623-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 118 2011 8 02 04 |
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10.1007/s00702-011-0623-8 doi (DE-627)SPR007677804 (SPR)s00702-011-0623-8-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Rainer, Michael verfasserin aut Memantine in moderate to severe Alzheimer’s disease: an observational post-marketing study 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Memantine is an N-methyl-d-aspartate (NMDA) receptor antagonist, approved for the treatment of moderate to severe Alzheimer’s disease (AD). We conducted a 4-month observational, post-marketing, Austrian study of memantine in 377 outpatients with moderate to severe AD. In this ‘real-life’ setting, memantine was well-tolerated, and produced benefits in cognition (Mini-Mental State Examination), activities of daily living (Activities of Daily Living score), and global function (Clinical Global Impression scale). Treatment effects were apparent in both pre-treated and treatment-naïve patient subgroups. Alzheimer’s disease (dpeaa)DE-He213 Dementia (dpeaa)DE-He213 Memantine (dpeaa)DE-He213 Activities of daily living (dpeaa)DE-He213 Post-marketing (dpeaa)DE-He213 ‘Real-life’ setting (dpeaa)DE-He213 Wuschitz, A. verfasserin aut Jagsch, C. verfasserin aut Erb, C. verfasserin aut Chirikdjian, J.-J. verfasserin aut Mucke, H. A. M. verfasserin aut Enthalten in Journal of neural transmission Wien [u.a.] : Springer, 1950 118(2011), 8 vom: 02. Apr. (DE-627)300185901 (DE-600)1481655-6 1435-1463 nnns volume:118 year:2011 number:8 day:02 month:04 https://dx.doi.org/10.1007/s00702-011-0623-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 118 2011 8 02 04 |
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Enthalten in Journal of neural transmission 118(2011), 8 vom: 02. Apr. volume:118 year:2011 number:8 day:02 month:04 |
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Alzheimer’s disease Dementia Memantine Activities of daily living Post-marketing ‘Real-life’ setting |
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Journal of neural transmission |
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Rainer, Michael @@aut@@ Wuschitz, A. @@aut@@ Jagsch, C. @@aut@@ Erb, C. @@aut@@ Chirikdjian, J.-J. @@aut@@ Mucke, H. A. M. @@aut@@ |
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Rainer, Michael |
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Rainer, Michael ddc 610 bkl 44.90 misc Alzheimer’s disease misc Dementia misc Memantine misc Activities of daily living misc Post-marketing misc ‘Real-life’ setting Memantine in moderate to severe Alzheimer’s disease: an observational post-marketing study |
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610 ASE 44.90 bkl Memantine in moderate to severe Alzheimer’s disease: an observational post-marketing study Alzheimer’s disease (dpeaa)DE-He213 Dementia (dpeaa)DE-He213 Memantine (dpeaa)DE-He213 Activities of daily living (dpeaa)DE-He213 Post-marketing (dpeaa)DE-He213 ‘Real-life’ setting (dpeaa)DE-He213 |
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ddc 610 bkl 44.90 misc Alzheimer’s disease misc Dementia misc Memantine misc Activities of daily living misc Post-marketing misc ‘Real-life’ setting |
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ddc 610 bkl 44.90 misc Alzheimer’s disease misc Dementia misc Memantine misc Activities of daily living misc Post-marketing misc ‘Real-life’ setting |
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ddc 610 bkl 44.90 misc Alzheimer’s disease misc Dementia misc Memantine misc Activities of daily living misc Post-marketing misc ‘Real-life’ setting |
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Memantine in moderate to severe Alzheimer’s disease: an observational post-marketing study |
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Rainer, Michael Wuschitz, A. Jagsch, C. Erb, C. Chirikdjian, J.-J. Mucke, H. A. M. |
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memantine in moderate to severe alzheimer’s disease: an observational post-marketing study |
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Memantine in moderate to severe Alzheimer’s disease: an observational post-marketing study |
| abstract |
Abstract Memantine is an N-methyl-d-aspartate (NMDA) receptor antagonist, approved for the treatment of moderate to severe Alzheimer’s disease (AD). We conducted a 4-month observational, post-marketing, Austrian study of memantine in 377 outpatients with moderate to severe AD. In this ‘real-life’ setting, memantine was well-tolerated, and produced benefits in cognition (Mini-Mental State Examination), activities of daily living (Activities of Daily Living score), and global function (Clinical Global Impression scale). Treatment effects were apparent in both pre-treated and treatment-naïve patient subgroups. |
| abstractGer |
Abstract Memantine is an N-methyl-d-aspartate (NMDA) receptor antagonist, approved for the treatment of moderate to severe Alzheimer’s disease (AD). We conducted a 4-month observational, post-marketing, Austrian study of memantine in 377 outpatients with moderate to severe AD. In this ‘real-life’ setting, memantine was well-tolerated, and produced benefits in cognition (Mini-Mental State Examination), activities of daily living (Activities of Daily Living score), and global function (Clinical Global Impression scale). Treatment effects were apparent in both pre-treated and treatment-naïve patient subgroups. |
| abstract_unstemmed |
Abstract Memantine is an N-methyl-d-aspartate (NMDA) receptor antagonist, approved for the treatment of moderate to severe Alzheimer’s disease (AD). We conducted a 4-month observational, post-marketing, Austrian study of memantine in 377 outpatients with moderate to severe AD. In this ‘real-life’ setting, memantine was well-tolerated, and produced benefits in cognition (Mini-Mental State Examination), activities of daily living (Activities of Daily Living score), and global function (Clinical Global Impression scale). Treatment effects were apparent in both pre-treated and treatment-naïve patient subgroups. |
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Memantine in moderate to severe Alzheimer’s disease: an observational post-marketing study |
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https://dx.doi.org/10.1007/s00702-011-0623-8 |
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Wuschitz, A. Jagsch, C. Erb, C. Chirikdjian, J.-J. Mucke, H. A. M. |
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Wuschitz, A. Jagsch, C. Erb, C. Chirikdjian, J.-J. Mucke, H. A. M. |
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| doi_str |
10.1007/s00702-011-0623-8 |
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2024-07-03T14:29:28.342Z |
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| score |
7.399626 |