Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines

Abstract Blood pressure lowering per se provides a large proportion of the benefit associated with antihypertensive treatment. Blood pressure should be reduced to <140/90 mmHg in the general hypertensive population, but lower targets should be presumed in individuals at high cardiovascular risk....
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Mancia, Giuseppe [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2008

Anmerkung:	© Adis Data Information BV 2008

Übergeordnetes Werk:	Enthalten in: High blood pressure & cardiovascular prevention - [S.l.] : Springer International, 2003, 15(2008), 2 vom: Apr., Seite 85-90
Übergeordnetes Werk:	volume:15 ; year:2008 ; number:2 ; month:04 ; pages:85-90

Links:	Volltext

DOI / URN:	10.2165/00151642-200815020-00007

Katalog-ID:	SPR036345946

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520			\|a Abstract Blood pressure lowering per se provides a large proportion of the benefit associated with antihypertensive treatment. Blood pressure should be reduced to <140/90 mmHg in the general hypertensive population, but lower targets should be presumed in individuals at high cardiovascular risk. In this context, calcium-channel antagonists (CCAs) remain important antihypertensive drugs because of: (i) their ability to effectively lower BP in monotherapy as well as to optimally combine with other drugs when multiple drug treatment is needed; (ii) evidence from clinical trials indicates that their administration is accompanied by a reduction in cardiovascular morbidity and mortality; and (iii) their specific prospective properties on some types of subclinical organ damage of special importance for hypertension-related morbidity or mortality, i.e. atherosclerosis. This is in line with the modern view of cardiovascular prevention as a strategy that should delay the progression to high cardiovascular risk, which, once reached, is partly irreversible.
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912			\|a GBV_ILN_32
912			\|a GBV_ILN_39
912			\|a GBV_ILN_40
912			\|a GBV_ILN_60
912			\|a GBV_ILN_62
912			\|a GBV_ILN_63
912			\|a GBV_ILN_65
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912			\|a GBV_ILN_95
912			\|a GBV_ILN_100
912			\|a GBV_ILN_101
912			\|a GBV_ILN_105
912			\|a GBV_ILN_110
912			\|a GBV_ILN_120
912			\|a GBV_ILN_138
912			\|a GBV_ILN_150
912			\|a GBV_ILN_151
912			\|a GBV_ILN_161
912			\|a GBV_ILN_170
912			\|a GBV_ILN_171
912			\|a GBV_ILN_187
912			\|a GBV_ILN_206
912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
912			\|a GBV_ILN_230
912			\|a GBV_ILN_250
912			\|a GBV_ILN_266
912			\|a GBV_ILN_281
912			\|a GBV_ILN_285
912			\|a GBV_ILN_293
912			\|a GBV_ILN_370
912			\|a GBV_ILN_602
912			\|a GBV_ILN_636
912			\|a GBV_ILN_702
912			\|a GBV_ILN_2001
912			\|a GBV_ILN_2003
912			\|a GBV_ILN_2004
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2006
912			\|a GBV_ILN_2007
912			\|a GBV_ILN_2008
912			\|a GBV_ILN_2009
912			\|a GBV_ILN_2010
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2014
912			\|a GBV_ILN_2015
912			\|a GBV_ILN_2020
912			\|a GBV_ILN_2021
912			\|a GBV_ILN_2025
912			\|a GBV_ILN_2026
912			\|a GBV_ILN_2027
912			\|a GBV_ILN_2031
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2037
912			\|a GBV_ILN_2038
912			\|a GBV_ILN_2039
912			\|a GBV_ILN_2044
912			\|a GBV_ILN_2048
912			\|a GBV_ILN_2049
912			\|a GBV_ILN_2050
912			\|a GBV_ILN_2055
912			\|a GBV_ILN_2057
912			\|a GBV_ILN_2059
912			\|a GBV_ILN_2061
912			\|a GBV_ILN_2064
912			\|a GBV_ILN_2065
912			\|a GBV_ILN_2068
912			\|a GBV_ILN_2088
912			\|a GBV_ILN_2093
912			\|a GBV_ILN_2106
912			\|a GBV_ILN_2107
912			\|a GBV_ILN_2108
912			\|a GBV_ILN_2110
912			\|a GBV_ILN_2111
912			\|a GBV_ILN_2112
912			\|a GBV_ILN_2113
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912			\|a GBV_ILN_2147
912			\|a GBV_ILN_2148
912			\|a GBV_ILN_2152
912			\|a GBV_ILN_2153
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912			\|a GBV_ILN_2336
912			\|a GBV_ILN_2446
912			\|a GBV_ILN_2470
912			\|a GBV_ILN_2472
912			\|a GBV_ILN_2507
912			\|a GBV_ILN_2522
912			\|a GBV_ILN_2548
912			\|a GBV_ILN_4035
912			\|a GBV_ILN_4037
912			\|a GBV_ILN_4046
912			\|a GBV_ILN_4112
912			\|a GBV_ILN_4125
912			\|a GBV_ILN_4242
912			\|a GBV_ILN_4246
912			\|a GBV_ILN_4249
912			\|a GBV_ILN_4251
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4306
912			\|a GBV_ILN_4307
912			\|a GBV_ILN_4313
912			\|a GBV_ILN_4322
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912			\|a GBV_ILN_4324
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912			\|a GBV_ILN_4326
912			\|a GBV_ILN_4333
912			\|a GBV_ILN_4334
912			\|a GBV_ILN_4335
912			\|a GBV_ILN_4336
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952			\|d 15 \|j 2008 \|e 2 \|c 04 \|h 85-90

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publishDate	2008
allfields	10.2165/00151642-200815020-00007 doi (DE-627)SPR036345946 (SPR)00151642-200815020-00007-e DE-627 ger DE-627 rakwb eng Mancia, Giuseppe verfasserin aut Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Adis Data Information BV 2008 Abstract Blood pressure lowering per se provides a large proportion of the benefit associated with antihypertensive treatment. Blood pressure should be reduced to <140/90 mmHg in the general hypertensive population, but lower targets should be presumed in individuals at high cardiovascular risk. In this context, calcium-channel antagonists (CCAs) remain important antihypertensive drugs because of: (i) their ability to effectively lower BP in monotherapy as well as to optimally combine with other drugs when multiple drug treatment is needed; (ii) evidence from clinical trials indicates that their administration is accompanied by a reduction in cardiovascular morbidity and mortality; and (iii) their specific prospective properties on some types of subclinical organ damage of special importance for hypertension-related morbidity or mortality, i.e. atherosclerosis. This is in line with the modern view of cardiovascular prevention as a strategy that should delay the progression to high cardiovascular risk, which, once reached, is partly irreversible. Enthalten in High blood pressure & cardiovascular prevention [S.l.] : Springer International, 2003 15(2008), 2 vom: Apr., Seite 85-90 (DE-627)490226264 (DE-600)2192466-1 1179-1985 nnns volume:15 year:2008 number:2 month:04 pages:85-90 https://dx.doi.org/10.2165/00151642-200815020-00007 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_65 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_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 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_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_2118 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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 15 2008 2 04 85-90
spelling	10.2165/00151642-200815020-00007 doi (DE-627)SPR036345946 (SPR)00151642-200815020-00007-e DE-627 ger DE-627 rakwb eng Mancia, Giuseppe verfasserin aut Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Adis Data Information BV 2008 Abstract Blood pressure lowering per se provides a large proportion of the benefit associated with antihypertensive treatment. Blood pressure should be reduced to <140/90 mmHg in the general hypertensive population, but lower targets should be presumed in individuals at high cardiovascular risk. In this context, calcium-channel antagonists (CCAs) remain important antihypertensive drugs because of: (i) their ability to effectively lower BP in monotherapy as well as to optimally combine with other drugs when multiple drug treatment is needed; (ii) evidence from clinical trials indicates that their administration is accompanied by a reduction in cardiovascular morbidity and mortality; and (iii) their specific prospective properties on some types of subclinical organ damage of special importance for hypertension-related morbidity or mortality, i.e. atherosclerosis. This is in line with the modern view of cardiovascular prevention as a strategy that should delay the progression to high cardiovascular risk, which, once reached, is partly irreversible. Enthalten in High blood pressure & cardiovascular prevention [S.l.] : Springer International, 2003 15(2008), 2 vom: Apr., Seite 85-90 (DE-627)490226264 (DE-600)2192466-1 1179-1985 nnns volume:15 year:2008 number:2 month:04 pages:85-90 https://dx.doi.org/10.2165/00151642-200815020-00007 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_65 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_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 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_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_2118 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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 15 2008 2 04 85-90
allfields_unstemmed	10.2165/00151642-200815020-00007 doi (DE-627)SPR036345946 (SPR)00151642-200815020-00007-e DE-627 ger DE-627 rakwb eng Mancia, Giuseppe verfasserin aut Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Adis Data Information BV 2008 Abstract Blood pressure lowering per se provides a large proportion of the benefit associated with antihypertensive treatment. Blood pressure should be reduced to <140/90 mmHg in the general hypertensive population, but lower targets should be presumed in individuals at high cardiovascular risk. In this context, calcium-channel antagonists (CCAs) remain important antihypertensive drugs because of: (i) their ability to effectively lower BP in monotherapy as well as to optimally combine with other drugs when multiple drug treatment is needed; (ii) evidence from clinical trials indicates that their administration is accompanied by a reduction in cardiovascular morbidity and mortality; and (iii) their specific prospective properties on some types of subclinical organ damage of special importance for hypertension-related morbidity or mortality, i.e. atherosclerosis. This is in line with the modern view of cardiovascular prevention as a strategy that should delay the progression to high cardiovascular risk, which, once reached, is partly irreversible. Enthalten in High blood pressure & cardiovascular prevention [S.l.] : Springer International, 2003 15(2008), 2 vom: Apr., Seite 85-90 (DE-627)490226264 (DE-600)2192466-1 1179-1985 nnns volume:15 year:2008 number:2 month:04 pages:85-90 https://dx.doi.org/10.2165/00151642-200815020-00007 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_65 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_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 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_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_2118 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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 15 2008 2 04 85-90
allfieldsGer	10.2165/00151642-200815020-00007 doi (DE-627)SPR036345946 (SPR)00151642-200815020-00007-e DE-627 ger DE-627 rakwb eng Mancia, Giuseppe verfasserin aut Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Adis Data Information BV 2008 Abstract Blood pressure lowering per se provides a large proportion of the benefit associated with antihypertensive treatment. Blood pressure should be reduced to <140/90 mmHg in the general hypertensive population, but lower targets should be presumed in individuals at high cardiovascular risk. In this context, calcium-channel antagonists (CCAs) remain important antihypertensive drugs because of: (i) their ability to effectively lower BP in monotherapy as well as to optimally combine with other drugs when multiple drug treatment is needed; (ii) evidence from clinical trials indicates that their administration is accompanied by a reduction in cardiovascular morbidity and mortality; and (iii) their specific prospective properties on some types of subclinical organ damage of special importance for hypertension-related morbidity or mortality, i.e. atherosclerosis. This is in line with the modern view of cardiovascular prevention as a strategy that should delay the progression to high cardiovascular risk, which, once reached, is partly irreversible. Enthalten in High blood pressure & cardiovascular prevention [S.l.] : Springer International, 2003 15(2008), 2 vom: Apr., Seite 85-90 (DE-627)490226264 (DE-600)2192466-1 1179-1985 nnns volume:15 year:2008 number:2 month:04 pages:85-90 https://dx.doi.org/10.2165/00151642-200815020-00007 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_65 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_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 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_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_2118 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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 15 2008 2 04 85-90
allfieldsSound	10.2165/00151642-200815020-00007 doi (DE-627)SPR036345946 (SPR)00151642-200815020-00007-e DE-627 ger DE-627 rakwb eng Mancia, Giuseppe verfasserin aut Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Adis Data Information BV 2008 Abstract Blood pressure lowering per se provides a large proportion of the benefit associated with antihypertensive treatment. Blood pressure should be reduced to <140/90 mmHg in the general hypertensive population, but lower targets should be presumed in individuals at high cardiovascular risk. In this context, calcium-channel antagonists (CCAs) remain important antihypertensive drugs because of: (i) their ability to effectively lower BP in monotherapy as well as to optimally combine with other drugs when multiple drug treatment is needed; (ii) evidence from clinical trials indicates that their administration is accompanied by a reduction in cardiovascular morbidity and mortality; and (iii) their specific prospective properties on some types of subclinical organ damage of special importance for hypertension-related morbidity or mortality, i.e. atherosclerosis. This is in line with the modern view of cardiovascular prevention as a strategy that should delay the progression to high cardiovascular risk, which, once reached, is partly irreversible. Enthalten in High blood pressure & cardiovascular prevention [S.l.] : Springer International, 2003 15(2008), 2 vom: Apr., Seite 85-90 (DE-627)490226264 (DE-600)2192466-1 1179-1985 nnns volume:15 year:2008 number:2 month:04 pages:85-90 https://dx.doi.org/10.2165/00151642-200815020-00007 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_65 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_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 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_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_2118 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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 15 2008 2 04 85-90
language	English
source	Enthalten in High blood pressure & cardiovascular prevention 15(2008), 2 vom: Apr., Seite 85-90 volume:15 year:2008 number:2 month:04 pages:85-90
sourceStr	Enthalten in High blood pressure & cardiovascular prevention 15(2008), 2 vom: Apr., Seite 85-90 volume:15 year:2008 number:2 month:04 pages:85-90
format_phy_str_mv	Article
institution	findex.gbv.de
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container_title	High blood pressure & cardiovascular prevention
authorswithroles_txt_mv	Mancia, Giuseppe @@aut@@
publishDateDaySort_date	2008-04-01T00:00:00Z
hierarchy_top_id	490226264
id	SPR036345946
language_de	englisch
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author	Mancia, Giuseppe
spellingShingle	Mancia, Giuseppe Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines
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title	Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines
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title_full	Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines
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title_sort	dihydropiridinic calcium-channel antagonists in the 2007 esh/esc hypertension guidelines
title_auth	Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines
abstract	Abstract Blood pressure lowering per se provides a large proportion of the benefit associated with antihypertensive treatment. Blood pressure should be reduced to <140/90 mmHg in the general hypertensive population, but lower targets should be presumed in individuals at high cardiovascular risk. In this context, calcium-channel antagonists (CCAs) remain important antihypertensive drugs because of: (i) their ability to effectively lower BP in monotherapy as well as to optimally combine with other drugs when multiple drug treatment is needed; (ii) evidence from clinical trials indicates that their administration is accompanied by a reduction in cardiovascular morbidity and mortality; and (iii) their specific prospective properties on some types of subclinical organ damage of special importance for hypertension-related morbidity or mortality, i.e. atherosclerosis. This is in line with the modern view of cardiovascular prevention as a strategy that should delay the progression to high cardiovascular risk, which, once reached, is partly irreversible. © Adis Data Information BV 2008
abstractGer	Abstract Blood pressure lowering per se provides a large proportion of the benefit associated with antihypertensive treatment. Blood pressure should be reduced to <140/90 mmHg in the general hypertensive population, but lower targets should be presumed in individuals at high cardiovascular risk. In this context, calcium-channel antagonists (CCAs) remain important antihypertensive drugs because of: (i) their ability to effectively lower BP in monotherapy as well as to optimally combine with other drugs when multiple drug treatment is needed; (ii) evidence from clinical trials indicates that their administration is accompanied by a reduction in cardiovascular morbidity and mortality; and (iii) their specific prospective properties on some types of subclinical organ damage of special importance for hypertension-related morbidity or mortality, i.e. atherosclerosis. This is in line with the modern view of cardiovascular prevention as a strategy that should delay the progression to high cardiovascular risk, which, once reached, is partly irreversible. © Adis Data Information BV 2008
abstract_unstemmed	Abstract Blood pressure lowering per se provides a large proportion of the benefit associated with antihypertensive treatment. Blood pressure should be reduced to <140/90 mmHg in the general hypertensive population, but lower targets should be presumed in individuals at high cardiovascular risk. In this context, calcium-channel antagonists (CCAs) remain important antihypertensive drugs because of: (i) their ability to effectively lower BP in monotherapy as well as to optimally combine with other drugs when multiple drug treatment is needed; (ii) evidence from clinical trials indicates that their administration is accompanied by a reduction in cardiovascular morbidity and mortality; and (iii) their specific prospective properties on some types of subclinical organ damage of special importance for hypertension-related morbidity or mortality, i.e. atherosclerosis. This is in line with the modern view of cardiovascular prevention as a strategy that should delay the progression to high cardiovascular risk, which, once reached, is partly irreversible. © Adis Data Information BV 2008
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title_short	Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines
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Dihydropiridinic Calcium-Channel Antagonists in the 2007 ESH/ESC Hypertension Guidelines

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