The Metabolic Syndrome is characterized by the variable combination of visceral obesity and alterations in glucose metabolism, lipid metabolism, and BP. It has a high prevalence in the middle age and elderly population. Subjects with the Metabolic Syndrome also have a higher prevalence of microalbuminuria.
The Metabolic Syndrome is characterized by the variable combination of visceral obesity and alterations in glucose metabolism, lipid metabolism, and BP. It has a high prevalence in the middle age and elderly population. Subjects with the Metabolic Syndrome also have a higher prevalence of microalbuminuria.
The Metabolic Syndrome is characterized by the variable combination of visceral obesity and alterations in glucose metabolism, lipid metabolism, and BP. It has a high prevalence in the middle age and elderly population. Subjects with the Metabolic Syndrome also have a higher prevalence of microalbuminuria.
4. Perguruan Tinggi Strata I : Fak.Kedokteran UNDIP , lulus 1982 Strata II : Program Pendidikan Dokter Spesialis I Jantung dan Pembuluh Darah FK UNAIR , lulus 1995
5. 1983 - 1990 Kepala Puskesmas Kec. Mojolaban Kab. Sukoharjo Jateng 6. 1990 - 1995 PPDS I Jantung di FK UNAIR / RSUD Dr. Soetomo Surabaya 7. 1996 - Sekarang SMF / Lab. Kardiologi RSUD Dr.Moewardi / FK UNS 8. 1998 - 2006 Wakil Kepala Instalasi Perawatan Intensive RSUD Dr. Moewardi Surakarta 9. 2004 - Sekarang Ketua Panitia Kredensial Komite Medik RSUD Dr. Moewardi Surakarta 10. 2006 - Sekarang Ketua PERKI Cabang Surakarta THE ROLE OF ANTIHYPERTENSIVE AGENT IN HYPERTENSION PATIENTS WITH METABOLIC SYNDROME Dr.TRISULO WASYANTO,Sp JP (K),FIHA DEPT OF CARDIOLOGY & VASCULAR MEDICINE UNIV OF SEBELAS MARET / Dr MOEWARDI HOSPITAL S U R A K A R T A The Metabolic Syndrome The metabolic syndrome is characterized by the variable combination of visceral obesity and alterations in glucose metabolism, lipid metabolism, and BP. It has a high prevalence in the middle age and elderly population. Subjects with the metabolic syndrome also have a higher prevalence of microalbuminuria, LVH and arterial stiffness than those without metabolic syndrome. Their CV risk is high and the chance of developing diabetes markedly increased. Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension. Eur Heart J 2007;28:1462-1536 Vascular Damage The presence of the Metabolic Syndrome is associated with increased CAD and Total mortality Definition and Classification of Hypertension : JNC VII Hypertension is defined as blood pressure 140/90 mmHg Category Systolic (mmHg) Diastolic (mmHg) Normal <120 and <80 Prehypertension 120-139 or 80-89 Stage 1 hypertension 140-159 or 90-99 Stage 2 hypertension 160 or 100 JNC VII. J AMA 2003;289:2560-2572 JNC VII : Management of Hypertension by JNC VII : Management of Hypertension by Blood Pressure Classification Blood Pressure Classification ACE-I = angiotensin-converting enzyme inhibitor; ARB = angiotensin-receptor blocker; BB = beta blocker; CCB = calcium channel blocker. Chobanian Chobanian AV et al. AV et al. J AMA. J AMA. 2003;289:2560 2003;289:2560- -2572. 2572. Drug(s) for the compelling indications; other antihypertensive drugs (diuretics, ACE-I, ARB, BB, CCB) as needed Drug(s) for the compelling indications; other antihypertensive drugs (diuretics, ACE-I, ARB, BB, CCB) as needed BP Classification Lifestyle Modification Initial Drug Therapy Without Compelling Indication With Compelling Indication Normal <120/80 mm Hg Prehypertension 120-139/80-89 mm Hg Stage 1 hypertension 140-159/90-99 mm Hg Stage 2 hypertension 160/100 mm Hg Encourage Yes Yes Yes No drug indicated Drug(s) for the compelling indications Thiazide-type diuretics for most; may consider ACE-I, ARB, BB, CCB, or combination 2-drug combination for most (usually thiazide-type diuretic and ACE-I, ARB, BB, or CCB) Hypertension treatment strategy : JNC VII Lifestyle modifications Not at goal blood pressure (<140/90 mmHg) (<130/80 mmHg for patients with diabetes or chronic kidney disease) Initial drug choices Without compelling indications With compelling indications Stage 1 hypertension (SBP 140-159 or DBP 90-99 mmHg) Thiazide-type diuretics for most. May consider ACE-I, ARB, BB, CCB or combination Stage 2 hypertension (SBP 160 or DBP 100 mmHg) Two-drug combination for most (usually thiazide-type diuretic and ACE-I or ARB, or BB, or CCB) Drug(s) for the compelling indications
Other antihypertensive Drugs (diuretics, ACE- I, ARB, BB, CCB) as needed Not at blood pressure goal Optimize dosages or add additional drugs until goal blood pressure is achieved. Consider consultation with hypertension specialist. JNC VII. J AMA 2003;289:2560-2572 SBP, systolic blood pressure; DBP, diastolic blood pressure; ACE-I, angiotensin-converting enzyme inhibitor; ARB, angiotensin II receptor blocker; BB, beta-blocker; CCB, calcium-channel blocker JNC VII & ESH/ESC 2003: Treatment Considerations Most patients with hypertension will require 2 or more antihypertensive drugs to achieve BP goals According to baseline BP and presence or absence of complications, therapy can be initiated either with a low dose of a single agent or with a low-dose combination of 2 agents When BP is >20/10 mm Hg above goal, consideration should be given to initiating 2 drugs, either as separate prescriptions or in fixed-dose combinations, one of which should be a thiazide- type diuretic
Chobanian AV et al. J AMA. 2003;289:2560-2572. Guidelines Committee. J Hypertens. 2003;21:1011-1053. Definitions and Classifications of Blood Pressure : ESH/ESC 2007 Category Systolic Diastolic Optimal < 120 and < 80 Normal 120-129 and/or 80-84 High normal 130-139 and/or 85-89 Grade 1 hypertension 140-159 and/or 90-99 Grade 2 hypertension 160-179 and/or 100-109 Grade 3 hypertension 180 and/or 110 Isolated systolic hypertension and < 90 140 Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension. Eur Heart J 2007;28:1462-1536 Initiation of Antihypertensive treatment : ESC 2OO7 Other risk factors, OD, or disease Normal SBP 120-129 or DBP 80-84 High normal SBP 130-139 or DBP 85-89 Grade 1 HT SBP 140-159 or DBP 90-99 Grade 2 HT SBP 160-179 or DBP 100-109 Grade 3 HT SBP 180 or DBP 110 No other risk factors No BP intervention No BP intervention Lifestyle changes for several months then drug treatment if BP uncontrolled Lifestyle changes for several weeks then drug treatment if BP uncontrolled Lifestyle changes + immediate drug treatment 1-2 risk factors Lifestyle changes Lifestyle changes
Lifestyle changes for several weeks then drug treatment if BP uncontrolled Lifestyle changes for several weeks then drug treatment if BP uncontrolled Lifestyle changes + immediate drug treatment 3 risk factors, MS or OD Lifestyle changes Lifestyle changes and consider drug treatment Lifestyle changes + drug treatment Lifestyle changes + drug treatment
Lifestyle changes + immediate drug treatment Diabetes Lifestyle changes Lifestyle changes + drug treatment Lifestyle changes + drug treatment Lifestyle changes + drug treatment Lifestyle changes + immediate drug treatment Established CV or renal disease Lifestyle changes + immediate drug treatment Lifestyle changes + immediate drug treatment Lifestyle changes + immediate drug treatment Lifestyle changes + immediate drug treatment Lifestyle changes + immediate drug treatment Conditions favouring the use of some Antihypertensive drugs versus other SUBCLINICAL ORGAN DAMAGE LVH ACEI, CA, ARB Asymptomatic atherosclerosis CA, ACEI Microalbuminuria ACEI, ARB Renal Dysfunction ACEI, ARB CLINICAL EVENT Previous stroke Any BP lowering agent Previous MI BB, ACEI, ARB Angina pectoris BB, CA Heart failure Diuretics, BB, ACEI, ARB, Anti - aldosterone agents Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension. Eur Heart J 2007;28:1462-1536 Continued.. Atrial fibrillation Recurrent ARB, ACEI Permanent BB, non - dihydropiridine CA Tachyarrhytmias BB ESRD / proteinuria ACEI, ARB, loop diuretics Peripheral artery disease CA LV dysfunction ACEI Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension. Eur Heart J 2007;28:1462-1536 Continued.. CONDITION ISH (elderly) Diuretics, CA Metabolic syndrome ACEI, ARB, CA Diabetes mellitus ACEI, ARB Pregnancy CA, methyldopa, BB Black people Diuretics, CA Glaucoma ACEI induced cough BB ARB Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension. Eur Heart J 2007;28:1462-1536 Contra-indications to use certain Antihypertensive drugs Compelling contra- indications Possible contra- indications Thiazide diuretics Gout -Metabolic syndrome -Glucose intolerance -Pregnancy Beta-blockers Asthma
A-V block (grade 2 or 3) -Peripheral artery disease -Metabolic syndrome -Athletes and physically active patients -Chronic obstructive pulmonary disease Calcium antagonists (dihydropiridine) -Tachyarrhytmias -Heart failure Calcium antagonists (verapamil, diltiazem) A-V block (grade 2 or 3) Heart failure Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension. Eur Heart J 2007;28:1462-1536 Continued.. Compelling contra- indications
Possible contra- indications ACE-inhibitors Pregnancy Angioneurotic edema Hyperkalaemia Bilateral renal artery stenosis Angiotensin receptor blockers Pregnancy Hyperkalaemia Bilateral renal artery stenosis Diuretics (antialdosterone) Renal failure hyperkalaemia Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension. Eur Heart J 2007;28:1462-1536 Diuretics ARBs CCBs ACE-Inhibitors -Blockers -Blockers European Society of Hypertension 2007 Possible Combination of Different Classes of Anti Hypertension Drugs Preferred combinations Proven bene- ficial in trials
Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension Mild BP elevation Low/Moderate CV risk Conventional BP Target Marked BP elevation High/very high CV Risk Lower BP target Choose between Single Agent at low Dose Two Drugs Combination at low Dose Previous Agent at Full Dose Two Three drug combination at full dose Switch to different agent at low dose Two-to Three drug Combination at full dose Full Dose Monotherapy Monotherapy versus combination therapy strategies Previous combination at full dose Add a Third drug at low dose If Goal BP Not Achieved If Goal BP Not Achieved Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension Comparison of tight BP vs tight Glucose control in UKPDS 5 -50 -40 -30 -20 -10 0 Tight glucose control Tight BP control Microvascular endpoints * Stroke Any diabetes- related endpoint Diabetes-related deaths * * * * p<0.02, tight BP control (achieved BP 144/82 mmHg) vs less tight control (achieved BP 154/87 mmHg).
p<0.03, intensive glucose control (achieved HbA
1c 7.0%) vs less intensive control (achieved HbA 1c 7.9%). R i s k
r e d u c t i o n
( % )
UKPDS 38. BMJ 1998;317:703-713; UKPDS 33. Lancet 1998;352:837-853 BP, blood pressure; UKPDS, United Kingdom Prospective Diabetes Study 44 12 24 10 32 32 37 Gaede P, et al. N Engl J Med 2003;348:383-393 Steno-2: Patients who reached intensive- treatment goals at a mean of 7.8 years HbA 1c <6.5% P a t i e n t s
( % )
20 30 40 50 60 70 10 80 Cholesterol <175 mg/dL Triglycerides <150 mg/dL Systolic BP <130 mmHg Diastolic BP <80 mmHg p=0.06 p<0.001 p=0.19 p=0.001 p=0.21 Intensive therapy Conventional therapy 0 Good BP control reduces risk of cardiovascular events BP, blood pressure Steno-2: Composite CV endpoints P r i m a r y
c o m p o s i t e
e n d p o i n t *
( % )
0 0 36 12 96 60 48 84 72 24 60 30 40 20 10 50 Intensive therapy BP 132/73 mmHg Conventional therapy BP 146/78 mmHg Months of follow-up p=0.007 Hazard ratio=0.47 (95% CI, 0.24 to 0.73; p=0.008) Gaede P, et al. N Engl J Med 2003;348:383-393 * Primary composite endpoint = composite of death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, revascularization and amputation Treatment of Hypertension in MS Some anti-hypertensives (diuretics, beta- blockers) worsen glycemic control and may not be suitable for long-term use in MS Drugs of choice in MS may be ACE-inhibitors, and possibly ARBs ACE-inhibitors (and ARBs) are free of potentially diabetogenic side-effects and seem to have pleiotropic antidiabetic properties Use of ACE-inhibitors with beta-blockers and/or diuretics may cancel out the diabetogenic effects of the latter Adapted from www.biophoenic.com In patients with metabolic syndrome diagnostic procedures should include a more in-depth assessment of subclinical organ damage. In all individuals with metabolic syndrome intense lifestyle measures should be adopted. When there is hypertension drug treatment should start with a drug unlikely to facilitate onset to diabetes. Therefore a blocker of the renin- angiotensin system should be used and followed, if needed, by the addition of a calcium antagonists or a low-doze thiazide diuretics. It appears desirable to bring BP to the normal range. CONCLUTIONS (1) Lack of evidence from specific clinical trials prevents firm recommendations on use of antihypertensive drugs in all metabolic syndrome subjects with a high normal BP. There is some evidence that blocking the renin- angiotensin system may also delay incident hypertension. CONCLUTIONS ( 2 )