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DAFTAR RIWAYAT HIDUP 1. Nama : Dr .H.Trisulo Wasyanto, Sp JP (K), FIHA 2. Tempat & tanggal lahir : Poso , 8    2 - 1956 3. Pangkat / Golongan : Pembina Utama Muda / IV C 4. Per gur uan Ti ngg i 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 Kep ala Puskesmas Kec. Moj olaban Kab. Sukoharjo   Jateng 6. 1990 - 1995 PPDS I Jan tung di FK UNAIR / RSUD Dr . Soetomo Surabaya 7. 1996 - Sek arang SMF / Lab. Kardiolog i RSUD Dr .Moewardi / FK UNS 8. 1998 - 2006 Waki l Kepala Ins tala si Per awatan Intens ive RSUD Dr . Moewardi Surakarta 9. 2004 - Sekarang Ketua Panitia Kredensial Komite Medik RSUD Dr . Moewardi Suraka rta 10. 2006 - Sekarang Ketua PERKI Cabang Surakarta

Dr. Trisulo, HT Dan Metabolik Sindrome

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    DAFTAR RIWAYAT HIDUP

    1. Nama : Dr.H.Trisulo Wasyanto, Sp JP (K), FIHA

    2. Tempat & tanggal lahir : Poso , 8

    2 - 1956

    3. Pangkat / Golongan : Pembina Utama Muda / IV C

    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. SukoharjoJateng

    6. 1990 - 1995 PPDS I Jantung di FK UNAIR / RSUD Dr. Soetomo Surabaya

    7. 1996 - Sekarang SMF / Lab. Kardiologi RSUD Dr.Moewardi / FK UNS8. 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

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    THE ROLE OF ANTIHYPERTENSIVE AGENTIN HYPERTENSION PATIENTS WITH METABOLIC SYNDROM

    Dr.TRISULO WASYANTO,Sp JP (K),FIHADEPT OF CARDIOLOGY & VASCULAR MEDICINE

    UNIV OF SEBELAS MARET / Dr MOEWARDI HOSPITAL

    S U R A K A R T A

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    The Metabolic Syndrome The metabolic syndrome is characterized by

    the variable combination of visceral obesity

    and alterations inglucose 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 highandthe 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

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    Vascular amage

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    The presence of the Metabolic Syndrome is associated

    with increased CAD and Total mortality

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    Definition and Classification of

    Hypertension : JNC VII

    Hypertension is defined as blood pressure 140/90 mmHg

    Category Systolic

    (mmHg)

    Diastolic

    (mmHg)

    Normal

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    JNC VII : Management of Hypertension byJNC VII : Management of Hypertension byBlood Pressure ClassificationBlood Pressure Classification

    ACE-I = angiotensin-converting enzyme inhibitor; ARB = angiotensin-receptor blocker; BB = beta blocker;

    CCB = calcium channel blocker.ChobanianChobanian AV et al.AV et al. JAMA.JAMA. 2003;289:25602003;289:2560--2572.2572.

    Drug(s) for the compellingindications; otherantihypertensive drugs(diuretics, ACE-I, ARB,BB, CCB) as needed

    Drug(s) for the compellingindications; otherantihypertensive drugs(diuretics, ACE-I, ARB, BB,

    CCB) as needed

    BP Classification

    Lifestyle

    Modification

    Initial Drug Therapy

    Without Compelling

    Indication

    With Compelling

    Indication

    Normal

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    Hypertension treatment strategy : JNC VIILifestyle modifications

    Not at goal blood pressure (

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    JNC VII & ESH/ESC 2003:

    Treatment Considerations

    Most patients with hypertensionwill require 2 ormore 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 athiazide-

    type diureticChobanian AV et al. JAMA. 2003;289:2560-2572.Guidelines Committee. J Hypertens.2003;21:1011-1053.

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    Definitions and Classifications of

    Blood Pressure : ESH/ESC 2007

    Category Systolic DiastolicOptimal < 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 3hypertension

    180 and/or 110Isolated

    systolic

    hypertension

    and < 90 140

    Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension.Eur Heart J 2007;28:1462-1536

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    Initiation of Antihypertensive treatment : ESC 2OO7Other 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 orDBP 110

    No other risk

    factors

    No BP

    intervention

    No BP

    intervention

    Lifestyle

    changes forseveral months

    then drug

    treatment if BP

    uncontrolled

    Lifestyle

    changes forseveral weeks

    then drug

    treatment if BP

    uncontrolled

    Lifestyle

    changes +immediate drug

    treatment

    1-2 risk factors Lifestyle

    changes

    Lifestyle

    changes

    Lifestyle

    changes for

    several weeksthen drug

    treatment if BP

    uncontrolled

    Lifestyle

    changes for

    several weeksthen drug

    treatment if BP

    uncontrolled

    Lifestyle

    changes +

    immediate drugtreatment

    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

    treatmentDiabetes 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 drugtreatment

    Lifestyle

    changes +

    immediate drugtreatment

    Lifestyle

    changes +

    immediate drugtreatment

    Lifestyle

    changes +

    immediate drugtreatment

    Lifestyle

    changes +

    immediate drugtreatment

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    Conditions favouring the use of some

    Antihypertensive drugs versus otherSUBCLINICAL 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, ARBAngina 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

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    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 HypertensionAdapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension.Eur Heart J 2007;28:1462-1536

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    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

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    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

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    Continued..

    Compelling contra-

    indications

    Possible contra-

    indications

    ACE-inhibitors Pregnancy

    Angioneurotic edema

    HyperkalaemiaBilateral renal artery

    stenosis

    Angiotensin receptor

    blockers

    Pregnancy

    Hyperkalaemia

    Bilateral renal arterystenosis

    Diuretics

    (antialdosterone)

    Renal failure

    hyperkalaemia

    Adapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension.Eur Heart J 2007;28:1462-1536

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    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 trialsAdapted From 2007 ESH-ESC Guidelines for the Management of Arterial Hypertension

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    Mild BP elevation

    Low/Moderate CV risk

    ConventionalBP Target

    Marked BP elevation

    High/very high CV RiskLower 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

    Ada ted From 2007 ESH-ESC Guidelines for the Mana ement of Arterial H ertension

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    Comparison of tight BP vs tight Glucose control

    in UKPDS

    5

    -50

    -40

    -30

    -20

    -10

    0

    Tight glucose controlTight BP control

    Microvascularendpoints

    *

    Stroke Any diabetes-related endpoint Diabetes-relateddeaths

    *

    *

    *

    * p

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    Gaede P, et al. N Engl J Med2003;348:383-393

    Steno-2: Patients who reached intensive-

    treatment goals at a mean of 7.8 years

    HbA1c

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    Steno-2: Composite CV endpoints

    Primaryco

    mposite

    endpoin

    t*(%)

    0

    0 3612 966048 847224

    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 Med2003;348:383-393

    * Primary composite endpoint = composite of death from cardiovascular causes,nonfatal myocardial infarction, nonfatal stroke, revascularization and amputation

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    Treatment of Hypertension in MS

    Some anti-hypertensives (diuretics, beta-blockers) worsen glycemic controland may

    not be suitable for long-term use in MS

    Drugs of choice in MS may beACE-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

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    In patients with metabolic syndrome diagnosticprocedures 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 hypertensiondrug treatmentshould

    start with a drug unlikely to facilitate onset to

    diabetes.Therefore ablocker of the renin-

    angiotensin system should be usedand 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)

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    Lack of evidence from specific clinical trialsprevents firm recommendations on use of

    antihypertensive drugs in all metabolic

    syndrome subjects with a high normal BP.

    There is some evidence thatblocking the renin-angiotensin system may also delay incident

    hypertension.

    CONCLUTIONS ( 2 )

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