Title: 1999 WHO-ISH Hypertension Practice Guidelines for Primary Care Physicians
11999 WHO-ISHHypertension Practice Guidelinesfor
Primary Care Physicians
- World Health Organization
- INTERNATIONAL SOCIETY OF HYPERTENSION
2Working Group Practice Guidelines
- John Chalmers (Australia, Chairman)
- Paul Chusid (USA)
- Jay N Cohn (USA)
- Lars H Lindholm (Sweden, Writing Coordinator)
- Ingrid Martin (WHO, Switzerland)
- Karl-Heinz Rahn (ISH, Germany)
- Peter Sleight (WHL, UK)
3WHO-ISH HypertensionGuidelines Subcommittee
- Michael Alderman (USA)
- Kikuo Arakawa (Japan)
- Lawrie Beilin (Australia)
- John Chalmers(Australia, Chairman)
- Serap Erdine (Turkey)
- Masatoshi Fujishima (Japan)
- Pavel Hamet (Canada)
- Lennart Hansson (Sweden)
- Lewis Landsberg (USA)
- Frans Leenen (Canada)
- Lars H Lindholm (Sweden)
Liu Lisheng (China) AFB Mabadeje
(Nigeria) Stephen MacMahon (Australia) Giuseppe
Mancia (Italy) Ingrid Martin (Switzerland) Albert
Mimran (France) Karl-Heinz Rahn (Germany) Arturo
Ribeiro (Brazil) Peter Sleight (UK) Judith
Whitworth (Australia) Alberto Zanchetti (Italy)
4- The WHO-ISH Guidelines are written for a global
audience from communities that vary widely in the
nature of their health system and in the
availability of resources. - The goal, however, remains universally the same,
that is to lower BP and other risk factors in
order to reduce the risk of CVD.
4
1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
PRIMARY CARE PHYSICIANS
5Global Goal
5
1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
PRIMARY CARE PHYSICIANS
6What is the Goalof the Practice Guidelines?
- To lower blood pressure (BP) and other risk
factors in order to reduce the risk of
cardiovascular disease (CVD)
6
1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
PRIMARY CARE PHYSICIANS
7Why is Hypertension Management Needed? (1)
- 600 million hypertensives in the world
- 3 million die annually as a direct result of
hypertension
8Why is Hypertension Management Needed? (2)
- The Rule of Halves
- Only 1/2 have been diagnosed
- Only 1/2 of those diagnosed have been treated
- Only 1/2 of those treated are adequately
controlled - Thus, only 12.5 overall are adequately controlled
9What is New?
1999 WHO-ISH 1993 WHO-ISH JNC-VI Definition of
gt 140/90 gt140/90 gt140/90 hypertension Levels Gra
de 1,2,3 Mild, Moderate, Stage
1,2,3 Severe Decision Not based on BP BP to
treat BP alone, but assessment of total CV
risk Target BPs lt130/85 lt130/80 lt140/90 lt140/90
(elderly) lt140/90 (elderly)
9
10What is New?
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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11Why BP lt130/85 mm Hgand Not lt140/90 mm Hg? (1)
- The relationship between CV risk and BP is
continuous - Today, more than 50 of all hypertensives have BP
gt160/90 mm Hg and 75 have BP gt140/90 - The major determinant of the risk reduction
conferred by antihypertensive therapy is the BP
level attained
12Why BP lt130/85 mm Hgand Not lt140/90 mm Hg? (2)
- In diabetics, there is a clear benefit of
lowering BP lt85 mm Hg - The HOT Study showed that lowering BP lt 85 mm Hg
did not increase CV risk - The goal should be to attain normal BP (lt130/85
mm Hg)
13Questions to be Answered (1)
- What is high blood pressure?
- Clinical evaluation - what should be done?
- Which factors influence prognosis?
- Do patients benefit from antihypertensive
treatment? - How should hypertension be managed?
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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14Questions to be Answered (2)
- Which drug treatments should be used?
- What treatment goal should be set and how should
patients be followed up? - How should hypertension during pregnancy be
handled? - How should hypertension in Type-2 diabetics be
handled?
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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15What is High Blood Pressure?
- BP levels are continuously related to the risk of
CVD - Definition of hypertension or raised BP is
arbitrary - Even within the normotensive range, people with
the lowest BP levels have the lowest rates of CVD
16Relative Risk of CHD and Stroke in Relation to
Patients Usual Diastolic BP
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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17New (1999) WHO-ISH Definitionsand Classification
of BP Levels
Category Systolic BP Diastolic BP (mm Hg) (mm
Hg) Optimal BP lt120 lt80 Normal
BP lt130 lt85 High-Normal 130-139 85-89 Grade 1
Hypertension (mild) 140-159 90-99 Subgroup
Borderline 140-149 90-94 Grade 2 Hypertension
(moderate) 160-179 100-109 Grade 3 Hypertension
(severe) gt180 gt110 Isolated Systolic
Hypertension gt140 lt90 Subgroup
Borderline 140-149 lt90
18Clinical Evaluation - What Should Be Done?
- Confirm elevation of BP
- Exclude or identify secondary causes of
hypertension - Determine presence of target organ damage and
quantify extent - Search for other CV risk factors and clinical
conditions that may influence prognosis and
treatment
19How to Record BP (1)
- Measure BP several times on separate occasions
with the patient in sitting position - Use a mercury sphygmomanometer or other
non-invasive device
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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20How to Record BP (2)
- Measure BP several times on several occasions
- Allow the patient to sit for several minutes
before measuring BP - Use a cuff with a bladder that is 12-13 cm X 35
cm, larger for fat arms - Use phase 5 Korotkoff sounds (disappearance) to
measure diastolic BP - Measure BP in both arms at first visit
- Measure BP in standing position in elderly
subjects and diabetic patients - Place sphygmomanometer cuff at heart level,
whatever the position of the patient
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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21Multiple BP Measurements Recommended
- Because BP is characterized by large spontaneous
variations, diagnosis should be based on multiple
BP measurements taken on several separate
occasions
21
22Minimum RoutineInvestigations
- Clinical and family history
- Full physical examination as described in medical
textbooks - Laboratory investigations, including
- urinalyses for blood, protein, and glucose
- microscopic examination of the urine
- blood chemistry for potassium, creatinine,
fasting glucose, and total cholesterol - Electrocardiography (ECG)
22
23Isolated Office Hypertension
- In some patients office BP is persistently
elevated whereas daytime BP outside clinic
environment is not. Continuing debate whether
isolated office hypertension (white coat
hypertension) is an innocent phenomenon or
carries an increased risk of CVD
23
24Ambulatory BP Monitorings Should be Considered,
if
- Unusual variability of BP over the same or
different visits - Isolated office (white coat) hypertension in
subjects with low CV risk - Symptoms suggesting hypotensive episodes
- Hypertension resistant to drug treatment
24
25Ambulatory BP Monitoring
- BP values obtained by home measurement or
ambulatory monitoring are several mm Hg lower
than office measurement - Average 24 hour or home BP values around 125/80
mm Hg office BP 140/90 mm Hg - Reliable information about long-term prognostic
value of ambulatory and home monitoring is awaited
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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26Which Factors Influence Prognosis? (1)
- Decisions should not be made on BP alone, but
also on presence of other risk factors, target
organ damage, and concomitant diseases, as well
as on other aspects of patients personal,
medical, social, economic, ethnic, and cultural
characteristics
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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27Which Factors Influence Prognosis? (2)
- Risk factors of CVD
- I. Used for risk stratification
- II. Other factors adversely influencing
prognosis - Target organ damage (TOD)
- Associated clinical conditions (ACC)
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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28Which Factors Influence Prognosis? (3)
Risk factors for CVD
- I. Used for risk stratification
- Levels of systolic and diastolic blood pressure
(Grades 1-3) - Men gt55 years
- Women gt65 years
- Smoking
- Total cholesterol gt6.5 mmol/L (250 mg/dl)
- Diabetes
- Family history of premature cardiovascular disease
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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29Which Factors Influence Prognosis? (4)
Risk factors for CVD
- II. Other factors adversely influencing prognosis
- Reduced HDL cholesterol
- Raised LDL cholesterol
- Microalbuminuria in diabetes
- Impared glucose tolerance
- Obesity
- Sedentary lifestyle
- Raised fibrinogen
- High risk socioeconomic group
- High risk ethnic group
- High risk geographic region
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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30Which Factors Influence Prognosis? (5)
Target organ damage (TOD)
- Left ventricular hypertrophy (electrocardiogram,
echocardiogram, or radiogram) - Proteinuria and/or slight elevation of plasma
creatinine concentration 106-177 mmol/L (1.2-2.0
mg/dl) - Ultrasound or radiological evidence of
atherosclerotic plaque (carotid, iliac, and
femoral arteries, aorta) - Generalised or focal narrowing of the retinal
arteries
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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31Which Factors Influence Prognosis? (6)
Associated clinical conditions (ACC)
- Cerebrovascular disease
- Ischaemic stroke
- Cerebral haemorrhage
- Transient ischaemic attack (TIA)
- Heart disease
- Myocardial infarction
- Angina pectoris
- Coronary revascularisation
- Congestive heart failure
1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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31
32Which Factors Influence Prognosis? (7)
Associated clinical conditions (ACC)
- Renal disease
- Diabetic nephropathy
- Renal failure, plasma creatinine concentration
gt177 mmol/L (gt2.0 mg/dl) - Vascular disease
- Dissecting aneurysm
- Symptomatic arterial disease
- Advanced hypertensive retinopathy
- Haemorrhages or exudates
- Papilloedema
1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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32
33Which FactorsInfluence Prognosis? (8)
Typical 10 year risk of stroke or myocardial
infarction
- Low risk lt15 percent
- Medium risk 15-20 percent
- High risk 20-30 percent
- Very high risk 30 percent or higher
33
34Which FactorsInfluence Prognosis? (9)
- Example 1
- 65-year old man with diabetes, TIAs, and BP of
145/90 mm Hg will have annual risk of major CVD
event 20 times greater than 40-year old man with
same BP but without diabetes or history of CVD
34
35Which FactorsInfluence Prognosis? (10)
- Example 2
- 40-year old man with BP of 170/105 mm Hg will
have risk of major CV event 2-3 times greater
than man of same age with BP of 145/90 mm Hg and
similar other risk factors
35
36Stratifying Risk - Quantifying Prognosis
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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37Do Patients Benefit from Antihypertensive
Treatment? (1)
- Yes, the randomized trials conducted to date have
shown clear evidence of a lower incidence of
major CVD events after high BP was treated with
anti-hypertensive drugs.
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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38Do Patients Benefit from Antihypertensive
Treatment? (2)
- There is as yet no evidence that the main benefit
of treating hypertension is due to a particular
drug property rather than to lowering BP per se.
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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39Effects of Antihypertensive Treatment in
Randomised Controlled Trials
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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40Absolute Effects of Antihypertensive Treatment
10/5 mm Hg 20/10 mm Hg Low risk
patients lt5 lt9 Medium risk patients 5-7 8-11
High risk patients 7-10 11-17 Very high risk
patients gt10 gt17
Patient Group Absolute treatment effects
(CVD events prevented per 1000 patients years)
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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41Larger Risk Reductions?
- The estimates of antihypertensive benefits shown
were reported from trials of about 5 years
duration. - It is possible that long-term treatment over
decades might produce larger risk reductions.
41
1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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42Management Strategy (1)
- Initiate lifestyle measures wherever appropriate
in all patients, including those who require drug
treatment - Smoking cessation
- Weight reduction
- Moderation of alcohol consumption
- Reduction of salt intake
- Increased physical activity
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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43Management Strategy (2)
Very High Risk
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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44Management Strategy (3)
Very High
Begin drug treatment
Begin drug treatment
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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45Management Strategy (4)
Medium
Low
Monitor BP other risk factors for 3-6 months
Monitor BP other risk factors for 6-12 months
SBP gt140 or DBP gt90 Begin drug treatment
SBP lt140 or DBP lt90 Continue to monitor
SBP gt150 or DBP gt95 Begin drug treatment
SBP lt150 or DBP lt95 Continue to monitor
45
1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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46Principles of Drug Treatment (1)
- Use a low dose of one drug to initiate therapy
- If good response and tolerability but inadequate
control increase the dose of the first drug - If little response or poor tolerability change to
another drug class
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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47Principles of Drug Treatment (2)
- It is often preferrable to add a small dose of a
second drug rather than increase the dose of the
first drug - Use long-acting drugs providing 24-hour efficacy
on a once daily basis. Improves adherence to
therapy and minimizes BP variability.
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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48Principles of Drug Treatment (3)
- More evidence of beneficial CVD effects with
older drugs (e.g., diuretics and beta-blockers) - Evidence of benefit with newer drugs (e.g., ACE
inhibitors and calcium antagonists) is
accumulating.
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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49Principles of Drug Treatment (4)
- There are six maindrug classes used worldwide -
diuretics, beta-blockers, ACE inhibitors, calcium
antagonists, alpha blockers, and angiotensin II
antagonists.
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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50Principles of Drug Treatment (5)
- All 6 classes are suitable for the initiation and
maintenance of BP lowering therapy, but the
choiceof drugs will be influenced by cost and by
many factors for special groupsof patients. In
some parts of the world, reserpine and methyldopa
arealso used frequently.
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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51Indications
Compelling PossibleHeart failure DiabetesElderly
patients Systolic hypertension
Diuretics
Contraindications
Compelling PossibleGout Dyslipidaemia Sexually
active males
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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52Indications
Compelling PossibleAngina Heart failureAfter
myocardial infarct PregnancyTachyarrhythmias Diab
etes
Contraindications
Beta-Blockers
Compelling PossibleAsthma and Dyslipidaemia
Chronic obstructive Athletes and Pulmonary
disease Physically activeHeart block (AV
2,3) Patients Peripheral vascular disease
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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53Indications
Compelling PossibleAngina PeripheralElderly
patients Vascular disease Systolic
hypertension
Calcium Antagonists
Contraindications
Compelling PossibleHeart block (AV 2,3) Heart
failure
verapimil or diltiazem
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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54Indications
Compelling PossibleHeart failure Left
ventricular dysfunctAfter myocardial
infarctDiabetic nephropathy
ACE Inhibitors
Contraindications
Compelling PossiblePregnancyBilateral renal
artery stenosisHyperkalaemia
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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55Indications
Compelling PossibleProstatic Hypertrophy Glucose
intolerance Dyslipidaemia
Alpha-Blockers
Contraindications
Compelling Possible Orthostatic
hypotension
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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56Indications
Compelling PossibleACE-I cough Heart failure
Angiotensin II Antagonists
Contraindications
Compelling PossiblePregnancyBilateral renal
Artery stenosisHyperkalaemia
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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57Combination Therapy (1)
- In most patients, appropriate combination therapy
produces BP reductions that are twice as great as
those obtained with monotherapy, for example,
12-22 mm Hg systolic BP and 7-14 mm Hg diastolic
BP for patients with initial BP of gt160/95 mm Hg
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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58Combination Therapy (2)
- Effective drug combinations to treat hypertension
are - diuretic and beta-blocker
- diuretic and ACE inhibitor (or Angiotensin II
antagonist) - calcium antagonist (dihydropyridine) and
beta-blocker - calcium antagonist and ACE inhibitor
- alpha-blocker and beta-blocker
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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59Other Drugs to Consider in Hypertension
- Aspirin
- Cholesterol lowering therapy
59
60Treatment Goal (1)
Reduce total CVD risk
- Requires treatment of all reversible risk
factors, such as smoking, raised cholesterol, or
diabetes, and the management of associated
clinical conditions, as well as treatment of
raised BP
60
61Treatment Goal (2)
- The goal of antihypertensive treatment should be
to achieve optimal or normal BP in young,
middle-aged, or diabetic subjects (below 130/85
mm Hg), and at least high-normal BP in elderly
patients (below 140/90 mm Hg)
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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62Follow-Up (1)
- Follow-up during evaluation and stabilisation of
treatment should be frequent to monitor BP and
other risk factors - Follow-up is important to establish good
relations with the patient and to educate the
patient, so that he/she takes responsibility for
the life-long control
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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63Follow-up (2)
- Good communication between physician and patient
is essential because treatment of hypertension is
for life - Adequate information about BP and high BP, about
risks and prognosis, about expected benefits of
treatment, and about risks and side effects of
treatment are essential for satisfactory
life-long control of hypertension which is poor
in many countries today
63
1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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64How Should HypertensionDuring Pregnancy be
Diagnosed?
- Usually defined by absolute levelof BP (for
example, 140/90 mm Hg or over) or an increase in
BP from pre-conception or first trimester (for
example, SBP rise of gt25 mm Hg and/or DBP rise of
gt15 mm Hg)
64
65How Should HypertensionDuring Pregnancy be
Defined?
- Hypertension in pregnancy usually defined as
- pre-existing chronic hypertension
- de novo diagnosed, gestational hypertension or
pre-eclampsia - pre-eclampsia superimposed on chronic hypertension
65
66How Should HypertensionDuring Pregnancy be
Handled?
- BP above 170/110 mm Hg should be lowered to
protect mother from risk of stroke or eclampsia - Opinion is divided on the need for drug treatment
for BP below this level
66
67Antihypertensive DrugsMost Widely Used
AcutelyDuring Pregnancy
- Nifedipine
- Labetalol
- Hydralazine
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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68Antihypertensive DrugsMost Widely Used
ChronicallyDuring Pregnancy
- Beta-blockers
- oxprenolol, pindolol, labetalol
- atenolol, however, is associated with fetal
growth retardation when used long-term throughout
pregnancy - Methyldopa
- Prazosin, hydralazine, nifedipine, and isradipine
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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69Drugs Most WidelyAvoided During Pregnancy
- ACE inhibitors (associated with possible adverse
fetal effects) - Angiotensin ll antagonists (effects may be
similar to ACE inhibitors) - Diuretics used infrequently because of concerns
of reducing already compromised plasma volume
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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70Hypertensionin Type-2 Diabetics (1)
- Diabetes and hypertension are multiplicative risk
factors for CVD - Absence of hypertension in diabetes is associated
with a better long-term survival
70
71Hypertensionin Type-2 Diabetics (2)
- Progressive decline in glomerular function can be
slowed with antihypertensive treatment - Similar lifestyle measures are recommended for
hypertension and diabetes
71
72Hypertensionin Type-2 Diabetics (3)
- Good evidence for reductionin CVD events in
diabetic patients treated with antihypertensivedr
ugs, including diuretics,and more recently,
beta-blockersand ACE inhibitors
72
73Hypertensionin Type-2 Diabetics (4)
- The goal of antihypertensive treatment in Type-2
diabetics should be to achieve optimal or
normal BP (that is below 130/85 mm Hg)
73
74What is the ImplementationPlan for Practice
Guidelines? (1)
- Publication in as many national medical journals
as possible - Over 2 million brochures to be printed in English
and several other languages - Distribution worldwide with assistance of
national hypertension and GP societies
74
75What is the ImplementationPlan for Practice
Guidelines? (2)
- Funding by multiple pharmaceutical companies with
no-strings-attached unrestricted educational
grants - Presentations at symposia, congresses, medical
meetings, hospitals, medical schools, etc.
75
76Summary (1)
- The goal of the 1999 WHO-ISH Hypertension
Practice Guidelines is to lower BP and other risk
factors in order to reducethe risk of CVD
76
77Summary (2)
- The goal of the 1999 WHO-ISH Hypertension
Practice Guidelinesis to lower BP and other risk
factors in order to reduce the risk of CVD -- in
primary care settings outside the hospital
77
78- How to Get Additional Copiesof Practice
Guidelines - Contact your nationalsociety/league of
hypertension, or - Write to World Health Organization Cardi
ovascular Diseases Programme CH-1211 Geneva 27,
Switzerland
- Fax 41 22 791 4151
- E-mail watsonm_at_who.ch
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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79No-strings-attached UnrestrictedGrant Funding
for Practice Guidelinesby Following Companies
- Bayer
- Bristol-Myers Squibb
- Glaxo Wellcome
- Merck (MSD)
- Novartis
- Pfizer
- Roche
- Searle
- Zeneca
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1999 WHO-ISH HYPERTENSION PRACTICE GUIDELINES FOR
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