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BETA BLOCKER USE IN
CARDIOVASCULAR DISEASES
Dr. dr. Hendro Darmawan, SpJP,
FIHA
PIT VI IDI Kota Bogor, 9 Nopember
2013
CVD (focused on) :
Classification of β-blockers
Table 6: Classification of ß-blockers

1st Generation

Non-selective

Propranolol

2nd Generation

β1-selective

Atenolol
Metoprolol
Betaxolol
Bisoprolol

3rd Generation

Additional
properties, for
example
vasodilation

Carvedilol
Nebivolol
1-selectivity of various blockers
Bisoprolol
1:75

Atenolol

Betaxolol

1:35

1:35

Metoprolol

increasing
ß 1-selectivity

1:20

no
selectivity

1.8:1
Propranolol

increasing
ß 2-selectivity

300:1
ICI
118.551

Ratio of constants of inhibition

Wellstein A et al. J Cardiovasc Pharmacol 1986; 8 (Suppl. 11): 36-40
Wellstein A et al. Eur Heart J 1987; 8 (Suppl. M): 3–8
Beta 1 VS Beta 2 Selectivity
Elimination routes of various beta
blockers from body
MECHANISM OF BETA BLOCKERS
IN HEART FAILURE
 Upregulation of β receptors and improved β







adrenergic signaling.
Reducing the hyperphosphorylation of calcium
release channels of sarcoplasmic reticulum and
normalizing their function
Bradycardia (↑ coronary blood flow and
decreased myocardial oxygen demand).
Protection from catecholamine myocyte toxicity.
Suppression of ventricular arrhythmias.
Anti-apoptosis. β2 receptors, which are relatively
increased, are coupled to inhibitory G protein & block
apoptosis.
Mechanism of β-blocker benefits
in ischemic heart disease

• Reduction in myocardial oxygen
requirements via a decrease in
heart rate, blood pressure and
ventricular contractility.
• Slowing of the heart rate
prolongs coronary diastolic
filling period.
• Redistribution of coronary
Mechanism of β-blocker benefits
in ischemic heart disease

• Increases threshold to
ventricular fibrillation.
• Reduction in infarct size and
reduction in the risk of cardiac
rupture.
• Reduction in the rate of
reinfarction.
• Regression of the atheromatous
Summary of Trials of Beta-Blocker Therapy
Phase of
Treatment

Total No.
Patients

RR (95% CI)

Acute
treatment

28,970

0.87 (0.77-0.98)

Secondary
prevention

24,298

0.77 (0.70-0.84)

Overall

53,268

0.81 (0.75-0.87)

2
1
0.5
Relative risk (RR) of death
Placebo
Beta blocker
better
better

Antman E, Braunwald E. Acute Myocardial Infarction. In:
Braunwald E, Zipes DP, Libby P, eds. Heart Disease: A
textbook of Cardiovascular Medicine, 6th ed.,
Philadelphia, PA: W.B. Sanders, 2001, 1168.
MAINTATE

Usefulness of beta-blocker therapy in patients with
diabetes mellitus and CAD (BIP)

1.00

0.90
0.85

Mortality
42%

Withß-blockers
Withoutß-blockers

0.80
P = 0.0001

0.75
1

14.417 pts

2

3

Year

4

5

Jonas et al. Am J Cardiol 1996; 77: 1273 et seqq.

Survival rate

0.95
BP and -BLOCKERS

Central
effects
Baroreceptor
reflexes



Carotid sinus
?

Stellate
ganglion

NE




E



Renin



Sinus rate
Stroke volume
Cardiac output

Terminal
neurone

Angio I
Angio II

Systemic
vascular
resistance

NE


Initial rise
then fall
BisoDIAS

Endgültig

28

Bisoprolol: Long-term treatment of hypertension

140

SBP(mm Hg)

100

DBP(mm Hg)
HR(beats/min)

60

0
n = 102

12

15

18

21

24

27

30

33

36 months

102

97

102

101

102

102

102

100

102

Giesecke HG et al. J Cardiovasc Pharmacol 1990; 16 (Suppl 5): 175

180
This is how braunwald’s textbook
summarizes the use of betablockers in
hypertension
 “Beta blockers are specifically recommended for

hypertensive patients with concomitant coronary
disease, particularly after a myocardial infarction,
congestive heart failure, or tachyarrhythmias.”
 “If a beta blocker is chosen, the agents that are more
cardioselective offer the likelihood of fewer
perturbations of lipid and carbohydrate metabolism
and, because of fewer side effects (except for
bradycardia), better adherence to therapy.”
 “Long-acting formulations are better for once-daily
dosing.”
Page 945 braunwald’s
textbook of medicine 9th edition
From: Cardiovascular Protection Using Beta-Blockers: A Critical Review of the Evidence

J Am Coll Cardiol. 2007;50(7):563-572. doi:10.1016/j.jacc.2007.04.060

Figure Legend:
Proposed Use of Beta-Blockers for Hypertension

In patients with uncomplicated hypertension, beta-blockers should not be used as
first-line agents. However, in patients with uncontrolled hypertension on various
other antihypertensive agents and in those with complicated hypertension, betablockers should be considered in the armamentarium of treatment. CHF = chronic
heart failure; MI = myocardial infarction. College of Cardiology.
Copyright © The American
All rights reserved.
Bisoprolol experience in
Indian patients
Mar
2012
Bisoprolol in hypertension
Objectives:

This study was aimed to evaluate the
efficacy and tolerability of
bisoprolol, in Indian patients
diagnosed with stage I essential
hypertension as first line drug.
Primary and secondary outcomes measures:

The primary outcome measure was
percentage of patients achieving
blood pressure (BP) <140/90 mm Hg
at the end of 12 weeks, while
Channaraya V, Marya RK, Somasundaram M, et al. BMJ Open 2012;2:e000683
multiple secondary outcome

RESULT

2131 (96.44%) patients n: 2418
achieved BP control.
Different beta blockers and sexual
dysfunction versus placebo
Conclusion:
Cardioselective beta-blockers
(Bisoprolol) is important part of CVD
management
THANK YOU!

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Launching Simposium PIT IDI Kota Bogor 2013

  • 1. BETA BLOCKER USE IN CARDIOVASCULAR DISEASES Dr. dr. Hendro Darmawan, SpJP, FIHA PIT VI IDI Kota Bogor, 9 Nopember 2013
  • 3. Classification of β-blockers Table 6: Classification of ß-blockers 1st Generation Non-selective Propranolol 2nd Generation β1-selective Atenolol Metoprolol Betaxolol Bisoprolol 3rd Generation Additional properties, for example vasodilation Carvedilol Nebivolol
  • 4. 1-selectivity of various blockers Bisoprolol 1:75 Atenolol Betaxolol 1:35 1:35 Metoprolol increasing ß 1-selectivity 1:20 no selectivity 1.8:1 Propranolol increasing ß 2-selectivity 300:1 ICI 118.551 Ratio of constants of inhibition Wellstein A et al. J Cardiovasc Pharmacol 1986; 8 (Suppl. 11): 36-40 Wellstein A et al. Eur Heart J 1987; 8 (Suppl. M): 3–8
  • 5. Beta 1 VS Beta 2 Selectivity
  • 6. Elimination routes of various beta blockers from body
  • 7.
  • 8. MECHANISM OF BETA BLOCKERS IN HEART FAILURE  Upregulation of β receptors and improved β      adrenergic signaling. Reducing the hyperphosphorylation of calcium release channels of sarcoplasmic reticulum and normalizing their function Bradycardia (↑ coronary blood flow and decreased myocardial oxygen demand). Protection from catecholamine myocyte toxicity. Suppression of ventricular arrhythmias. Anti-apoptosis. β2 receptors, which are relatively increased, are coupled to inhibitory G protein & block apoptosis.
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.
  • 18.
  • 19.
  • 20. Mechanism of β-blocker benefits in ischemic heart disease • Reduction in myocardial oxygen requirements via a decrease in heart rate, blood pressure and ventricular contractility. • Slowing of the heart rate prolongs coronary diastolic filling period. • Redistribution of coronary
  • 21. Mechanism of β-blocker benefits in ischemic heart disease • Increases threshold to ventricular fibrillation. • Reduction in infarct size and reduction in the risk of cardiac rupture. • Reduction in the rate of reinfarction. • Regression of the atheromatous
  • 22. Summary of Trials of Beta-Blocker Therapy Phase of Treatment Total No. Patients RR (95% CI) Acute treatment 28,970 0.87 (0.77-0.98) Secondary prevention 24,298 0.77 (0.70-0.84) Overall 53,268 0.81 (0.75-0.87) 2 1 0.5 Relative risk (RR) of death Placebo Beta blocker better better Antman E, Braunwald E. Acute Myocardial Infarction. In: Braunwald E, Zipes DP, Libby P, eds. Heart Disease: A textbook of Cardiovascular Medicine, 6th ed., Philadelphia, PA: W.B. Sanders, 2001, 1168.
  • 23. MAINTATE Usefulness of beta-blocker therapy in patients with diabetes mellitus and CAD (BIP) 1.00 0.90 0.85 Mortality 42% Withß-blockers Withoutß-blockers 0.80 P = 0.0001 0.75 1 14.417 pts 2 3 Year 4 5 Jonas et al. Am J Cardiol 1996; 77: 1273 et seqq. Survival rate 0.95
  • 24.
  • 25. BP and -BLOCKERS Central effects Baroreceptor reflexes  Carotid sinus ? Stellate ganglion NE   E  Renin  Sinus rate Stroke volume Cardiac output Terminal neurone Angio I Angio II Systemic vascular resistance NE  Initial rise then fall
  • 26.
  • 27.
  • 28. BisoDIAS Endgültig 28 Bisoprolol: Long-term treatment of hypertension 140 SBP(mm Hg) 100 DBP(mm Hg) HR(beats/min) 60 0 n = 102 12 15 18 21 24 27 30 33 36 months 102 97 102 101 102 102 102 100 102 Giesecke HG et al. J Cardiovasc Pharmacol 1990; 16 (Suppl 5): 175 180
  • 29. This is how braunwald’s textbook summarizes the use of betablockers in hypertension  “Beta blockers are specifically recommended for hypertensive patients with concomitant coronary disease, particularly after a myocardial infarction, congestive heart failure, or tachyarrhythmias.”  “If a beta blocker is chosen, the agents that are more cardioselective offer the likelihood of fewer perturbations of lipid and carbohydrate metabolism and, because of fewer side effects (except for bradycardia), better adherence to therapy.”  “Long-acting formulations are better for once-daily dosing.” Page 945 braunwald’s textbook of medicine 9th edition
  • 30. From: Cardiovascular Protection Using Beta-Blockers: A Critical Review of the Evidence J Am Coll Cardiol. 2007;50(7):563-572. doi:10.1016/j.jacc.2007.04.060 Figure Legend: Proposed Use of Beta-Blockers for Hypertension In patients with uncomplicated hypertension, beta-blockers should not be used as first-line agents. However, in patients with uncontrolled hypertension on various other antihypertensive agents and in those with complicated hypertension, betablockers should be considered in the armamentarium of treatment. CHF = chronic heart failure; MI = myocardial infarction. College of Cardiology. Copyright © The American All rights reserved.
  • 31. Bisoprolol experience in Indian patients Mar 2012
  • 32. Bisoprolol in hypertension Objectives: This study was aimed to evaluate the efficacy and tolerability of bisoprolol, in Indian patients diagnosed with stage I essential hypertension as first line drug. Primary and secondary outcomes measures: The primary outcome measure was percentage of patients achieving blood pressure (BP) <140/90 mm Hg at the end of 12 weeks, while Channaraya V, Marya RK, Somasundaram M, et al. BMJ Open 2012;2:e000683 multiple secondary outcome 
  • 33. RESULT 2131 (96.44%) patients n: 2418 achieved BP control.
  • 34. Different beta blockers and sexual dysfunction versus placebo