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The Choise of Antihypertensive Drug Therapy

 

Hypertension is now seen as an integrated system of cardiovascular risk factors.(Weber M.1993.). The danger of coronary heart diseases increases with the number of risk factors (Kannel WB.1992.)

Prevalence of other coronary risk factors in hypertensives (Kaplan NM.,1993.)

Risk factor

%

Smoking

35

Hypercholesterolemia >240mg/dl>200mg/dl

40/85¹

Decreased HDL-cholesterol<40mg/dl

25

Obesity

40

Diabetes

15

Hyperinsulinaemia

50

Left ventricular hypertrophy

30

Sedentary lifestyle

>50

¹Hypercholesterolaemia >24omg/dl >200mg/dl, 85% (Poulter NR.,1991.)

Effects of antihypertensive agents on coronary risk factors (Kaplan NM.,1993.)

Coronary risk
factor

ACE
inhibitors

Calcium
Antag.

Beta
blockers

Diuretics

Alpha-
blockers

Blood pressure

+

+

+

+

+

Cholesterol

0

0

0

-

+

HDL chol.

0

0

-

0

0

Glucose
intolerance

+

0

-

-

0

Hiperinsulinemia

+

0

-

-

+

LVH

+

+

+

+/0

+

+ positive effect

0 neutral effect

- negative effect

 

Antihypertensive Drug Therapy

   

Drug Therapy

Indications

Contraindications

Diuretics

Congestive heart failure

Diabetes
Gout
Hypercholesterolemia

Central alpha agonists

 

Liver disease(methydopa)
Autoimmune disease
Depression

Alpha blockers

Hypercholesterolemia
Prostatis

 

Beta blockers

Coronary heart disease
Tachyarrhythmias
Migraine
Anxiety

Bronchospastic disease
Diabetes requiring insulin
Bradyarrhythmias
Congestive heart failure
Peripherial vascular disease

ACE inhibitors

Congestive heart failure
Post-myocardial infarctus
Diabetes nephropathy

Renal failure
Renovascular hypertension
Volumen depletion

Calcium antagonists

Angina pectoris
(Amlodipin)
Renal insufficiency
Tachyarrhythmias
(Verapamil,Diltiazem)
Peripheral vascular disease

Bradiarrhythmias
(Diltiazem,Verapamil)

 

References
Cardiovascular Drugs and therapy.11th international Congress on Cardiovascular Pharmacotherapy, Montreal, QC, Canada, 18-21 May 2002.
J Intern Med 1993; 234:317-323 JAMA 1990; 263:407-413. Clin Ther 1994;16:88-102.
Ann Intern Med 1992;116:238-244.
 

OUR INVESTIGATION

Effects of Lisinopril on left ventricular function

Andjelija Necin, Jelena Stamenkovic - Rebic, Zivojin Stamenkovic
Cardiovascular Dispensary, Novi Sad. Yugoslavia; Cardiovascular Institute, S.Kamenica, Yugoslavia (Serbia)

The Aim of the study was to asses the effects of Lisinoptil (L) on left ventricular performance in hypertensive patients (pts). 20 hypertensive pts 95<DBP>115 mmHg with left ventricular (LV) hypetrophy, mean age 50±10,7 yrs, were treated with L. (5 mg -2o mg once daily)for 6 months.

Methods: All pts underwent complete echocardiographic examination before and after treatment with L. We have measured: LV end diastolic diameter (LVEDD) and end systolic diameter (LVESD),the interventricular septal (IVS) and posterior wall (PLW) thicknees, LV mass (LVM), LVM index (LVMI), early pack velocity (E), late pack velocity (A), the E/A ration, mitral flow deceleration time (DT) and ejection fraction (RF).

Results are presented on the table:
 

 

Before th

After th

P

LVEDD (cm)

5.12 ± 0.42

4.96 ± o.41

NS

LVESD (cm)

3.18 ± 0.41

3.11 ± 0.38

NS

IVS (cm)

1.35 ± 0.11

1.01 ± 0.11

<0.001

PLW (cm)

1.29 ± 0.12

1.1 ± 0.12

<0.001

LVN (g)

153 ± 20.1

115 ±18.2

<0.001

LVMI (g/m²)

148 ± 13.4

137 ± 12.9

<0.005

E/A ratio

0.8 ± o.2o

1.57 ± 0.25

<0.001

F (%)

64 ± 8

68 ± 10

<0.005

 

After 12 weeks of treatment L. induced a significant reduction in blood pressure in the study group from 16o ± 2.0/85 ± 1.2 mmHg to 134 ± 1.8/78 ± 1.4 (p<0.001).

Conclusion: L induced a significant reduction in blood pressure and reduced LV hypertrophy and mass.L improved diastolic and systolic function of LV.

Abstract at 11th International Congress on Cardiovascular Pharnacotherapy,Montreal,QC,Canada,18-21 May,2002.P337.
 

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