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IONOTROPES AND IVC
DIAMETER
Dr.D.S.NIVETHAA
POST GRADUATE DEPARTMENT OF ANAESTHESIOLOGY
RECEPTOR DISTRIBUTION
EFFECTS OF SPECIFIC ADRENERGIC RECEPTOR
STIMULATION
EPINEPHRINE
Prototype sympathomimetic
synthesized stored andreleased from adrenal medulla
oral administration not effective- rapid metabolism in GI mucosaand liver
RECEPTORS STIMULATED-Beta 1-myocardium-raises BP, cardiac
output,myocardial oxygen demand by increasing contractility
Alpha 1- decreases splanchnic and renal blood flow but increases cpp by
increasing aortic diastolic bp
Beta 2- vasodilation in sk. muscle
ROUTES- SC/IV/IM
DOSE- to improve myocardial contractility 2-20 Mic/min(0.04-0.4
mic/kg/min)-4mic/ml dilution
Available preparation-1:1000(1mg/ml)
prefilled syringe 1:10000
1 in 1 lakh for paediatric use(10 mic/ml)
USES
1. Life threatening anaphylaxis-100-500 mcg
2. Severe asthma and bronchospasm- nebulization -5ml of 1:1000 (max 5 mg)
3. Cardiac arrest- 1mg every 3-5 mins
NOREPINEPHRINE
Precursor of epinephrine
Direct alpa 1 , beta 1 with little beta 2 activity
Beta 1 – myocardial contractility- inc BP
infusion- 2-20 mic/min(0.01-0.4mic/kg/min
should be infused in 5 D ( acidity-prevent oxidation of catecholamine)
DOC in septic shock-inc MAP,PVR
DOPAMINE
Precursor of norepinephrine
direct and indirect adrenergic and dopaminergic agonist
renal dose-0.5-3 mic/kg/min-DA1
3-10 mic/kg/min-beta 1
>10 mic/kg/min-PVR inc- alpha 1
used to improve cardiac output, maintain renal function
ISOPROTERENOL
Pure beta agonist
Beta 1-inc HR,CO,CONTRACTILITY,SBP
Beta 2-dec PVR,DBP
Dose- 1-5 mic/min
Metabolism-COMT in liver
Effective in patient with heart block
DOBUTAMINE
Synthetic catecholamine
Derived from isoproterenol
Potent alpha 1 agonist
Weak beta 1 &2 agonist
<5mic/kg/min-beta 1, alpha 1
>5mic/kg/min-alpha 1
>10 mic/kg/min- prone for arrhythmia
EPHEDRINE
Indirect acting synthetic sympathomimetic- alpha and beta
5-10 mg IV
Tachyphylaxis can occur
IV – inc HR,SBP
Hypotension due to Regional blockade and GA induction
Oral- treat bronchial asthma
IM-0.5 mg/kg- antiemetic
PHENYLEPHRINE
Hydroxy phenylethylamine
Direct alpha 1
Inc PVR,MAP
50-200 mic iv bolus
Infusion-20-100 mic/min
Nasal -1%-decongestant
DIGOXIN
Cardiac glycoside
Extracted from foxglove plant
60-80% oral bioavailability
Peak plasma conc- 1-3 hours following oral administration
100% iv bioavailability-attain peak plasma conc immediately
Excreted entirely by kidneys
Half life -1-2 days- inversely proportional to GFR(inc with age and renal
disease.
ORAL IV
ONSET OF ACTION 0.5-2hrs 10-30mins
PEAK EFFECT 6hrs 2-4hrs
Mechanism of action-selective and reversible cardiac sarcolemmal Na+_K+ ATPase
inhibitor
Increases intracellular calcium –responsible for ionotropic action
• Other benefits-
1. No change in heart rate
2. Decrease in LV preload and afterload
3. Decrease in wall tension
4. Decrease in oxygen consumption in failing heart
ECG findings obtained at therapeutic plasma concentrations include
 Prolonged PR interval-delayed Av nodal conduction
 Shortened QTc intervals-rapid ventricular repolarization
 ST depression-scaphoid/scooped out-decreased phase 3 depolarization of
cardiac action potentials.
 Diminished /inverted T wave
NARROW THERAPEUTIC RANGE
Digoxin toxicity
20% of patients treated with cardiac glycosides –report digitalis toxicity
AT RISK INDIVIDUALS:
-Renal dysfunction
-Diuretics-potassium depletion-arrhythmia
-Hyperventilation-decrease potassium 0.5mEq/L for 10mmHg decrease in
PaCO2
-Electrolyte imbalance –Hypokalemia,Hypercalcemia,Hypomagnesemia
-Hypoxemia induced sympathetic nervous system activity
Plasma conc < 0.5ng/ml-no toxicity
Therapeutic range-0.5-2.5ng/ml
Toxic range>3.0ng/ml
Treatment
- treat the underlying cause
-treat cardiac dysrhythmias
Phenytoin-0.5-1.5mg/kg IV over 5 mins
Lidocaine-1-2mg/kg IV
Atropine-35-70mic/kg IV
K+ supplementation-0.025-0.050 mEq/L
-Life threatening toxicity- digoxin antibodies
-Temporary artificial transvenous cardiac pacemaker-if complete heart
block is present.
THANK YOU

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IONOTROPES.pptx

  • 1. IONOTROPES AND IVC DIAMETER Dr.D.S.NIVETHAA POST GRADUATE DEPARTMENT OF ANAESTHESIOLOGY
  • 2.
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 10. EFFECTS OF SPECIFIC ADRENERGIC RECEPTOR STIMULATION
  • 11.
  • 12. EPINEPHRINE Prototype sympathomimetic synthesized stored andreleased from adrenal medulla oral administration not effective- rapid metabolism in GI mucosaand liver RECEPTORS STIMULATED-Beta 1-myocardium-raises BP, cardiac output,myocardial oxygen demand by increasing contractility Alpha 1- decreases splanchnic and renal blood flow but increases cpp by increasing aortic diastolic bp Beta 2- vasodilation in sk. muscle
  • 13. ROUTES- SC/IV/IM DOSE- to improve myocardial contractility 2-20 Mic/min(0.04-0.4 mic/kg/min)-4mic/ml dilution Available preparation-1:1000(1mg/ml) prefilled syringe 1:10000 1 in 1 lakh for paediatric use(10 mic/ml) USES 1. Life threatening anaphylaxis-100-500 mcg 2. Severe asthma and bronchospasm- nebulization -5ml of 1:1000 (max 5 mg) 3. Cardiac arrest- 1mg every 3-5 mins
  • 14. NOREPINEPHRINE Precursor of epinephrine Direct alpa 1 , beta 1 with little beta 2 activity Beta 1 – myocardial contractility- inc BP infusion- 2-20 mic/min(0.01-0.4mic/kg/min should be infused in 5 D ( acidity-prevent oxidation of catecholamine) DOC in septic shock-inc MAP,PVR
  • 15. DOPAMINE Precursor of norepinephrine direct and indirect adrenergic and dopaminergic agonist renal dose-0.5-3 mic/kg/min-DA1 3-10 mic/kg/min-beta 1 >10 mic/kg/min-PVR inc- alpha 1 used to improve cardiac output, maintain renal function
  • 16. ISOPROTERENOL Pure beta agonist Beta 1-inc HR,CO,CONTRACTILITY,SBP Beta 2-dec PVR,DBP Dose- 1-5 mic/min Metabolism-COMT in liver Effective in patient with heart block
  • 17. DOBUTAMINE Synthetic catecholamine Derived from isoproterenol Potent alpha 1 agonist Weak beta 1 &2 agonist <5mic/kg/min-beta 1, alpha 1 >5mic/kg/min-alpha 1 >10 mic/kg/min- prone for arrhythmia
  • 18. EPHEDRINE Indirect acting synthetic sympathomimetic- alpha and beta 5-10 mg IV Tachyphylaxis can occur IV – inc HR,SBP Hypotension due to Regional blockade and GA induction Oral- treat bronchial asthma IM-0.5 mg/kg- antiemetic
  • 19. PHENYLEPHRINE Hydroxy phenylethylamine Direct alpha 1 Inc PVR,MAP 50-200 mic iv bolus Infusion-20-100 mic/min Nasal -1%-decongestant
  • 20. DIGOXIN Cardiac glycoside Extracted from foxglove plant 60-80% oral bioavailability Peak plasma conc- 1-3 hours following oral administration 100% iv bioavailability-attain peak plasma conc immediately Excreted entirely by kidneys Half life -1-2 days- inversely proportional to GFR(inc with age and renal disease.
  • 21. ORAL IV ONSET OF ACTION 0.5-2hrs 10-30mins PEAK EFFECT 6hrs 2-4hrs Mechanism of action-selective and reversible cardiac sarcolemmal Na+_K+ ATPase inhibitor Increases intracellular calcium –responsible for ionotropic action • Other benefits- 1. No change in heart rate 2. Decrease in LV preload and afterload 3. Decrease in wall tension 4. Decrease in oxygen consumption in failing heart
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  • 23. ECG findings obtained at therapeutic plasma concentrations include  Prolonged PR interval-delayed Av nodal conduction  Shortened QTc intervals-rapid ventricular repolarization  ST depression-scaphoid/scooped out-decreased phase 3 depolarization of cardiac action potentials.  Diminished /inverted T wave NARROW THERAPEUTIC RANGE
  • 24. Digoxin toxicity 20% of patients treated with cardiac glycosides –report digitalis toxicity AT RISK INDIVIDUALS: -Renal dysfunction -Diuretics-potassium depletion-arrhythmia -Hyperventilation-decrease potassium 0.5mEq/L for 10mmHg decrease in PaCO2 -Electrolyte imbalance –Hypokalemia,Hypercalcemia,Hypomagnesemia -Hypoxemia induced sympathetic nervous system activity
  • 25. Plasma conc < 0.5ng/ml-no toxicity Therapeutic range-0.5-2.5ng/ml Toxic range>3.0ng/ml Treatment - treat the underlying cause -treat cardiac dysrhythmias Phenytoin-0.5-1.5mg/kg IV over 5 mins Lidocaine-1-2mg/kg IV Atropine-35-70mic/kg IV K+ supplementation-0.025-0.050 mEq/L -Life threatening toxicity- digoxin antibodies -Temporary artificial transvenous cardiac pacemaker-if complete heart block is present.
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