Monday, February 16, 2009

Management of Heart Failure By MOH


Posted by:Dr.Zharif




Investigation

Blood test – FBC, renal function, liver function, glucose, lipid profile

urinalysis – proteinuria, glycosuria

Other important investigations include:

• echocardiogram – to identify structural abnormalities and assess LV systolic

and diastolic dysfunction

natriuretic peptides or their precursors (especially BNP and NT-proBNP) – If available, this investigation is useful in the evaluation of patients presenting IIa.A with acute dyspnoea in the urgent care setting in whom the clinical diagnosis of HF is uncertain. A low-normal concentration of this marker in an untreated patient makes the diagnosis of HF unlikely.Thus it is a useful “rule–out” test in doubtful cases.

Additional investigations when indicated;

Blood tests:

– cardiac biomarkers – thyroid function tests

– C-reactive protein (to look for inflammation)

Tests for myocardial ischemia and/or viability: – treadmill exercise test

– stress echocardiography (exercise or pharmacological)

– radionuclide studies

– cardiac magnetic resonance imaging (CMR)

Invasive tests:

– coronary angiography – cardiac catheterization – endomyocardial biopsy

Others:

– Holter electrocardiography, loop recorders and long-time ECG recording – pulmonary function tests


Management

The principles of management are:

Rapid recognition of the condition

Stabilization of hemodynamics

Improvement in clinical symptoms and signs

Identification and treatment of the

– underlying cause

– precipitating / aggravating factors.

The initial management includes a combination of the following first line therapy:

Oxygen – 5 to 6 liters/minute, by mask with the aim of achieving oxygen saturation of more than 95% in order to maximize tissue oxygenation and to prevent end organ dysfunction or multi organ failure. Elective ventilation using non invasive positive pressure ventilation (Continuous Positive Airway Pressure [CPAP] or Bi-level Positive Airway Pressure [BiPAP])should be considered early if necessary Should the oxygen saturation be inadequate or the patient develop respiratory muscle fatigue, then endotracheal intubation and mechanical ventilation is necessary.

Frusemide – Intravenous (i.v.) frusemide 40 – 100mg. The dose should be

individualized depending on the severity of the clinical condition

Administration of a loading dose followed by a continuous infusion has been

shown to be more effective than repeated bolus injections alone .The

dose should be titrated according to clinical response and renal function.

Morphine sulphate – i.v. 3 – 5 mg bolus (repeated if necessary, up to a total maximum of 10mg). It reduces pulmonary venous congestion and sympathetic drive. It is most useful in patients who are dyspnoeic and restless. Intravenous anti-emetics (metoclopramide 10mg or prochlorperazine 12.5mg) should be administered concomitantly. Care must be exercised in patients with chronic respiratory diseases.

Nitrates - If the BP is adequate (SBP > 100 mmHg), nitrates are indicated as first line therapy in AHF. It should be administered sublingually or intravenously. The i.v. route is more effective and preferable. Patients should be closely monitored for hypotension. This commonly occurs with concomitant diuretic therapy. Studies have shown that the combination of i.v. nitrate and low dose frusemide is more efficacious than high dose diuretic treatment alone .

Extreme caution should be exercised in patients with aortic and mitral stenosis.

Nitrates are contraindicated in severe valvular stenosis



Route of

Dosages



Admin


Diuretics




Frusemide

IV

40mg – 100mg



Infusion

5 – 40mg/hour (better than very high bolus




doses)






Vasodilators




Nitroglycerin

Infusion

5ug/min increasing at intervals of 3 – 5 min




by 5ug/min increments up to 100 – 200




ug/min


Nitroprusside

Infusion

0.1 – 5ug/kg/min






Sympathomimetics




Dobutamine

Infusion

2 – 20ug/kg/min


Dopamine

Infusion

<2>




2 – 10ug/kg/min – inotropic doses




10 – 20ug/kg/min –




peripheral vasoconstriction


Noradrenaline

Infusion

0.02 – 1ug/kg/min till desired BP is




attained






Phosphodiesterase-




3- Inhibitors




Milrinone

Infusion

50ug/kg bolus then 0.375 – 0.75ug/kg/min








Grading of Recommendations of Therapies in the Management of AHF


Intervention

Grades of

Level of



Recommen-

Comments



Evidence



dation








INITIAL MANAGEMENT CONSISTS OF :





Maintain the oxygen saturation above


Oxygen

I

C


95%











Diuretics

I

B

Indicated for fluid retention







Nitrates

I

B

Contraindicated if SBP<>


with caution in valvular stenosis.











Morphine

IIb

C

Indicated in pts who are dyspnoeic and


restless











NOT RESPONSIVE TO INITIAL TREATMENT AND SBP≥100mmHg





continuous infusion; combination with






Diuretics

IIb

C

nitrates, dopamine, dobutamine or





thiazide


Dobutamine

IIa

C

Indicated for peripheral hypoperfusion +/-


pulmonary congestion











Dopamine

IIb

C

To improve renal perfusion and promote


(<2>µg/kg/min)

diuresis










Milrinone

IIb

C

Improves symptoms and hemodynamics.







Sodium

I

C

Indicated in hypertensive crisis and acute


Nitroprusside

valvular regurgitation










NOT RESPONSIVE TO INITIAL TREATMENT AND SBP<100mmhg





Indicated to increase the BP


Dopamine

IIa

C


(>2µg/kg/min)











Noradrenaline

IIb

C

Indicated to increase the BP










Indicated as a bridge till myocardial


IABP

I

B

recovery or heart transplant







Ventricular



Indicated as a bridge till myocardial


Assist Device




IIa

B

recovery or heart transplant


(VAD)









For more detail Information about Management of Heart Failure By MOH
u can download the pdf file HERE

2 comments:

Unknown said...

В исследовании Brown et al. (1986) на изолированных мышечных волокнах было показано, что оубаин (G-строфантин) потенцирует инотропные эффекты милринона. В исследовании Bohm et al. (1988) было показано, что предварительная обработка мышечных волокон миокарда изопреналином у пациентов с ЗСН ФК II-IV по NYHA приводила к усилению инотропного действия милринона, что по крайней мере теоретически может свидетельствовать о возможной клиническую эффективность комбинированного применения катехоламинергичних препаратов (изопреналин) и ингибиторов фосфодиэстеразы (милринона) у пациентов с терминальными стадиями ЗСН.
http://vetconsultplus.ru/032016/Milrinon-instrukcija-primeneniju-gumannoj-veterinarnoj-medicine-otzyvy-sobakam-koshkam.html

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