Volume administration Overload Hypovolemia. Volume and the failing RV Volume overload Increased wall tension Reduced contractility.

Slides:



Advertisements
Similar presentations
Pediatric Septic Shock
Advertisements

Dr Bronwyn Avard, July 2010  To understand the basic physiology of shock  To understand the pharmacodynamics and pharmacokinetics of vasoactive drugs.
Hemodynamic Monitoring
 Heart failure is a complex clinical syndrome Can result from:  structural or functional cardiac disorder  impairs the ability of the ventricle to.
Haemodynamic Monitoring
Pulmonary Hypertension and Congestive Heart Failure
PERIOPERATIVE HYPERTENSION The Role of DA-1 Agonists (Fenoldopam) R. Sheinbaum M.D. O. Wenker M.D.
Cardioanaesthesia. Coronary artery disease O 2 delivery Coronary blood flow = directly related to coronary perfusion pressure (CPP) CPP = aortic diastolic.
Cardiovascular Medications PICU Resident Talk Stanford School of Medicine Pediatric Critical Care Medicine June 2010.
Pharmacology DOR 101 Abdelkader Ashour, Ph.D. 9 th Lecture.
Cardiogenic Shock and Hemodynamics. Outline Overview of shock – Hemodynamic Parameters – PA catheter, complications – Differentiating Types of Shock Cardiogenic.
Drugs Used In the Treatment of Congestive Heart Failure(Cont) Garrett J. Gross, Ph.D. Drugs Used In the Treatment of Congestive Heart Failure(Cont) Garrett.
Chapter 15 Assessment of Cardiac Output
Pressure, Flow, and Resistance Understanding the relationship among pressure, flow and resistance can help you understand how cardiac output and vascular.
1 Cardiac Pathophysiology Part B. 2 Heart Failure The heart as a pump is insufficient to meet the metabolic requirements of tissues. Can be due to: –
MODULE F – HEMODYNAMIC MONITORING. Topics to be Covered Cardiac Output Determinants of Stroke Volume Hemodynamic Measurements Pulmonary Artery Catheterization.
Bio-Med 350 Normal Heart Function and Congestive Heart Failure.
CORONARY CIRCULATION DR. Eman El Eter.
CURRENT STATUS OF STRESS TESTING JOHN HAMATY D.O..
Hemodynamic Monitoring By Nancy Jenkins RN,MSN. What is Hemodynamic Monitoring? It is measuring the pressures in the heart.
The Vexing Problem of Vasoplegia
Heart Failure, HF CHF develops when plasma volume increases and fluid accumulates in the lungs, abdominal organs (liver especially), and peripheral tissues.
Congenital Heart Defects Functional Overview
Drugs for CCF Heart failure is the progressive inability of the heart to supply adequate blood flow to vital organs. It is classically accompanied by significant.
CONCEPTS OF NORMAL HEMODYNAMICS AND SHOCK
PHARMAKOLOGY VASOPRESSOR DRUGS DJUDJUK RAHMAD BASUKI Lab.Anestesi dan Terapi Intensive RSSA Malang.
Vasoactive Drugs and Shock
Causes Myocardial dysfunction eg IHD, CM Volume overload eg AR, MR Obstruction eg AS, HCM Diastolic dysfunction eg Constriction Mechanical problems eg.
Medical Progress: Heart Failure. Primary Targets of Treatment in Heart Failure. Treatment options for patients with heart failure affect the pathophysiological.
Vasopressors and Inotropes in Canadian Emergency Departments
CARDIAC DISEASE IN PREGNANCY. Physiologic Changes of Pregnancy Blood volume and cardiac output rise in pregnancy to a peak that is 150% of normal by 24.
Hemodynamic Monitoring
Chapter 16 Assessment of Hemodynamic Pressures
Heart failure Dr Rafat Mosalli. Objectives Definition Definition Pathophysiology Pathophysiology Age specific Causes Age specific Causes Clinical pictures.
Cardiac Failure Richard Price Richard Price Consultant, Intensive Care, RAH. Consultant, Intensive Care, RAH.
Nursing and heart failure
Bipyridines :(Amrinone,Milrinone ) only available in parenteral form. Half-life 3-6hrs. Excreted in urine.
PICU Resident Talk Stanford School of Medicine Pediatric Critical Care Medicine June 2014.
Inferior/Right Ventricular Infarction CLINICAL PRESENTATION AND TREATMENT Lady Minto Hospital Emergency Rounds February 2015 Prepared by Shane Barclay.
Do you want a Fluid Bolus?. Why give fluid – The theory? Increase preload, increase cardiac output, increase oxygen delivery.
Cardiogenic Shock Dr. Belal Hijji, RN, PhD October 12 & 15, 2011.
Copyright 2008 Society of Critical Care Medicine
Diagnosis and Management of Shock Dr. Anas Khan Consultant, EM MBBS, MHA, ArBEM.
Definition and Classification of Shock
How and when should we monitor CO and SV in shock? When would I want to measure CO or SV in shock ? Alexandre Mebazaa, MD, PhD University Paris 7 Anesthesiology.
Giving our patients the best chance to survive shock Erik Diringer, DO Intensivist – Kenmore Mercy Hospital.
Systolic Versus Diastolic Failure. Forms of Heart Failure Sytolic Failure Inability of the ventricle to contract normally and expel sufficient blood Inadequate.
Copyright © 2008 Thomson Delmar Learning CHAPTER 15 Hemodynamic Measurements.
Differentiate Pulmonary arterial hypertension from pulmonary venous congestion.
Intensive Care Cardiovascular Pharmacology
 Introduction  Classification of inotropes  Postoperative myocardial dysfunction.  Choice of inotrope  Indications in specific settings.
– Dr. J. Satish Kumar, MD, Department of Basic & Medical Sciences, AUST General Medicine CVS Name:________________________________________ Congestive Heart.
Overview of Receptors and Drugs
Exercise Management Chronic Heart Failure Chapter 12.
1 Special circulations, Coronary, Pulmonary… Faisal I. Mohammed, MD,PhD.
Hemodynamic Monitoring John Nation RN, MSN Thanks to Nancy Jenkins.
PHARMACOLOGIC THERAPY  Standard First-Line Therapies Angiotensin-Converting Enzyme Inhibitors (ACEI) β Blockers Diuretics Digoxin  Second line Therapies.
Shock and its treatment Jozsef Stankovics Department of Paediatrics, Medical University of Pécs 2008.
N Engl J Med 2010;362: R3 CHAE JUNGMIN/ Prof KIM MYENGGON.
Melanie Tan C is for Circulation Locum Consultant in Anaesthesia, UCLH.
신장내과 R4 강혜란 Cardiorenal syndrome (CRS).  Patients with heart failure (HF) who have a reduced GFR -> Mortality ↑  Patients with chronic kidney disease.
Heart Failure NURS 241 Chapter 35 (p.797).
Drugs Used to Treat Heart Failure
Use of High Flow Nasal Cannula and Aerosolized Epoprostenol as a Bridge to Lung Transplantation Sherwin Morgan, RRT, Steve Mosakowski, RRT, Stephanie Ostrawski,
Pulmonary Vascular Disease Anaesthetic implications and strategies
Treatment of Congestive Heart Failure
Traditional parenteral antihypertensive treatment
Definition and Classification of Shock
Dr Satti Abdelrahim Satti Pediatric Consultant
Inhaled iloprost in patients with chronic thromboembolic pulmonary hypertension: effects before and after pulmonary thromboendarterectomy  Thorsten Kramm,
Presentation transcript:

Volume administration Overload Hypovolemia

Volume and the failing RV Volume overload Increased wall tension Reduced contractility

 41 acutely ill patients receiving 300 cc albumin over 30 minutes  All patients had an RVEF-capable Swan-Ganz catheter  Measurements included RVEDVI, calculated from (CI/HR) / RVEF Chest 1990;98:1450-4

Volume challenge and RV response

Findings  Patients with high baseline RVEDVI did not benefit from volume loading  In all other patients RVESVI and RVEDVI did increase similarly with volume  CVP is a poor predictor of volume responsiveness  (Normal) RV output is preload-dependent  In the failing RV, judicious volume management is necessary, and fluid removal may eventually help with recovery

Volume status  Gentle volume challenge in the early stage of RV failure (only shown for acute PE)  Close monitoring of fluid status either with echo or using the CVP waveform, trend(, and number)  Excessive volume loading may worsen RV performance (RV distention, TR, ventricular interdependence)  Diuretics or ultrafiltration may be indicated, but have not been studied in this population  Loop diuretic resistance in chronic heart failure sometimes requires addition of a thiazide diuretic drug

Cardiac output Contractility Cardiac output Tachyarrhythmia Increased afterload (Systemic hypotension)

Sympathomimetic inotropes  Improves contractility (RVSWI and RVEF) despite an increase in mPAP  Never studied in patients with pulmonary hypertension  Up to 5 mcg/kg/min  Increases CO, reduces PVR and SVR  Less tachycardiac than dopamine  Higher doses can cause systemic hypotension EpinephrineDobutamine Intensive Care Med 1997;23: Crit Care Med 2003;31:1140-6

Sympathomimetic inotropes  Primarily chronotropic agent  Described in the heart transplant population  Can cause significant arrhythmias  Dopamine increases CO  Almost always causes (at least) mild tachycardia  Increases PVR/SVR ratio IsoproterenolDopamine Crit Care Med 1991;19:60-7 Br Heart J 1975;37:482-5 J Pediatr 2002;140:373-5

PDE inhibitors

 They all augment contractility and produce vasodilation  Mild tachycardia is common  Good human data exists for LV dysfunction, but is somewhat scarce for RV failure  Potential advantage is pulmonary vasodilation, which is via PDE3-receptors and not specific  Can cause significant systemic hypotension Ann Thorac Surg 1997;63: Clin Transplant 2010;24:515-9

Cardiac output  Dobutamine should be used for RV failure; the dose should not be higher than 10 mcg/kg/min  Higher doses may cause tachycardia, arrhythmias, and systemic hypotension  Epinephrine is probably preferred in the setting of low arterial blood pressure  PDE inhibitors like milrinone are probably similar to dobutamine, but act via a different receptor system and are more potent pulmonary vasodilators

Pulmonary vascular resistance  RV is a high-volume low-pressure chamber  It has about 1/6 of the LV’s muscle mass  There is little tolerance to acute increases in afterload (From Braunwald, 1984)

Targets for reducing PVR N Engl J Med 2004;351: Inhaled agents are always preferred in the acute setting

Nitric oxide  Rapid half-life, inactivated by hemoglobin  Virtually no systemic vasodilation, need for continuous application  Studied in a variety of perioperative settings, small studies  NO improves hemodynamics, but has not been shown to improve outcomes  High cost (for how long?)

Nitric oxide in LVAD patients?  150 patients undergoing LVAD with increased preoperative PVR  NO versus placebo, option of open-label NO in the presence of RV failure  Primary endpoint: RV failure  Secondary endpoints:  Length-of-stay  RVAD rate  No significant differences J Heart Lung Transplant 2011;30:870-8

Alternatives  Safe and effective in the setting of cardiac surgery  Easy to administer  Potential cost-saver  PDE5 inhibitor  Relatively selective  As effective as NO  Synergistic effect  No differences in systemic blood pressure Inhaled epoprostenolOral sildenafil J Thorac Cardiovasc Surg 2004;127: NO = $3000 vs. EPO = $150 NO = $3000 vs. EPO = $150 Circulation 2002;105:

 58 patients with increased PVR  Comparison of hemodynamic effects  NO and prostacyclin equally lowered PVR, mPAP, and TPG as well as they increased CO  Nitroprusside lowered PVR, but also SVR and had to be discontinued in 62% of the cases due to low systemic blood pressure J Card Surg 2005;20:171-6

Am J Respir Crit Care Med 1996;153: Circles = S a O 2 Diamonds = MAP Squares = F i O 2

Importance of maintaining systemic blood pressure  RCA perfusion throughout the cardiac cycle  As PVR approaches SVR, coronary perfusion will decrease  Adequate perfusion pressure needed to prevent RV ischemia  Maintain positive SVR/PVR or MAP/mPAP ratio Aortic pressure Coronary flow

Which vasopressor?  Potential vasoconstriction, but improved PVR/SVR ratio in most studies  Additional positive inotropic effect via beta- receptor  Improved coronary blood flow during exercise by endogenous norepinephrine  Some small, but promising studies  Potent peripheral vasoconstrictor  Potential pulmonary vasodilation NorepinephrineVasopressin Anaesthesia 2002;57:9-14 Exp Biol Med 2002;227: Eur J Cardiothorac Surg 2006;29:952-6 Am J Physiol 1994;267:H2413-9

Anesthesiology 1984;60:132-5 In the presence of increased RV afterload, volume expansion causes deterioration of ventricular function likely due to increased wall stress Distention imposes increased wall stress, this can cause RV ischemia Volume-induced RV dysfunction was reversed by norepinephrine Ventricular interdependence caused SV to decrease despite constant or slightly increased LVEDP

Summary I Pulmonary hypertension is a serious disease associated with increased perioperative mortality Worsening RV dysfunction determines of symptoms and outcome Important to distinguish pulmonary arterial and pulmonary venous hypertension

Summary II Treatment of underlying disease and influencing factors is mandatory Supportive therapy includes: Careful ptimization of volume status Maintenance of RV perfusion pressure Enhancing RV contractility Reduction of RV afterload

Thank you!