Acute Vasodilator Testing in Pulmonary Hypertension: What, When, and How?

Similar documents
Pulmonary Hypertension in 2012

22nd Annual Heart Failure 2018 an Update on Therapy. Pulmonary Arterial Hypertension: Contemporary Approach to Treatment

Update in Pulmonary Arterial Hypertension

Cardiac Catheterization is Unnecessary in the Evaluation of Patients with Pulmonary Hypertension: CON

Pulmonary Hypertension. Murali Chakinala, M.D. Washington University School of Medicine

Effective Strategies and Clinical Updates in Pulmonary Arterial Hypertension

ADCIRCA (tadalafil) The World Health Organization (WHO) has classified pulmonary hypertension into five different groups: (2)

PVDOMICS. Study Introduction. Kristin Highland, MD Gerald Beck, PhD. NHLBI Pulmonary Vascular Disease Phenomics Program

Approach to Pulmonary Hypertension in the Hospital

REVATIO (sildenafil)

Pulmonary Hypertension: Clinical Features & Recent Advances

The World Health Organization (WHO) has classified pulmonary hypertension into five different groups: (2)

Anjali Vaidya, MD, FACC, FASE, FACP Associate Director, Pulmonary Hypertension, Right Heart Failure, and Pulmonary Thromboendarterectomy Program

The World Health Organization (WHO) has classified pulmonary hypertension into five different groups: (2)

PDE5 INHIBITOR POWDERS Sildenafil powder, Tadalafil powder

PVDOMICS. Study Introduction. Kristin Highland, MD Gerald Beck, PhD. NHLBI Pulmonary Vascular Disease Phenomics Program

Recruitment and Consenting

Pulmonary arterial hypertension. Pulmonary arterial hypertension: newer therapies. Definition of PH 12/18/16. WHO Group classification of PH

The World Health Organization (WHO) has classified pulmonary hypertension into five different groups: (2)

Pulmonary Arterial Hypertension - Overview

Pulmonary Arterial Hypertension - Overview

Pulmonary Hypertension: Definition and Unmet Needs

The World Health Organization (WHO) has classified pulmonary hypertension into five different groups: (3)

The World Health Organization (WHO) has classified pulmonary hypertension into five different groups: (2)

Pulmonary Hypertension: Another Use for Viagra

The World Health Organization (WHO) has classified pulmonary hypertension into five different groups: (2)

The World Health Organization (WHO) has classified pulmonary hypertension into five different groups: (2)

Paediatric PAH in the current era

MACITENTAN DEVELOPMENT IN CHILDREN WITH PULMONARY HYPERTENSION (PAH)

Pulmonary Hypertension Due to Left Heart Disease

PULMONARY HYPERTENSION RESPIRATORY & CRITICAL CARE CONFERENCE APRIL 21, 2016 LAURA G. HOOPER

Disclosure. Pulmonary Hypertension (PH) Pulmonary Arterial Hypertension: Diagnosis and Novel Management Strategies. Objectives

The World Health Organization (WHO) has classified pulmonary hypertension into five different groups: (2)

Pulmonary Hypertension Perioperative Management

Pulmonary Hypertension: When to Initiate Advanced Therapy. Jonathan D. Rich, MD Associate Professor of Medicine Northwestern University

Update on pulmonary HTN

ADVANCED THERAPIES FOR PHARMACOLOGICAL TREATMENT OF PULMONARY HYPERTENSION

A Best Practices Approach to Treating Pulmonary Hypertension for the ED and Acute Care Provider. Disclosures

Pulmonary Hypertension and Left Heart Disease: What s good for the goose is not necessary good for the gander

Pulmonary Hypertension A-Z

Teaching Round Claudio Sartori

Pulmonary Arterial Hypertension: The Approach to Management in 2019

Disclosures. Objectives 6/16/2016. A Look at the Other Side: Focus on the Right Ventricle and Pulmonary Hypertension

Disclosures. Objectives. RV vs LV. Structure and Function 9/25/2016. A Look at the Other Side: Focus on the Right Ventricle and Pulmonary Hypertension

Oral Therapies for Pulmonary Arterial Hypertension

Pharmacy Management Drug Policy

1. Phosphodiesterase Type 5 Enzyme Inhibitors: Sildenafil (Revatio), Tadalafil (Adcirca)

PULMONARY HYPERTENSION

Pulmonary Hypertension. Pulmonary Arterial Hypertension Diagnosis, Impact and Outcomes

THERAPEUTICS IN PULMONARY ARTERIAL HYPERTENSION Evidences & Guidelines

Therapeutic approaches in P(A)H and the new ESC Guidelines

Pulmonary Heart Disease: Evaluation and Management

Anjali Vaidya, MD, FACC, FASE, FACP Associate Director, Pulmonary Hypertension, Right Heart Failure, Pulmonary Thromboendarterectomy Program Advanced

Neonatal and Pediatric Pulmonary Vascular Disease

Recent Treatment of Pulmonary Artery Hypertension. Cardiology Division Yonsei University College of Medicine

The Hemodynamics of PH Interpreting the numbers

The Case of Marco Nazzareno Galiè, M.D.

Pharmacy Coverage Guidelines are subject to change as new information becomes available.

Clinical implication of exercise pulmonary hypertension: when should we measure it?

Pulmonary Hypertension in Chronic Obstructive Pulmonary Disease

Sotatercept PULSAR Phase 2 PAH Webinar. March 28, 2018

Real-world experience with riociguat in CTEPH

Right Ventricular Failure and Pulmonary Hypertension 2011

Filtering through the Facts: Portopulmonary Hypertension Saturday, September 19, :15 10:05 a.m.

4/14/2010. Pulmonary Hypertension: An Update. Tim Williamson, MD, FCCP. University of Kansas Hospital. Normal Physiology

2015 State-of-the-Art Management of Pulmonary Hypertension Based on an Understanding of the Various Etiologies

Identifying Appropriate Treatment & Management Strategies in Pulmonary Arterial Hypertension

Patient Case. Patient Case 6/1/2013. Treatment of Pulmonary Hypertension in a Community

Pulmonary Hypertension: Evolution and

Pulmonary Arterial Hypertension (PAH): Emerging Therapeutic Strategies

Corporate Medical Policy

Pharmacy Management Drug Policy

Pulmonary vascular remodelling: causes, mechanisms and consequences

Pharmacy Management Drug Policy

CONUNDRUMS IN PULMONARY ARTERIAL HYPERTENSION

Navigating the identification, diagnosis and management of pulmonary hypertension using the updated ESC/ERS guidelines

Ειδικές θεραπείες σε µη-αρτηριακή πνευµονική υπέρταση, πότε; - Στέλλα Μπρίλη Α Πανεπιστηµιακή Καρδιολογική Κλινική Ιπποκράτειο Νοσοκοµείο Αθηνών

Where are we now in the longterm. of PAH and CTEPH? Hits and misses of medical treatment. Hap Farber Boston University School of Medicine, Boston, USA

The Circle of New Life for Pulmonary Hypertension Patients: Where does Palliative Care have a role in the new treatment era?

Pulmonary Hypertension: ICD-10 I27.0, I27.2

Treatment of Paediatric Pulmonary Hypertension

Pulmonary Arterial Hypertension in Pa)ents with HIV Infec)on: New Thoughts, BeGer Outcomes

Clinical Policy: Macitentan (Opsumit) Reference Number: ERX.SPMN.88

PULMONARY ARTERIAL HYPERTENSION AGENTS

Combination therapy in the treatment of pulmonary arterial hypertension 2015 update

Phosphodiesterase Type 5 Inhibitors: ADCIRCA (tadalafil) oral tablet REVATIO (sildenafil) oral suspension and tablet

Clinical Policy: Ambrisentan (Letairis) Reference Number: ERX.SPMN.84 Effective Date: 07/16

Pulmonary Arterial Hypertension Drug Prior Authorization Protocol

Multimodality imaging for PAH: Is CT better than MRI?

Pediatric Pulmonary Hypertension: Inside Out

NATIONAL INSTITUTE FOR HEALTH AND CLINICAL EXCELLENCE. Health Technology Appraisal. Drugs for the treatment of pulmonary arterial hypertension

PULMONARY HYPERTENSION For Cardiologists

Wednesday, April 25 Screening Diagnosis and Treatment of PAH: An Overview

2017 UnitedHealthcare Services, Inc.

Valutazione del neonato con sospetta ipertensione polmonare

Emerging Challenges in Primary Care: Evolving Strategies of Care in Pulmonary Arterial Hypertension: Integrating the Data into Practice

Drug Class Monograph. Policy/Criteria:

Transcription:

Acute Vasodilator Testing in Pulmonary Hypertension: What, When, and How? Teresa De Marco, MD University of California, San Francisco Disclosures: Grants/Research: United Therapeutics, Lung Biotechnology, Pfizer, Reata Consultant/Honoraria: Actelion, Gilead, Bayer. Cardiokinetics, Bellepharon I will discuss off-label use of drugs Review: Objectives Definition and classification of pulmonary hypertension (PH) The role of right heart catheterization and acute vasodilator testing in: Pulmonary arterial hypertension (WHO Group 1) PH due to left heart disease (WHO Group 2) How to perform and interpret results of the testing 1

Pulmonary Hypertension (PH) Sustained elevation of mean pulmonary artery pressure*: > 25 mmhg (Normal: 8-20 mmhg) * MPAP= 1/3(PAs-PAd) + Pad epasp echo Doppler > 40 mmhg Simonneau G, et al. J Am Coll Cardiol. 2004:43:5S-12 Simonneau G, et al, J Am Coll Cardiol. 2009;54:S43-54. 5 th WSPH Updated Classification of Pulmonary Hypertension, Nice 2013 GROUP 1 Pulmonary Arterial Hypertension (PAH) 1.1 Idiopathic PAH 1.2 Heritable PAH 1.3 Drug- and Toxin-Induced 1.4 Associated with: 1.4.1 Connective Tissue Disease 1.4.2 Human Immunodeficiency Virus (HIV) Infection 1.4.3 Portal Hypertension 1.4.4 Congenital Heart Disease 1.4.5 Schistosomiasis 1 PVOD and/or PCH 1 Persistent PH of the Newborn (PPHN) GROUP 2 PH Due to Left Heart Disease 2.1 LV Systolic Dysfunction 2.2 LV Diastolic Dysfunction 2.3 Valvular Disease 2.4 Congenital/Acquired Left Heart Inflow/ Outflow Tract Obstruction and Congenital Cardiomyopathies Simmoneau G, et al. JACC. 2013; 62:D34-41. GROUP 3 PH Due to Lung Disease and/or Hypoxia 3.1 Chronic Obstructive Pulmonary Disease 3.2 Interstitial Lung Disease 3.3 Other Pulmonary Diseases With Mixed Restrictive and Obstructive Pattern 3.4 Sleep-disordered Breathing 3.5 Alveolar Hypoventilation Disorders 3.6 Chronic Exposure to High Altitude 3.7 Developmental Lung Diseases GROUP 4 Chronic Thromboembolic PH (CTEPH) GROUP 5 PH With Unclear Multifactorial Mechanisms 5.1 Hematologic Disorders: Chronic Hemolytic Anemia, Myeloproliferative Disorders, Splenectomy 5.2 Systemic Disorders: Sarcoidosis, Pulmonary Histiocytosis, Lymphangioleiomyomatosis 5.3 Metabolic Disorders: Glycogen Storage Disease, Gaucher Disease, Thyroid Disorders 5.4 Others: Tumoral Obstruction, Fibrosing Mediastinitis, Chronic Renal Failure, Segmental PH 2

Etiology of PH on Echocardiogram Single center study from Australia 6,994 screened 936 pts (9.1%) with PH on ECHO (defined as epasp >40 mmhg) Strange G et al. Heart 2012;98:1806-1811. PH Diagnostic Guidelines Echocardiography Indicates PH Right Heart Catheterization Establish diagnosis based on hemodynamics Ascertain etiology Establish severity & prognosis Evaluate vasoreactivity Guide treatment Adapted from McGoon M, et al. Chest. 2004;126:14S-34S. 3

PAWP: Normal 4-12 mmhg TPG= mpap - PAWP Normal < 10 mmhg DPG= dpap PAWP Normal < 5 mmhg PVR= mpap - PAWP/CO Normal < 1 Wu PH Hemodynamic Profiles: Where is the lesion? (mean PAP > 25 mmhg) Pre-capillary PH Isolated post-capillary (Passive PH ) VC RA RV PA PV PC LA LV Ao Vachiery JL et al, J Am Coll Cardiol 2013;62: D100-8 Fang J et al, J Heart Lung Transplant 2012;31:913 33 Galie N et al, Eur Respir J 2009;34(6):1219-63 Combined post- & pre-capillary PH (Mixed PH) High flow PH nl range or PVR (CHD, AV fistula, thyrotoxicosis, chronic anemia) PH: Where is the lesion? (mean PAP > 25 mmhg) Pre-capillary PH PAWP < 15 mmhg TPG > 12; DPG > 7 mmhg PVR > 3 Wu VC RA RV PA PV PC LA LV Ao Group 1 PAH Modified from: Galie N et al. Eur Respir J. 2009. 34(6):1219-63 Fang J et al. J Heart Lung Transplant 2012;31:913 33 Vachiery JL et al, J Am Coll Cardiol 2013;62: D100-8 4

Algorithm for Assessment of Vasoreactivity in Patients with PAH (I/H/D) mpa 10 mmhg mpa < 40 mmhg No CO Right Heart Catheterization With Acute Vasoreactivity Testing (ino, epoprostenol, adenosine) Responder (<15%) [Better prognosis] Non - responder Consider: Hemodynamicallymonitored trial of Calcium Channel Blocker [<10% respond long-term] Consider: Oral ERAs/PDE5-I/sGC stim. IV Epoprostenol Inhaled Iloprost SQ/IV/inhaled/po Treprostinil Therapeutic Targets for PAH Endothelin pathway Endothelin cells Nitric oxide pathway Vessel lumen Prostacyclin pathway Pre-proendothelin Proendothelin Arachidonic acid Prostaglandin I 2 Endothelin receptor A Endothelin receptor antagonists Endothelin 1 Vasoconstriction and proliferation Endothelin receptor B L-arginine L-citrulline Phosphodiesterase type 5 Nitric oxide cgmp + Exogenous nitric oxide sgc stimul. Vasodilation and antiproliferation Prostacyclin (prostaglandin I 2 ) camp + Vasodilation and antiproliferation Prostacyclin derivatives Smooth muscle cells Phosphodiesterase type 5 inhibitor Humbert M, Sitbon O, Simonneau G. N Engl J Med 2004;351:1425-36 5

FDA-Approved Specific Therapies for PAH Endothelin Receptor Antagonists (oral) Bosentan Ambrisentan Macitentan Phosphodiesterase Type-5 Inhibitors (oral) Sildenafil Tadalafil Soluble Guanylate Cyclase Stimulators (oral) Riociguat (also approved for CTEPH) Prostacyclin Derivatives Epoprostenol: IV Iloprost: inhalational Treprostinil: inhalational, oral, SQ or IV FDA-Approved Specific Therapies for PAH Endothelin Receptor Antagonists Bosentan Ambrisentan Macitentan Phosphodiesterase Type-5 Inhibitors Sildenafil: Tadalafil Soluble Guanylate Cyclase Stimulators Riociguat (also approved for CTEPH) Prostacyclin Derivatives Epoprostenol: IV Iloprost: inhalational Treprostinil: inhalational,oral, SQ or IV 6

PH Classification Group 2: PH due to left heart disease LV Systolic dysfunction LV Diastolic dysfunction Valvular disease LH obstruction & Congenital CMP PH: Where is the lesion? (mean PAP > 25 mmhg) Isolated Post-Capillary PH PAWP>15 mmhg TPG < 12; DPG < 7 mmhg PVR nl range VC RA RV PA PC Simonneau G et al, J Am Coll Cardiol 2013;62:D34-41 Vachiery JL et al, J Am Coll Cardiol 2013;62: D100-8 Fang J et al, J Heart Lung Transplant 2012;31:913 33 Galie N et al, Eur Respir J 2009;34(6):1219-63 PV LA PVP LAP MR LV LVEDP Ao Systemic HTN AoV Disease Myocardial Disease Dilated CMP-ischemic/non-isc. Obesity-related CMP Hypertrophic CMP Restrictive/infiltrative CMP Pericardial disease PH: Where is the Isolated Post-Capillary PH lesion? PAWP>15; TPG <12; DPG <7 mmhg PVR nl range Atrial Myxoma Cor Triatriatum VC RA RV PA PV PC PVP LA LAP LV Ao MV Disease VC RA RV PA PV PC PVP Simonneau et al, J Am Coll Cardiol 2013;62:D34-41 Vachiery JL et al, J Am Coll Cardiol 2013;62: D100-8 Fang J et al, J Heart Lung Transplant 2012;31:913 33 Galie N et al, Eur Respir J 2009;34(6):1219-63 PV compression LA LV Ao 7

PH: Where is the lesion? Left sided filling pressure Neurohormones, cytokines, other mediators VC RA RV PA PC PV LA PVP LAP LV LVEDP Ao Simonneau et al, J Am Coll Cardiol 2013;62:D34-41 Vachiery JL et al, J Am Coll Cardiol 2013;62: D100-8 Fang J et al, J Heart Lung Transplant 2012;31:913 33 Galie N et al, Eur Respir J 2009;34(6):1219-63 Combined post- & pre-capillary (Cpc) PH Mixed hemodynamic profile PAWP > 15 mmhg TPG>12-15; DPG > 7 PVR > 3 Wu Responsive vs. Not-responsive Reversible vs. Irreversible (Diuretics,NTP, Inodilators, Sildenafil, Other agents) Moraes et al, Circ 2000; 1718 PH due to Left HF: Prevalence & Prognosis Prevalence: 25% to 80% in HF population (definition of PH is highly variable; referral bias; HFrEF vs HFpEF; acute vs chronic HF; mild vs severe HF) Cpc or Mixed PH: 47% in ADHF (ESCAPE); 35% in other series PH complicating left HF: Worse prognosis due to RV failure Increases morbidity and mortality (2X PVR > 3 Wu) Associated with exercise capacity Inverse relationship: peak VO 2 and resting mean PAP or PVR Positive correlation: resting RV ejection fraction and peak VO 2 in heart transplant candidates Pre- heart transplant, acutely irreversible, mixed PH is associated with high post-transplant mortality (up to 40%) Butler et al, J Am Coll Cardiol; 1999;34:1802 Cappola et al, Circ 2002;105:1663 Costard-Jackle et al. J Am Coll Cardiol;1992;19:48 Erickson et al. J Heart Transpl 1990;9:526 DiSalvo et al. J Am Coll Cardiol; 1995;25:1143 Kirklin et al. J Heart Lung Transpl 1988: 7:331 Khush et al. Am Heart J; 2009;157:1026 Abramson et al, Ann Int Med; 1992;116:888 Ghio et al, J Am Coll Cardiol;2001;37:183 Moraes et al, Circ 2000; 1718 8

Severity of Cpc* or Mixed PH in Left HD Mean PAP (mmhg) TPG (mmhg) PVR (Wood units) Mild 25-34 10-12 2.5-3.4 Moderate 35-44 13-15 3.5-4.9 Severe >45 >15 >5 In OHT: Morbidity & mortality risk is a continuous risk that increases with progressive elevation in MPAP, TPG, PVR * Combined post- & pre- capillary PH Murali S. Advances in PH 2006; 5:30 Kirklin et al. J Heart Lung Transpl 1988: 7:331 Proposed Algorithm For Management of Mixed PH in Left HF Cpc-PH or Mixed PH due to Left HF On standard, guidelines directed therapy Acute/Subacute Vasoreactivity Testing (NTP, Milrinone) Vasoreactive/Reversible PAsP < 50 mmhg TPG <15 mmhg;pvr < 2.5-3 Wu SAP >85 mmhg (q 3-6 mos RHC) Transplant eligible Heart transplant PH resolves or becomes vasoreactive (Frequent RHC) Adapted from Murali S, Adv in PH 2006;5:33 Mehra et al. J Heart Lung Transplant 2006; 25:1024 Not vasoreactive Irreversible Aggressive chronic pharmacologic rx (IV inodilators, po PDE5-I*) MCS,VAD (RV) Combination rx * Persistent PH<1% Not transplant eligible Consider heart-lung transplantation Continue HF rx Invest. trials DT VAD (RV) * Investigational/ Off -label 9

Summary PH is characterized by different hemodynamic profiles depending on the underlying pathophysiology Right heart catheterization is an important modality in the evaluation of PH Goals of vasodilator testing in PH: Assess prognosis & severity of disease Guide therapy Therapeutic modalities are variable depending on etiology of PH 10