Real-world experience with riociguat in CTEPH

Size: px
Start display at page:

Download "Real-world experience with riociguat in CTEPH"

Transcription

1 Real-world experience with riociguat in CTEPH Matthias Held Center of Pulmonary Hypertension and Pulmonary Vascular Disease, Medical Mission Hospital, Würzburg, Germany Tuesday, 29 September ERS International Congress 2015

2 Disclosures Honoraria for lectures: Actelion, Bayer HealthCare, Berlin Chemie, Boehringer Ingelheim, GSK, Novartis, Pfizer Honoraria for advisory board activities: Actelion, Bayer HealthCare, GSK Participation in clinical trials: Actelion, Bayer HealthCare, GSK, Pfizer, United Therapeutics Research funding: Actelion

3 Overview Treatment of CTEPH: PEA, medical treatment or BPA? Medical therapy of CTEPH in inoperable patients before approval of riociguat Follow-up of patients after PEA, and detection of persistent/recurrent CTEPH Medical therapy in patients with persistent/recurrent CTEPH Medical therapy of CTEPH in inoperable patients after approval of riociguat BPA, balloon pulmonary angioplasty; PEA, pulmonary endarterectomy.

4 CTEPH treatment algorithm Diagnosis confirmed by CTEPH expert center Lifelong anticoagulation Operability assessment by a multidisciplinary CTEPH team Acceptable risk:benefit ratio Technically operable Technically non-operable Copyright protected content. Please view original Non-acceptable content in the following reference: Galiè N et al. Eur Heart risk:benefit J 2015:doi: /eurheart/ehv317 ratio a Targeted medical therapy Pulmonary endarterectomy Persistent symptomatic PH Consider BPA in expert center b Consider lung transplantation Persistent severe symptomatic PH a Technically operable patients with non-acceptable risk/benefit ratio can also be considered for BPA. b In some centers medical therapy and BPA are initiated concurrently. BPA, balloon pulmonary angioplasty. Galiè N et al. Eur Heart J 2015:doi: /eurheart/ehv317.

5 Case study CASE STUDY October year-old female; history of PE 2007 Parameter Nov 2009 PAP (mmhg) 101/45 (65) PVR (dyn sec m 5 ) 1222 CI (L/min/m 2 ) 2.1 CTEPH Board decision 2009/2010: Unsuitable for PEA: Poor benefit:risk ratio Medical treatment: Off-label PAH therapy Sequential combination: ERA + PDE5 inhibitor CI, cardiac index; ERA, endothelin receptor antagonist; PDE5, phosphodiesterase type 5; PE, pulmonary embolism; PEA, pulmonary endarterectomy; PAP, pulmonary arterial pressure; PVR, pulmonary vascular resistance.

6 PEA Oct 2010; ERA stopped, PDE5 inhibitor continued CASE STUDY Pre-PEA Week 6 post-pea Month 18 post-pea Jul 2010 Jan 2011 May 2012 ERA, endothelin receptor antagonist; PDE5, phosphodiesterase type 5; PEA, pulmonary endarterectomy.

7 Overview Treatment of CTEPH: PEA, medical treatment or BPA? Medical therapy of CTEPH in inoperable patients before approval of riociguat Follow-up of patients after PEA, and detection of persistent/recurrent CTEPH Medical therapy in patients with persistent/recurrent CTEPH Medical therapy of CTEPH in inoperable patients after approval of riociguat BPA, balloon pulmonary angioplasty; PEA, pulmonary endarterectomy.

8 Follow-up after PEA CASE STUDY Improvement in FC ERA stopped post-pea PDE5 inhibitor continued PEA Parameter Sept 2010 Jan 2011 May 2012 Apr 2014 WHO FC IV II I I 6MWD (m) Echo spap (mmhg) 88 n/a n/a n/a April 2014: Riociguat is the only approved medical treatment for inoperable CTEPH, and persistent/recurrent CTEPH post-pea 6MWD, 6-minute walking distance; Echo, echocardiography; ERA, endothelin receptor antagonist; FC, functional class; n/a, not applicable; PDE5, phosphodiesterase type 5; PEA, pulmonary endarterectomy; spap, systolic pulmonary arterial pressure; WHO, World Health Organization. Bayer HealthCare. Adempas EU Summary of Product Characteristics, July 2015.

9 What would you recommend? 1. No action, follow up in 6 months 2. Stop PDE5 inhibitor 3. Perform RHC VOTE NOW! PDE5, phosphodiesterase type 5; RHC, right heart catheterization.

10 Importance of RHC in follow-up after PEA PEA CASE STUDY Sept 2010 Jan 2011 May 2012 Apr 2014 WHO FC IV II I I 6MWD (m) Echo spap (mmhg) 88 n/a n/a n/a RHC mpap (mmhg) PVR (dyn sec m 5 ) CO (L/min) Follow-up after PEA: Echo can miss the diagnosis of persistent/recurrent CTEPH RHC required 6MWD, 6-minute walking distance; CO, cardiac output; Echo, echocardiography; FC, functional class; n/a, not applicable; mpap, mean pulmonary arterial pressure; PEA, pulmonary endarterectomy; PVR, pulmonary vascular resistance; RHC, right heart catheterization; spap, systolic pulmonary arterial pressure; WHO FC, World Health Organization functional class.

11 What would you recommend? 1. Stay on PDE5 inhibitor 2. Transition to riociguat 3. Add on riociguat VOTE NOW! PDE5, phosphodiesterase type 5.

12 Improvements seen following transition from PDE5 inhibitor to riociguat CASE STUDY PEA Riociguat transition Sept 2010 Jan 2011 May 2012 Apr 2014 Jul 2015 WHO FC IV II I I I I Sep MWD (m) Echo spap (mmhg) 88 n/a n/a n/a n/a n/a RHC mpap (mmhg) PVR (dyn sec m 5 ) CO (L/min) MWD, 6-minute walking distance; CO, cardiac output; Echo, echocardiography; FC, functional class; mpap, mean pulmonary arterial pressure; n/a, not applicable; PEA, pulmonary endarterectomy; PVR, pulmonary vascular resistance; RHC, right heart catheterization; spap, systolic pulmonary arterial pressure; WHO FC, World Health Organization functional class.

13 Overview Treatment of CTEPH: PEA, medical treatment or BPA? Medical therapy of CTEPH in inoperable patients before approval of riociguat Follow-up of patients after PEA, and detection of persistent/recurrent CTEPH Medical therapy in patients with persistent/recurrent CTEPH Medical therapy of CTEPH in inoperable patients after approval of riociguat BPA, balloon pulmonary angioplasty; PEA, pulmonary endarterectomy.

14 Experience achieving treatment goals: Scenarios for CTEPH in clinical reality Data to be included in manuscript currently in preparation ERA, endothelin receptor antagonist; i.v., intravenous; PDE5i, phosphodiesterase type 5 inhibitor. Held M et al. Manuscript in preparation.

15 Riociguat is a PH-targeted therapy with proven efficacy in CTEPH Class Drug Randomized pivotal clinical trials in CTEPH Primary endpoint met sgc stimulator Riociguat CHEST-1 and Prostanoid Epoprostenol Treprostinil Iloprost (AIR 4 ) Selexipag Bosentan BENEFiT 5 ERA PDE5 inhibitor Ambrisentan (AMBER I 6 ) Macitentan recruiting MERIT-1 7 Sildenafil Tadalafil ERA, endothelin receptor antagonist; PDE5, phosphodiesterase type 5; sgc, soluble guanylate cyclase. 1. Ghofrani HA et al. N Engl J Med 2013;369: Simonneau G et al. Eur Respir J 2015;45: Simonneau G et al. Eur Respir J 2014;44(Suppl.58): Olschewski H et al. N Engl J Med 2002;347: Jaïs X et al. J Am Coll Cardiol 2008;52: GlaxoSmithKline. AMBER I. Available at: (accessed Sept 2015). 7. Actelion. MERIT-1. Available at: (accessed Aug 2015).

16 Real-world data: The clinical reality in patients with CTEPH Single-center experience with riociguat beyond clinical studies Medical Mission Hospital, Würzburg Apr 2014 May 2015: N=56 Data overall: Prevalent patients (change of existing therapy) Incident Data patients to be included (initiation in manuscript of new therapy) currently in preparation Held M et al. Manuscript in preparation.

17 Mean 6MWD (m) Mean NT-proBNP (pg/ml) Improvements in 6MWD and NT-proBNP 3 months after transitioning to riociguat Overall CTEPH population m (p=0.003) pg/ml (p=0.04) Data to be included in manuscript currently in preparation n=56 50 n=56 n=56 n=56 n= Baseline Follow-up (3 months) 0 Baseline Follow-up (3 months) 6MWD, 6-minute walking distance; NT-proBNP, N-terminal prohormone of brain natriuretic peptide. Held M et al. Manuscript in preparation.

18 Are symptoms observed in CTEPH necessarily side effects of treatment? (I) Data to be included in manuscript currently in preparation bpm, beats per minute; DBP, diastolic blood pressure; HR, heart rate; SBP, systolic blood pressure. Held M et al. Manuscript in preparation.

19 Are symptoms observed in CTEPH necessarily side effects of treatment? (II) Data to be included in manuscript currently in preparation *Adverse events occurring in 5% of patients in either group. 1. Ghofrani et al. N Engl J Med 2013;369:319 29; 2. Held M et al. Manuscript in preparation.

20 How to deal with symptoms and potential side effects (I) CASE STUDY Case 60-year-old patient on riociguat with syncope BP (right arm) 155/85 mmhg Medication Riociguat 2.5 mg tid Ramipril 5/25 mg comp qd/bid Nevibolol 5 mg qd Atorvastatin 10 mg qd L-thyroxin 75 µg qd Omeprazole 40 mg qd Dreisafer (Fe [II] sulfate monohydrate) 100 mg qd ASA 100 mg qd ASA, acetylsalicylic acid; BP, blood pressure; bid; twice daily; qd, once daily; tid, three times daily.

21 What would you recommend? 1. Watch and wait 2. Stop riociguat 3. Explore and investigate VOTE NOW!

22 How to deal with symptoms and potential side effects (II) CASE STUDY Flow acceleration in the subclavian artery subclavian stenosis Medication continued Stenting performed Symptoms and potential side effects require a careful diagnostic work-up!

23 Summary of single-center experience with riociguat beyond clinical studies Medical Mission Hospital, Würzburg High efficacy Mean change in 6MWD: +40 m Mean change in NT-proBNP: 891 pg/ml Good tolerability 64% of patients (n=56) on riociguat 2.5 mg tid Data to be included in manuscript currently in preparation 2% had intermittent treatment interruption Single case of syncope Not riociguat-related Caused by subclavian artery stenosis 6MWD, 6-minute walking distance; NT-proBNP, N-terminal prohormone of brain natriuretic peptide; tid, three times daily. Held M et al. Manuscript in preparation.

24 Summary: CTEPH and riociguat in the real world Riociguat consistently demonstrates clinically meaningful improvements in patients with inoperable CTEPH or persistent/recurrent CTEPH post-pea In a goal-orientated approach, scheduled follow-up of patients post-pea that includes RHC is important to accurately detect and treat persistent/recurrent CTEPH Careful diagnostic work-up of side effects is essential for correct identification of their cause Patients on historic off-label pretreatment should be carefully assessed PEA, pulmonary endarterectomy; RHC, right heart catheterization.

25 Thank you

Chronic Thromboembolic Pulmonary Hypertention CTEPH

Chronic Thromboembolic Pulmonary Hypertention CTEPH Chronic Thromboembolic Pulmonary Hypertention CTEPH Medical Management Otto Schoch, Prof. Dr. Klinik für Pneumologie und Schlafmedizin Kantonsspital St.Gallen CTEPH: Medical Management Diagnostic aspects

More information

*Division of Pulmonary, Sleep, and Critical Care Medicine, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI, USA

*Division of Pulmonary, Sleep, and Critical Care Medicine, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI, USA The Relationship between NO Pathway Biomarkers and Response to Riociguat in the RESPITE Study of Patients with PAH Not Reaching Treatment Goals with Phosphodiesterase 5 Inhibitors James R Klinger,* Raymond

More information

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

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 Where are we now in the longterm management of PAH and CTEPH? Hits and misses of medical treatment Hap Farber Boston University School of Medicine, Boston, USA Monday, 28 September ERS International Congress

More information

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

Therapeutic approaches in P(A)H and the new ESC Guidelines Therapeutic approaches in P(A)H and the new ESC Guidelines Jean-Luc Vachiéry, FESC Head Pulmonary Vascular Diseases and Heart Failure Clinic Hôpital Universitaire Erasme Université Libre de Bruxelles Belgium

More information

SATELLITE SYMPOSIUM OF MSD. sgc Stimulation for the treatment of PH. Real life management of PAH: case presentation

SATELLITE SYMPOSIUM OF MSD. sgc Stimulation for the treatment of PH. Real life management of PAH: case presentation SATELLITE SYMPOSIUM OF MSD sgc Stimulation for the treatment of PH Real life management of PAH: case presentation Eftychia Demerouti MD, MSc, PhD Cardiologist Onassis Cardiac Surgery Center Conflict of

More information

Oral Therapies for Pulmonary Arterial Hypertension

Oral Therapies for Pulmonary Arterial Hypertension Oral Therapies for Pulmonary Arterial Hypertension Leslie Wooten, PharmD PGY2 Internal Medicine Pharmacy Resident University of Cincinnati Medical Center April 30 th, 2018 Objectives Pharmacist Objectives

More information

Pulmonary Arterial Hypertension: The Approach to Management in 2019

Pulmonary Arterial Hypertension: The Approach to Management in 2019 Pulmonary Arterial Hypertension: The Approach to Management in 2019 Munir S. Janmohamed M.D. FACC Medical Director Mechanical Circulatory Support/Heart Failure Program Mercy General Hospital/Mercy Medical

More information

ΔΙΑΓΝΩΣΗ ΚΑΙ ΘΕΡΑΠΕΙΑ ΤΗΣ ΧΡΟΝΙΑΣ ΘΡΟΜΒΟΕΜΒΟΛΙΚΗΣ ΥΠΕΡΤΑΣΗΣ (CTEPH)

ΔΙΑΓΝΩΣΗ ΚΑΙ ΘΕΡΑΠΕΙΑ ΤΗΣ ΧΡΟΝΙΑΣ ΘΡΟΜΒΟΕΜΒΟΛΙΚΗΣ ΥΠΕΡΤΑΣΗΣ (CTEPH) Aristotle University of Thessaloniki Cardiology Clinic, AHEPA Hospital ΔΙΑΓΝΩΣΗ ΚΑΙ ΘΕΡΑΠΕΙΑ ΤΗΣ ΧΡΟΝΙΑΣ ΘΡΟΜΒΟΕΜΒΟΛΙΚΗΣ ΥΠΕΡΤΑΣΗΣ (CTEPH) Charalampos I. Karvounis, MD Professor of Cardiology Aristotle

More information

The Case of Marco Nazzareno Galiè, M.D.

The Case of Marco Nazzareno Galiè, M.D. The Case of Marco Nazzareno Galiè, M.D. DIMES Disclosures Consulting fees and research support from Actelion Pharmaceuticals Ltd, Bayer HealthCare, Eli Lilly and Co, GlaxoSmithKline and Pfizer Ltd Clinical

More information

Updates in Pulmonary Hypertension Pharmacotherapy. Ziad Sadik PharmD BCPS

Updates in Pulmonary Hypertension Pharmacotherapy. Ziad Sadik PharmD BCPS Updates in Pulmonary Hypertension Pharmacotherapy Ziad Sadik PharmD BCPS Disclosure Information I have no financial relationship to disclose AND I will not discuss off label use and/or investigational

More information

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

Pulmonary Hypertension: When to Initiate Advanced Therapy. Jonathan D. Rich, MD Associate Professor of Medicine Northwestern University Pulmonary Hypertension: When to Initiate Advanced Therapy Jonathan D. Rich, MD Associate Professor of Medicine Northwestern University Disclosures Medtronic, Abbott: Consultant Hemodynamic Definition of

More information

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

Anjali Vaidya, MD, FACC, FASE, FACP Associate Director, Pulmonary Hypertension, Right Heart Failure, and Pulmonary Thromboendarterectomy Program Anjali Vaidya, MD, FACC, FASE, FACP Associate Director, Pulmonary Hypertension, Right Heart Failure, and Pulmonary Thromboendarterectomy Program Advanced Heart Failure & Cardiac Transplant Temple University

More information

Progress in PAH. Gerald Simonneau

Progress in PAH. Gerald Simonneau Progress in PAH Gerald Simonneau National Reference center for Pulmonary Hypertension Bicetre University Hospital, INSERM U 999 Paris-Sud University Le Kremlin Bicêtre France Clinical Classification of

More information

Pharmacy Management Drug Policy

Pharmacy Management Drug Policy SUBJECT: Pulmonary Arterial Hypertension (PAH) POLICY NUMBER: Pharmacy-42 Clinical criteria used to make utilization review decisions are based on credible scientific evidence published in peer reviewed

More information

PULMONARY ARTERIAL HYPERTENSION AGENTS

PULMONARY ARTERIAL HYPERTENSION AGENTS Approvable Criteria: PULMONARY ARTERIAL HYPERTENSION AGENTS Brand Name Generic Name Length of Authorization Adcirca tadalafil Calendar Year Adempas riociguat Calendar Year Flolan epoprostenol sodium Calendar

More information

2017 UnitedHealthcare Services, Inc.

2017 UnitedHealthcare Services, Inc. UnitedHealthcare Pharmacy Clinical Pharmacy Programs Program Number 2017 P 2020-10 Program Prior Authorization/Medical Necessity PAH Agents Medication Adcirca (tadalafil), Adempas (riociguat), Letairis

More information

THERAPEUTICS IN PULMONARY ARTERIAL HYPERTENSION Evidences & Guidelines

THERAPEUTICS IN PULMONARY ARTERIAL HYPERTENSION Evidences & Guidelines THERAPEUTICS IN PULMONARY ARTERIAL HYPERTENSION Evidences & Guidelines Vu Nang Phuc, MD Dinh Duc Huy, MD Pham Nguyen Vinh, MD, PhD, FACC Tam Duc Cardiology Hospital Faculty Disclosure No conflict of interest

More information

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

Pulmonary arterial hypertension. Pulmonary arterial hypertension: newer therapies. Definition of PH 12/18/16. WHO Group classification of PH Pulmonary arterial hypertension Pulmonary arterial hypertension: newer therapies Ramona L. Doyle, MD Clinical Professor of Medicine, UCSF Attending Physician UCSF PH Clinic Definition and classification

More information

Drug Class Monograph. Policy/Criteria:

Drug Class Monograph. Policy/Criteria: Drug Class Monograph Class: Pulmonary Arterial Hypertension Agents Drugs: Adcirca (tadalafil), Adempas (riociguat), Flolan (epoprostenol), Letairis (ambrisentan), Opsumit (macitentan), Orenitram (treprostinil),

More information

Pulmonary Arterial Hypertension Drug Prior Authorization Protocol

Pulmonary Arterial Hypertension Drug Prior Authorization Protocol Pulmonary Arterial Hypertension Drug Prior Authorization Protocol Line of Business: Medicaid P&T Approval Date: February 21, 2018 Effective Date: April 1, 2018 This policy has been developed through review

More information

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

Anjali Vaidya, MD, FACC, FASE, FACP Associate Director, Pulmonary Hypertension, Right Heart Failure, Pulmonary Thromboendarterectomy Program Advanced Anjali Vaidya, MD, FACC, FASE, FACP Associate Director, Pulmonary Hypertension, Right Heart Failure, Pulmonary Thromboendarterectomy Program Advanced Heart Failure & Cardiac Transplant Temple University

More information

The Case of Lucia Nazzareno Galiè, M.D.

The Case of Lucia Nazzareno Galiè, M.D. The Case of Lucia Nazzareno Galiè, M.D. DIMES Disclosures Consulting fees and research support from Actelion Pharmaceuticals Ltd, Bayer HealthCare, Eli Lilly and Co, GlaxoSmithKline and Pfizer Ltd Clinical

More information

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

1. Phosphodiesterase Type 5 Enzyme Inhibitors: Sildenafil (Revatio), Tadalafil (Adcirca) This policy has been developed through review of medical literature, consideration of medical necessity, generally accepted medical practice standards, and approved by the IEHP Pharmacy and Therapeutic

More information

Real life management of CTEPH: patient case

Real life management of CTEPH: patient case 2 nd International Congress on cardiovascular imaging in clinical practice k Real life management of CTEPH: patient case Anastasia Anthi Pulmonary Hypertension Clinic, Attikon University Hospital, Athens

More information

Teaching Round Claudio Sartori

Teaching Round Claudio Sartori Teaching Round 14.03.2017 Claudio Sartori Cas clinique Femme 47 ans, connue pour un BPCO, asthénie, douleurs thoraciques, dyspnée à l effort, œdèmes membres inférieurs, deux syncopes. Tabac, BMI 31 kg/m2

More information

Case Presentation : Pulmonary Hypertension: Diagnosis and Imaging

Case Presentation : Pulmonary Hypertension: Diagnosis and Imaging Case Presentation 9.40-11.20: Pulmonary Hypertension: Diagnosis and Imaging Eftychia Demerouti MD, MSc, PhD Cardiologist Onassis Cardiac Surgery Center Conflicts of interest Consulting fees and fees for

More information

ADVANCED THERAPIES FOR PHARMACOLOGICAL TREATMENT OF PULMONARY HYPERTENSION

ADVANCED THERAPIES FOR PHARMACOLOGICAL TREATMENT OF PULMONARY HYPERTENSION Status Active Medical and Behavioral Health Policy Section: Medicine Policy Number: II-107 Effective Date: 04/21/2014 Blue Cross and Blue Shield of Minnesota medical policies do not imply that members

More information

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

PULMONARY HYPERTENSION RESPIRATORY & CRITICAL CARE CONFERENCE APRIL 21, 2016 LAURA G. HOOPER PULMONARY HYPERTENSION RESPIRATORY & CRITICAL CARE CONFERENCE APRIL 21, 2016 LAURA G. HOOPER OUTLINE Brief review of WHO Group Classification Scheme Subgroups we ll focus on: WHO Group I Pulmonary Arterial

More information

Riociguat for chronic thromboembolic pulmonary hypertension

Riociguat for chronic thromboembolic pulmonary hypertension Riociguat for chronic thromboembolic pulmonary hypertension This technology summary is based on information available at the time of research and a limited literature search. It is not intended to be a

More information

ACCP PAH Medical Therapy Guidelines: 2007 Update. David Badesch, MD University of Colorado School of Medicine Denver, CO

ACCP PAH Medical Therapy Guidelines: 2007 Update. David Badesch, MD University of Colorado School of Medicine Denver, CO ACCP PAH Medical Therapy Guidelines: 2007 Update David Badesch, MD University of Colorado School of Medicine Denver, CO Disclosure of Commercial Interest Dr. Badesch has received grant/research support

More information

Treatment of Paediatric Pulmonary Hypertension

Treatment of Paediatric Pulmonary Hypertension Treatment of Paediatric Pulmonary Hypertension Dunbar Ivy, MD The Children s Hospital Heart Institute University of Colorado School of Medicine 1 Disclosures I have the following financial relationships

More information

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

Clinical Policy: Macitentan (Opsumit) Reference Number: ERX.SPMN.88 Clinical Policy: (Opsumit) Reference Number: ERX.SPMN.88 Effective Date: 07/16 Last Review Date: 06/16 Coding Implications Revision Log See Important Reminder at the end of this policy for important regulatory

More information

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

Navigating the identification, diagnosis and management of pulmonary hypertension using the updated ESC/ERS guidelines Navigating the identification, diagnosis and management of pulmonary hypertension using the updated ESC/ERS guidelines Host: Marc Humbert Speaker: Simon Gibbs Marc HUMBERT, MD, PhD Professor of Respiratory

More information

Update in Pulmonary Arterial Hypertension

Update in Pulmonary Arterial Hypertension Update in Pulmonary Arterial Hypertension Michael J Sanley, MD April 12, 2018 Disclosures I have nothing to disclose 2 1 Case Presentation 67 yo male with atrial fibrillation, CLL on IVIG, presents with

More information

HARVARD PILGRIM HEALTH CARE RECOMMENDED MEDICATION REQUEST GUIDELINES

HARVARD PILGRIM HEALTH CARE RECOMMENDED MEDICATION REQUEST GUIDELINES Generic Brand HICL GCN Exception/Other SELEXIPAG UPTRAVI 42922 TREPROSTINIL ORENITRAM ER 40827 If the caller wishes to initiate a request then a MRF must be completed. This drug requires a written request

More information

Approach to Pulmonary Hypertension in the Hospital

Approach to Pulmonary Hypertension in the Hospital Approach to Pulmonary Hypertension in the Hospital Todd M Bull MD Professor of Medicine Director Pulmonary Vascular Disease Center Director Center for Lungs and Breathing Division of Pulmonary Sciences

More information

Medical Management of CTEPH: What is its role?

Medical Management of CTEPH: What is its role? Medical Management of CTEPH: What is its role? Nick H. Kim, MD University of California, San Diego Disclosures Consultant/Speakers Bureau: Actelion, Bayer Healthcare Research Support: Aires, Gilead Sciences,

More information

Pharmacy Management Drug Policy

Pharmacy Management Drug Policy SUBJECT: POLICY NUMBER: PHARMACY-42 EFFECTIVE DATE: 6/2005 LAST REVIEW DATE: 4/19/2018 If the member s subscriber contract excludes coverage for a specific service or prescription drug, it is not covered

More information

Role of Combination PAH Therapies

Role of Combination PAH Therapies Role of Combination PAH Therapies Ronald J. Oudiz, MD, FACP, FACC Associate Professor of Medicine, David Geffen School of Medicine at UCLA Director, Liu Center for Pulmonary Hypertension Los Angeles Biomedical

More information

In focus The paediatric PAH population Clinicians Perspectives

In focus The paediatric PAH population Clinicians Perspectives In focus The paediatric PAH population Clinicians Perspectives Maurice Beghetti Pediatric Cardiology University Children s Hospital HUG and CHUV Pulmonary Hypertension Program HUG Centre Universitaire

More information

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

22nd Annual Heart Failure 2018 an Update on Therapy. Pulmonary Arterial Hypertension: Contemporary Approach to Treatment 22nd Annual Heart Failure 2018 an Update on Therapy Pulmonary Arterial Hypertension: Contemporary Approach to Treatment Ronald J. Oudiz, MD, FACP, FACC, FCCP Professor of Medicine The David Geffen School

More information

Therapeutic Categories Outlook

Therapeutic Categories Outlook Equity Research Health Care Therapeutic Categories Outlook Comprehensive Study February 2017 Alzheimer s Disease Bone Diseases Cardiovascular Central Nervous System Dermatology Diabetes/Obesity Epilepsy

More information

Επεμβατικές στρατηγικές στην πνευμονική υπέρταση

Επεμβατικές στρατηγικές στην πνευμονική υπέρταση Επεμβατικές στρατηγικές στην πνευμονική υπέρταση Παναγιώτης Καρυοφύλλης Καρδιολόγος Ωνάσειο Καρδιοχειρουργικό Κέντρο Mortality in PAH 2015 ESC/ERS Guidelines. Treatment algorithm Since BAS is performed

More information

Pharmacy Management Drug Policy

Pharmacy Management Drug Policy SUBJECT: POLICY NUMBER: PHARMACY-42 EFFECTIVE DATE: 6/2005 LAST REVIEW DATE: 10/1/2018 If the member s subscriber contract excludes coverage for a specific service or prescription drug, it is not covered

More information

Combination therapy in the treatment of pulmonary arterial hypertension 2015 update

Combination therapy in the treatment of pulmonary arterial hypertension 2015 update Journal of Rare Cardiovascular Diseases 2015; 2 (4): 103 107 www.jrcd.eu REVIEW ARTICLE Rare diseases of pulmonary circulation Combination therapy in the treatment of pulmonary arterial hypertension 2015

More information

Contreversies in the management of PH What is controversial in treatment?

Contreversies in the management of PH What is controversial in treatment? Contreversies in the management of PH What is controversial in treatment? Service de Pneumologie et Réanimation National reference center for pulmonary hypertension Université Paris Sud Hôpital Antoine

More information

A Patient s Guide to Understanding Pulmonary Arterial Hypertension in Systemic Sclerosis

A Patient s Guide to Understanding Pulmonary Arterial Hypertension in Systemic Sclerosis A Patient s Guide to Understanding Pulmonary Arterial Hypertension in Systemic Sclerosis Compared with the general population, patients with systemic sclerosis (also known as scleroderma) have a higher

More information

Clinical Commissioning Policy: Selexipag for treating pulmonary arterial hypertension (all ages)

Clinical Commissioning Policy: Selexipag for treating pulmonary arterial hypertension (all ages) Clinical Commissioning Policy: Selexipag for treating pulmonary arterial hypertension (all ages) NHS England Reference: 170065P 1 NHS England INFORMATION READER BOX Directorate Medical Operations and Information

More information

Φαρµακοθεραπεία στη Πνευµονική Αρτηριακή Υπέρταση: Αρχική ή διαδοχική συνδυαστική θεραπεία

Φαρµακοθεραπεία στη Πνευµονική Αρτηριακή Υπέρταση: Αρχική ή διαδοχική συνδυαστική θεραπεία 37 ο Πανελλήνιο Καρδιολογικό Συνέδριο Αθήνα, Οκτώβριος 2016 k Φαρµακοθεραπεία στη Πνευµονική Αρτηριακή Υπέρταση: Αρχική ή διαδοχική συνδυαστική θεραπεία Αναστασία Ανθη Β Κλιν. Εντατικής Θεραπείας & Διακλινικό

More information

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

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

More information

Disclosures. Inhaled Therapy in Pediatric Pulmonary Hypertension. Inhaled Prostacyclin: Rationale. Outline

Disclosures. Inhaled Therapy in Pediatric Pulmonary Hypertension. Inhaled Prostacyclin: Rationale. Outline Disclosures Inhaled Therapy in Pediatric Pulmonary Hypertension The University of Colorado receives fees for Dr Ivy to be a consultant for Actelion, Gilead, Lilly, Pfizer, and United Therapeutics Dunbar

More information

Pulmonary Arterial Hypertension (PAH): Emerging Therapeutic Strategies

Pulmonary Arterial Hypertension (PAH): Emerging Therapeutic Strategies Pulmonary Arterial Hypertension (PAH): Emerging Therapeutic Strategies Nick H. Kim, M.D. Clinical Professor of Medicine Director, Pulmonary Vascular Medicine Clinical Service Chief, PCCSM La Jolla Pulmonary,

More information

Medical Therapy for Chronic Thromboembolic Pulmonary Hypertension

Medical Therapy for Chronic Thromboembolic Pulmonary Hypertension Medical Therapy for Chronic Thromboembolic Pulmonary Hypertension Josanna Rodriguez-Lopez, MD Pulmonary Hypertension and Thromboendarterectomy Program Massachusetts General Hospital Harvard Medical School

More information

Effective Strategies and Clinical Updates in Pulmonary Arterial Hypertension

Effective Strategies and Clinical Updates in Pulmonary Arterial Hypertension Effective Strategies and Clinical Updates in Pulmonary Arterial Hypertension Hap Farber Director, Pulmonary Hypertension Center Boston University School of Medicine Disclosures 1) Honoria: Actelion, Gilead,

More information

Pulmonary Hypertension: Evolution and

Pulmonary Hypertension: Evolution and Management of Pulmonary Hypertension: Evolution and Controversies VERMONT CARDIAC NETWORK SPRING CONFERENCE MAY 10, 2018 MARYELLEN ANTKOWIAK, MD, PULMONARY & CRITICAL CARE MEDICINE, UVMMC WHO classification

More information

Pulmonary Hypertension in 2012

Pulmonary Hypertension in 2012 Pulmonary Hypertension in 2012 Evan Brittain, MD December 7, 2012 Kingston, Jamaica VanderbiltHeart.com Disclosures None VanderbiltHeart.com Outline Definition and Classification of PH Hemodynamics of

More information

Chronic Thromboembolic Pulmonary Hypertension (CTEPH): A Review

Chronic Thromboembolic Pulmonary Hypertension (CTEPH): A Review Chronic Thromboembolic Pulmonary Hypertension (CTEPH): A Review Jeffrey Wilt, MD; Cassandra Lickert, MD; Michele Cole, PharmD, MS; and Janis Pruett, EdD, RN, MSN, FNP-BC Introduction Chronic thromboembolic

More information

Therapy Update: ERAs. Review of Mechanism. Disclosure Statements. Outline. Disclosure: Research support from United Therapeutics

Therapy Update: ERAs. Review of Mechanism. Disclosure Statements. Outline. Disclosure: Research support from United Therapeutics 1 Therapy Update: ERAs Disclosure Statements Disclosure: Research support from United Therapeutics Most of the medications discussed in this presentation are off-label usage Nidhy Varghese, MD Pulmonary

More information

Clinical Commissioning Policy: National policy for targeted therapies for the treatment of pulmonary hypertension in adults

Clinical Commissioning Policy: National policy for targeted therapies for the treatment of pulmonary hypertension in adults Clinical Commissioning Policy: National policy for targeted therapies for the treatment of pulmonary hypertension in adults Reference: NHS England A11/P/c 1 Clinical Commissioning Policy: National policy

More information

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

Cardiac Catheterization is Unnecessary in the Evaluation of Patients with Pulmonary Hypertension: CON Cardiac Catheterization is Unnecessary in the Evaluation of Patients with Pulmonary Hypertension: CON Dunbar Ivy, MD The Children s s Hospital Heart Institute 1 Diagnostic Evaluation: Right Heart Cardiac

More information

Updates on Pulmonary Hypertension Treatment

Updates on Pulmonary Hypertension Treatment Updates on Pulmonary Hypertension Treatment Dane Mellgren, PharmD PGY-1 Pharmacy Practice Resident Hennepin County Medical Center 04/27/18 Disclosure I have no disclosures to be made regarding the content

More information

Advanced Therapies for Pharmacological Treatment of Pulmonary Hypertension

Advanced Therapies for Pharmacological Treatment of Pulmonary Hypertension Advanced Therapies for Pharmacological Treatment of Pulmonary Hypertension Applies to all products administered or underwritten by Blue Cross and Blue Shield of Louisiana and its subsidiary, HMO Louisiana,

More information

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

Clinical Policy: Ambrisentan (Letairis) Reference Number: ERX.SPMN.84 Effective Date: 07/16 Clinical Policy: (Letairis) Reference Number: ERX.SPMN.84 Effective Date: 07/16 Last Review Date: 06/16 Revision Log See Important Reminder at the end of this policy for important regulatory and legal

More information

Management of Pulmonary Arterial Hypertension: Evolution in Management

Management of Pulmonary Arterial Hypertension: Evolution in Management Management of Pulmonary Arterial Hypertension: Evolution in Management Stephen C. Mathai, MD MHS The Johns Hopkins Pulmonary Hypertension Program Assistant Professor of Medicine Johns Hopkins University

More information

Abstract Book. Inspiring Approaches to Clinical Challenges in Pulmonary Hypertension

Abstract Book. Inspiring Approaches to Clinical Challenges in Pulmonary Hypertension Inspiring Approaches to Clinical Challenges in Pulmonary Hypertension Abstract Book A symposium sponsored by Bayer Schering Pharma at ERS 2008 Annual Congress www.ventavis.com Welcome Dear Colleague, It

More information

National Horizon Scanning Centre. Tadalafil for pulmonary arterial hypertension. October 2007

National Horizon Scanning Centre. Tadalafil for pulmonary arterial hypertension. October 2007 Tadalafil for pulmonary arterial hypertension October 2007 This technology summary is based on information available at the time of research and a limited literature search. It is not intended to be a

More information

See Important Reminder at the end of this policy for important regulatory and legal information.

See Important Reminder at the end of this policy for important regulatory and legal information. Clinical Policy: (Adcirca) Reference Number: HIM.PA.SP23 Effective Date: 05/17 Last Review Date: Line of Business: Health Insurance Marketplace Coding Implications Revision Log See Important Reminder at

More information

Πνευμονική Υπέρταση: Μια ΚΡΙΤΙΚΗ ματιά στις κλινικές μελέτες - AMBITION. Αναστασία Ανθη

Πνευμονική Υπέρταση: Μια ΚΡΙΤΙΚΗ ματιά στις κλινικές μελέτες - AMBITION. Αναστασία Ανθη Πανελλήνια Σεμινάρια Ομάδων Εργασίας 2017 k Πνευμονική Υπέρταση: Μια ΚΡΙΤΙΚΗ ματιά στις κλινικές μελέτες - AMBITION Αναστασία Ανθη Β Κλιν. Εντατικής Θεραπείας & Διακλινικό Ιατρείο Πνευμ. Υπέρτασης Π.Γ.Ν.

More information

Class Update with New Drug Evaluation: Drugs for Pulmonary Arterial Hypertension

Class Update with New Drug Evaluation: Drugs for Pulmonary Arterial Hypertension Copyright 2012 Oregon State University. All Rights Reserved Drug Use Research & Management Program Oregon State University, 500 Summer Street NE, E35 Salem, Oregon 97301-1079 Phone 503-947-5220 Fax 503-947-1119

More information

Start of Phase IIIb Study with Bayer s Riociguat in PAH Patients Who Demonstrate an Insufficient Response to PDE-5 Inhibitors

Start of Phase IIIb Study with Bayer s Riociguat in PAH Patients Who Demonstrate an Insufficient Response to PDE-5 Inhibitors Investor News Not intended for U.S. and UK Media Bayer AG Investor Relations 51368 Leverkusen Germany www.investor.bayer.com Pulmonary Arterial Hypertension (PAH): Start of Phase IIIb Study with Bayer

More information

Advances in Pharmacotherapy of PAH

Advances in Pharmacotherapy of PAH 24 th Annual Advances in Heart Disease Advances in Pharmacotherapy of PAH Gabriel Gregoratos, MD 12/14/2007 UCSF Cardiology 1 Faculty Disclosure Statement for Gabriel Gregoratos, MD Nothing to disclose

More information

Pulmonary Hypertension: Another Use for Viagra

Pulmonary Hypertension: Another Use for Viagra Pulmonary Hypertension: Another Use for Viagra Kathleen Tong, MD Director, Heart Failure Program Assistant Clinical Professor University of California, Davis Disclosures I have no financial conflicts A

More information

Pharmacy Medical Necessity Guidelines: Pulmonary Hypertension Medications

Pharmacy Medical Necessity Guidelines: Pulmonary Hypertension Medications Pharmacy Medical Necessity Guidelines: Pulmonary Hypertension Medications Effective: January 15, 2018 Prior Authorization Required Type of Review Care Management Not Covered Type of Review Clinical Review

More information

Chronic post-embolic pulmonary hypertension: a new target for medical therapies?

Chronic post-embolic pulmonary hypertension: a new target for medical therapies? REVIEW RARE DISEASE AND ORPHAN DRUGS Chronic post-embolic pulmonary hypertension: a new target for medical therapies? Marion Delcroix Affiliations: Respiratory Division, University Hospitals and Dept of

More information

La terapia dell ipertensione arteriosa polmonare oggi

La terapia dell ipertensione arteriosa polmonare oggi La terapia dell ipertensione arteriosa polmonare oggi PneumoTrieste 2017 Trieste 3 5 Aprile 2017 Sergio Harari U.O. di Pneumologia e UTIR Servizio di Emodinamica e Fisiopatologia Respiratoria Ospedale

More information

Prognostic value of echocardiographic parameters in patients with pulmonary arterial hypertension (PAH) treated with targeted therapies

Prognostic value of echocardiographic parameters in patients with pulmonary arterial hypertension (PAH) treated with targeted therapies Prognostic value of echocardiographic parameters in patients with pulmonary arterial hypertension (PAH) treated with targeted therapies E. Beciani, M. Palazzini, C. Bachetti, F. Sgro, E. Conficoni, E.

More information

Update on the Management of Pulmonary Hypertension

Update on the Management of Pulmonary Hypertension Update on the Management of Pulmonary Hypertension Weston Bush, PharmD, BCPS Clinical Pharmacy Specialist, SICU University Hospitals Case Medical Center Disclosures None Treatment (Conventional/Supportive)

More information

NHS England. Evidence review: Balloon pulmonary angioplasty for inoperable chronic thromboembolic pulmonary hypertension (CTEPH)

NHS England. Evidence review: Balloon pulmonary angioplasty for inoperable chronic thromboembolic pulmonary hypertension (CTEPH) NHS England Evidence review: Balloon pulmonary angioplasty for inoperable chronic thromboembolic pulmonary hypertension (CTEPH) 1 NHS England Evidence review: Balloon pulmonary angioplasty for inoperable

More information

Clinical Policy: Treprostinil (Orenitram, Remodulin, Tyvaso) Reference Number: ERX.SPA.36 Effective Date:

Clinical Policy: Treprostinil (Orenitram, Remodulin, Tyvaso) Reference Number: ERX.SPA.36 Effective Date: Clinical Policy: (Orenitram, Remodulin, Tyvaso) Reference Number: ERX.SPA.36 Effective Date: 07.01.16 Last Review Date: 02.18 Revision Log See Important Reminder at the end of this policy for important

More information

Pulmonary Hypertension Essentials. PD Dr. med. Silvia Ulrich Somaini University Hospital of Zurich

Pulmonary Hypertension Essentials. PD Dr. med. Silvia Ulrich Somaini University Hospital of Zurich Pulmonary Hypertension Essentials PD Dr. med. Silvia Ulrich Somaini University Hospital of Zurich Agenda Basics and Presentation Classification Diagnosis Pathogenesis Diagnosis Treatment Pathogenesis and

More information

Αγγειοπλαστική των πνευμονικών αρτηριών στην χρόνια θρομβοεμβολική πνευμονική υπέρταση. Παρόν και μέλλον

Αγγειοπλαστική των πνευμονικών αρτηριών στην χρόνια θρομβοεμβολική πνευμονική υπέρταση. Παρόν και μέλλον Αγγειοπλαστική των πνευμονικών αρτηριών στην χρόνια θρομβοεμβολική πνευμονική υπέρταση. Παρόν και μέλλον Παναγιώτης Καρυοφύλλης Επιμελητής Β Ωνάσειο Καρδιοχ/κό Κέντρο CTEPH is an obstructive disease Pulmonary

More information

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

2015 State-of-the-Art Management of Pulmonary Hypertension Based on an Understanding of the Various Etiologies 2015 State-of-the-Art Management of Pulmonary Hypertension Based on an Understanding of the Various Etiologies Vallerie V. McLaughlin, MD, FACC, FAHA Kim A Eagle MD Endowed Professor of Cardiovascular

More information

Riociguat for the treatment of pulmonary arterial hypertension: a long-term extension study (PATENT-2)

Riociguat for the treatment of pulmonary arterial hypertension: a long-term extension study (PATENT-2) ORIGINAL ARTICLE PULMONARY VASCULAR DISEASES Riociguat for the treatment of pulmonary arterial hypertension: a long-term extension study () Lewis J. Rubin 1, Nazzareno Galiè 2, Friedrich Grimminger 3,4,

More information

National Horizon Scanning Centre. Oral and inhaled treprostinil for pulmonary arterial hypertension: NYHA class III. April 2008

National Horizon Scanning Centre. Oral and inhaled treprostinil for pulmonary arterial hypertension: NYHA class III. April 2008 Oral and inhaled treprostinil for pulmonary arterial hypertension: NYHA class April 2008 This technology summary is based on information available at the time of research and a limited literature search.

More information

MACITENTAN DEVELOPMENT IN CHILDREN WITH PULMONARY HYPERTENSION (PAH)

MACITENTAN DEVELOPMENT IN CHILDREN WITH PULMONARY HYPERTENSION (PAH) MACITENTAN DEVELOPMENT IN CHILDREN WITH PULMONARY HYPERTENSION (PAH) ORPHAN DRUG AND RARE DISEASE 11 MAY 2017 Catherine Lesage, MD, Pediatrics Program Head, Actelion Copyright AGENDA Pulmonary Arterial

More information

Clinical Policy: Treprostinil (Orenitram, Remodulin, Tyvaso) Reference Number: ERX.SPA.36 Effective Date:

Clinical Policy: Treprostinil (Orenitram, Remodulin, Tyvaso) Reference Number: ERX.SPA.36 Effective Date: Clinical Policy: (Orenitram, Remodulin, Tyvaso) Reference Number: ERX.SPA.36 Effective Date: 07.01.16 Last Review Date: 02.19 Revision Log See Important Reminder at the end of this policy for important

More information

Prior Authorization Required Type of Review Care Management Not Covered Type of Review Clinical Review

Prior Authorization Required Type of Review Care Management Not Covered Type of Review Clinical Review Pharmacy Medical Necessity Guidelines: Effective: July 11, 2017 Prior Authorization Required Type of Review Care Management Not Covered Type of Review Clinical Review Pharmacy (RX) or Medical (MED) Benefit

More information

Commissioning Policy: Targeted Therapies for use in Pulmonary Hypertension in Adults

Commissioning Policy: Targeted Therapies for use in Pulmonary Hypertension in Adults Commissioning Policy: Targeted Therapies for use in Pulmonary Hypertension in Adults Reference: NHS England A11/P/c NHS England INFORMATION READER BOX Directorate Medical Commissioning Operations Patients

More information

Pulmonary Arterial Hypertension - Overview

Pulmonary Arterial Hypertension - Overview Pulmonary Arterial Hypertension - Overview J. Shaun Smith, MD Co-Director, Pulmonary Vascular Disease Program Assistant Professor of Medicine Division of Pulmonary, Critical Care and Sleep Medicine The

More information

Pulmonary Arterial Hypertension - Overview

Pulmonary Arterial Hypertension - Overview Pulmonary Arterial Hypertension - Overview J. Shaun Smith, MD Co-Director, Pulmonary Vascular Disease Program Assistant Professor of Medicine Division of Pulmonary, Critical Care and Sleep Medicine The

More information

Paediatric Pulmonary Arterial Hypertension (PAH)

Paediatric Pulmonary Arterial Hypertension (PAH) Paediatric Pulmonary Arterial Hypertension (PAH) Regulators perspective on a Global challenge EMA FDA HC paediatric PAH workshop 12 th June 2017 Cécile Ollivier European Medicines Agency Science and Innovation

More information

Medical management of chronic thromboembolic pulmonary hypertension

Medical management of chronic thromboembolic pulmonary hypertension REVIEW CHRONIC THROMBOEMBOLIC PULMONARY HYPERTENSION Medical management of chronic thromboembolic pulmonary hypertension Joanna Pepke-Zaba 1, Hossein-Ardeschir Ghofrani 2 and Marius M. Hoeper 3 Affiliations:

More information

See Important Reminder at the end of this policy for important regulatory and legal information.

See Important Reminder at the end of this policy for important regulatory and legal information. Clinical Policy: (Revatio) Reference Number: CP.PHAR.197 Effective Date: 03.16 Last Review Date: 02.18 Line of Business: Commercial, Health Insurance Marketplace, Medicaid Revision Log See Important Reminder

More information

See Important Reminder at the end of this policy for important regulatory and legal information.

See Important Reminder at the end of this policy for important regulatory and legal information. Clinical Policy: (Revatio) Reference Number: CP.PHAR.197 Effective Date: 03.16 Last Review Date: 02.19 Line of Business: Commercial, HIM*, Medicaid Revision Log See Important Reminder at the end of this

More information

IV PGI2 vs. Inhaled PGI2 in chronic lung disease

IV PGI2 vs. Inhaled PGI2 in chronic lung disease Inhaled Therapies for PAH Erika Berman Rosenzweig, MD Associate Professor of Clinical Pediatrics (in Medicine) Director, Pulmonary Hypertension Center Columbia University Medical Center Disclosures Has

More information

Pulmonary Hypertension: Clinical Features & Recent Advances

Pulmonary Hypertension: Clinical Features & Recent Advances Pulmonary Hypertension: Clinical Features & Recent Advances Lisa J. Rose-Jones, MD Assistant Professor of Medicine, Division of Cardiology Advanced Heart Failure/Cardiac Transplantation & Pulmonary Hypertension

More information

Advanced Therapies for Pharmacological Treatment of Pulmonary Arterial Hypertension

Advanced Therapies for Pharmacological Treatment of Pulmonary Arterial Hypertension Advanced Therapies for Pharmacological Treatment of Pulmonary Arterial Hypertension Policy Number: 5.01.09 Last Review: 01/2018 Origination: 6/2013 Next Review: 02/2019 Policy Blue Cross and Blue Shield

More information

Pulmonary hypertension (PH) represents

Pulmonary hypertension (PH) represents Mædica - a Journal of Clinical Medicine MAEDICA a Journal of Clinical Medicine 2014; 9(2): 198-203 CASE REPORTS Complete Therapeutical Approach in Pulmonary Arterial Hypertension: from Vasodilators to

More information

Comparison between adult and pediatric populations with I/HPAH and PAH-CHD in the Bologna ARCA registry

Comparison between adult and pediatric populations with I/HPAH and PAH-CHD in the Bologna ARCA registry nazzareno.galie@unibo.it Comparison between adult and pediatric populations with I/HPAH and PAH-CHD in the Bologna ARCA registry Nazzareno Galiè, MD, FESC, FRCP (Hon), DIMES 2 Comprehensive clinical classification

More information