Pulmonary Arterial Hypertension
Conditions
Keywords
PAH prognosis, PAH outcomes, PAH survival, PAH risk status
Brief summary
In this study researchers want to learn more about Pulmonary Arterial Hypertension, a type of high blood pressure in the lungs related to the narrowing of the small blood vessels in the lungs (group 1 according to WHO classification). Goal of the study is to describe the signs and risk factors of the illness at study start and the chances of survival.
Detailed description
The primary objective of the study is to describe baseline clinical characteristics and overall survival in a cohort of patients with pulmonary arterial hypertension (PAH) of WHO functional class I in Argentina. Secondary objectives are to study the discriminatory ability of the risk assessment tool presented in the European Society of Cardiology and European Respiratory Society (ESC/ERS) 2015 guidelines and to explore the potential prognostic advantage of a low-risk profile at follow-up as treatment goal.
Interventions
DRUGPAH medication
Any PAH-targeted medication
Sponsors
Bayer
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Consecutive newly diagnosed patients by Right heart catheterization (RHC) from 01-Jan-2012 to 31-Dec-2017, belonging to one of the following of Group 1 PAH subgroups: Idiopathic (IPAH), or Heritable (HPAH), or Drug or toxin induced, or Associated (APAH) with one of the following: Connective tissue disease; Congenital heart disease with simple systemic to pulmonary shunt at least 1 year after surgical repair; Portal Hypertension or HIV infection. * Diagnosis of PAH by RHC exhibiting a mean pulmonary artery pressure (MPAP) ≥ 25 mmHg and a pulmonary artery wedge pressure (PAWP) ≤15 mmHg at normal or reduced cardiac output, according to European Society of Cardiology and European Respiratory Society (ESC/ERS) 2009 guidelines or MPAP ≥ 25 mmHg and a PAWP ≤15 mmHg and a pulmonary vascular resistance (PVR) \> 3 WU according to ESC/ERS 2015 guidelines. * Patients with at least one year documented follow up or that have died or received transplant before 1 year of follow up after baseline RHC and that have initiated treatment with a PAH-targeted medication.
Exclusion criteria
* Patients with severe concomitant left heart disease (left ventricular ejection fraction \<35%). * Patients with restrictive lung disease (Forced vital capacity (FVC) \<60% predicted) other than connective tissue disease or obstructive lung disease (forced expiratory volume (FEV) \<60% predicted, with FEV1/FVC\<70%). * Clinical or radiological evidence of Pulmo-Veno-Occlusive Disease (PVOD) or Pulmonary Capillary Haemangiomatosis (PCH). * Hypertrophic obstructive cardiomyopathy. * Severe proven or suspected coronary artery disease. * Congenital or acquired valvular or myocardial disease if clinically significant apart from tricuspid valvular insufficiency due to pulmonary hypertension. * Underlying medical disorders at baseline with an anticipated life expectancy below 2 years (e.g. active cancer disease with localized and/or metastasized tumor mass) or Clinical relevant hepatic dysfunction (Child-Pugh B and C) or Renal insufficiency (glomerular filtration rate \<30 mL/min). * Diagnosis of a pulmonary hypertension from WHO groups 2, 3, 4 or 5.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Time from diagnosis to death from any cause | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Sex | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Ethnicity | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Descriptive analysis of comorbidities at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| PAH-subgroup at baseline as assessed by physician | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | PAH-subgroups may be idiopathic, heritable, drug- or toxin-induced, or associated PAH (with CTD or HIV or portopulmonary hypertension or repaired congenital heart disease). |
| Right atrial pressure at baseline by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary artery pressure at baseline by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary vascular resistance at baseline by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary artery wedge pressure (PAWP) at baseline by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Cardiac Index (CI) at baseline by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Mixed venous oxygen saturation (SvO2) at baseline by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary vasoreactivity at baseline by pulmonary artery pressure | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Yes / No - variable |
| Peak oxygen consumption by cardiopulmonary exercise test at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Right atrial area at baseline by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pericardial effusion at baseline by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Patients may have no, mild, moderate or severe pericardial effusion. |
| Right ventricular function at baseline by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Patients may have a normal, mild, moderate and severe right ventricular function. |
| Tricuspid annular plane systolic excursion (TAPSE) at baseline by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary artery systolic pressure at baseline by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Left ventricular ejection fraction at baseline by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| 6-minute walking distance at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary hypertension functional class according to WHO classification at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Four functional classes ranging from Class I (Pulmonary hypertension without limited physical activity) to Class IV (Pulmonary hypertension with strongly limited physical activity). |
| Time from onset of diagnostic symptoms to PAH-diagnosis | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Symptoms progression at baseline assessed by physician | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Patient may display no, a slow or rapid progression of symptoms. |
| Syncope frequency at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | No, occasional or repeated syncope |
| Systolic blood pressure at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Body mass index at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Concentration of diagnostic markers for heart failure in blood at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Used diagnostic marker are either Brain natriuretic Peptide (BNP) or N-terminal pro b-type Natriuretic Peptide (NT-proBNP). |
| Drug class of supportive PAH treatment | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Supportive treatments for PAH are assigned to four drug classes: diuretics, anticoagulants, oxygen and other. |
| Drug class of PAH-treatment after diagnosis | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | PAH-treatments are assigned to six drug classes: endothelin receptor antagonists (ERA), PDE5 inhibitors, prostanoides, prostacyclin receptor agonists, soluble guanylate cyclase (sGC) stimulants and calcium blockers. |
| PAH risk status at baseline according to ESC/ERS 2015 guidelines | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Patients may have a low, intermediate or high risk for PAH according to the European Society of Cardiology and European Respiratory Society 2015 guidelines. |
| Overall survival rate | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Body height at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Heart rate at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Body weight at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Age at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pulmonary artery pressure at follow-up by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary vascular resistance at follow-up by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary artery wedge pressure (PAWP) at follow-up by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Cardiac Index (CI) at follow-up by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Mixed venous oxygen saturation (SvO2) at follow-up by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Peak oxygen consumption by cardiopulmonary exercise test at follow-up | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Right atrial area at follow-up by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pericardial effusion at follow-up by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Right ventricular function at follow-up by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Tricuspid annular plane systolic excursion (TAPSE) at follow-up by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary artery systolic pressure at follow-up by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Left ventricular ejection fraction at follow-up by echocardiography | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| 6-minute walking distance at follow-up | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary hypertension functional class according to WHO classification at baseline | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Four functional classes ranging from Class I (Pulmonary hypertension without limited physical activity) to Class IV (Pulmonary hypertension with strongly limited physical activity). |
| Symptoms progression at follow-up | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Syncope frequency at follow-up | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Concentration of diagnostic markers for heart failure in blood at follow-up | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Used diagnostic marker are either Brain natriuretic Peptide (BNP) or N-terminal pro b-type Natriuretic Peptide (NT-proBNP). |
| PAH risk status at follow-up according to ESC/ERS 2015 guidelines | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Patients may have low, intermediate and high risk for PAH according to the European Society of Cardiology and European Respiratory Society 2015 guidelines. |
| Cause of death | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Time from diagnosis to death from any cause | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Pulmonary transplant | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Yes or No |
| Time from diagnosis to pulmonary transplant | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Time from diagnosis to first hospitalization due to PAH-progression | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Number of hospitalizations per year due to PAH-progression | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Proportion of patients with low PAH risk | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Risk status is assessed according to the Society of Cardiology and European Respiratory Society (ESC/ERS) 2015 guidelines. |
| Proportion of patients with intermediate+high PAH risk | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Risk status is assessed according to the Society of Cardiology and European Respiratory Society (ESC/ERS) 2015 guidelines. |
| Survival rate of patients with low risk for PAH | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| Survival rate of patients with intermediate or high risk for PAH | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
| PAH risk status of patients without transplant being alive at the date of latest medical records according to ESC/ERS 2015 guidelines | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | Patients may have low, intermediate and high risk for PAH according to the European Society of Cardiology and European Respiratory Society 2015 guidelines. |
| Right atrial pressure at follow-up by right heart catheterization hemodynamics | Retrospective analysis of data from 01-Jan-2012 to 31-Dec-2018 | — |
Countries
Argentina
Outcome results
None listed