The TOPP-2 registry is an international, non-interventional, prospective registry including children and adolescents newly diagnosed with pulmonary hypertension (PH) to gain further insights in the disease course and long-term outcome of PH in childhood. Patients will undergo clinical assessments and receive standard medical care, as determined by treating physicians in their daily clinical practice. The TOPP-2 registry is specifically designed to capture the variables that have been proposed as treatment goals in PePH and the reasons for changes in treatment strategy. The TOPP-2 registry uses the new clinical classification of PH as outlined at the 5th World Symposium for Pulmonary Hypertension (WSPH) in Nice 2013 and includes new characterizations for children with PH. The registry is planned and implemented under the scientific leadership of the Association for Pediatric Pulmonary Hypertension (PePH), independently from the financial sponsors. All enrolled patients will have a follow-up period of 18 months.
Study Type
OBSERVATIONAL
Enrollment
388
Stanford Children's Hospital
Palo Alto, California, United States
University of Colorado Denver School of Medicine, Children's Hospital Colorado
Aurora, Colorado, United States
Children's National Medical Center
Washington D.C., District of Columbia, United States
Emory University
Atlanta, Georgia, United States
Boston Children's Hospital
Boston, Massachusetts, United States
Death
Time frame: Over registry run-time (5.5 years)
Transplantation
Time frame: Over registry run-time (5.5 years)
Adverse events
Time frame: Over registry run-time (5.5 years)
Hospitalisation related to pulmonary arterial hypertension (PAH)
Time frame: Over registry run-time (5.5 years)
Use/initiation of i.v./s.c. prostanoids
Time frame: Over registry run-time (5.5 years)
Atrial septostomy
Time frame: Over registry run-time (5.5 years)
Potts shunt
Time frame: Over registry run-time (5.5 years)
Time to clinical worsening
Various composites of above parameters
Time frame: Over registry run-time (5.5 years)
Decline in 6-minute walk test (6MWT)
Time frame: Over registry run-time (5.5 years)
Type of treatment
Type of treatment (drug, mono/combination, administration route)
Time frame: Over registry run-time (5.5 years)
Switch in treatment
Time frame: Over registry run-time (5.5 years)
Escalation of treatment
Time frame: Over registry run-time (5.5 years)
Reasons for treatment change
Time frame: Over registry run-time (5.5 years)
Decline in WHO functional class
Time frame: Over registry run-time (5.5 years)
Decline in Panama functional class
Time frame: Over registry run-time (5.5 years)
Worsening of echocardiographic parameters (ECHO)
Parameters encompass TAPSE and RV/LV dimension ratio
Time frame: Over registry run-time (5.5 years)
Increase in Brain Natriuretic Peptide (BNP)
Time frame: Over registry run-time (5.5 years)
Increase in N-terminal-proBNP (NT-proBNP)
Time frame: Over registry run-time (5.5 years)
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St Louis Children's Hospital
St Louis, Missouri, United States
University of Nebraska Medical Center
Omaha, Nebraska, United States
Columbia University Medical Center
New York, New York, United States
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, United States
Vanderbilt University Children's Hospital
Nashville, Tennessee, United States
...and 22 more locations