Acute vasoreactivity testing in pediatric idiopathic pulmonary arterial hypertension: an international survey on current practice. (1st November 2019)
- Record Type:
- Journal Article
- Title:
- Acute vasoreactivity testing in pediatric idiopathic pulmonary arterial hypertension: an international survey on current practice. (1st November 2019)
- Main Title:
- Acute vasoreactivity testing in pediatric idiopathic pulmonary arterial hypertension: an international survey on current practice
- Authors:
- Caicedo, Lina
Hopper, Rachel
Garcia Aguilar, Humberto
Ivy, Dunbar
Haag, Dora
Fineman, Jeff
Humpl, Tillman
Al‐Tamimi, Omar
Feinstein, Jeff A.
Berger, Rolf
Rosenzweig, Erika
Kashour, Tarek
Diaz, Gabriel Fernando
Mendoza, Alberto
Krishnan, Usha
Bobhate, Prashant
Handler, Stephanie
Lopes, Antonio Augusto
Kumar Rahit, Manoj
Barward, Parag
Labrandero de Lera, Carlos
Adatia, Ian
Moledina, Shahin
Abman, Steven
del Cerro, Maria Jesus - Abstract:
- Abstract : The aim of this study was to determine practice patterns and inter‐institutional variability in how acute vasoreactivity testing (AVT) is performed and interpreted in pediatrics throughout the world. A survey was offered to physicians affiliated with the Pediatric & Congenital Heart Disease Taskforce of the Pulmonary Vascular Research Institute (PVRI), the Pediatric Pulmonary Hypertension Network (PPHNET), or the Spanish Registry for Pediatric Pulmonary Hypertension (REHIPED), from February to December 2016. The survey requested data about the site‐specific protocol for AVT and subsequent management of pediatric patients with idiopathic pulmonary arterial hypertension (IPAH) or heritable PAH (HPAH). Twenty‐eight centers from 13 countries answered the survey. AVT is performed in most centers using inhaled nitric oxide (iNO). Sitbon criteria was used in 39% of the centers, Barst criteria in 43%, and other criteria in 18%. First‐line therapy for positive AVT responders in functional class (FC) I/II was calcium channel blocker (CCB) in 89%, but only in 68% as monotherapy. Most centers (71%) re‐evaluated AVT‐positive patients hemodynamics after 6–12 months; 29% of centers re‐evaluated based only on clinical criteria. Most centers (64%) considered a good response as remaining in FC I or II, with near normalization of pulmonary arterial pressure and pulmonary vascular resistance, but a stable FC I/II alone was sufficient criteria in 25% of sites. Protocols and diagnosticAbstract : The aim of this study was to determine practice patterns and inter‐institutional variability in how acute vasoreactivity testing (AVT) is performed and interpreted in pediatrics throughout the world. A survey was offered to physicians affiliated with the Pediatric & Congenital Heart Disease Taskforce of the Pulmonary Vascular Research Institute (PVRI), the Pediatric Pulmonary Hypertension Network (PPHNET), or the Spanish Registry for Pediatric Pulmonary Hypertension (REHIPED), from February to December 2016. The survey requested data about the site‐specific protocol for AVT and subsequent management of pediatric patients with idiopathic pulmonary arterial hypertension (IPAH) or heritable PAH (HPAH). Twenty‐eight centers from 13 countries answered the survey. AVT is performed in most centers using inhaled nitric oxide (iNO). Sitbon criteria was used in 39% of the centers, Barst criteria in 43%, and other criteria in 18%. First‐line therapy for positive AVT responders in functional class (FC) I/II was calcium channel blocker (CCB) in 89%, but only in 68% as monotherapy. Most centers (71%) re‐evaluated AVT‐positive patients hemodynamics after 6–12 months; 29% of centers re‐evaluated based only on clinical criteria. Most centers (64%) considered a good response as remaining in FC I or II, with near normalization of pulmonary arterial pressure and pulmonary vascular resistance, but a stable FC I/II alone was sufficient criteria in 25% of sites. Protocols and diagnostic criteria for AVT, and therapeutic approaches during follow‐up, were highly variable across the world. Reported clinical practice is not fully congruent with current guidelines, suggesting the need for additional studies that better define the prognostic value of AVT for pediatric IPAH patients. … (more)
- Is Part Of:
- Pulmonary circulation. Volume 9:Number 4(2019)
- Journal:
- Pulmonary circulation
- Issue:
- Volume 9:Number 4(2019)
- Issue Display:
- Volume 9, Issue 4 (2019)
- Year:
- 2019
- Volume:
- 9
- Issue:
- 4
- Issue Sort Value:
- 2019-0009-0004-0000
- Page Start:
- 1
- Page End:
- 9
- Publication Date:
- 2019-11-01
- Subjects:
- Pediatric pulmonary hypertension -- idiopathic pulmonary arterial hypertension -- cardiac catheterization -- acute vasoreactivity testing -- calcium channel blockers
Pulmonary circulation -- Periodicals
Pulmonary circulation
Electronic journals -- Sciences
Periodicals
616.24005 - Journal URLs:
- http://www.jstor.org/action/showPublication?journalCode=pulmcirc ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/1644 ↗
http://www.pulmonarycirculation.org/ ↗
https://uk.sagepub.com/en-gb/eur/pulmonary-circulation/journal202599 ↗
https://onlinelibrary.wiley.com/journal/20458940 ↗
http://www.sagepublications.com/ ↗ - DOI:
- 10.1177/2045894019857533 ↗
- Languages:
- English
- ISSNs:
- 2045-8932
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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