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The clinical case of sildenafil administration in a very premature infant with pulmonary hypertension
We report the use of oral sildenafil in a 7-month-old preterm newborn with severe bronchopulmonary dysplasia and pulmonary arterial hypertension refractory to captopril and inhaled budesonide, and need of consistent oxygenation. Sildenafil was prepared as a powder for oral administration. Oral silde...
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Published in: | Journal of pediatric and neonatal individualized medicine 2015-04, Vol.4 (1), p.e040108-e040108 |
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container_title | Journal of pediatric and neonatal individualized medicine |
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creator | Galina A. Alyamovskaya Elena S. Keshishian Elena G. Verchenko Vera V. Bereznitskaya |
description | We report the use of oral sildenafil in a 7-month-old preterm newborn with severe bronchopulmonary dysplasia and pulmonary arterial hypertension refractory to captopril and inhaled budesonide, and need of consistent oxygenation. Sildenafil was prepared as a powder for oral administration. Oral sildenafil treatment was continued for 11 months. Oxygen supplement was suspended after 4 months and captopril administration was finished after 7 months of sildenafil treatment. There were no adverse effects during the treatment period. The respiratory failure decreased significantly and pulmonary arterial pressure became normal after 7 months of sildenafil treatment. |
doi_str_mv | 10.7363/040108 |
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Alyamovskaya ; Elena S. Keshishian ; Elena G. Verchenko ; Vera V. Bereznitskaya</creator><creatorcontrib>Galina A. Alyamovskaya ; Elena S. Keshishian ; Elena G. Verchenko ; Vera V. Bereznitskaya</creatorcontrib><description>We report the use of oral sildenafil in a 7-month-old preterm newborn with severe bronchopulmonary dysplasia and pulmonary arterial hypertension refractory to captopril and inhaled budesonide, and need of consistent oxygenation. Sildenafil was prepared as a powder for oral administration. Oral sildenafil treatment was continued for 11 months. Oxygen supplement was suspended after 4 months and captopril administration was finished after 7 months of sildenafil treatment. There were no adverse effects during the treatment period. 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The respiratory failure decreased significantly and pulmonary arterial pressure became normal after 7 months of sildenafil treatment.</description><subject>bronchopulmonary dysplasia</subject><subject>premature infants</subject><subject>pulmonary arterial hypertension</subject><subject>sildenafil</subject><issn>2281-0692</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNotjltLwzAYhoMgOOb8DfkD1RzaNL2U4WEw2M28Ll-SLy4jTUuaKfv3FvXqheflPRDywNljK5V8YjXjTN-QlRCaV0x14o5s5vnMGOM1V0rLFcHjCamNIQULkVqYkY6eziE6TOBDpOCGxZxLhhLGREOiQL8wX-mUcYByybgwD6nQ71BOdLrEYUyw-KfrhLlgmpfYPbn1EGfc_OuafLy-HLfv1f7wtts-7yvHG14qrzlr0TRWojQouxoE6zx0vnaNkN6YWnjvmtajYdx0wlrZqdZygVpJVEauye6v141w7qcchuVJP0Lof8GYP3vIJdiIvQJsjXToNS71jgO34LTmzsnaL7vyB78pZUs</recordid><startdate>20150401</startdate><enddate>20150401</enddate><creator>Galina A. Alyamovskaya</creator><creator>Elena S. 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Alyamovskaya</creatorcontrib><creatorcontrib>Elena S. Keshishian</creatorcontrib><creatorcontrib>Elena G. Verchenko</creatorcontrib><creatorcontrib>Vera V. Bereznitskaya</creatorcontrib><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of pediatric and neonatal individualized medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Galina A. Alyamovskaya</au><au>Elena S. Keshishian</au><au>Elena G. Verchenko</au><au>Vera V. Bereznitskaya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The clinical case of sildenafil administration in a very premature infant with pulmonary hypertension</atitle><jtitle>Journal of pediatric and neonatal individualized medicine</jtitle><date>2015-04-01</date><risdate>2015</risdate><volume>4</volume><issue>1</issue><spage>e040108</spage><epage>e040108</epage><pages>e040108-e040108</pages><eissn>2281-0692</eissn><abstract>We report the use of oral sildenafil in a 7-month-old preterm newborn with severe bronchopulmonary dysplasia and pulmonary arterial hypertension refractory to captopril and inhaled budesonide, and need of consistent oxygenation. Sildenafil was prepared as a powder for oral administration. Oral sildenafil treatment was continued for 11 months. Oxygen supplement was suspended after 4 months and captopril administration was finished after 7 months of sildenafil treatment. There were no adverse effects during the treatment period. The respiratory failure decreased significantly and pulmonary arterial pressure became normal after 7 months of sildenafil treatment.</abstract><pub>Hygeia Press di Corridori Marinella</pub><doi>10.7363/040108</doi><oa>free_for_read</oa></addata></record> |
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subjects | bronchopulmonary dysplasia premature infants pulmonary arterial hypertension sildenafil |
title | The clinical case of sildenafil administration in a very premature infant with pulmonary hypertension |
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