Efficacy of Surfactant-TA, Calfactant and Poractant Alfa for Preterm Infants with Respiratory Distress Syndrome: A Retrospective Study
To compare the efficacy of the new drug calfactant with the commonly used drugs surfactant-TA and poractant alfa. A total of 332 preterm infants at 24-31 weeks' gestation with respiratory distress syndrome (RDS) were enrolled and allocated to three groups according to the surfactant instilled;...
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Published in | Yonsei medical journal Vol. 56; no. 2; pp. 433 - 439 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
Yonsei University College of Medicine
01.03.2015
연세대학교의과대학 |
Subjects | |
Online Access | Get full text |
ISSN | 0513-5796 1976-2437 1976-2437 |
DOI | 10.3349/ymj.2015.56.2.433 |
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Abstract | To compare the efficacy of the new drug calfactant with the commonly used drugs surfactant-TA and poractant alfa.
A total of 332 preterm infants at 24-31 weeks' gestation with respiratory distress syndrome (RDS) were enrolled and allocated to three groups according to the surfactant instilled; Group 1 (n=146, surfactant-TA), Group 2 (n=96, calfactant), and Group 3 (n=90, poractant alfa). The diagnosis of RDS and the decision to replace the pulmonary surfactant were left to the attending physician and based on patient severity determined by chest radiography and blood gas analysis. Data were collected and reviewed retrospectively using patient medical records.
Demographic factors including gestational age, birth weight, Apgar score, clinical risk index for babies II score, and maternal status before delivery were not different between the study groups. Instances of surfactant redosing and pulmonary air leaks, as well as duration of mechanical ventilation, were also not different. Rates of patent ductus arteriosus, intraventricular hemorrhage (≥grade III), periventricular leukomalacia, high stage retinopathy of prematurity, necrotizing enterocolitis (≥stage II), and mortality were also similar, as was duration of hospital stay. Cases of pulmonary hemorrhage and moderate to severe bronchopulmonary dysplasia were increased in Group 3.
Calfactant is equally as effective as surfactant-TA and poractant alfa. This was the first study comparing the efficacy of surfactant-TA, calfactant, and poractant alfa in a large number of preterm infants in Korea. Further randomized prospective studies on these surfactants are needed. |
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AbstractList | Purpose: To compare the efficacy of the new drug calfactant with the commonly used drugs surfactant-TA and poractant alfa. Materials and Methods: A total of 332 preterm infants at 24‒31 weeks’ gestation with respiratory distress syndrome (RDS) were enrolled and allocated to three groups according to the surfactant instilled;Group 1 (n=146, surfactant-TA), Group 2 (n=96, calfactant), and Group 3 (n=90, poractant alfa). The diagnosis of RDS and the decision to replace the pulmonarysurfactant were left to the attending physician and based on patient severitydetermined by chest radiography and blood gas analysis. Data were collected and reviewed retrospectively using patient medical records. Results: Demographic factors including gestational age, birth weight, Apgar score, clinical risk index for babies II score, and maternal status before delivery were not different between the study groups. Instances of surfactant redosing and pulmonary air leaks, as well as duration of mechanical ventilation, were also not different. Rates of patent ductus arteriosus, intraventricular hemorrhage (≥grade III), periventricular leukomalacia, high stage retinopathy of prematurity, necrotizing enterocolitis (≥stage II), and mortality were also similar, as was duration of hospital stay. Cases of pulmonary hemorrhage and moderate to severe bronchopulmonary dysplasia were increased in Group 3. Conclusion: Calfactant is equally as effective as surfactant-TA and poractantalfa. This was the first study comparing the efficacy of surfactant-TA, calfactant,and poractant alfa in a large number of preterm infants in Korea. Further randomized prospective studies on these surfactants are needed. KCI Citation Count: 8 To compare the efficacy of the new drug calfactant with the commonly used drugs surfactant-TA and poractant alfa. A total of 332 preterm infants at 24-31 weeks' gestation with respiratory distress syndrome (RDS) were enrolled and allocated to three groups according to the surfactant instilled; Group 1 (n=146, surfactant-TA), Group 2 (n=96, calfactant), and Group 3 (n=90, poractant alfa). The diagnosis of RDS and the decision to replace the pulmonary surfactant were left to the attending physician and based on patient severity determined by chest radiography and blood gas analysis. Data were collected and reviewed retrospectively using patient medical records. Demographic factors including gestational age, birth weight, Apgar score, clinical risk index for babies II score, and maternal status before delivery were not different between the study groups. Instances of surfactant redosing and pulmonary air leaks, as well as duration of mechanical ventilation, were also not different. Rates of patent ductus arteriosus, intraventricular hemorrhage (≥grade III), periventricular leukomalacia, high stage retinopathy of prematurity, necrotizing enterocolitis (≥stage II), and mortality were also similar, as was duration of hospital stay. Cases of pulmonary hemorrhage and moderate to severe bronchopulmonary dysplasia were increased in Group 3. Calfactant is equally as effective as surfactant-TA and poractant alfa. This was the first study comparing the efficacy of surfactant-TA, calfactant, and poractant alfa in a large number of preterm infants in Korea. Further randomized prospective studies on these surfactants are needed. To compare the efficacy of the new drug calfactant with the commonly used drugs surfactant-TA and poractant alfa.PURPOSETo compare the efficacy of the new drug calfactant with the commonly used drugs surfactant-TA and poractant alfa.A total of 332 preterm infants at 24-31 weeks' gestation with respiratory distress syndrome (RDS) were enrolled and allocated to three groups according to the surfactant instilled; Group 1 (n=146, surfactant-TA), Group 2 (n=96, calfactant), and Group 3 (n=90, poractant alfa). The diagnosis of RDS and the decision to replace the pulmonary surfactant were left to the attending physician and based on patient severity determined by chest radiography and blood gas analysis. Data were collected and reviewed retrospectively using patient medical records.MATERIALS AND METHODSA total of 332 preterm infants at 24-31 weeks' gestation with respiratory distress syndrome (RDS) were enrolled and allocated to three groups according to the surfactant instilled; Group 1 (n=146, surfactant-TA), Group 2 (n=96, calfactant), and Group 3 (n=90, poractant alfa). The diagnosis of RDS and the decision to replace the pulmonary surfactant were left to the attending physician and based on patient severity determined by chest radiography and blood gas analysis. Data were collected and reviewed retrospectively using patient medical records.Demographic factors including gestational age, birth weight, Apgar score, clinical risk index for babies II score, and maternal status before delivery were not different between the study groups. Instances of surfactant redosing and pulmonary air leaks, as well as duration of mechanical ventilation, were also not different. Rates of patent ductus arteriosus, intraventricular hemorrhage (≥grade III), periventricular leukomalacia, high stage retinopathy of prematurity, necrotizing enterocolitis (≥stage II), and mortality were also similar, as was duration of hospital stay. Cases of pulmonary hemorrhage and moderate to severe bronchopulmonary dysplasia were increased in Group 3.RESULTSDemographic factors including gestational age, birth weight, Apgar score, clinical risk index for babies II score, and maternal status before delivery were not different between the study groups. Instances of surfactant redosing and pulmonary air leaks, as well as duration of mechanical ventilation, were also not different. Rates of patent ductus arteriosus, intraventricular hemorrhage (≥grade III), periventricular leukomalacia, high stage retinopathy of prematurity, necrotizing enterocolitis (≥stage II), and mortality were also similar, as was duration of hospital stay. Cases of pulmonary hemorrhage and moderate to severe bronchopulmonary dysplasia were increased in Group 3.Calfactant is equally as effective as surfactant-TA and poractant alfa. This was the first study comparing the efficacy of surfactant-TA, calfactant, and poractant alfa in a large number of preterm infants in Korea. Further randomized prospective studies on these surfactants are needed.CONCLUSIONCalfactant is equally as effective as surfactant-TA and poractant alfa. This was the first study comparing the efficacy of surfactant-TA, calfactant, and poractant alfa in a large number of preterm infants in Korea. Further randomized prospective studies on these surfactants are needed. |
Author | Jeon, Ga Won Oh, Minkyung Sin, Jong Beom |
AuthorAffiliation | 2 Department of Pharmacology and Clinical Trial Center, Inje University Busan Paik Hospital, Busan, Korea 1 Department of Pediatrics, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea |
AuthorAffiliation_xml | – name: 1 Department of Pediatrics, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea – name: 2 Department of Pharmacology and Clinical Trial Center, Inje University Busan Paik Hospital, Busan, Korea |
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Keywords | Pulmonary surfactants respiratory distress syndrome poractant alfa beractant calfactant |
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Snippet | To compare the efficacy of the new drug calfactant with the commonly used drugs surfactant-TA and poractant alfa.
A total of 332 preterm infants at 24-31... To compare the efficacy of the new drug calfactant with the commonly used drugs surfactant-TA and poractant alfa.PURPOSETo compare the efficacy of the new drug... Purpose: To compare the efficacy of the new drug calfactant with the commonly used drugs surfactant-TA and poractant alfa. Materials and Methods: A total of... |
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SubjectTerms | Biological Products - administration & dosage Biological Products - therapeutic use Birth Weight Bronchopulmonary Dysplasia - drug therapy Female Gestational Age Humans Infant, Newborn Infant, Premature Male Original Phospholipids - administration & dosage Phospholipids - therapeutic use Pulmonary Surfactants - administration & dosage Pulmonary Surfactants - therapeutic use Republic of Korea Respiration, Artificial Respiratory Distress Syndrome, Newborn - drug therapy Retrospective Studies Risk Treatment Outcome Ventilator Weaning 의학일반 |
Title | Efficacy of Surfactant-TA, Calfactant and Poractant Alfa for Preterm Infants with Respiratory Distress Syndrome: A Retrospective Study |
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