Impact of Palliation Strategy on Interstage Feeding and Somatic Growth for Infants With Ductal‐Dependent Pulmonary Blood Flow: Results from the Congenital Catheterization Research Collaborative
Background In infants with ductal-dependent pulmonary blood flow, the impact of palliation strategy on interstage growth and feeding regimen is unknown. Methods and Results This was a retrospective multicenter study of infants with ductal-dependent pulmonary blood flow palliated with patent ductus a...
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Published in | Journal of the American Heart Association Vol. 9; no. 1; p. e013807 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley and Sons Inc
07.01.2020
Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 2047-9980 2047-9980 |
DOI | 10.1161/JAHA.119.013807 |
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Abstract | Background In infants with ductal-dependent pulmonary blood flow, the impact of palliation strategy on interstage growth and feeding regimen is unknown. Methods and Results This was a retrospective multicenter study of infants with ductal-dependent pulmonary blood flow palliated with patent ductus arteriosus (PDA) stent or Blalock-Taussig shunt (BTS) from 2008 to 2015. Subjects with a defined interstage, the time between initial palliation and subsequent palliation or repair, were included. Primary outcome was change in weight-for-age
-score. Secondary outcomes included % of patients on: all oral feeds, feeding-related medications, higher calorie feeds, and feeding-related readmission. Propensity score was used to account for baseline differences. Subgroup analysis was performed in 1- (1V) and 2-ventricle (2V) groups. The cohort included 66 PDA stent (43.9% 1V) and 195 BTS (54.4% 1V) subjects. Prematurity was more common in the PDA stent group (
=0.051). After adjustment, change in weight-for-age
-score did not differ between groups over the entire interstage. However, change in weight-for-age
-score favored PDA stent during the inpatient interstage (
=0.005) and BTS during the outpatient interstage (
=0.032). At initial hospital discharge, PDA stent treatment was associated with all oral feeds (
<0.001) and absence of feeding-related medications (
=0.002). Subgroup analysis revealed that 2V but not 1V patients demonstrated significant increase in weight-for-age
-score. In the 2V cohort, feeding-related readmissions were more common in the BTS group (
=0.008). Conclusions In infants with ductal-dependent pulmonary blood flow who underwent palliation with PDA stent or BTS, there was no difference in interstage growth. PDA stent was associated with a simpler feeding regimen and fewer feeding-related readmissions. |
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AbstractList | Background In infants with ductal-dependent pulmonary blood flow, the impact of palliation strategy on interstage growth and feeding regimen is unknown. Methods and Results This was a retrospective multicenter study of infants with ductal-dependent pulmonary blood flow palliated with patent ductus arteriosus (PDA) stent or Blalock-Taussig shunt (BTS) from 2008 to 2015. Subjects with a defined interstage, the time between initial palliation and subsequent palliation or repair, were included. Primary outcome was change in weight-for-age
-score. Secondary outcomes included % of patients on: all oral feeds, feeding-related medications, higher calorie feeds, and feeding-related readmission. Propensity score was used to account for baseline differences. Subgroup analysis was performed in 1- (1V) and 2-ventricle (2V) groups. The cohort included 66 PDA stent (43.9% 1V) and 195 BTS (54.4% 1V) subjects. Prematurity was more common in the PDA stent group (
=0.051). After adjustment, change in weight-for-age
-score did not differ between groups over the entire interstage. However, change in weight-for-age
-score favored PDA stent during the inpatient interstage (
=0.005) and BTS during the outpatient interstage (
=0.032). At initial hospital discharge, PDA stent treatment was associated with all oral feeds (
<0.001) and absence of feeding-related medications (
=0.002). Subgroup analysis revealed that 2V but not 1V patients demonstrated significant increase in weight-for-age
-score. In the 2V cohort, feeding-related readmissions were more common in the BTS group (
=0.008). Conclusions In infants with ductal-dependent pulmonary blood flow who underwent palliation with PDA stent or BTS, there was no difference in interstage growth. PDA stent was associated with a simpler feeding regimen and fewer feeding-related readmissions. Background In infants with ductal‐dependent pulmonary blood flow, the impact of palliation strategy on interstage growth and feeding regimen is unknown. Methods and Results This was a retrospective multicenter study of infants with ductal‐dependent pulmonary blood flow palliated with patent ductus arteriosus (PDA) stent or Blalock‐Taussig shunt (BTS) from 2008 to 2015. Subjects with a defined interstage, the time between initial palliation and subsequent palliation or repair, were included. Primary outcome was change in weight‐for‐age Z‐score. Secondary outcomes included % of patients on: all oral feeds, feeding‐related medications, higher calorie feeds, and feeding‐related readmission. Propensity score was used to account for baseline differences. Subgroup analysis was performed in 1‐ (1V) and 2‐ventricle (2V) groups. The cohort included 66 PDA stent (43.9% 1V) and 195 BTS (54.4% 1V) subjects. Prematurity was more common in the PDA stent group (P=0.051). After adjustment, change in weight‐for‐age Z‐score did not differ between groups over the entire interstage. However, change in weight‐for‐age Z‐score favored PDA stent during the inpatient interstage (P=0.005) and BTS during the outpatient interstage (P=0.032). At initial hospital discharge, PDA stent treatment was associated with all oral feeds (P<0.001) and absence of feeding‐related medications (P=0.002). Subgroup analysis revealed that 2V but not 1V patients demonstrated significant increase in weight‐for‐age Z‐score. In the 2V cohort, feeding‐related readmissions were more common in the BTS group (P=0.008). Conclusions In infants with ductal‐dependent pulmonary blood flow who underwent palliation with PDA stent or BTS, there was no difference in interstage growth. PDA stent was associated with a simpler feeding regimen and fewer feeding‐related readmissions. Background In infants with ductal-dependent pulmonary blood flow, the impact of palliation strategy on interstage growth and feeding regimen is unknown. Methods and Results This was a retrospective multicenter study of infants with ductal-dependent pulmonary blood flow palliated with patent ductus arteriosus (PDA) stent or Blalock-Taussig shunt (BTS) from 2008 to 2015. Subjects with a defined interstage, the time between initial palliation and subsequent palliation or repair, were included. Primary outcome was change in weight-for-age Z-score. Secondary outcomes included % of patients on: all oral feeds, feeding-related medications, higher calorie feeds, and feeding-related readmission. Propensity score was used to account for baseline differences. Subgroup analysis was performed in 1- (1V) and 2-ventricle (2V) groups. The cohort included 66 PDA stent (43.9% 1V) and 195 BTS (54.4% 1V) subjects. Prematurity was more common in the PDA stent group (P=0.051). After adjustment, change in weight-for-age Z-score did not differ between groups over the entire interstage. However, change in weight-for-age Z-score favored PDA stent during the inpatient interstage (P=0.005) and BTS during the outpatient interstage (P=0.032). At initial hospital discharge, PDA stent treatment was associated with all oral feeds (P<0.001) and absence of feeding-related medications (P=0.002). Subgroup analysis revealed that 2V but not 1V patients demonstrated significant increase in weight-for-age Z-score. In the 2V cohort, feeding-related readmissions were more common in the BTS group (P=0.008). Conclusions In infants with ductal-dependent pulmonary blood flow who underwent palliation with PDA stent or BTS, there was no difference in interstage growth. PDA stent was associated with a simpler feeding regimen and fewer feeding-related readmissions.Background In infants with ductal-dependent pulmonary blood flow, the impact of palliation strategy on interstage growth and feeding regimen is unknown. Methods and Results This was a retrospective multicenter study of infants with ductal-dependent pulmonary blood flow palliated with patent ductus arteriosus (PDA) stent or Blalock-Taussig shunt (BTS) from 2008 to 2015. Subjects with a defined interstage, the time between initial palliation and subsequent palliation or repair, were included. Primary outcome was change in weight-for-age Z-score. Secondary outcomes included % of patients on: all oral feeds, feeding-related medications, higher calorie feeds, and feeding-related readmission. Propensity score was used to account for baseline differences. Subgroup analysis was performed in 1- (1V) and 2-ventricle (2V) groups. The cohort included 66 PDA stent (43.9% 1V) and 195 BTS (54.4% 1V) subjects. Prematurity was more common in the PDA stent group (P=0.051). After adjustment, change in weight-for-age Z-score did not differ between groups over the entire interstage. However, change in weight-for-age Z-score favored PDA stent during the inpatient interstage (P=0.005) and BTS during the outpatient interstage (P=0.032). At initial hospital discharge, PDA stent treatment was associated with all oral feeds (P<0.001) and absence of feeding-related medications (P=0.002). Subgroup analysis revealed that 2V but not 1V patients demonstrated significant increase in weight-for-age Z-score. In the 2V cohort, feeding-related readmissions were more common in the BTS group (P=0.008). Conclusions In infants with ductal-dependent pulmonary blood flow who underwent palliation with PDA stent or BTS, there was no difference in interstage growth. PDA stent was associated with a simpler feeding regimen and fewer feeding-related readmissions. |
Author | Goldstein, Bryan H. Petit, Christopher J. Aggarwal, Varun Nicholson, George T. Gartenberg, Ari J. Qureshi, Athar M. Ligon, R. Allen Kelleman, Michael Bauser‐Heaton, Holly Meadows, Jeffery J. McCracken, Courtney Glatz, Andrew C. Kwakye, Derek B. |
AuthorAffiliation | 4 Sibley Heart Center Cardiology Department of Pediatrics Children's Healthcare of Atlanta Emory University School of Medicine Atlanta GA 1 Division of Cardiology Department of Pediatrics Vanderbilt University School of Medicine Nashville TN 5 Division of Cardiology Department of Pediatrics University of California San Francisco School of Medicine San Francisco CA 6 The Heart Institute Cincinnati Children's Hospital Medical Center Department of Pediatrics University of Cincinnati College of Medicine Cincinnati OH 2 Department of Pediatrics The Cardiac Center Children's Hospital of Philadelphia Perelman School of Medicine at the University of Pennsylvania Philadelphia PA 3 Lillie Frank Abercrombie Section of Cardiology Department of Pediatrics Texas Children's Hospital Baylor College of Medicine Houston TX |
AuthorAffiliation_xml | – name: 1 Division of Cardiology Department of Pediatrics Vanderbilt University School of Medicine Nashville TN – name: 2 Department of Pediatrics The Cardiac Center Children's Hospital of Philadelphia Perelman School of Medicine at the University of Pennsylvania Philadelphia PA – name: 6 The Heart Institute Cincinnati Children's Hospital Medical Center Department of Pediatrics University of Cincinnati College of Medicine Cincinnati OH – name: 5 Division of Cardiology Department of Pediatrics University of California San Francisco School of Medicine San Francisco CA – name: 4 Sibley Heart Center Cardiology Department of Pediatrics Children's Healthcare of Atlanta Emory University School of Medicine Atlanta GA – name: 3 Lillie Frank Abercrombie Section of Cardiology Department of Pediatrics Texas Children's Hospital Baylor College of Medicine Houston TX |
Author_xml | – sequence: 1 givenname: George T. surname: Nicholson fullname: Nicholson, George T. organization: Division of Cardiology Department of Pediatrics Vanderbilt University School of Medicine Nashville TN – sequence: 2 givenname: Andrew C. surname: Glatz fullname: Glatz, Andrew C. organization: Department of Pediatrics The Cardiac Center Children's Hospital of Philadelphia Perelman School of Medicine at the University of Pennsylvania Philadelphia PA – sequence: 3 givenname: Athar M. surname: Qureshi fullname: Qureshi, Athar M. organization: Lillie Frank Abercrombie Section of Cardiology Department of Pediatrics Texas Children's Hospital Baylor College of Medicine Houston TX – sequence: 4 givenname: Christopher J. surname: Petit fullname: Petit, Christopher J. organization: Sibley Heart Center Cardiology Department of Pediatrics Children's Healthcare of Atlanta Emory University School of Medicine Atlanta GA – sequence: 5 givenname: Jeffery J. surname: Meadows fullname: Meadows, Jeffery J. organization: Division of Cardiology Department of Pediatrics University of California San Francisco School of Medicine San Francisco CA – sequence: 6 givenname: Courtney surname: McCracken fullname: McCracken, Courtney organization: Sibley Heart Center Cardiology Department of Pediatrics Children's Healthcare of Atlanta Emory University School of Medicine Atlanta GA – sequence: 7 givenname: Michael surname: Kelleman fullname: Kelleman, Michael organization: Sibley Heart Center Cardiology Department of Pediatrics Children's Healthcare of Atlanta Emory University School of Medicine Atlanta GA – sequence: 8 givenname: Holly surname: Bauser‐Heaton fullname: Bauser‐Heaton, Holly organization: Sibley Heart Center Cardiology Department of Pediatrics Children's Healthcare of Atlanta Emory University School of Medicine Atlanta GA – sequence: 9 givenname: Ari J. surname: Gartenberg fullname: Gartenberg, Ari J. organization: Department of Pediatrics The Cardiac Center Children's Hospital of Philadelphia Perelman School of Medicine at the University of Pennsylvania Philadelphia PA – sequence: 10 givenname: R. Allen surname: Ligon fullname: Ligon, R. Allen organization: Sibley Heart Center Cardiology Department of Pediatrics Children's Healthcare of Atlanta Emory University School of Medicine Atlanta GA – sequence: 11 givenname: Varun surname: Aggarwal fullname: Aggarwal, Varun organization: Lillie Frank Abercrombie Section of Cardiology Department of Pediatrics Texas Children's Hospital Baylor College of Medicine Houston TX – sequence: 12 givenname: Derek B. surname: Kwakye fullname: Kwakye, Derek B. organization: The Heart Institute Cincinnati Children's Hospital Medical Center Department of Pediatrics University of Cincinnati College of Medicine Cincinnati OH – sequence: 13 givenname: Bryan H. surname: Goldstein fullname: Goldstein, Bryan H. organization: The Heart Institute Cincinnati Children's Hospital Medical Center Department of Pediatrics University of Cincinnati College of Medicine Cincinnati OH |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31852418$$D View this record in MEDLINE/PubMed |
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Snippet | Background In infants with ductal-dependent pulmonary blood flow, the impact of palliation strategy on interstage growth and feeding regimen is unknown.... Background In infants with ductal‐dependent pulmonary blood flow, the impact of palliation strategy on interstage growth and feeding regimen is unknown.... |
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SubjectTerms | Age Factors Blalock-Taussig Procedure - adverse effects Body Height Cardiac Catheterization - adverse effects Cardiac Catheterization - instrumentation Child Development Child, Preschool congenital heart disease Ductus Arteriosus - diagnostic imaging Ductus Arteriosus - physiopathology Feeding Methods - adverse effects Female Heart Defects, Congenital - diagnostic imaging Heart Defects, Congenital - physiopathology Heart Defects, Congenital - surgery Humans Infant Infant, Newborn Male Original Research outcomes research Palliative Care Pulmonary Circulation Retrospective Studies Stents surgery Time Factors Treatment Outcome United States Weight Gain |
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Title | Impact of Palliation Strategy on Interstage Feeding and Somatic Growth for Infants With Ductal‐Dependent Pulmonary Blood Flow: Results from the Congenital Catheterization Research Collaborative |
URI | https://www.ncbi.nlm.nih.gov/pubmed/31852418 https://www.proquest.com/docview/2328773550 https://pubmed.ncbi.nlm.nih.gov/PMC6988161 https://doaj.org/article/49df09428f354bc2b4006cb1e44c2d8b |
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