Intestinal Function in Neonates With Complex Congenital Heart Disease
Primary Purpose
Congenital Heart Defects, Growth Failure
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Arm 1: NPO by mouth pre-operative
Arm 2: Fresh Breast Milk pre-operative
Sponsored by
About this trial
This is an interventional treatment trial for Congenital Heart Defects focused on measuring congenital heart defects, growth failure
Eligibility Criteria
Inclusion Criteria:
- Study subjects will be male and female neonates admitted to MUSC PCICU or NICU prior to 72 hours of life who are gestational age ≥ 37 weeks.
- inpatient status at MUSC for a minimum of 48 hours prior to planned surgery and have a postnatal diagnosis of complex congenital heart disease - defined as a structural heart defect requiring cardiac surgery (reparative or palliative) prior to hospital discharge.
Exclusion Criteria:
- Infants with hemodynamic instability in the pre-operative period requiring mechanical circulatory support or
- who have the presence of lactate > 3 after the first 24 hours of admission
- admission from home
- major congenital extracardiac abnormalities (i.e. renal, brain, GI)
- cardiac surgery will not be performed at MUSC, and
- mother does not plan to pump breastmilk during the infant's first week of life.
Sites / Locations
- Medical University of South Carolina
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Active Comparator
Arm Label
Arm 1: NPO pre-operative
Arm 2: Fresh Breast Milk pre-operative
Arm Description
1) Current care - NPO (nothing by mouth) postnatal intestinal function of neonates with complex CHD who receive enteral trophic breastmilk (10cc/kg/day) feeds (intervention) vs NPO (nothing by mouth) in the pre-operative period.
2) Intervention - Trophic mother's own fresh (non-frozen) breastmilk gavage feeds via nasogastric tube every 3 hours at 10 cc/kg/day
Outcomes
Primary Outcome Measures
Change in urine lactulose/mannitol ratio over time
Specific Aim 1: compare decrease in intestinal permeability by urine lactulose: mannitol ratios of the trophic breastmilk fed group (intervention) vs. NPO (nothing by mouth) group (current care) amongst neonates with complex CHD over 3 different time points (postnatal day 3-4, post-operative day 7-8, and post-operative day 13-14).
Secondary Outcome Measures
Enteral Feeds
Specific Aim 2: To compare the duration (in days) until goal enteral feeds are successfully achieved in the trophic breastmilk fed group vs. NPO group.
H1: Infants who receive trophic breastmilk feeds in the pre-operative period will successfully achieve goal enteral feeds in a shorter duration of time compared to those infants who were strictly NPO in the pre-operative period.
Intestinal Microflora Pattern
Specific Aim 3: To qualitatively compare the intestinal microflora pattern over the first postpartum month as determined by stool microbiota of the trophic breastmilk fed group vs. NPO group.
H1: The microbiota patterns of those infants who receive trophic breastmilk feeds in the pre-operative period will differ from those infants who were strictly NPO in the pre-operative period.
Full Information
NCT ID
NCT01475357
First Posted
October 6, 2011
Last Updated
October 14, 2014
Sponsor
Medical University of South Carolina
1. Study Identification
Unique Protocol Identification Number
NCT01475357
Brief Title
Intestinal Function in Neonates With Complex Congenital Heart Disease
Official Title
Intestinal Function in Neonates With Complex Congenital Heart Disease
Study Type
Interventional
2. Study Status
Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
March 2014 (Actual)
Study Completion Date
April 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of South Carolina
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Postnatal intestinal function in cardiac infants. The overall goal of this proposal is to address a widespread health problem in the pediatric cardiac infant population - poor postnatal growth - through a collaborative effort between pediatric cardiology, cardiothoracic surgery, neonatology, microbiology, and immunology. The hypothesis is that term neonates with complex congenital heart disease (CHD) who receive trophic breastmilk feeds in the pre-operative period will show improved gut function than neonates who were strictly NPO (nothing by mouth) in the pre-operative period.
Detailed Description
The overall goal of this proposal is to address a widespread health problem in the pediatric cardiac infant population - poor postnatal growth - through a collaborative effort between pediatric cardiology, cardiothoracic surgery, neonatology, microbiology, and immunology. The foundational hypothesis of this proposal is that term neonates (≥ 37 weeks gestation) with complex congenital heart disease (CHD) are vulnerable to disturbances in intestinal mucosal function, permeability, microflora, and local immune function, which ultimately result in feeding intolerance and poor somatic growth. By identifying biologic targets for perioperative intestinal protection, this project has the potential to shift and improve the paradigm of perioperative care for neonates with complex CHD. This pilot study will generate the data necessary to pursue K23 and R01 funding to further investigate postnatal intestinal maturation and function in neonates with complex CHD and cyanosis, specifically as it pertains to local immune function and inflammatory response.
The objectives of this proposal are to perform a single-center (MUSC), prospective, randomized pilot trial to investigate postnatal intestinal function in cardiac infants through the following Specific Aims:
Specific Aim 1: To compare the decrease in intestinal permeability as determined by urine lactulose: mannitol ratios of the trophic breastmilk fed group (intervention) vs. NPO (nothing by mouth) group (current care) amongst neonates with complex CHD over 3 different time points (postnatal day 3-4, post-operative day 7-8, and post-operative day 13-14).
H1: Infants who receive trophic breastmilk feeds in the pre-operative period will demonstrate a more rapid decrease in intestinal permeability (improved postnatal intestinal maturation) over the first 2 weeks of life compared to those infants who were strictly NPO in the pre-operative period.
Specific Aim 2: To compare the duration (in days) until goal enteral feeds are successfully achieved in the trophic breastmilk fed group vs. NPO group.
H1: Infants who receive trophic breastmilk feeds in the pre-operative period will successfully achieve goal enteral feeds in a shorter duration of time compared to those infants who were strictly NPO in the pre-operative period.
Specific Aim 3: To qualitatively compare the intestinal microflora pattern over the first postpartum month as determined by stool microbiota of the trophic breastmilk fed group vs. NPO group.
H1: The microbiota patterns of those infants who receive trophic breastmilk feeds in the pre-operative period will differ from those infants who were strictly NPO in the pre-operative period.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Defects, Growth Failure
Keywords
congenital heart defects, growth failure
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
27 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Arm 1: NPO pre-operative
Arm Type
Other
Arm Description
1) Current care - NPO (nothing by mouth) postnatal intestinal function of neonates with complex CHD who receive enteral trophic breastmilk (10cc/kg/day) feeds (intervention) vs NPO (nothing by mouth) in the pre-operative period.
Arm Title
Arm 2: Fresh Breast Milk pre-operative
Arm Type
Active Comparator
Arm Description
2) Intervention - Trophic mother's own fresh (non-frozen) breastmilk gavage feeds via nasogastric tube every 3 hours at 10 cc/kg/day
Intervention Type
Other
Intervention Name(s)
Arm 1: NPO by mouth pre-operative
Intervention Description
Current treatment for infants born with cardiac defects awaiting surgery is to keep them NPO pre-operatively. Arm 1 will make no changes to this current policy.
Intervention Type
Other
Intervention Name(s)
Arm 2: Fresh Breast Milk pre-operative
Intervention Description
Infants randomized to Arm 2 of the study will receive their mother's own breast milk pre-operatively.
Primary Outcome Measure Information:
Title
Change in urine lactulose/mannitol ratio over time
Description
Specific Aim 1: compare decrease in intestinal permeability by urine lactulose: mannitol ratios of the trophic breastmilk fed group (intervention) vs. NPO (nothing by mouth) group (current care) amongst neonates with complex CHD over 3 different time points (postnatal day 3-4, post-operative day 7-8, and post-operative day 13-14).
Time Frame
post-natal day 3-4 (baseline), post-op days 7 and 14
Secondary Outcome Measure Information:
Title
Enteral Feeds
Description
Specific Aim 2: To compare the duration (in days) until goal enteral feeds are successfully achieved in the trophic breastmilk fed group vs. NPO group.
H1: Infants who receive trophic breastmilk feeds in the pre-operative period will successfully achieve goal enteral feeds in a shorter duration of time compared to those infants who were strictly NPO in the pre-operative period.
Time Frame
Duration (in days) until goal enteral feeds are achieved, an expected average of 3 weeks
Title
Intestinal Microflora Pattern
Description
Specific Aim 3: To qualitatively compare the intestinal microflora pattern over the first postpartum month as determined by stool microbiota of the trophic breastmilk fed group vs. NPO group.
H1: The microbiota patterns of those infants who receive trophic breastmilk feeds in the pre-operative period will differ from those infants who were strictly NPO in the pre-operative period.
Time Frame
30 days 1st post-partum month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
37 Weeks
Maximum Age & Unit of Time
40 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Study subjects will be male and female neonates admitted to MUSC PCICU or NICU prior to 72 hours of life who are gestational age ≥ 37 weeks.
inpatient status at MUSC for a minimum of 48 hours prior to planned surgery and have a postnatal diagnosis of complex congenital heart disease - defined as a structural heart defect requiring cardiac surgery (reparative or palliative) prior to hospital discharge.
Exclusion Criteria:
Infants with hemodynamic instability in the pre-operative period requiring mechanical circulatory support or
who have the presence of lactate > 3 after the first 24 hours of admission
admission from home
major congenital extracardiac abnormalities (i.e. renal, brain, GI)
cardiac surgery will not be performed at MUSC, and
mother does not plan to pump breastmilk during the infant's first week of life.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sinai C Zyblewski, MD
Organizational Affiliation
Medical University of South Carolina
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University of South Carolina
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
19619784
Citation
Anderson JB, Beekman RH 3rd, Border WL, Kalkwarf HJ, Khoury PR, Uzark K, Eghtesady P, Marino BS. Lower weight-for-age z score adversely affects hospital length of stay after the bidirectional Glenn procedure in 100 infants with a single ventricle. J Thorac Cardiovasc Surg. 2009 Aug;138(2):397-404.e1. doi: 10.1016/j.jtcvs.2009.02.033. Epub 2009 May 23.
Results Reference
background
PubMed Identifier
16500550
Citation
Kelleher DK, Laussen P, Teixeira-Pinto A, Duggan C. Growth and correlates of nutritional status among infants with hypoplastic left heart syndrome (HLHS) after stage 1 Norwood procedure. Nutrition. 2006 Mar;22(3):237-44. doi: 10.1016/j.nut.2005.06.008.
Results Reference
background
PubMed Identifier
14472142
Citation
MEHRIZI A, DRASH A. Growth disturbance in congenital heart disease. J Pediatr. 1962 Sep;61:418-29. doi: 10.1016/s0022-3476(62)80373-4. No abstract available.
Results Reference
background
PubMed Identifier
19321898
Citation
Owens JL, Musa N. Nutrition support after neonatal cardiac surgery. Nutr Clin Pract. 2009 Apr-May;24(2):242-9. doi: 10.1177/0884533609332086.
Results Reference
background
PubMed Identifier
19116405
Citation
Schwalbe-Terilli CR, Hartman DH, Nagle ML, Gallagher PR, Ittenbach RF, Burnham NB, Gaynor JW, Ravishankar C. Enteral feeding and caloric intake in neonates after cardiac surgery. Am J Crit Care. 2009 Jan;18(1):52-7. doi: 10.4037/ajcc2009405.
Results Reference
background
PubMed Identifier
16488706
Citation
Jeffries HE, Wells WJ, Starnes VA, Wetzel RC, Moromisato DY. Gastrointestinal morbidity after Norwood palliation for hypoplastic left heart syndrome. Ann Thorac Surg. 2006 Mar;81(3):982-7. doi: 10.1016/j.athoracsur.2005.09.001.
Results Reference
background
PubMed Identifier
19403484
Citation
Pickard SS, Feinstein JA, Popat RA, Huang L, Dutta S. Short- and long-term outcomes of necrotizing enterocolitis in infants with congenital heart disease. Pediatrics. 2009 May;123(5):e901-6. doi: 10.1542/peds.2008-3216.
Results Reference
background
PubMed Identifier
16474253
Citation
del Castillo SL, Moromisato DY, Dorey F, Ludwick J, Starnes VA, Wells WJ, Jeffries HE, Wong PC. Mesenteric blood flow velocities in the newborn with single-ventricle physiology: modified Blalock-Taussig shunt versus right ventricle-pulmonary artery conduit. Pediatr Crit Care Med. 2006 Mar;7(2):132-7. doi: 10.1097/01.PCC.0000200999.89777.92.
Results Reference
background
PubMed Identifier
15982432
Citation
Harrison AM, Davis S, Reid JR, Morrison SC, Arrigain S, Connor JT, Temple ME. Neonates with hypoplastic left heart syndrome have ultrasound evidence of abnormal superior mesenteric artery perfusion before and after modified Norwood procedure. Pediatr Crit Care Med. 2005 Jul;6(4):445-7. doi: 10.1097/01.PCC.0000163674.53466.CA.
Results Reference
background
PubMed Identifier
11061778
Citation
McElhinney DB, Hedrick HL, Bush DM, Pereira GR, Stafford PW, Gaynor JW, Spray TL, Wernovsky G. Necrotizing enterocolitis in neonates with congenital heart disease: risk factors and outcomes. Pediatrics. 2000 Nov;106(5):1080-7. doi: 10.1542/peds.106.5.1080.
Results Reference
background
PubMed Identifier
1561008
Citation
Bernstein D, Bell JG, Kwong L, Castillo RO. Alterations in postnatal intestinal function during chronic hypoxemia. Pediatr Res. 1992 Mar;31(3):234-8. doi: 10.1203/00006450-199203000-00008.
Results Reference
background
PubMed Identifier
19014824
Citation
Willis L, Thureen P, Kaufman J, Wymore E, Skillman H, da Cruz E. Enteral feeding in prostaglandin-dependent neonates: is it a safe practice? J Pediatr. 2008 Dec;153(6):867-9. doi: 10.1016/j.jpeds.2008.04.074.
Results Reference
background
PubMed Identifier
19307819
Citation
Braudis NJ, Curley MA, Beaupre K, Thomas KC, Hardiman G, Laussen P, Gauvreau K, Thiagarajan RR. Enteral feeding algorithm for infants with hypoplastic left heart syndrome poststage I palliation. Pediatr Crit Care Med. 2009 Jul;10(4):460-6. doi: 10.1097/PCC.0b013e318198b167.
Results Reference
background
PubMed Identifier
19838139
Citation
del Castillo SL, McCulley ME, Khemani RG, Jeffries HE, Thomas DW, Peregrine J, Wells WJ, Starnes VA, Moromisato DY. Reducing the incidence of necrotizing enterocolitis in neonates with hypoplastic left heart syndrome with the introduction of an enteral feed protocol. Pediatr Crit Care Med. 2010 May;11(3):373-7. doi: 10.1097/PCC.0b013e3181c01475.
Results Reference
background
PubMed Identifier
20453528
Citation
Natarajan G, Reddy Anne S, Aggarwal S. Enteral feeding of neonates with congenital heart disease. Neonatology. 2010;98(4):330-6. doi: 10.1159/000285706. Epub 2010 May 7.
Results Reference
background
PubMed Identifier
18034198
Citation
Johnson BA, Mussatto K, Uhing MR, Zimmerman H, Tweddell J, Ghanayem N. Variability in the preoperative management of infants with hypoplastic left heart syndrome. Pediatr Cardiol. 2008 May;29(3):515-20. doi: 10.1007/s00246-007-9022-1. Epub 2007 Nov 22.
Results Reference
background
PubMed Identifier
1809006
Citation
Bines JE, Walker WA. Growth factors and the development of neonatal host defense. Adv Exp Med Biol. 1991;310:31-9. doi: 10.1007/978-1-4615-3838-7_3. No abstract available.
Results Reference
background
PubMed Identifier
10749395
Citation
Walker WA. Role of nutrients and bacterial colonization in the development of intestinal host defense. J Pediatr Gastroenterol Nutr. 2000;30 Suppl 2:S2-7.
Results Reference
background
PubMed Identifier
15384575
Citation
Walker WA. The dynamic effects of breastfeeding on intestinal development and host defense. Adv Exp Med Biol. 2004;554:155-70. doi: 10.1007/978-1-4757-4242-8_15.
Results Reference
background
PubMed Identifier
14599042
Citation
Fanaro S, Chierici R, Guerrini P, Vigi V. Intestinal microflora in early infancy: composition and development. Acta Paediatr Suppl. 2003 Sep;91(441):48-55. doi: 10.1111/j.1651-2227.2003.tb00646.x.
Results Reference
background
PubMed Identifier
16882802
Citation
Penders J, Thijs C, Vink C, Stelma FF, Snijders B, Kummeling I, van den Brandt PA, Stobberingh EE. Factors influencing the composition of the intestinal microbiota in early infancy. Pediatrics. 2006 Aug;118(2):511-21. doi: 10.1542/peds.2005-2824.
Results Reference
background
PubMed Identifier
19385995
Citation
Tanaka S, Kobayashi T, Songjinda P, Tateyama A, Tsubouchi M, Kiyohara C, Shirakawa T, Sonomoto K, Nakayama J. Influence of antibiotic exposure in the early postnatal period on the development of intestinal microbiota. FEMS Immunol Med Microbiol. 2009 Jun;56(1):80-7. doi: 10.1111/j.1574-695X.2009.00553.x. Epub 2009 Apr 6.
Results Reference
background
PubMed Identifier
18081456
Citation
Goldman AS. The immune system in human milk and the developing infant. Breastfeed Med. 2007 Dec;2(4):195-204. doi: 10.1089/bfm.2007.0024.
Results Reference
background
PubMed Identifier
17145901
Citation
Pietz J, Achanti B, Lilien L, Stepka EC, Mehta SK. Prevention of necrotizing enterocolitis in preterm infants: a 20-year experience. Pediatrics. 2007 Jan;119(1):e164-70. doi: 10.1542/peds.2006-0521. Epub 2006 Dec 4.
Results Reference
background
PubMed Identifier
17284759
Citation
Raiten DJ, Kalhan SC, Hay WW Jr. Maternal nutrition and optimal infant feeding practices: executive summary. Am J Clin Nutr. 2007 Feb;85(2):577S-583S. doi: 10.1093/ajcn/85.2.577S.
Results Reference
background
PubMed Identifier
3277090
Citation
Klagsbrun M. Nutrition Classics. Proceedings of the National Academy of Sciences of the United States of America, October 1978, Volume 75, Number 10: Human milk stimulates DNA synthesis and cellular proliferation in cultured fibroblasts. By Michael Klagsbrun. Nutr Rev. 1988 Jan;46(1):21-3. doi: 10.1111/j.1753-4887.1988.tb05349.x. No abstract available.
Results Reference
background
PubMed Identifier
16798726
Citation
Clark JA, Doelle SM, Halpern MD, Saunders TA, Holubec H, Dvorak K, Boitano SA, Dvorak B. Intestinal barrier failure during experimental necrotizing enterocolitis: protective effect of EGF treatment. Am J Physiol Gastrointest Liver Physiol. 2006 Nov;291(5):G938-49. doi: 10.1152/ajpgi.00090.2006. Epub 2006 Jun 22.
Results Reference
background
PubMed Identifier
15528252
Citation
Clark JA, Lane RH, Maclennan NK, Holubec H, Dvorakova K, Halpern MD, Williams CS, Payne CM, Dvorak B. Epidermal growth factor reduces intestinal apoptosis in an experimental model of necrotizing enterocolitis. Am J Physiol Gastrointest Liver Physiol. 2005 Apr;288(4):G755-62. doi: 10.1152/ajpgi.00172.2004. Epub 2004 Nov 4.
Results Reference
background
PubMed Identifier
20105663
Citation
Dvorak B. Milk epidermal growth factor and gut protection. J Pediatr. 2010 Feb;156(2 Suppl):S31-5. doi: 10.1016/j.jpeds.2009.11.018.
Results Reference
background
PubMed Identifier
19196035
Citation
Taylor SN, Basile LA, Ebeling M, Wagner CL. Intestinal permeability in preterm infants by feeding type: mother's milk versus formula. Breastfeed Med. 2009 Mar;4(1):11-5. doi: 10.1089/bfm.2008.0114.
Results Reference
background
PubMed Identifier
9691155
Citation
Garofalo RP, Goldman AS. Cytokines, chemokines, and colony-stimulating factors in human milk: the 1997 update. Biol Neonate. 1998;74(2):134-42. doi: 10.1159/000014019.
Results Reference
background
PubMed Identifier
3880886
Citation
Hanson LA, Ahlstedt S, Andersson B, Carlsson B, Fallstrom SP, Mellander L, Porras O, Soderstrom T, Eden CS. Protective factors in milk and the development of the immune system. Pediatrics. 1985 Jan;75(1 Pt 2):172-6.
Results Reference
background
PubMed Identifier
8540428
Citation
Xanthou M, Bines J, Walker WA. Human milk and intestinal host defense in newborns: an update. Adv Pediatr. 1995;42:171-208.
Results Reference
background
PubMed Identifier
12496227
Citation
van Elburg RM, Fetter WP, Bunkers CM, Heymans HS. Intestinal permeability in relation to birth weight and gestational and postnatal age. Arch Dis Child Fetal Neonatal Ed. 2003 Jan;88(1):F52-5. doi: 10.1136/fn.88.1.f52.
Results Reference
background
PubMed Identifier
8583288
Citation
Catassi C, Bonucci A, Coppa GV, Carlucci A, Giorgi PL. Intestinal permeability changes during the first month: effect of natural versus artificial feeding. J Pediatr Gastroenterol Nutr. 1995 Nov;21(4):383-6. doi: 10.1097/00005176-199511000-00003.
Results Reference
background
PubMed Identifier
3123630
Citation
Weaver LT, Laker MF, Nelson R, Lucas A. Milk feeding and changes in intestinal permeability and morphology in the newborn. J Pediatr Gastroenterol Nutr. 1987 May-Jun;6(3):351-8. doi: 10.1097/00005176-198705000-00008.
Results Reference
background
PubMed Identifier
12516776
Citation
He F, Morita H, Ouwehand AC, Hosoda M, Hiramatsu M, Kurisaki J, Isolauri E, Benno Y, Salminen S. Stimulation of the secretion of pro-inflammatory cytokines by Bifidobacterium strains. Microbiol Immunol. 2002;46(11):781-5. doi: 10.1111/j.1348-0421.2002.tb02765.x.
Results Reference
background
PubMed Identifier
3081865
Citation
Walsh MC, Kliegman RM. Necrotizing enterocolitis: treatment based on staging criteria. Pediatr Clin North Am. 1986 Feb;33(1):179-201. doi: 10.1016/s0031-3955(16)34975-6.
Results Reference
background
PubMed Identifier
6424583
Citation
Weaver LT, Laker MF, Nelson R. Intestinal permeability in the newborn. Arch Dis Child. 1984 Mar;59(3):236-41. doi: 10.1136/adc.59.3.236.
Results Reference
background
PubMed Identifier
18607263
Citation
Dvorak B, Khailova L, Clark JA, Hosseini DM, Arganbright KM, Reynolds CA, Halpern MD. Comparison of epidermal growth factor and heparin-binding epidermal growth factor-like growth factor for prevention of experimental necrotizing enterocolitis. J Pediatr Gastroenterol Nutr. 2008 Jul;47(1):11-8. doi: 10.1097/MPG.0b013e3181788618.
Results Reference
background
PubMed Identifier
25962930
Citation
Zyblewski SC, Nietert PJ, Graham EM, Taylor SN, Atz AM, Wagner CL. Randomized Clinical Trial of Preoperative Feeding to Evaluate Intestinal Barrier Function in Neonates Requiring Cardiac Surgery. J Pediatr. 2015 Jul;167(1):47-51.e1. doi: 10.1016/j.jpeds.2015.04.035. Epub 2015 May 8.
Results Reference
derived
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Intestinal Function in Neonates With Complex Congenital Heart Disease
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