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Continuous Versus Intermittent Bolus Feeding in Very Preterm Infants - Effect on Respiratory Morbidity (CONFER)

Primary Purpose

Chronic Lung Disease of Prematurity, Bronchopulmonary Dysplasia

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Method of feeding; continuous feeding OR bolus feeding
Sponsored by
National University Hospital, Singapore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Chronic Lung Disease of Prematurity focused on measuring Prematurity, Randomised control trial (RCT), BPD, CLD, continuous feeding

Eligibility Criteria

1 Day - 3 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants with a birth weight <1250g and a gestational age of between 24+0 - 33+6 weeks

Exclusion Criteria:

  1. Major congenital malformation
  2. Chromosomal abnormality
  3. 10-minute Apgar score of =3
  4. Not expected to survive beyond 72 hours of age
  5. Bilateral grade 4 intraventricular haemorrhage (IVH)
  6. Did not consent / Consent not available

Sites / Locations

  • NICU, Universiti Kebangsaan MalaysiaRecruiting
  • NICU, National University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Continuous feeding (CF)

Bolus feeding (BF)

Arm Description

Infants fed through a naso or orogastric tube in a continuous fashion using syringe pump. Each feed cycle is of 4 hours (3 hrs continuous feeding and 1 hour rest). 6 feed cycles in a day. Feed volume increment per day is as per departmental protocol and same as comparator arm.

Infants fed through a naso or orogastric tube in a gravity dependent bolus feeding every 2-3 hours. Each feed would take approximately 10 minutes. Feed volume increment per day is as per departmental protocol and same as experimental arm.

Outcomes

Primary Outcome Measures

Incidence of BPD
BPD as defined by 2001 NICHD criteria
Incidence of Death
Death occurring before 36 weeks post menstrual age or 28 days of life

Secondary Outcome Measures

Invasive Ventilatory requirements
Days on invasive ventilation
Any Ventilatory requirements
Days on any ventilatory (invasive or non invasive) support
Supplemental Oxygen support
Days on supplemental oxygen
Feed tolerance
Time (days) from randomization to achievement of full feeds (defined as 150ml/Kg/Day)
Weight outcomes
Z-scores for weight (grams)
Length outcomes
Z-scores for length (cm)
Head Growth outcomes
Z-scores for head circumference (cm)

Full Information

First Posted
May 15, 2019
Last Updated
January 14, 2020
Sponsor
National University Hospital, Singapore
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1. Study Identification

Unique Protocol Identification Number
NCT03961139
Brief Title
Continuous Versus Intermittent Bolus Feeding in Very Preterm Infants - Effect on Respiratory Morbidity
Acronym
CONFER
Official Title
Continuous Versus Intermittent Bolus Feeding in Very Preterm Infants - Effects on Respiratory Morbidity: A Multicentre Randomised Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Unknown status
Study Start Date
December 3, 2019 (Actual)
Primary Completion Date
June 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National University Hospital, Singapore

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Chronic Lung Disease (CLD) of Prematurity is a common yet challenging co-morbidity affecting extremely premature newborns. Multifactorial influences leading to this co-morbidity is known and targeted in various research studies. Gastroesophageal reflux (GER) is common among the same cohort of patients. The investigators hypothesize that recurrent milk reflux into the airways of the premature babies worsen the inflammation of premature lungs and is a major contributor of CLD. The investigators hypothesize that Continuous feeding (CF) minimises GER and micro-aspiration, thereby reducing the incidence and severity of CLD in high-risk infants. Our aim is to compare the effect of intermittent bolus versus continuous intra-gastric feeding on the incidence and severity of CLD in very low birth weight infants ≤ 1250 grams.
Detailed Description
The pathogenesis of bronchopulmonary dysplasia (BPD) is complex and multifactorial. As a result of premature birth, developmental arrest during a critical period of fetal lung development compounded by mechanical, oxidative and other injuries sustained during neonatal respiratory care forms the basis of pathogenesis. BPD affects up to 50% of infants with birth weight less than 1000 g. Between 2000 and 2009, despite advancement of neonatal care, annual BPD rates reported by Vermont Oxford Network among very low birth weight infants varied from 26.2% to 30.4% without any decline. Severely affected infants often require prolonged ventilation, high oxygen use, alternative airway and several potent medications over the first few months to years of their lives. High mortality rates, neurodevelopmental delay, respiratory morbidity and growth failure are associated with BPD. Treatment of severe BPD with or without pulmonary hypertension is challenging. Prolonging the pregnancy in the face of premature labour, treating perinatal infections, augmenting pulmonary maturity with corticosteroids, judicious oxygen use, lung protective ventilation and optimizing nutrition to promote growth are important and well established measures to prevent or modify the progress of the chronic lung disease. It is common to find infants with BPD also having significant symptoms of reflux. Gastroesophageal reflux (GER) is a well-known co-morbidity among preterms and ex-preterms on chronic ventilation, many of whom go on to require surgical fundoplication to stop the reflux thus preventing further lung damage. Some have reported dramatic respiratory improvement after resolution of GER. In the early days of a preterm baby with respiratory distress, GER is common and silent. Among infants, diagnosis of pathologic GER from a benign one is difficult. Many neonatal intensive care units (NICUs) would investigate for GER only when faced with moderate to severe BPD to achieve better respiratory symptom control. However GER has not been studied well as a factor precipitating the development of BPD among VLBW neonates. This is the focus of the study. Aspiration of gastric contents into the lung is a widespread phenomenon in mechanically ventilated preterm infants. In animal models of gastric aspiration, gastric particulates altered the pulmonary mechanics, increased pulmonary inflammatory cells, released pro-inflammatory mediators, and inactivated surfactant. Development of bacterial pneumonia is a well-recognized complication following aspiration of gastric contents. The investigators hypothesize that repeated aspirations would aggravate and accelerate an inflammatory response in the lung finally leading on to BPD. In addition oxygen mediated damage and mechanical ventilation potentiate lung injury due to aspiration. Logically, if GER and aspiration could be minimized, it could decrease the incidence and severity of BPD. Certain positioning of the baby, small volume of feed increment, keeping a close watch on feed tolerance are practical ways of improving feeding tolerance and reducing GER. The intermittent bolus intra-gastric feeding method is commonly used to feed premature babies. Other alternatives are continuous intra-gastric (feed volume is slowly infused in the stomach over couple of hours through the nasogastric tube) and continuous transpyloric feeding (feeding tube passes beyond the stomach to the duodenum and feed volume is slowly infused over hours). Transpyloric continuous feeding as compared to intermittent gastric bolus feeding, has been found to significantly reduce ventilatory support requirements in extremely low birth weight (ELBW) infants, possibly via its effect of minimising GER. In this study, none of the babies who received transpyloric feeding developed significant BPD and in addition babies with significant BPD improved after switching to transpyloric method. Transpyloric feeding tubes however are challenging to insert, and intestinal perforation is an uncommon but significant adverse effect. This feeding method is also not physiological as it bypasses the stomach. It remains to be seen if continuous gastric feeds, which is easily administered and safer, would yield some of the advantages of continuous transpyloric feeds over intermittent gastric feeding. A Cochrane review in 2011 of continuous intra-gastric versus intermittent bolus intra-gastric feeding for premature infants found conflicting results, and was unable to make recommendations regarding the benefits and risks of these feeding methods. Clinical outcomes of interest from these trials were related to growth, feeding tolerance and gastrointestinal complications. The Cochrane review importantly found no significant difference in somatic growth and incidence of necrotising enterocolitis (NEC) between either feeding methods. Another Cochrane review in 2014 did not identify any randomised trial that evaluated the effects of continuous versus intermittent bolus intragastric tube feeding on gastro-oesophageal reflux disease in preterm and low birth weight infants and opined that well-designed and adequately powered trials are needed in this field. There were no studies comparing the effect of the above feeding methods on respiratory outcomes either. Trial objectives Aim: To compare the effect of intermittent bolus versus continuous intra-gastric feeding on the incidence and severity of BPD in very low birth weight infants (≤ 1250 grams). Hypothesis: Continuous feeding (CF) minimises silent GER and micro-aspiration, thereby reducing the incidence and severity of bronchopulmonary dysplasia (BPD) in high-risk infants when compared to intermittent bolus feeding (BF). Statistical considerations Sample size calculation: based on 2015 data from the Singapore National Very-Low-Birth-Weight (VLBW) Infant Network for infants ≤ 1250 grams, mortality rate was 12.9% and BPD rate (defined as any oxygen supplementation or any respiratory support at 36 weeks post-conceptional age) was 29.4%. Thus the composite primary outcome rate was 42.3%. For a primary outcome rate reduction from 45% to 22.5%, with a type 1 error rate of 5% and a power of 80%, a sample size of 68 infants in each arm is required, giving a total sample size of 136 infants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Lung Disease of Prematurity, Bronchopulmonary Dysplasia
Keywords
Prematurity, Randomised control trial (RCT), BPD, CLD, continuous feeding

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomised-controlled trial with 2 parallel groups (1:1 ratio). Control group: intermittent bolus intra-gastric tube feeding (BF), Intervention group: continuous intra-gastric tube feeding (CF). Not blinded. Stratified randomization along following birth weight groups: </=750 g 751 - 1000 g 1001 -1250 g Method of randomisation: Computer generated randomization codes stored in sealed opaque envelopes. Intervention started by 72 hours of life (more than trophic feed volume achieved) and continued until an infant reaches a weight of 1.6 kg and is determined by the attending Neonatologist to be ready to commence oral feeding by breast or bottle, or when an infant attains a post-conceptional age of 36 weeks, whichever is earlier. Continuous fed is delivered through a nasogastric tube by a syringe pump over 3hrs with 1 hour of break - 6 cycles a day. Feed volume, type of feed, feed increment regulated by the clinical team. Intention to treat analysis.
Masking
None (Open Label)
Masking Description
na. Open label
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Continuous feeding (CF)
Arm Type
Experimental
Arm Description
Infants fed through a naso or orogastric tube in a continuous fashion using syringe pump. Each feed cycle is of 4 hours (3 hrs continuous feeding and 1 hour rest). 6 feed cycles in a day. Feed volume increment per day is as per departmental protocol and same as comparator arm.
Arm Title
Bolus feeding (BF)
Arm Type
Active Comparator
Arm Description
Infants fed through a naso or orogastric tube in a gravity dependent bolus feeding every 2-3 hours. Each feed would take approximately 10 minutes. Feed volume increment per day is as per departmental protocol and same as experimental arm.
Intervention Type
Other
Intervention Name(s)
Method of feeding; continuous feeding OR bolus feeding
Intervention Description
CF: Infants fed through a naso or orogastric tube in a continuous fashion using syringe pump. Each feed cycle is of 4 hours (3 hrs continuous feeding and 1 hour rest). 6 feed cycles in a day. BF: Infants fed through a naso or orogastric tube in a gravity dependent bolus feeding every 2-3 hours. Each feed would take approximately 10 minutes.
Primary Outcome Measure Information:
Title
Incidence of BPD
Description
BPD as defined by 2001 NICHD criteria
Time Frame
occurring before 36 weeks post menstrual age or 28 days of life
Title
Incidence of Death
Description
Death occurring before 36 weeks post menstrual age or 28 days of life
Time Frame
occurring before 36 weeks post menstrual age or 28 days of life
Secondary Outcome Measure Information:
Title
Invasive Ventilatory requirements
Description
Days on invasive ventilation
Time Frame
36 weeks post menstrual age or 28 days of life
Title
Any Ventilatory requirements
Description
Days on any ventilatory (invasive or non invasive) support
Time Frame
36 weeks post menstrual age or 28 days of life
Title
Supplemental Oxygen support
Description
Days on supplemental oxygen
Time Frame
36 weeks post menstrual age or 28 days of life
Title
Feed tolerance
Description
Time (days) from randomization to achievement of full feeds (defined as 150ml/Kg/Day)
Time Frame
36 weeks post menstrual age or 28 days of life
Title
Weight outcomes
Description
Z-scores for weight (grams)
Time Frame
birth, 36 weeks and 40 weeks post menstrual age
Title
Length outcomes
Description
Z-scores for length (cm)
Time Frame
birth, 36 weeks and 40 weeks post menstrual age
Title
Head Growth outcomes
Description
Z-scores for head circumference (cm)
Time Frame
birth, 36 weeks and 40 weeks post menstrual age

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
3 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants with a birth weight <1250g and a gestational age of between 24+0 - 33+6 weeks Exclusion Criteria: Major congenital malformation Chromosomal abnormality 10-minute Apgar score of =3 Not expected to survive beyond 72 hours of age Bilateral grade 4 intraventricular haemorrhage (IVH) Did not consent / Consent not available
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Agnihotri Biswas, MRCPCH
Phone
+65 67725075
Email
biswas_agnihotri@nuhs.edu.sg
First Name & Middle Initial & Last Name or Official Title & Degree
Jiun Lee, MRCPCH
Phone
+65 67725076
Email
lee_jiun@nuhs.edu.sg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Agnihotri Biswas, MRCPCH
Organizational Affiliation
Senior Consultant Neonatologist, NUH Singapore
Official's Role
Principal Investigator
Facility Information:
Facility Name
NICU, Universiti Kebangsaan Malaysia
City
Kuala Lumpur
ZIP/Postal Code
56000
Country
Malaysia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fook-Choe Cheah, FRCPCH
Phone
+60 3 91456637
Email
cheahfc@ppukm.ukm.edu.my
Facility Name
NICU, National University Hospital
City
Singapore
ZIP/Postal Code
119074
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Agnihotri Biswas, MRCPCH
Phone
67725075
Email
biswas_agnihotri@nuhs.edu.sg
First Name & Middle Initial & Last Name & Degree
Jiun Lee, MRCPCH
Phone
67725075
Email
lee_jiun@nuhs.edu.sg

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
12667831
Citation
Bancalari E, Claure N, Sosenko IR. Bronchopulmonary dysplasia: changes in pathogenesis, epidemiology and definition. Semin Neonatol. 2003 Feb;8(1):63-71. doi: 10.1016/s1084-2756(02)00192-6.
Results Reference
background
PubMed Identifier
20732945
Citation
Stoll BJ, Hansen NI, Bell EF, Shankaran S, Laptook AR, Walsh MC, Hale EC, Newman NS, Schibler K, Carlo WA, Kennedy KA, Poindexter BB, Finer NN, Ehrenkranz RA, Duara S, Sanchez PJ, O'Shea TM, Goldberg RN, Van Meurs KP, Faix RG, Phelps DL, Frantz ID 3rd, Watterberg KL, Saha S, Das A, Higgins RD; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Neonatal outcomes of extremely preterm infants from the NICHD Neonatal Research Network. Pediatrics. 2010 Sep;126(3):443-56. doi: 10.1542/peds.2009-2959. Epub 2010 Aug 23.
Results Reference
background
PubMed Identifier
22614775
Citation
Horbar JD, Carpenter JH, Badger GJ, Kenny MJ, Soll RF, Morrow KA, Buzas JS. Mortality and neonatal morbidity among infants 501 to 1500 grams from 2000 to 2009. Pediatrics. 2012 Jun;129(6):1019-26. doi: 10.1542/peds.2011-3028. Epub 2012 May 21.
Results Reference
background
PubMed Identifier
16322158
Citation
Ehrenkranz RA, Walsh MC, Vohr BR, Jobe AH, Wright LL, Fanaroff AA, Wrage LA, Poole K; National Institutes of Child Health and Human Development Neonatal Research Network. Validation of the National Institutes of Health consensus definition of bronchopulmonary dysplasia. Pediatrics. 2005 Dec;116(6):1353-60. doi: 10.1542/peds.2005-0249.
Results Reference
background
PubMed Identifier
21169836
Citation
Jobe AH. The new bronchopulmonary dysplasia. Curr Opin Pediatr. 2011 Apr;23(2):167-72. doi: 10.1097/MOP.0b013e3283423e6b.
Results Reference
background
PubMed Identifier
23918888
Citation
Cristea AI, Carroll AE, Davis SD, Swigonski NL, Ackerman VL. Outcomes of children with severe bronchopulmonary dysplasia who were ventilator dependent at home. Pediatrics. 2013 Sep;132(3):e727-34. doi: 10.1542/peds.2012-2990. Epub 2013 Aug 5.
Results Reference
background
PubMed Identifier
15973322
Citation
Walsh MC, Morris BH, Wrage LA, Vohr BR, Poole WK, Tyson JE, Wright LL, Ehrenkranz RA, Stoll BJ, Fanaroff AA; National Institutes of Child Health and Human Development Neonatal Research Network. Extremely low birthweight neonates with protracted ventilation: mortality and 18-month neurodevelopmental outcomes. J Pediatr. 2005 Jun;146(6):798-804. doi: 10.1016/j.jpeds.2005.01.047.
Results Reference
background
PubMed Identifier
18055675
Citation
Khemani E, McElhinney DB, Rhein L, Andrade O, Lacro RV, Thomas KC, Mullen MP. Pulmonary artery hypertension in formerly premature infants with bronchopulmonary dysplasia: clinical features and outcomes in the surfactant era. Pediatrics. 2007 Dec;120(6):1260-9. doi: 10.1542/peds.2007-0971.
Results Reference
background
PubMed Identifier
7813274
Citation
Radford PJ, Stillwell PC, Blue B, Hertel G. Aspiration complicating bronchopulmonary dysplasia. Chest. 1995 Jan;107(1):185-8. doi: 10.1378/chest.107.1.185.
Results Reference
background
PubMed Identifier
21252395
Citation
Demirel G, Yilmaz Y, Uras N, Erdeve O, Ulu HO, Oguz SS, Dilmen U. Dramatical recovery of a mechanical ventilatory dependent extremely low birth weight premature infant after Nissen fundoplication. J Trop Pediatr. 2011 Dec;57(6):484-6. doi: 10.1093/tropej/fmq125. Epub 2011 Jan 19.
Results Reference
background
PubMed Identifier
27355979
Citation
Gien J, Kinsella J, Thrasher J, Grenolds A, Abman SH, Baker CD. Retrospective Analysis of an Interdisciplinary Ventilator Care Program Intervention on Survival of Infants with Ventilator-Dependent Bronchopulmonary Dysplasia. Am J Perinatol. 2017 Jan;34(2):155-163. doi: 10.1055/s-0036-1584897. Epub 2016 Jun 29.
Results Reference
background
PubMed Identifier
2774613
Citation
Newell SJ, Booth IW, Morgan ME, Durbin GM, McNeish AS. Gastro-oesophageal reflux in preterm infants. Arch Dis Child. 1989 Jun;64(6):780-6. doi: 10.1136/adc.64.6.780.
Results Reference
background
PubMed Identifier
8949695
Citation
Ewer AK, Durbin GM, Morgan ME, Booth IW. Gastric emptying and gastro-oesophageal reflux in preterm infants. Arch Dis Child Fetal Neonatal Ed. 1996 Sep;75(2):F117-21. doi: 10.1136/fn.75.2.f117.
Results Reference
background
PubMed Identifier
11773535
Citation
Peter CS, Sprodowski N, Bohnhorst B, Silny J, Poets CF. Gastroesophageal reflux and apnea of prematurity: no temporal relationship. Pediatrics. 2002 Jan;109(1):8-11. doi: 10.1542/peds.109.1.8.
Results Reference
background
PubMed Identifier
16831894
Citation
Lopez-Alonso M, Moya MJ, Cabo JA, Ribas J, del Carmen Macias M, Silny J, Sifrim D. Twenty-four-hour esophageal impedance-pH monitoring in healthy preterm neonates: rate and characteristics of acid, weakly acidic, and weakly alkaline gastroesophageal reflux. Pediatrics. 2006 Aug;118(2):e299-308. doi: 10.1542/peds.2005-3140. Epub 2006 Jul 10.
Results Reference
background
PubMed Identifier
10879336
Citation
Fuloria M, Hiatt D, Dillard RG, O'Shea TM. Gastroesophageal reflux in very low birth weight infants: association with chronic lung disease and outcomes through 1 year of age. J Perinatol. 2000 Jun;20(4):235-9. doi: 10.1038/sj.jp.7200352.
Results Reference
background
PubMed Identifier
21730816
Citation
Jadcherla SR, Peng J, Chan CY, Moore R, Wei L, Fernandez S, DI Lorenzo C. Significance of gastroesophageal refluxate in relation to physical, chemical, and spatiotemporal characteristics in symptomatic intensive care unit neonates. Pediatr Res. 2011 Aug;70(2):192-8. doi: 10.1203/PDR.0b013e31821f704d.
Results Reference
background
PubMed Identifier
18245400
Citation
Farhath S, He Z, Nakhla T, Saslow J, Soundar S, Camacho J, Stahl G, Shaffer S, Mehta DI, Aghai ZH. Pepsin, a marker of gastric contents, is increased in tracheal aspirates from preterm infants who develop bronchopulmonary dysplasia. Pediatrics. 2008 Feb;121(2):e253-9. doi: 10.1542/peds.2007-0056.
Results Reference
background
PubMed Identifier
15371091
Citation
Knight PR, Davidson BA, Nader ND, Helinski JD, Marschke CJ, Russo TA, Hutson AD, Notter RH, Holm BA. Progressive, severe lung injury secondary to the interaction of insults in gastric aspiration. Exp Lung Res. 2004 Oct-Nov;30(7):535-57. doi: 10.1080/01902140490489162.
Results Reference
background
PubMed Identifier
15757954
Citation
Davidson BA, Knight PR, Wang Z, Chess PR, Holm BA, Russo TA, Hutson A, Notter RH. Surfactant alterations in acute inflammatory lung injury from aspiration of acid and gastric particulates. Am J Physiol Lung Cell Mol Physiol. 2005 Apr;288(4):L699-708. doi: 10.1152/ajplung.00229.2004.
Results Reference
background
PubMed Identifier
9404761
Citation
Nader-Djalal N, Knight PR, Davidson BA, Johnson K. Hyperoxia exacerbates microvascular lung injury following acid aspiration. Chest. 1997 Dec;112(6):1607-14. doi: 10.1378/chest.112.6.1607.
Results Reference
background
PubMed Identifier
9661561
Citation
Nader-Djalal N, Knight PR 3rd, Thusu K, Davidson BA, Holm BA, Johnson KJ, Dandona P. Reactive oxygen species contribute to oxygen-related lung injury after acid aspiration. Anesth Analg. 1998 Jul;87(1):127-33. doi: 10.1097/00000539-199807000-00028.
Results Reference
background
PubMed Identifier
15614133
Citation
Hermon MM, Wassermann E, Pfeiler C, Pollak A, Redl H, Strohmaier W. Early mechanical ventilation is deleterious after aspiration-induced lung injury in rabbits. Shock. 2005 Jan;23(1):59-64. doi: 10.1097/01.shk.0000143417.28273.6d.
Results Reference
background
PubMed Identifier
22071802
Citation
Premji SS, Chessell L. Continuous nasogastric milk feeding versus intermittent bolus milk feeding for premature infants less than 1500 grams. Cochrane Database Syst Rev. 2011 Nov 9;2011(11):CD001819. doi: 10.1002/14651858.CD001819.pub2.
Results Reference
background
PubMed Identifier
25030383
Citation
Richards R, Foster JP, Psaila K. Continuous versus bolus intragastric tube feeding for preterm and low birth weight infants with gastro-oesophageal reflux disease. Cochrane Database Syst Rev. 2014 Jul 17;(7):CD009719. doi: 10.1002/14651858.CD009719.pub2.
Results Reference
background
PubMed Identifier
9665103
Citation
de Ville K, Knapp E, Al-Tawil Y, Berseth CL. Slow infusion feedings enhance duodenal motor responses and gastric emptying in preterm infants. Am J Clin Nutr. 1998 Jul;68(1):103-8. doi: 10.1093/ajcn/68.1.103.
Results Reference
background
PubMed Identifier
11401896
Citation
Jobe AH, Bancalari E. Bronchopulmonary dysplasia. Am J Respir Crit Care Med. 2001 Jun;163(7):1723-9. doi: 10.1164/ajrccm.163.7.2011060. No abstract available.
Results Reference
background

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Continuous Versus Intermittent Bolus Feeding in Very Preterm Infants - Effect on Respiratory Morbidity

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