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| ID | Type | Description | Link |
|---|---|---|---|
| 1025465 | Other Grant/Funding Number | Canadian Institutes of Health Research |
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| Name | Class |
|---|---|
| Canadian Institutes of Health Research (CIHR) | OTHER_GOV |
| Imperial College London | OTHER |
| Imperial Clinical Trials Unit (ICTU) | UNKNOWN |
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The WHEAT International trial is a comparative effectiveness trial exploring whether withholding enteral feeds around the time of blood transfusion in very premature infants (<30 weeks) will reduce the occurrence of Necrotizing Enterocolitis (NEC). Currently both continued feeding and withholding feeding are approved care practices. The current study will randomize infants from Neonatal Intensive Care Units (NICUs) across Canada and the United Kingdom (UK) into one of the two care approaches (withholding or continued feeds) to determine if any significant outcomes are found.
BACKGROUND: Necrotizing enterocolitis (NEC) is a devastating disease that affects mostly the intestine of premature infants. The wall of the intestine is invaded by bacteria, which cause local infection and inflammation that can ultimately destroy the wall of the bowel (intestine). NEC is among the most potentially devastating neonatal diseases and has a mortality of up to 33%, the most severe form (requiring surgery or resulting in death) affects about 5% of infants born at less than 30 gestational weeks; survivors are at high risk of long-term health and developmental problems. Prevention of NEC has been identified as one of the most important research uncertainties in the field of preterm birth. A temporal association between red cell transfusion and the subsequent development of the disease is well described. This 'transfusion-associated NEC' may also be more severe with higher mortality. Very preterm or extremely low birth weight infants are among the most frequently transfused patients: between 56% and 90-95% have at least one transfusion, and those transfused received an average of 5 transfusions in their neonatal stay. Withholding milk feeds during red cell transfusion may reduce the risk of NEC by decreasing postprandial mesenteric ischemia but there may be harmful effects of pausing enteral feeds. However, due to a lack of good quality evidence, there is no consensus regarding the optimal feeding strategy during a blood transfusion.
Both comparator pathways of care are standard practice in Canada and the UK; the WHEAT trial is a comparative effectiveness trial. The two care pathways that will be compared are:
Infants will remain allocated to the same care pathway until 34(+6) weeks(+days) gestational age.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Withholding feeds around transfusion | Active Comparator | All enteral feeds will be discontinued (the infant will be placed nil by mouth) for 4 hours prior to packed red cell transfusion, during the transfusion and until 4 hours post transfusion. During this period, hydration and blood glucose will be maintained according to local practice, commonly by providing parenteral nutrition or intravenous dextrose. Four hours after the red cell transfusion has finished, feeds will be recommenced to how they were being received prior to the decision to transfuse. This duration of withholding feeds will follow the approach used in other trials and observational studies, and identified as the most acceptable in a survey of UK neonatal units. It gives time for milk in the small bowel to transit into the large bowel before the transfusion and for the circulation to stabilize after the transfusion before milk feeds given into the stomach pass through into the small intestine. |
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| Continuing feeds around transfusion | Active Comparator | Enteral feeds will continue to be given prior, during and after the packed red cell transfusion, in the manner in which they were being given prior to the decision to transfuse. Infants will remain allocated to the same care pathway until 34(+6) weeks(+days) gestational age. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Withholding feeds around transfusion | Other | Withholding enteral feeds for preterm infants (<30 weeks) around the time of blood transfusions to determine if any impact on the development and/or severity of Necrotizing Enterocolitis. |
| Measure | Description | Time Frame |
|---|---|---|
| NEC Stage II | Stage II or greater NEC recorded after the first trial blood transfusion; defined according to the modified Bell staging criteria: based on clinical features and abdominal imaging findings, or on surgical or histological findings of NEC. | From randomization to 40 weeks postmenstrual age |
| Measure | Description | Time Frame |
|---|---|---|
| Severe NEC | Histologically or surgically confirmed or recorded on the death certificate. These infants will be identified as described in Battersby et al. which will include infants recorded as being transferred for surgery. | From randomization to 40 weeks postmenstrual age |
| Death |
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Inclusion Criteria:
1. Preterm birth at <30+0 gestational weeks + days
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Cari-Lee Carnell | Contact | 9024706630 | cari-lee.carnell@iwk.nshealth.ca | |
| Tara Hatfield | Contact | 9024706630 | tara.hatfield@iwk.nshealth.ca |
| Name | Affiliation | Role |
|---|---|---|
| Balpreet Singh, MD | IWK Health, Canada | Principal Investigator |
| Jon Dorling, MD | Princess Anne Hospital, UK | Principal Investigator |
| Chris Gale, MD |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| IWK Health | Recruiting | Halifax | Nova Scotia | B3K 6R8 | Canada |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 28404014 | Background | Battersby C, Longford N, Mandalia S, Costeloe K, Modi N; UK Neonatal Collaborative Necrotising Enterocolitis (UKNC-NEC) study group. Incidence and enteral feed antecedents of severe neonatal necrotising enterocolitis across neonatal networks in England, 2012-13: a whole-population surveillance study. Lancet Gastroenterol Hepatol. 2017 Jan;2(1):43-51. doi: 10.1016/S2468-1253(16)30117-0. Epub 2016 Nov 8. | |
| 20447649 |
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The WHEAT trial is a randomised controlled, unblinded, international, multicentre, parallel-group superiority trial comparing two clinical pathways. Participants will be randomised to either pathway.
In the United Kingdom, the trial is running across 77 neonatal units.
In Canada, the trial is running at 15 neonatal sites, all of which participate in recruitment, intervention delivery, and follow-up procedures in line with the study protocol.
Across both countries, participant recruitment will continue until 31 December 2026. The last participant randomised is expected to complete the trial participation period by 31 March 2027, following completion of the follow-up period defined as neonatal unit discharge or 40+0 weeks postmenstrual age, whichever occurs first.
Analysis of trial data will take place after completion of follow-up, with results anticipated to be communicated by September 2027.
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| Continued feeds around transfusion | Other | Continued enteral feeds |
|
All-cause mortality |
| From randomization to 40 weeks postmenstrual age |
| Late onset sepsis | Culture positive sepsis, onset after 72 hours of life | From randomization to 40 weeks postmenstrual age |
| Number of days with a central venous line in situ | Number of days with a central venous line in situ | From birth to date of discharge home |
| Number of central line associated bloodstream infections | Number of central line associated bloodstream infections: Positive blood culture confirmed bloodstream infection | From randomization to 40 weeks postmenstrual age |
| Duration of any parenteral nutrition in days | Duration of any parenteral nutrition in days | From birth to 40 weeks postmenstrual age |
| Growth | Weight and head circumference z score. | At date of discharge home |
| Spontaneous Intestinal Perforation | Histologically or surgically confirmed or recorded in the death certificate. | From randomization to 40 weeks postmenstrual age |
| Duration of hospital stay | Total duration of neonatal care in days including all levels of care (intensive care, high dependency care, special care and ordinary care) | From birth to date of discharge home |
| Bronchopulmonary Dysplasia (BPD)/Chronic Lung Disease | Requiring respiratory support at 36 weeks gestation | At 36 weeks postmenstrual age |
| Retinopathy of prematurity (ROP) | ROP requiring treatment | From randomization to 40 weeks postmenstrual age |
| Severe Brain Injury | Intraventricular haemorrhage (IVH) grade 3 or 4 or cystic periventricular leukomalacia (PVL) | At 40 weeks postmenstrual age |
| Imperial College London, UK |
| Principal Investigator |
| Norfolk & Norwich University Hospitals NHS Foundation Trust (Norfolk & Norwich University Hospital) | Recruiting | Norwich | England | United Kingdom |
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| The Hillingdon Hospitals NHS Foundation Trust (Hillingdon Hospital) | Recruiting | Hillingdon | UK | United Kingdom |
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| Barts Health NHS Trust (3 Hospitals: Royal London Hospital, Whipps Cross Hospital, Newham General Hospital) | Recruiting | London | UK | United Kingdom |
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| Chelsea and Westminster Hospital NHS Foundation Trust (Chelsea and Westminster Hospital) | Recruiting | London | UK | United Kingdom |
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| Imperial College Healthcare NHS Trust (2 Hospitals: St Mary's Hospital & Queen Charlotte's and Chelsea Hospital) | Recruiting | London | UK | United Kingdom |
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| Bedfordshire Hospitals NHS Foundation Trust (Luton & Dunstable University Hospital) | Recruiting | Luton | UK | United Kingdom |
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| East Kent University Hospitals NHS Foundation Trust (William Harvey Hospital) | Recruiting | Ashford | United Kingdom |
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| Buckinghamshire Healthcare NHS Trust (Stoke Mandeville Hospital) | Recruiting | Aylesbury | United Kingdom |
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| Barnsley Hospital NHS Foundation Trust | Recruiting | Barnsley | United Kingdom |
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| Birmingham Women's and Children's NHS Foundation Trust (Birmingham Women's Hospital NICU) | Recruiting | Birmingham | United Kingdom |
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| University Hospitals Birmingham NHS Trust (2 Hospitals: Heartland's Hospital & Good Hope Hospital) | Recruiting | Birmingham | United Kingdom |
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| Bradford Teaching Hospitals NHS Foundation Trust (Bradford Royal Infirmary) | Recruiting | Bradford | United Kingdom |
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| North Bristol NHS Trust (Southmead Hospital) | Recruiting | Bristol | United Kingdom |
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| East and North Essex NHS Foundation Trust - Colchester Hospital | Recruiting | Colchester | United Kingdom |
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| University Hospital Coventry & Warwickshire NHS Trust (University Hospital Coventry) | Recruiting | Coventry | United Kingdom |
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| University Hospitals of Derby and Burton NHS Trust (Royal Derby Hospital) | Recruiting | Derby | United Kingdom |
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| NHS Tayside (Ninewells Hospital) | Recruiting | Dundee | United Kingdom |
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| Medway Hospital NHS Foundation Trust (Oliver Fisher Neonatal Unit, Medway Maritime Hospital) | Recruiting | Gillingham | United Kingdom |
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| Gloucestershire Hospitals NHS Foundation Trust (Gloucestershire Royal Hospital) | Recruiting | Gloucester | United Kingdom |
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| Calderdale & Huddersfield NHS Foundation Trust (Calderdale Royal Hospital) | Recruiting | Halifax | United Kingdom |
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| East and North Essex NHS Foundation Trust - Ipswich Hospital | Recruiting | Ipswich | United Kingdom |
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| Leeds Teaching Hospitals NHS Trust (Leeds General Infirmary & St James' University Hospital) | Recruiting | Leeds | United Kingdom |
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| University Hospitals of Leicester NHS Trust (Leicester Royal Infirmary) | Recruiting | Leicester | United Kingdom |
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| Liverpool Women's Hospital NHS Foundation Trust (Liverpool Women's Hospital) | Recruiting | Liverpool | United Kingdom |
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| North West London NHS Trust (Northwick Park Hospital) | Recruiting | London | United Kingdom |
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| Manchester University NHS Foundation Trust (2 Hospitals: St Mary's Hospital - Oxford Road, North Manchester General) | Recruiting | Manchester | United Kingdom |
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| Manchester University NHS Foundation Trust (Wythenshawe) | Recruiting | Manchester | United Kingdom |
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| The Newcastle Upon Tyne Hospitals NHS Foundation Trust (Royal Victoria Infirmary) | Recruiting | Newcastle upon Tyne | United Kingdom |
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| Nottingham University Hospitals NHS Trust (2 Hospitals: City Hospital, Queen's Medical Centre) | Recruiting | Nottingham | United Kingdom |
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| Oxford University Hospitals NHS FT (John Radcliffe Hospital) | Recruiting | Oxford | United Kingdom |
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| North West Anglia NHS Trust (Peterborough City Hospital) | Recruiting | Peterborough | United Kingdom |
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| Portsmouth University Hospitals NHS Trust (Queen Alexandra Hospital) | Recruiting | Portsmouth | United Kingdom |
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| Lancashire Teaching Hospitals NHS Foundation Trust (Royal Preston Hospital) | Recruiting | Preston | United Kingdom |
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| The Shrewsbury & Telford Hospitals NHS Trust (Royal Shrewsbury Hospital) | Recruiting | Shrewsbury | United Kingdom |
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| University Hospital Southampton NHS Foundation Trust (Southampton General Hospital) | Recruiting | Southampton | United Kingdom |
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| Betsi Cadwaladr University Health Board (Glan Cwyd Hospital) | Recruiting | Wales | United Kingdom |
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| Walsall Healthcare NHS Trust (Walsall Manor Hospital) | Recruiting | Walsall | United Kingdom |
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| West Hertfordshire Hospitals NHS Trust (Watford General Hospital) | Recruiting | Watford | United Kingdom |
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| Royal Wolverhampton NHS Trust (New Cross Hospital) | Recruiting | Wolverhampton | United Kingdom |
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| Background |
| Duro D, Kalish LA, Johnston P, Jaksic T, McCarthy M, Martin C, Dunn JC, Brandt M, Nobuhara KK, Sylvester KG, Moss RL, Duggan C. Risk factors for intestinal failure in infants with necrotizing enterocolitis: a Glaser Pediatric Research Network study. J Pediatr. 2010 Aug;157(2):203-208.e1. doi: 10.1016/j.jpeds.2010.02.023. Epub 2010 May 6. |
| 15741374 | Background | Hintz SR, Kendrick DE, Stoll BJ, Vohr BR, Fanaroff AA, Donovan EF, Poole WK, Blakely ML, Wright L, Higgins R; NICHD Neonatal Research Network. Neurodevelopmental and growth outcomes of extremely low birth weight infants after necrotizing enterocolitis. Pediatrics. 2005 Mar;115(3):696-703. doi: 10.1542/peds.2004-0569. |
| 16984980 | Background | Rees CM, Pierro A, Eaton S. Neurodevelopmental outcomes of neonates with medically and surgically treated necrotizing enterocolitis. Arch Dis Child Fetal Neonatal Ed. 2007 May;92(3):F193-8. doi: 10.1136/adc.2006.099929. Epub 2006 Sep 19. |
| 24931684 | Background | Duley L, Uhm S, Oliver S; Preterm Birth Priority Setting Partnership Steering Group. Top 15 UK research priorities for preterm birth. Lancet. 2014 Jun 14;383(9934):2041-2042. doi: 10.1016/S0140-6736(14)60989-2. No abstract available. |
| 6279816 | Background | Seges RA, Kenny A, Bird GW, Wingham J, Baals H, Stauffer UG. Pediatric surgical patients with severe anaerobic infection: report of 16 T-antigen positive cases and possible hazards of blood transfusion. J Pediatr Surg. 1981 Dec;16(6):905-10. doi: 10.1016/s0022-3468(81)80844-5. |
| 22447991 | Background | Stritzke AI, Smyth J, Synnes A, Lee SK, Shah PS. Transfusion-associated necrotising enterocolitis in neonates. Arch Dis Child Fetal Neonatal Ed. 2013 Jan;98(1):F10-4. doi: 10.1136/fetalneonatal-2011-301282. Epub 2012 Mar 23. |
| 21067771 | Background | Blau J, Calo JM, Dozor D, Sutton M, Alpan G, La Gamma EF. Transfusion-related acute gut injury: necrotizing enterocolitis in very low birth weight neonates after packed red blood cell transfusion. J Pediatr. 2011 Mar;158(3):403-9. doi: 10.1016/j.jpeds.2010.09.015. Epub 2010 Nov 10. |
| 17009195 | Background | Mally P, Golombek SG, Mishra R, Nigam S, Mohandas K, Depalhma H, LaGamma EF. Association of necrotizing enterocolitis with elective packed red blood cell transfusions in stable, growing, premature neonates. Am J Perinatol. 2006 Nov;23(8):451-8. doi: 10.1055/s-2006-951300. Epub 2006 Sep 28. |
| 28601308 | Background | Cunningham KE, Okolo FC, Baker R, Mollen KP, Good M. Red blood cell transfusion in premature infants leads to worse necrotizing enterocolitis outcomes. J Surg Res. 2017 Jun 1;213:158-165. doi: 10.1016/j.jss.2017.02.029. Epub 2017 Feb 28. |
| 25652740 | Background | Keir AK, Yang J, Harrison A, Pelausa E, Shah PS; Canadian Neonatal Network. Temporal changes in blood product usage in preterm neonates born at less than 30 weeks' gestation in Canada. Transfusion. 2015 Jun;55(6):1340-6. doi: 10.1111/trf.12998. Epub 2015 Feb 5. |
| 16939737 | Background | Kirpalani H, Whyte RK, Andersen C, Asztalos EV, Heddle N, Blajchman MA, Peliowski A, Rios A, LaCorte M, Connelly R, Barrington K, Roberts RS. The Premature Infants in Need of Transfusion (PINT) study: a randomized, controlled trial of a restrictive (low) versus liberal (high) transfusion threshold for extremely low birth weight infants. J Pediatr. 2006 Sep;149(3):301-307. doi: 10.1016/j.jpeds.2006.05.011. |
| 28916576 | Background | Jasani B, Rao S, Patole S. Withholding Feeds and Transfusion-Associated Necrotizing Enterocolitis in Preterm Infants: A Systematic Review. Adv Nutr. 2017 Sep 15;8(5):764-769. doi: 10.3945/an.117.015818. Print 2017 Sep. |
| 30890001 | Background | Sahin S, Gozde Kanmaz Kutman H, Bozkurt O, Yavanoglu Atay F, Emre Canpolat F, Uras N, Suna Oguz S, Underwood MA. Effect of withholding feeds on transfusion-related acute gut injury in preterm infants: a pilot randomized controlled trial. J Matern Fetal Neonatal Med. 2020 Dec;33(24):4139-4144. doi: 10.1080/14767058.2019.1597844. Epub 2019 Mar 28. |
| 8614608 | Background | Neu J. Necrotizing enterocolitis: the search for a unifying pathogenic theory leading to prevention. Pediatr Clin North Am. 1996 Apr;43(2):409-32. doi: 10.1016/s0031-3955(05)70413-2. |
| 28046187 | Background | Battersby C, Longford N, Costeloe K, Modi N; UK Neonatal Collaborative Necrotising Enterocolitis Study Group. Development of a Gestational Age-Specific Case Definition for Neonatal Necrotizing Enterocolitis. JAMA Pediatr. 2017 Mar 1;171(3):256-263. doi: 10.1001/jamapediatrics.2016.3633. |
| ID | Term |
|---|---|
| D020345 | Enterocolitis, Necrotizing |
| D047928 | Premature Birth |
| ID | Term |
|---|---|
| D004760 | Enterocolitis |
| D005759 | Gastroenteritis |
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
| D007410 | Intestinal Diseases |
| D007752 | Obstetric Labor, Premature |
| D007744 | Obstetric Labor Complications |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
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