Operationalising kangaroo Mother care before stabilisation amongst low birth Weight Neonates in Africa (OMWaNA): protocol for a randomised controlled trial to examine mortality impact in Uganda.
Critical Pathways
Female
Hospitalization
/ statistics & numerical data
Humans
Infant
Infant Care
/ methods
Infant Mortality
Infant, Low Birth Weight
/ growth & development
Infant, Newborn
Kangaroo-Mother Care Method
/ methods
Male
Multicenter Studies as Topic
Outcome Assessment, Health Care
Survival Analysis
Uganda
/ epidemiology
Weight Gain
Kangaroo care
Low birthweight
Neonatal mortality
Newborn
Pragmatic
Preterm
Randomised controlled trial
Skin-to-skin contact
Journal
Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253
Informations de publication
Date de publication:
31 Jan 2020
31 Jan 2020
Historique:
received:
13
11
2019
accepted:
30
12
2019
entrez:
2
2
2020
pubmed:
2
2
2020
medline:
20
11
2020
Statut:
epublish
Résumé
There are 2.5 million neonatal deaths each year; the majority occur within 48 h of birth, before stabilisation. Evidence from 11 trials shows that kangaroo mother care (KMC) significantly reduces mortality in stabilised neonates; however, data on its effect among neonates before stabilisation are lacking. The OMWaNA trial aims to determine the effect of initiating KMC before stabilisation on mortality within seven days relative to standard care. Secondary objectives include exploring pathways for the intervention's effects and assessing incremental costs and cost-effectiveness between arms. We will conduct a four-centre, open-label, individually randomised, superiority trial in Uganda with two parallel groups: an intervention arm allocated to receive KMC and a control arm receiving standard care. We will enrol 2188 neonates (1094 per arm) for whom the indication for KMC is 'uncertain', defined as receiving ≥ 1 therapy (e.g. oxygen). Admitted singleton, twin and triplet neonates (triplet if demise before admission of ≥ 1 baby) weighing ≥ 700-≤ 2000 g and aged ≥ 1-< 48 h are eligible. Treatment allocation is random in a 1:1 ratio between groups, stratified by weight and recruitment site. The primary outcome is mortality within seven days. Secondary outcomes include mortality within 28 days, hypothermia prevalence at 24 h, time from randomisation to stabilisation or death, admission duration, time from randomisation to exclusive breastmilk feeding, readmission frequency, daily weight gain, infant-caregiver attachment and women's wellbeing at 28 days. Primary analyses will be by intention-to-treat. Quantitative and qualitative data will be integrated in a process evaluation. Cost data will be collected and used in economic modelling. The OMWaNA trial aims to assess the effectiveness of KMC in reducing mortality among neonates before stabilisation, a vulnerable population for whom its benefits are uncertain. The trial will improve understanding of pathways underlying the intervention's effects and will be among the first to rigorously compare the incremental cost and cost-effectiveness of KMC relative to standard care. The findings are expected to have broad applicability to hospitals in sub-Saharan Africa and southern Asia, where three-quarters of global newborn deaths occur, as well as important policy and programme implications. ClinicalTrials.gov, NCT02811432. Registered on 23 June 2016.
Sections du résumé
BACKGROUND
BACKGROUND
There are 2.5 million neonatal deaths each year; the majority occur within 48 h of birth, before stabilisation. Evidence from 11 trials shows that kangaroo mother care (KMC) significantly reduces mortality in stabilised neonates; however, data on its effect among neonates before stabilisation are lacking. The OMWaNA trial aims to determine the effect of initiating KMC before stabilisation on mortality within seven days relative to standard care. Secondary objectives include exploring pathways for the intervention's effects and assessing incremental costs and cost-effectiveness between arms.
METHODS
METHODS
We will conduct a four-centre, open-label, individually randomised, superiority trial in Uganda with two parallel groups: an intervention arm allocated to receive KMC and a control arm receiving standard care. We will enrol 2188 neonates (1094 per arm) for whom the indication for KMC is 'uncertain', defined as receiving ≥ 1 therapy (e.g. oxygen). Admitted singleton, twin and triplet neonates (triplet if demise before admission of ≥ 1 baby) weighing ≥ 700-≤ 2000 g and aged ≥ 1-< 48 h are eligible. Treatment allocation is random in a 1:1 ratio between groups, stratified by weight and recruitment site. The primary outcome is mortality within seven days. Secondary outcomes include mortality within 28 days, hypothermia prevalence at 24 h, time from randomisation to stabilisation or death, admission duration, time from randomisation to exclusive breastmilk feeding, readmission frequency, daily weight gain, infant-caregiver attachment and women's wellbeing at 28 days. Primary analyses will be by intention-to-treat. Quantitative and qualitative data will be integrated in a process evaluation. Cost data will be collected and used in economic modelling.
DISCUSSION
CONCLUSIONS
The OMWaNA trial aims to assess the effectiveness of KMC in reducing mortality among neonates before stabilisation, a vulnerable population for whom its benefits are uncertain. The trial will improve understanding of pathways underlying the intervention's effects and will be among the first to rigorously compare the incremental cost and cost-effectiveness of KMC relative to standard care. The findings are expected to have broad applicability to hospitals in sub-Saharan Africa and southern Asia, where three-quarters of global newborn deaths occur, as well as important policy and programme implications.
TRIAL REGISTRATION
BACKGROUND
ClinicalTrials.gov, NCT02811432. Registered on 23 June 2016.
Identifiants
pubmed: 32005286
doi: 10.1186/s13063-019-4044-6
pii: 10.1186/s13063-019-4044-6
pmc: PMC6995072
doi:
Banques de données
ClinicalTrials.gov
['NCT02811432']
Types de publication
Clinical Trial Protocol
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
126Subventions
Organisme : NICHD NIH HHS
ID : K23 HD092611
Pays : United States
Organisme : Medical Research Council
ID : MR/R010161/1
Pays : United Kingdom
Organisme : Eunice Kennedy Shriver National Institute of Child Health and Human Development
ID : K23HD092611
Organisme : Medical Research Council
ID : MR/S004971/1
Pays : United Kingdom
Références
J Glob Health. 2018 Jun;8(1):010701
pubmed: 29497509
MCN Am J Matern Child Nurs. 2013 Nov-Dec;38(6):385-90
pubmed: 24145494
Early Hum Dev. 2009 Sep;85(9):561-7
pubmed: 19505775
Pediatrics. 2016 Jan;137(1):
pubmed: 26702029
Acta Paediatr. 2010 Jun;99(6):827-35
pubmed: 20121708
J Perinatol. 2011 Apr;31 Suppl 1:S49-56
pubmed: 21448204
Lancet Glob Health. 2014 Nov;2(11):e635-44
pubmed: 25442688
PLoS One. 2018 Nov 21;13(11):e0207156
pubmed: 30462671
J Trop Pediatr. 2005 Apr;51(2):93-7
pubmed: 15840760
J Med Ethics. 2006 Aug;32(8):439-43
pubmed: 16877621
BMC Med. 2016 Jan 18;14:5
pubmed: 26782822
J Biomed Inform. 2009 Apr;42(2):377-81
pubmed: 18929686
J Pediatr. 1991 Sep;119(3):417-23
pubmed: 1880657
Arch Pediatr Adolesc Med. 2006 Jul;160(7):681-5
pubmed: 16818832
J Glob Health. 2016 Jun;6(1):010701
pubmed: 27231546
BMC Pregnancy Childbirth. 2015;15 Suppl 2:S7
pubmed: 26391335
Rev Panam Salud Publica. 2013 Sep;34(3):176-82
pubmed: 24233110
Trials. 2015 Nov 04;16:502
pubmed: 26537492
Acta Paediatr. 2006 May;95(5):529-34
pubmed: 16825131
Lancet. 2012 Jun 9;379(9832):2162-72
pubmed: 22682464
Int J Tuberc Lung Dis. 2016 May;20(5):696-703
pubmed: 27084827
Lancet. 2014 Jul 26;384(9940):347-70
pubmed: 24853604
Lancet Glob Health. 2019 Jan;7(1):e37-e46
pubmed: 30389451
Implement Sci. 2012 Aug 13;7:75
pubmed: 22889113
Ann Trop Paediatr. 2000 Mar;20(1):22-6
pubmed: 10824209
J Hum Lact. 2014 Feb;30(1):41-6
pubmed: 24212300
BMJ. 2015 Mar 19;350:h1258
pubmed: 25791983
J Human Dev Capabil. 2018;19(3):271-288
pubmed: 29973972
Trop Med Int Health. 2010 Oct;15(10):1140-7
pubmed: 20723185
Acta Paediatr. 1998 Sep;87(9):976-85
pubmed: 9764894
BMJ. 2014 Mar 07;348:g1687
pubmed: 24609605
Biol Res Nurs. 2018 Jan;20(1):54-62
pubmed: 29017336
Value Health. 2016 Dec;19(8):921-928
pubmed: 27987641
Early Hum Dev. 2015 Jan;91(1):63-70
pubmed: 25545453
J Perinatol. 2008 Oct;28(10):685-90
pubmed: 18580881
Cochrane Database Syst Rev. 2016 Aug 23;(8):CD002771
pubmed: 27552521
BMC Med. 2013 Jan 31;11:24
pubmed: 23369256
Pediatr Res. 2010 Jan;67(1):1-8
pubmed: 19816235
Lancet. 2000 Dec 16;356(9247):2045-51
pubmed: 11145490
Acta Paediatr. 2018 Mar 30;:null
pubmed: 29603791
Lancet. 1994 Sep 17;344(8925):782-5
pubmed: 7916073
Lancet Glob Health. 2019 Jul;7(7):e849-e860
pubmed: 31103470
Lancet. 2014 Jul 12;384(9938):189-205
pubmed: 24853593
J Neonatal Perinatal Med. 2013;6(3):243-9
pubmed: 24246597
Pediatr Res. 2013 Dec;74 Suppl 1:17-34
pubmed: 24366461
BMC Pregnancy Childbirth. 2015;15 Suppl 2:S5
pubmed: 26391115
BMC Health Serv Res. 2014 Jul 08;14:293
pubmed: 25001366
Child Care Health Dev. 2013 Jan;39(1):20-6
pubmed: 22680250
J Clin Epidemiol. 2017 Jun;86:91-100
pubmed: 27989952
Pediatrics. 1997 Oct;100(4):682-8
pubmed: 9310525
Pediatr Clin North Am. 2013 Feb;60(1):49-74
pubmed: 23178060