Dopamine vs. Norepinephrine for Hypotension in Very Preterm Infants With Late-onset Sepsis
Late-Onset Neonatal Sepsis | Extreme Prematurity | Neonatal HypotensionFluid-unresponsive hypotension needing cardiotropic drug treatment is a serious complication in very preterm neonates with suspected late-onset sepsis (LOS; defined as culture positive or negative bloodstream infection or necrotizing enterocolitis occurring \>48 hours of age). In Canada, \~250 very preterm neonates receive cardiotropic drugs for LOS related fluid-unresponsive hypotension every year; of these \~35-40% die. Unlike for adult patients, there is little evidence to inform practice. While several medications are used by clinicians, the most frequently used medications are Dopamine (DA) and Norepinephrine (NE). However, their relative impact on patient outcomes and safety is not known resulting in significant uncertainty and inter- and intra-unit variability in practice. Conducting large randomized trials in this subpopulation can be operationally challenging and expensive. Comparative effectiveness research (CER), is a feasible alternative which can generate high-quality real-world evidence using real-world data, by comparing the impact of different clinical practices.
Aim: To conduct an international CER study, using a pragmatic clinical trial design, in conjunction with the existing infrastructure of the Canadian Neonatal Network to identify the optimal management of hypotension in very preterm neonates with suspected LOS.
Objective: To compare the relative effectiveness and safety of pharmacologically equivalent dosages of DA versus NE for primary pharmacotherapy for fluid-unresponsive hypotension in preterm infants born ≤ 32 weeks gestational age with suspected LOS.
Hypothesis: Primary treatment with NE will be associated with a lower mortality
Methods: This CER project will compare management approach at the unit-level allowing inclusion of all eligible patients admitted during the study period. 15 centers in Canada, 4 centers in Ireland, 2 centers in Israel and 6 centers in the United States have agreed to standardize their practice. All eligible patients deemed circulatory insufficient will receive fluid therapy (minimum 10-20 cc/kg). If hypotension remains unresolved:
Dopamine Units: start at 5mics/kg/min, increase every 16-30 minutes by 5 mics/kg/min to a maximum dose of 15 mics/kg/min or adequate response
Norepinephrine Units: start at 0.05 mics/kg/min, increase every 16-30 minutes by 0.05 mics/kg/min to maximum dose of 0.15/mics/kg/min or adequate response
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Conditions de participation
-
Sexe:
ALL -
Âges admissibles:
21 to 32
Critères de participation
Inclusion Criteria:
* ≤32 weeks gestational age and \> 48 hours of life
* Receiving primary vasopressor therapy with Dopamine or Norepinephrine in the context of suspected late-onset sepsis or necrotizing enterocolitis with systemic hypotension (defined as: culture positive or negative bloodstream infection)
Exclusion Criteria:
* Known chromosomal or genetic anomalies
* Receiving primary therapy with agents other than Dopamine or Norepinephrine
Lieu de l'étude
St.Boniface Hospital
St.Boniface HospitalWinnipeg, Manitoba
Canada
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Yasser ElSayed
London Health Sciences Centre
London Health Sciences CentreLondon, Ontario
Canada
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Soume Bhattacharya
Sunnybrook Health Sciences Centre
Sunnybrook Health Sciences CentreToronto, Ontario
Canada
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Montreal Children's Hospital
Montreal Children's HospitalMontréal, Quebec
Canada
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Gabriel Altit
BC Women's Hospital
BC Women's HospitalVancouver, British Columbia
Canada
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Michael Castaldo
McMaster Children's Hospital
McMaster Children's HospitalHamilton, Ontario
Canada
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Amneet Sidhu
Mount Sinai Hospital
Mount Sinai HospitalToronto, Ontario
Canada
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Jewish General Hospital
Jewish General HospitalMontréal, Quebec
Canada
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Nina Nouraeyan
Winnipeg Health Sciences Centre
Winnipeg Health Sciences CentreWinnipeg, Manitoba
Canada
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Deepak Louis
Children's Hospital of Eastern Ontario
Children's Hospital of Eastern OntarioOttawa, Ontario
Canada
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Laurent Renesme
Windsor Regional Hospital
Windsor Regional HospitalWindsor, Ontario
Canada
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Sajit Augustine
Foothill's Medical Centre
Foothill's Medical CentreCalgary, Alberta
Canada
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IWK Health Centre
IWK Health CentreHalifax, Nova Scotia
Canada
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Hospital for Sick Children
Hospital for Sick ChildrenToronto, Ontario
Canada
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CHU Sainte- Justine
CHU Sainte- JustineMontréal, Quebec
Canada
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- Étude parrainée par
- Mount Sinai Hospital, Canada
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT05347238