Dopamine vs. Norepinephrine for Hypotension in Very Preterm Infants With Late-onset Sepsis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age21-32
SponsorMount Sinai Hospital, Canada

About this trial

Fluid-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. 16 centers in Canada, 2 centers in Ireland, 1 center in each of Israel, Spain and the UK, 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

Eligibility criteria

Qualifiers

≤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)

Disqualifiers

Known chromosomal or genetic anomalies

Receiving primary therapy with agents other than Dopamine or Norepinephrine

Trial design

Treatments tested in this trial

  • Dopamine
  • Norepinephrine

Treatment groups

550 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Mount Sinai Hospital, Canada

Lead sponsor

Sunnybrook Health Sciences Centre

Collaborator

The Hospital for Sick Children

Collaborator

London Health Sciences Centre

Collaborator

Windsor Regional Hospital

Collaborator

Foothills Medical Centre

Collaborator

Health Sciences Centre, Winnipeg, Manitoba

Collaborator

St. Boniface Hospital

Collaborator

Jewish General Hospital

Collaborator

St. Justine's Hospital

Collaborator

IWK Health Centre

Collaborator

University College Cork

Collaborator

Coombe Women and Infants University Hospital

Collaborator

Island Health, Victoria, BC

Collaborator

Assaf-Harofeh Medical Center

Collaborator

Dayton Children's Hospital

Collaborator

Banner University Medical Center

Collaborator

Methodist Healthcare - Memphis

Collaborator

Hospital Universitario La Paz

Collaborator

McMaster Children's Hospital

Collaborator

Children's Hospital of Eastern Ontario

Collaborator

BC Women's Hospital & Health Centre

Collaborator

Stony Brook University

Collaborator

Children's Hospital at Montefiore

Collaborator

Golisano Children's Hospital

Collaborator