Hypoxic-Ischemic Encephalopathy
Conditions
Brief summary
The purpose of this study is to investigate the efficacy and safety of umbilical cord milking in depressed neonates at birth for prevention of hypoxic ischemic encephalopathy.
Detailed description
Hypoxic-ischemic encephalopathy (HIE) is a brain injury caused by inadequate supply of oxygen and blood to the brain of a newborn baby. Therapeutic hypothermia is the only proven therapy for these infants. Even after receiving therapeutic hypothermia, 50% of all infants with moderate and severe HIE die or develop neurological and functional impairment. There is a need for a new intervention for neonatal HIE, which is readily available in developing countries and can complement hypothermia. The American College of Obstetricians and Gynecologists and American Academy of Pediatrics recommend a delay in umbilical cord clamping in vigorous term and preterm infants for at least 30-60 seconds after birth. Immediate umbilical cord clamping is contraindicated in maternal hemodynamic instability, need for immediate resuscitation of the newborn and in conditions where placental circulation is not intact. Umbilical cord milking (UCM) is a simple method of delivering volume and possibly stem cells to those neonates, where resuscitation cannot be postponed for obtaining the benefits of delayed cord clamping. We hypothesize that depressed neonates who receive umbilical cord milking will have lower incidence and severity of hypoxic ischemic encephalopathy compared to depressed neonates who receive immediate cord clamping.We propose to investigate the safety and effectiveness of UCM in term and late preterm (≥35 week's gestation) infants who are depressed at birth, in preventing the development and/or progression of hypoxic ischemic encephalopathy. The need for immediate resuscitation measures, abnormal parameters (clinical, hematological and biochemical) and neuroimaging will be compared in depressed neonates with and without UCM. If UCM is found to be safe and beneficial, it can be a useful substitute for delayed cord clamping in depressed neonates worldwide. Conditions: Depressed neonate, Hypoxic-ischemic encephalopathy Intervention: Umbilical cord milking Study Design Study Type: Interventional Study Design: Allocation: Randomized Endpoint Classification: Efficacy/Safety Study Intervention Model: Parallel Assignment Number of Arms: 2 Masking: Single Blind (Subject) Primary Purpose: Prevention Enrollment: 400 \[Anticipated\] Arms and Interventions: Arms:2, Assigned Interventions: 1. Experimental: Umbilical Cord Milking and 2. No Intervention: Immediate Umbilical Cord Clamping 1. Experimental: Umbilical Cord Milking,Other Name: Umbilical cord stripping Umbilical Cord Milking involves milking a 30 cm long segment of umbilical cord at birth, after initiation of ventilation Procedure: Umbilical Cord Milking (UCM) At birth the umbilical cord of a depressed newborn is clamped immediately and cut 30 cm from the umbilicus and the neonate placed on the resuscitation table. After completion of initial steps, if the baby does not have adequate spontaneous respirations and a heart rate of 100 bpm or higher, positive pressure ventilation (PPV) is given for 30 seconds, along with UCM. The cord is untwisted and held in a vertical position. It is milked 3 times towards the baby at a speed of 10 cm/s and then clamped 3 cm from the umbilicus. The time of cord clamping will be recorded using a timer. After completion of PPV along with UCM, if the baby requires further resuscitation, the NRP 2015 guidelines will be followed. Depressed newborns who respond to initial steps of resuscitation with normal breathing and heart rate of 100 bpm or higher, will receive UCM after this. 2. No Intervention: Immediate Umbilical Cord Clamping, Other Name: routine clamping of the umbilical cord Procedure: Immediate Cord Clamping, At birth the umbilical cord of a depressed newborn is clamped immediately (current recommendation) and cut 3 cm from the umbilicus and the neonate placed on the resuscitation table. The time of cord clamping will be recorded using a timer. After completion of initial steps, if the baby requires further resuscitation, the NRP 2015 guidelines will be followed.
Interventions
PROCEDUREUmbilical Cord Milking
At birth the cord of a depressed newborn is clamped immediately and cut 30 cm from the umbilicus. After completion of initial steps, if required, positive pressure ventilation (PPV) is given for 30 seconds, along with UCM. The cord is untwisted and held in a vertical position. It is milked 3 times towards the baby at a speed of 10 cm/s and then clamped 3 cm from the umbilicus. After completion of PPV along with UCM, if the baby requires further resuscitation, the NRP 2015 guidelines will be followed. Depressed newborns who respond to initial steps of resuscitation with normal breathing and heart rate of 100 bpm or higher, will receive UCM after this.
Sponsors
Jubilee Mission Medical College and Research Institute
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)
Masking description
Single Blind (Subject)
Eligibility
Sex/Gender
ALL
Age
1 Minutes to 24 Weeks
Healthy volunteers
No
Inclusion criteria
• Neonates of ≥35 week's gestation and born depressed (defined by NRP 2015 criteria: as those neonates who doesn't cry or breathe at birth and whose tone is poor) in the hospital
Exclusion criteria
* MCDA Twin pregnancy (DCDA twins are included) * Triplet or quadruplet pregnancy * Presence of IUGR in antenatal scans (\< 10th Centile) * Short umbilical cord length (\<30 cm) * Rh-negative or retrovirus positive mothers * Major chromosomal or congenital anomalies * Hydrops fetalis * Severe placental abruption * Cord prolapse and cord abnormalities such as true knots * Culture positive early onset neonatal sepsis
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence and severity of HIE in depressed neonates with and without umbilical cord milking | 72 hours | The severity of HIE if any will be assessed by modified Sarnat staging which is based on level of consciousness, spontaneous activity, neuromuscular control, primitive reflexes, autonomic function and seizures. \[Designated as safety issue: No\]; Ref:Sarnat HB, Sarnat MS. Neonatal encephalopathy following fetal distress. A clinical and electroencephalographic study. Arch Neurol. 1976; 33:696-705. PMID: 987769 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The resuscitation interventions required and the short term outcomes for depressed newborns with and without umbilical cord milking. | 20 minutes after delivery | The resuscitation interventions required (use of CPAP, oxygen, mask and bag ventilation, endotracheal intubation and ventilation, chest compressions, drugs, and fluid boluses) and the short term outcomes of resuscitation will be assessed using the validated Combined Apgar score (consisting of the Expanded and Specified Apgar scoring systems) introduced by Rudiger et al, in depressed neonates with and without UCM. \[Designated as safety issue: No\]; Ref:Dalili H, Nili F, Sheikh M, Hardani AK, Shariat M, Nayeri F (2015) Comparison of the Four Proposed Apgar Scoring Systems in the Assessment of Birth Asphyxia and Adverse Early Neurologic Outcomes. PLoS ONE 10(3): e0122116 |
| Requirement of Neonatal Intensive Care Unit (NICU) admission | 1st 24 hours after delivery | Requirement of Neonatal Intensive Care Unit (NICU) admission \[Designated as safety issue: No\] |
| Blood lactate at 24 hours | 1st 24 hours after delivery | Lactate in the peripheral blood at 24 hours after birth in neonates with any grade of HIE. \[Designated as safety issue: No\] |
| CD34+ stem cell count at 24 hours | 24 hours after birth | CD34+ stem cell count in the peripheral blood at 24 hours after birth in neonates with any grade of HIE. \[Designated as safety issue: No\] |
| The number of neonates with symptomatic polycythemia | 48 hours after birth | The number of neonates with symptomatic polycythemia defined as lethargy, plethora, jitteriness, tachycardia, tachypnea and with venous hematocrit \> 65%. \[Designated as safety issue: No\]; |
| The number of neonates with hyperbilirubinemia requiring phototherapy or exchange transfusion. | 72 hours after birth | Neonates requiring phototherapy or exchange transfusion will be evaluated according to the NICE/AAP guidelines and serum bilirubin levels will be interpreted according to the baby's age in hours. Physicians who assess the neonate and advice phototherapy or exchange transfusion will be blinded to the intervention. \[Designated as safety issue: No\] |
| The number of neonates with anemia | 2 hours after birth | The number of neonates with anemia defined as venous hemoglobin \< 12.5 g/dL \[Designated as safety issue: No\]; |
| MRI changes in the brain of neonates with moderate and severe degrees of HIE who underwent whole body hypothermia. | 14 days after birth | MRI examination will be performed in neonates who underwent whole body hypothermia 7-14 days after birth and the changes in brain scored as per a validated MR scoring system (Barkovich et al, Am J Neuroradiol 1998;19:143-9) by a neuroradiologist blinded to the intervention. \[Designated as safety issue: No\]; Ref:Barkovich AJ, Hajnal BL, Vigneron D, Sola A, Partridge JC, Allen F, et al. Prediction of neuromotor outcome in perinatal asphyxia: evaluation of MR scoring systems. Am J Neuroradiol 1998;19:143-9. \[PubMed: 9432172\] |
| Duration of hospital stay in neonates with any grade of HIE. | Duration of hospital stay, an expected average of 7-14 days | Duration of hospital stay in neonates with any grade of HIE. \[Designated as safety issue: No\] |
| Survival at 6 weeks of age | 6 weeks after birth | Survival at 6 weeks of age \[Designated as safety issue: No\] |
| Haemoglobin levels at 6 weeks of age | 6 weeks after birth | Haemoglobin levels at 6 weeks of age \[Designated as safety issue: No\] |
| Serum ferritin levels at 6 weeks of age | 6 weeks after birth | Serum ferritin levels at 6 weeks of age \[Designated as safety issue: No\] |
Countries
India
Contacts
Primary ContactManoj Varanattu, M D
Backup ContactVarghese PR, Ph D
Outcome results
None listed