Effect Of Intrapartum Oropharyngeal (IP-OP) Suction on Meconium Aspiration Syndrome (MSAF-OPS)
Meconium Aspiration Syndrome
About this trial
This is an interventional prevention trial for Meconium Aspiration Syndrome focused on measuring Neonates, Intrapartum Oropharyngeal Suctioning, Meconium Aspiration Syndrome
Eligibility Criteria
Inclusion Criteria:
- Gestation >/= 37 weeks
- Meconium staining of amniotic fluid
- Cephalic presentation
- Singleton pregnancy
Exclusion Criteria:
- Babies with major congenital malformations (if known antenatally)
- Hydrops fetalis
- Refusal of consent
- Chromosomal anomalies
Sites / Locations
- Kalawati Saran children's Hospital, Lady Hardinge Medical College
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
No Intrapartum Oropharyngeal (IP-OP) Suction
Intrapartum Oropharyngeal (IP-OP) suction
Neonates randomized to No IP-OP group received supportive treatment as per standard unit protocols. They were also assessed as vigorous or non-vigorous and received care according to NRP 2005.
The neonates randomized to IP-OP group were provided oropharyngeal suctioning at the delivery of head before the delivery of shoulder, using suction machine at a negative pressure of 100mm of Hg or Dee Lee's suction trap in the event of electricity failure or non availability of suction machine.Subsequently, all the neonates born through MSAF were assessed by pediatrician as vigorous or non vigorous and provided care as per NRP guidelines 2005.