Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium
Conditions
Interventions
Intervention1: Nil: Nil
Sponsors
Vijayanagar institute of medical sciences Contonment ballari
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients more than 18 years 2.Patient who is having term pregnancy (37 week) undergoing cesarean delivery in department of VIMS , ballari due to various maternal and fetal indications. 3.Patients who categorized as ASA physical status class 2 and above 4.All booked and non-booked patient 5.Patients who are willing to participate will be included in this study after an informed and written consent
Exclusion criteria
Exclusion criteria: 1.Patients who refuse to participate in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the incidence of peri operative anaesthesia related maternal adverse events in patients undergoing cesarean delivery.Timepoint: From intra operative period to 24 hours postoperatively after cesarean delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To assess the type of anaesthesia related adverse events including hypoxia, desaturation, hypotension, hypocarbia, pain, hypothermia, post operative nausea & vomiting, need for o2 supplementation, any other form of ventilatory support 2)Assess for correlation with types of anaesthetic drugs, obstetric history, medical history and co-morbidities. 3)To assess the incidence of anaesthesia related neonatal adverse outcomes in terms of APGAR score at 1 min and 5 mins, umblical cord blood gas analysis, NICU admission Timepoint: 1 year | — |
Countries
India
Contacts
Public ContactDr Anuradha h
Vijayanagar institute of medical sciences
Outcome results
None listed