Caesarean section. Delivery by elective caesarean section
Conditions
Interventions
This semi- experimental study was performed on 92 candidates for cesarean section by spinal anesthesia referring to the operating room of Ali ibn Abi Talib (Zahedan) Hospital in 1396. 46 patients will
Prevention
Sponsors
Zahedan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 40 Years
Inclusion criteria
Inclusion criteria: Spinal anesthesia No intake of corticosteroid No administration of non-steroidal anti-spasm and magnesium sulfate No underlying disease (thyroid, diabetes, cardiovascular disease and chronic hypertension and preeclampsia) Ending pregnancy at the time of the term (37 to 42 weeks). No fever, addiction, rupture of amniotic sac, polyhydramnios and oligohydroamnios. No constraint for controlling body temperature through tympanic curves.
Exclusion criteria
Exclusion criteria: Occurrence of any situation where the process Natural anesthetic and surgical treatment of the patient. Receiving blood during surgery. Significant loss of blood pressure during surgery. Blood pressure 20% greater than before anesthesia Prolonged surgical time (more than an hour).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Central body temperature. Timepoint: Pre-intervention-during intervention-after intervention. Method of measurement: Based on degrees C and using the tympanic thermometer.;Chill. Timepoint: During intervention - after intervention. Method of measurement: Based on Crossley classification. Grade 1 = No shivering, Grade 2 = Mild shivering (Hair straightening, Peripheral cyanosis visible without vibration), Grade 3 = Medium shiver (visible muscle tremor in a group of muscles), Grade 4 = Severe chills (Muscle vibration in All muscles of the body). | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: Before intervention - during intervention - after intervention. Method of measurement: Systolic and diastolic blood pressure using a monitor based on mm of mercury.;Pulse rate. Timepoint: Before intervention - during intervention - after intervention. Method of measurement: Using the monitor and based on the number in minutes.;Respiratory rate. Timepoint: Before intervention - during intervention - after intervention. Method of measurement: Using the monitor and based on the number in minutes.;Arterial blood oxygen saturation. Timepoint: Before intervention - during intervention - after intervention. Method of measurement: Using the monitor and percentage basis. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Bammeri
Zahedan University of Medical Sciences
Outcome results
None listed