Evaluation of the Effect on Optic Nerve Sheath Diameter in Patients Undergoing Cesarean Section (EONSDCS)

Abant Izzet Baysal University

Status: Unknown

Conditions: Intracranial Pressure

Treatments: Procedure: USG guided ONSD measurement preepidural

Study type: Interventional

Funder types: Other

Identifiers

NCT03853889

ABANTIBU 6

Details and patient eligibility

About

Depending on the physiology of pregnancy, the risk of increased aspiration, difficult airway, increased oxygen consumption and reduced functional residual capacity, breathing problems make general anesthesia application risky. In obstetric operations, neuraxial anesthesia is preferred because of both maternal and maternal mortality and morbidity. Epidural area has decreased due to pregnancy physiology. Previous studies have shown that the blood given to the epidural area increases the intracranial pressure by compressing the dura mater.Optic nerve diameter measurements ultrasound guided is a non-invasive and reliable method for detecting intracranial pressure increase.

In this study, aimed to compare the optic nerve sheath diameter before and after epidural anesthesia with USG.

Full description

Epidural anesthesia will be performed at L2 level and sitting position in all patients. Patients will be measured and recorded for optic nerve sheath diameter at 15 min (T2), 30 min (T3) and 60 min (T4) immediately after epidural anesthesia (T0) and after epidural anesthesia.. Measurement of the optic nerve sheath diameter will be done with the help of a linear probe without applying high pressure to the eyeball while the patient is in supine position and the eyelids are closed. The optic nerve sheath diameter will be measured 3 mm beyond the optical disc. The measurements shall be applied in both transverse and sagittal planes for both eyes and the arithmetic mean of the four measured values.

Enrollment: 35 estimated patients

Sex: Female

Ages: 18 to 40 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• epidural anesthesia patients
• 18-40 years patients
• American Society of Anesthesiologists status I-II patients

Exclusion criteria

• Patients with allergy to any of the drugs to be used in the study,
• patients with severe heart failure,
• atrial and ventricular arrhythmias,
• severe valve disease,
• electrolyte disorder,
• renal failure, preeclampsia, eclampsia

Trial design

Primary purpose: Other

Allocation: Non-Randomized

Interventional model: Sequential Assignment

Masking: None (Open label)

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35 participants in 2 patient groups

preepidural ONSD

Active Comparator group

Description:

The diameter of the optic nerve sheath to be measured(ONSD) with the help of ultrasonography before epidural anesthesia(pre epidural ONSD). The measurement will be measured 3 mm behind the optical disc. The measurements shall be applied in both transverse and sagittal planes for both eyes and the arithmetic mean of the four measured values.

Treatment:

Procedure: USG guided ONSD measurement preepidural

post epidural ONSD

Experimental group

Description:

The diameter of the optic nerve sheath to be measured with the help of ultrasonography Immediately after epidural anesthesia(post epidural ONSD) (T1), 15 minutes (T2), 30 min (T3), 60. min (T4) epidural anesthesia. The measurement will be measured 3 mm behind the optical disc. The measurements shall be applied in both transverse and sagittal planes for both eyes and the arithmetic mean of the four measured values.

Treatment:

Procedure: USG guided ONSD measurement preepidural