The sniffing position defined as neck flexion with upper cervical extension, is traditionally recommended for general anesthesia induction, as it improves laryngoscopic views. However, the head elevation beyond the sniffing position, also known as ramped position or head elevated laryngoscopy position, usually achieved by specially designed pillows such as the Oxford head elevating laryngoscopy pillow (Alma Medical,Oxford, UK) or the Troop® elevation pillow (Mercury Medical, Clearwater, FL, USA)has been shown to not only increase respiratory reserve but also to improve laryngeal views in patients undergoing bariatric surgery. Additionally it helps in pre-oxygenating the patient more efficiently by keeping the airway patent and provides easier bag-mask ventilation. It may also benefit the term parturient in a similar way by improving functional residual capacity (FRC), ventilation and comfort. However, this positon may affect the cephalad spread of the intrathecal local anesthetic. Two earlier studies looked at the intrathecal local anesthetic spread in obstetric patients when placed in the head elevated laryngoscopy position, and both suggested poor cephalad spread, with patients requiring higher supplementation. However, both studies excluded morbidly obese patients. The Investigators hypothesized that in obese parturients with BMI more than or equal 40, higher intra-abdominal pressures and possibly lower CSF volumes will counteract the poor cephalad spread associated with this position. The aim of this study is to determine the effect of a ramped position on intrathecal local anesthetic spread in the morbidly obese term parturients with BMI more than or equal 40 undergoing elective Cesarean delivery(CD).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
90
ramped position, also known as head elevated laryngoscopy position,
Hamad Medical Corporation
Doha, Qatar
The sensory level (loss of cold and pin prick sensation) at 15 min after the intrathecal administration of the medication in the parturient
Time frame: From date of randomization until the date of first documented progression, assessed up to 48 months
Incidence of inadequate block level at 15 min and need for epidural supplements
Secondary Outcomes: I. Incidence of inadequate block level at 15 min II. The need for epidural supplementation. III. Dosage of epidural local anesthetics to achieve adequate block level following the spinal anesthetic. IV. The need and dosage of iv opioids for intraoperative supplemental analgesia V. The incidence of pain throughout the procedure (by the use of NRS). VI. The use and dosage of vasopressor. VII. The rate of conversion to general anesthesia. VIII. Maternal satisfaction with the position. IX. Neonatal outcomes (Birth weight in kilograms, APGAR scores, umbilical cord gases and lactate)
Time frame: From date of randomization until the date of first documented progression, assessed up to 48 months
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