Influence of Body Positioning on the Identification of Tuffier's Line Using the Palpation Method: An Ultrasound Study

Pregnant Women Clinical Trial

Official title:

Influence of Body Positioning on the Identification of Tuffier's Line Using the Traditional Palpation Method: An Ultrasound Study.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03128541
• Other study ID #: 218764
• Status: Recruiting
• Phase: N/A
• First received: April 20, 2017
• Last updated: July 31, 2017
• Start date: April 14, 2017
• Est. completion date: December 2017

Study information

• Verified date: July 2017
• Source: Guy's and St Thomas' NHS Foundation Trust
• Contact: Nhathien Nguyen-Lu, FRCA
• Phone: 0207 188 7188
• Email: nat.nguyen-lu[@]gstt.nhs.uk
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

The study aims to ascertain whether being placed in a sitting or lateral decubitus position, influences identification of the midpoint of the L4/L5 intervertebral space, using manual demarcation of Tuffier's line. Participants will be randomly assigned to a sitting or lateral decubitus position. The mid-point of the L4/L5 intervertebral space will be identified using anatomical palpation and compared to the "true" mid-point measured by ultrasound. The procedure will be repeated in both positions on the same participant.The study will be a prospective, randomized, double blinded, crossover trial

Description:

Anaesthetists insert epidurals or spinal anaesthetics (collectively called central neuraxial blocks) to patients during childbirth to provide pain relief and anaesthesia. A spinal anaesthetic involves the injection of pain relieving medicines directly into the sac of fluid that surrounds the spinal cord. An epidural uses a different technique to place a thin plastic tube into the fatty tissues that surround this sac. Spinal anaesthesia must be placed below where the spinal cord ends to avoid nerve trauma. Doctors have traditionally been taught to identify a safe level, by feeling the top of a patients hips and drawing an imaginary line between these two points across the patients back known as Tuffier's line. This identifies L4/5 interspace, below which anaesthetists avoids the termination of the spinal cord. The same blind "anatomical rule" is used throughout anaesthetics, whether the patient is male or female, young or old, pregnant or non-pregnant, supine or lateral, an approach that is clearly far from robust. The physiological changes of pregnancy such as fluid retention and weight gain can further make identification of the standard landmarks challenging. Advances in ultrasound technology have allowed direct visualisation of the bones in the back. Studies have shown that the conventional anatomical based method for locating the point of needle insertion is unreliable even amongst experienced anaesthetists.

Spinal or epidural anaesthesia can be performed with the patient either sitting or lying on their side. The investigators aim to determine whether a difference exists between the perceived mid-point of the L4/L5 intervertebral space, identified using manual demarcation of Tuffier's line, in these two positions. Ultrasound will then be used to ascertain the distance from the "true" midpoint.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 80
• Est. completion date: December 2017
• Est. primary completion date: December 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 16 Years to 65 Years

Eligibility

Inclusion Criteria:

• >37 weeks gestation

• BMI<40

• Singleton pregnancy

• Aged 16 to 65 years old.

• Latent phase of labour (<4cm cervix dilatation).

Exclusion Criteria:

• Previous spinal surgery

• Scoliosis

• Age<16

• Patient unable to tolerate positions

• Degenerative disease of the spine

• Patient refusal or inability to provide informed consent

• Patient in established labour (i.e. >4cm cervical dilatation)

Related Conditions & MeSH terms

• Pregnant Women

Intervention

Diagnostic Test:
• Ultrasound spine
A ultrasound of the lumbar spine of each patient will be performed in both positions to identify vertebral levels

Locations

Country	Name	City	State
United Kingdom	St Thomas' Hospital	London

Sponsors (1)

Lead Sponsor	Collaborator
Guy's and St Thomas' NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Discrepancy in distance between palpation vs. ultrasound midpoint of L4/5. interspace.	Distance (mm) between the mid-point of the L4/L5 intervertebral space in sitting and lateral decubitus positions, identified through manual palpation compared to the "true" mid-point measured by ultrasound.	15-30 minutes
Secondary	Discrepancy in distance between ultrasound midpoint of L4/5 in sitting vs. lateral position	Distance (mm) between the mid-point of the L4/L5 intervertebral space identified by ultrasound in sitting versus lateral decubitus positions.	15-30 minutes