Programmed Intermittent Epidural Bolus (PIEB) Techniques for Labour Analgesia

Analgesia Clinical Trial

— PIEB  

Official title:

Programmed Intermittent Epidural Bolus (PIEB) Techniques for Labour Analgesia; Finding the Optimum Combination

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06266767
• Other study ID #: MRC-01-18-157
• Status: Not yet recruiting
• Phase: Phase 4
• Start date: February 20, 2024
• Est. completion date: April 30, 2024

Study information

• Verified date: August 2023
• Source: Hamad Medical Corporation
• Contact: Roshan Fernando, MD
• Phone: 0097444392219
• Email: RFernando1[@]hamad.qa
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Epidural Analgesia remains the most effective form of pain relief in labour. After initiating epidural analgesia, there are many epidural drug regimens that can be employed to maintain analgesia for the duration of labour using an epidural catheter. Due to recent advances in medical technology, new epidural pumps, which allow both patient controlled epidural analgesia boluses (PCEA, a common standard of care in many hospitals) and programmed intermittent epidural boluses (PIEB, automatic boluses given in addition to the PCEA bolus), are now available. In this randomized double-blind trial, we aim to evaluate the effects of different combinations of PIEB (epidural bolus volume) and PIEB (bolus volume and time interval) on labour patient-controlled epidural analgesia (PCEA) usage. In theory, the more effective the PIEB combination (the ideal drug volume and ideal time interval), the less PCEA boluses (extra epidural drug) will be used as well as less clinician boluses and less lower limb weakness (motor block) as assessed by the Bromage Score.

Description:

Many women experience severe pain during labour. There are many forms of pain relief methods available to women in developed countries. Labour epidural analgesia remains the most effective form of pain relief. It is also the least depressive to the central nervous system of the mother and the baby. After initiating epidural analgesia, there are many regimens that can be employed to maintain analgesia for the duration of labour.

Traditionally, epidural analgesia (using low dose mixtures of local anaesthetic and opioid) has been administered by nurse or midwife-controlled manual boluses or as continuous infusion via a dedicated epidural pump (once the epidural catheter has been placed by an anaesthetist). Although these regimens provide an effective form of labour analgesia, patient satisfaction is not always achieved because of the associated lower limb motor block (leg weakness) and the increased risk of requiring instrumental delivery such as a forceps delivery. Due to recent advances in medical technology, new epidural pumps, which allow patient controlled epidural analgesia (PCEA) boluses and programmed intermittent epidural (PIEB) boluses, are now available.

Bolus injection through an epidural catheter may result in better distribution of anaesthetic solution in the epidural space when compared with continuous infusion of the same low dose local anaesthetic / opioid mixture. Capogna et al carried out a randomized double-blind study to compare the effects of a programmed intermittent epidural bolus (PIEB) regimen with a continuous epidural infusion (CEI). Motor block was reported in 37% in the CEI group and in only 2.7% in the PIEB group (P < 0.001). The incidence of instrumental delivery was 20% for the CEI group and 7% for the PIEB group (P = 0.03). The total local anaesthetic consumption, number of patients requiring additional PCEA boluses, and mean number of PCEA boluses per patient were also found to be lower in the PIEB group (P < 0.001). There were no differences in pain scores and duration of labour analgesia. (Capogna et al, 2011) Another randomized controlled study published by Wong et al compared total local anaesthetic (bupivacaine was used in this study) consumption, need for supplemental epidural analgesia, quality of analgesia, and patient satisfaction in women who received programmed intermittent epidural boluses (PIEB) compared with continuous epidural infusion (CEI) for maintenance of labour epidural analgesia. The median total bupivacaine dose per hour of analgesia was significantly less in the PIEB (n = 63) (10.5 mg/h; 95% confidence interval, 9.5-11.8 mg/h) when compared with the CEI group (n = 63) (12.3 mg/h; 95% confidence interval, 10.5-14.0 mg/h) (P < 0.01). Patient satisfaction scores were also higher in the PIEB group. The authors concluded that PIEB combined with patient controlled epidural analgesia (PCEA) provided similar analgesia, but with a smaller bupivacaine dose and better patient satisfaction compared with CEI with PCEA for maintenance of epidural labour analgesia. (Wong et al, 2006) Wong et al carried out another study to evaluate bupivacaine consumption and other analgesic outcomes when the programmed intermittent bolus time interval and volume were manipulated during the maintenance of epidural labour analgesia. They found that extending the programmed intermittent bolus interval and volume from 15 minutes to 60 minutes, and 2.5 mL to 10 mL, respectively, decreased bupivacaine consumption without decreasing patient comfort or satisfaction. (Wong et al, 2011) In our study, we aim to compare the effects of different combinations of PIEB bolus volume and PIEB time interval on the number of PCEA demands / clinician boluses, pain score, local anaesthetic consumption and patient satisfaction in order to find the optimal PIEB volume and PIEB time interval for labour pain relief when used together with a fixed (pre-determined) PCEA regimen.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 200
• Est. completion date: April 30, 2024
• Est. primary completion date: April 20, 2024
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Age 18 to 50 yrs

• In active labour

• ASA 2 patients (pregnant patients are considered to be ASA 2)

• Singleton pregnancy

• > 37 weeks gestation

• Booking BMI 18 to 35

Exclusion Criteria:

• BMI < 18

• BMI > 35

• Systemic opioids within the previous 6 hours

• Presence of a fetal anomaly

• Pre-eclampsia

• Bleeding disorders (including coagulation disorders)

• Recent spinal surgery

• Spinal injury

• Elevated intracranial pressure (ICP)

• Neuraxial disorders of any description

• Signs of local or systemic infection

• Patient refusal for neuraxial analgesia

Related Conditions & MeSH terms

• Analgesia
• Labor Pain
• Obstetric Pain

Intervention

Drug:
• Levobupivacaine and Fentanyl
Programmed Intermittent Epidural Bolus

Locations

Country	Name	City	State
Qatar	Hamad Medical Corporation (HMC)	Doha

Sponsors (1)

Lead Sponsor	Collaborator
Hamad Medical Corporation

Country where clinical trial is conducted

Qatar, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The volume of local anaesthetic mixture for breakthrough pain (PCEA + clinician bolus) + the Bromage Score	The (composite) primary outcome will identify the 2 best performing groups	From the siting of the epidural block to the delivery of the fetus (maximum 24 hrs)
Secondary	Pain score	Numeric Rating Scale (NRS). Patient self-reported pain scale. 0 (No Pain) to 10 (Worst possible pain)	From the siting of the epidural block to the delivery of the fetus (maximum 24 hrs)
Secondary	Total local anesthetic consumption	Initial Epidural Bolus + Total volume PIEB + Total volume PCEA + Clinician bolus volume	From the siting of the epidural block to the delivery of the fetus (maximum 24 hrs)
Secondary	Need for supplementary epidural analgesia	Total volume PCEA + Total volume clinician Bolus	From the siting of the epidural block to the delivery of the fetus (maximum 24 hrs)
Secondary	Bromage score (lower limb weakness score)	Bromage Score -1: Free movement of legs and feet, 2: Just able to flex knees, able to move feet, 3: Unable to flex knees, able to move feet, 4 :Unable to move legs or feet	From the siting of the epidural block to the delivery of the fetus (maximum 24 hrs)
Secondary	Type of delivery	Normal vaginal delivery, cesarean delivery, forceps and vacuum delivery	From the siting of the epidural block to the delivery of the fetus (maximum 24 hrs)
Secondary	Sensory block	Assessed with cold spray (ethyl chloride)	From the siting of the epidural block for 3 hours
Secondary	Fetal Outcome	Umbilical cord blood gases + Apgar scores	At the time of birth and 5 minutes after delivery