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Spinal Versus Epidural Analgesia in Laparotomic Liver Surgery

Not Applicable
Conditions
Liver Diseases
Liver Neoplasms
Secondary Malignant Neoplasm of Liver
Interventions
Procedure: Spinal analgesia
Procedure: Epidural analgesia
Procedure: Transversus Abdominis Plane block
Procedure: Surgical wound infiltration
Registration Number
NCT02647047
Lead Sponsor
Ospedale San Raffaele
Brief Summary

The purpose of this study is to evaluate the efficacy of spinal analgesia for minor laparotomic hepatectomy compared with epidural analgesia, monitoring visual analog scale (VAS). The investigators expect at least the same post-operative pain control in the two groups (non inferiority of pain control with spinal analgesia compared to epidural analgesia). Second endpoint is to verify whether after spinal analgesia there is a decrease in patient's length of hospitalization according to enhanced recovery after surgery (ERAS) principles.

Detailed Description

Liver surgery is performed under general anesthesia. Loco-regional analgesia is generally performed before general anesthesia induction to obtain the best post-operative pain control,in association with intravenous analgesic drug administration.

For minor laparotomic surgery (defined as the resection of up to three hepatic segments), if not contraindicated, in our hospital loco-regional analgesia is performed through the placement of a thoracic (T7-T8 or T8-T9) epidural catheter in which a local anesthetic (usually ropivacaine) and an opioid (usually sufentanil) are administered for the first three post-operative days. This is still considered the gold-standard for pain management in this surgery. In our institute, there is a dedicated acute pain service (APS) for pain management in the post-operative period. APS is also responsible for monitoring, registering and treating all side effects related to both the procedure and the drugs used.

In laparoscopic abdominal surgery, instead of epidural analgesia, if not contraindicated, spinal analgesia with low dose morphine before general anesthesia induction is performed. This technique is actually considered efficacy and safe in these type of surgeries.

The investigators therefore decided to test the efficacy of spinal analgesia versus epidural analgesia for minor liver surgery since anterior hepatic segments resection is less painful than major liver surgery because it requires less liver manipulation without significant involvement of the Glisson's capsule. This might imply a less incidence of procedure-related side effects such as post-dural puncture headache or site infections. Moreover, spinal analgesia may allow a earlier post-operative patients mobilization and thus a earlier hospital discharge.

In this randomized controlled trial, the investigators therefore aim to randomize 40 consecutive patients into 2 arms. The experimental group will receive spinal analgesia (morphine 0.2 mg) for post-operative pain control while the control group will receive epidural analgesia (bolus of ropivacaine 0.2% 4-6 mL followed by continuous epidural infusion of ropivacaine 0.2%: 99 mL + sufentanil 50 mcg/mL: 1 mL).

Randomization will be performed with closed opaque envelopes. During surgery, patients will be monitored as usual. Intraoperative blood losses and fluids administration will be recorded.

Patients randomized into the epidural group will not receive local anesthetic administration through the epidural catheter during the hepatic resection phase to avoid hemodynamic instability. Once the hepatic resection phase is finished and euvolemic status is recovered, epidural analgesia will be administered as mentioned before.

In patients in the spinal group, transversus abdominis plane (TAP) block with ropivacaine 0.375% 20 mL bilaterally or surgical wound infiltration with ropivacaine 0.75% 10- 20 mL will also be performed before anesthesia recovery.

In both groups, post-operative pain control will be managed with intravenous acetaminophen 1000 mg 40 minutes before ending of surgery followed by intravenous administration of acetaminophen 1000 mg every 8 hours and a non-steroidal antinflammatory drug (ketorolac 30 mg) as a rescue therapy in the post-operative period if not contraindicated.

Patients will be monitored every 24 hours until the achievement of the "ready to discharge" status defined as:

* appropriate oral alimentation;

* optimal pain control with drugs administered orally;

* adequate ability in walking and personal care;

* clinical, laboratory and instrumental absence of any post-operative complication;

* intestinal function recovery;

* patient consent to discharge.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Age > 18 years old
  • Hospitalized patients
  • Surgical indication for minor laparotomic anterior liver resection (II, III, IV and V hepatic segment resection)
  • Surgical indication for laparotomic liver metastasectomy
  • Ability to provide an informed consent
Exclusion Criteria
  • Patient refusal to provide informed consent
  • Chronical therapy with opioids
  • Pregnancy or breastfeeding
  • Alcohol or drug abuse
  • Planned or unplanned post-operative intensive care unit admission
  • Contraindication to spinal/epidural analgesia
  • Severe liver or renal failure
  • Cognitive disorders, mental retard or psychiatric disorders
  • Allergy to any drug used

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SpinalAcetaminophenPatients will receive spinal analgesia (morphine 0.2 mg) before general anesthesia for minor laparotomic liver resection.
SpinalTransversus Abdominis Plane blockPatients will receive spinal analgesia (morphine 0.2 mg) before general anesthesia for minor laparotomic liver resection.
EpiduralSufentanilPatients will receive epidural analgesia (bolus of ropivacaine 0.2% 4-6 mL followed by continuous epidural infusion of ropivacaine 0.2% 99 mL + sufentanil 50 mcg/mL 1 mL) before general anesthesia for minor laparotomic liver resection.
SpinalSpinal analgesiaPatients will receive spinal analgesia (morphine 0.2 mg) before general anesthesia for minor laparotomic liver resection.
SpinalSurgical wound infiltrationPatients will receive spinal analgesia (morphine 0.2 mg) before general anesthesia for minor laparotomic liver resection.
EpiduralEpidural analgesiaPatients will receive epidural analgesia (bolus of ropivacaine 0.2% 4-6 mL followed by continuous epidural infusion of ropivacaine 0.2% 99 mL + sufentanil 50 mcg/mL 1 mL) before general anesthesia for minor laparotomic liver resection.
SpinalRopivacainePatients will receive spinal analgesia (morphine 0.2 mg) before general anesthesia for minor laparotomic liver resection.
SpinalKetorolacPatients will receive spinal analgesia (morphine 0.2 mg) before general anesthesia for minor laparotomic liver resection.
EpiduralKetorolacPatients will receive epidural analgesia (bolus of ropivacaine 0.2% 4-6 mL followed by continuous epidural infusion of ropivacaine 0.2% 99 mL + sufentanil 50 mcg/mL 1 mL) before general anesthesia for minor laparotomic liver resection.
EpiduralAcetaminophenPatients will receive epidural analgesia (bolus of ropivacaine 0.2% 4-6 mL followed by continuous epidural infusion of ropivacaine 0.2% 99 mL + sufentanil 50 mcg/mL 1 mL) before general anesthesia for minor laparotomic liver resection.
EpiduralRopivacainePatients will receive epidural analgesia (bolus of ropivacaine 0.2% 4-6 mL followed by continuous epidural infusion of ropivacaine 0.2% 99 mL + sufentanil 50 mcg/mL 1 mL) before general anesthesia for minor laparotomic liver resection.
Primary Outcome Measures
NameTimeMethod
Assessment of postoperative pain control by mean of the visual analog scale early after surgeryWithin 1 hour after surgery

Visual analog scale (VAS) will be assessed and compared between the two groups.

Assessment of postoperative pain control by mean of the visual analog scale one day after surgery24 hours after surgery

Visual analog scale (VAS) will be assessed and compared between the two groups.

Assessment of postoperative pain control by mean of the visual analog scale six hours after surgery6 hours after surgery

Visual analog scale (VAS) will be assessed and compared between the two groups.

Assessment of postoperative pain control by mean of the visual analog scale three days after surgery72 hours after surgery

Visual analog scale (VAS) will be assessed and compared between the two groups.

Assessment of postoperative pain control by mean of the visual analog scale at hospital dischargeUp to 30 days after surgery

Visual analog scale (VAS) will be assessed and compared between the two groups.

Assessment of postoperative pain control by mean of the visual analog scale two days after surgery48 hours after surgery

Visual analog scale (VAS) will be assessed and compared between the two groups.

Secondary Outcome Measures
NameTimeMethod
Ready to discharge statusUp to 30 days after surgery

The postoperative day in which patients reach the "ready to discharge" status will be recorded and compared between the two groups.

Trial Locations

Locations (1)

Ospedale San Raffaele

🇮🇹

Milano, MI, Italy

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