Nalbuphine Versus Fentanyl As Additives To Bupivacaine In Spinal Anaesthesia For Internal FixationI Of Tibia

The Efficacy Of Nalbuphine Versus Fentanyl As Additives To Bupivacaine In Spinal Anaesthesia For Internal FixationI Of Tibia

The Efficacy Of Nalbuphine Versus Fentanyl As Additives To Bupivacaine In Spinal Anaesthesia For Internal FixationI Of Tibia

Study Overview

• Status: Completed
• Conditions: Pain, Postoperative
• Intervention / Treatment: Drug: Fentanyl/Hyperbaric bupivacaine; Drug: Nalbuphine/Hyperbaric bupivacaine

Detailed Description

The Efficacy Of Nalbuphine Versus Fentanyl As Additives To Bupivacaine In Spinal Anaesthesia For Internal FixationI Of Tibia

INTRODUCTION Regional techniques, such as spinal anaesthesia may offer advantages over general anaesthesia including reduced stress response to surgery and analgesia extending into the postoperative period.(1,2) Adequate pain management to facilitate rehabilitation and to accelerate functional recovery after lower limb orthopedic surgery is essential to enable patients to resume normal activity as soon as possible.(3) To increase the duration of analgesia produced by local anesthetic, a number of adjuvants have been added through the central neuraxial route.(4) The profound segmental anti-nociception produced by neuraxial opioids in doses much smaller than would be required for comparable anti-nociception if administered systemically has made them very popular and effective in the treatment of many painful states.(5)The anti-nociception is also devoid of motor, sensory and autonomic blockade so there is no paralysis or hypotension. Furthermore, the availability of a specific opioid receptor antagonist naloxone to reverse their action when necessary has made the use of opioids more acceptable.(6) Opioids work in the intrathecal space by activating opioid- receptors in the dorsal gray matter of spinal cord, which modulates the function of afferent pain fibers.(7)Intrathecal and epidural narcotics seem to modulate pain primarily at the spinal cord rather than in the brain as do intravenous narcotics.(8) Site of action in the spinal cord may provide analgesia with less sedation, confusion and nausea, which are adverse effects associated with intravenous narcotics.(9) Various opioids have been used along with bupivacaine to prolong its effect, to improve the quality of analgesia and minimize the requirement of postoperative analgesics.(10,11) The main obstacles for optimal use of opioids are their side effects which include pruritis, nausea/ emesis, constipation, urinary retention, respiratory depression, undesirable sedation and the development of tolerance/ dependence. Though some side effects may be benign but others like respiratory depression can prove to be life threatening.(12-14) Nalbuphine is a semisynthetic opioid with mixed mu antagonist and kappa agonist properties. When used singly or in combination with other agents it has the potential to maintain or even enhance opioid based analgesia while simultaneously mitigating the common mu-opioid side effects. (15) Nalbuphine binds readily to both mu- and kappa-receptors. The binding of nalbuphine to mu receptors only serves to competitively displace other mu-agonists from the receptor, without itself displaying any agonist activity.(16)When nalbuphine binds to kappa-receptors, however, it has an agonist effect. Kappa-opioid receptors are distributed throughout brain and spinal cord involved in nociception. Nalbuphine binds avidly to kappa-receptors in these areas to produce analgesia. This pattern of binding and effects defines nalbuphine as a mixed agonist-antagonist.(17) Fentanyl, a lipophilic opioid has rapid onset of action, It does not tend to migrate intrathecally to the 4th ventricle in sufficient concentration to cause delayed respiratory depression.(18,19)

AIM OF THE WORK The aim of our study is to compare the effect of intrathecal nalbuphine versus intrathecal fentanyl as adjuvants to bupivacaine, as regard the intra-operative and post-operative analgesia, the hemodynamic stability, the onset of sensory/motor block and the duration of action in patients undergoing internal fixation of tibia.

PATIENTS This study will be carried out in El-Hadara University Hospital on sixty patients aged 18-50 years; belonging to American Society of Anesthesiologists (ASA) physical status I and II, scheduled for elective internal fixation of tibia, of expected duration less than 3 h, under subarachnoid block, this prospective study will be done in a double-blinded, randomized way.

Exclusion criteria:

• Patients with significant co-existing conditions such as hepatic, renal and cardiovascular diseases.
• Patients with contraindications to regional anesthesia like local infection or bleeding disorders.
• Patients with allergy to opioids, long-term opioids use, and a history of chronic pain.

After approval from the local ethical committee, a written consent will be obtained from each patient.

Patients will be randomly allocated into two groups according to intrathecal drug injected using closed envelope method.

Group F:

Patients will receive intrathecal injection of 2 ml of 0.5% hyperbaric bupivacaine plus 1 ml fentanyl (50μg).

Group N:

Patients will receive intrathecal injection of 2 ml of 0.5% hyperbaric bupivacaine plus 1ml nalbuphine hydrochloride (1.6 mg); (nalufin 20 mg in 1 ml ampoule, Amoun Pharmaceutical Co. Cairo, Egypt).

METHODS

1. Preoperative preparation:

   Preoperative screening of all patients including:

   • History taking.
   • Complete physical examination.

   • Laboratory investigation:

     • Complete blood picture (CBC)
     • Prothrombin time (PT), partial thromboplastin time (PTT), Prothrombin activity and INR.
     • Liver enzymes: Aspartate transaminase, Alanine transaminase.
     • Serum urea and creatinine.
     • Fasting blood sugar. Nothing per month in previous 6 hours.

2. Monitoring:

   All patients will be monitored by:

   • Electrocardiogram (ECG) for heart rate (beat/min).
   • Non-invasive arterial blood pressure: mean arterial blood pressure (MAP), systolic blood pressure (SAP) and diastolic arterial blood pressure (DAP).
   • Pulse oximeter for arterial oxygen saturation (SaO2).

3. Intraoperative procedure:

   • After securing intravenous (18G) access in the non-dominant hand, preloading with Ringer's solution 10 ml/kg in 15 min will be done.
   • Subarachnoid block will be performed with 3 ml of the study drug injected in L3/4 intervertebral space, using a 25 gauge Quincke spinal needle, in the sitting position, maintaining aseptic precautions, according to the standard institutional protocol.
   • The patients will be randomized using close envelope method equally into two groups according to the additive (fentanyl or nalbuphine), and all patients will receive the same amount of local anesthetic (2 ml 0.5% heavy bupivacaine).

   Thereafter, patients will be placed in the supine position for surgery, elevation of the head by a pillow and oxygen mask will be applied.

   Advanced equipment and drugs for resuscitation, airway management and ventilation will be ready.

   MEASUREMENTS 1. Hemodynamic parameters:

   • Patient heart rate and mean arterial blood pressure will be monitored and recorded at the following periods:
   • 5 minutes before the intrathecal injection.
   • At 2, 4, 6, 8 and 10 minutes after the injection.

   • Every 15 min until the patient will be moved to the post anaesthesia care unit (PACU).

     2. Assessment of sensory blockade:

   • The onset of sensory block is defined as the time in minutes to reach highest sensory level (20), it will be evaluated by ice at midclavicular level bilaterally every 2min for 15 min.
   • The duration of sensory block will be defined as the time it takes for sensory level to decrease to dermatomal level 12 measured from the highest sensory level evaluated by ice every 15 minutes. (21)

   • The maximal level of sensory block will be evaluated by 20 min after the completion of injection.

     3. Assessment of the motor block:

   • Onset time of motor block will be assessed immediately after sensory block assessment using modified Bromage scale.(22)

   Modified Bromage scale

   • The onset of motor block will be defined as the time from intrathecal injection to Bromage score 3 tested every 2min for 15 min. (23)
   • Duration of motor block will be evaluated every 15 minutes intraoperative from Bromage score 3 then every 30 minutes in the post anaesthesia care unit (PACU) until full recovery of motor function.

4. post operative analgesia:

   1. Duration of analgesia:

      • The duration of analgesia will be defined as the period from spinal injection to the first time when the patient complained of pain in the postoperative period.
      • Patients will be assessed using Visual analogue scale (VAS), in the immediate postoperative period, then every 2hours for the first 8hours, then every 6hours for the rest of the first 24hours.

      Visual analogue scale (VAS)

      - It ranges from 0 indicating no pain till 10 indicating severe intolerable pain with variable degrees of ascending pain in between.(24)

   2. Postoperative analgesic requirements:

      • The time of the first request analgesia will be recorded and treated by intramuscular diclofenac sodium (75mg) in a dose of 1mg/kg and repeated after 1 hour if needed up to 2 ampoules.
      • Paracetamol 1 g IV every 8 hours will be given for analgesia to all patients starting immediately postoperative (time zero).
      • Total dose of analgesic requirements will be calculated and elaborated statistically.
   3. Postoperative Complication:

Any complication will be recorded and managed such as hypotension, bradycardia, nausea, vomiting, pruritus, shivering and respiratory depression.

• Hypotension will be defined as systolic blood pressure less than 90mmHg and\or a decrease of more than 20% from baseline blood pressure. (25)
• Bradycardia will be defined as HR<50 beat\min.
• Respiratory depression will be defined as respiratory rate <10 breath\min.

ETHICS OF RESEARCH Prospective study: Informed consent will be taken from patients. In case of incompetent patients the informed consent will be taken from the guardians.

• Study Type: Interventional
• Enrollment (Actual): 50
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Egypt
  • Alexandria, Egypt, 21111
    • Alexandria Faculty of Medicine

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 50 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• patients aged 18-50 years
• American Society of Anesthesiologists (ASA) physical status I and II
• Scheduled for elective internal fixation of tibia, of expected duration less than 3 h, under subarachnoid block

Exclusion Criteria:

• Patients with significant co-existing conditions such as hepatic, renal and cardiovascular diseases.
• Patients with contraindications to regional anesthesia like local infection or bleeding disorders.
• Patients with allergy to opioids, long-term opioids use, and a history of chronic pain.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Fentanyl/Hyperbaric Bupivacaine; Group F: Patients will receive intrathecal injection of 2 ml of 0.5% hyperbaric bupivacaine plus 1 ml fentanyl (50μg) and will have Tibial internal fixation.	Drug: Fentanyl/Hyperbaric bupivacaine; Intrathecal Fentanyl/Hyperbaric bupivacaine and Tibial internal fixation.; Other Names: Spinal Fentanyl/Hyperbaric bupivacaine
Active Comparator: Nalbuphine/Hyerbaric Bupivacaine; Group N: Patients will receive intrathecal injection of 2 ml of 0.5% hyperbaric bupivacaine plus 1ml nalbuphine hydrochloride (1.6 mg); (nalufin 20 mg in 1 ml ampoule, Amoun Pharmaceutical Co. Cairo, Egypt) and will have Tibial internal fixation.	Drug: Nalbuphine/Hyperbaric bupivacaine; Intrathecal Nalbuphine/Hyperbaric bupivacaine and Tibial internal fixation.; Other Names: Spinal Nalbuphine/Hyperbaric bupivacaine

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Pain Postoperative	VAS 0-10	24 hours

Collaborators and Investigators

• Sponsor: University of Alexandria

Study record dates

Study Major Dates

• Study Start (Actual): November 4, 2017
• Primary Completion (Actual): August 19, 2018
• Study Completion (Actual): August 20, 2018

Study Registration Dates

• First Submitted: May 12, 2018
• First Submitted That Met QC Criteria: May 22, 2018
• First Posted (Actual): May 24, 2018

Study Record Updates

• Last Update Posted (Actual): January 23, 2019
• Last Update Submitted That Met QC Criteria: January 19, 2019
• Last Verified: January 1, 2019

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Postoperative Complications; Pain; Neurologic Manifestations; Pain, Postoperative; Physiological Effects of Drugs; Central Nervous System Depressants; Peripheral Nervous System Agents; Analgesics; Sensory System Agents; Anesthetics, Intravenous; Anesthetics, General; Anesthetics; Analgesics, Opioid; Narcotics; Adjuvants, Anesthesia; Anesthetics, Local; Fentanyl; Bupivacaine; Nalbuphine
• Other Study ID Numbers: 050108393

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No