Comparing Reversal With Neostigmine and Sugammadex in Paediatric (JS)

Comparison Between the Efficacy of Neostigmine Versus Sugammadex Reversal of Rocuronium Induced Neuromuscular Blockade In Paediatric Patients.

A reversal agent is commonly given to improve neuromuscular function after intra-operative administration of non-depolarizing neuromuscular blocking agents. The administration of conventional reversal agent neostigmine is associated with many undesirable side effects. For almost a decade, a new novel drug sugammadex has been used to specifically antagonize the effect of aminosteroidal neuromuscular blocking agents.

A total of 80 paediatric patients planned for general anaesthesia were divided into two groups and were given either neostigmine+atropine, or sugammadex for reversal once the operation had completed.

Study Overview

• Status: Completed
• Conditions: Neuromuscular Blockade
• Intervention / Treatment: Drug: Neostigmine; Drug: Sugammadex Sodium

Detailed Description

RESEARCH HYPOTHESIS

1. Sugammadex has a shorter recovery time (from TOF count of 2 or 3 to TOF ratio of more than 0.9) as compared to neostigmine.
2. Sugammadex has a more stable haemodynamic profile as compared to neostigmine when used to reverse rocuronium induced neuromuscular blockade in paediatric patients.
3. Sugammadex causes less complications or side effects when used in paediatric patients as a reversal for rocuronium induced neuromuscular blockade when compared to neostigmine.

This study was a prospective, double blinded, randomized control study involving 80 selected paediatric patients undergoing various surgeries under general anaesthesia in the operation theatre of Hospital University Sains Malaysia (USM), Kubang Kerian.

Sample size The sample size for this study was calculated using Power and Sample Size Calculation Programme Version 3.0.10.software based on different each respective objectives.

1. To compare the recovery time from Train of four (TOF) count of 2 or 3 to TOF ratio of more than 0.9 between neostigmine and sugammadex in reversal of rocuronium induced neuromuscular blockade in paediatric patients.

   • For objective 1, 33 participants in each respective groups are needed to detect the difference of 8 minutes (480 seconds) in time taken to achieve TOF ratio of 0.9 post-administration of reversal agent (SD was 590, according to Olzem Sacan et al) with 90% power, alpha 0.05. 20% is added for drop out participant. Therefore sample size, n = 33 + (0.2 x 33) = 40 patients.

2. To compare the haemodynamic changes between neostigmine and sugammadex in reversal of rocuronium induced neuromuscular blockade in paediatric patients.

   • For objective 2 (referring to blood pressure), 22 participants in each respective groups are needed to detect the difference of 10 mmHg in mean arterial blood pressure 5 minutes post-administration of reversal agent (SD was 10, according to Olzem Sacan et al) with 90% power, alpha 0.05. 20% is added for drop out participant. Therefore sample size, n = 22 + (0.2 x 22) = 26 patients.
   • For objective 2 (referring to heart rate), 22 participants in each respective groups are needed to detect the difference of 8 beats per minute in heart rate, 5 minutes post-administration of reversal agent (SD was 8, according to Olzem Sacan et al) with 90% power, alpha 0.05. 20% is added for drop out participant. Therefore sample size, n = 22 + (0.2 x 22) = 26 patients.

Therefore the total patients in each group will be 40 patients per group. Total sample size is 80 patients.

After gaining approval from USM Research Ethics Committee, the study was conducted in the Operation Theatre Hospital University Sains Malaysia (HUSM).

Parents of patients who fulfilled the inclusion criteria for this study were counselled, and those who agreed to participate in the study were given full explanation about the study and written consent was taken.

Randomization Subjects were divided into two groups using allocation sequence generated from online randomisation software (http://www.randomization.com). These respective allocations were concealed in sealed envelopes, which were not opened until it was time to administer the respective reversal agents in the Operation Theatre after completion of surgery. Patients were randomised to receive either 'Drug A' or 'Drug B' to reverse rocuronium induced neuromuscular blockade.

The randomization generated by the computer was only known to the anaesthetic assistant nurse, who is not involved in recruiting patients or carrying out the study.

Blinding This is a double blinded study. There were 2 important measures taken to ensure this. For this purpose, a specific anaesthetic assistant nurse is allocated before the study was carried out. This nurse is not involved in recruiting the subjects or carrying out the study, and is not related to the researcher.

Step 1 : Prior to sample collection, all subjects have already been randomized according to a sequence derived from online computer randomization. The anaesthetic assistant nurse prepares 80 envelopes, each respectively numbered 1-80, and 80 cards that will fit into the envelope, 40 labelled 'A' and 40 labelled 'B'. The cards were inserted into the envelopes and sealed according to the sequence that was derived from computer randomization. For example if subject 1 falls under group A, the card labelled 'A' is inserted into the envelope labelled 1, and firmly sealed. This is continued until all 80 cards have been inserted into all 80 numbered envelopes according to the determined sequence, all being firmly sealed. This process is carried out without the presence of the researcher.

Step 2 : On the day of surgery, prior to inducing the patient under general anaesthesia, the anaesthetic assistant nurse had prepares the reversal agents labelled 'Drug A' and 'Drug B'. To ensure desired double blinding, both reversal agents had to be diluted into similar volumes for equivalent dose for each respective drug for reversal of moderate block of Rocuronium induced neuromuscular blockade (TOF count 2 or 3)

• 1 mg of Atropine (1ml) was mixed with 2.5mg of Neostigmine (1ml) and diluted into 10 mls with Normal Saline 0.9% in a 10ml standard syringe. This would be a solution of 0.1 mg/ml Atropine with 0.25 mg/ml Neostigmine. A normal standard reversal dose for TOF count of 2 to 3 would be 0.05 mg/kg of Neostigmine with 0.02 mg/kg of Atropine. Therefore the volume would be 0.2mls per kg.
• 100 mg Sugammadex (1ml) is diluted into 10mls in a standard 10mls syringe with Normal Saline 0.9%. This will provide a new solution of 10mg/ml. The required dose for reversal of reversal of Rocuronium induced neuromuscular blockade with a TOF count of 2 or 3 would be 2mg/kg. This will also be equivalent to a volume of 0.2mls per kg.

This process was also done without the presence of the researcher. All medications were discarded by the end of the day.

Only the anaesthetic assistant nurse is aware which drug, either Neostigmine-Atropine combination or Sugammadex belongs to either group A (drug A) and group B (drug B), till all 80 samples have been collected. After completion of the study, the researcher is informed which drug was labelled as 'Drug A' and 'Drug B' respectively.

Study Protocol In the operating room, the patient was put under routine monitoring for general anaesthesia, including non-invasive blood pressure, electrocardiography, pulse oxymetry, end tidal carbon dioxide. The TOF Watch Sx, was also placed at the patients hand appropriately along the ulnar groove to monitor the neurotransmission activity of ulnar nerve . TOF reading was not taken at this time.

Paediatric Bispectral Index (BIS) monitoring was also placed on the patient's forehead, to ensure the patient was adequately induced prior to any painful stimulation for example intravenous access placement or TOF monitoring.

The patient was induced via sevoflurane gaseous induction, with a fresh gas flow rate of 8 litres per min of oxygen. Sevoflurane was dialled between 4 to 6 percent, to ensure hemodynamic parameters were within acceptable range, and BIS count achieved was 40-50.

Once the patient was fully relaxed and induced, a good functioning appropriate sized peripheral intravenous access was obtained.

2 mcg/kg of fentanyl was given for analgesia. After administration of fentanyl, the TOF Watch Sx was calibrated and a baseline TOF reading was taken and recorded.The patient was paralyzed with 0.6 mg/kg of rocuronium, and intubation of the trachea was done once TOF count was less than 1.

TOF monitoring was assessed at 15 minute intervals once patient was under general anaesthesia. Boluses of intravenous rocuronium 0.2 mg/kg was administered intermittently to maintain a TOF count of 2-3.

The baseline haemodynamic values (blood pressure, heart rate, pulse oxymetry, end tidal carbon dioxide) were documented prior to induction, post-intubation and the subsequent 15 minutes interval, to obtain a baseline and mean reading. The TOF readings were documented prior to Rocuronium administration (post-induction), post-intubation, then every 15 minutes interval, and just prior to reversal.

All patients were given suppositories paracetamol 20-30mg/kg for analgesia. No further opioids were served other than on induction. Where applicable, regional blocks or local infiltration at the surgical site were given for analgesia.

Prior to administration of the reversal agent as determined by randomization, it was ensured that the TOF reading was 2-3.

The following time was taken and recorded :

• from administration of reversal agent to TOF ratio more than 0.9
• from administration of reversal to spontaneous ventilation
• from administration of reversal to adequate ventilation (tidal volume at least 6mls/kg and adequate respiratory rate for age)
• from administration of reversal to extubation The haemodynamic parameters (blood pressure, heart rate, pulse oxymetry, respiratory rate, tidal volume, end tidal carbon dioxide) were documented in 5 minute intervals upon administration of the reversal agent.

Haemodynamic parameters in the recovery bay (blood pressure, heart rate, pulse oxymetry, respiratory rate) were also documented.

Patients were also observed for any complications or side effects post-extubation such as nausea, vomiting, secretions, respiratory distress, etc in the recovery bay.

• Study Type: Interventional
• Enrollment (Actual): 80
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Malaysia
  • Kelantan
    • Kubang Kerian, Kelantan, Malaysia, 16150
      • University of Science Malaysia Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 8 months to 10 years (Child)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• American Society of Anaesthesiologist (ASA) physical status 1 and 2.
• Paediatric patients within the above criteria whom require rocuronium induced neuromuscular blockage for general anaesthesia

Exclusion Criteria:

• Active or recent upper respiratory tract infection (within 2 weeks)
• Haemodynamically unstable patients for example trauma, haemorrhage, sepsis, thyrotoxic or cardiac failure
• Patients with pre-existing neuromuscular disorders
• Patients with renal failure, with creatinine clearance of less than 30mmol/L
• Patients requiring post-operative ventilation
• Patients with known allergy to sugammadex or neostigmine

Study Plan

How is the study designed?

Design Details

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

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Neostigmine; 1 mg of Atropine (1ml) was mixed with 2.5mg of Neostigmine (1ml) and diluted into 10mls with Normal Saline 0.9% in a 10ml standard syringe.	Drug: Neostigmine; The TOF Watch Sx, and Paediatric Bispectral Index (BIS) monitoring were put on patient. Gaseous induction, with oxygen and Sevoflurane was given until BIS was 40-50, then a intravenous line was obtained. 2 mcg/kg of fentanyl was given for analgesia. then,the TOF Watch Sx was calibrated.The patient was paralyzed with 0.6mg/kg of rocuronium, and intubation of the trachea was done once TOF count was less than 1. A maintenance of 0.2 mg/kg of Rocuronium was given boluses every 30 minutes to maintain TOF count between 2-3. At the end of surgery, TOF count was checked to ensure it was between 2-3. Then a reversal dose for TOF count of 2 to 3 was 0.05 mg/kg of Neostigmine with 0.02 mg/kg of Atropine. Therefore the volume would be 0.2 mls per kg is to be administered.; Other Names: Prostigmine
Experimental: Sugammadex sodium; 100mg Sugammadex (1ml) is diluted into 10mls in a standard 10mls syringe with Normal Saline 0.9%.	Drug: Sugammadex Sodium; The TOF Watch Sx, and Paediatric Bispectral Index (BIS) monitoring were put on patient. Gaseous induction, with oxygen and Sevoflurane was given until BIS was 40-50, then a intravenous line was obtained. 2 mcg/kg of fentanyl was given for analgesia. then,the TOF was calibrated.The patient was paralyzed with 0.6mg/kg of rocuronium, and intubation of the trachea was done once TOF count was less than 1. A maintenance of 0.2 mg/kg of Rocuronium was given boluses every 30 minutes to maintain TOF count between 2-3. At the end of surgery, TOF count was checked to ensure it between 2-3. Then the dose for reversal of sugammadex with a TOF count of 2 or 3 would be 2 mg/kg. This will also be equivalent to a volume of 0.2 mls per kg and given at the end of surgery.; Other Names: Bridion

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Recovery time	To assess the recovery time from TOF count of 2 or 3 to TOF ratio of more than 0.9 between neostigmine or sugammadex in reversal of rocuronium induced neuromuscular blockade in paediatric patients.	From the time the reversal drugs (neostigmine or sugammadex) were given at TOF count of 2-3 till the TOF ratio is more than 0.9 up to 5 minutes after the operation finished

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Adequate ventilation	To evaluate the time from administration of reversal to adequate ventilation (tidal volume at least 6mls/kg and adequate respiratory rate for age)	From the time of the reversal drugs (neostigmine or sugammadex) were given till patient achieved good ventilation (tidal volume 6 ml/kg) up to 5 minutes after the operation finished
Extubation time	To evaluate the time from administration of reversal to extubation	From the time of the reversal drugs (neostigmine or sugammadex) were given till the patient is extubated up to 5 minutes after the operation finished.
Blood Pressure	Blood pressure was documented in 5 minute intervals upon administration of the reversal agent and in the the recovery bay.	From the time of the reversal drugs (neostigmine or sugammadex) were given till the patient is discharged throughout the time the patient stays at the recovery bay up to 30 minutes.
Heart Rate	Heart rate was documented in 5 minute intervals upon administration of the reversal agent and in the the recovery bay.	From the time of the reversal drugs (neostigmine or sugammadex) were given till the patient is discharged throughout the time the patient stays at the recovery bay up to 30 minutes.
Oxygen saturation	Oxygen saturation was documented in 5 minute intervals upon administration of the reversal agent and in the the recovery bay.	From the time of the reversal drugs (neostigmine or sugammadex) were given till the patient is discharged throughout the time the patient stays at the recovery bay up to 30 minutes.
Number of patients with treatment related-adverse event as assessed by clinical observation	To monitor any incidence of treatment related-adverse event post extubation	From the time of the patient extubated until the patient is discharged throughout the time the patient stays at the recovery bay up to 30 minutes.

Collaborators and Investigators

• Sponsor: Universiti Sains Malaysia
• Investigators: Principal Investigator: rhendra hardy Mohamad Zaini, MD, Universiti Sains Malaysia

Publications and helpful links

General Publications

• Khuenl-Brady KS, Wattwil M, Vanacker BF, Lora-Tamayo JI, Rietbergen H, Alvarez-Gomez JA. Sugammadex provides faster reversal of vecuronium-induced neuromuscular blockade compared with neostigmine: a multicenter, randomized, controlled trial. Anesth Analg. 2010 Jan 1;110(1):64-73. doi: 10.1213/ane.0b013e3181ac53c3. Epub 2009 Aug 27.
• Blobner M, Eriksson LI, Scholz J, Motsch J, Della Rocca G, Prins ME. Reversal of rocuronium-induced neuromuscular blockade with sugammadex compared with neostigmine during sevoflurane anaesthesia: results of a randomised, controlled trial. Eur J Anaesthesiol. 2010 Oct;27(10):874-81. doi: 10.1097/EJA.0b013e32833d56b7.
• Plaud B, Meretoja O, Hofmockel R, Raft J, Stoddart PA, van Kuijk JH, Hermens Y, Mirakhur RK. Reversal of rocuronium-induced neuromuscular blockade with sugammadex in pediatric and adult surgical patients. Anesthesiology. 2009 Feb;110(2):284-94. doi: 10.1097/ALN.0b013e318194caaa.
• Sacan O, White PF, Tufanogullari B, Klein K. Sugammadex reversal of rocuronium-induced neuromuscular blockade: a comparison with neostigmine-glycopyrrolate and edrophonium-atropine. Anesth Analg. 2007 Mar;104(3):569-74. doi: 10.1213/01.ane.0000248224.42707.48.

Study record dates

Study Major Dates

• Study Start (Actual): December 1, 2014
• Primary Completion (Actual): June 30, 2016
• Study Completion (Actual): June 30, 2016

Study Registration Dates

• First Submitted: April 16, 2017
• First Submitted That Met QC Criteria: May 1, 2017
• First Posted (Actual): May 2, 2017

Study Record Updates

• Last Update Posted (Actual): May 2, 2017
• Last Update Submitted That Met QC Criteria: May 1, 2017
• Last Verified: May 1, 2017

More Information

Terms related to this study

• Keywords: Rocuronium; Sugammadex; Neostigmine; Paediatric general anaesthesia
• Additional Relevant MeSH Terms: Physiological Effects of Drugs; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Autonomic Agents; Peripheral Nervous System Agents; Cholinergic Agents; Enzyme Inhibitors; Cholinesterase Inhibitors; Parasympathomimetics; Neostigmine
• Other Study ID Numbers: JEPeM/281.3(3)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

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