Glossopharyngeal and Maxillary Nerve Blocks in Adenotonsillectomy (Pediatrics)
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About
This study aims to compare of bilateral ultrasound-guided glossopharyngeal nerve (UGGNB) and ultrasound-guided maxillary nerve (UGMNB) versus conventional multimodal analgesia for tonsillectomy operations.
Full description
Patients will be premedicated with oral midazolam 0.5 mg/kg prior to arriving in the operating room 30 min before the procedure.
Standard monitoring will be maintained throughout the procedure included electrocardiography, noninvasive arterial pressure, arterial oxygen saturation.
. If intravenous access is present, Fentanyl 1 μg/kg IV will be given and anesthesia will be induced using propofol 2-3 mg/kg and atracurium 0.5 mg/kg. If intravenous access is not present, anesthesia will be induced with inhalation of 8% sevoflurane in 100% oxygen under spontaneous ventilation and IV access will be established, fentanyl 1 µg/kg IV and atracurium 0.5 m g/kg IV will be given after achieving IV access. Endotracheal intubation will be done using an appropriate size endotracheal tube (ETT) and capnography attached. IV dexamethasone 150 μg/kg will be given. Anesthesia will be maintained using a 50:50 mixture of air and oxygen along with isoflurane 1.2% and the maintenance dose of atracurium 0.1 mg/kg each 20 minutes. Pressure-controlled ventilation and low fresh gas flows will be used. All patients will receive intraoperative analgesia in the form of single dose paracetamol 15 mg/kg.
Patients will be randomly allocated into two equal groups:
Block Group: patients will receive combined bilateral ultrasound-guided glossopharyngeal nerve (UGGNB) and bilateral ultrasound-guided maxillary nerve (UGMNB) immediately after the induction of anesthesia and prior to surgical incision by an expert anesthesiologist in ultrasound guided regional anesthesia who is not a part of the study using Philips Model HD5 Diagnostic ultrasound system a the scanning probe will be the linear ultrasound probe (4-12MHz) for glossopharyngeal nerve block and a curvilinear ultrasound probe (5-7 MHz) for maxillary nerve block using fine needle as described with aid of ultrasound.
Conventional Group: patients will receive multimodal analgesia for tonsillectomy operations in the form of single dose of IV paracetamol 15 mg/kg.
Tonsillectomies will be carried out by expert surgeon using the same electro-dissection surgical technique.
In block group:
Technique of ultrasound-guided glossopharyngeal nerve block (UGSGNB): posterior mandibular ramus approach For the procedure, anesthesiologist will turn patient face carefully toward the clinician, and a linear ultrasound probe will be placed in the neck to check the surrounding target structures: the sternocleidomastoid muscle, the common carotid artery, and the internal jugular vein. After the sternocleidomastoid muscle has been identified, a linear ultrasound probe will be placed parallel to the sternocleidomastoid muscle fiber direction just caudal to the mandibular ramus. The stylohyoid muscle is easily visualized by tiling the linear ultrasound probe toward the mandibular ramus. In this area, the stylohyoid muscle is positioned under the sternocleidomastoid muscle, and both can be observed under ultrasound guidance. A 25-gauge, 25-mm needle will be inserted deeply under the stylohyoid muscle through the sternocleidomastoid muscle via an out-of-plane approach. An ultrasound-guided nerve block will be performed with 3 mL of 0.25% bupivacaine after the absence of blood backflow is confirmed. The same procedure will be then repeated on the contralateral side.
Technique of ultrasound-guided maxillary nerve (UGMNB): Suprazygomatic maxillary nerve blocks The curvilinear ultrasound probe will be placed in the infrazygomatic area, over the maxilla, angled 45° cephalad. This probe position allows visualization of the pterygopalatine fossa, limited anteriorly by the maxilla and posteriorly by the greater wing of the sphenoid. A 22- gauge, 5-cm nerve block needle will be inserted perpendicularly to the skin following aseptic preparation of the skin at the frontozygomatic angle formed by the posterior orbital rim and zygomatic . Once contact was made with the greater wing of the sphenoid, the needle will be redirected caudally and medially, and advances through the pterygomaxillary fissure into the pterygomaxillary fossa. The needle will be advanced using an out-of-plane approach, and the needle tip can usually be identified during movements.
Needle placement will be verified by real-time ultrasound guidance and negative aspiration before administration of 3-4 ml of 0.25 % bupivacaine. The same procedure will be then repeated on the contralateral side.
In both groups Baseline hemodynamics in the form of: non-invasive BP, HR, oxygen saturation will be recorded before induction of anesthesia. the intraoperative hemodynamics will be recorded at 15 minute intervals in addition to continuous monitoring of HR and oxygen saturation. If heart rate (HR) increases more than 20% of baseline an additional dose of fentanyl 1 µg/kg will be given , if blood pressure exceeding 20% from baseline an additional dose of fentanyl 1 µg/kg will be given with a maximum total dose of 5 mcg/kg if additional doses are required , if bradycardic atropine 0.01 mg/kg will be given. At the end of the surgery , Inhalational anesthesia will be discontinued and muscle relaxation will be reversed by atropine (0.02 mg/Kg) and neostigmine (0.05 mg/Kg) after the restoration of the patient's spontaneous breathing. The patient will be transferred to the post-anesthesia care unit (PACU) for 1 hours to complete recovery and monitoring and then will be sent to the ward. Quality of analgesia will be assessed using the Wong-Baker FACES scale for children more than 3 years of age up to 8 years of age and VAS score for older children every 30 minutes for 1 hours after recovery from anesthesia in PACU and every 2, 4, 8, 12, and 24 hours postoperative after transferring to the ward.
For postoperative pain therapy, If the pain scale scores are ≥ 4, first will be IV ibuprofen 7.5 mg/kg immediately postoperative.
Regarding that maximum single dose of ibuprofen is 400mg , maximum daily dose is 40mg/kg .
Paracetamol will not be given within 6 hour of intraoperative administration. After 15 mins if the pain scale scores still ≥ 4, patients will receive pethidine 0.5 mg/kg I.V. as rescue analgesia, which may be repeated, taking in consideration that the total daily dose should not exceed 1.5 mg/kg(11), regarding that minimum period of pethidine rescue analgesic doses are from 2 to 4 hours and. The analgesic effect occurs after about 10 minutes following parenteral administration.
Antiemetics (IV 1.25 mg/kg dimenhydrinate or 0.15 mg/kg of metoclopramide or 0.1 mg/kg ondansetron) will be given in the case of postoperative nausea and vomiting .
The patient will be discharged when the pain is controlled as the pain scale < 3 and there is no nausea, vomiting, and/or bleeding. Post discharge, the FACES and VAS scales will be explained to the parents for further assessment of pain score post-operative day for 24 hrs.
The parents will be contacted by phone numbers to asses pain score and the dose of paracetamol & ibuprofen will be documented.
Possible complications of local anesthetic toxicity will appear as hemodynamic instability in the form of hypotension and bradycardia and will be managed using bolus of crystalloids (20ml/kg),ephedrine (1-3mg) boluses and atropine (0.01mg/kg).
Any complications resulting from peripheral nerve blockade like: bleeding, infection or neuropathy, will be recorded and managed accordingly.
Enrollment
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Inclusion criteria
- Pediatric patients aged 5 to 13 years
- American Society of Anesthesiologists (ASA) physical status I-II scheduled for adenotonsillectomy.
Exclusion criteria
- Parents Refusal
- Cognitive impairment or developmental delays.
- Infection at injection site.
- Recent upper respiratory tract infection.
- Post-tonsillectomy bleeding, allergy to local anesthetics.
- American Society of Anesthesiologists (ASA) class III and IV.
- Morbid obesity.
- Those receiving regular analgesia within the last week before surgery.
Trial design
Primary purpose
Allocation
Interventional model
Masking
40 participants in 2 patient groups, including a placebo group
Trial contacts and locations
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Central trial contact
Nagy Malak, MD; Atef Salama, MD
Data sourced from clinicaltrials.gov
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