Transsphenoidal surgery is considered safe and effective and is currently the procedure of choice for the removal of intrasellar lesions. Direct transnasal access to the sphenoid sinus, without the need for detachment of the nasal septum, provides less postoperative morbidity compared to traditional methods. Sphenopalatine ganglion block is known for its efficacy in otorhinolaryngological surgeries in which the sinuses are approached by transnasal endoscopy, as an important part of postoperative analgesia. However, in a neurosurgical environment, specifically in the treatment of tumors of the sella turcica, the use of the blockade of the referred ganglion to produce postoperative analgesia has been used in a scarce way in the literature. The primary objective of the study is to verify whether blocking the sphenopalatine nerve ganglion in the nasopharynx posterior wall provides better postoperative pain control in surgeries with nasal access for transsphenoidal approach, compared to the placebo group. As secondary objectives, the investigators will observe the consumption of opioids in the intraoperative period, in addition to the incidence of nausea, vomiting and postoperative headache also within 24 hours. Forty patients with physical status P1, P2 or P3 will be prospectively analyzed by the American Society of Anesthesiology (ASA) to undergo microsurgery for tumors with a sellar and / or suprasellar location, with transsphenoidal access, in patients with an age range between 18 and 64 years old, including men and women.
Transsphenoidal surgery is considered safe and effective and is currently the procedure of choice for the removal of intrasellar lesions. Direct transnasal access to the sphenoid sinus, without the need for detachment of the nasal septum, provides less postoperative morbidity compared to traditional methods. Sphenopalatine ganglion block is known for its efficacy in otorhinolaryngological surgeries in which the sinuses are approached by transnasal endoscopy, as an important part of postoperative analgesia. However, in a neurosurgical environment, specifically in the treatment of tumors of the sella turcica, the use of the blockade of the referred ganglion to produce postoperative analgesia has been used in a scarce way in the literature. The primary objective of the study is to verify whether blocking the sphenopalatine nerve ganglion in the nasopharynx posterior wall provides better postoperative pain control in surgeries with nasal access for transsphenoidal approach, compared to the placebo group. As secondary objectives, the investigators will observe the consumption of opioids in the intraoperative period, in addition to the incidence of nausea, vomiting and postoperative headache also within 24 hours. Forty patients with physical status P1, P2 or P3 will be prospectively analyzed by the American Society of Anesthesiology (ASA) to undergo microsurgery for tumors with a sellar and / or suprasellar location, with transsphenoidal access, in patients with an age range between 18 and 64 years old, including men and women. As for the surgical technique, both the use of the microscope and the endoscope will be considered. They will be randomly allocated to a placebo group (group P; 0.9% saline, n = 20) and a test group (group R; ropivacaine 1%, n = 20).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
40
The block of the sphenopalatine ganglion will be performed bilaterally, using a cotton bud soaked with 1% ropivacaine, placed in the mucosa of the posterior wall of the nasal cavity, through both nostrils. Once placed in the proper position, the swab will remain for about 20 minutes to absorb the local anesthetic from the mucosa.
Instituto Estadual do Cérebro Paulo Niemeyer
Rio de Janeiro, Brazil
Evaluation of postoperative analgesia using the visual analogue pain scale (VAS pain)
To verify whether blocking the sphenopalatine nerve ganglion in the posterior nasopharynx wall provides change in postoperative pain control, assessed using the visual analogue pain scale, in surgeries with nasal access for transsphenoidal approach, compared to the placebo group.
Time frame: Immediately after awakening from anesthesia
Evaluation of postoperative analgesia using the visual analogue pain scale (VAS pain)
To verify whether blocking the sphenopalatine nerve ganglion in the posterior nasopharynx wall provides change in postoperative pain control, assessed using the visual analogue pain scale, in surgeries with nasal access for transsphenoidal approach, compared to the placebo group.
Time frame: 2 hours postoperative
Evaluation of postoperative analgesia using the visual analogue pain scale (VAS pain)
To verify whether blocking the sphenopalatine nerve ganglion in the posterior nasopharynx wall provides change in postoperative pain control, assessed using the visual analogue pain scale, in surgeries with nasal access for transsphenoidal approach, compared to the placebo group.
Time frame: 6 hours postoperative
Evaluation of postoperative analgesia using the visual analogue pain scale (VAS pain)
To verify whether blocking the sphenopalatine nerve ganglion in the posterior nasopharynx wall provides change in postoperative pain control, assessed using the visual analogue pain scale, in surgeries with nasal access for transsphenoidal approach, compared to the placebo group.
Time frame: 12 hours postoperative
Evaluation of postoperative analgesia using the visual analogue pain scale (VAS pain)
To verify whether blocking the sphenopalatine nerve ganglion in the posterior nasopharynx wall provides change in postoperative pain control, assessed using the visual analogue pain scale, in surgeries with nasal access for transsphenoidal approach, compared to the placebo group.
Time frame: 24 hours postoperative
Change the consumption of intraoperative opioids
Check the change in total opioid consumption in the intraoperative period
Time frame: Intraoperative time
Use of complementary opioids
Assess the number of rescue doses with opioids in pos operative period for for adequate analgesia (it is understood as insufficient analgesia classification on the visual analog scale of pain greater than or equal to 3)
Time frame: Immediately after awakening from anesthesia
Use of complementary opioids
Assess the number of rescue doses with opioids in pos operative period for for adequate analgesia (it is understood as insufficient analgesia classification on the visual analog scale of pain greater than or equal to 3)
Time frame: 2 hours postoperative
Use of complementary opioids
Assess the number of rescue doses with opioids in pos operative period for for adequate analgesia (it is understood as insufficient analgesia classification on the visual analog scale of pain greater than or equal to 3)
Time frame: 6 hours postoperative
Use of complementary opioids
Assess the number of rescue doses with opioids in pos operative period for for adequate analgesia (it is understood as insufficient analgesia classification on the visual analog scale of pain greater than or equal to 3)
Time frame: 12 hours postoperative
Use of complementary opioids
Assess the number of rescue doses with opioids in pos operative period for for adequate analgesia (it is understood as insufficient analgesia classification on the visual analog scale of pain greater than or equal to 3)
Time frame: 24 hours postoperative
Postoperative nausea and vomiting;
Check the incidence of postoperative nausea and vomiting
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Time frame: Immediately after awakening from anesthesia
Postoperative nausea and vomiting;
Check the incidence of postoperative nausea and vomiting
Time frame: 2 hours postoperative
Postoperative nausea and vomiting;
Check the incidence of postoperative nausea and vomiting
Time frame: 6 hours postoperative
Postoperative nausea and vomiting;
Check the incidence of postoperative nausea and vomiting
Time frame: 12 hours postoperative
Postoperative nausea and vomiting;
Check the incidence of postoperative nausea and vomiting
Time frame: 24 hours postoperative
Postoperative headache
Check the incidence of postoperative headache
Time frame: Immediately after awakening from anesthesia
Postoperative headache
Check the incidence of postoperative headache
Time frame: 2 hours postoperative
Postoperative headache
Check the incidence of postoperative headache
Time frame: 6 hours postoperative
Postoperative headache
Check the incidence of postoperative headache
Time frame: 12 hours postoperative
Postoperative headache
Check the incidence of postoperative headache
Time frame: 24 hours postoperative