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This study aims to evaluate the influence of ultrasound-guided erector spinae plane block on postoperative pain and diaphragmatic dysfunction in pediatric patients undergoing thoracoscopic sympathectomy.
Pain may occur after pediatric thoracic surgery in cases such as skin incision creation, rib traction, and drain placement, and in other cases, such as rib nerve injury. Such pain is highly unfavorable to pediatric patients' recovery as it may lead to reduced cough strength for clearing secretions, decreased functional residual capacity, and pulmonary complications such as atelectasis and pneumonia.
Erector spinae plane block (ESPB) is a novel trunk block to relieve chronic neuropathic pain. Since then, it has gained prominence as a regional anesthesia technique with the potential to revolutionize postoperative pain management, and it has been effectively administered not only for the management of perioperative pain for a wide variety of surgeries but also for the management of acute post-traumatic pain and chronic pain.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Erector spinae plane block group | Experimental | Patients will receive bilateral erector spinae plane block after the induction of general anesthesia as a study group. |
|
| Control group | Active Comparator | Patients will not receive the block after the induction of general anesthesia as a control group. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Erector spinae plane block | Other | Patients will receive bilateral erector spinae plane block after the induction of general anesthesia as a study group. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Degree of pain | Postoperative pain assessment with the numeric rating scale (NRS) score. NRS (0 represents "no pain" while 10 represents "the worst pain imaginable"). NRS will be assessed on arrival at the post-anesthesia care unit (PACU), 1, 2, 4, 8, 12, and 24 h postoperatively. | 24 hours postoperatively |
| Measure | Description | Time Frame |
|---|---|---|
| Total analgesic consumption | Total analgesic consumption will be recorded. | 24 hours postoperatively |
| Anesthetic consumption: minimum alveolar concentration | Anesthetic consumption: minimum alveolar concentration (MAC) of sevoflurane every 10 min using Anesthetic Consumption = Flow Rate × Concentration of Anesthetic in Vapor. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Safaa M Sallam, Master | Contact | 00201001876902 | safaa.sallam@med.menofia.edu.eg |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Menoufia University | Recruiting | Shibīn al Kawm | Menoufia | 32511 | Egypt |
The data will be available upon a reasonable request from the corresponding author after the end of study for one year.
After the end of study for one year.
The data will be available upon a reasonable request from the corresponding author.
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| ID | Term |
|---|---|
| D000768 | Anesthesia, General |
| ID | Term |
|---|---|
| D000758 | Anesthesia |
| D000760 | Anesthesia and Analgesia |
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| General anesthesia | Other | Patients will not receive the block after the induction of general anesthesia as a control group. |
|
| Intraoperatively |
| Diaphragmatic excursion | Diaphragmatic excursion will be recorded using ultrasound preoperatively and postoperatively. | 24 hours postoperatively |
| Time to the first request for the rescue analgesia | Time to the first request for the rescue analgesia will be recorded from the end of surgery till first dose of meperidine administrated. | 24 hours postoperatively |
| Incidence of complications | Incidence of complications such as local anesthetic systemic toxicity (LAST), bradycardia, hypotension, nausea, vomiting, and respiratory depression will be recorded. | 24 hours postoperatively |
| Recovery profile | Recovery profile will be recorded using Richmond Agitation and Sedation Scale (RASS) was required to be between - 3 and + 4 for a delirium classification (ISMV 4 only; RASS not collected in ISMV 3. | 24 hours postoperatively |