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Scoliosis correction surgery in children is a complex procedure with significant risks, including postoperative pain, inflammatory response, and potential neurological complications. Effective pain control and minimizing inflammation are critical for faster recovery and improved patient outcomes. Dexamethasone is commonly used as an adjuvant in regional anesthesia due to its anti-inflammatory effects and ability to prolong analgesia. However, limited research exists on the optimal route of dexamethasone administration (intravenous vs. perineural) and the best local anesthetic concentration for pain management, inflammatory response, and neuromonitoring during surgery.
This study aims to compare the effects of different dexamethasone administration routes and local anesthetic concentrations on postoperative pain, inflammation (NLR, PLR), and neuromonitoring in pediatric scoliosis surgery. Results may improve regional anesthesia protocols, enhance patient safety, and offer valuable insights for clinical practice.
Scoliosis correction surgery in children is a complex procedure associated with a significant risk of postoperative pain, inflammatory response, and potential neurological complications. Ensuring optimal pain control and minimizing adverse inflammatory responses is crucial for shortening the recovery period, improving patient comfort, and reducing the risk of long-term complications. In clinical practice, dexamethasone is frequently used as an adjuvant in regional anesthesia techniques due to its anti-inflammatory properties and its potential to prolong the analgesic effect.
Although the use of dexamethasone as an adjuvant in regional anesthesia is well known, there is limited research focusing on the impact of its route of administration (local versus intravenous) and the optimal concentration of local anesthetic agents on the effectiveness of pain control, inflammatory response, and neuromonitoring parameters during surgical procedures in children. Understanding these aspects is particularly important in complex procedures such as scoliosis correction surgery, where precise neurological function monitoring is essential for patient safety.
The objective of the proposed study is to evaluate the impact of different dexamethasone administration routes (intravenous and perineural) and varying concentrations of local anesthetic agents on postoperative pain, inflammatory response (measured using NLR and PLR indices), and neuromonitoring parameters in children undergoing scoliosis correction surgery. The findings from this study may contribute to the development of more effective and safer regional anesthesia and analgesia protocols for this patient group.
Conducting this study will provide new insights into the optimization of anesthesia in pediatric spinal surgery, potentially leading to improved treatment outcomes and patient safety, as well as valuable data for clinical practice regarding the selection of anesthetic strategies.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| perineural Dexamethasone | Active Comparator | Erector Spinae Plane Block with 0.2% ropivacaine with perineural 0.1mg/kg dexamethasne |
|
| intravenous dexamethasne | Active Comparator | Erector Spinae Plane Block with 0.2% ropivacaine with intravenous 0.1mg/kg dexamethasne |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| perineural Dexamethasone | Drug | Erector Spinae Plane Block with 0.2% Ropivacaine + 0.1mg/kg perineural Dexamethasone |
|
| Measure | Description | Time Frame |
|---|---|---|
| Time to first rescue opioid analgesia | Time to first rescue opioid analgesia | 48 hours after surgery |
| Measure | Description | Time Frame |
|---|---|---|
| intraoperative requirement for propofol | intraoperative requirement for propofol in mg/kg | durring surgery |
| intraoperative requirement for remifentanil | intraoperative requirement for remifentanil in ug/kg |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Malgorzata Reysner, M.D. Ph.D. | Contact | +48608762068 | mdomagalska@ump.edu.pl |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Poznan University of Medical Sciences | Recruiting | Poznan | 60-701 | Poland |
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| intravenous Dexamethasone | Drug | Erector Spinae Plane Block with 0.2% Ropivacaine + 0.1mg/kg intravenous Dexamethasone |
|
| durring surgery |
| MEP | Motor evoced potentials durring surgery | durring surgery |
| Total opioid consumption | Total opioid consumption in milliequivalents of morphine per kg | 48 after surgery |
| NRS | The numeric rating scale (NRS) with zero meaning "no pain" and 10 meaning "the worst pain imaginable" | 6 hours after surgery |
| NRS | The numeric rating scale (NRS) with zero meaning "no pain" and 10 meaning "the worst pain imaginable" | 12 hours after surgery |
| NRS | The numeric rating scale (NRS) with zero meaning "no pain" and 10 meaning "the worst pain imaginable" | 24 hours after surgery |
| NRS | The numeric rating scale (NRS) with zero meaning "no pain" and 10 meaning "the worst pain imaginable" | 36 hours after surgery |
| NRS | The numeric rating scale (NRS) with zero meaning "no pain" and 10 meaning "the worst pain imaginable" | 48 hours after surgery |
| NLR | Neutrophile-to-lymphocyte ratio | 12 hours after surgery |
| NLR | Neutrophile-to-lymphocyte ratio | 48 hours after surgery |
| PLR | Platelet-to-lymohocyte ratio | 12 hours after surgery |
| PLR | Platelet-to-lymohocyte ratio | 24 hours after surgery |
| PLR | Platelet-to-lymohocyte ratio | 48 hours after surgery |
| ID | Term |
|---|---|
| D012600 | Scoliosis |
| ID | Term |
|---|---|
| D013121 | Spinal Curvatures |
| D013122 | Spinal Diseases |
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
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