Dexamethasone at Lower Concentration Ropivacaine in the Supraclavicular Nerve Block
Märksõnad
Abstraktne
Kirjeldus
The supraclavicular brachial plexus block is widely used in upper limb surgery below the shoulder. Although it is easier and more stable than axillary nerve block and subclavian brachial plexus block, long-acting local anesthetics are used for long-term blockade with traditional block methods. However, this can easily lead to long-term motor nerve blockage, Horner's syndrome, phrenic nerve paralysis or systemic poisoning, and even serious side effects such as cardiac arrest.
Ropivacaine is a novel long-acting topical amine amine topical anesthetics that lasts long and has anesthetic and analgesic effects. Its pharmacological characteristics are low cardiotoxicity, sensory block and motor block separation at low concentrations more obvious, and with the external peripheral vasoconstriction. Therefore, the drug is especially suitable for postoperative analgesia. Dexamethasone is a synthetic corticosteroid for the treatment of a wide range of symptoms including rheumatic diseases, certain skin diseases, severe allergies, asthma, chronic obstructive pulmonary disease, cerebral edema, and may also be combined with antibiotics for tuberculosis patients. It is becoming more common to use steroids as an adjunct to local anesthetics in brachial plexus block. Steroids have neurological blockade effects by blocking the nociceptive transmission of pith-type C-fibers and inhibiting the release of ectopic neurons. Dexamethasone, as a local anesthetic adjuvant in peripheral nerve block, has also been widely studied recently.
In order to reduce the incidence of long-acting topical anesthetics from the nerve block in the supraclavicular arm, reducing the local anesthetic concentration is a feasible method, but this will also result in a shorter time to neurological block. The investigators hypothesized that the addition of Dexamethasone 5 mg to low concentrations (0.25%) of Ropivacaine would prolong postoperative analgesia. Therefore, the purpose of this study was to compare the postoperative analgesia and the side effects of postoperative supraclavicular brachial plexus blockade with the addition of Dexamethasone 5mg to Ropivacaine (0.5%) alone and Ropivacaine (0.25%) in low concentrations.
Kuupäevad
| Viimati kinnitatud: | 03/31/2018 |
| Esmalt esitatud: | 06/02/2018 |
| Hinnanguline registreerumine on esitatud: | 06/26/2018 |
| Esmalt postitatud: | 06/27/2018 |
| Viimane värskendus on esitatud: | 06/26/2018 |
| Viimati värskendus postitatud: | 06/27/2018 |
| Õppe tegelik alguskuupäev: | 04/12/2018 |
| Eeldatav esmane lõpetamise kuupäev: | 12/30/2020 |
| Eeldatav uuringu lõpetamise kuupäev: | 12/30/2020 |
Seisund või haigus
Sekkumine / ravi
Drug: Group Ropivacaine High (RH)
Drug: Group Ropivacaine Low (RL)
Drug: Group Ropivacaine Low + Dexamethasone (RLD)
Faas
Käerühmad
| Arm | Sekkumine / ravi |
|---|---|
| Sham Comparator: Group Ropivacaine High (RH) Ultrasound-guided supraclavicular brachial plexus block with Ropivacaine 0.5% 20ml + N/S 1.6mL. | Drug: Group Ropivacaine High (RH) In Group RH, participants received supraclavicular brachial plexus block with ropivacaine 0.5% 20ml at the end of surgery. |
| Placebo Comparator: Group Ropivacaine Low (RL) Ultrasound-guided supraclavicular brachial plexus block with Ropivacaine 0.25% 20ml + N/S 1.6mL. | Drug: Group Ropivacaine Low (RL) In Group RL, participants received supraclavicular brachial plexus block with ropivacaine 0.25% 20ml at the end of surgery. |
| Experimental: Group Ropivacaine Low + Dexamethasone (RLD) Ultrasound-guided supraclavicular brachial plexus block with Ropivacaine 0.25% 20ml + Dexamethasone 8mg (1.6mL). | Drug: Group Ropivacaine Low + Dexamethasone (RLD) In Group RLD, participants received supraclavicular brachial plexus block with ropivacaine 0.25% 20ml + dexamethasone 8mg at the end of surgery. |
Abikõlblikkuse kriteeriumid
| Õppimiseks sobivad vanused | 20 Years To 20 Years |
| Uuringuks kõlblikud sood | All |
| Võtab vastu tervislikke vabatahtlikke | Jah |
| Kriteeriumid | Inclusion Criteria: - American society of Anesthesiology classification: I ~ III - patients who have undergone arm surgery for blockage of the upper clavicle from nerve block Exclusion Criteria: - Patients had brachial plexus degeneration, coagulation abnormalities, obvious heart, lung, liver or kidney disease, body mass index less than 18.5 or greater than 35, body weight greater than 80 kg, pregnancy, regular use of steroids or opiates Opioids, chronic medication or alcohol abuse, as well as previous allergies or adverse reactions to opiates, dexamethasone, or the use of topical anesthetic Ropivacaine, were excluded from this study. |
Tulemus
Esmased tulemusnäitajad
1. analgesic effects (the intensity of pain) [24 hours after the end of surgery]
Sekundaarsed tulemusmõõdud
1. blood pressure [1 hour after the end of surgery]
2. motor block [24 hours after the end of surgery]
3. heart rate [1 hour after the end of surgery]
Muud tulemusmeetmed
1. postoperative nausea [24 hours after the end of surgery]
2. postoperative vomiting [24 hours after the end of surgery]
