Effect of intravenous dexmedetomidine on sensory block duration in spinal anesthesia for lower limb surgery: a randomized controlled trial
Efeito da dexmedetomidina intravenosa na duração do bloqueio sensorial em anestesia espinhal para cirurgia de membros inferiores: um ensaio clínico randomizado
Simran Chahal, Anju R. Bhalotra, Rahil Singh, Shweta Dhiman, Snigdha Singh
Abstract
Study objective
To study the effect of Intravenous (IV) dexmedetomidine during spinal anesthesia on duration of sensory block and postoperative analgesia in patients undergoing lower limb orthopedic surgery.
Design
Prospective randomized double blind controlled trial.
Intervention
Patients in intervention (DX) group received 0.5 mcg.kg⁻¹ IV dexmedetomidine over 10 min. Spinal anesthesia was administered and an infusion of dexmedetomidine 0.5 mcg.kg⁻¹.h⁻¹ was given throughout surgery.
Measurements
Onset time of sensory and motor block, maximum height of sensory block and duration of sensory and motor block were assessed. Intraoperative Heart Rate (HR), Blood Pressure (BP), Peripheral Oxygen Saturation (SpO₂), sedation scores, postoperative pain scores, time to requirement of first analgesic and analgesic consumption over first 24h were noted.
Results
Data of 58 ASA I/II adults was analyzed. Duration of sensory block, defined as time to two-dermatome regression, was 137.03 ± 25.02 min in DX group and 79.45 ± 11.27 min in the NS group (p = 0.000). Onset of sensory and motor block and maximum height of sensory block were similar. Postoperative VAS scores were lower in the DX group at 4h and 24h (p = 0.001, p = 0.0001) and comparable at 0h, 8h and 12h. Time to requirement of postoperative analgesia was longer in the DX group (p < 0.001) and requirement of postoperative analgesics was higher in the NS group. Sedation scores and incidence of bradycardia were higher in the DX group, but hypotension was similar.
Conclusion
IV dexmedetomidine (0.5 mcg.kg⁻¹ followed by 0.5 mcg.kg⁻¹.h⁻¹) resulted in extended sensory and motor block, prolonged postoperative analgesia and reduced postoperative analgesic consumption with minimal side effects.
Keywords
Resumo
Introdução
Investigar o efeito da dexmedetomidina intravenosa (IV) durante anestesia espinhal sobre a duração do bloqueio sensorial e analgesia pós-operatória em pacientes submetidos à cirurgia ortopédica de membros inferiores.
Desenho do estudo
Ensaio clínico prospectivo, randomizado, duplo-cego e controlado.
Intervenção
Os pacientes do grupo intervenção (DX) receberam dexmedetomidina IV 0,5 mcg.kg⁻¹ ao longo de 10 minutos. A anestesia espinhal foi administrada e uma infusão contínua de dexmedetomidina 0,5 mcg.kg⁻¹.h⁻¹ foi mantida durante toda a cirurgia.
Medições
Foram avaliados o tempo de início do bloqueio sensorial e motor, altura máxima do bloqueio sensorial e duração do bloqueio sensorial e motor. Também foram monitorados: frequência cardíaca (FC), pressão arterial (PA), saturação periférica de oxigênio (SpO₂), escores de sedação, escores de dor pós-operatória, tempo até a necessidade do primeiro analgésico e consumo de analgésicos nas primeiras 24 horas.
Resultados
Os dados de 58 adultos ASA I/II foram analisados. A duração do bloqueio sensorial, definida como o tempo para regressão de dois dermátomos, foi de 137,03 ± 25,02 min no grupo DX e 79,45 ± 11,27 min no grupo NS (p = 0,000). O início do bloqueio sensorial e motor e a altura máxima do bloqueio sensorial foram semelhantes entre os grupos. Os escores de dor pós-operatória (VAS) foram menores no grupo DX aos intervalos de 4h e 24h (p = 0,001, p = 0,0001) e comparáveis aos de 0h, 8h e 12h. O tempo até a necessidade de analgesia pós-operatória foi maior no grupo DX (p < 0,001) e o consumo de analgésicos pós-operatórios foi maior no grupo NS. Os escores de sedação e a incidência de bradicardia foram mais altos no grupo DX, mas a hipotensão foi semelhante.
Conclusão
A dexmedetomidina IV (0,5 mcg.kg⁻¹ seguida de infusão de 0,5 mcg.kg⁻¹.h⁻¹) prolongou o bloqueio sensorial e motor, aumentou a duração da analgesia pós-operatória e reduziu o consumo de analgésicos pós-operatórios, com efeitos colaterais mínimos.
Palavras-chave
References
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Submitted date:
01/25/2025
Accepted date:
07/31/2025