Comparative study between Dexmedetomidine and Ondansteron for prevention of post spinal shivering. A randomized controlled trial

Joseph Makram Botros, Atef Mohamed Sayed Mahmoud, Safaa Gaber Ragab, Mohammed Awad Alsaeid Ahmed, Hany Maher Salib Roushdy, Hany Mahmoud Yassin, Maged Labib Bolus, Abeer Shaban Goda, Joseph Makram Botros, Atef Mohamed Sayed Mahmoud, Safaa Gaber Ragab, Mohammed Awad Alsaeid Ahmed, Hany Maher Salib Roushdy, Hany Mahmoud Yassin, Maged Labib Bolus, Abeer Shaban Goda

Abstract

Background: Regional anesthesia could affect the homeostatic system functions resulting frequently in perioperative hypothermia and consequently shivering. The objective of this trial was to evaluate the efficacy of dexmedetomidine and ondansetron to reduce the incidence and severity of shivering after intrathecal blocks.

Methods: This randomized placebo-controlled trial included 120 patients allocated equally in three groups. All patients were anesthetized by standard intrathecal blocks for surgical procedure at lower half of the body and received one of the study drugs intravenously (IV) according to the group assignments. Group S patients (placebo) were administered saline, Group O (ondansetron) were given 8 mg ondansetron, and Group D (dexmedetomidine) were given 1 μg/kg of dexmedetomidine. Shivering incidence and scores, sedation scores, core body temperature, hemodynamic variables, and incidence of complications (nausea, vomiting, hypotension, bradycardia, over-sedation, and desaturation) were recorded.

Results: The incidence and 95% confidence interval (95% CI) of shivering in group S 57.5% (42.18-72.82%) was significantly higher than that of both group O 17.5% (5.73-29.27%), P < 0.001 and group D 27.5% (13.66-41.34%), P = 0.012. However, the difference in the incidence of shivering between group O and group D was comparable, P = 0.425. The sedation scores were significantly higher in group D than those of both group S and group O, P < 0.001. Sedation scores between group S and group O were comparable, P = 0.19. Incidences of adverse effects were comparable between the three groups.

Conclusion: Prophylactic administrations of dexmedetomidine or ondansetron efficiently decrease the incidence and severity of shivering after spinal anesthesia as compared to placebo without significant difference between their efficacies when compared to each other.

Trial registration: Pan African Clinical Trial Registry (PACTR) under trial number (PACTR201710002706318). 18-10-2017. 'retrospectively registered'.

Keywords: Dexmedetomidine; Intraoperative hypothermia; Ondansetron; Shivering; Spinal anesthesia.

Conflict of interest statement

Ethics approval and consent to participate

The local ethical committee approval was obtained from Fayoum University Hospitals (R 64). Each participant was informed about the study protocol in details and complete written informed consents were signed before enrollment in the study.

Consent for publication

Consent for publication was obtained from the participants’ if appropriate.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
The percentage of patients at each grade of shivering among the three groups. Group S: Saline group, Group O: Ondansetron group, Group D: Dexmedetomidine group
Fig. 2
Fig. 2
The heart rate values among the three groups. Group S: Saline group, Group O: Ondansetron group, Group D: Dexmedetomidine group. *P < 0.001
Fig. 3
Fig. 3
Systolic blood pressure values among the three groups Group S: Saline group, Group O: Ondansetron group, Group D: Dexmedetomidine group
Fig. 4
Fig. 4
Diastolic blood pressure values among the three groups. Group S: Saline group, Group O: Ondansetron group, Group D: Dexmedetomidine group
Fig. 5
Fig. 5
Body temperature measurements at the predefined time points between the three groups. Group S: Saline group, Group O: Ondansetron group, Group D: Dexmedetomidine group

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Source: PubMed

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