Abstract

Introduction: Uncooperative child does not allow completion of procedures, denying valuable data required for clinicians.
 Material and Methods: An open labelled parallel group prospective randomized control study was conducted at zonal hospital Jorhat. We evaluated 200 children randomized into two groups using computer based randomization. Participants aged 3 months to 5 years (n=200) were randomized to receive 50 mg/kg Triclofos sodium orally or intranasal spray of midazolam 0.2 mg/kg.
 Results: Adequate sedation (Ramsay reactivity score of 3 and 4) was obtained in 86% children in midazolam group as compared to 80% in triclofos group with p value of 0.138. Mean duration for onset of sedation was 20 min ± 5.4 min in Trichlophos group and 12 min ± 4.5 min with Intranasal Midazolam which was statistically significant with p-value of <0.001. The mean duration of post procedural sedation was found to be 24.00 ± 9.21 min in midazolam group and 49.00 ± 16.99 min in triclofos group (p=<0.001) which was statistically significant. No significant difference was seen for side effects frequency between the two drugs (15% in Triclofos, 10% in Midazolam group; p=0.285).
 Conclusion: We conclude that intranasal midazolam is more effective than oral trichlophos with a comparable safety profile.
 CTRI Trial Number: /2017/08/009448.

Highlights

  • Uncooperative child does not allow completion of procedures, denying valuable data required for clinicians

  • Midazolam in current times has emerged as an ideal drug for procedural sedation having all the desirable properties in this regard

  • Midazolam has been used by several routes like IV, IM, rectal and Intranasal for sedation

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Summary

Introduction

Uncooperative child does not allow completion of procedures, denying valuable data required for clinicians. Participants aged 3 months to 5 years (n=200) were randomized to receive 50 mg/kg Triclofos sodium orally or intranasal spray of midazolam 0.2 mg/kg. Mean duration for onset of sedation was 20 min +/- 5.4 min in Trichlophos group and 12 min +/- 4.5 min with Intranasal Midazolam which was statistically significant with p-value of

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