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XyloFUNS: Xylocaine to freeze during unpleasant nasopharyngeal swabs in children-a randomized controlled trial.
Gagnon, François; Gravel, Jocelyn; Duranceau, Camille; Vallieres, Emilie; Bhatt, Maala; Harman, Stuart; Trottier, Evelyne D.
  • Gagnon F; Division of Pediatric Emergency Medicine, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Gravel J; Division of Pediatric Emergency Medicine, CHU Ste-Justine, Université de Montréal, Montreal, Quebec, Canada.
  • Duranceau C; Division of Pediatric Emergency Medicine, CHU Ste-Justine, Université de Montréal, Montreal, Quebec, Canada.
  • Vallieres E; Division of Microbiology, Clinical Laboratory Medicine Department, Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montreal, Quebec, Canada.
  • Bhatt M; Division of Infectious Diseases, Pediatrics Department, Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montreal, Quebec, Canada.
  • Harman S; Division of Pediatric Emergency Medicine, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Trottier ED; Division of Pediatric Emergency Medicine, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
Paediatr Child Health ; 27(8): 469-475, 2022 Dec.
Article in English | MEDLINE | ID: covidwho-2070157
ABSTRACT

Objectives:

To evaluate the efficacy of intranasal vaporized lidocaine in reducing pain for children undergoing a nasopharyngeal (NP) swab in the Emergency Department (ED). Study

Design:

A randomized blinded clinical trial was conducted in a paediatric ED. Both participants and the researcher evaluating the primary outcome were blinded. Children aged 6 to 17 years old requiring a NP swab were eligible. Participants were randomly allocated to receive intranasal lidocaine or a sham treatment prior to their NP swab. The primary outcome measure was pain during the swab as assessed by the visual analog scale. Secondary outcome measures were pain using the verbal numeric rating scale, fear using the children fear scale, and adverse effects of the intervention.

Results:

Eighty-eight participants were enrolled-45 in the lidocaine group and 43 controls. The mean visual analog scale scores for pain were 46 mm in the lidocaine group and 53 mm in the control group (mean difference 7 mm; 95% CI -5 to 19 mm). No serious adverse events were observed.

Conclusions:

Intranasal lidocaine administered prior to NP swabs in the ED failed to show an improvement in pain scores for school-aged children and youth.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Language: English Journal: Paediatr Child Health Year: 2022 Document Type: Article Affiliation country: Pch

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Language: English Journal: Paediatr Child Health Year: 2022 Document Type: Article Affiliation country: Pch