ADV6209 for Premedication in Pediatric Anesthesia: A Double-Blinded, Randomized Controlled Trial

ADV6209, a new formulation of midazolam with the addition of γ-cyclodextrin for oral use, has recently been licensed as the first pediatric sedative in the European Union. We compared the clinical efficacy of ADV6209 to the standard formulation of midazolam in premedication to reduce anxiety in chil...

Full description

Saved in:
Bibliographic Details
Main Authors: Markus Zadrazil (Author), Peter Marhofer (Author), Werner Schmid (Author), Daniela Marhofer (Author), Philipp Opfermann (Author)
Format: Book
Published: MDPI AG, 2022-09-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_fda23c409afc4ca6b46e7c2d9ab6f726
042 |a dc 
100 1 0 |a Markus Zadrazil  |e author 
700 1 0 |a Peter Marhofer  |e author 
700 1 0 |a Werner Schmid  |e author 
700 1 0 |a Daniela Marhofer  |e author 
700 1 0 |a Philipp Opfermann  |e author 
245 0 0 |a ADV6209 for Premedication in Pediatric Anesthesia: A Double-Blinded, Randomized Controlled Trial 
260 |b MDPI AG,   |c 2022-09-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics14102062 
500 |a 1999-4923 
520 |a ADV6209, a new formulation of midazolam with the addition of γ-cyclodextrin for oral use, has recently been licensed as the first pediatric sedative in the European Union. We compared the clinical efficacy of ADV6209 to the standard formulation of midazolam in premedication to reduce anxiety in children before anesthesia induction in a randomized, double-blinded controlled trial. Eighty children (ASA I/II; age: 2-8 years) scheduled for elective surgery were randomized to receive 0.25 mg kg<sup>−1</sup> of either conventional midazolam or ADV6209. Assessment tools included the modified Yale Preoperative Anxiety Scale-Short Form (mYPAS-SF) as well as scores for oral acceptance of the premedication and facemask acceptance during inhalational anesthesia induction. Mann-Whitney U and Pearson's chi-square tests were used for comparisons of outcome parameters. The primary outcome parameter of the study (mYPAS-SF anxiety score 30 min after the drug administration) did not reveal any significant intergroup difference between the ADV6209 group and the conventional midazolam group. Both drugs revealed their efficacy in reducing anxiety and in providing adequate sedation. The premedication dose was accepted by all children in the ADV6209 but rejected by 15% in the conventional midazolam group (<i>p</i> = 0.037). Acceptance of facemask placement was not found to differ significantly. No adverse events related to the study medications were noted. ADV6209 was better orally accepted than the conventional midazolam preparation and proved its efficacy in reducing preoperative anxiety. This clinically interesting preparation may alleviate the premedication process of 2−8 year-old children and obviates off-label drug use. 
546 |a EN 
690 |a anesthesia 
690 |a child 
690 |a premedication 
690 |a midazolam 
690 |a pharmacology 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 14, Iss 10, p 2062 (2022) 
787 0 |n https://www.mdpi.com/1999-4923/14/10/2062 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/fda23c409afc4ca6b46e7c2d9ab6f726  |z Connect to this object online.