Evidence map›Paper›PMID 42493553›Full record

ArticlePediatric research2026

Effect of sustained inflation on pharmacokinetics and pharmacodynamics of endotracheal and supraglottic airway epinephrine in a neonatal piglet model.

Ming Zhou, Jiang-Qin Liu, Marwa Ramsie, Po-Yin Cheung, Raza Hyderi, Shrieya Praveen, Tze-Fun Lee, Megan O'Reilly, Chenguang Xu, Georg M Schmölzer

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Article in Pediatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

10 authors.

Ming ZhouDepartment of Neonatology, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, China.
Jiang-Qin LiuDepartment of Neonatology, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, China.
Marwa RamsieCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada.
Po-Yin CheungCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada.
Raza HyderiCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada.
Shrieya PraveenCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada.
Tze-Fun LeeCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada.
Megan O'ReillyCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada.
Chenguang XuDepartment of Pediatrics, The University of Hong Kong - Shenzhen Hospital, Hong Kong, China.
Georg M SchmölzerCentre for the Studies of Asphyxia and Resuscitation, Neonatal Research Unit, Royal Alexandra Hospital, Edmonton, AB, Canada. georg.schmoelzer@me.com.ORCID http://orcid.org/0000-0001-9798-2415

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDuring neonatal resuscitation, the preferred route is intravenous (IV) or intraosseous (IO) administration, while endotracheal (ETT) delivery is a temporary solution. Supraglottic airway (SGA) devices are an alternative route to ETT administration. We compared the pharmacokinetics (PK) and pharmacodynamics (PD) of epinephrine administered via ETT and SGA, as well as the impact of a sustained inflation to enhance drug absorption by pushing the drug into the lung.

methodsThirty newborn anesthetized normoxic piglets (1-4 days old, 1.7-2.4 kg) were randomized to receive 0.1 mg/kg epinephrine via ETT, SGA (top or bottom placement), or combined with SI. Hemodynamic parameters (heart rate [HR], mean arterial pressure [MAP], and carotid blood flow [CBF]) and plasma epinephrine concentrations were measured at baseline and 1-10 min post-administration.

resultETT administration resulted in significantly higher HR, CBF, MAP, and plasma epinephrine concentrations compared to SGA routes (all p < 0.05), with peak concentrations achieved within 2 min versus the delayed, lower peaks in the SGA groups. SI did not enhance PK/PD outcomes in either the ETT or SGA groups.

conclusionETT administration resulted in significantly higher hemodynamic parameters compared to SGA, An SI did not enhance pharmacokinetic or pharmacodynamic outcomes in either the ETT or SGA groups. IMPACT: Endotracheal (ETT) epinephrine administration produced significantly higher plasma concentrations and stronger hemodynamic responses than supraglottic airway (SGA) delivery in a newborn piglet model. This study is the first to directly compare pharmacokinetics and pharmacodynamics of epinephrine delivered via ETT versus multiple SGA positions, with and without sustained inflation (SI). SGA administration resulted in delayed and lower epinephrine absorption, indicating limited effectiveness for rapid drug delivery during neonatal resuscitation. Sustained inflation did not enhance drug absorption or hemodynamic response for either ETT or SGA routes, challenging assumptions that SI might improve pulmonary drug uptake.

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