Effect of Minimally Invasive Surfactant Therapy on Lung Volume and Ventilation in Preterm Infants - 25/02/16
Abstract |
Objective |
To assess the changes in (regional) lung volume and gas exchange during minimally invasive surfactant therapy (MIST) in preterm infants with respiratory distress syndrome.
Study design |
In this prospective observational study, infants requiring a fraction of inspired oxygen (FiO2) ≥0.30 during nasal continuous positive airway pressure of 6 cmH2O were eligible for MIST. Surfactant (160-240 mg/kg) was administered in supine position in 1-3 minutes via an umbilical catheter placed 2 cm below the vocal cords. Changes in end-expiratory lung volume (EELV), tidal volume, and its distribution were recorded continuously with electrical impedance tomography before and up to 60 minutes after MIST. Changes in transcutaneous oxygen saturation (SpO2) and partial carbon dioxide pressure, FiO2, respiratory rate, and minute ventilation were recorded.
Results |
A total of 16 preterm infants were included. One patient did not finish study protocol because of severe apnea 10 minutes after MIST. In the remaining infants (gestational age 29.8 ± 2.8 weeks, body weight 1545 ± 481 g) EELV showed a rapid and sustained increase, starting in the dependent lung regions, followed by the nondependent regions approximately 5 minutes later. Oxygenation, expressed as the SpO2/FiO2 ratio, increased from 233 (IQR 206-257) to 418 (IQR 356-446) after 60 minutes (P < .001). This change was significantly correlated with the change in EELV (ρ = 0.70, P < .01). Tidal volume and minute volume decreased significantly after MIST, but transcutaneous partial carbon dioxide pressure was comparable with pre-MIST values. Ventilation distribution remained unchanged.
Conclusions |
MIST results in a rapid and homogeneous increase in EELV, which is associated with an improvement in oxygenation.
Le texte complet de cet article est disponible en PDF.Keyword : AU, EELV, ΔEELV, EIT, fEIT, FiO2, MIST, nCPAP, RDS, SpO2, TcPCO2, ΔZ
Plan
Supported by Chiesi Pharmaceutical, Rijswijk, The Netherlands. The EIT device was provided by CareFusion, Yorba Linda, CA. I.F. has received reimbursement for congress and travel expenses and speaking fees from Dräger and Swisstom. A.v.K. has received travel expenses and speaking fees from CareFusion, Yorba Linda, CA. The other authors declare no conflicts of interest. |
Vol 170
P. 67-72 - mars 2016 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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