TY - JOUR
T1 - High-frequency oscillation versus conventional ventilation following surfactant administration and partial liquid ventilation
AU - Mrozek, Jeanne D.
AU - Bing, Dennis R.
AU - Meyers, Pat A.
AU - Connett, John E
AU - Mammel, Mark C.
PY - 1998/7
Y1 - 1998/7
N2 - Surfactant followed by partial liquid ventilation (PLV) with perfluorocarbon (PFC; LiquiVent® improves oxygenation, lung compliance, and lung pathology in lung-injured animals receiving conventional ventilation (CV). In this study, we hypothesize that high-frequency oscillation (HFO) and CV will provide equivalent oxygenation in lung-injured animals following surfactant repletion and PLV, once lung volume is optimized. After saline- lavage lung injury during CV, newborn piglets were randomized to either HFO (n = 10) or CV (n = 9). HFO animals were stabilized over 15 min without optimization of lung volume; CV animals continued treatment with time- cycled, pressure-limited, volume-targeted ventilation. All animals then received 100 mg/kg of surfactant (Survanta®). Thirty minutes later, all received intratracheal PFC to approximate functional residual capacity. Thirty minutes after PLV began, mean airway pressure (MAP) in both groups was increased to improve oxygenation. MAP was directly adjusted during HFO; PEEP and PIP were adjusted during IMV, maintaining a pressure sufficient to deliver 15 mL/kg tidal volume. Animals were treated for 4 h. The CV group showed improved oxygenation following surfactant administration (O1:26.79 ± 1.98 vs. 8.59 ± 6.29, P < 0.0004), with little further improvement following PFC administration or adjustments in MAP. Oxygenation in HFO-treated animals did not improve following surfactant, but did improve following PFC (O1:27.78 ± 6.84 vs. 15.86 ± 5.53, P < 0.005) and adjustments in MAP (O1:15.86 ± 5.53 vs. 8.96 ± 2.18, P < 0.03). After MAP adjustments, there were no significant intergroup differences in oxygenation. Animals in the CV group required lower MAP than animals in the HFO group to maintain similar oxygenation. We conclude that surfactant repletion followed by PLV improves oxygenation during both CV and HFO. The initial response to administration of surfactant and PFC was different for the conventional and high-frequency oscillation groups, likely reflecting the ventilation strategy used; animals in the CV group responded most to surfactant, whereas animals in the HFO group responded most after PFC instillation. The ultimately similar oxygenation of the two groups once lung volume had been optimized suggests that HFO may be used effectively during administration of, and treatment with, surfactant and perfluorocarbon.
AB - Surfactant followed by partial liquid ventilation (PLV) with perfluorocarbon (PFC; LiquiVent® improves oxygenation, lung compliance, and lung pathology in lung-injured animals receiving conventional ventilation (CV). In this study, we hypothesize that high-frequency oscillation (HFO) and CV will provide equivalent oxygenation in lung-injured animals following surfactant repletion and PLV, once lung volume is optimized. After saline- lavage lung injury during CV, newborn piglets were randomized to either HFO (n = 10) or CV (n = 9). HFO animals were stabilized over 15 min without optimization of lung volume; CV animals continued treatment with time- cycled, pressure-limited, volume-targeted ventilation. All animals then received 100 mg/kg of surfactant (Survanta®). Thirty minutes later, all received intratracheal PFC to approximate functional residual capacity. Thirty minutes after PLV began, mean airway pressure (MAP) in both groups was increased to improve oxygenation. MAP was directly adjusted during HFO; PEEP and PIP were adjusted during IMV, maintaining a pressure sufficient to deliver 15 mL/kg tidal volume. Animals were treated for 4 h. The CV group showed improved oxygenation following surfactant administration (O1:26.79 ± 1.98 vs. 8.59 ± 6.29, P < 0.0004), with little further improvement following PFC administration or adjustments in MAP. Oxygenation in HFO-treated animals did not improve following surfactant, but did improve following PFC (O1:27.78 ± 6.84 vs. 15.86 ± 5.53, P < 0.005) and adjustments in MAP (O1:15.86 ± 5.53 vs. 8.96 ± 2.18, P < 0.03). After MAP adjustments, there were no significant intergroup differences in oxygenation. Animals in the CV group required lower MAP than animals in the HFO group to maintain similar oxygenation. We conclude that surfactant repletion followed by PLV improves oxygenation during both CV and HFO. The initial response to administration of surfactant and PFC was different for the conventional and high-frequency oscillation groups, likely reflecting the ventilation strategy used; animals in the CV group responded most to surfactant, whereas animals in the HFO group responded most after PFC instillation. The ultimately similar oxygenation of the two groups once lung volume had been optimized suggests that HFO may be used effectively during administration of, and treatment with, surfactant and perfluorocarbon.
KW - Animal disease models
KW - Fluorocarbons
KW - High frequency ventilation
KW - Mechanical ventilation
KW - Pulmonary surfactant
KW - Respiratory distress syndrome
UR - http://www.scopus.com/inward/record.url?scp=0031879637&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0031879637&partnerID=8YFLogxK
U2 - 10.1002/(SICI)1099-0496(199807)26:1<21::AID-PPUL5>3.0.CO;2-L
DO - 10.1002/(SICI)1099-0496(199807)26:1<21::AID-PPUL5>3.0.CO;2-L
M3 - Article
C2 - 9710276
AN - SCOPUS:0031879637
SN - 8755-6863
VL - 26
SP - 21
EP - 29
JO - Pediatric pulmonology
JF - Pediatric pulmonology
IS - 1
ER -