Adult Respiratory Distress Syndrome in Full-Term Newborns

PEDIATRICS ◽  
1989 ◽  
Vol 83 (6) ◽  
pp. 971-976
Author(s):  
Roger G. Faix ◽  
Rose M. Viscardi ◽  
Michael A. DiPietro ◽  
Joanne J. Nicks

Since 1984, 11 newborns with severe respiratory distress have been treated whose clinical characteristics appear distinctive. Characteristics of these neonates were as follows: (1) they were full term by obstetric and neonatal criteria, (2) they had diffuse bilateral alveolar opacification on chest radiographs during the acute illness, (3) each had an acute perinatal triggering insult, (4) the neonates required continuous positive pressure ventilation for at least 48 hours with Fio2 > 0.50 for at least 12 hours, (5) they needed positive end-expiratory pressure of 6 cm of H2O or greater within three days of the triggering event, (6) there were no other known causes of these clinical conditions. Ten (91%) neonates had evidence of other organ dysfunction in addition to the lungs. Trials of hyperventilation in nine and tolazoline in five failed to improve oxygenation. Ten infants who underwent trials of increased positive end-expiratory pressure ≥6 cm of H2O without other concurrent changes in ventilator settings responded with prompt increases in PaO2 (median increase 84 mm Hg, range 22 to 196 mm Hg). All 11 babies survived but required prolonged mechanical ventilation and supplemental oxygen. We suggest that adult respiratory distress syndrome can and does occur in newborns. A trial of positive end-expiratory pressure ≥6 cm of H2O should be considered in full-term infants with severe respiratory distress in whom other causes can be excluded.

PEDIATRICS ◽  
1994 ◽  
Vol 93 (3) ◽  
pp. 538-538
Author(s):  
L. Gortner ◽  
F. Pohlandt ◽  
P. Bartmann

Kammash and co-workers described the effects of natural surfactant (BLSE) in full-term neonates1 suffering from adult respiratory distress syndrome (ARDS)-like disorders.2 Due to paucity of further published data,3 we would like to confirm the aforementioned studies by our observations in neonates. Full-term newborns were eligible for the pilot trial, if severe ARDS-like disorder was diagnosed: Fio2 0.9 to 1.0 for Pao2 >50 mm Hg; peak inspiratory pressure (PIP) 35 cm H2O for Paco2 50 mm Hg.


2004 ◽  
Vol 101 (3) ◽  
pp. 620-625 ◽  
Author(s):  
Wolfgang Oczenski ◽  
Christoph Hörmann ◽  
Christian Keller ◽  
Norbert Lorenzl ◽  
Anton Kepka ◽  
...  

Background Recruitment maneuvers performed in early adult respiratory distress syndrome remain a matter of dispute in patients ventilated with low tidal volumes and high levels of positive end-expiratory pressure (PEEP). In this prospective, randomized controlled study the authors evaluated the impact of recruitment maneuvers after a PEEP trial on oxygenation and venous admixture (Qs/Qt) in patients with early extrapulmonary adult respiratory distress syndrome. Methods After a PEEP trial 30 consecutive patients ventilated with low tidal volumes and high levels of PEEP were randomly assigned to either undergo a recruitment maneuver or not. Data were recorded at baseline, 3 min after the recruitment maneuver, and 30 min after baseline. Recruitment maneuvers were performed with a sustained inflation of 50 cm H2O maintained for 30 s. Results Compared with baseline the ratio of the arterial oxygen partial pressure to the fraction of inspired oxygen (Pao2/Fio2) and Qs/Qt improved significantly at 3 min after the recruitment maneuver (Pao2/Fio2, 139 +/- 46 mm Hg versus 246 +/- 111 mm Hg, P < 0.001; Qs/Qt, 30.8 +/- 5.8% versus 21.5 +/- 9.7%, P < 0.005), but baseline values were reached again within 30 min. No significant differences in Pao2/Fio2 and Qs/Qt were detected between the recruitment maneuver group and the control group at baseline and after 30 min (recruitment maneuver group [n = 15]: Pao2/Fio2, 139 +/- 46 mm Hg versus 138 +/- 39 mm Hg; Qs/Qt, 30.8 +/- 5.8% versus 29.2 +/- 7.4%; control group: [n = 15]: Pao2/Fio2, 145 +/- 33 mm Hg versus 155 +/- 52 mm Hg; Qs/Qt, 30.2 +/- 8.5% versus 28.1 +/- 5.4%). Conclusion In patients with early extrapulmonary adult respiratory distress syndrome who underwent a PEEP trial, recruitment maneuvers failed to induce a sustained improvement of oxygenation and venous admixture.


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