Multicenter randomized controlled trial of the effects of inhaled nitric oxide therapy on gas exchange in children with acute hypoxemic respiratory failure

Citation
El. Dobyns et al., Multicenter randomized controlled trial of the effects of inhaled nitric oxide therapy on gas exchange in children with acute hypoxemic respiratory failure, J PEDIAT, 134(4), 1999, pp. 406-412
Citations number
19
Categorie Soggetti
Pediatrics,"Medical Research General Topics
Journal title
JOURNAL OF PEDIATRICS
ISSN journal
00223476 → ACNP
Volume
134
Issue
4
Year of publication
1999
Pages
406 - 412
Database
ISI
SICI code
0022-3476(199904)134:4<406:MRCTOT>2.0.ZU;2-X
Abstract
Objectives and background: To determine whether inhaled nitric oxide (iNO) therapy can attenuate the progression of lung disease in acute hypoxemic re spiratory failure, we performed a multicenter, randomized, masked, controll ed study of the effects of prolonged iNO therapy on oxygenation. We hypothe sized that iNO therapy would improve oxygenation in an acute manner, slow t he rate of decline in gas exchange, and decrease the number of patients who meet pre-established oxygenation failure criteria. Study design: A total of 108 children (median age 2.5 years) with severe ac ute hypoxemic respiratory failure from 7 centers were enrolled. After conse nt was obtained, patients were randomized to treatment with iNO (10 ppm) or mechanical ventilation alone for at least 72 hours. Patients with an oxyge nation index greater than or equal to 40 for 3 hours or greater than or equ al to 25 for 6 hours were considered treatment failures and exited the stud y. Results: Patient age, primary diagnosis, pediatric risk of mortality score, mode of ventilation, and median oxygenation index (35 +/- 22 vs 30 +/- 15; iNO vs control; mean +/- SEM) were not different between groups at study e ntry. Comparisons of oxygenation indexes during the first 12 hours demonstr ated an acute improvement in oxygenation in the;NO group at 4 hours (-10.2 vs -2.7 mean values; P < .014) and at 12 hours (-9.2 vs -2.8; P < .007). At 12 hours 36% of the control group met failure criteria in contrast with 16 % in the iNO group (P < .05). During prolonged therapy the failure rate was reduced in the iNO group in patients whose entry oxygenation index was gre ater than or equal to 25 (P < .04) and in immunocompromised patients (P < . 03). Conclusions: We conclude that iNO causes an acute improvement in oxygenatio n in children with severe AHRF Two subgroups (immunocompromised and an entr y oxygen index greater than or equal to 25) appear to have a more sustained improvement in oxygenation, and we speculate that these subgroups may bene fit from prolonged therapy.