Elsevier

The Journal of Pediatrics

Volume 117, Issue 6, December 1990, Pages 939-946
The Journal of Pediatrics

High-frequency oscillatory ventilation compared with conventional intermittent mechanical ventilation in the treatment of respiratory failure in preterm infants: Neurodevelopmental status at 16 to 24 months of postterm age*

https://doi.org/10.1016/S0022-3476(05)80142-8Get rights and content

The High-Frequency intervention Trial was a 10-center randomized clinical trial to test the efficacy and safety of high-frequency oscillatory ventilation (HFO) in the treatment of neonates welghing 750 to 2000 gm; 327 infants were assigned to HFO and 346 to conventional intermittent mechanical ventilation (IMV). Survival and lung morbidity rates were the same in the two groups. Bayley psychometric evaluations and CNS examination were performed at 16 to 24 months of postterm age in 77% of the survivors (185HFO and 201 IMV). There was no difference in growth or respiratory status at follow-up, Cerebral paisy was diagnosed in 19 (10%) HFO-treated infants and 23 (11%) IMV-treated infants. There was no difference in severity between the two groups. A signifiantly higher incidence of hydrocephalus (12% vs 6%) was present in the HFO group (p<0.05). Bayley index scores>83 were scored in 57% of HFO-treated infants compared with 66% of IMV-treated infants. The proportion of children atfollow-up with a normal neuro-developmental status (i.e., Bayley score>83 and no major CNS defect) was significantly less in the HFO than in the IMV group (54 vs 65%; p<0.05). Both treatment groups showed a strong association between the presence of grade 3 or 4 intraventricular hemorrhage and the development of major CNS or cognitive defects. No significant long-term beneficial or deleterious effects were demonstrated in the use of HFO versus IMV for the treatment of respiratory failure in low birth weight premature infants, except that there were slightly more neurologic deficits in the HFO group related to the higher proportion of survivors with major intraventricular hemorrhage.

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*

Supported by contracts (Nos. NO1HR46001 and NO1HR46003-46012) from the Division of Lung Diseases, National Heart, Lung, and Blood Institute Bethesda, Md.

***

Members of the HIFI Study Group are as follows: University of California (San Diego): F. Mannino, G. Heldt, Y. Vaucher; Case Western Reserve (Cleveland, Ohio): R. Martin, W. Carlo, M. Hack; University of Manitoba, (Winnipeg): H. Rigatto, M. Davi, O. Casiro; University of Miami (Miami, Fla.): R. Goldberg, E. Bancalari, C. Bauer: University of Pennsylvania (Philadelphia): W. Fox, A. Spitzer, S, Abbasi, J. Bernbaum, J. Gerdes: University of Toronto (Toronto, Ontario): P. Fitzhardinge, P. Swyer, H. Whyte; Tufts University School of Medicine (Boston, Mass.): I. D. Frantz, B. Boynton, R. Delollis; Vanderbilt University (Nashville, Tenn.): R. Cotton, T. Hazinski; University of Washington (Seattle): W. A. Hodson, W. Truog, F. C. Bennett; University of Wisconsin (Madison): G. Gutcher, R. Perelman; Research Triangle Institute (Research Triangle Park, N. C.): W. K. Poole, A. V. Rao, M. Jordan; Division of Lung Diseases (Bethesda, Md.): E. Sinnett.

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