Delivery Room Management of the Apparently Vigorous Meconium-stained Neonate: Results of the Multicenter, International Collaborative Trial

Author:

Wiswell Thomas E.1,Gannon Catherine M.1,Jacob Jack2,Goldsmith Leonard3,Szyld Edgardo4,Weiss Kerry5,Schutzman David6,Cleary Gerard M.1,Filipov Panayot7,Kurlat Isabel8,Caballero Carlos L.9,Abassi Soraya10,Sprague Daniel11,Oltorf Charles12,Padula Michael1

Affiliation:

1. From the Neonatology services at Thomas Jefferson University, Philadelphia, Pennsylvania;

2. Providence Alaska Medical Center, Anchorage, Alaska;

3. West Jersey Hospital, Voorhees, New Jersey;

4. Diego Paroissien Hospital, Buenos Aires, Argentina;

5. Mercer Medical Center, Trenton, New Jersey;

6. Fitzgerald Mercy Hospital, Darby, Pennsylvania;

7. Flushing Hospital, Flushing, New York;

8. University Hospital, Buenos Aires, Argentina;

9. Clinicas Hospital, Asúncion, Paraguay;

10. Pennsylvania Hospital, Philadelphia, Pennsylvania;

11. Desert Samaritan Medical Center, Phoenix, Arizona; and

12. Scott and White Memorial Hospital, Temple, Texas.

Abstract

Objective. Disagreement exists concerning the appropriate delivery room management of the airway of vigorous meconium-stained infants. Some suggest a universal approach to intubation and suctioning of the airway in all such neonates, whereas others advocate a selective approach. We performed this investigation: 1) to assess whether intubation and suctioning of apparently vigorous, meconium-stained neonates would reduce the incidence of meconium aspiration syndrome (MAS); and 2) to determine the frequency of complications from delivery room intubation and suctioning of such infants. Methods. Inclusion criteria included: 1) gestational age ≥37 weeks; 2) birth through meconium-stained amniotic fluid of any consistency; and 3) apparent vigor immediately after birth. Subjects were randomized to be intubated and suctioned (INT) or to expectant management (EXP). Primary outcome measures included: 1) the incidence of respiratory distress, including MAS, and 2) the incidence of complications from intubation. Results. A total of 2094 neonates were enrolled from 12 participating centers (1051 INT and 1043 EXP). Meconium-stained amniotic fluid consistency was similar in both groups. Of the 149 (7.1%) infants that subsequently demonstrated respiratory distress, 62 (3.0%) had MAS and 87 (4.2%) had findings attributed to other disorders. There were no significant differences between groups in the occurrence of MAS (INT = 3.2%; EXP = 2.7%) or in the development of other respiratory disorders (INT = 3.8%; EXP = 4.5%). Of 1098 successfully intubated infants, 42 (3.8%) had a total of 51 complications of the procedure. In all cases, the complications were mild and transient in nature. Conclusions. Compared with expectant management, intubation and suctioning of the apparently vigorous meconium-stained infant does not result in a decreased incidence of MAS or other respiratory disorders. Complications of intubation are infrequent and short-lived.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Reference29 articles.

1. Meconium staining and the meconium aspiration syndrome: unresolved issues.;Wiswell;Pediatr Clin North Am,1993

2. Meconium-stained amniotic fluid and the meconium aspiration syndrome: an update.;Cleary;Pediatr Clin North Am,1998

3. Meconium aspiration in infants: a prospective study.;Gregory;J Pediatr,1974

4. Tracheal suction in meconium aspiration.;Ting;Am J Obstet Gynecol,1975

5. Meconium aspiration syndrome: have we made a difference?;Wiswell;Pediatrics,1990

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