Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Nangia S, Sunder S, Biswas R, Saili A. Aug 2016 India | 175 term non-vigorous infants. | Pilot RCT | Occurrence of MAS | MAS present in 23/88 (26.1%) vs. 28/87 (32.3%) neonates in ‘No ET Suction’ and ‘ET Suction’ groups respectively (OR 0.4 (0.12-1.4); p = 0.14) | |
Chettri S, Adhisivam B, Bhat BV. May 2015 India | 162 term, nonvigorous, born through MSAF | RCT | Incidence of MAS | Overall, 39 (32%) neonates developed MAS. | |
Kelleher J, Bhat R, Salas AA, Addis D, Mills EC, Mallick H, Tripathi A, Pruitt EP, Roane C, McNair T July 2013 USA | 488 neonates born at median of 39 weeks’ gestation. | Randomised Equivalency Trial | Respiratory rate in first 24 hours. | Mean RR was 51 breaths per minutes in the wipe group and 50 in the suction group (95% CI -2 to 0, p <0.001) | |
Wiswell TE, Gannon CM, Jacob J, Goldsmith L, Szyld E, Weiss K, Schutzman D, Cleary GM, Filipov P, Ku Jan 2000 USA | 2094 neonates gestational age ?37 weeks, birth through MSAF of any consistency with apparent vigor immediately after birth. | Multicenter, international collaborative trial. | Incidence of respiratory distress, including MAS. | No significant differences between groups in the occurrence of MAS (INT = 3.2%; EXP = 2.7%) INT = Intubation & Suction EXP = Expectant Management | |
Linder N, Aranda JV et al Apr 1988 Israel | 572 ‘normal’ newborns born through MSAF with 1 minute Apgar 8+. | Prospective Study | Development of respiratory distress | No mortality among infants in the study, but morbidity, mainly pulmonary and laryngeal disorders, occurred in six of the suctioning group (6/308) | |
Ting P, Brady JP. July 1975 USA | 125 infants born through MSAF | Retrospective Study | Development of respiratory distress | 28 infants who did not receive immediate tracheal suction, 16 became symptomatic and seven died of massive meconium aspiration pneumonitis (P less than 0.001) |