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Antenatal Dexamethasone for Early Preterm Birth in Low-Resource Countries.

Authors :
Oladapo OT
Vogel JP
Piaggio G
Nguyen MH
Althabe F
Gülmezoglu AM
Bahl R
Rao SPN
De Costa A
Gupta S
Baqui AH
Khanam R
Shahidullah M
Chowdhury SB
Ahmed S
Begum N
D Roy A
Shahed MA
Jaben IA
Yasmin F
Rahman MM
Ara A
Khatoon S
Ara G
Akter S
Akhter N
Dey PR
Sabur MA
Azad MT
Choudhury SF
Matin MA
Goudar SS
Dhaded SM
Metgud MC
Pujar YV
Somannavar MS
Vernekar SS
Herekar VR
Bidri SR
Mathapati SS
Patil PG
Patil MM
Gudadinni MR
Bijapure HR
Mallapur AA
Katageri GM
Chikkamath SB
Yelamali BC
Pol RR
Misra SS
Das L
Nanda S
Nayak RB
Singh B
Qureshi Z
Were F
Osoti A
Gwako G
Laving A
Kinuthia J
Mohamed H
Aliyan N
Barassa A
Kibaru E
Mbuga M
Thuranira L
Githua NJ
Lusweti B
Ayede AI
Falade AG
Adesina OA
Agunloye AM
Iyiola OO
Sanni W
Ejinkeonye IK
Idris HA
Okoli CV
Irinyenikan TA
Olubosede OA
Bello O
Omololu OM
Olutekunbi OA
Akintan AL
Owa OO
Oluwafemi RO
Eniowo IP
Fabamwo AO
Disu EA
Agbara JO
Adejuyigbe EA
Kuti O
Anyabolu HC
Awowole IO
Fehintola AO
Kuti BP
Isah AD
Olateju EK
Abiodun O
Dedeke OF
Akinkunmi FB
Oyeneyin L
Adesiyun O
Raji HO
Ande ABA
Okonkwo I
Ariff S
Soofi SB
Sheikh L
Zulfiqar S
Omer S
Sikandar R
Sheikh S
Giordano D
Gamerro H
Carroli G
Carvalho J
Neilson J
Molyneux E
Yunis K
Mugerwa K
Chellani HK
Source :
The New England journal of medicine [N Engl J Med] 2020 Dec 24; Vol. 383 (26), pp. 2514-2525. Date of Electronic Publication: 2020 Oct 23.
Publication Year :
2020

Abstract

Background: The safety and efficacy of antenatal glucocorticoids in women in low-resource countries who are at risk for preterm birth are uncertain.<br />Methods: We conducted a multicountry, randomized trial involving pregnant women between 26 weeks 0 days and 33 weeks 6 days of gestation who were at risk for preterm birth. The participants were assigned to intramuscular dexamethasone or identical placebo. The primary outcomes were neonatal death alone, stillbirth or neonatal death, and possible maternal bacterial infection; neonatal death alone and stillbirth or neonatal death were evaluated with superiority analyses, and possible maternal bacterial infection was evaluated with a noninferiority analysis with the use of a prespecified margin of 1.25 on the relative scale.<br />Results: A total of 2852 women (and their 3070 fetuses) from 29 secondary- and tertiary-level hospitals across Bangladesh, India, Kenya, Nigeria, and Pakistan underwent randomization. The trial was stopped for benefit at the second interim analysis. Neonatal death occurred in 278 of 1417 infants (19.6%) in the dexamethasone group and in 331 of 1406 infants (23.5%) in the placebo group (relative risk, 0.84; 95% confidence interval [CI], 0.72 to 0.97; P = 0.03). Stillbirth or neonatal death occurred in 393 of 1532 fetuses and infants (25.7%) and in 444 of 1519 fetuses and infants (29.2%), respectively (relative risk, 0.88; 95% CI, 0.78 to 0.99; P = 0.04); the incidence of possible maternal bacterial infection was 4.8% and 6.3%, respectively (relative risk, 0.76; 95% CI, 0.56 to 1.03). There was no significant between-group difference in the incidence of adverse events.<br />Conclusions: Among women in low-resource countries who were at risk for early preterm birth, the use of dexamethasone resulted in significantly lower risks of neonatal death alone and stillbirth or neonatal death than the use of placebo, without an increase in the incidence of possible maternal bacterial infection. (Funded by the Bill and Melinda Gates Foundation and the World Health Organization; Australian and New Zealand Clinical Trials Registry number, ACTRN12617000476336; Clinical Trials Registry-India number, CTRI/2017/04/008326.).<br /> (Copyright © 2020 Massachusetts Medical Society.)

Details

Language :
English
ISSN :
1533-4406
Volume :
383
Issue :
26
Database :
MEDLINE
Journal :
The New England journal of medicine
Publication Type :
Academic Journal
Accession number :
33095526
Full Text :
https://doi.org/10.1056/NEJMoa2022398