Artículo
Antenatal dexamethasone for early preterm birth in low-resource countries
Oladapo, Olufemi T.; Vogel, Joshua P.; Piaggio, Gilda; Nguyen, My-Huong; Althabe, Fernando
; Metin Gülmezoglu, A.; Bahl, Rajiv; Rao, Suman P.N.; de Costa, Ayesha; Gupta, Shuchita; Shahidullah, Mohammod; Chowdhury, Saleha B.; Ara, Gulshan; Akter, Shaheen; Akhter, Nasreen; Dey, Probhat R.; Abdus Sabur, M.; Azad, Mohammad T.; Choudhury, Shahana F.; Matin, M.A.; Goudar, Shivaprasad S.; Dhaded, Sangappa M.; Metgud, Mrityunjay C.; Pujar, Yeshita V.; Somannavar, Manjunath S.; Vernekar, Sunil S.; Herekar, Veena R.; Bidri, Shailaja R.; Mathapati, Sangamesh S.; Patil, Preeti G.; Patil, Mallanagouda M.; Gudadinni, Muttappa R.; Bijapure, Hidaytullah R.; Mallapur, Ashalata A.; Katageri, Geetanjali M.; Chikkamath, Sumangala B.; Yelamali, Bhuvaneshwari C.; Pol, Ramesh R.; Misra, Sujata S.; Das, Leena
Fecha de publicación:
12/2020
Editorial:
Massachusetts Medical Society
Revista:
New England Journal of Medicine
ISSN:
0028-4793
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
BACKGROUND: The safety and efficacy of antenatal glucocorticoids in women in low-resource countries who are at risk for preterm birth are uncertain. 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. 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. 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.
Palabras clave:
Dexamethasone
,
Early preterm birth
,
Low-resource countries
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Articulos(CIESP)
Articulos de CENTRO DE INVESTIGACIONES EN EPIDEMIOLOGIA Y SALUD PUBLICA
Articulos de CENTRO DE INVESTIGACIONES EN EPIDEMIOLOGIA Y SALUD PUBLICA
Citación
Oladapo, Olufemi T.; Vogel, Joshua P.; Piaggio, Gilda; Nguyen, My-Huong; Althabe, Fernando; et al.; Antenatal dexamethasone for early preterm birth in low-resource countries; Massachusetts Medical Society; New England Journal of Medicine; 383; 26; 12-2020; 2514-2525
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