TY - JOUR
T1 - A population-based, multifaceted strategy to implement antenatal corticosteroid treatment versus standard care for the reduction of neonatal mortality due to preterm birth in low-income and middle-income countries
T2 - The ACT cluster-randomised trial
AU - Althabe, Fernando
AU - Belizán, José M.
AU - McClure, Elizabeth M.
AU - Hemingway-Foday, Jennifer
AU - Berrueta, Mabel
AU - Mazzoni, Agustina
AU - Ciganda, Alvaro
AU - Goudar, Shivaprasad S.
AU - Kodkany, Bhalachandra S.
AU - Mahantshetti, Niranjana S.
AU - Dhaded, Sangappa M.
AU - Katageri, Geetanjali M.
AU - Metgud, Mrityunjay C.
AU - Joshi, Anjali M.
AU - Bellad, Mrutyunjaya B.
AU - Honnungar, Narayan V.
AU - Derman, Richard J.
AU - Saleem, Sarah
AU - Pasha, Omrana
AU - Ali, Sumera
AU - Hasnain, Farid
AU - Goldenberg, Robert L.
AU - Esamai, Fabian
AU - Nyongesa, Paul
AU - Ayunga, Silas
AU - Liechty, Edward A.
AU - Garces, Ana L.
AU - Figueroa, Lester
AU - Hambidge, K. Michael
AU - Krebs, Nancy F.
AU - Patel, Archana
AU - Bhandarkar, Anjali
AU - Waikar, Manjushri
AU - Hibberd, Patricia L.
AU - Chomba, Elwyn
AU - Carlo, Waldemar A.
AU - Mwiche, Angel
AU - Chiwila, Melody
AU - Manasyan, Albert
AU - Pineda, Sayury
AU - Meleth, Sreelatha
AU - Thorsten, Vanessa
AU - Stolka, Kristen
AU - Wallace, Dennis D.
AU - Koso-Thomas, Marion
AU - Jobe, Alan H.
AU - Buekens, Pierre M.
N1 - Funding Information:
This trial was funded by grants from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (U01 HD058322, U01 HD040477, U01 HD043464, U01 HD040657, U01 HD042372, U01 HD040607, U01 HD058326, and U01 HD040636) . Support was also provided by the WHO Department of Reproductive Health and Research. Syringes were donated by Becton Dickinson. Members of the ACT group are listed in the appendix (pp 11–12) .
Publisher Copyright:
© 2015 Elsevier Ltd.
PY - 2015/2/14
Y1 - 2015/2/14
N2 - Background Antenatal corticosteroids for pregnant women at risk of preterm birth are among the most effective hospital-based interventions to reduce neonatal mortality. We aimed to assess the feasibility, effectiveness, and safety of a multifaceted intervention designed to increase the use of antenatal corticosteroids at all levels of health care in low-income and middle-income countries. Methods In this 18-month, cluster-randomised trial, we randomly assigned (1:1) rural and semi-urban clusters within six countries (Argentina, Guatemala, India, Kenya, Pakistan, and Zambia) to standard care or a multifaceted intervention including components to improve identification of women at risk of preterm birth and to facilitate appropriate use of antenatal corticosteroids. The primary outcome was 28-day neonatal mortality among infants less than the 5th percentile for birthweight (a proxy for preterm birth) across the clusters. Use of antenatal corticosteroids and suspected maternal infection were additional main outcomes. This trial is registered with ClinicalTrials.gov, number NCT01084096. Findings The ACT trial took place between October, 2011, and March, 2014 (start dates varied by site). 51 intervention clusters with 47 394 livebirths (2520 [5%] less than 5th percentile for birthweight) and 50 control clusters with 50 743 livebirths (2258 [4%] less than 5th percentile) completed follow-up. 1052 (45%) of 2327 women in intervention clusters who delivered less-than-5th-percentile infants received antenatal corticosteroids, compared with 215 (10%) of 2062 in control clusters (p<0·0001). Among the less-than-5th-percentile infants, 28-day neonatal mortality was 225 per 1000 livebirths for the intervention group and 232 per 1000 livebirths for the control group (relative risk [RR] 0·96, 95% CI 0·87-1·06, p=0·65) and suspected maternal infection was reported in 236 (10%) of 2361 women in the intervention group and 133 (6%) of 2094 in the control group (odds ratio [OR] 1·67, 1·33-2·09, p<0·0001). Among the whole population, 28-day neonatal mortality was 27·4 per 1000 livebirths for the intervention group and 23·9 per 1000 livebirths for the control group (RR 1·12, 1·02-1·22, p=0·0127) and suspected maternal infection was reported in 1207 (3%) of 48 219 women in the intervention group and 867 (2%) of 51 523 in the control group (OR 1·45, 1·33-1·58, p<0·0001). Interpretation Despite increased use of antenatal corticosteroids in low-birthweight infants in the intervention groups, neonatal mortality did not decrease in this group, and increased in the population overall. For every 1000 women exposed to this strategy, an excess of 3·5 neonatal deaths occurred, and the risk of maternal infection seems to have been increased. Funding Eunice Kennedy Shriver National Institute of Child Health and Human Development.
AB - Background Antenatal corticosteroids for pregnant women at risk of preterm birth are among the most effective hospital-based interventions to reduce neonatal mortality. We aimed to assess the feasibility, effectiveness, and safety of a multifaceted intervention designed to increase the use of antenatal corticosteroids at all levels of health care in low-income and middle-income countries. Methods In this 18-month, cluster-randomised trial, we randomly assigned (1:1) rural and semi-urban clusters within six countries (Argentina, Guatemala, India, Kenya, Pakistan, and Zambia) to standard care or a multifaceted intervention including components to improve identification of women at risk of preterm birth and to facilitate appropriate use of antenatal corticosteroids. The primary outcome was 28-day neonatal mortality among infants less than the 5th percentile for birthweight (a proxy for preterm birth) across the clusters. Use of antenatal corticosteroids and suspected maternal infection were additional main outcomes. This trial is registered with ClinicalTrials.gov, number NCT01084096. Findings The ACT trial took place between October, 2011, and March, 2014 (start dates varied by site). 51 intervention clusters with 47 394 livebirths (2520 [5%] less than 5th percentile for birthweight) and 50 control clusters with 50 743 livebirths (2258 [4%] less than 5th percentile) completed follow-up. 1052 (45%) of 2327 women in intervention clusters who delivered less-than-5th-percentile infants received antenatal corticosteroids, compared with 215 (10%) of 2062 in control clusters (p<0·0001). Among the less-than-5th-percentile infants, 28-day neonatal mortality was 225 per 1000 livebirths for the intervention group and 232 per 1000 livebirths for the control group (relative risk [RR] 0·96, 95% CI 0·87-1·06, p=0·65) and suspected maternal infection was reported in 236 (10%) of 2361 women in the intervention group and 133 (6%) of 2094 in the control group (odds ratio [OR] 1·67, 1·33-2·09, p<0·0001). Among the whole population, 28-day neonatal mortality was 27·4 per 1000 livebirths for the intervention group and 23·9 per 1000 livebirths for the control group (RR 1·12, 1·02-1·22, p=0·0127) and suspected maternal infection was reported in 1207 (3%) of 48 219 women in the intervention group and 867 (2%) of 51 523 in the control group (OR 1·45, 1·33-1·58, p<0·0001). Interpretation Despite increased use of antenatal corticosteroids in low-birthweight infants in the intervention groups, neonatal mortality did not decrease in this group, and increased in the population overall. For every 1000 women exposed to this strategy, an excess of 3·5 neonatal deaths occurred, and the risk of maternal infection seems to have been increased. Funding Eunice Kennedy Shriver National Institute of Child Health and Human Development.
UR - http://www.scopus.com/inward/record.url?scp=84923078802&partnerID=8YFLogxK
U2 - 10.1016/S0140-6736(14)61651-2
DO - 10.1016/S0140-6736(14)61651-2
M3 - Article
C2 - 25458726
AN - SCOPUS:84923078802
SN - 0140-6736
VL - 385
SP - 629
EP - 639
JO - The Lancet
JF - The Lancet
IS - 9968
ER -