TY - JOUR
T1 - Shared Placental and Asphyxial Pathways in Preterm Stillbirths and Neonatal Deaths
T2 - The Prospective Observational PURPOSe Study
AU - Goldenberg, Robert L.
AU - Nausheen, Sidrah
AU - Masheer, Shazia
AU - Uddin, Zeeshan
AU - Bann, Carla M.
AU - Goudar, Shivaprasad S.
AU - Guruprasad, Gowder
AU - Ahmed, Imran
AU - Ghanchi, Najia K.
AU - Tikmani, Shiyam Sunder
AU - Dhaded, Sangpappa
AU - Kulkarni, Vardendra
AU - Yasmin, Haleema
AU - Saleem, Sarah
AU - McClure, Elizabeth M.
N1 - Publisher Copyright:
© 2025 John Wiley & Sons Ltd.
PY - 2026/1
Y1 - 2026/1
N2 - Objective: To evaluate similarities in pathways leading to preterm stillbirth and preterm neonatal death. Design: Prospective observational study. Setting: Study hospitals in India and Pakistan. Population: Preterm stillbirths and neonatal deaths ≥ 1000 g delivered in a study facility and evaluated by an expert panel for cause of death. Methods: An observational study of stillbirths and preterm neonatal deaths. Main Outcome Measures: Asphyxia, placental maternal vascular malperfusion (MVM), maternal hypertension, fetal growth restriction (FGR). Results: There were 398 preterm stillbirths and 582 preterm neonatal deaths in our study population. Of these, the panel determined asphyxia as a cause of death for 80.2% of the preterm stillbirths and 57.4% of the preterm neonatal deaths. Of the 319 preterm stillbirths with asphyxia, 62.4% also had placental MVM, while only 38.0% of the preterm stillbirths without birth asphyxia had MVM. Maternal hypertension was present among 44.5% of the stillbirths and FGR in 35.2%. Among the stillbirths with hypertension, 64.4% had asphyxia and MVM compared to 38.5% among those without hypertension. Similar patterns were seen among neonatal deaths. Conclusions: Both MVM and birth asphyxia were commonly present among stillbirths and neonatal deaths, especially those associated with hypertension and FGR compared to stillbirths and neonatal deaths without those conditions. These findings suggest that MVM and fetal asphyxia are part of a common pathway for stillbirth and preterm neonatal deaths.
AB - Objective: To evaluate similarities in pathways leading to preterm stillbirth and preterm neonatal death. Design: Prospective observational study. Setting: Study hospitals in India and Pakistan. Population: Preterm stillbirths and neonatal deaths ≥ 1000 g delivered in a study facility and evaluated by an expert panel for cause of death. Methods: An observational study of stillbirths and preterm neonatal deaths. Main Outcome Measures: Asphyxia, placental maternal vascular malperfusion (MVM), maternal hypertension, fetal growth restriction (FGR). Results: There were 398 preterm stillbirths and 582 preterm neonatal deaths in our study population. Of these, the panel determined asphyxia as a cause of death for 80.2% of the preterm stillbirths and 57.4% of the preterm neonatal deaths. Of the 319 preterm stillbirths with asphyxia, 62.4% also had placental MVM, while only 38.0% of the preterm stillbirths without birth asphyxia had MVM. Maternal hypertension was present among 44.5% of the stillbirths and FGR in 35.2%. Among the stillbirths with hypertension, 64.4% had asphyxia and MVM compared to 38.5% among those without hypertension. Similar patterns were seen among neonatal deaths. Conclusions: Both MVM and birth asphyxia were commonly present among stillbirths and neonatal deaths, especially those associated with hypertension and FGR compared to stillbirths and neonatal deaths without those conditions. These findings suggest that MVM and fetal asphyxia are part of a common pathway for stillbirth and preterm neonatal deaths.
KW - Asia
KW - birth asphyxia
KW - maternal vascular malperfusion
KW - neonatal death
KW - stillbirth
UR - https://www.scopus.com/pages/publications/105016807079
U2 - 10.1111/1471-0528.70017
DO - 10.1111/1471-0528.70017
M3 - Article
C2 - 40976260
AN - SCOPUS:105016807079
SN - 1470-0328
VL - 133
SP - 320
EP - 325
JO - BJOG: An International Journal of Obstetrics and Gynaecology
JF - BJOG: An International Journal of Obstetrics and Gynaecology
IS - 2
ER -