Characteristics of fetal and neonatal deaths registered in San Martín, Peru, 2011–2025
DOI:
https://doi.org/10.59594/iicqp.2026.v4n2.180Keywords:
Fetal Death, Perinatal Death, Infant MortalityAbstract
Objective: To describe the clinical and epidemiological characteristics of fetal and neonatal deaths registered in San Martín, Peru, from 2011 to 2025 and to evaluate the association between neonatal death characteristics and timing of death.
Methods: This observational analytical study was based on publicly available regional data. Clinical, obstetric, geographic, and temporal variables were summarized using frequencies, percentages, medians, and interquartile ranges. Among neonatal deaths with classifiable timing of death, characteristics were compared according to timing of death: less than 24 hours, 1–6 days, and 7–27 days. Adjusted prevalence ratios (aPRs) were estimated using Poisson regression with robust variance.
Results: A total of 3,084 deaths were analyzed: 1,423 (46.1%) fetal and 1,661 (53.9%) neonatal. Among neonatal deaths, 1,130 (68.0%) occurred in preterm newborns and 1,127 (67.9%) in newborns with low birth weight. The most frequent causes of neonatal death were other causes (28.0%), prematurity-immaturity (27.7%), and infections (24.6%). Among the 1,637 neonatal deaths with classifiable timing of death, 572 occurred within the first 24 hours, 715 at 1–6 days, and 350 at 7–27 days. Among neonatal deaths, the proportion occurring within the first 24 hours was higher in records with a gestational age of less than 28 weeks (aPR = 1.88; 95% CI: 1.55–2.28), asphyxia and related causes (aPR = 3.25; 95% CI: 2.58–4.11), congenital malformations or lethal congenital malformation (aPR = 2.74; 95% CI: 2.11–3.56), and prematurity-immaturity (aPR = 1.76; 95% CI: 1.37–2.26).
Conclusions: Neonatal deaths were concentrated among preterm and low-birth-weight newborns. Deaths occurring within the first 24 hours showed a profile characterized by extreme prematurity, asphyxia and related causes, and congenital or lethal malformations. These findings describe differences in the timing of death and do not estimate mortality risk among live-born infants.
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