BMC Public Health (Jun 2022)

Clusters of preterm live births and respiratory distress syndrome-associated neonatal deaths: spatial distribution and cooccurrence patterns

  • Ana Sílvia Scavacini Marinonio,
  • Daniela Testoni Costa-Nobre,
  • Milton Harumi Miyoshi,
  • Rita de Cassia Xavier Balda,
  • Kelsy Catherina Nema Areco,
  • Tulio Konstantyner,
  • Mandira Daripa Kawakami,
  • Adriana Sanudo,
  • Paulo Bandiera-Paiva,
  • Rosa Maria Vieira de Freitas,
  • Lilian Cristina Correia Morais,
  • Mônica La Porte Teixeira,
  • Bernadette Cunha Waldvogel,
  • Maria Fernanda Branco de Almeida,
  • Ruth Guinsburg,
  • Carlos Roberto Veiga Kiffer

DOI
https://doi.org/10.1186/s12889-022-13629-4
Journal volume & issue
Vol. 22, no. 1
pp. 1 – 10

Abstract

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Abstract Background Prematurity and respiratory distress syndrome (RDS) are strongly associated. RDS continues to be an important contributor to neonatal mortality in low- and middle-income countries. This study aimed to identify clusters of preterm live births and RDS-associated neonatal deaths, and their cooccurrence pattern in São Paulo State, Brazil, between 2004 and 2015. Methods Population-based study of all live births with gestational age ≥ 22 weeks, birthweight ≥ 400 g, without congenital anomalies from mothers living in São Paulo State, Brazil, during 2004–2015. RDS-associated neonatal mortality was defined as deaths < 28 days with ICD-10 codes P22.0 or P28.0. RDS-associated neonatal mortality and preterm live births rates per municipality were submitted to first- and second-order spatial analysis before and after smoothing using local Bayes estimates. Spearman test was applied to identify the correlation pattern between both rates. Results Six hundred forty-five thousand two hundred seventy-six preterm live births and 11,078 RDS-associated neonatal deaths in São Paulo State, Brazil, during the study period were analyzed. After smoothing, a non-random spatial distribution of preterm live births rate (I = 0.78; p = 0.001) and RDS-associated neonatal mortality rate (I = 0.73; p = 0.001) was identified. LISA maps confirmed clusters for both, with a negative correlation (r = -0.24; p = 0.0000). Clusters of high RDS-associated neonatal mortality rates overlapping with clusters of low preterm live births rates were detected. Conclusions Asymmetric cluster distribution of preterm live births and RDS-associated neonatal deaths may be helpful to indicate areas for perinatal healthcare improvement.

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