Skip to main content
Springer Nature - PMC COVID-19 Collection logoLink to Springer Nature - PMC COVID-19 Collection
. 2021 Apr 13;90(1):20–21. doi: 10.1038/s41390-021-01507-5

Improving VLBW infant outcomes with big data analytics

F Sessions Cole 1,
PMCID: PMC8042621  PMID: 33850292

Big data analytic strategies applied to routinely acquired, continuously assessed physiologic monitoring parameters in the neonatal intensive care unit (NICU) have provided clinically useful, predictive algorithms that reduce neonatal morbidities through detection of vital sign patterns associated with adverse outcomes.16 For example, based on large clinical trials carried out in low birth weight infants,710 NICU guidelines target gestational and chronologic age-specific oxygen saturation limits that reduce risk of neurologic morbidities, retinopathy of prematurity, oxygen radical injury, necrotizing enterocolitis, and death.5,6,11 These studies highlight the usefulness of standardized, predictive analytic algorithms and the need to continue to increase the sensitivity and specificity of these algorithms.

For future development of predictive algorithms, Zimmet et al. highlight the importance of using data from multiple NICUs. They extracted heart rate, pulse rate derived from pulse oximetry, and oxygen saturation obtained from continuous monitoring of 1168 very low birth weight infants in 3 institutionally unrelated NICUs from birth through day 42 (35,238 infant-days of data). Their data suggest that vital sign patterns can be impacted not only by onset of illness but also by NICU-specific care practices, monitor management and hardware, and socioeconomic/race/ethnicity characteristics of infants. Using vital sign data from a single NICU risks development of predictive algorithms that reflect NICU-specific characteristics and are not generalizable across NICUs. The ability to detect inter-NICU differences from vital sign data also suggests their usefulness for generation of multi-component, predictive algorithms that can identify, standardize, and monitor best practices across NICUs.

The vital sign signatures observed by Zimmet et al. identified both consistent patterns across NICUs and inter-NICU differences associated with differences in care delivery, monitor management and hardware, and infant characteristics. They found consistent vital sign patterns across all 3 NICUs in heart rate and oxygen saturation metrics, in heart rate increases of ~10 beats/minute (from 150 to 160 beats/min) over the first 2 weeks of life, and in lack of clinically significant differences in vital signs between sexes after correction for birth weight, gestational age, and institution. Their heart rate data confirm and extend prior observations in full-term infants12 and in preterm infants from a single NICU.13 Consistency of heart rate metrics across the 3 NICUs in the first 2 weeks of life suggests that caffeine use is similar although no patient-specific data are available. The consistency of mean oxygen saturation over time (~94%) in all 3 NICUs reflects the use of standardized NICU guideline targets based on large clinical trials.710 However, in contrast to the consistency of these vital sign patterns, the frequencies of bradycardia (heart rate <100 beats/min for ≥4 s) and desaturation (oxygen saturation <80% for ≥10 s) events differed in the first 2 weeks of life among the 3 nurseries: infants at one NICU had up to twice as many bradycardia events per day during the first 2 weeks of life, while infants at another NICU had about half as many desaturation events. The inter-NICU differences in bradycardia events were not detectable after 3 weeks of age, while the differences in daily number of desaturation events between sites increased from birth to 6 weeks of age. The authors speculate that the lower number of bradycardia events at one of the NICUs is associated with differences in ventilator care practices: the NICU with lower use of mechanical ventilation and greater use of nasal continuous positive airway pressure had a greater number of bradycardia events. Although this speculation is supported by differences in the average number of days on mechanical ventilation per infant among the 3 NICUs (10 days vs. 35 days vs. 33 days in 2017–2018), confirmation in this study was not possible due to lack of availability of patient-specific, daily respiratory support data. The authors point to differences in alarm alert management and in socioeconomic/race/ethnicity characteristics of infants among the NICUs to explain the differences in desaturation events.

For future development of vital sign-based, standardized predictive algorithms that can be used across NICUs, this report highlights the importance of using data from NICUs with differing infant demographics, clinical practices, and monitor management and characteristics. In addition, vital sign data described by Zimmet et al. highlight their usefulness for identification of inter-NICU differences in nursing- and physician-based care practice, infant race/ethnicity, outcome, and infant socioeconomic characteristics. Linkage of vital sign data with other accessible sources of electronic data can advance discovery of standardized best practices across NICUs, reduce preventable harm, and improve outcomes.14,15 For example, the California Perinatal Quality Care Collaborative (CPQCC) and the Vermont Oxford Network have provided standardized quality metrics that have measurably and consistently improved outcomes through inter-NICU comparisons and best practice identification.16,17 However, the data in the manuscript by Zimmet et al. provide an example of the importance of including race/ethnicity and socioeconomic data linked to social determinants of health for future development of predictive algorithms. While the CPQCC publishes a health equity dashboard and has observed racial and/or ethnic variation in quality of care,18,19 other predictive analytic algorithms have not systematically included race/ethnicity or social determinants of health metrics.20 For example, the impact of omission of race/ethnicity data on bronchopulmonary dysplasia (BPD) risk estimation in the National Institute of Child Health and Human Development (NICHD) BPD Outcome Estimator21,22 was recently described.23,24 Specifically, Whitehead et al. illustrate a paradox of the NICHD BPD Risk Estimator that resulted from omission of recognized disparities in preterm birth risk and mortality between African- and European-descent preterm infants. This omission leads to a sufficiently high mortality projection for African-descent infants that the threshold risk of moderate-to-severe BPD is never attained despite high severity of illness. The authors point out that, without adjustment for race-based disparities in mortality risk, prediction algorithms run the risk of erroneous risk estimation due to the competing risk of increased mortality. Inclusion of race/ethnicity and social determinants of health data in predictive algorithms will be important in identifying NICU strategies to reduce racial disparities in multiple infant health outcomes.22,25,26

Nursing practice data are also critical for inter-NICU comparisons of clinical care delivery processes27 but are not routinely included in large clinical data sets used for predictive algorithm development. The diversity of nursing practice data collection platforms among NICUs and the vendor-specific, proprietary differences between platforms have reduced electronic access to standardized nursing practice data collection.28 Future predictive analytic algorithms should take advantage of open-source data dictionaries for data collection that include intentional integration of nursing practice data.28 Zimmet et al. highlight the importance of using vital sign data from multiple NICUs for future development of predictive risk algorithms with improved sensitivity and specificity. Their work also suggests the importance of integrating vital sign-based analytics with other NICU-specific characteristics of physician- and nurse-based care delivery, monitor management and hardware, infant socioeconomic status, unit culture, and race/ethnicity to accelerate discovery and implementation of standardized best practices across NICUs that will improve infant outcomes through regional, national, and international collaboration.14,15,2931

Competing interests

The author declares no competing interests.

Footnotes

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Kumar N, Akangire G, Sullivan B, Fairchild K, Sampath V. Continuous vital sign analysis for predicting and preventing neonatal diseases in the twenty-first century: big data to the forefront. Pediatr. Res. 2020;87:210–220. doi: 10.1038/s41390-019-0527-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Moorman JR, et al. Mortality reduction by heart rate characteristic monitoring in very low birth weight neonates: a randomized trial. J. Pediatr. 2011;159:900–6 e1. doi: 10.1016/j.jpeds.2011.06.044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Stone ML, et al. Abnormal heart rate characteristics before clinical diagnosis of necrotizing enterocolitis. J. Perinatol. 2013;33:847–850. doi: 10.1038/jp.2013.63. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Griffin MP, Lake DE, O’Shea TM, Moorman JR. Heart rate characteristics and clinical signs in neonatal sepsis. Pediatr. Res. 2007;61:222–227. doi: 10.1203/01.pdr.0000252438.65759.af. [DOI] [PubMed] [Google Scholar]
  • 5.Fairchild KD, et al. Vital signs and their cross-correlation in sepsis and NEC: a study of 1,065 very-low-birth-weight infants in two NICUs. Pediatr. Res. 2017;81:315–321. doi: 10.1038/pr.2016.215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Saria S, Rajani AK, Gould J, Koller D, Penn AA. Integration of early physiological responses predicts later illness severity in preterm infants. Sci. Transl. Med. 2010;2:48ra65. doi: 10.1126/scitranslmed.3001304. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Saugstad OD, Aune D. Optimal oxygenation of extremely low birth weight infants: a meta-analysis and systematic review of the oxygen saturation target studies. Neonatology. 2014;105:55–63. doi: 10.1159/000356561. [DOI] [PubMed] [Google Scholar]
  • 8.Askie LM, et al. Association between oxygen saturation targeting and death or disability in extremely preterm infants in the neonatal oxygenation prospective meta-analysis collaboration. JAMA. 2018;319:2190–2201. doi: 10.1001/jama.2018.5725. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Poets CF, et al. Association between intermittent hypoxemia or bradycardia and late death or disability in extremely preterm infants. JAMA. 2015;314:595–603. doi: 10.1001/jama.2015.8841. [DOI] [PubMed] [Google Scholar]
  • 10.Di Fiore JM, et al. Patterns of oxygenation, mortality, and growth status in the surfactant positive pressure and oxygen trial cohort. J. Pediatr. 2017;186:49–56 e1. doi: 10.1016/j.jpeds.2017.01.057. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Sullivan BA, et al. Early pulse oximetry data improves prediction of death and adverse outcomes in a two-center cohort of very low birth weight infants. Am. J. Perinatol. 2018;35:1331–1338. doi: 10.1055/s-0038-1654712. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Fleming S, et al. Normal ranges of heart rate and respiratory rate in children from birth to 18 years of age: a systematic review of observational studies. Lancet. 2011;377:1011–1018. doi: 10.1016/S0140-6736(10)62226-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Alonzo CJ, et al. Heart rate ranges in premature neonates using high resolution physiologic data. J. Perinatol. 2018;38:1242–1245. doi: 10.1038/s41372-018-0156-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Kaempf, J., Morris, M., Steffen, E., Wang, L. & Dunn, M. Continued improvement in morbidity reduction in extremely premature infants. Arch. Dis. Child. Fetal Neonatal Ed. 10.1136/archdischild-2020-319961 (2020). [DOI] [PubMed]
  • 15.Lee, H. C. et al. Comparison of collaborative versus single-site quality improvement to reduce NICU length of stay. Pediatrics142, e20171395 (2018). [DOI] [PubMed]
  • 16.Lee, H. C., Liu, J., Profit, J., Hintz, S. R. & Gould, J. B. Survival without major morbidity among very low birth weight infants in California. Pediatrics146, e20193865 (2020). [DOI] [PMC free article] [PubMed]
  • 17.Edwards EM, Ehret DEY, Soll RF, Horbar JD. Vermont Oxford Network: a worldwide learning community. Transl. Pediatr. 2019;8:182–192. doi: 10.21037/tp.2019.07.01. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Gould, J. B. Building the first statewide quality improvement collaborative, the CPQCC: a historic perspective. Children7, 177 (2020). [DOI] [PMC free article] [PubMed]
  • 19.Profit, J. et al. Racial/ethnic disparity in NICU quality of care delivery. Pediatrics140, e20170918 (2017). [DOI] [PMC free article] [PubMed]
  • 20.Rysavy MA, et al. Assessment of an updated neonatal research network extremely preterm birth outcome model in the Vermont Oxford Network. JAMA Pediatr. 2020;174:e196294. doi: 10.1001/jamapediatrics.2019.6294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Laughon MM, et al. Prediction of bronchopulmonary dysplasia by postnatal age in extremely premature infants. Am. J. Respir. Crit. Care Med. 2011;183:1715–1722. doi: 10.1164/rccm.201101-0055OC. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Davis JM, Pursley DM, Pediatric Policy C. Preventing long-term respiratory morbidity in preterm neonates: is there a path forward? Pediatr. Res. 2020;87:9–10. doi: 10.1038/s41390-019-0641-z. [DOI] [PubMed] [Google Scholar]
  • 23.Whitehead HV, et al. The challenge of risk stratification of infants born preterm in the setting of competing and disparate healthcare outcomes. J. Pediatr. 2020;223:194–196. doi: 10.1016/j.jpeds.2020.04.043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Vesoulis ZA, McPherson CC, Whitehead HV. Racial disparities in calculated risk for bronchopulmonary dysplasia: a dataset. Data Brief. 2020;30:105674. doi: 10.1016/j.dib.2020.105674. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Litt, J. S., Fraiman, Y. S. & Pursley, D. M. Health equity and the social determinants: putting newborn health in context. Pediatrics145, e20200817 (2020). [DOI] [PMC free article] [PubMed]
  • 26.Beck AF, et al. The color of health: how racism, segregation, and inequality affect the health and well-being of preterm infants and their families. Pediatr. Res. 2020;87:227–234. doi: 10.1038/s41390-019-0513-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Lake ET, Staiger D, Edwards EM, Smith JG, Rogowski JA. Nursing care disparities in neonatal intensive care units. Health Serv. Res. 2018;53:3007–3026. doi: 10.1111/1475-6773.12762. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Singh H, et al. Development of data dictionary for neonatal intensive care unit: advancement towards a better critical care unit. JAMIA Open. 2020;3:21–30. doi: 10.1093/jamiaopen/ooz064. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Lui, K. et al. Inter-center variability in neonatal outcomes of preterm infants: a longitudinal evaluation of 298 neonatal units in 11 countries. Semin. Fetal Neonatal Med. 10.1016/j.siny.2021.101196 (2021). [DOI] [PubMed]
  • 30.Pursley DM, McCormick MC. Bending the arc for the extremely low gestational age newborn. Pediatr. Res. 2018;83:751–753. doi: 10.1038/pr.2018.18. [DOI] [PubMed] [Google Scholar]
  • 31.Profit J, et al. The correlation between neonatal intensive care unit safety culture and quality of care. J. Patient Saf. 2020;16:e310–e316. doi: 10.1097/PTS.0000000000000546. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Pediatric Research are provided here courtesy of Nature Publishing Group

RESOURCES