Near Infrared Spectroscopy as a Biomarker for Necrotising Enterocolitis following Red Blood Cell Transfusion. Issue 6 (December 2014)

• Record Type: Journal Article
• Authors: Sood, Beena G.; Cortez, Josef; McLaughlin, Kathleen; Gupta, Meenakshi; Amaram, Arun; Kolli, Madhuri; Zajac, Maryellen; Pizzino, Janet; Schoettle, Bonnie; Chen, Xinguang
• Is Part Of: Journal of near infrared spectroscopy. Volume 22:Issue 6(2014)
• Page Start: 375
• Page End: 388
• Publication Date: 2014-12
• Subjects: near infrared spectroscopy -- biomarkers -- tissue oxygenation -- neonatal -- necrotising enterocolitis -- red blood cell transfusions -- prematurity -- time-series data; Near infrared spectroscopy -- Periodicals; 543.5
• DOI: 10.1255/jnirs.1135
• Languages: English
• ISSNs: 0967-0335

Abstract

Red blood cell transfusions (RBCTs) have been associated with necrotising enterocolitis (NEC) in preterm infants (PTIs). The objective of this report is to evaluate the use of regional cerebral (cRSO2 ) and splanchnic (sRSO2 ) tissue oximetry measured using near infrared (NIR) spectroscopy as biomarkers to evaluate the association between RBCT and NEC in a secondary analysis of a hypothesis-generating Phase I exploratory study of biomarker development. cRSO2 and sRSO2 were monitored in PTIs receiving RBCTs. Three time periods were defined: pre-RBCT (12 h prior to RBCT), during RBCT and post-RBCT (24 h after RBCT). Three groups were defined: absence of NEC within ±7 days of index RBCT (Group 1); NEC within 7 days prior (Group 2) and within 7 days after RBCT (Group 3). Mean hourly sRSO2 and cRSO2 were compared between groups across RBCT periods using the mixed effect method. Neonatal postnatal morbidities and treatments were included as covariates. Fifty-seven infants (median gestational age 27 weeks) received 147 RBCTs (Group 1 = 120, Group 2 = 19, and Group 3 = 8) during NIR spectroscopy monitoring. In the adjusted analysis, there was a significant change in sRSO2 during the course of RBCT ( p = 0.0405) with significant interaction with group ( p < 0.0001) such that in Groups 1 and 2, sRSO2 increased over RBCT periods, whereas in Group 3, sRSO2 declined over RBCT periods. cRSO2 increased during the course of the RBCT ( p < 0.0001) with significant interaction with group ( p = 0.0258). cRSO2 and sRSO2 increased significantly following RBCT in infants without NEC or NEC diagnosed prior to RBCT. Post-RBCT sRSO2 decreased in infants who were subsequently diagnosed with NEC in this exploratory secondary analysis of a Phase I Biomarker study. sRSO2 response may potentially be a biomarker to identify infants who are likely to develop NEC post-RBCT that needs to be validated in larger prospective "hypothesis-testing" randomised controlled trials.