Hematologic Risk Factors for the Development of Retinopathy of Prematurity-A Retrospective Study
- PMID: 36980125
- PMCID: PMC10047256
- DOI: 10.3390/children10030567
Hematologic Risk Factors for the Development of Retinopathy of Prematurity-A Retrospective Study
Abstract
(1) Background: Retinopathy of prematurity (ROP) can cause severe visual impairment or even blindness. We aimed to assess the hematological risk factors that are associated with different stages of ROP in a cohort of preterm newborns, and to compare the clinical characteristics and therapeutic interventions between groups. (2) Methods: This retrospective study included 149 preterm newborns from a tertiary maternity hospital in Romania between January 2018 and December 2018, who were segregated into: Group 1 (with ROP, n = 59 patients), and Group 2 (without ROP, n = 90 patients). The patients that were affected by ROP were subsequently divided into the following subgroups: Subgroup 1 (Stage 1, n = 21), Subgroup 2 (Stage 2, n = 35), and Subgroup 3 (Stage 3, n = 25). The associations were analyzed using multivariate logistic regression and sensitivity analysis. (3) Results: Platelet mass indexes (PMI) that were determined in the first, seventh, and tenth days of life were significantly associated with Stage 1 ROP. PMI determined in the first day of life was also significantly associated with Stage 2 ROP. The sensitivity and specificity of these parameters were modest, ranging from 44 to 57%, and 59 to 63%. (4) Conclusions: PMI has a modest ability to predict the development of ROP.
Keywords: hematological parameters; platelet mass index; retinopathy of prematurity; risk factor identification.
Conflict of interest statement
The authors declare no conflict of interest.
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References
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- Gerull R., Brauer V., Bassler D., Laubscher B., Pfister R.E., Nelle M., Muller B., Gerth-Kahlert C., Adams M., Swiss Neonatal Network and Follow-up Group Incidence of retinopathy of prematurity (ROP) and ROP treatment in Switzerland 2006–2015: A population-based analysis. Arch. Dis. Child. Fetal Neonatal Ed. 2018;103:337–342. doi: 10.1136/archdischild-2017-313574. - DOI - PubMed
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