Implementation of a Clinical Prediction Model Using Daily Postnatal Weight Gain, Birth Weight, and Gestational Age to Risk Stratify ROP
Abstract
Purpose:
To develop a simple prognostic model using postnatal weight gain, birth weight, and gestational age to identify infants at risk for developing severe retinopathy of prematurity (ROP).
Methods:
Medical records from two tertiary referral centers with the diagnosis code “Retinopathy of Prematurity” were evaluated. Those with a birth weight of 1,500 g or less, gestational age of 30 weeks or younger, and unstable clinical courses were included. Multivariate regression analysis was applied to transform three independent variables into a growth rate algorithm.
Results:
Seventeen of 191 neonates had severe ROP. Weight gain of at least 23 g/d was determined as a protective cut-off value against development of severe ROP. This value maintained 100% sensitivity with 62% specificity to ensure all neonates who require treatment would be captured. Overall, the Omaha (OMA)-ROP model calculated a 58% reduction in eye examinations within the cohort.
Conclusions:
Inclusion of postnatal growth rate in risk stratification will minimize the number of eye examinations performed without increasing adverse visual outcomes. The OMA-ROP model predicts neonates who gain less than 23 g/d are at higher risk for developing severe ROP. Although promising, larger cohort studies may be necessary to validate and implement new screening practices among preterm infants.
[J Pediatr Ophthalmol Strabismus. 2018;55(5):326-334.]
- 1.Binenbaum G, Ying GS, Quinn GE, The CHOP postnatal weight gain, birth weight, and gestational age retinopathy of prematurity risk model. Arch Ophthalmol. 2012; 130:1560–1565.
10.1001/archophthalmol.2012.2524 > Crossref MedlineGoogle Scholar - 2.Gilbert C, Fielder A, Gordillo L, International NO-ROP Group. Characteristics of infants with severe retinopathy of prematurity in countries with low, moderate, and high levels of development: implications for screening programs. Pediatrics. 2005; 115:e518–e525.
10.1542/peds.2004-1180 > Crossref MedlineGoogle Scholar - 3.Gilbert C, Foster A. Blindness in children: control priorities and research opportunities. Br J Ophthalmol. 2001; 85:1025–1027.
10.1136/bjo.85.9.1025 > Crossref MedlineGoogle Scholar - 4.Section on Ophthalmology American Academy of PediatricsAmerican Academy of OphthalmologyAmerican Association for Pediatric Ophthalmology and Strabismus. Screening examination of premature infants for retinopathy of prematurity. Pediatrics. 2006; 117:572–576.
10.1542/peds.2005-2749 > Crossref MedlineGoogle Scholar - 5.Cryotherapy for Retinopathy of Prematurity Cooperative Group. Multicenter trial of cryotherapy for retinopathy of prematurity: preliminary results. Arch Ophthalmol. 1988; 106:471–479.
10.1001/archopht.1988.01060130517027 > Crossref MedlineGoogle Scholar - 6.Cryotherapy for Retinopathy of Prematurity Cooperative Group. Multicenter trial of cryotherapy for retinopathy of prematurity: three-month outcome. Arch Ophthalmol. 1990; 108:195–204.
10.1001/archopht.1990.01070040047029 > Crossref MedlineGoogle Scholar - 7.Early Treatment For Retinopathy of Prematurity Cooperative Group. Revised indications for the treatment of retinopathy of prematurity: results of the early treatment for retinopathy of prematurity randomized trial. Arch Ophthalmol. 2003; 121:1684–1694.
10.1001/archopht.121.12.1684 > Crossref MedlineGoogle Scholar - 8.Promelle V, Milazzo S. Retinopathy of prematurity [article in French]. J Fr Ophtalmol. 2017; 40:430–437.
10.1016/j.jfo.2016.12.013 > Crossref MedlineGoogle Scholar - 9.Cryotherapy for Retinopathy of Prematurity Cooperative Group. The natural ocular outcome of premature birth and retinopathy: status at 1 year. Arch Ophthalmol. 1994; 112:903–912.
10.1001/archopht.1994.01090190051021 > Crossref MedlineGoogle Scholar - 10.Chiang MF, Arons RR, Flynn JT, Starren JB. Incidence of retinopathy of prematurity from 1996 to 2000: analysis of a comprehensive New York state patient database. Ophthalmology. 2004; 111:1317–1325.
10.1016/j.ophtha.2003.10.030 > Crossref MedlineGoogle Scholar - 11.Haines L, Fielder AR, Scrivener R, Wilkinson ARRoyal College of Paediatrics and Child Health; the Royal College of Ophthalmologists; British Association of Perinatal Medicine. Retinopathy of prematurity in the UK I: the organisation of services for screening and treatment. Eye (Lond). 2002; 16:33–38.
10.1038/sj.eye.6700030 > Crossref MedlineGoogle Scholar - 12.Lee SK, Normand C, McMillan D, Canadian Neonatal Network. Evidence for changing guidelines for routine screening for retinopathy of prematurity. Arch Pediatr Adolesc Med. 2001; 155:387–395.
10.1001/archpedi.155.3.387 > Crossref MedlineGoogle Scholar - 13.Palmer EA, Flynn JT, Hardy RJ, The Cryotherapy for Retinopathy of Prematurity Cooperative Group. Incidence and early course of retinopathy of prematurity. Ophthalmology. 1991; 98:1628–1640.
10.1016/S0161-6420(91)32074-8 > Crossref MedlineGoogle Scholar - 14.Wilkinson AR, Haines L, Head K, Fielder ARGuideline Development Group of the Royal College of Paediatrics and Child Health; Royal College of Ophthalmologists; British Association of Perinatal Medicine. UK retinopathy of prematurity guideline. Eye (Lond). 2009; 23:2137–2139.
10.1038/eye.2008.128 > Crossref MedlineGoogle Scholar - 15.Binenbaum G. Algorithms for the prediction of retinopathy of prematurity based on postnatal weight gain. Clin Perinatol. 2013; 40:261–270.
10.1016/j.clp.2013.02.004 > Crossref MedlineGoogle Scholar - 16.Hellström A, Engstrom E, Hard A, Postnatal serum insulin-like growth factor I deficiency is associated with retinopathy of prematurity and other complications of premature birth. Pediatrics. 2003; 112:1016–1020.
10.1542/peds.112.5.1016 > Crossref MedlineGoogle Scholar - 17.Löfqvist C, Andersson E, Sigurdsson J, Longitudinal postnatal weight and insulin-like growth factor I measurements in the prediction of retinopathy of prematurity. Arch Ophthalmol. 2006; 124:1711–1718.
10.1001/archopht.124.12.1711 > Crossref MedlineGoogle Scholar - 18.Hellström A, Perruzzi C, Ju M, Low IGF-I suppresses VEGF-survival signaling in retinal endothelial cells: direct correlation with clinical retinopathy of prematurity. Proc Natl Acad Sci U S A. 2001; 98:5804–5808.
10.1073/pnas.101113998 > Crossref MedlineGoogle Scholar - 19.Smith LE, Shen W, Perruzzi C, Regulation of vascular endothelial growth factor-dependent retinal neovascularization by insulin-like growth factor-1 receptor. Nat Med. 1999; 50:1390–1395.
10.1038/70963 > CrossrefGoogle Scholar - 20.Fierson WMAmerican Academy of Pediatrics Section on Ophthalmology; American Academy of Ophthalmology; American Association for Pediatric Ophthalmology and Strabismus; American Association of Certified Orthoptists. Screening examination of premature infants for retinopathy of prematurity. Pediatrics. 2013; 131:189–195.
10.1542/peds.2012-2996 > Crossref MedlineGoogle Scholar - 21.Movsas TZ, Spitzer AR, Gewolb IH. Trisomy 21 and risk of retinopathy of prematurity. Pediatrics. 2015; 136:e441–e447.
10.1542/peds.2015-0623 > Crossref MedlineGoogle Scholar - 22.Binenbaum G, Ying G, Quinn G, Premature Infants in Need of Transfusion Study Group. A clinical prediction model to stratify retinopathy of prematurity risk using postnatal weight gain. Pediatrics. 2011; 127:e607–e614.
10.1542/peds.2010-2240 > Crossref MedlineGoogle Scholar - 23.Ehrenkranz RA, Younes N, Lemons JA, Longitudinal growth of hospitalized very low birth weight infants. Pediatrics. 1999; 104:280–289.
10.1542/peds.104.2.280 > Crossref MedlineGoogle Scholar - 24.Patel AL, Engstrom JL, Meier PP, Kimura RE. Accuracy of methods for calculating postnatal growth velocity for extremely low birth weight infants. Pediatrics. 2005; 116:1466–1473.
10.1542/peds.2004-1699 > Crossref MedlineGoogle Scholar - 25.Moons KG, Altman DG, Vergouwe Y, Royston P. Prognosis and prognostic research: application and impact of prognostic models in clinical practice. BMJ. 2009; 338:b606.
10.1136/bmj.b606 > Crossref MedlineGoogle Scholar - 26.Wu C, Vanderveen D, Hellstrom A, Lofqvist C, Smith L. Longitudinal postnatal weight measurements for the prediction of retinopathy of prematurity. Arch Ophthalmol. 2010; 128:443–447.
10.1001/archophthalmol.2010.31 > Crossref MedlineGoogle Scholar - 27.Cao JH, Wagner BD, Mccourt EA, The Colorado–retinopathy of prematurity model (CO-ROP): postnatal weight gain screening algorithm. J AAPOS. 2016; 20:19–24.
10.1016/j.jaapos.2015.10.017 > Crossref MedlineGoogle Scholar - 28.Cao JH, Wagner BD, Cerda A, Colorado retinopathy of prematurity model: a multi-institutional validation study. J AAPOS. 2016; 20:220–225.
10.1016/j.jaapos.2016.01.017 > Crossref MedlineGoogle Scholar - 29.Smith WJ, Underwood LE, Keyes L, Clemmons DR. Use of insulin-like growth factor I (IGF-I) and IGF-binding protein measurements to monitor feeding of premature infants. J Clin Endocrinol Metab. 1997; 82:3982–3988. > MedlineGoogle Scholar
- 30.Hård AL, Lӧfqvist C, Fortes Filho JB, Procianoy RS, Smith L, Hellström A. Predicting proliferative retinopathy in a Brazilian population of preterm infants with the screening algorithm WINROP. Arch Ophthalmol. 2010; 128:1432–1436.
10.1001/archophthalmol.2010.255 > Crossref MedlineGoogle Scholar - 31.Gursoy H, Basmak H, Bilgin B, Erol N, Colak E. The effects of mild-to-severe retinopathy of prematurity on the development of refractive errors and strabismus. Strabismus. 2014; 22:68–73.
10.3109/09273972.2014.904899 > Crossref MedlineGoogle Scholar - 32.Smith BT, Tasman WS. Retinopathy of prematurity: late complications in the baby boomer generation (1946–1964). Trans Am Ophthalmol Soc. 2005; 103:225–234. > MedlineGoogle Scholar