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dc.contributor.authorLundgren, Pia
dc.date.accessioned2015-01-07T10:34:38Z
dc.date.available2015-01-07T10:34:38Z
dc.date.issued2015-01-07
dc.identifier.isbn978-91-628-9204-3 (printed)
dc.identifier.isbn978-91-628-9205-0 (e-pub)
dc.identifier.urihttp://hdl.handle.net/2077/37528
dc.description.abstractBackground: Retinopathy of prematurity (ROP) is a sight-threatening disease that affects extremely preterm and very preterm infants. Approximately 5–10% of infants screened for ROP go on to develop severe ROP that requires treatment. To minimize unnecessary screening procedures, which can be stressful for these fragile infants, it is important to identify new risk factors and predictors that better determine which infants are at high risk for ROP. The objective of this study was to investigate growth pattern (peri- and postnatal weight gain) and nutritional intake as risk factors for severe ROP. Methods: WINROP (Weight, insulin-like growth factor 1, neonatal, retinopathy of prematurity) is a web-based surveillance system that aims to identify infants at high risk of ROP based on their birth weight (BW), gestational age (GA), and postnatal weight gain. In all cohorts that we studied, BW, GA, gender, and maximum ROP stage and ROP treatment were retrospectively retrieved from hospital records. In Paper I, we validated WINROP in a Swedish population-based cohort of extremely preterm infants (born at GA <27 weeks) (n=407). This cohort, called the EXPRESS cohort, was further evaluated in Paper IV in relation to nutritional intake and the correlation with severe ROP. In Paper II, the association between infant weight standard deviation scores (WSDS) at first sign of ROP and ROP requiring treatment was evaluated in a Gothenburg cohort screened for ROP (n=147). In Paper III, the birth weight standard deviations score (BWSDS) was calculated in 5 cohorts (n=2941) that were previously included in WINROP studies; Paper III assessed the impact of low birth weight as a risk factor for severe ROP. Results: WINROP correctly identified 96% (45/47) of infants who required treatment for ROP in an extremely preterm cohort. Low weight (p=0.001) and low WSDS at first detection of ROP (p=0.002) were risk factors for severe ROP. Low BWSDS (p<0.001) was a risk factor for severe ROP for all preterm infants; however, the impact of low BWSDS increased with increasing GA. In addition, low energy intake (p<0.01) during the first four weeks of life was associated with the development of severe ROP (p<0.01). Conclusions: Weight at birth and postnatal weight gain can be useful predictors for severe ROP as can weight at first detection of ROP. In addition, low energy intake during the first four weeks of a preterm infant’s life may be associated with later severe ROP.sv
dc.language.isoengsv
dc.relation.haspartI. Lundgren P, Stoltz Sjöstrom E, Domellöf M, Källen K, Holmström G, Hård AL, Smith LE, Löfqvist C, Hellström A. WINROP identifies severe retinopathy of prematurity at an early stage in a nation-based cohort of extremely preterm infants. PLoS One. 2013 Sep 12;8(9):e73256 ::PMID::24069180sv
dc.relation.haspartII. Lundgren P, Wilde Å, Löfqvist C, Smith LE, Hård AL, Hellström A. Weight at first detection of retinopathy of prematurity predicts disease severity. Br J Ophthalmol. 2014 Nov;98(11):1565–9 ::PMID::24963022sv
dc.relation.haspartIII. Lundgren P, Kistner A, Andersson EM, Hansen-Pupp I, Holmström G, Ley D, Niklasson A, Smith LE, Wu C, Hellström A, Löfqvist C. Low birth weight is a risk factor for severe retinopathy of prematurity depending on gestational age. PLoS One. 2014 Oct 15;9(10):e109460 ::PMID::25330287sv
dc.relation.haspartIV. Stoltz Sjöström E, Lundgren P, Öhlund I, Holmström G, Hellström A, Domellöf M. Low energy intake during the first four weeks of life increases the risk for severe retinopathy of prematurity in extremely preterm infants. Submitted for publicationsv
dc.subjectRetinopathy of prematuritysv
dc.subjectPreterm infantsv
dc.subjectBirth weightsv
dc.subjectRisk factorsv
dc.subjectNutritionsv
dc.subjectWeight gainsv
dc.titleGrowth pattern and nutritional intake as predictors for retinopathy of prematuritysv
dc.typetexteng
dc.type.svepDoctoral thesiseng
dc.gup.mailpia.lundgren@gu.sesv
dc.type.degreeDoctor of Philosophy (Medicine)sv
dc.gup.originUniversity of Gothenburg. Sahlgrenska Academysv
dc.gup.departmentInstitute of Neuroscience and Physiology. Department of Clinical Neuroscience and Rehabilitationsv
dc.gup.defenceplaceFredagen den 23 januari 2015, kl 9.00, Sal Tallen, Drottning Silvias barn och ungdoms sjukhus, Göteborgsv
dc.gup.defencedate2015-01-23
dc.gup.dissdb-fakultetSA


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