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Perinatal risk factors for development of retinopathy of prematurity in a tertiary neonatal intensive care unit
OBJECTIVE: Retinopathy of prematurity (ROP) is a vasoproliferative disorder that is one of the main preventable causes of blindness among preterm neonates. This study aimed to determine the incidence of ROP and investigate the relationship between perinatal risk factors and ROP development. METHODS:...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taibah University
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694889/ https://www.ncbi.nlm.nih.gov/pubmed/31435422 http://dx.doi.org/10.1016/j.jtumed.2019.05.001 |
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author | Nugud, Alaa A. Nugud, Shomous Nugud, Ahmed Nugud, Assmaa A. Kathamuthu, Raja Jalal, Mahmoud |
author_facet | Nugud, Alaa A. Nugud, Shomous Nugud, Ahmed Nugud, Assmaa A. Kathamuthu, Raja Jalal, Mahmoud |
author_sort | Nugud, Alaa A. |
collection | PubMed |
description | OBJECTIVE: Retinopathy of prematurity (ROP) is a vasoproliferative disorder that is one of the main preventable causes of blindness among preterm neonates. This study aimed to determine the incidence of ROP and investigate the relationship between perinatal risk factors and ROP development. METHODS: This retrospective, non-interventional, non-comparative, hospital-based study was conducted at a tertiary-level neonatal intensive care unit. A total of 163 consecutive patients who met the inclusion criteria were recruited in this study. RESULTS: ROP prevalence was 0.01. During the study period, 44 patients developed ROP (27%), and 119 (73%) did not. Stage I ROP was detected in 8 patients (4.9%); stage II ROP without plus-disease in 26 patients (16%); stage II disease with comorbidities in 1 patient (0.6%); and stage III disease in 9 patients (5.5%). None of the patients showed stage IV and V disease. The mean gestational age was 27.7 ± 2.08 weeks in babies who had ROP and 29.59 ± 1.80 weeks in the other group. Neonates with ROP required more frequent blood transfusion (average, 4.89 ± 3.164 transfusions) compared to their counterparts who received an average of 1.19 ± 1.733 transfusions. Intracranial haemorrhage was identified in 55 (33.7%) patients, of whom 14.1% had ROP. Moreover, neonatal seizures occurred in 23 (14.11%) babies and were more common among babies who had ROP (n = 14). CONCLUSION: This study identified key factors associated with ROP, such as intracranial haemorrhage with or without neonatal seizures and a high frequency of blood transfusions. |
format | Online Article Text |
id | pubmed-6694889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taibah University |
record_format | MEDLINE/PubMed |
spelling | pubmed-66948892019-08-21 Perinatal risk factors for development of retinopathy of prematurity in a tertiary neonatal intensive care unit Nugud, Alaa A. Nugud, Shomous Nugud, Ahmed Nugud, Assmaa A. Kathamuthu, Raja Jalal, Mahmoud J Taibah Univ Med Sci Original Article OBJECTIVE: Retinopathy of prematurity (ROP) is a vasoproliferative disorder that is one of the main preventable causes of blindness among preterm neonates. This study aimed to determine the incidence of ROP and investigate the relationship between perinatal risk factors and ROP development. METHODS: This retrospective, non-interventional, non-comparative, hospital-based study was conducted at a tertiary-level neonatal intensive care unit. A total of 163 consecutive patients who met the inclusion criteria were recruited in this study. RESULTS: ROP prevalence was 0.01. During the study period, 44 patients developed ROP (27%), and 119 (73%) did not. Stage I ROP was detected in 8 patients (4.9%); stage II ROP without plus-disease in 26 patients (16%); stage II disease with comorbidities in 1 patient (0.6%); and stage III disease in 9 patients (5.5%). None of the patients showed stage IV and V disease. The mean gestational age was 27.7 ± 2.08 weeks in babies who had ROP and 29.59 ± 1.80 weeks in the other group. Neonates with ROP required more frequent blood transfusion (average, 4.89 ± 3.164 transfusions) compared to their counterparts who received an average of 1.19 ± 1.733 transfusions. Intracranial haemorrhage was identified in 55 (33.7%) patients, of whom 14.1% had ROP. Moreover, neonatal seizures occurred in 23 (14.11%) babies and were more common among babies who had ROP (n = 14). CONCLUSION: This study identified key factors associated with ROP, such as intracranial haemorrhage with or without neonatal seizures and a high frequency of blood transfusions. Taibah University 2019-06-03 /pmc/articles/PMC6694889/ /pubmed/31435422 http://dx.doi.org/10.1016/j.jtumed.2019.05.001 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Nugud, Alaa A. Nugud, Shomous Nugud, Ahmed Nugud, Assmaa A. Kathamuthu, Raja Jalal, Mahmoud Perinatal risk factors for development of retinopathy of prematurity in a tertiary neonatal intensive care unit |
title | Perinatal risk factors for development of retinopathy of prematurity in a tertiary neonatal intensive care unit |
title_full | Perinatal risk factors for development of retinopathy of prematurity in a tertiary neonatal intensive care unit |
title_fullStr | Perinatal risk factors for development of retinopathy of prematurity in a tertiary neonatal intensive care unit |
title_full_unstemmed | Perinatal risk factors for development of retinopathy of prematurity in a tertiary neonatal intensive care unit |
title_short | Perinatal risk factors for development of retinopathy of prematurity in a tertiary neonatal intensive care unit |
title_sort | perinatal risk factors for development of retinopathy of prematurity in a tertiary neonatal intensive care unit |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694889/ https://www.ncbi.nlm.nih.gov/pubmed/31435422 http://dx.doi.org/10.1016/j.jtumed.2019.05.001 |
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