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Published on: August 16, 2013
Chronic Placental Inflammation as a Risk Factor of Severe Retinopathy of Prematurity
Chae Young Kim1, Euiseok Jung1, Eun Na Kim2
1Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Insights
Chronic placental inflammation (CPI) is linked to severe retinopathy of prematurity (ROP) in very low-birth-weight (VLBW) infants. This inflammation increases the likelihood of ROP requiring laser treatment.
Area of Science:
- Neonatalogy
- Perinatal Medicine
- Pathology
Background:
- Chronic placental inflammation (CPI) is a suspected factor in premature infant diseases.
- Retinopathy of prematurity (ROP) is a leading cause of vision impairment in preterm and very low-birth-weight (VLBW) infants.
Purpose of the Study:
- To investigate the association between chronic placental inflammation (CPI) and the development of retinopathy of prematurity (ROP) in VLBW infants.
Main Methods:
- A retrospective review of clinical records for VLBW infants born between 2013 and 2016.
- Analysis of placental pathology, including CPI, using logistic regression to assess infant morbidities.
Main Results:
- The study included 402 VLBW infants (mean gestational age 28.5 weeks).
- ROP incidence was 24.1%. CPI was present in 22.4% of infants, with 28.9% of those developing ROP.
- CPI was independently associated with an increased risk of severe ROP requiring laser photocoagulation (aOR 2.739, p=.029), after adjusting for gestational age, birth weight, and oxygen exposure.
Conclusions:
- Chronic placental inflammation is a significant risk factor for severe retinopathy of prematurity in VLBW infants.
- CPI is associated with ROP requiring laser treatment, highlighting its clinical importance.
Background:
Chronic placental inflammation (CPI) has been implicated in the pathogenesis of diseases in premature infants, whereas retinopathy of prematurity (ROP) is a major complication primarily affecting preterm and very low-birth-weight (VLBW) infants. This study aims to investigate the association between CPI and ROP in VLBW infants.
Methods:
We performed a retrospective review of clinical records of VLBW infants born between 2013 and 2016. Placental pathology findings including CPI cases were analyzed using logistic regression to study infants' morbidities and other clinical characteristics.
Results:
A total of 402 infants with a mean (standard deviation) gestational age of 28.5 (2.8) weeks and birth weight of 1,027.2 (304.4) g were included. The incidence of ROP was 24.1%. CPI was found in 90 infants (22.4%), among which 28.9% (26 of 90) developed ROP, and 21.1% (19 of 90) underwent laser photocoagulation. Lower gestational age, lower birth weight, longer duration of oxygen supply, and presence of CPI were associated with the development of ROP. After adjustment for gestational age, birth weight, sex, duration of oxygen supply, and other overlapping placental pathology, CPI was associated with the odds for type 1 ROP that required laser photocoagulation (adjusted odds ratio, 2.739; 95% confidence interval, 1.112 to 6.749; p = .029).
Conclusions:
CPI was associated with severe ROP requiring treatment with laser photocoagulation in VLBW infants.
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