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Research Article | Volume 18 Issue 6 (June, 2026) | Pages 180 - 183
Comparative assessment of incidence of retinopathy in anaemic and non-anaemic subjects to assess the role of anaemia in retinopathy
 ,
 ,
 ,
1
Associate professor, Department of Preventive Social Medicine, Prasad Institute of Medical Sciences, Lucknow, Uttar Pradesh
2
Assistant Professor, Department of Ophthalmology, Atal Bihari Vajpayee Government Medical College, Vidisha, Madhya Pradesh
3
Senior Resident, Department of Ophthalmology, Atal Bihari Vajpayee Government Medical College, Vidisha, Madhya Pradesh
4
PG 2nd Year Resident, Department of Ophthalmology, Atal Bihari Vajpayee Government Medical College, Vidisha, Madhya Pradesh
Under a Creative Commons license
Open Access
Received
May 16, 2026
Revised
May 28, 2026
Accepted
June 10, 2026
Published
June 14, 2026
Abstract

Introduction: ROP (retinopathy of prematurity) in premature infants has higher and significant association with low birth weight and lesser gestational age at birth. Anaemia in these infants is also known to have association with the high risk of ROP. Aim: The present study was aimed to comparatively assess the incidence of retinopathy in anaemic and non-anaemic subjects in India to assess the role of anaemia in retinopathy. Methods: The present study assessed 200 premature babies with consecutive birth at the Institute within the defined study period with the gestational age at birth <34 weeks or birth weight <200 grams were assessed to study the retinopathy of prematurity. The incidence of ROP was also assessed in neonates with anaemia and non-anaemic babies. Results: Among 200 subjects, 48 babies had ROP and rest 152 babies had zone 3A vascularized retina. Most common stage was stage 2 in 24 babies, stage 1 in 10 subjects, stage 3 in 8 subjects, and stage 4 in 2 babies. APROP (Aggressive Posterior ROP) was seen in 4 babies. Stage 5 was not seen in any study subject. In 48 babies with ROP, 25% (n=12) subjects needed treatment and 75% (n=36) babies had spontaneous regression. Among 32 babies, 50% (n=16) subjects had ROP. In remaining 168 babies without anaemia, 19% (n=32) babies had ROP. Among 200 study subjects, 22 had received blood transfusion where 54.5% (n=12) had ROP. In remaining 178 babies that did not get blood transfusion, 20.2% (n=36) babies had ROP. Conclusion: The present study concludes that anaemia is a vital risk factor that affects the incidence of ROP. Anaemia must be hence, managed and avoided in premature babies for management of retinopathy of prematurity.

Keywords
INTRODUCTION

ROP (retinopathy of prematurity) is a disease of the developing blood vessels in the retina in the infants that are born preterm. The vital pathological factor in ROP is the ischemia of the avascular retina which ultimately result in the neovascularization.1

 

Retinopathy of prematurity is one of the most vital and key factors for managing the preventable blindness in the child subjects. Despite the well-established records of birth weight and gestational age as the two main risk factors in causing the retinopathy of prematurity, however, anaemia is yet not established as an independent risk factor in causing the retinopathy of prematurity.2

 

Literature data is substantial concerning retinopathy of prematurity and the associated risk factors as gestational age and birth weight. However, existing literature data is scarce concerning the role of anaemia in causing retinopathy of prematurity.3,4 Hence, the present study was aimed to comparatively assess the incidence of retinopathy in anaemic and non-anaemic subjects in India to assess the role of anaemia in retinopathy.

MATERIAL AND METHODS

The present prospective observational study was aimed to comparatively assess the incidence of retinopathy in anaemic and non-anaemic subjects in India to assess the role of anaemia in retinopathy. The study was done at Department of Ophthalmology, Atal Bihari Vajpayee Government Medical College, Vidisha, Madhya Pradesh. The study subjects were from Department of Ophthalmology of the Institute. Verbal and written informed consent were taken from all the subjects and school authorities before study participation. The study included 200 babies that met the inclusion criteria for the study. Following the standards of inclusion, all the premature babies in birth weight of 2 kg or lesser and the gestational age of <34 weeks. The exclusion criteria for the study were subjects with birth weight >2.5kgs, gestational age <34 weeks, with any congenital anomaly, and were not willing to participate in the study. The gestational age and birth weight at the time of birth was noted in all the subjects. All the needed risk factors were recorded including the blood transfusion. In both the eyes of all the subjects, 2.5% phenylephrine and 0.5% diluted tropicamide was instilled thrice for nearly an hours before assessment of pupil dilatation. To decrease the discomfort while testing, 0.5% paracaine as topical anesthetic was used after full dilation of the pupil. For keeping the eyelids apart, sterile eye speculum was inserted. Indirect ophthalmoscope with a 20 D lens and scleral depressor was used for examination of peripheral retina. Findings of the fungus were documented including severity, stag, zone, and vascularity of the retinopathy of prematurity. Diagnosis was made using the guidelines of ICROP.5 Treatment was planned for subjects with type 1 ROP. Parents were counselled and explained for procedure concerning the importance of treatment and follow-up. Last follo w-up visit was done at 41 weeks after the conception age. The variables assessed were exchange transfusion, blood transfusion, anaemia, birth weight, gestational age, twin pregnancy, and gender of the subjects. The gathered data from the study subjected was assessed with statistical evaluation using the chi-square test, Fisher’s exact test, Mann Whitney U test, and SPSS (Statistical Package for the Social Sciences) software version 24.0 (IBM Corp., Armonk. NY, USA) using ANOVA, chi-square test, and student's t-test. The significance level was considered at a p-value of <0.05.

RESULTS

The present prospective observational study was aimed to comparatively assess the incidence of retinopathy in anaemic and non-anaemic subjects in India to assess the role of anaemia in retinopathy. The present study assessed 200 premature babies with consecutive birth at the Institute within the defined study period with the gestational age at birth <34 weeks or birth weight <200 grams were assessed to study the retinopathy of prematurity. The incidence of ROP was also assessed in neonates with anaemia and non-anaemic babies. Among 200 babies, there were 108 males and 92 females. The birth weight was in the range of 940-2000 grams and gestational age at birth was 28-34 weeks.

 

It was seen that for profile and prevalence assessment for ROP, ROP was seen in 48 subjects among total 200 babies included in the study. The remaining 152 subjects depicted 3A vascularized retina on subsequent three follow-ups. Stage 2 of ROP was most commonly seen in 24 babies, stage 1 ROP in 10 subjects, stage 3 in 8 subjects, and stage 4 in 2 babies of the study. APROP (Aggressive Posterior ROP) was seen in 2 babies. Stage 5 ROP was not seen in any study subject. In 48 subjects with ROP, 25% (n=12) babied needed treatment and other 75% (n=36) subjects showed spontaneous regression.

 

The study results showed that for association of ROP and anaemia, in 200 babies included and screened in the study, 32 subjects had anaemia. Among 32 babies, 50% (n=16) babies had ROP. Among remaining 168 subjects without anaemia, 19% (n=32) babies had ROP. On statistical assessment, a significant association was seen in incidence of ROP and anaemia in study subjects with p=0.006 (Table 1).

 

Concerning the assessment of ROP and blood transfusion in study subjects among 200 subjects included in the study subjects, 22 babies were given blood transfusion where 54.5% (n=12) babies had retinopathy of prematurity. In the remaining 178 babies that were not given blood transfusion, 20.2% (n=36) babies had retinopathy of prematurity (Table 2). On statistical assessment, significant association was seen in incidence of ROP and blood transfusion in study subjects with p=0.01.

 

Table 1: Distribution od anaemia and ROP in study subjects

S. No

Anaemia

ROP negative

ROP positive

Total

n

%

n

%

1.       

Absent

136

80.95

32

19.04

168

2.       

Present

16

50

16

50

16

3.       

Total

152

76

48

48

200

Table 2: ROP and blood transfusion in study subjects

S. No

Anaemia

ROP negative

ROP positive

Total

n

%

n

%

1.       

Not given

142

79.77

36

20.22

178

2.       

Given

10

45.4

12

54.5

22

3.       

Total

152

76

48

48

200

DISCUSSION

The present study assessed 200 premature babies with consecutive birth at the Institute within the defined study period with the gestational age at birth <34 weeks or birth weight <200 grams were assessed to study the retinopathy of prematurity. The incidence of ROP was also assessed in neonates with anaemia and non-anaemic babies. Among 200 babies, there were 108 males and 92 females. The birth weight was in the range of 940-2000 grams and gestational age at birth was 28-34 weeks. These data were comparable to the previous studies of Hellgren G et al6 in 2021 and Cakir B et al7 in 2018 where authors assessed subjects with demographic data comparable to the present study in their respective studies.

 

The study results showed that for profile and prevalence assessment for ROP, ROP was seen in 48 subjects among total 200 babies included in the study. The remaining 152 subjects depicted 3A vascularized retina on subsequent three follow-ups. Stage 2 of ROP was most commonly seen in 24 babies, stage 1 ROP in 10 subjects, stage 3 in 8 subjects, and stage 4 in 2 babies of the study. APROP (Aggressive Posterior ROP) was seen in 2 babies. Stage 5 ROP was not seen in any study subject. In 48 subjects with ROP, 25% (n=12) babied needed treatment and other 75% (n=36) subjects showed spontaneous regression. These results were consistent with the findings of Parrozzani R et al8 in 2021 and Bishnoi K et al9 in 2024 where for profile and prevalence assessment for ROP reported by the authors in their studies were comparable to the present study.

 

It was seen that for association of ROP and anaemia, in 200 babies included and screened in the study, 32 subjects had anaemia. Among 32 babies, 50% (n=16) babies had ROP. Among remaining 168 subjects without anaemia, 19% (n=32) babies had ROP. On statistical assessment, a significant association was seen in incidence of ROP and anaemia in study subjects with p=0.006. These findings were in agreement with the results of Tang W et al10 in 2024 and Erdöl H et al11 in 2017 where association of ROP and anaemia similar to the present study was also reported by the authors in their respective studies.

 

On assessing the ROP and blood transfusion in study subjects among 200 subjects included in the study subjects, 22 babies were given blood transfusion where 54.5% (n=12) babies had retinopathy of prematurity. In the remaining 178 babies that were not given blood transfusion, 20.2% (n=36) babies had retinopathy of prematurity (Table 2). On statistical assessment, significant association was seen in incidence of ROP and blood transfusion in study subjects with p=0.01. These results correlated with the findings of Prasad N et al12 in 2023 and Pinheiro AM et al13 in 2009 where ROP and blood transfusion results reported by the authors was comparable to the present study.

CONCLUSION

Considering its limitations, the present study concludes that anaemia is a vital risk factor that affects the incidence of ROP. Anaemia must be hence, managed and avoided in premature babies for management of retinopathy of prematurity. Further longitudinal studies with larger sample size and longer monitoring are needed to reach a definitive conclusion.

REFERENCES
  1. Rekha S, Battu RR. Retinopathy of prematurity: incidence and risk factors. Indian Pediatr. 1996;33:999–1003.
  2. Gopal L, Sharma T, Ramachandran S, Shanmugasundaram R, Asha V. Retinopathy of prematurity: a study. Indian J Ophthalmol. 1995;43:59–61.
  3. Wheatley CM, Dickinson JL, Mackey DA, Craig JE, Sale MM. Retinopathy of prematurity: recent advances in our understanding. Br J Ophthalmol. 2002;86:696–700.
  4. Coats DK, Aaron MM, Mohamed AH. Involution of retinopathy of prematurity after laser treatment: Factors associated with development of retinal detachment. Am J Ophthalmol. 2005;140:214–22.
  5. International Committee for the Classification of Retinopathy of Prematurity. The International Classification of Retinopathy of Prematurity revisited. Arch Ophthalmol. 2005;123:991–9.
  6. Hellgren G, Lundgren P, Pivodic A, Löfqvist C, Nilsson AK, Ley D, et al. Decreased Platelet Counts and Serum Levels of VEGF-A, PDGF-BB, and BDNF in Extremely Preterm Infants Developing Severe ROP. Neonatology. 2021;118:18–27.
  7. Cakir B, Liegl R, Hellgren G, Lundgren P, Sun Y, Klevebro S, et al. Thrombocytopenia is associated with severe retinopathy of prematurity. JCI Insight. 2018;3:e99448.
  8. Parrozzani R, Marchione G, Fantin A, Frizziero L, Salvadori S, Nardo D, et al. Thrombocytopenia as Type 1 ROP Biomarker: A Longitudinal Study. J Pers Med. 2021;11:1120.
  9. Bishnoi K, Prasad R, Upadhyay T, Mathurkar S. A Narrative Review on Managing Retinopathy of Prematurity: Insights into Pathogenesis, Screening, and Treatment Strategies. Cureus. 2024;16:e56168.
  10. Tang W, Zhang Y, Zhang H, Li K, Zhao Z, Ma H, et al. Progress in the study of association between hematological indicators and retinopathy of prematurity (Review). Biomed Rep. 2024;21:111.
  11. Erdöl H, Hacioglu D, Kola M, Türk A, Aslan Y. Investigation of the effect of hemoglobin F and A levels on development of retinopathy of prematurity. J AAPOS. 2017;21:136–40.
  12. Prasad N, Kumar K, Dubey A. Fetal hemoglobin, blood transfusion, and retinopathy of prematurity in preterm infants: An observational, prospective study. Indian J Ophthalmol. 2023;71:2803–7.
  13. Pinheiro AM, Silva WA, Bessa CGF, Cunha HM, Ferreira MAF, Gomes AHB. [Incidence and risk factors of retinopathy of prematurity in University Hospital Onofre Lopes, Natal (RN)- Brazil]. Arq Bras Oftalmol. 2009;72:451–6.

 

 

 

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