Abstract
Purpose
To review the incidence and risk factors for retinopathy of prematurity (ROP) King Faisal Specialist Hospital and King Abdulaziz University Hospital in Jeddah, Saudi Arabia.
Material and methods
In this prospective cohort study, preterm infants who were admitted to a neonatal intensive care unit from 2012 to 2013 were evaluated for ROP. Inclusion criteria were, preterm infants with gestational age <32 weeks and/or birth weight <1500 g. The risk factors that were assessed were intraventricular hemorrhage, patent ductus arteriosus (PDA), sepsis and hydrocephalus. The relative risk was used to measure the risk and logistic regression was used to adjust for confounding factors. Statistical significance was indicated by p < 0.05.
Results
Thirty-one of 92 (33.7%) preterm infants had unilateral or bilateral ROP. The mean gestational age was 26.7 weeks (range, 24–29 weeks) and mean birth weight was 0.843 kg (range, 0.606–1.450 kg). There were 7 infants with stage 1 ROP, 10 infants with stage 2, 14 infants with stage 3 and no cases of stage 4 or 5. Twelve (13%) infants had plus disease and received laser therapy within 72 h of diagnosis. Statistically significant risk factors for ROP were PDA (p = 0.0005) and intraventricular hemorrhage (p = 0.0005).
Conclusion
The incidence of ROP was 33.7% and risk factors were PDA and intraventricular hemorrhage. Laser therapy was very effective for the treatment of plus disease and preventing progression of ROP. Clinicians should assess for potential risk factors when monitoring premature infants.
Keywords: Retinopathy of prematurity (ROP), Plus disease, Threshold disease, Patent ductus arteriosus, Hydrocephalus, Intraventricular hemorrhage
Introduction
Retinopathy of prematurity (ROP) is an abnormal growth of retinal blood vessels that affect premature infants born at or before 32 weeks and weighing 1500 g or less at birth. ROP is usually bilateral and can lead to lifelong vision impairment or blindness.1 The smaller an infant at birth, the greater the likelihood of developing ROP. However, ROP can affect larger and more mature infants. A study of ROP in Riyadh, Saudi Arabia reported 56% of all premature births developed ROP and 15% of these patients had stage 3 disease (severe ROP).2 The mean gestational age (GA) of the ROP patients was 30 weeks.2
In 2010, approximately 184,700 (uncertainty range, 169,600–214,500) preterm infants developed ROP (all stages) worldwide. Twenty-thousand (range, 15,500–27,200) of these infants were severely visually impaired or blind. Additionally, 12,300 (8,300–18,400) preterm babies had mild to moderate visual impairment. Sixty-five percent of patients who are visually impaired due to ROP, were born in middle-income regions; 6.2% (4.3–8.9%) of all visually impaired infants with ROP were born later than 32 weeks gestational age.3 In the majority of cases, ROP regresses and improves with observation. However, a small percentage of infants develop severe ROP that warrants laser treatment.
This prospective study evaluates the incidence of ROP among highly vulnerable infants at 32 weeks (or younger) gestational age and/or weighing less than 1500 g at birth. Additionally, the risk factors for ROP that contributed to ROP in this Saudi Arabian study population were evaluated.
Material and methods
This prospective, cohort study evaluated the incidence of ROP at the two hospitals and investigated the risk factors for ROP. This study evaluated premature infants for ROP who are admitted to the neonatal intensive care unit (NICU) from September 2012 to October 2013 at King Faisal Specialist Hospital and King Abdulaziz University Hospital in Jeddah, Saudi Arabia. Both facilities are tertiary care hospitals that treat ROP cases referred from the entire country. The research committee and biomedical ethics unit at King Abdulaziz University Hospital approved this study.
Inclusion criteria were, all infants who born ⩽32 weeks gestational age and/or birth weight ⩽1500 g. Infants born before 27 weeks were screened at 30–31 weeks postmenstrual age (PMA). Infants born after 27 weeks or weighing <1500 g were screened at 28–35 days postnatal age and screened weekly or every 2 weeks.4 All infants were followed up till they developed ROP or the retina was fully vascularized.
All infants underwent indirect ophthalmoscopy after pupil dilation with 1% topical mydriacyl with a 28 D lens, insertion of a sterile lid speculum and scleral depression. Data were collected on gestational age, birth weight, risk factors, stage of ROP, zone of ROP, presence of plus disease, presence of threshold disease and the type of treatment.
A group of infants who did not develop ROP was compared to the group who developed ROP for the presence and absence of risk factors (Table 4). The risk factors that were assessed were, intraventricular hemorrhage, patent ductus arteriosus (PDA), sepsis, and hydrocephalus. The infants were assessed regularly until the retina was fully vascularized. Treatment was performed within 72 h of diagnosis. Infants who did not require laser treatment underwent routine vision screening, unless there was a specific concern. The indications for treatment of severe ROP were: zone I, any ROP with plus disease; zone I, stage 3 without plus disease; zone II, stage 3 with plus disease or; zone II, stage 2 with plus disease.5
Table 4.
Risk factors for retinopathy of prematurity in the study group and a control group.
| ROP group | No ROP group | Relative risk(RR) | 95% confidence interval | p-Value | |
|---|---|---|---|---|---|
| PDA | Yes: 16 No:15 |
Yes: 9 No: 52 |
2.86 | 1.8–4.9 | 0.0005 |
| IVH | Yes: 15 No: 16 |
Yes: 2 No: 59 |
4.13 | 2.6–6.6 | 0.0005 |
| Hydrocephalus | Yes: 5 No: 26 |
Yes: 1 No: 60 |
2.76 | 1.7–4.46 | 0.008 |
| Sepsis | Yes: 18 No: 13 |
Yes: 32 No: 29 |
1.163 | 0.649–2.085 | 0.610 |
ROP = retinopathy of prematurity
Statistical analysis
The data were collected for statistical analysis and entered into the statistical package for social sciences (IBM Corp., Armonk, NY, USA). The relative risk was used to measure the risk and logistic regression was used to adjust for confounding factors. A p value less than 0.05 was considered statistically significant.
Results
Ninety-two premature infants were screened for ROP. There were 31 (33.7%; 16 females and 15 males) infants diagnosed with ROP and 12 (13%) infants required laser treatment. The mean gestational age was 26.7 weeks (range, 24 weeks to 29 weeks) and the mean birth weight was 0.843 kg (range, 0.606–1.450 kg).
There were fourteen (45.2%) infants with stage 3 ROP which was the most common type of ROP in this study (Table 1). The majority of cases (20 infants; 64.5%) were found in zone 3 (Table 2). The fewest cases of ROP were in zone 1 (2 cases; 6.5%) (Table 2). All cases needing treatment received laser therapy within 72 h of diagnosis (Table 3).
Table 1.
Stages of the retinopathy of prematurity among premature infants from two tertiary care hospitals in Saudi Arabia.
| Stage of ROP | Frequency (infants) | Percentage (%) |
|---|---|---|
| 1 | 7 | 22.5 |
| 2 | 10 | 32.3 |
| 3 | 14 | 45.2 |
| Total | 31 | 100 |
ROP = retinopathy of prematurity
Table 2.
Frequency of retinopathy of prematurity classified by zone.
| Zone | Frequency (infants) | Percentage (%) |
|---|---|---|
| 1 | 2 | 6.5 |
| 2 | 9 | 29 |
| 3 | 20 | 64.5 |
| Total | 31 | 100 |
Table 3.
Plus disease among premature infants from two tertiary care hospitals in Saudi Arabia.
| Plus disease | Frequency (infants) | Percentage (%) |
|---|---|---|
| Yes | 12 | 38.7 |
| No | 19 | 61.3 |
| Total | 31 | 100 |
After adjusting for confounding factors with logistic regression, PDA and IVH had a significant effect on the occurrence of ROP. Hydrocephalus and sepsis were not significant risk factors for ROP (Table 4, Table 5). Laser photocoagulation was very effective in treating ROP. Out of all 31 patients with ROP, 19 cases regressed with observation and 12 cases regressed with laser therapy.
Table 5.
Risk factors for retinopathy of prematurity after adjustment for confounding factors with logistic regression analysis.
| p-Value | Odds ratio O.R | 95% confidence interval | |
|---|---|---|---|
| PDA | 0.003 | 6.201 | 1.850–20.780 |
| IVH | 0.000 | 29.968 | 5.515–162.828 |
| Hydrocephalus | 0.106 | 8.979 | 0.629–128.230 |
| Sepsis | 0.841 | 1.127 | 0.352–3.607 |
Intraventricular hemorrhage = IVH; patent ductus arteriosus = PDA
Discussion
The incidence of ROP is rising in developing countries and some premature infants with ROP are heavier than 1500 g. In Western countries, extremely low-birth-weight infants (⩽1000 g) are surviving due to advances in neonatal care. Hence there is an increase in the incidence of ROP in Western countries also. The mean birth weights of infants from highly developed countries ranged from 737 g to 763 g compared with values ranging from 903 g to 1527 g in less developed countries.6 Mean GAs of infants from highly developed countries ranged from 25.3 weeks to 25.6 weeks compared to 26.3–33.5 weeks in less developed countries.6
A 2003 study of infants at King Khalid University Hospital in Riyadh, Saudi Arabia, reported an incidence rate of 41% for infants weighing <1500 g and the mean gestational age was 28 weeks and the mean birth weight was 1103 g.7 Similarly, our study reported a relatively high incidence of ROP at 33.7% for infants weighing <1500 g with mean gestational age of 26.6 weeks and mean birth weight of 0.843 g. Another study in Saudi Arabia reported an incidence of ROP was 56% with a mean gestational age of 30 weeks for ROP patients and 15% of the patients were in stage 3 disease (severe ROP).2 However, in our study there were 13% of cases with severe ROP that received laser treatment. A study from King Fahad Medical City, Saudi Arabia evaluated premature infants born at gestational age (GA) 32 weeks or younger or birth weight (BW) 1500 g or less from January 1, 2007, until the end of December 2009.8 The study by Dr. Afaf reported an ROP incidence of 30% in infants with mean GA of 27 weeks (range, 23–35 weeks) and mean birth weight of 907 g (range, 530–1730 g).8
The incidence of ROP in the current study is well within the range reported for other countries in the region and elsewhere. For example the incidence of ROP in Kuwait is 38.9%,9 in Taiwan is 37.8%,10 in Iran is 32%,11 in Egypt is 19.2%,12 in Jordan is 28.6%13 and in Bahrain is 20.4%.14 Most of these countries are reporting an increased incidence of ROP in infants weighing less than 1500 g.
In our study, the risk factors that were statistically significantly associated to ROP were PDA and IVH. However, two studies one from Turkey and the other from India, reported a relationship between PDA and incidence of ROP in infants younger than 32 weeks.15, 16 Additionally, an Irish study reported that in 68 infants with IVH, ROP was present in 33 infants (48.5%).17 Another study from Saudi Arabia used predictive logistic regression model and reported intraventricular hemorrhage was a risk factor for ROP (OR = 2.90).8
Laser therapy is extremely effective for treatment of type 1 threshold ROP, with a success rate of 91–95% except for some zone 1 eyes.18 We found that 13% of ROP cases required treatment. However, other studies have reported ROP treatment rates of 6.6% in Jordan,13 15% in Saudi Arabia,2 19% in Saudi Arabia,7 6% in Bahrain,14 and 7.8% in Kuwait.9 In our study, the disease regressed in all infants who received laser therapy. Based on our experience in the current study, laser photocoagulation was very effective in treating ROP. All our patients regressed either with observation or laser treatment and none progressed to stage 4 or 5 disease.
Conclusions
The incidence of ROP was 33.7%. The significant risk factors for ROP were PDA and IVH. Twelve (13%) cases underwent laser therapy which was very effective in preventing progression of the disease. Therefore, clinicians should be aware of the presence of these risk factors when monitoring premature infants. Timely laser therapy can reduce the visual morbidity associated with ROP.
Conflict of interest
The authors declared that there is no conflict of interest.
Acknowledgements
Our appreciation to the Department of Ophthalmology and NICU at the two tertiary centers, King Faisal Specialist Hospital and King Abdulaziz University Hospital in Jeddah, Saudi Arabia.
Footnotes
Peer review under responsibility of Saudi Ophthalmological Society, King Saud University.
References
- 1.Crosse V.M., Evans P.J. Prevention of retrolental fibroplasia. AMA Arch Ophthalmol. 1952;48(1):83–87. doi: 10.1001/archopht.1952.00920010086012. [DOI] [PubMed] [Google Scholar]
- 2.Binkhathlan A.A., Almahmoud L.A., Saleh M.J., Srungeri S. Retinopathy of prematurity in Saudi Arabia: incidence, risk factors, and the applicability of current screening criteria. Br J Ophthalmol. 2008;92(2):167–169. doi: 10.1136/bjo.2007.126508. [DOI] [PubMed] [Google Scholar]
- 3.Blencowe Hannah, Lawn Joy E., Vazquez Thomas, Fielder Alistair, Gilbert Clare. Preterm-associated visual impairment and estimates of retinopathy of prematurity at regional and global levels for 2010. Pediatr Res. 2013;74(Suppl. 1):35–49. doi: 10.1038/pr.2013.205. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Wilkinson A.R., Haines L., Head K., Fielder A.R. Royal College of Ophthalmologists; United Kingdom: 2008. Guideline for the screening and treatment of retinopathy of prematurity. [Google Scholar]
- 5.Early Treatment for Retinopathy of Prematurity Cooperative Group. Revised indications for the treatment of retinopathy of prematurity: results of prematurity randomized trial. Arch Ophthalmol 2003;121(12):1684–94. [DOI] [PubMed]
- 6.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(5):e518–e525. doi: 10.1542/peds.2004-1180. [DOI] [PubMed] [Google Scholar]
- 7.Al-Amro S.A., Al-Kharfi T.M., Thabit A.A., Al-Mofada S.M. Retinopathy of prematurity at a University Hospital in Riyadh, Saudi Arabia. Saudi Med J. 2003;24(7):720–724. [PubMed] [Google Scholar]
- 8.Bin-Khathlan Afaf A., Al-Ballaa Fatin N., AlYahya Abdullah K. Ophthalmic short- and long-term outcomes for premature infants: results of an extended follow-up program in Saudi Arabia. Saudi J Ophthalmol. 2014;28(4):268–273. doi: 10.1016/j.sjopt.2014.05.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Wani V.B., Kumar N., Sabti K., Raizada S., Rashwan N., Shukkur M.M. Results of screening for retinopathy of prematurity in a large nursery in Kuwait: incidence and risk factors. Indian J Ophthalmol. 2010;58(3):204–208. doi: 10.4103/0301-4738.62644. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Li M.L., Hsu S.M., Chang Y.S., Shih M.H., Lin Y.C., Lin C.H. Retinopathy of prematurity in southern Taiwan: a 10-year tertiary medical center study. J Formos Med Assoc. 2013;112(8):445–453. doi: 10.1016/j.jfma.2012.03.002. [DOI] [PubMed] [Google Scholar]
- 11.Feghhi M., Altayeb S.M., Haghi F., Kasiri A., Farahi F., Dehdashtyan M. Incidence of retinopathy of prematurity and risk factors in the South-Western region of Iran. Middle East Afr J Ophthalmol. 2012;19(1):101–106. doi: 10.4103/0974-9233.92124. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Abdel H.A., Mohamed G.B., Othman M.F. Retinopathy of prematurity: a study of incidence and risk factors in NICU of Al-Minya University Hospital in Egypt. J Clin Neonatol. 2012;1(2):76–81. doi: 10.4103/2249-4847.96755. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Almutez Gharaibeh, Mohammed Khassawneh, Wadah Khriesat, Shadi Alkhatib, Yazan Migdadi. Adopting western retinopathy of prematurity screening programs in eastern countries, are we screening properly? Middle East Afr J Ophthalmol. 2011;18(3):209–213. doi: 10.4103/0974-9233.84047. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Al Alawi E.K., Al Omran M.S., Al Bahrana E.H. Incidence of retinopathy of prematurity in Bahrain, 2002–2011. Middle East Afr J Ophthalmol. 2015;22(3):335–339. doi: 10.4103/0974-9233.159750. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Sarikabadayi Y.U., Aydemir O., Ozen Z.T., Aydemir C., Tok L., Oguz S.S. Screening for retinopathy of prematurity in a large tertiary neonatal intensive care unit in Turkey: frequency and risk factors. Ophthalmic Epidemiol. 2011;18(6):269–274. doi: 10.3109/09286586.2011.615449. [DOI] [PubMed] [Google Scholar]
- 16.Kumar P., Sankar M.J., Deorari A., Azad R., Chandra P., Agarwal R. Risk factors for severe retinopathy of prematurity in preterm low birth weight neonates. Indian J Pediatr. 2011;78(7):812–816. doi: 10.1007/s12098-011-0363-7. [DOI] [PubMed] [Google Scholar]
- 17.O’Keefe M., Kafil-Hussain N., Flitcroft I., Lanigan B. Ocular significance of intraventricular haemorrhage in premature infants. Br J Ophthalmol. 2001;85(3):357–359. doi: 10.1136/bjo.85.3.357. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Hurley B.R., McNamara J.A., Fineman M.S. Laser treatment for retinopathy of prematurity: evolution in treatment technique over 15 years. Retina. 2006;26(7):S16–S17. doi: 10.1097/01.iae.0000244293.94251.20. [DOI] [PubMed] [Google Scholar]
