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Background
Pathophysiology
Retinopathy of prematurity primarily occurs in extremely low birth weight (ELBW)
infants. Most research suggests that a low birth weight, a young gestational age (GA; see
the Gestational Age from Estimated Date of Delivery calculator), and the severity of
illness (eg, respiratory distress syndrome [RDS], bronchopulmonary
dysplasia [BPD], sepsis) are associated factors. Recently, other associations have been
described. However, the severity of the illness appears to be a major predictor of severe
disease. The smallest, sickest, and most immature infants are at the highest risk for
serious disease. Black infants appear to have less severe retinopathy of prematurity.[1, 2]
Retinal vasculature begins to develop around 16 weeks' gestation. It grows
circumferentially and becomes fully mature at term. Premature birth results in the
cessation of normal retinal vascular maturation. Exposure of newborn premature infants
to hyperoxia downregulates retinal vascular endothelial growth factor (VEGF). Blood
vessels constrict and can become obliterated, resulting in delays of normal retinal
vascular development. This hyperoxia-vasocessation is known as stage I of retinopathy of
prematurity. See the image below.
Stage I retinopathy of
prematurity.
Early on, oxygen and nutrients can be delivered to the retina by means of diffusion from
the underlying choroid capillary bed. The retina continues to grow in thickness and
eventually outgrows its vascular supply. Over time, retinal hypoxia occurs and results in
an overgrowth of vessels; this hypoxia-vasoproliferation is stage II of retinopathy of
prematurity. See the image below.
Stage II retinopathy of
prematurity.
This process is mediated, in part, by VEGF and is affected by insulinlike growth factor-1
(IGF-1) and other cytokines. These changes in the retina result in retinopathy of
prematurity.
Dhaliwal et al found that retinopathy of prematurity occurred with significantly greater
frequency and severity in small-for-GA (SGA) infants compared with appropriate-for-GA
(AGA) infants.[3] In a review of 1413 infants with birth weight less than 1500 g and/or
GA of 26-31 weeks, infants with a birth weight below the tenth percentile for GA were
more likely to develop any stage of retinopathy of prematurity than their AGA peers (p<
0.01) and were more likely to develop severe retinopathy of prematurity (GA of 26-27
weeks, p< 0.01; GA of 28-31 weeks, p = 0.01).
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Epidemiology
Frequency
United States
The incidence varies with birth weight but is reported to be approximately 50-70% in
infants whose weight is less than 1250 g at birth.
Hussain et al reviewed the incidence and the need for surgery in neonates with
retinopathy of prematurity who were born at 22-36 weeks' gestation between July 1989
and June 30, 1997.[4] The incidences were 21.3% (202 of 950 patients) for retinopathy of
prematurity of any stage and 4.6% (44 of 950 patients) for retinopathy of prematurity at
stage III or worse. No retinopathy of prematurity was noted in infants born after 32
weeks' gestation. No infant born after 28 weeks' gestation needed retinal surgery in this
study. Despite the increased survival of ELBW infants, they found a considerable
reduction in the incidence and severity of retinopathy of prematurity compared with
reports from an earlier period. However, infants born before 28 weeks' gestation and
those with birth weights less than 1000 g were at risk to need retinal surgical treatment
for retinopathy of prematurity.
Investigators from the Supplemental Therapeutic Oxygen for Prethreshold Retinopathy of
Prematurity (STOP-ROP) multicenter trial concluded that maintaining oxygen saturation
in the high-90% range did not reduce the severity of the retinopathy when compared with
the saturations in the low-90% range.[5] However, it did result in more adverse pulmonary
events. In a subanalysis of infants who did not have plus disease (ie, tortuosity of vessels)
at the time of study entry, the progression to threshold was significantly decreased when
compared with the progression in infants with plus disease. Thus, a critical window for
oxygen administration may be determined.
International
Retinopathy of prematurity is prevalent worldwide and several reports have detailed the
incidence and risk factors associated with the disease.
A Korean study reported a 20.7% incidence (88 of 425 premature babies) and reported
that a GA of 28 weeks or less and a birth weight of 1000 g or less were the most
significant risk factors.[6] Another study from Singapore reported a 29.2% incidence (165
of 564 ELBW infants).[7] The median age of onset of retinopathy of prematurity was 35
weeks (range, 31-40 wk) postmenstrual age. The risk factors for development of
threshold retinopathy of prematurity by regression analysis were maternal preeclampsia,
birth weight, pulmonary hemorrhage, duration of ventilation, and duration of continuous
positive airway pressure (CPAP).
An observational study from United Kingdom designed to compare the characteristics of
infants with severe retinopathy of prematurity in countries with low, moderate, and high
levels of development found that the mean birth weights of infants from highly developed
countries was 737-763 g compared with 903-1527 g in less-developed countries.[8] Mean
GAs of infants from highly developed countries were 25.3-25.6 weeks compared with
26.3-33.5 weeks in less-developed countries. Thus, larger and more mature infants
seemed to be developing severe retinopathy of prematurity in less-developed nations.
This suggests that individual countries need to develop their own screening programs
with criteria suited to their local population.
Mortality/Morbidity
Long-term outcomes for serious disease include severe visual impairment and blindness.
In addition, myopia, amblyopia, and strabismus may occur. Repka et al described the
need for subsequent ophthalmic intervention in patients with retinopathy of prematurity.[9]
Race
Some reports indicate a decreased incidence of progression to threshold disease in black
infants. Most evidence comes from the Cryotherapy for Retinopathy of Prematurity
(CRYO-ROP) study.[10] Further evidence that black infants are less likely to develop
severe retinopathy of prematurity has been reported in studies of candidemia in ELBW
infants.[11] The exact mechanism for the decreased incidence of progression to surgery in
black infants has not been described. Bizzaro et al showed a strong genetic predisposition
to retinopathy of prematurity when comparing monozygotic twins with dizygotic twins.
[12]
Sex
Although some reports indicate a male predilection, the CRYO-ROP study revealed no
differences based on sex.[10]
Age
26. Good WV, Hardy RJ, Dobson V, et al. The incidence and course of retinopathy of
prematurity: findings from the earlytreatment for retinopathy of prematurity
study. Pediatrics. 2005 Jul. 116(1):15-23.[Medline].
27. Console V, Gagliardi L, De Giorgi A, De Ponti E. Retinopathy of prematurity and
antenatal corticosteroids. The Italian ROP Study Group. Acta Biomed Ateneo
Parmense. 1997. 68 Suppl 1:75-9.[Medline].
28. Wright KW, Sami D, Thompson L, Ramanathan R, Joseph R, Farzavandi S. A
physiologic reduced oxygen protocol decreases the incidence of threshold
retinopathy of prematurity. Trans Am Ophthalmol Soc. 2006. 104:7884. [Medline].
29. Wallace DK. Oxygen saturation levels and retinopathy of prematurity--are we on
target?. J AAPOS. 2006 Oct. 10(5):382-3. [Medline].
30. [Guideline] AAP, AAPOS, AAO. Screening examination of premature infants for
retinopathy of prematurity. A joint statement of the American Academy of
Pediatrics, the American Association for Pediatric Ophthalmology and
Strabismus, and the American Academy of Ophthalmology. Pediatrics. 1997 Aug.
100(2 Pt 1):273. [Medline]. [Full Text].
31. Bremer DL, Palmer EA, Fellows RR, et al. Strabismus in premature infants in the
first year of life. Cryotherapy for Retinopathy of Prematurity Cooperative
Group. Arch Ophthalmol. 1998 Mar. 116(3):329-33. [Medline].
32. Brooks SE, Marcus DM, Gillis D, et al. The effect of blood transfusion protocol
on retinopathy of prematurity: A prospective, randomized study. Pediatrics. 1999
Sep. 104(3 Pt 1):514-8. [Medline].
33. Committee for the Classification of Retinopathy of Prematurity. An international
classification of retinopathy of prematurity. Arch Ophthalmol. 1984 Aug.
102(8):1130-4. [Medline].
34. Connolly BP, McNamara JA, Sharma S, et al. A comparison of laser
photocoagulation with trans-scleral cryotherapy in the treatment of threshold
retinopathy of prematurity. Ophthalmology. 1998 Sep. 105(9):1628-31. [Medline].
35. Cryotherapy for Retinopathy of Prematurity Cooperative Group. Multicenter trial
of cryotherapy for retinopathy of prematurity: preliminary results. Pediatrics.
1988 May. 81(5):697-706. [Medline].
36. Dani C, Reali MF, Bertini G, et al. The role of blood transfusions and iron intake
on retinopathy of prematurity. Early Hum Dev. 2001 Apr. 62(1):57-63. [Medline].
48. Pearce IA, Pennie FC, Gannon LM, et al. Three year visual outcome for treated
stage 3 retinopathy of prematurity: cryotherapy versus laser. Br J Ophthalmol.
1998 Nov. 82(11):1254-9. [Medline].
49. Phelps DL. Retinopathy of prematurity. Pediatr Rev. 1995 Feb. 16(2):506. [Medline].
50. Quinn GE, Dobson V, Kivlin J, et al. Prevalence of myopia between 3 months and
5 1/2 years in preterm infants with and without retinopathy of prematurity.
Cryotherapy for Retinopathy of Prematurity Cooperative Group. Ophthalmology.
1998 Jul. 105(7):1292-300. [Medline].
51. Raju TN, Langenberg P, Bhutani V, Quinn GE. Vitamin E prophylaxis to reduce
retinopathy of prematurity: a reappraisal of published trials. J Pediatr. 1997 Dec.
131(6):844-50. [Medline].
52. Reynolds JD, Hardy RJ, Kennedy KA, et al. Lack of efficacy of light reduction in
preventing retinopathy of prematurity. Light Reduction in Retinopathy of
Prematurity (LIGHT-ROP) Cooperative Group [see comments]. N Engl J Med.
1998 May 28. 338(22):1572-6. [Medline].
53. Saunders RA, Donahue ML, Christmann LM, et al. Racial variation in retinopathy
of prematurity. The Cryotherapy for Retinopathy of Prematurity Cooperative
Group. Arch Ophthalmol. 1997 May. 115(5):604-8. [Medline].
54. Travassos A, Teixeira S, Ferreira P, et al. Intravitreal bevacizumab in aggressive
posterior retinopathy of prematurity. Ophthalmic Surg Lasers Imaging. 2007
May-Jun. 38(3):233-7. [Medline].
55. Vanderveen DK, Mansfield TA, Eichenwald EC. Lower oxygen saturation alarm
limits decrease the severity of retinopathy of prematurity. J AAPOS. 2006 Oct.
10(5):445-8. [Medline].
56. Wallace DK. Oxygen saturation levels and retinopathy of prematurity--are we on
target?. J AAPOS. 2006 Oct. 10(5):382-3. [Medline].
57. Young TL, Anthony DC, Pierce E, et al. Histopathology and vascular endothelial
growth factor in untreated and diode laser-treated retinopathy of prematurity. J
AAPOS. 1997 Jun. 1(2):105-10.[Medline].
Scheme of retina of right eye (RE) and left eye (LE) showing zone borders and clock
hours used to describe location and extent of retinopathy of prematurity.
Zone I retinopathy of prematurity.
Zone II retinopathy of prematurity.
Zone III retinopathy of prematurity.
Stage II retinopathy of prematurity.
Stage III retinopathy of prematurity.
Retinopathy of prematurity.
Retinopathy of prematurity.
Retinopathy of prematurity.
Retinopathy of prematurity.
Retinopathy of prematurity threshold, according to the Cryotherapy for Retinopathy of
Prematurity (CRYO-ROP) cooperative group.
Treatment guidelines, according to the Early Treatment for Retinopathy of Prematurity
(ET-ROP) study.
Laser photocoagulation.
Cryotherapy probe application.