Stages of ROP
Stage I — Mildly
abnormal blood vessel growth. Many children who develop stage I improve
with no treatment and eventually develop normal vision. The disease
resolves on its own without further progression.
Stage II — Moderately
abnormal blood vessel growth. Many children who develop stage II
improve with no treatment and eventually develop normal vision. The
disease resolves on its own without further progression.
Stage III — Severely
abnormal blood vessel growth. The abnormal blood vessels grow toward
the center of the eye instead of following their normal growth pattern
along the surface of the retina. Some infants who develop stage III
improve with no treatment and eventually develop normal vision.
However, when infants have a certain degree of Stage III and "plus
disease" develops, treatment is considered. "Plus disease" means that
the blood vessels of the retina have become enlarged and twisted,
indicating a worsening of the disease. Treatment at this point has a
good chance of preventing retinal detachment.
Stage IV — Partially
detached retina. Traction from the scar produced by bleeding, abnormal
vessels pulls the retina away from the wall of the eye.
Stage V — Completely
detached retina and the end stage of the disease. If the eye is left
alone at this stage, the baby can have severe visual impairment and
even blindness.
Most babies who develop ROP have stages I or II. However, in a small
number of babies, ROP worsens, sometimes very rapidly. Untreated ROP
threatens to destroy vision.
The Risk Factors associated with ROP:
In addition to birth weight and how
early a baby is born, other factors contributing to the risk of ROP
include anemia, blood transfusions, respiratory distress, breathing
difficulties, and the overall health of the infant.
An ROP epidemic occurred in the 1940s and early 1950s when hospital
nurseries began using excessively high levels of oxygen in incubators
to save the lives of premature infants. During this time, ROP was the
leading cause of blindness in children in the US. In 1954, scientists
funded by the National Institutes of Health determined that the
relatively high levels of oxygen routinely given to premature infants
at that time were an important risk factor, and that reducing the level
of oxygen given to premature babies reduced the incidence of ROP. With
newer technology and methods to monitor the oxygen levels of infants,
oxygen use as a risk factor has diminished in importance.
Although it had been suggested as a factor in the development of ROP,
researchers supported by the National Eye Institute determined that
lighting levels in hospital nurseries has no effect on the development
of ROP.
What is Plus disease?
As ROP progresses, more and more
shunting occurs in the neovascular tissue at the retinal
vascular-avascular junction. This increased retinal vascular blood flow
results in dilation and tortuosity of the major retinal arteries and
veins in the posterior pole - a development described as "plus
disease". For an eye to qualify as having plus disease, these vascular
changes must be present in at least two of the four quadrants around
the optic nerve.
What is Rush disease?
Rapidly progressive, very severe ROP in posterior zone I is a poor
prognostic sign and is frequently called "rush disease".


