Skip to main content
. Author manuscript; available in PMC: 2009 Jan 23.
Published in final edited form as: N Engl J Med. 2000 Feb 10;342(6):381–389. doi: 10.1056/NEJM200002103420603

Table 3.

Incidence of Worsening of Retinopathy between the End of the Dcct and After Four Years of the Edic Study.*

Retinal Change NO. of
Patients
Progression of
Retinopathy
Adjusted Odds
Reduction
(95% CI)§
P
Value
percent
Severe nonproliferative retinopathy or worse 76 (52-88) <0.001
Conventional therapy 556 10
Intensive therapy 589 2
Proliferative retinopathy 74 (46-87) <0.001
Conventional therapy 564 9
Intensive therapy 590 2
Clinically significant macular edema 77 (52-89) <0.001
Conventional therapy 564 8
Intensive therapy 582 2
Laser therapy (focal or scatter) 77 (45-91) 0.002
Conventional therapy 544 6
Intensive therapy 575 1
*

DCCT denotes Diabetes Control and Complications Trial, EDIC Epidemiology of Diabetes Intervention and Complications, and CI confidence interval.

Patients who underwent scatter photocoagulation after the DCCT were counted as having a progression of retinopathy; those who underwent focal photocoagulation were counted as having clinically significant macular edema.

The numbers of patients free of each specific type of worsening at the end of the DCCT are given.

§

The odds reduction is for former intensive therapy as compared with former conventional therapy on the basis of a logistic-regression analysis with adjustment for the level of severity of retinopathy at the end of the DCCT according to the Early Treatment Diabetic Retinopathy Study categories shown in Table 2, plus any previous laser therapy (focal or scatter).

P values were calculated by the likelihood-ratio test.