Ophthalmology
Volume 110, Issue 7 , Pages 1396-1402, July 2003

Long-term graft survival after penetrating keratoplasty

  • Robert W Thompson Jr., MD

      Affiliations

    • Price Vision Group, Indianapolis, Indiana, USA
  • ,
  • Marianne O Price, PhD

      Affiliations

    • Cornea Research Foundation of America, Indianapolis, Indiana, USA
  • ,
  • Patrick J Bowers, MD

      Affiliations

    • University of Tennessee College of Medicine, Chattanooga Unit, Chattanooga, Tennessee, USA
  • ,
  • Francis W Price Jr., MD

      Affiliations

    • Price Vision Group, Indianapolis, Indiana, USA
    • Corresponding Author InformationReprint requests to Francis W. Price, Jr., MD, Corneal Consultants of Indiana, 9002 N. Meridian Street, Suite #100, Indianapolis, IN 46260, USA.

Received 28 May 2002; accepted 13 January 2003.

Abstract 

Purpose

To determine long-term graft survival rates and causes of secondary graft failures for a large series of penetrating keratoplasties (PKPs).

Design

Retrospective, noncomparative case series.

Participants

Longitudinal review of 3992 consecutive eyes that underwent PKP at a large tertiary care referral center from 1982 through 1996. Data were collected retrospectively from August 1982 through December 1988 and prospectively thereafter.

Intervention

Three thousand six hundred forty primary grafts and 352 regrafts.

Main outcome measures

Corneal graft survival and etiology of graft failures. Patients were evaluated preoperatively and at 1, 3, 6, 9, 12, 18, and 24 months after transplant, then at yearly intervals.

Results

Mean recipient age was 67 years (range, 1–98 years). The predominant indications for PKP were pseudophakic bullous keratopathy (32%) and Fuchs’ dystrophy (23%). Graft failure occurred in 10% (385) of the eyes. The most common causes of secondary graft failure were endothelial failure (29%) or immunologic endothelial rejection (27%). Survival of first time grafts was 90% at 5 years and 82% at 10 years. Initial regrafts had significantly lower 5-year and 10-year survival rates, 53% and 41%, respectively. The highest 5-year and 10-year survival rates were noted in primary grafts for eyes with a preoperative diagnosis of keratoconus (97% and 92%, respectively), or Fuchs’ dystrophy (97% and 90%, respectively). Primary grafts for aphakic bullous keratopathy without intraocular lens placement had the lowest 5-year survival rate, 70%.

Conclusions

The 5-year and 10-year survival rates in this series demonstrate that PKP is a safe and effective treatment for the corneal diseases commonly transplanted in the United States. However, endothelial failure and immunologic graft rejection were persistent risks over the long term, supporting the need for continued patient follow-up. Regrafts, aphakic eyes without intraocular lens placement at the time of transplant, and corneas with deep stromal vascularization had reduced graft survival rates. Pseudophakic bullous keratopathy grafts with a retained posterior chamber intraocular lens were at increased risk of endothelial failure compared with primary grafts done for other causes or compared with pseudophakic bullous keratopathy grafts done with intraocular lens exchange.

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 Manuscript no. 220351.Supported by grants from the Indiana Lion’s Eye Bank, Indianapolis Indiana, and the Cornea Research Foundation of America, Indianapolis, Indiana.

PII: S0161-6420(03)00463-9

doi:10.1016/S0161-6420(03)00463-9

Ophthalmology
Volume 110, Issue 7 , Pages 1396-1402, July 2003