Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1995;22(2):138-44.

New developments in the diagnosis and management of cardiac allograft vasculopathy

Affiliations
Free PMC article
Review

New developments in the diagnosis and management of cardiac allograft vasculopathy

M R Mehra et al. Tex Heart Inst J. 1995.
Free PMC article

Abstract

The major cause of late death in cardiac transplant recipients is cardiac allograft vasculopathy, also referred to as cardiac transplant atherosclerosis, which occurs in as many as 45% of transplant recipients who survive longer than 1 year. It differs from typical atherosclerosis in that intimal hyperplasia is concentric and diffuse, the internal elastic lamina remains intact, calcification is rare, and the disease tends to develop rapidly. Intravascular ultrasound and coronary angioscopy are more sensitive diagnostic measures of cardiac allograft vasculopathy than is coronary angiography. Although retransplantation at present seems to be the only definitive therapy for cardiac allograft vasculopathy, it has shown only fair results. Recent studies have suggested that calcium entry blockers and angiotensin-converting enzyme inhibitors may play a beneficial role in delaying the progression of cardiac allograft vasculopathy.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Circulation. 1992 Jan;85(1):69-77 - PubMed
    1. Circulation. 1992 Mar;85(3):979-87 - PubMed
    1. Lab Invest. 1968 Jul;19(1):97-112 - PubMed
    1. Lancet. 1969 Nov 22;2(7630):1088-92 - PubMed
    1. Circulation. 1970 May;41(5):753-72 - PubMed

MeSH terms

Substances

LinkOut - more resources