Annals
Established in 1927 by the American College of Physicians
:
Advanced search
box Article
 arrow  Table of Contents                
space
box Services
 arrow  Send comment/rapid response letter
space
 arrow  Notify a friend about this article
space
 arrow  Alert me when this article is cited
space
 arrow  Add to Personal Archive
space
 arrow  Download to Citation Manager
space
 arrow  ACP Search                        
space
 arrow  Get Permissions
space
box Google Scholar
 arrow  Search for Related Content
space
box PubMed
Articles in PubMed by Author:
  arrow  Olin, J. W.
space
  arrow  Young, J. R.
space
 arrow  Related Articles in PubMed
space
 arrow  PubMed Citation
space
 arrow  PubMed
space

REPLY

Duplex Scanning of Renal Arteries for Stenosis

right arrow Jeffrey W. Olin, DO; Marion Piedmonte, MA; and Jess R. Young, MD

1 February 1996 | Volume 124 Issue 3 | Page 371


IN RESPONSE:

Dr. Chertow asserts that we erred in our calculations of positive and negative predictive values. Our definitions and our results, however, are correct. In fact, the formula provided by Dr. Chertow defines positive predictive value and negative predictive value exactly as we did.

Positive and negative predictive values depend heavily on disease prevalence; however, when sensitivity and specificity are high, as in our study (both more than 98%) [1], positive and negative predictive values will be very high, given prevalence rates between 20% and 80%. The positive predictive value will be poor only if renovascular disease is very rare. Similarly, the negative predictive value will be poor only if the prevalence of renovascular disease is extremely high.

As stated in our manuscript, our study cohort had a high pretest likelihood of disease [1]. Most patients who were studied had either hypertension that was difficult to control, unexplained azotemia, or both. In a previous study, we showed a disease prevalence of 70% among patients in whom renal artery stenosis was initially suspected. Fewer patients were evaluated because of associated peripheral vascular disease or abdominal aortic aneurysm. Similarly, we have shown that the prevalence of renal artery stenosis in this subgroup was approximately 40% [2]. Therefore, calculations of positive predictive value based on prevalence rates of 1%, 5%, and 10% seriously underestimate the prevalence of renovascular disease in our patient population.

We agree with Appel and colleagues that a normal (or even low) end diastolic velocity does not exclude critical renal artery stenosis. Appel and others have shown that in patients with parenchymal renal disease, the end diastolic velocity may not be elevated in the presence of severe renal artery stenosis. We believe that the increased resistance (resistive index) within the renal circulation may have prevented an increase in the end diastolic velocity. If the end diastolic velocity was 150 cm/sec or greater, 81% of the arteries had renal artery stenosis of 80% or greater [1]; however, an end diastolic velocity of less than 150 cm/sec does not exclude high-grade renal artery stenosis.


Author and Article Information
space
up arrowTop
dotAuthor & Article Info
down arrowReferences

Cleveland Clinic Foundation; Cleveland, OH 44195


References
space
up arrowTop
up arrowAuthor & Article Info
dotReferences

1. Olin JW, Piedmonte MR, Young JR, De Anna S, Grubb M, Childs MB. Utility of duplex ultrasound scanning of the renal arteries for diagnosing significant renal artery stenosis. Ann Intern Med. 1995; 122:833-8.

2. Olin JW, Melia M, Young JR, Graor RA, Risius B. Prevalence of atherosclerotic renal artery stenosis in patients with atherosclerosis elsewhere. Am J Med. 1990; 88:46N-51N.

About Letters
space

The Editors welcome submissions for possible publication in the Letters section. Authors of letters should:

•Include no more than 300 words of text, three authors, and five references

•Type with double-spacing

•Send three copies of the letter, an authors' form signed by all authors, and a cover letter describing any conflicts of interest related to the contents of the letter.

Letters commenting on an Annals article will be considered if they are received within 6 weeks of the time the article was published. Only some of the letters received can be published. Published letters are edited and may be shortened; tables and figures are included only selectively. Authors will be notified that the letter has been received. If the letter is selected for publication, the author will be notified about 3 weeks before the publication date. Unpublished letters cannot be returned.

Annals welcomes electronically submitted letters.





box Article
 arrow  Table of Contents                
space
box Services
 arrow  Send comment/rapid response letter
space
 arrow  Notify a friend about this article
space
 arrow  Alert me when this article is cited
space
 arrow  Add to Personal Archive
space
 arrow  Download to Citation Manager
space
 arrow  ACP Search                        
space
 arrow  Get Permissions
space
box Google Scholar
 arrow  Search for Related Content
space
box PubMed
Articles in PubMed by Author:
  arrow  Olin, J. W.
space
  arrow  Young, J. R.
space
 arrow  Related Articles in PubMed
space
 arrow  PubMed Citation
space
 arrow  PubMed
space


 Home | Current Issue | Past Issues | In the Clinic | ACP Journal Club | CME | Collections | Audio/Video | Mobile | Subscribe | Tools | Help | ACP Online