Annals of Diagnostic Pathology
Volume 14, Issue 2 , Pages 88-93, April 2010

Interobserver diagnostic variability at “moderate” agreement levels could significantly change the prognostic estimates of clinicopathologic studies: evaluation of the problem using evidence from patients with diffuse lung disease

Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center Los Angeles, CA 90048, USA

Abstract 

Does interobserver diagnostic variability (IODV) influence the accuracy of prognostic estimates of clinicopathologic studies? “Best evidence” from usual interstitial pneumonia (UIP) and nonspecific interstitial pneumonia (NSIP) patients was used to investigate the effects of IODV. Systematic literature review identified studies of UIP and NSIP providing “best evidence.” Survival proportions from studies were compared using χ2 and meta-analysis. Interobserver diagnostic variability was simulated in the data arbitrarily at 5% to 30% intervals. The various “diagnoses” were evaluated with κ, and χ2 statistics were used to evaluate the interobserver agreement and compare survival proportions. The survival proportions for UIP and NSIP patients in 7 retrospective level III studies ranged from 11% to 58% and 39% to 100%, respectively. Analysis of simulation results with κ and χ2 statistics showed that IODV greater than 10% resulted in significantly different survival proportion estimations. Interobserver diagnostic variability at moderate agreement levels significantly influences prognostic estimates. Evaluation and minimization of IODV in future clinicopathologic studies are indicated.

Keywords: Evidence based, Interobserver variability, Interstitial lung disease

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1092-9134(09)00151-8

doi:10.1016/j.anndiagpath.2009.12.002

Annals of Diagnostic Pathology
Volume 14, Issue 2 , Pages 88-93, April 2010