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Complying with STARD is likely to improve the quality of reporting
As a clinician, I need high quality evidence about
the usefulness, precision, and accuracy of diagnostic tests, and I need it now. Such evidence is rare even for the clinical examination, the
most critical component of the diagnostic process.
1 2
The
situation is getting worse with the exponential increase of diagnostic
tests, most of which have never been evaluated properly and can mislead
the diagnostic process. Although rigorous methodological standards in
research about diagnostic tests have been applied more rigorously in
the past decade, their reporting and methodological quality remain
inadequate.2-5 Against this background, the proposal in
this issue from the authors of Standards for Reporting of Diagnostic Accuracy (STARD) for reporting diagnostic research should be applauded (p 41).3
There is a precedent for a favourable effect of such standards in the
reporting of randomised trials. Since the development of the
Consolidated Standards of Reporting Trials (CONSORT)6 and
their adoption by the International Committee of Medical Journal Editors, the Council of Science Editors, and the World Association of
Medical Editors, the reporting of randomised trials has improved. Although some of this may be due to a growing sophistication among trialists in general, the quality of reports in journals that promoted
CONSORT (BMJ, JAMA, and Lancet) showed
greater improvement than in a journal that did not advocate its use
(New England Journal of Medicine).7 Similarly,
although Devereaux and colleagues found that six of 11 methodological
factors outlined in the CONSORT statement were still reported less than
50% of the time in 105 recently reported randomised trials published
in 29 journals,8 journals that promoted the CONSORT
statement did better than those that did not. Although these are
encouraging results, referees and editors of journals need to do a
better job in ensuring that their authors implement the CONSORT recommendations.
Given that precedent, the STARD criteria, if applied by investigators
and required by editors, may lead to more high quality evidence about
diagnostic tests. But if this evidence is to be used by busy
clinicians, it must be available quickly and in an easily
understandable form. The promise of the "more informative abstract"
has to be fulfilled by authors and journals.9 The STARD
methodological criteria provide the basis for more informative abstracts to accompany diagnostic articles.
Will the publication and recognition of the STARD statement have a
favourable impact on our clinical practice? Although I agree with the
authors of STARD that complete and informative reporting about
diagnostic tests can only lead to better health care, I am confident
that they would agree that the mere introduction of STARD is unlikely
significantly to improve the quality and reporting of diagnostic
research. Just as with the CONSORT statement, more intensive efforts to
apply the guidelines will have to be made by those who develop
diagnostic tests, fund and execute the studies that determine their
clinical usefulness, and report and disseminate their results. This
will not happen without substantial increases in the support of
diagnostic research and in the translation and presentation of its
results to the front lines of clinical care. Alliance between high
quality diagnostic studies that observe the STARD recommendations and
programmes of systematic reviews of diagnostic studies such as the one
initiated by Matthias Egger and Daniel Pewsner are welcome. Egger and
Pewsner have created the Bayes Library of Diagnostic Studies and
Reviews, an international consortium conducting rigorous systematic
reviews of studies of diagnostic accuracy. The alliance should provide
journal editors and translational services with the raw materials that
could give high quality evidence about the usefulness, precision, and
accuracy of diagnostic tests to clinicians, and give it to them now.
Toronto General Hospital, 200 Elizabeth Street, Toronto M5G
2C4, Canada (sstraus{at}mtsinai.on.ca)
Footnotes
Competing interests: SS attended the first STARD consensus conference but did not receive any honorariums.
| 1. | McAlister FA, Straus SE, Sackett DL, on behalf of the CARE-COAD1 Group. Why we need large, simple studies of the clinical examination: the problem and a proposed solution. Lancet 1999; 354: 1721-1724[CrossRef][ISI][Medline]. |
| 2. |
Lijmer JG, Mol BW, Heisterkamp S, Bonsel GJ, Prins MH, van der Meulen JH, et al.
Empirical evidence of design-related bias in studies of diagnostic tests.
JAMA
1999;
282:
1061-1066 |
| 3. |
Bossuyt PM, Reitsma JB, Bruns DE, Gatsonis CA, Glasziou PP, Irwig LM, et al.
Towards complete and accurate reporting of studies of diagnostic accuracy: the STARD initiative.
BMJ
2003;
326:
41-44 |
| 4. | Reid MC, Lachs MS, Feinstein A. Use of methodological standards in diagnostic test research. JAMA 1995; 274: 645-651[Abstract]. |
| 5. | Arroll B, Schechter MT, Sheps SB. The assessment of diagnostic tests: a comparison of medical literature in 1982 and 1985. J Gen Intern Med 1988; 3: 443-447[ISI][Medline]. |
| 6. |
Altman DG, Schulz KF, Moher D, Egger M, Davidoff F, Elbourne D, et al.
The revised CONSORT statement for reporting randomised trials: explanation and elaboration.
Ann Intern Med
2001;
134:
663-694 |
| 7. |
Moher D, Jones A, Lepage L, for the CONSORT group.
Use of the CONSORT statement and quality of reports of randomised trials. A comparative before-and-after evaluation.
JAMA
2001;
285:
1992-1995 |
| 8. | Devereaux PJ, Manns BJ, Ghali WA, Quan H, Guyatt GH. The reporting of methodological factors in randomised controlled trials and the association with a journal policy to promote adherence to the Consolidated Standards of Reporting Trials (CONSORT) checklist. Control Clin Trials 2002; 23: 380-388[CrossRef][ISI][Medline]. |
| 9. | Haynes RB. More informative abstracts: current status and evaluation. J Clin Epidemiol 1993; 46: 595-597[CrossRef][ISI][Medline]. |