Contributed by Lisa Olen| 10 October, 2005  21:28 GMT
 Mistakes in diagnosing cancer are common and often result in delays and additional costs that are harmful to patients.
Diagnosing cancer typically requires obtaining and examining tissue samples using procedures that are prone to error and consequently result in harm to the patient, according to a new study published in
Cancer, the journal of the
American Cancer Society.
In a study funded by the Agency for Healthcare Research and Quality, a government-mandated error detection method found up to 12 percent of reviewed specimens had an erroneous diagnosis.
Stephen S. Raab, MD, of the University of Pittsburgh School of Medicine and colleagues examined tissue specimens, pathologists' findings, and medical records from four institutions that diagnose precancerous and cancerous lesions in an effort to characterize the frequency, cause and impact of errors in cancer diagnosis.
Multiple Tests, Different Results
Patients often have multiple tests in order to diagnose cancer. The researchers reviewed cases when multiple tests produced different diagnoses for the same individual.
Errors were frequent and institution-dependent, they found.
Up to 9 percent of gynecologic specimen pairs (Pap test and cervical biopsy) were incorrect. Up to 12 percent of non-gynecologic specimen pairs contained an error.
Differences in institutional error rates most likely are related to bias in error reporting, the researchers suggest, although better methods may have resulted in fewer mistakes at some institutions.
Most of the errors were due to poor specimen collection. The proportion of errors attributed to pathologist misinterpretation ranged from 5-50 percent. Pathologists frequently disagreed with the assignment of error cause when reviewing specimens from other institutions.
Delayed Diagnoses
Gynecologic errors led to harm in 45 percent of cases, while non-gynecologic errors were harmful in 39 percent of cases, a review of medical records showed.
The most likely harm consists of diagnosis delays and costly additional testing. The researchers note that is very rare that unneeded procedures are performed for the false positive diagnosis of cancer.
Pathologists disagreed on the severity of harm resulting from an error in cancer diagnosis.
This study demonstrates a relatively high frequency of error, the researchers say. Also, variability in practice makes it difficult to understand what factors are causing the mistakes.
"The standardization and uniform reporting of errors in cancer diagnosis is a first step in improving safety," the authors conclude.
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