Electronic triggers yield speedier cancer diagnosis

Electronic triggers designed to search for key data were able to identify and reduce follow-up delays for patients being evaluated for a diagnosis of colon or prostate cancer.

The full study on the triggers, developed by researchers at Baylor College of Medicine and Michael E. DeBakey Veterans Affairs Medical Center, was published in the Journal of Clinical Oncology.

“Our computerized triggers scanned huge amounts of patient data in the electronic health record and flagged individuals at risk for delays in follow-up of cancer-related abnormal clinical findings,” Hardeep Singh, MD, MPH, associate professor of medicine at Baylor and chief of health policy, quality & informatics program for the Center for Innovations in Quality, Effectiveness and Safety at DeBakey, said in a release. “We created these trigger algorithms in the hopes of being able to leverage electronic health records to improve patient care and safety.”

The investigators’ analysis defined timely follow-up as 30 days for suspected lung cancer, 60 days for colon cancer and 90 days for prostate cancer. Many factors, including primary care workloads, time pressures, information overload, and lack of robust test result tracking systems can contribute to delays in evaluating patients whose original findings were suggestive of cancer, he said.

“There are few, if any, human- or technology-based solutions that efficiently identify such care delays,” said Daniel Murphy, MD, MBA, first author on the paper and instructor in the department of medicine and health services researcher at Baylor and the DeBakey Veterans Affairs Medical Center. “Triggers can act as safeguards as long as the information about potential delays can be communicated to clinicians taking care of these patients.”

Singh and participating researchers recruited 72 primary care clinicians at two study sites for this 15-month study and divided providers into intervention and control groups. In the control group, clinicians followed up suspicious findings through usual procedures whereas in the intervention group, the study team applied triggers twice a month to all patients under their care. Triggers consider the following test results as red flags if the patient did not receive timely follow-up:

  • Positive fecal occult blood test
  • Iron deficiency anemia
  • Elevated prostate specific antigen
  • Abnormal imaging suspicious for cancer

“While all patients flagged by the computerized trigger algorithm in the intervention group are considered at risk, we confirmed the presence of delay by manually reviewing their records and communicating to their clinicians only when necessary,” Singh said.

“Patients seeing clinicians who were notified of potential delays had more timely diagnostic evaluation for both prostate and colon cancer,” Murphy said. “Also, more patients in the intervention part of the study had received diagnostic evaluation by the time we completed our final review.”

“Missed or delayed diagnoses are among the most common patient safety concerns in outpatient settings, and measuring and reducing them are a high priority,” said Singh. “Solutions that harvest and put to use the vast amount of electronic clinical data being collected are essential."

Access the article.

 

Beth Walsh,

Editor

Editor Beth earned a bachelor’s degree in journalism and master’s in health communication. She has worked in hospital, academic and publishing settings over the past 20 years. Beth joined TriMed in 2005, as editor of CMIO and Clinical Innovation + Technology. When not covering all things related to health IT, she spends time with her husband and three children.

Around the web

The American College of Cardiology has shared its perspective on new CMS payment policies, highlighting revenue concerns while providing key details for cardiologists and other cardiology professionals. 

As debate simmers over how best to regulate AI, experts continue to offer guidance on where to start, how to proceed and what to emphasize. A new resource models its recommendations on what its authors call the “SETO Loop.”

FDA Commissioner Robert Califf, MD, said the clinical community needs to combat health misinformation at a grassroots level. He warned that patients are immersed in a "sea of misinformation without a compass."

Trimed Popup
Trimed Popup