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Policy makers, professional organizations, and patient advocates have called for systems to monitor the quality of cancer care. Cancer registries identify all patients diagnosed with cancer and collect information about their initial treatment. However, registry data are less accurate for ambulatory-based services than hospital-based services than ambulatory services. The more remote from the diagnostic hospital procedure, in both space and time, the less likely the registry is to have the information about the treatment. Cancer registries are uniquely situated to identify a population-based…mehr

Produktbeschreibung
Policy makers, professional organizations, and patient advocates have called for systems to monitor the quality of cancer care. Cancer registries identify all patients diagnosed with cancer and collect information about their initial treatment. However, registry data are less accurate for ambulatory-based services than hospital-based services than ambulatory services. The more remote from the diagnostic hospital procedure, in both space and time, the less likely the registry is to have the information about the treatment. Cancer registries are uniquely situated to identify a population-based sample of cancer patients and remain the best candidate to provide the infrastructure for measuring the quality of cancer care. A significant investment should be made to augment their data collection efforts so that they can reliably document cancer care delivered in the ambulatory setting.
Autorenporträt
Jennifer Malin, MD, PhD, is Associate Professor of Medicine at the University of California, Los Angeles, a health policy analyst at RAND, and a practicing medical oncologist. Her research focuses on evaluating the quality and effectiveness of cancer care and developing methods to evaluate and improve the efficiency of health care.