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Assessing impact of organised breast screening across small residential areas—development and internal validation of a prediction model
Authors:G. Farshid MBBS  MD   FRCPA  FFSc   G. Gill MBBS  MD   FRACS  J. Kollias FRACS  MD  B. Koczwara BM  BS   FRACP  MBioethics  C. Karapetis MBBS  FRACP   MMedSc  J. Adams MBBS  PhD   FRACP  MRCP   R. Joshi MBBS  MD   FRACP  D. Keefe PSM  MBBS   MD  FRACP   FRCP  T. Niyonsenga MSC  PhD  K. Powell BABus  K. Fusco BHlth Sci  DipBiomedSc  M. Eckert MPH  DNurs   MN  DipAppSc  K. Beckmann PhD  MPH   BSc  D. Roder DDSc    MPH  BDS
Affiliation:1. Centre for Population Health Research, University of South Australia, Adelaide, SA, Australia;2. SA Health, BreastScreen SA, Adelaide, SA, Australia;3. Breast Endocrine and Surgical Oncology Unit, RAH, Discipline of Surgery, University of Adelaide, North Terrace, Adelaide, SA, Australia;4. SA Health, Adelaide, SA, Australia;5. Department of Medical Oncology, Flinders University, Adelaide, SA, Australia;6. Medical Oncology, Lyell McEwin Hospital, Elizabeth Vale, SA, Australia;7. Royal Adelaide Hospital, Adelaide, SA, Australia;8. South Australian Health & Medical Research Institute, Adelaide, SA, Australia;9. Cancer Nursing, University of South Australia, Adelaide, SA, Australia
Abstract:Monitoring screening mammography effects in small areas is often limited by small numbers of deaths and delayed effects. We developed a risk score for breast cancer death to circumvent these limitations. Screening, if effective, would increase post‐diagnostic survivals through lead‐time and related effects, as well as mortality reductions. Linked cancer and BreastScreen data at four hospitals (n = 2,039) were used to investigate whether screened cases had higher recorded survivals in 13 small areas, using breast cancer deaths as the outcome (M1), and a risk of death score derived from TNM stage, grade, histology type, hormone receptor status, and related variables (M2). M1 indicated lower risk of death in screened cases in 12 of the 13 areas, achieving statistical significance (p < .05) in 5. M2 indicated lower risk scores in screened cases in all 13 areas, achieving statistical significance in 12. For cases recently screened at diagnosis (<6 months), statistically significant reductions applied in 8 areas (M1) and all 13 areas (M2). Screening effects are more detectable in small areas using these risk scores than death itself as the outcome variable. An added advantage is the application of risk scores for providing a marker of screening effect soon after diagnosis.
Keywords:breast screening  effect monitoring  small areas
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