2013
DOI: 10.1002/bjs.9166
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Population-based data from the Swedish Colon Cancer Registry

Abstract: These population-based data represent good-quality reference points.

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citations
Cited by 91 publications
(86 citation statements)
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References 18 publications
(21 reference statements)
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“…Due to the few cases of CRC, a simplified model was used to calculate losses of QALYs due to CRC. We made an approximation of stage-specific survival rates based on data from the Swedish Colorectal Cancer Registry (SCRCR) 2007-2011 [19]: Stages I and II -100% survival; Stage III -50% deceased on year five after one year of terminal care; and Stage IV -100% deceased after one year of palliative care. Stage distribution at CRC diagnosis was also based on data from the SCRCR.…”
Section: Calculation Of Qalysmentioning
confidence: 99%
“…Due to the few cases of CRC, a simplified model was used to calculate losses of QALYs due to CRC. We made an approximation of stage-specific survival rates based on data from the Swedish Colorectal Cancer Registry (SCRCR) 2007-2011 [19]: Stages I and II -100% survival; Stage III -50% deceased on year five after one year of terminal care; and Stage IV -100% deceased after one year of palliative care. Stage distribution at CRC diagnosis was also based on data from the SCRCR.…”
Section: Calculation Of Qalysmentioning
confidence: 99%
“…A further problem can be accurate identification and timing of the primary diagnosis, leading to incorrect times to future health outcome events (such as treatment, readmission or death) 43 . The process by which individuals are identified for inclusion in the database can also result in subtle biases (such as lead-time bias as a consequence of a screening programme) 2 . Procedure codes, at least as far as is necessary for clinical management or reimbursement purposes, may be more accurately recorded than diagnostic coding in administrative databases, although they tend to lack detail 15 .…”
Section: Data Qualitymentioning
confidence: 99%
“…Additionally, the main challenges associated with using these data sources for research purposes are considered. Clinical databases come in two main forms ( Table 1) 2,12,13 : administrative databases (for example, HES in England 14 or insurance claims data in the USA, such as Medicare 15 ), set up to collect management and/or reimbursement data; and clinical registries focusing on a disease (Swedish Colon Cancer Registry 2 ), or device/procedure-based registries (UK Transcatheter Aortic Valve Implantation (TAVI) registry 16 ) that tend to focus primarily on quality improvement and enable research as a secondary process. The main advantages of using such data sources are: their comprehensive nature (some provide complete coverage for an entire population 2 ); the relatively large number of patients, allowing subgroups and rare events to be investigated; and the ability to compare healthcare providers, at both the institution and individual healthcare-professional level.…”
Section: Introductionmentioning
confidence: 99%
“…Results are similarly improved in rectal cancer, potentially also challenging routines developed based upon studies performed in the past. More intensive staging at diagnosis, better surgery, more careful pathological examinations and discussions at multidisciplinary team meetings all contribute to improved outcomes overall and in the separate stages, so called stage migration [56][57][58].…”
Section: Modifying the Time Interval To Surgerymentioning
confidence: 99%