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Title: Electronic reminders for pathologists promote recognition of patients at risk for Lynch syndrome: cluster-randomised controlled trial.
Author(s): Overbeek, L.I.H. (29898315X)
Hermens, R.P.M.G. (242577334)
Krieken, J.H.J.M. van (071431772)
Adang, E.M.M. (153669063)
Casparie, M.
Nagengast, F.M. (073940569)
Ligtenberg, M.J.L. (088914763)
Hoogerbrugge-van der Linden, N. (101110200)
Publication year: 2010
Document type: Article / Letter to editor
Journal: Virchows Archiv
ISSN: 0945-6317
Volume: vol. 456
Issue: iss. 6
Start page: p. 653
End page: p. 659
Abstract: We investigated success factors for the introduction of a guideline on recognition of Lynch syndrome in patients recently diagnosed with colorectal cancer (CRC) below age 50 or a second CRC below age 70. Pathologists were asked to start microsatellite instability (MSI) testing and report to surgeons with the advice to consider genetic counselling when MSI test or family history was positive. A multicentre cluster-randomised controlled trial (ClinicalTrials.gov, number NCT00141466) was performed in 12 pathology laboratories (clusters), serving 29 community hospitals. All received an introduction to the new guideline. In the intervention group, surgeons received education and tumour test result reminders; pathologists were provided with inclusion criteria cards, an electronic patient inclusion reminder system and feedback on inclusion. Two hundred sixty-six CRC patients were eligible for recognition as at risk for Lynch syndrome. The actual recognition was 18% more successful in the intervention as compared to the control arm (77% (120 of 156) compared to 59% (65 of 110)), with an adjusted odds ratio (OR) = 2.8 (95% confidence interval (CI) 1.1-7.0). The electronic reminder system for pathologists was most strongly associated with recognition of high-risk patients, OR = 4.2 (95% CI 1.7-10.1). An electronic reminder system for pathologists appeared effective for adherence to a new complex guideline and will enhance the recognition of Lynch syndrome.
Subject: IGMD 2: Molecular gastro-enterology and hepatology
IGMD 3: Genomic disorders and inherited multi-system disorders
NCEBP 1: Molecular epidemiology
NCEBP 4: Quality of hospital and integrated care
NCMLS 3A: Genetics and epigenetic pathways of disease
ONCOL 1: Hereditary cancer and cancer-related syndromes
ONCOL 3: Translational research
ONCOL 4: Quality of Care
ONCOL 5: Aetiology, screening and detection
Organization: Human Genetics
IQ Healthcare
Pathology
Epidemiology, Biostatistics & HTA
UMCN Extern
Gastroenterology
Medical Oncology
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/88721

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