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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004216naa a2200469 4500
001oai:DiVA.org:uu-323754
003SwePub
008170612s2017 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:135808081
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3237542 URI
024a https://doi.org/10.1002/ijc.307252 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1358080812 URI
040 a (SwePub)uud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Baltzer, Nicholasu Uppsala universitet,Beräkningsbiologi och bioinformatik,Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Stockholm County, Sweden4 aut0 (Swepub:uu)nicba902
2451 0a Risk stratification in cervical cancer screening by complete screening history :b Applying bioinformatics to a general screening population
264 c 2017-04-24
264 1b Wiley,c 2017
338 a print2 rdacarrier
520 a Women screened for cervical cancer in Sweden are currently treated under a one-size-fits-all programme, which has been successful in reducing the incidence of cervical cancer but does not use all of the participants' available medical information. This study aimed to use women's complete cervical screening histories to identify diagnostic patterns that may indicate an increased risk of developing cervical cancer. A nationwide case-control study was performed where cervical cancer screening data from 125,476 women with a maximum follow-up of 10 years were evaluated for patterns of SNOMED diagnoses. The cancer development risk was estimated for a number of different screening history patterns and expressed as Odds Ratios (OR), with a history of 4 benign cervical tests as reference, using logistic regression. The overall performance of the model was moderate (64% accuracy, 71% area under curve) with 61-62% of the study population showing no specific patterns associated with risk. However, predictions for high-risk groups as defined by screening history patterns were highly discriminatory with ORs ranging from 8 to 36. The model for computing risk performed consistently across different screening history lengths, and several patterns predicted cancer outcomes. The results show the presence of risk-increasing and risk-decreasing factors in the screening history. Thus it is feasible to identify subgroups based on their complete screening histories. Several high-risk subgroups identified might benefit from an increased screening density. Some low-risk subgroups identified could likely have a moderately reduced screening density without additional risk.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Cancer och onkologi0 (SwePub)302032 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cancer and Oncology0 (SwePub)302032 hsv//eng
650 7a NATURVETENSKAPx Data- och informationsvetenskapx Bioinformatik0 (SwePub)102032 hsv//swe
650 7a NATURAL SCIENCESx Computer and Information Sciencesx Bioinformatics0 (SwePub)102032 hsv//eng
653 a bioinformatics
653 a cervical cancer
653 a screening
653 a personalized medicine
653 a machine learning
700a Sundström, Karinu Karolinska Institutet4 aut
700a Nygård, Jan F.u Canc Registry Norway, Dept Registry Informat, Oslo, Oslo County, Norway.4 aut
700a Dillner, Joakimu Karolinska Institutet4 aut
700a Komorowski, Janu Uppsala universitet,Beräkningsbiologi och bioinformatik,Polish Acad Sci, Inst Comp Sci, Warsaw, Warsaw County, Poland.4 aut0 (Swepub:uu)jakom133
710a Uppsala universitetb Beräkningsbiologi och bioinformatik4 org
773t International Journal of Cancerd : Wileyg 141:1, s. 200-209q 141:1<200-209x 0020-7136x 1097-0215
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ijc.30725
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-323754
8564 8u https://doi.org/10.1002/ijc.30725
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:135808081

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