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180702 r ||| eng |
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|a Self-collected versus clinician collected samples for sexually transmitted infection testing in women
|h Elektronische Ressource
|b a review of comparative clinical effectiveness cost-effectiveness, and guidelines
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|a CADTH Rapid Response Service
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|a Ottawa (ON)
|b Canadian Agency for Drugs and Technologies in Health
|c 2016, 22 June 2016
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|a 1 PDF file (38 pages)
|b illustrations
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|a Includes bibliographical references
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|a Comparative Effectiveness Research
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|a Sexually Transmitted Diseases / diagnosis
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|a Canada
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|a Cost-Benefit Analysis
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| 653 |
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|a Women's Health
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|a Treatment Outcome
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| 653 |
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|a Specimen Handling / methods
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|a Self Care
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|a Canadian Agency for Drugs and Technologies in Health
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|a eng
|2 ISO 639-2
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|b NCBI
|a National Center for Biotechnology Information
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|a Rapid response report: summary with critical appraisal
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|u https://www.ncbi.nlm.nih.gov/books/NBK373480
|3 Volltext
|n NLM Bookshelf Books
|3 Volltext
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|a 610
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|a The purpose of this report is to examine the clinical effectiveness, cost-effectiveness, and evidence-based guidelines regarding the use self-collected samples for sexually transmitted infections (STI) testing, as compared with samples collected by clinicians
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