Background: Multitarget stool DNA (mt-sDNA) is an increasingly utilized noninvasive option for colorectal cancer screening; however, its impact is limited by imperfect test adherence. Tailored patient navigation (TPN) improves adherence for other cancer screening tests, but its role in mt-sDNA is not known.
Aim: Determine whether TPN improves mt-sDNA completion and reduces sample could not be processed (SCNBP) result rates.
Setting: A large, urban, academic primary care clinic serving a medically vulnerable population.
Participants: All patients who received mt-sDNA order in 2022 and 2023.
Program Description: A patient navigator outreached all patients ordered mt-sDNA to support test completion during the 12-month intervention period in 2023.
Program Evaluation: Rates of mt-sDNA completion within 90 days and SCNBP results were compared between the 12-month intervention and pre-intervention periods using generalized estimating equations. A total of 2694 patients received 3297 orders during the study. TPN was significantly associated with improved rates of 90-day mt-sDNA completion (51% vs. 39%, OR 1.67, p < .001) and SCNBP results (4% vs. 5%, OR 0.55, p < .001).
Discussion: Tailored patient navigation was associated with improved rates of mt-sDNA completion and SCNBP results despite built-in navigation services provided by the manufacturer. TPN for mt-sDNA is a promising strategy for enhancing colorectal cancer screening uptake.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1007/s11606-024-09201-y | DOI Listing |
J Gen Intern Med
November 2024
Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Background: Multitarget stool DNA (mt-sDNA) is an increasingly utilized noninvasive option for colorectal cancer screening; however, its impact is limited by imperfect test adherence. Tailored patient navigation (TPN) improves adherence for other cancer screening tests, but its role in mt-sDNA is not known.
Aim: Determine whether TPN improves mt-sDNA completion and reduces sample could not be processed (SCNBP) result rates.
J Gastrointest Cancer
October 2024
Digestive Disease Research Center, Medical University of South Carolina, Charleston, SC, USA.
Background: Multitarget stool DNA (MT-sDNA) tests (here, Cologuard®) are currently used in average-risk patients as a primary method of screening for colorectal cancer. However, MT-sDNA testing has also been used in patients who previously underwent colonoscopy who wish to avoid repeat colonoscopy. Here, in a large primary care practice setting, our aim was to evaluate the diagnostic performance of MT-sDNA testing in patients with a previously normal colonoscopy.
View Article and Find Full Text PDFJ Cancer Educ
July 2024
Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
BMJ Open Gastroenterol
July 2024
Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.
Objective: To identify the optimal incentive protocol for maximising participation while managing study costs during the Voyage trial.
Design: Prospective cohort (Voyage trial) of colorectal cancer (CRC) incidence and mortality outcomes in individuals screened with multitarget stool DNA (mt-sDNA) served as the population. A subset was randomised to receive postage stamps as a pre-consent incentive, or as a post-consent incentive after completion of the consent and questionnaire.
Soc Sci Med
January 2024
Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Colorectal cancer (CRC) screening continues to be underutilized in the US despite the availability of multiple effective, guideline-recommended screening options. Provider recommendation has been consistently shown to improve screening completion. Yet, available literature provides little information as to how specific information providers communicate influence patient decision-making about CRC screening.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!