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Meta-Analysis
. 2021 Jun:5:775-788.
doi: 10.1200/CCI.21.00004.

Leveraging Health Information Technology to Collect Family Cancer History: A Systematic Review and Meta-Analysis

Affiliations
Meta-Analysis

Leveraging Health Information Technology to Collect Family Cancer History: A Systematic Review and Meta-Analysis

Xuan Li et al. JCO Clin Cancer Inform. 2021 Jun.

Abstract

Purpose: Collection of family cancer histories (FCHs) can identify individuals at risk for familial cancer syndromes. The aim of this study is to evaluate the literature on existing strategies whereby providers use information technology to assemble FCH.

Methods: A systematic search of online databases (Ovid MEDLINE, Cochrane, and Embase) between 1980 and 2020 was performed. Statistical heterogeneity was assessed through the chi-square test (ie, Cochrane Q test) and the inconsistency statistic (I2). A random-effects analysis was used to calculate the pooled proportions and means.

Results: The comprehensive search produced 4,005 publications. Twenty-eight studies met inclusion criteria. Twenty-seven information technology tools were evaluated. Eighteen out of 28 studies were electronic surveys administered before visits (18, 64.3%). Five studies administered tablet surveys in offices (5, 17.8%). Four studies collected electronic survey via kiosk before visits (4, 14.3%), and one study used animated virtual counselor during visits (1, 3.6%). Among the studies that use an FCH tool, the pooled estimate of the overall completion rate was 86% (CI, 72% to 96%), 84% (CI, 65% to 97%) for electronic surveys before visits, 89% (CI, 0.74 to 0.98) for tablet surveys, and 85% (CI, 0.66 to 0.98) for surveys via kiosk. Mean time required for completion was 31.0 minutes (CI, 26.1 to 35.9), and the pooled estimate of proportions of participants referred to genetic testing was 12% (CI, 4% to 23%).

Conclusion: Our review found that electronic FCH collection can be completed successfully by patients in a time-efficient manner with high rates of satisfaction.

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Conflict of interest statement

Charlene ThomasTravel, Accommodations, Expenses: Inovio Pharmaceuticals, Nektar, Pfizer Kevin HolcombResearch Funding: Fujirebio DiagnosticsExpert Testimony: Johnson and Johnson Inc Melissa K. FreyResearch Funding: InvitaeNo other potential conflicts of interest were reported.

Figures

FIG 1.
FIG 1.
Preferred Reporting Items for Systematic Reviews and Meta-Analyses flow diagram of search strategy and study selection. FCH, family cancer history.
FIG 2.
FIG 2.
Four strategies for family cancer history collection.
FIG 3.
FIG 3.
(A) Pooled proportion of patients completing any collection tool. (B) Pooled proportion of participants completing tablet collection tool. (C) Pooled proportion of participants completing online survey collection tool. (D) Pooled proportion of participants completing kiosk survey collection tool. (E) Pooled mean time to completion of family cancer histories collection tool. (F) Pooled proportion of participants referred to genetic testing. MRAW, pooled raw means.
FIG 4.
FIG 4.
(A) Pooled proportion of patients completing any collection tool funnel plot. (B) Pooled proportion of participants completing tablet collection tool funnel plot. (C) Pooled proportion of participants completing online survey collection tool funnel plot. (D) Pooled proportion of participants completing kiosk survey collection tool funnel plot. (E) Pooled mean time to completion of family cancer histories collection tool funnel plot. (F) Pooled proportion of participants referred to genetic testing funnel plot.

References

    1. Offit K, Tkachuk KA, Stadler ZK, et al. Cascading after peridiagnostic cancer genetic testing: An alternative to population-based screening J Clin Oncol 381398–14082020 - PMC - PubMed
    1. Childers CP, Childers KK, Maggard-Gibbons M, et al. National estimates of genetic testing in women with a history of breast or ovarian cancer J Clin Oncol 353800–38062017 - PMC - PubMed
    1. Welch BM, Kensaku K.Clinical decision support for genetically guided personalized medicine: A systematic review J Am Med Inform Assoc 20388–4002013 - PMC - PubMed
    1. Frey MK, Kahn RM, Lipkin K, et al. Prospective feasibility trial of a novel strategy of facilitated cascade genetic testing using telephone counseling and mailed saliva kit genetic testing. Gynecol Oncol. 2019;154:281. - PMC - PubMed
    1. Daly MB, Pilarski R, Yurgelun MB, et al. NCCN guidelines insights: Genetic/familial high-risk assessment: Breast, ovarian, and pancreatic, version 1.2020 J Natl Compr Canc Netw 18380–3912020 - PubMed

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