Communicating incidental and reportable findings from research MRIs: considering factors beyond the findings in an underrepresented pediatric population

Kiley B Vander Wyst, Micah L Olson, Smita S Bailey, Ana Martinez Valencia, Armando Peña, Jeffrey Miller, Mitchell Shub, Lee Seabrooke, Janiel Pimentel, Kiri Olsen, Robert B Rosenberg, Gabriel Q Shaibi, Kiley B Vander Wyst, Micah L Olson, Smita S Bailey, Ana Martinez Valencia, Armando Peña, Jeffrey Miller, Mitchell Shub, Lee Seabrooke, Janiel Pimentel, Kiri Olsen, Robert B Rosenberg, Gabriel Q Shaibi

Abstract

Background: The application of advanced imaging in pediatric research trials introduces the challenge of how to effectively handle and communicate incidental and reportable findings. This challenge is amplified in underserved populations that experience disparities in access to healthcare as recommendations for follow-up care may be difficult to coordinate. Therefore, the purpose of the present report is to describe the process for identifying and communicating findings from a research MRI to low-income Latino children and families.

Methods: Latino adolescents (n = 86) aged 12-16 years old with obesity and prediabetes underwent a research MRI (3 Tesla Philips Ingenia®) as part of a randomized controlled diabetes prevention trial. The research MRIs were performed at baseline and 6 months to assess changes in whole-abdominal fat distribution and organ fat in response to the intervention. An institutional pathway was developed for identifying and reporting findings to participants and families. The pathway was developed through a collaborative process with hospital administration, research compliance, radiology, and the research team. All research images were reviewed by a board-certified pediatric radiologist who conveyed findings to the study pediatrician for determination of clinical actionability and reportability to children and families. Pediatric sub-specialists were consulted as necessary and a primary care practitioner (PCP) from a free community health clinic agreed to receive referrals for uninsured participants.

Results: A total of 139 images (86 pre- and 53 post-intervention) were reviewed with 31 findings identified and 23 deemed clinically actionable and reportable. The only reportable finding was severely elevated liver fat (> 10%, n = 14) with the most common and concerning incidental findings being horseshoe kidney (n = 1) and lung lesion (n = 1). The remainder (n = 7) were less serious. Of youth with a reportable or incidental finding, 18 had a PCP but only 7 scheduled a follow-up appointment. Seven participants without a PCP were referred to a safety-net clinic for follow-up.

Conclusions: With the increased utilization of high-resolution imaging in pediatric research, additional standardization is needed on what, when, and how to return incidental and reportable findings to participants, particularly among historically underrepresented populations that may be underserved in the community.

Trial registration: Preventing Diabetes in Latino Youth, NCT02615353.

Conflict of interest statement

The authors declare that they have no competing interests.

© 2021. The Author(s).

Figures

Fig. 1
Fig. 1
Preventing Diabetes in Latino Youth CONSORT Flow Diagram
Fig. 2
Fig. 2
Timeline of Major Events Leading to Development of an Institutional Pathway
Fig. 3
Fig. 3
Institutional Pathway for Identification and Reporting Incidental (IFs) and Reportable Findings

References

    1. Wong CA, Hernandez AF, Califf RM. Return of research results to study participants uncharted and untested. JAMA. 2018;320:435–436. doi: 10.1001/jama.2018.7898.
    1. Office for Human Research Protections. Attachment F - Recommendations on Reporting Incidental Findings.
    1. Presidential Commission for the Study of Bioethical Issues. ANTICIPATE and COMMUNICATE: Ethical Management of Incidental and Secondary Findings in the Clinical , Research , and Direct-to-Consumer Contexts. Washington, D.C.; 2013.
    1. Li Y, Thompson WK, Reuter C, Nillo R, Jernigan T, Dale A, et al. Rates of incidental findings in brain magnetic resonance imaging in children. JAMA Neurol. 2021;78:578–587. doi: 10.1001/jamaneurol.2021.0306.
    1. Meacham MC, Starks H, Burke W, Edwards K. Researcher perspectives on disclosure of incidental findings in genetic research. J Empir Res Hum Res Ethics. 2010;5:31–41. doi: 10.1525/jer.2010.5.3.31.
    1. Wolf SM. Introduction: the challenge of incidental findings. J Law Med Ethics. 2008;36:216–218. doi: 10.1038/jid.2014.371.
    1. Cheng TL, Emmanuel MA, Levy DJ, Jenkins RR. Child health disparities: what can a clinician do? Pediatrics. 2015;136:962–968.
    1. Butler AM. Social determinants of health and racial/ethnic disparities in type 2 diabetes in youth. Curr Diab Rep. 2017;17:2–5. doi: 10.1007/s11892-017-0885-0.
    1. Mackay D. Returning incidental findings in low-resource settings: a case of rescue? Hast Cent Rep. 2018;48:28–30. doi: 10.1002/hast.852.
    1. Sullivan HK, Berkman BE. Incidental findings in low-resource settings. Hast Cent Rep. 2018;48:20–28. doi: 10.1002/hast.851.
    1. Merritt MW, Taylor HA, Mullany LC. Ancillary care in community-based public health intervention research. Am J Public Health. 2010;100:211–216. doi: 10.2105/AJPH.2009.168393.
    1. Pérez-Escamilla R. Health care access among Latinos: implications for social and health care reforms. J Hispanic High Educ. 2010;9:43–60. doi: 10.1177/1538192709349917.
    1. Flores G, Vega LR. Barriers to health care access for Latino children: a review. Fam Med. 1998;30:196–205.
    1. Cyr ME, Etchin AG, Guthrie BJ, Benneyan JC. Access to specialty healthcare in urban versus rural US populations: a systematic literature review. BMC Health Serv Res. 2019;19:1–17. doi: 10.1186/s12913-019-4815-5.
    1. Sanchez-Birkhead AC, Kennedy HP, Callister LC, Miyamoto TP. Navigating a new health culture: experiences of immigrant hispanic women. J Immigr Minor Health. 2011;13:1168–1174. doi: 10.1007/s10903-010-9369-x.
    1. Bade E, Evertsen J, Smiley S, Banerjee I. Navigating the health care system: a view from the urban medically underserved. Wis Med J. 2008;107:374–379.
    1. Madden EF. Cultural health capital on the margins: cultural resources for navigating healthcare in communities with limited access. Soc Sci Med. 2015;133:145–152. doi: 10.1016/j.socscimed.2015.04.006.
    1. Vega WA, Rodriguez MA, Gruskin E. Health disparities in the latino population. Epidemiol Rev. 2009;31:99–112. doi: 10.1093/epirev/mxp008.
    1. Marciano L, Camerini AL, Schulz PJ. The role of health literacy in diabetes knowledge, self-care, and glycemic control: a Meta-analysis. J Gen Intern Med. 2019;34:1007–1017. doi: 10.1007/s11606-019-04832-y.
    1. Parker RM, Ratzan SC, Lurie N. Health literacy: a policy challenge for advancing high-quality health care. Health Aff. 2003;22:147–153. doi: 10.1377/hlthaff.22.4.147.
    1. Clark LT, Watkins L, Piña IL, Elmer M, Akinboboye O, Gorham M, et al. Increasing diversity in clinical trials: overcoming critical barriers. Curr Probl Cardiol. 2019;44:148–172. doi: 10.1016/j.cpcardiol.2018.11.002.
    1. Gibson LM, Paul L, Chappell FM, Macleod M, Whiteley WN, Salman RAS, et al. Potentially serious incidental findings on brain and body magnetic resonance imaging of apparently asymptomatic adults: systematic review and meta-analysis. BMJ. 2018;363.
    1. Hegenscheid K, Seipel R, Puls R. Potentially relevant incidental findings on research whole-body MRI in the general adult population : frequencies and management 2013;:816–826.
    1. Rangel EK. The Management of Incidental Findings in Neuro-imaging research. Framework Recommendations. 2010.
    1. Gur RE, Kaltman D, Melhem ER, Ruparel K, Prabhakaran K, Riley M, et al. Incidental findings in youths volunteering for brain MRI research. Am J Neuroradiol. 2013;34:2021–2025. doi: 10.3174/ajnr.A3525.
    1. Jansen PR, Dremmen M, van den Berg A. Incidental findings on brain imaging in the general pediatric population. N Engl J Med. 2017;377:19–21. doi: 10.1056/NEJMc1710724.
    1. Anastasova V, Mahalatchimy A, Rial-Sebbag E, Antó Boqué JM, Keil T, Sunyer J, et al. Communication of results and disclosure of incidental findings in longitudinal paediatric research. Pediatr Allergy Immunol. 2013;24:389–394. doi: 10.1111/pai.12087.
    1. Kaiser D, Leach J, Vannest J, Schapiro M, Holland S. Unanticipated findings in pediatric neuroimaging research: prevalence of abnormalities and process for reporting and clinical follow-up. Brain Imaging Behav. 2015;9:32–42. doi: 10.1007/s11682-014-9327-7.
    1. Kovanlikaya A, Mittelman SD, Ward A, Geffner ME, Dorey F, Gilsanz V. Obesity and fat quantification in lean tissues using three-point Dixon MR imaging. Pediatr Radiol. 2005;35:601–607. doi: 10.1007/s00247-005-1413-y.
    1. Samara A, Ventura EE, Alfadda AA, Goran MI. Use of MRI and CT for fat imaging in children and youth: what have we learned about obesity, fat distribution and metabolic disease risk? Obes Rev. 2012;13:723–732. doi: 10.1111/j.1467-789X.2012.00994.x.
    1. Pacifico L, di Martino M, Catalano C, Panebianco V, Bezzi M, Anania C, et al. T1-weighted dual-echo MRI for fat quantification in pediatric nonalcoholic fatty liver disease. World J Gastroenterol. 2011;17:3012–3019. doi: 10.3748/wjg.v17.i25.3012.
    1. Soltero EG, Konopken YP, Olson ML, Keller CS, Castro FG, Williams AN, et al. Preventing diabetes in obese Latino youth with prediabetes: a study protocol for a randomized controlled trial. BMC Public Health. 2017;17:1–12. doi: 10.1186/s12889-017-4174-2.
    1. Vander Wyst KB, Olson ML, Hooker E, Soltero EG, Konopken YP, Keller CS, et al. Yields and costs of recruitment methods with participant phenotypic characteristics for a diabetes prevention research study in an underrepresented pediatric population. Trials. 2020;21:1–11. doi: 10.1186/s13063-020-04658-8.
    1. Sarrami M, Ridley W, Nightingale S, Wright T, Kumar R. Adolescent gallstones—need for early intervention in symptomatic idiopathic gallstones. Pediatr Surg Int. 2019;35:569–574. doi: 10.1007/s00383-019-04461-w.
    1. Weizer AZ, Silverstein AD, Auge BK, Delvecchio FC, Raj G, Albala DM, et al. Determining the incidence of horseshoe kidney from radiographic data at a single institution. J Urol. 2003;170:1722–1726. doi: 10.1097/01.ju.0000092537.96414.4a.
    1. Borhani AA, Wiant A, Heller MT. Cystic hepatic lesions: a review and an algorithmic approach. Am J Roentgenol. 2014;203:1192–1204. doi: 10.2214/AJR.13.12386.
    1. Kwatra S, Krishnappa V, Mhanna C, Murray T, Novak R, Sethi SK, et al. Cystic diseases of childhood: a review. Urology. 2017;110:184–191. doi: 10.1016/j.urology.2017.07.040.
    1. Escobar-Morreale HF. Polycystic ovary syndrome: definition, aetiology, diagnosis and treatment. Nat Rev Endocrinol. 2018;14:270–284. doi: 10.1038/nrendo.2018.24.
    1. Schwimmer JB, Deutsch R, Kahen T, Lavine JE, Stanley C, Behling C. Prevalence of fatty liver in children and adolescents. Pediatrics. 2006;118:1388–1393. doi: 10.1542/peds.2006-1212.
    1. Seki A, Uchiyama H, Fukushi T, Sakura O, Tatsuya K. Incidental findings of brain magnetic resonance imaging study in a pediatric cohort in Japan and recommendation for a model management protocol. J Epidemiol. 2010;20(SUPPL.2):498–504. doi: 10.2188/jea.JE20090196.
    1. Kim BS, Illes J, Kaplan RT, Reiss A, Atlas SW. Incidental findings on pediatric MR images of the brain. Am J Neuroradiol. 2002;23:1674–1677.
    1. Pietro NC Di, Illes J. Disclosing Incidental Findings in Brain Research : The Rights of Minors in Decision-Making 2013;1013:1009–1013.
    1. Zadig P, von Brandis E, Lein RK, Rosendahl K, Avenarius D, Ording Müller LS. Whole-body magnetic resonance imaging in children – how and why? A systematic review. Pediatr Radiol. 2020.
    1. Anupindi SA, Bedoya MA, Lindell RB, Rambhatla SJ, Zelley K, Nichols KE, et al. Diagnostic performance of whole-body MRI as a tool for cancer screening in children with genetic cancer-predisposing conditions. Am J Roentgenol. 2015;205:400–408. doi: 10.2214/AJR.14.13663.
    1. Welsh JA, Karpen S, Vos MB. Increasing prevalence of nonalcoholic fatty liver disease among United States adolescents, 1988-1994 to 2007-2010. J Pediatr. 2013;162:496–500.e1. doi: 10.1016/j.jpeds.2012.08.043.
    1. Betancourt-Garcia MM, Arguelles A, Montes J, Hernandez A, Singh M, Forse RA. Pediatric nonalcoholic fatty liver disease: the rise of a lethal disease among Mexican American Hispanic children. Obes Surg. 2017;27:236–244. doi: 10.1007/s11695-016-2440-5.
    1. Pan JJ, Fallon MB. Gender and racial differences in nonalcoholic fatty liver disease. World J Hepatol. 2014;6:274–283. doi: 10.4254/wjh.v6.i5.274.
    1. Vos MB, Abrams SH, Barlow SE, Caprio S, Daniels SR, Kohli R, et al. NASPGHAN clinical practice guideline for the diagnosis and treatment of nonalcoholic fatty liver disease in. Children. 2017.
    1. Wilfond BS, Carpenter KJ. Incidental findings in pediatric research. J Law Med Ethics. 2008;36:332–340. doi: 10.1111/j.1748-720X.2008.00277.x.
    1. Sanders LM, Shaw JS, Guez G, Baur C, Rudd R. Health literacy and child health promotion: implications for research, clinical care, and public policy. Pediatrics. 2009;124(SUPPL):3.
    1. Guntzviller LM, Jensen JD, Carreno LM. Latino children’s ability to interpret in health settings: a parent–child dyadic perspective on child health literacy. Commun Monogr. 2017;84:143–163. doi: 10.1080/03637751.2016.1214871.
    1. Banas JR, Ball JW, Wallis LC, Gershon S. The adolescent health care broker—adolescents interpreting for family members and themselves in health care. J Community Health. 2017;42:739–747. doi: 10.1007/s10900-016-0312-5.
    1. Manganello JA. Health literacy and adolescents: a framework and agenda for future research. Health Educ Res. 2008;23:840–847. doi: 10.1093/her/cym069.
    1. Oh SS, Galanter J, Thakur N, Pino-Yanes M, Barcelo NE, White MJ, et al. Diversity in clinical and biomedical research: a promise yet to be fulfilled. PLoS Med. 2015;12:1–9. doi: 10.1371/journal.pmed.1001918.
    1. Royal JM, Peterson BS. The risks and benefits of searching for incidental findings in MRI research scans Jason. J Law Med Ethics. 2008;36:301–212. doi: 10.1038/jid.2014.371.
    1. Schaefer GO, Savulescu J. The right to know: a revised standard for reporting incidental findings. Hast Cent Rep. 2018;48:22–32. doi: 10.1002/hast.836.

Source: PubMed

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