Location via proxy:   [ UP ]  
[Report a bug]   [Manage cookies]                
skip to main content
research-article

Unpacking the Use of Laboratory Test Results in an Online Health Community throughout the Medical Care Trajectory

Published: 11 November 2022 Publication History

Abstract

While easy patient access to laboratory test results is necessary for patient engagement in their healthcare, it is not sufficient to enable patients to thrive in this role ? they must be able to understand and act upon these data. In this study, we analyzed posts to an online health community (OHC) that contained a patient's laboratory test results. The objective was to understand the nature of patients' questions related to these data to gain insights into how to better support patients as they individually and collaboratively make sense of their data. We found that patients seek help on the OHC to understand and use their laboratory test results at multiple points in the medical care trajectory. Specifically, in the diagnosis phase, patients tend to be focused on comprehending their data, to be receiving emotionally charged results and, of course, to be engaging the OHC in naming their medical issues. In the treatment phase, patients are often using their laboratory test results to ask more focused questions to identify treatment options, to seek treatment guidance from peers, and to predict the likely course of their disease. Throughout both phases, individuals are highly engaged in the medical process and put in substantial effort to proactively prepare for their care and interactions with doctors. They enlist the OHC in these efforts for many reasons such as a lack of confidence in their doctor. We discuss how gaps in the provision of healthcare services lead to the significant work involved in managing the complex and dynamic interplay between OHCs and the healthcare system. We offer design recommendations both for technologies that provide patients with access to their medical records and for OHCs that will likely continue to play an important role in filling gaps in healthcare services.

References

[1]
J.M. Alpert, A.H. Krist, R.A. Aycock, and G.L. Kreps. 2016. Applying multiple methods to comprehensively evaluate a patient portal's effectiveness to convey information to patients. Journal of Medical Internet Research 18, 5.
[2]
J.S. Ancker, M.C. Miller, V. Patel, and R. Kaushal. 2014. Sociotechnical challenges to developing technologies for patient access to health information exchange data. Journal of the American Medical Informatics Association 21, 4: 664--670.
[3]
Tariq Andersen, Pernille Bjørn, Finn Kensing, and Jonas Moll. 2011. Designing for collaborative interpretation in telemonitoring: Re-introducing patients as diagnostic agents. International Journal of Medical Informatics 80, 8: e112--e126. https://doi.org/10.1016/j.ijmedinf.2010.09.010
[4]
Tariq Osman Andersen, Jørgen Peter Bansler, Finn Kensing, Jonas Moll, Troels Mønsted, Karen Dam Nielsen, Olav Wendelboe Nielsen, Helen Høgh Petersen, and Jesper Hastrup Svendsen. 2018. Aligning Concerns in Telecare: Three Concepts to Guide the Design of Patient-Centred E-Health. Computer Supported Cooperative Work (CSCW) 27, 3--6: 1181--1214. https://doi.org/10.1007/s10606-018--9309--1
[5]
McHale O. Anderson, Sara L. Jackson, Natalia V. Oster, Sue Peacock, Janice D. Walker, Galen Y. Chen, and Joann G. Elmore. 2017. Patients Typing Their Own Visit Agendas Into an Electronic Medical Record: Pilot in a Safety-Net Clinic. The Annals of Family Medicine 15, 2: 158--161. https://doi.org/10.1370/afm.2036
[6]
Onur Asan, Jeanne Tyszka, and Bradley Crotty. 2018. The electronic health record as a patient engagement tool: mirroring clinicians' screen to create a shared mental model. JAMIA Open 1, 1: 42--48. https://doi.org/10.1093/jamiaopen/ooy006
[7]
Amid Ayobi, Paul Marshall, Anna L. Cox, and Yunan Chen. 2017. Quantifying the Body and Caring for the Mind: Self-Tracking in Multiple Sclerosis. 6889--6901. https://doi.org/10.1145/3025453.3025869
[8]
Susanne Barth and Menno D.T. de Jong. 2017. The privacy paradox -- Investigating discrepancies between expressed privacy concerns and actual online behavior -- A systematic literature review. Telematics and Informatics 34, 7: 1038--1058. https://doi.org/10.1016/j.tele.2017.04.013
[9]
Suzanne Bonamici. 2016. 21st Century Cures Act. Retrieved from https://www.congress.gov/bill/114th-congress/house-bill/34/
[10]
Claus Bossen, Kathleen H Pine, Federico Cabitza, Gunnar Ellingsen, and Enrico Maria Piras. 2019. Data work in healthcare: An Introduction. Health Informatics Journal 25, 3: 465--474. https://doi.org/10.1177/1460458219864730
[11]
John Bowers, Graham Button, and Wes Sharrock. 1995. Workflow From Within and Without: Technology and Cooperative Work on the Print Industry Shopfloor. In Proceedings of the Fourth European Conference on Computer-Supported Cooperative Work ECSCW '95, Hans Marmolin, Yngve Sundblad and Kjeld Schmidt (eds.). Springer Netherlands, Dordrecht, 51--66. https://doi.org/10.1007/978--94-011-0349--7_4
[12]
Geoffrey C. Bowker, Stefan Timmermans, Adele E. Clarke, and Ellen Balka (eds.). 2015. Boundary objects and beyond: working with Leigh Star. The MIT Press, Cambridge, Massachusetts.
[13]
Lauren Bussey and Elizabeth Sillence. 2017. (How) do People Negotiate Online Information into their Decision Making with Healthcare Professionals? In Proceedings of the 2017 International Conference on Digital Health - DH '17, 1--5. https://doi.org/10.1145/3079452.3079495
[14]
Ayse G. Büyüktür and Mark S. Ackerman. 2017. Information Work in Bone Marrow Transplant: Reducing Misalignment of Perspectives. In Proceedings of the 2017 ACM Conference on Computer Supported Cooperative Work and Social Computing, 1740--1752. https://doi.org/10.1145/2998181.2998361
[15]
Yunan Chen. 2011. Health Information Use in Chronic Care Cycles. In Proceedings of the ACM 2011 Conference on Computer Supported Cooperative Work (CSCW '11), 485--488. https://doi.org/10.1145/1958824.1958898
[16]
Yunan Chen, Victor Ngo, Sidney Harrison, and Victoria Duong. 2011. Unpacking exam-room computing: negotiating computer-use in patient-physician interactions. In Proceedings of the SIGCHI Conference on Human Factors in Computing Systems, 3343--3352. https://doi.org/10.1145/1978942.1979438
[17]
Yunan Chen and Kathleen Pine. 2014. When Medical Expertise Meets Record Expertise: The Practices of Patient Accessible Medical Records in China. In COOP 2014 - Proceedings of the 11th International Conference on the Design of Cooperative Systems, 27--30 May 2014, Nice (France), Chiara Rossitto, Luigina Ciolfi, David Martin and Bernard Conein (eds.). Springer International Publishing, Cham, 409--426. https://doi.org/10.1007/978--3--319-06498--7_25
[18]
Katherine Y. Chuang and Christopher C. Yang. 2010. Helping you to help me: Exploring supportive interaction in online health community. Proceedings of the American Society for Information Science and Technology 47, 1: 1--10. https://doi.org/10.1002/meet.14504701140
[19]
Chia-Fang Chung, Kristin Dew, Allison M Cole, Jasmine Zia, James A Fogarty, Julie A Kientz, and Sean A Munson. 2016. Boundary Negotiating Artifacts in Personal Informatics: Patient-Provider Collaboration with Patient-Generated Data. 768--784. https://doi.org/10.1145/2818048.2819926
[20]
Andrea Civan and Wanda Pratt. 2007. Threading together patient expertise. AMIA Annual Symposium Proceedings: 140--144.
[21]
Andrea Civan, Meredith M. Skeels, Anna Stolyar, and Wanda Pratt. 2006. Personal health information management: consumers' perspectives. AMIA Annual Symposium Proceedings: 156--160.
[22]
Josephine M. Clayton, Phyllis N. Butow, Martin H.N. Tattersall, Rhonda J. Devine, Judy M. Simpson, Ghauri Aggarwal, Katherine J. Clark, David C. Currow, Louise M. Elliott, Judith Lacey, Philip G. Lee, and Michael A. Noel. 2007. Randomized Controlled Trial of a Prompt List to Help Advanced Cancer Patients and Their Caregivers to Ask Questions About Prognosis and End-of-Life Care. Journal of Clinical Oncology 25, 6: 715--723. https://doi.org/10.1200/JCO.2006.06.7827
[23]
S.A. Collins, D.K. Vawdrey, R. Kukafka, and G.J. Kuperman. 2011. Policies for patient access to clinical data via PHRs: Current state and recommendations. Journal of the American Medical Informatics Association 18, SUPPL. 1: 2--7.
[24]
Clifton F. Conrad. 1978. A Grounded Theory of Academic Change. Sociology of Education 51, 2: 101. https://doi.org/10.2307/2112242
[25]
Juliet M. Corbin and Anselm L. Strauss. 1988. Unending work and care: managing chronic illness at home. Jossey-Bass Publishers, San Francisco.
[26]
Juliet Corbin and Anselm Strauss. 1985. Managing chronic illness at home: Three lines of work. Qualitative Sociology 8, 3: 224--247. https://doi.org/10.1007/BF00989485
[27]
Mayara Costa Figueiredo, Clara Caldeira, Elizabeth Victoria Eikey, Melissa Mazmanian, and Yunan Chen. 2018. Engaging with Health Data: The Interplay Between Self-Tracking Activities and Emotions in Fertility Struggles. Proceedings of the ACM on Human-Computer Interaction 2, CSCW: 1--20. https://doi.org/10.1145/3274309
[28]
Mayara Costa Figueiredo, Clara Caldeira, Tera L. Reynolds, Sean Victory, Kai Zheng, and Yunan Chen. 2017. Self-Tracking for Fertility Care: Collaborative Support for a Highly Personalized Problem. Proceedings of the ACM on Human-Computer Interaction 1, CSCW: 1--21. https://doi.org/10.1145/3134671
[29]
Mayara Costa Figueiredo and Yunan Chen. 2021. Health Data in Fertility Care: An Ecological Perspective. In Proceedings of the 2021 CHI Conference on Human Factors in Computing Systems, 1--17. https://doi.org/10.1145/3411764.3445189
[30]
S.R. Cotten and S.S. Gupta. 2004. Characteristics of online and offline health information seekers and factors that discriminate between them. Social Science and Medicine 59, 9: 1795--1806.
[31]
Elizabeth V. Eikey and Madhu C. Reddy. 2017. ?It's Definitely Been a Journey": A Qualitative Study on How Women with Eating Disorders Use Weight Loss Apps. In Proceedings of the 2017 CHI Conference on Human Factors in Computing Systems, 642--654. https://doi.org/10.1145/3025453.3025591
[32]
Arthur S. Elstein, Lee S. Shulman, and Sarah A. Sprafka. 1978. Medical Problem Solving: An Analysis of Clinical Reasoning. Harvard University Press. https://doi.org/10.4159/harvard.9780674189089
[33]
Sindhu Kiranmai Ernala, Kathan H. Kashiparekh, Amir Bolous, Asra Ali, John M. Kane, Michael L. Birnbaum, and Munmun De Choudhury. 2021. A Social Media Study on Mental Health Status Transitions Surrounding Psychiatric Hospitalizations. Proceedings of the ACM on Human-Computer Interaction 5, CSCW1: 1--32. https://doi.org/10.1145/3449229
[34]
Jordan Eschler, Zakariya Dehlawi, and Wanda Pratt. 2015. Self-Characterized Illness Phase and Information Needs of Participants in an Online Cancer Forum. In Proceedings of the International AAAI Conference on Web and Social Media (1), 101--109. Retrieved from https://ojs.aaai.org/index.php/ICWSM/article/view/14611
[35]
Juan Espinoza, Kelly Crown, and Omkar Kulkarni. 2020. A Guide to Chatbots for COVID-19 Screening at Pediatric Health Care Facilities. JMIR Public Health and Surveillance 6, 2: e18808. https://doi.org/10.2196/18808
[36]
Xiangmin Fan, Daren Chao, Zhan Zhang, Dakuo Wang, Xiaohua Li, and Feng Tian. 2021. Utilization of Self-Diagnosis Health Chatbots in Real-World Settings: Case Study. Journal of Medical Internet Research 23, 1: e19928. https://doi.org/10.2196/19928
[37]
Paolo Fraccaro, Markel Vigo, Panagiotis Balatsoukas, Sabine N. van der Veer, Lamiece Hassan, Richard Williams, Grahame Wood, Smeeta Sinha, Iain Buchan, and Niels Peek. 2018. Presentation of laboratory test results in patient portals: influence of interface design on risk interpretation and visual search behaviour. BMC Medical Informatics and Decision Making 18, 1: 11. https://doi.org/10.1186/s12911-018-0589--7
[38]
D. L. Frosch, S. G. May, K. A. S. Rendle, C. Tietbohl, and G. Elwyn. 2012. Authoritarian Physicians And Patients' Fear Of Being Labeled ?Difficult" Among Key Obstacles To Shared Decision Making. Health Affairs 31, 5: 1030--1038. https://doi.org/10.1377/hlthaff.2011.0576
[39]
P.M. Gee, D.A. Paterniti, D. Ward, and L.M.S. Miller. 2015. e-Patients perceptions of using personal health records for self-management support of chronic illness. CIN - Computers Informatics Nursing 33, 6: 229--237.
[40]
Traber D Giardina, Jessica Baldwin, Daniel T Nystrom, Dean F Sittig, and Hardeep Singh. 2018. Patient perceptions of receiving test results via online portals: a mixed-methods study. Journal of the American Medical Informatics Association 25, 4: 440--446. https://doi.org/10.1093/jamia/ocx140
[41]
Traber Davis Giardina, Varsha Modi, Danielle E. Parrish, and Hardeep Singh. 2015. The patient portal and abnormal test results: An exploratory study of patient experiences. Patient Experience Journal 2, 1: 148--154.
[42]
V. Gilchrist. 2005. Physician Activities During Time Out of the Examination Room. The Annals of Family Medicine 3, 6: 494--499. https://doi.org/10.1370/afm.391
[43]
A. Griffin, A. Skinner, J. Thornhill, and M. Weinberger. 2016. Patient Portals: Who uses them? What features do they use? And do they reduce hospital readmissions? Applied Clinical Informatics 7, 2: 489--501. https://doi.org/10.4338/ACI-2016-01-RA-0003
[44]
Lisa V Grossman, Ruth M Masterson Creber, Natalie C Benda, Drew Wright, David K Vawdrey, and Jessica S Ancker. 2019. Interventions to increase patient portal use in vulnerable populations: a systematic review. Journal of the American Medical Informatics Association. https://doi.org/10.1093/jamia/ocz023
[45]
Xinning Gui and Yunan Chen. 2019. Making Healthcare Infrastructure Work: Unpacking the Infrastructuring Work of Individuals. In Proceedings of the 2019 CHI Conference on Human Factors in Computing Systems, 1--14. https://doi.org/10.1145/3290605.3300688
[46]
M.J. Hall, M.M. Herda, E.A. Handorf, C.C. Rybak, C.A. Keleher, M. Siemon, and M.B. Daly. 2014. Direct-to-patient disclosure of results of mismatch repair screening for Lynch syndrome via electronic personal health record: A feasibility study. Genetics in Medicine 16, 11: 854--861.
[47]
Andrea Hartzler and Wanda Pratt. 2011. Managing the personal side of health: how patient expertise differs from the expertise of clinicians. Journal of Medical Internet Research 13, 3: e62. https://doi.org/10.2196/jmir.1728
[48]
J.N. Haun, J.D. Lind, S.L. Shimada, T.L. Martin, R.M. Gosline, N. Antinori, M. Stewart, and S.R. Simon. 2014. Evaluating user experiences of the secure messaging tool on the veterans affairs' patient portal system. Journal of Medical Internet Research 16, 3.
[49]
Judith H. Hibbard and Peter J. Cunningham. 2008. How engaged are consumers in their health and health care, and why does it matter? Research Brief, 8: 1--9.
[50]
Katrina L. Hinson. 2017. Framing illness through Facebook enabled online support groups. Communication Design Quarterly 4, 2b: 22--31. https://doi.org/10.1145/3068755.3068758
[51]
Inger Holmström and Marta Röing. 2010. The relation between patient-centeredness and patient empowerment: A discussion on concepts. Patient Education and Counseling 79, 2: 167--172. https://doi.org/10.1016/j.pec.2009.08.008
[52]
Jina Huh and Mark S. Ackerman. 2012. Collaborative help in chronic disease management: supporting individualized problems. In Proceedings of the ACM 2012 conference on Computer Supported Cooperative Work - CSCW '12, 853. https://doi.org/10.1145/2145204.2145331
[53]
Jos-Marien Jansen, Karin Niemantsverdriet, Anne Wil Burghoorn, Peter Lovei, Ineke Neutelings, Eva Deckers, and Simon Nienhuijs. 2020. Design for Co-responsibility: Connecting Patients, Partners, and Professionals in Bariatric Lifestyle Changes. In Proceedings of the 2020 ACM Designing Interactive Systems Conference, 1537--1549. https://doi.org/10.1145/3357236.3395469
[54]
Natalie Joseph-Williams, Glyn Elwyn, and Adrian Edwards. 2014. Knowledge is not power for patients: A systematic review and thematic synthesis of patient-reported barriers and facilitators to shared decision making. Patient Education and Counseling 94, 3: 291--309. https://doi.org/10.1016/j.pec.2013.10.031
[55]
Dmitri S. Katz, Blaine A. Price, Simon Holland, and Nicholas Sheep Dalton. 2018. Data, Data Everywhere, and Still Too Hard to Link: Insights from User Interactions with Diabetes Apps. In Proceedings of the 2018 CHI Conference on Human Factors in Computing Systems, 1--12. https://doi.org/10.1145/3173574.3174077
[56]
Michelle M Kelly, Peter L.T. Hoonakker, and Shannon M Dean. 2016. Using an inpatient portal to engage families in pediatric hospital care. Journal of the American Medical Informatics Association: ocw070. https://doi.org/10.1093/jamia/ocw070
[57]
Ariella Kelman, Caroline Robinson, Elisenda Cochin, Nina Ahluwalia, Julia Braverman, Emil Chiauzzi, and Kristina Simacek. 2016. Communicating laboratory test results for rheumatoid factor: what do patients and physicians want? Patient Preference and Adherence Volume 10: 2501--2517. https://doi.org/10.2147/PPA.S104396
[58]
P. Klemm, K. Reppert, and L. Visich. 1998. A nontraditional cancer support group. The Internet. Computers in Nursing 16, 1: 31--36.
[59]
Yubo Kou and Xinning Gui. 2018. Entangled with Numbers: Quantified Self and Others in a Team-Based Online Game. Proceedings of the ACM on Human-Computer Interaction 2, CSCW: 1--25. https://doi.org/10.1145/3274362
[60]
Matthew D Krasowski, Caleb V Grieme, Brian Cassady, Nicholas R Dreyer, Karolyn A Wanat, Maia Hightower, and Kenneth G Nepple. 2017. Variation in results release and patient portal access to diagnostic test results at an academic medical center. Journal of Pathology Informatics 8, 1: 45. https://doi.org/10.4103/jpi.jpi_53_17
[61]
S. Lindsay, S. Smith, P. Bellaby, and R. Baker. 2009. The health impact of an online heart disease support group: a comparison of moderated versus unmoderated support. Health Education Research 24, 4: 646--654. https://doi.org/10.1093/her/cyp001
[62]
Xi Lu, Tera L. Reynolds, Eunkyung Jo, Hwajung Hong, Xinru Page, Yunan Chen, and Daniel A. Epstein. 2021. Comparing Perspectives Around Human and Technology Support for Contact Tracing. In Proceedings of the 2021 CHI Conference on Human Factors in Computing Systems, 1--15. https://doi.org/10.1145/3411764.3445669
[63]
Geneviève Mák, Heather Smith Fowler, Chad Leaver, Simon Hagens, and Jennifer Zelmer. 2015. The Effects of Web-Based Patient Access to Laboratory Results in British Columbia: A Patient Survey on Comprehension and Anxiety. Journal of Medical Internet Research 17, 8: e191. https://doi.org/10.2196/jmir.4350
[64]
Lena Mamykina, Drashko Nakikj, and Noemie Elhadad. 2015. Collective Sensemaking in Online Health Forums. 3217--3226. https://doi.org/10.1145/2702123.2702566
[65]
Lena Mamykina, Arlene M. Smaldone, and Suzanne R. Bakken. 2015. Adopting the sensemaking perspective for chronic disease self-management. Journal of Biomedical Informatics 56: 406--417. https://doi.org/10.1016/j.jbi.2015.06.006
[66]
Joshua C Mandel, David A Kreda, Kenneth D Mandl, Isaac S Kohane, and Rachel B Ramoni. 2016. SMART on FHIR: a standards-based, interoperable apps platform for electronic health records. Journal of the American Medical Informatics Association 23, 5: 899--908. https://doi.org/10.1093/jamia/ocv189
[67]
Philipp Mayring. 2000. Qualitative Content Analysis. Forum Qualitative Sozialforschung / Forum: Qualitative Social Research 1, 2.
[68]
D. Mechanic, D. D. McAlpine, and M. Rosenthal. 2001. Are patients' office visits with physicians getting shorter? The New England Journal of Medicine 344, 3: 198--204. https://doi.org/10.1056/NEJM200101183440307
[69]
Anne Moen and Patricia Flatley Brennan. 2005. Health@Home: The Work of Health Information Management in the Household (HIMH): Implications for Consumer Health Informatics (CHI) Innovations. Journal of the American Medical Informatics Association 12, 6: 648--656. https://doi.org/10.1197/jamia.M1758
[70]
Priya Nambisan. 2011. Information seeking and social support in online health communities: impact on patients' perceived empathy. Journal of the American Medical Informatics Association 18, 3: 298--304. https://doi.org/10.1136/amiajnl-2010-000058
[71]
Lisa Neal, Kate Oakley, Gitte Lindgaard, David Kaufman, Jan Marco Leimeister, and Ted Selker. 2007. Online health communities. In CHI '07 extended abstracts on Human factors in computing systems - CHI '07, 2129. https://doi.org/10.1145/1240866.1240965
[72]
Lynn Nielsen-Bohlman, Allison M. Panzer, and David A. Kindig. 2004. Introduction. National Academies Press (US). Retrieved September 19, 2016 from http://www.ncbi.nlm.nih.gov/books/NBK216033/
[73]
Danielle Ofri. 2018. What patients say, what doctors hear.
[74]
Aisling Ann O'Kane and Helena Mentis. 2012. Sharing medical data vs. health knowledge in chronic illness care. In Proceedings of the 2012 ACM annual conference extended abstracts on Human Factors in Computing Systems Extended Abstracts - CHI EA '12, 2417. https://doi.org/10.1145/2212776.2223812
[75]
Sharoda A. Paul and Madhu C. Reddy. 2010. Understanding Together: Sensemaking in Collaborative Information Seeking. In Proceedings of the 2010 ACM Conference on Computer Supported Cooperative Work (CSCW '10), 321--330. https://doi.org/10.1145/1718918.1718976
[76]
Carol Peckham. 2016. Medscape Physician Compensation Report 2016: Minutes Personally Spent with Each Patient. Retrieved February 23, 2017 from http://www.medscape.com/features/slideshow/compensation/2016/public/overview#page=26
[77]
Anja Perlich and Christoph Meinel. 2016. Patient-Provider Teamwork via Cooperative Note Taking on Tele-Board MED. Studies in Health Technology and Informatics 228: 117--121.
[78]
Adam T. Perzynski, Mary Joan Roach, Sarah Shick, Bill Callahan, Douglas Gunzler, Randall Cebul, David C. Kaelber, Anne Huml, John Daryl Thornton, and Douglas Einstadter. 2017. Patient portals and broadband internet inequality. Journal of the American Medical Informatics Association 24, 5: 927--932. https://doi.org/10.1093/jamia/ocx020
[79]
Adrienne Pichon, Kayla Schiffer, Emma Horan, Bria Massey, Suzanne Bakken, Lena Mamykina, and Noemie Elhadad. 2021. Divided We Stand: The Collaborative Work of Patients and Providers in an Enigmatic Chronic Disease. Proceedings of the ACM on Human-Computer Interaction 4, CSCW3: 1--24. https://doi.org/10.1145/3434170
[80]
Catherine Plaisant, Richard Mushlin, Aaron Snyder, Jia Li, Dan Heller, and Ben Shneiderman. 2003. LifeLines: Using Visualization to Enhance Navigation and Analysis of Patient Records. In The Craft of Information Visualization. Elsevier, 308--312. https://doi.org/10.1016/B978--155860915-0/50038-X
[81]
Shriti Raj, Mark W. Newman, Joyce M. Lee, and Mark S. Ackerman. 2017. Understanding Individual and Collaborative Problem-Solving with Patient-Generated Data: Challenges and Opportunities. Proceedings of the ACM on Human-Computer Interaction 1, CSCW: 1--18. https://doi.org/10.1145/3134723
[82]
Madhu C. Reddy, Paul Dourish, and Wanda Pratt. 2006. Temporality in Medical Work: Time also Matters. Computer Supported Cooperative Work (CSCW) 15, 1: 29--53. https://doi.org/10.1007/s10606-005--9010-z
[83]
Tera L Reynolds, N Ali, E McGregor, T O'Brien, C Longhurst, AL Rosenberg, SE Rudkin, and K Zheng. 2017. Understanding Patient Questions about their Medical Records in an Online Health Forum: Opportunity for Patient Portal Design. In AMIA Annual Symposium Proceedings. https://doi.org/29854216
[84]
Tera L. Reynolds, Nida Ali, and Kai Zheng. 2020. What Do Patients and Caregivers Want? A Systematic Review of User Suggestions to Improve Patient Portals. In AMIA Annual Symposium Proceedings. https://doi.org/33936483
[85]
D. R. Rhoades, K. F. McFarland, W. H. Finch, and A. O. Johnson. 2001. Speaking and interruptions during primary care office visits. Family Medicine 33, 7: 528--532.
[86]
William C Richardson, Donald M Berwick, JC Bisgard, LR Bristow, CR Buck, CK Cassel, and others. 2001. Crossing the quality chasm: a new health system for the 21st century. Institute of Medicine, National Academy Press Washington, DC.
[87]
Sean Robinson, Melissa Reed, Travis Quevillon, and Ed Hirvi. 2019. Patient perceptions and interactions with their web portal-based laboratory results. BMJ Health & Care Informatics 26, 1: e000012. https://doi.org/10.1136/bmjhci-2019-000012
[88]
Douglas J. Rupert, Rebecca R. Moultrie, Jennifer Gard Read, Jacqueline B. Amoozegar, Alexandra S. Bornkessel, Amie C. O'Donoghue, and Helen W. Sullivan. 2014. Perceived healthcare provider reactions to patient and caregiver use of online health communities. Patient Education and Counseling 96, 3: 320--326. https://doi.org/10.1016/j.pec.2014.05.015
[89]
U. Sarkar, A.J. Karter, J.Y. Liu, N.E. Adler, R. Nguyen, A. López, and D. Schillinger. 2010. The literacy divide: Health literacy and the use of an internet-based patient portal in an integrated health system-results from the diabetes study of Northern California (DISTANCE). Journal of Health Communication 15, SUPPL. 2: 183--196.
[90]
Kjeld Schmidt and Liam Bannon. 1992. Taking CSCW seriously: Supporting articulation work. Computer Supported Cooperative Work (CSCW) 1, 1--2: 7--40. https://doi.org/10.1007/BF00752449
[91]
Woosuk Seo, Ayse G. Buyuktur, Sung Won Choi, Laura Sedig, and Sun Young Park. 2021. Challenges in the Parent-Child Communication of Health-related Information in Pediatric Cancer Care. Proceedings of the ACM on Human-Computer Interaction 5, CSCW1: 1--24. https://doi.org/10.1145/3449184
[92]
Woosuk Seo, Ayse G. Buyuktur, Sanya Verma, Hyeryoung Kim, Sung Won Choi, Laura Sedig, and Sun Young Park. 2021. Learning from Healthcare Providers' Strategies: Designing Technology to Support Effective Child Patient-Provider Communication. In Proceedings of the 2021 CHI Conference on Human Factors in Computing Systems, 1--15. https://doi.org/10.1145/3411764.3445120
[93]
Johanna Shapiro. 1993. The use of narrative in the doctor-patient encounter. Family Systems Medicine 11, 1: 47--53. https://doi.org/10.1037/h0089128
[94]
Tamar Sharon. 2017. Self-Tracking for Health and the Quantified Self: Re-Articulating Autonomy, Solidarity, and Authenticity in an Age of Personalized Healthcare. Philosophy & Technology 30, 1: 93--121. https://doi.org/10.1007/s13347-016-0215--5
[95]
Heather L Shepherd, Alexandra Barratt, Anna Jones, Deborah Bateson, Karen Carey, Lyndal J Trevena, Kevin McGeechan, Chris B Del Mar, Phyllis N Butow, Ronald M Epstein, Vikki Entwistle, and Edith Weisberg. 2016. Can consumers learn to ask three questions to improve shared decision making? A feasibility study of the ASK (AskShareKnow) Patient-Clinician Communication Model® intervention in a primary health-care setting. Health Expectations 19, 5: 1160--1168. https://doi.org/10.1111/hex.12409
[96]
Edward H. Shortliffe and James J. Cimino (eds.). 2013. Biomedical informatics: computer applications in health care and biomedicine. Springer, New York.
[97]
Jamie Skipper. 2012. Individuals' Access to Their Own Health Information. The Office of the National Coordinator for Health Information Technology.
[98]
Jacob Solomon, Aaron M. Scherer, Nicole L. Exe, Holly O. Witteman, Angela Fagerlin, and Brian J. Zikmund-Fisher. 2016. Is This Good or Bad?: Redesigning Visual Displays of Medical Test Results in Patient Portals to Provide Context and Meaning. In Proceedings of the 2016 CHI Conference Extended Abstracts on Human Factors in Computing Systems (CHI EA '16), 2314--2320. https://doi.org/10.1145/2851581.2892523
[99]
Stephanie B. Steinhardt and Steven J. Jackson. 2015. Anticipation Work: Cultivating Vision in Collective Practice. In Proceedings of the 18th ACM Conference on Computer Supported Cooperative Work & Social Computing, 443--453. https://doi.org/10.1145/2675133.2675298
[100]
B.D. Steitz, R.M. Cronin, S.E. Davis, E. Yan, and G.P. Jackson. 2017. Long-term patterns of patient portal use for pediatric patients at an academic medical center. Applied Clinical Informatics 8, 3: 779--793. https://doi.org/10.4338/ACI-2017-01-RA-0005
[101]
Anselm L. Strauss, Shizuko Fagerhaugh, Barbara Suczek, and Carolyn Wiener. 1997. Social organization of medical work. Transaction Publishers, New Brunswick, N.J., U.S.A.
[102]
Si Sun, Xiaomu Zhou, Joshua C. Denny, Trent Rosenbloom, and Hua Xu. 2012. Understanding patient-provider communication entered via a patient portal system. Proceedings of the American Society for Information Science and Technology 49, 1: 1--4. https://doi.org/10.1002/meet.14504901387
[103]
Christine M. Swoboda, Matthew J. DePuccio, Naleef Fareed, Ann Scheck McAlearney, and Daniel M. Walker. 2021. Patient Portals: Useful for Whom and for What? A Cross-Sectional Analysis of National Survey Data. Applied Clinical Informatics 12, 03: 573--581. https://doi.org/10.1055/s-0041--1731339
[104]
M.J.W. Thomas. 2002. Learning within incoherent structures: the space of online discussion forums: Learning within incoherent structures. Journal of Computer Assisted Learning 18, 3: 351--366. https://doi.org/10.1046/j.0266--4909.2002.03800.x
[105]
Alexandra Dundas Todd and Sue Fisher (eds.). 1993. The Social organization of doctor-patient communication. Ablex Pub. Corp, Norwood, N.J.
[106]
Tiffany C. Veinot, Jessica S. Ancker, Heather Cole-Lewis, Elizabeth D. Mynatt, Andrea G. Parker, Katie A. Siek, and Lena Mamykina. 2019. Leveling Up: On the Potential of Upstream Health Informatics Interventions to Enhance Health Equity. Medical Care 57: S108--S114. https://doi.org/10.1097/MLR.0000000000001032
[107]
Xi Wang, Kang Zhao, and Nick Street. 2017. Analyzing and Predicting User Participations in Online Health Communities: A Social Support Perspective. Journal of Medical Internet Research 19, 4: e130. https://doi.org/10.2196/jmir.6834
[108]
Karl E. Weick. 1995. Sensemaking in Organizations. SAGE.
[109]
Jennifer L. Welbourne, Anita L. Blanchard, and Marla D. Boughton. 2009. Supportive communication, sense of virtual community and health outcomes in online infertility groups. In Proceedings of the fourth international conference on Communities and technologies - C&T '09, 31. https://doi.org/10.1145/1556460.1556466
[110]
Frank H. Wians. 2009. Clinical Laboratory Tests: Which, Why, and What Do The Results Mean? Laboratory Medicine 40, 2: 105--113. https://doi.org/10.1309/LM404L0HHUTWWUDD
[111]
Thomas Ashby Wills. 1985. Supportive functions of interpersonal relationships. In Social support and health. Academic Press, San Diego, CA, 61--82.
[112]
Qian Yang, John Zimmerman, Aaron Steinfeld, Lisa Carey, and James F. Antaki. 2016. Investigating the Heart Pump Implant Decision Process: Opportunities for Decision Support Tools to Help. In Proceedings of the 2016 CHI Conference on Human Factors in Computing Systems, 4477--4488. https://doi.org/10.1145/2858036.2858373
[113]
Alyson L. Young and Andrew D. Miller. 2019. ?This Girl is on Fire": Sensemaking in an Online Health Community for Vulvodynia. In Proceedings of the 2019 CHI Conference on Human Factors in Computing Systems, 1--13. https://doi.org/10.1145/3290605.3300359
[114]
Michael J. Young, Ethan Scheinberg, and Harold Bursztajn. 2014. Direct-to-Patient Laboratory Test Reporting: Balancing Access With Effective Clinical Communication. JAMA 312, 2: 127. https://doi.org/10.1001/jama.2014.5823
[115]
Jing Zhang. 2017. Supporting Information Needs of Transitional Phases in Diabetes Management Through Online Health Communities. In Companion of the 2017 ACM Conference on Computer Supported Cooperative Work and Social Computing, 107--111. https://doi.org/10.1145/3022198.3024942
[116]
Zhan Zhang, Yegin Genc, Dakuo Wang, Mehmet Eren Ahsen, and Xiangmin Fan. 2021. Effect of AI Explanations on Human Perceptions of Patient-Facing AI-Powered Healthcare Systems. Journal of Medical Systems 45, 6: 64. https://doi.org/10.1007/s10916-021-01743--6
[117]
Zhan Zhang, Yu Lu, Yubo Kou, Danny T. Y. Wu, Jina Huh-Yoo, and Zhe He. 2019. Understanding Patient Information Needs About Their Clinical Laboratory Results: A Study of Social Q&A Site. Studies in Health Technology and Informatics 264: 1403--1407. https://doi.org/10.3233/SHTI190458
[118]
B.J. Zikmund-Fisher, N.L. Exe, and H.O. Witteman. 2014. Numeracy and literacy independently predict patients' ability to identify out-of-range test results. Journal of Medical Internet Research 16, 8: e187.
[119]
Brian J Zikmund-Fisher, Aaron M Scherer, Holly O Witteman, Jacob B Solomon, Nicole L Exe, Beth A Tarini, and Angela Fagerlin. 2017. Graphics help patients distinguish between urgent and non-urgent deviations in laboratory test results. Journal of the American Medical Informatics Association 24, 3: 520--528. https://doi.org/10.1093/jamia/ocw169
[120]
2009. Health Information Technology for Economic and Clinical Health (HITECH) Act in American Recovery and Reinvestment Act of 2009. Retrieved July 10, 2017 from https://www.gpo.gov/fdsys/pkg/PLAW-111publ5/html/PLAW-111publ5.htm
[121]
2021. Trends and Disparities in Patient Portal Use. National Institutes of Health (NIH). Retrieved from https://hints.cancer.gov/docs/Briefs/HINTS_Brief_45.pdf
[122]
Health Literacy. National Library of Medicine. Retrieved from https://nnlm.gov/initiatives/topics/health-literacy
[123]
Thyroglobulin. MedlinePlus. Retrieved from https://medlineplus.gov/lab-tests/thyroglobulin/

Cited By

View all
  • (2024)Creating Safe Places: Understanding the Lived Experiences of Families Managing Cystic Fibrosis in Young ChildrenProceedings of the 2024 CHI Conference on Human Factors in Computing Systems10.1145/3613904.3642334(1-18)Online publication date: 11-May-2024
  • (2024)Data work and practices in healthcare: A scoping reviewInternational Journal of Medical Informatics10.1016/j.ijmedinf.2024.105348184(105348)Online publication date: Apr-2024

Index Terms

  1. Unpacking the Use of Laboratory Test Results in an Online Health Community throughout the Medical Care Trajectory

      Recommendations

      Comments

      Information & Contributors

      Information

      Published In

      cover image Proceedings of the ACM on Human-Computer Interaction
      Proceedings of the ACM on Human-Computer Interaction  Volume 6, Issue CSCW2
      CSCW
      November 2022
      8205 pages
      EISSN:2573-0142
      DOI:10.1145/3571154
      Issue’s Table of Contents
      Permission to make digital or hard copies of all or part of this work for personal or classroom use is granted without fee provided that copies are not made or distributed for profit or commercial advantage and that copies bear this notice and the full citation on the first page. Copyrights for components of this work owned by others than the author(s) must be honored. Abstracting with credit is permitted. To copy otherwise, or republish, to post on servers or to redistribute to lists, requires prior specific permission and/or a fee. Request permissions from [email protected].

      Publisher

      Association for Computing Machinery

      New York, NY, United States

      Publication History

      Published: 11 November 2022
      Published in PACMHCI Volume 6, Issue CSCW2

      Permissions

      Request permissions for this article.

      Check for updates

      Author Tags

      1. medical care trajectory
      2. medical records
      3. online health community

      Qualifiers

      • Research-article

      Contributors

      Other Metrics

      Bibliometrics & Citations

      Bibliometrics

      Article Metrics

      • Downloads (Last 12 months)81
      • Downloads (Last 6 weeks)12
      Reflects downloads up to 10 Nov 2024

      Other Metrics

      Citations

      Cited By

      View all
      • (2024)Creating Safe Places: Understanding the Lived Experiences of Families Managing Cystic Fibrosis in Young ChildrenProceedings of the 2024 CHI Conference on Human Factors in Computing Systems10.1145/3613904.3642334(1-18)Online publication date: 11-May-2024
      • (2024)Data work and practices in healthcare: A scoping reviewInternational Journal of Medical Informatics10.1016/j.ijmedinf.2024.105348184(105348)Online publication date: Apr-2024

      View Options

      Get Access

      Login options

      Full Access

      View options

      PDF

      View or Download as a PDF file.

      PDF

      eReader

      View online with eReader.

      eReader

      Media

      Figures

      Other

      Tables

      Share

      Share

      Share this Publication link

      Share on social media