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Nearly 40 percent of individuals will be diagnosed with cancer at some point in their lifetime. For these individuals, access, exchange, and use of electronic health information is critical to managing their complex health needs. Patient access to online medical records enable these individuals to track their health information, communicate with their care team, and request refills of medications. In 2016, the President’s Cancer Panel sought to improve cancer-related outcomes with connected health by calling attention to enabling individuals to manage their health information and participate in their care across the cancer continuum. This data brief uses the National Cancer Institute’s nationally representative Health Information National Trends Survey (HINTS) to examine the access and use of health information technology by individuals diagnosed with cancer. To achieve a robust sample, we have combined data from the 2017 and 2018 surveys.
Figure 1: Percent of individuals who were offered access to their online medical record by a health care provider or insurer by individual’s cancer status, 2017-2018 combined sample.

Figure 2: Frequency of viewing an online medical record within the past year among those who had been offered an online medical record by a health care provider or insurer by cancer status, 2017-2018 combined sample.

Table 1: Reasons for not accessing online medical record as reported by individuals who did not view their online medical record within the past year by cancer status, 2017-2018 combined sample.
| Previous Cancer Diagnosis | |||
|---|---|---|---|
| Reason for Not Using Online Record | Never Had Cancer | Recent Cancer Diagnosis | Cancer Survivor |
| Prefer to speak to health care provider directly | 73% | 88%^ | 80% |
| Did not have a need to use your online medical record | 62% | 55% | 60% |
| Concerned about the privacy/security of online medical record | 20% | 24% | 19% |
| No longer have an online medical record | 16% | 12% | 15% |
| Do not have a way to access the website | 15% | 11% | 12% |
Figure 3: Types of information reported in individuals’ online medical record amongst those who were offered and accessed their record at least once by cancer status, 2017-2018 combined sample.

Table 2: Reported online medical record functionalities used by individuals who were offered and accessed their record at least once by cancer status, 2017-2018 combine sample.
| Previous Cancer Diagnosis | |||
|---|---|---|---|
| Use of Online Medical Record | Never Had Cancer | Recent Cancer Diagnosis | Cancer Survivor |
| Convenience Functions | |||
| Request refill of medications | 38% | 41% | 45% |
| Fill out forms or paperwork related to your health care | 41% | 49% | 32% |
| Updating Medical Record | |||
| Request correction of inaccurate information | 7% | 7% | 4% |
| Add health information | 22% | 22% | 22% |
| Communicating with Health Care Provider | |||
| Securely message health care provider and staff (e.g., e-mail) | 51% | 47% | 41% |
| Download or Transmit | |||
| Download online medical record | 21% | 22% | 23% |
| Transmit data to outside party (e.g., healthcare provider, caregiver, service, or app) | 15% | 23% | 15% |
| Self-Management and Decision Making | |||
| Help you make a decision about how to treat an illness or condition | 22% | 27% | 18% |
Table 3: Socio-demographic and health-related characteristics of individuals by cancer status, 2017-2018 combined sample.
| Previous Cancer Diagnosis | ||||
|---|---|---|---|---|
| Characteristic | Never Had Cancer (reference) | Recent Cancer Diagnosis | Cancer Survivor | |
| Gender | Male | 49% | 47% | 40%* |
| Female | 51% | 53% | 60%* | |
| Age | 18-34 | 25% | 4%* | 3%* |
| 35-46 | 22% | 8%* | 8%* | |
| 47-64 | 37% | 42% | 36% | |
| 65+ | 17% | 46%* | 53%* | |
| Race/Ethnicity | Hispanic | 16% | 9%* | 8%* |
| Non-Hispanic Asian | 6% | < 1%* | 2%* | |
| Non-Hispanic Black | 12% | 7%* | 8%* | |
| Non-Hispanic White | 63% | 80%* | 80%* | |
| Non-Hispanic Other | 3% | 3% | 2% | |
| Annual Household Income | $0 to $34,999 | 29% | 30% | 29% |
| $35,000 to $74,999 | 33% | 33% | 35% | |
| $75,000 or more | 38% | 37% | 36% | |
| Education | College Degree or more | 33% | 31% | 29% |
| Less than College | 67% | 69% | 71% | |
| Internet access and use | Yes | 83% | 80% | 78%* |
| No | 17% | 20% | 22%* | |
| Geography | Urban | 86% | 82% | 85% |
| Rural | 14% | 18% | 15% | |
| Doctor Visit in Past Year | Yes | 81% | 97%* | 93%* |
| No | 19% | 3%* | 7%* | |
| Health Insurance Coverage | Yes | 91% | 99%* | 97%* |
| No | 9% | 1%* | 3%* | |
| Have a Chronic Condition | Yes | 60% | 75%* | 77%* |
| No | 40% | 25%* | 23%* | |
Table 4: Percent of individuals who reported having a smartphone, tablet, electronic monitoring device, or health and wellness app, 2017-2018 combined sample.
| Previous Cancer Diagnosis | |||
|---|---|---|---|
| Type of Device | Never Had Cancer | Recent Cancer Diagnosis | Cancer Survivor |
| Electronic Monitoring Device (e.g. Fitbit, blood glucose meter, blood pressure device) | 35% | 33% | 39% |
| Tablet | 60% | 61% | 56% |
| Smartphone | 81% | 71%* | 66%* |
| Tablet or Smartphone | 85% | 77%* | 74%* |
| Health & Wellness App (among those with a tablet or smartphone) | 47% | 44% | 41%^ |
Table 5: Percent of individuals who reported using their health and wellness app or other electronic monitoring device to help discuss, track, and/or make decisions regarding their health by cancer status, 2017-2018 combined sample.
| Previous Cancer Diagnosis | |||
|---|---|---|---|
| Use of Electronic Device | Never Had Cancer | Recent Cancer Diagnosis | Cancer Survivor |
| Individuals with a health & wellness app1 | |||
| Track progress on a health-related goal e.g. quit smoking, lose weight, increase physical activity) | 73% | 62%^ | 67% |
| Make a decision about how to treat an illness or condition | 47% | 44% | 48% |
| Discuss your health with your health care provider | 44% | 53% | 47% |
| Individuals with a health & wellness app or other electronic monitoring device2 | |||
| Shared information from a smartphone, tablet, or other electronic monitoring device with a health professional | 27% | 25% | 37%* |
Figure 4: Percent of individuals who reported a gap in information exchange by cancer status, 2017-2018 combined sample.

There are almost 17 million cancer survivors in the United States. Today, individuals with a previous cancer diagnosis represent a growing segment of the population (3). Access to online medical records can enable cancer patients and survivors to manage complex and ongoing health information needs (4). Approximately 60 percent of individuals with a previous cancer diagnosis reported being offered access to their online medical record by a healthcare provider or insurer. Among individuals who were offered access, five in 10 cancer survivors and seven in 10 individuals with a recent diagnosis reported viewing their online medical record at least once within the past year (5).
Individuals with a previous cancer diagnosis were offered access to their online medical records at higher rates compared to those who never had cancer. This is consistent with previous research that shows individuals who have chronic conditions, visit their doctor regularly, and are insured report higher rates of being offered access to an online medical record (5). Individuals recently diagnosed with cancer viewed their record at higher rates compared to those never diagnosed with cancer. However, there were no differences in rates of viewing an online medical record between cancer survivors and those never diagnosed.
This analysis highlights missed opportunities for many individuals with cancer to benefit from access and use of online medical records. Approximately forty percent of individuals with a previous cancer history reported not being offered access to their online medical record. Additionally, a substantial portion of individuals with a previous cancer diagnosis did not view their online medical records when access was offered. Common reasons for not viewing one’s online medical record included preferring to speak directly with a healthcare provider, reporting not having a need to use an online medical record, and concerns about privacy and security of online medical records.
Furthermore, although rates of viewing online medical records were higher among those with a recent cancer diagnosis, online medical records appear to be underutilized by these individuals. This group did not report greater use of most functions of online medical records (such as help in making a medical decision about an illness) compared to individuals without cancer. Online medical records can serve as important tools for managing complex health information needs and ensuring that individuals with cancer are not lost in their transition from patient to survivor (6). Individuals with cancer are more likely to see multiple healthcare providers. As a result, those recently diagnosed are more likely to experience gaps as information is exchanged, which may result in additional burden to the patient (e.g., having to bring a test result such as an X-ray or MRI to an appointment). This population may benefit from more information about the functions of online medical records for healthcare management, such as the ability to exchange secure messages with a provider, correct inaccurate information, or add new information to a medical record. These results also indicate that individuals with a previous cancer diagnosis may also have technology needs and preferences that differ from the general population. For example, individuals with a prior cancer diagnosis are less likely to use smartphones.
To encourage engagement, healthcare practitioners should consider the unique characteristics, information needs, and technology preferences of this population when developing patient-facing medical records and related digital tools to support the health of all individuals affected by cancer (4). Previous work has shown that individuals are more likely to use their online medical record when encouraged by a healthcare provider (7). Educating providers on the benefits of using online medical records for cancer patients could increase utilization of these tools. The Patient Engagement Playbook and the Guide to Getting and Using your Health Record deliver tips to providers and patients for making this process easier.
Definitions for variables derived by ONC during this analysis are described below:
Offered access to an online medical record: Individuals were considered to be offered access to an online medical record if they responded “yes” to either health care provider or insurer for the question, “Have you ever been offered online access to your medical records by: a) health care provider? b) health insurer?”
Recent cancer diagnosis: Individuals who reported that their first cancer diagnosis occurred less than five years ago.
Cancer survivor: Individuals who reported that their first cancer diagnosis occurred more than five years ago.
Never had cancer: Individuals who reported that they have never been diagnosed with cancer.
Data are from the National Cancer Institute’s (NCI) Health Information National Trends Survey (HINTS). Since 2003, NCI has sponsored HINTS to assess the impacts of health communication, specifically measuring: how people access and use health information, how people use information technology to manage their health and health information, and the degree to which people are engaged in health behaviors.
ONC staff, working with the National Partnership of Women and Families and NCI, developed the survey content related to health IT use for HINTS 5. HINTS 5, Cycle 1 (2017) data were collected from January through May, 2017. HINTS 5, Cycle 2 (2018) data were collected from January through May 2018. The sample design for HINTS 5, Cycle 1 (2017) and Cycle 2 (2018) consisted of a single-mode mail survey, using the Next Birthday Method for respondent selection.
The sample design for the HINTS 5, Cycle 1 (2017) and Cycle 2 (2018) surveys consisted of two-stages. In the first stage, a stratified sample of addresses was selected from a file of residential addresses. In the second-stage, one adult was selected within each sampled household. The sampling frame consisted of a database of addresses used by Marketing Systems Group (MSG) to provide random samples addresses. Complete data were collected from 3,527 respondents. The response rate was in 33%, and results were weighted to account for non-response and generate national estimates.
The analyses conducted in this data brief primarily focused on questions from sections B and D. The questions asked in the HINTS 5, Cycle 1 (2017) and Cycle 2 (2018) survey can be found at https://hints.cancer.gov/docs/Instruments/HINTS5_Cycle1_Annotated_Instrument_English.pdf.
1. National Cancer Institute. Cancer Statistics. (April 2018). Available here: https://www.cancer.gov/about-cancer/understanding/statistics
2. President’s Cancer Panel. (November 2016). Improving Cancer-Related Outcomes with Connected Health: A Report to the President of the United States from the President’s Cancer Panel. Bethesda, Maryland.
3. Bluethmann et al. (July 2016). Anticipating the ”Silver Tsunami”: Prevalence Trajectories and Comorbidity Burden among Older Cancer Survivors in the United States. Cancer Epidemiol Biomarkers Prev. 25:1029-1036.
4. Kent et al. (November 2012). Health information needs and health-related quality of life in a diverse population of long-term cancer survivors. Patient Ed Couns. 89:345-352.
5. Patel V & Johnson C. (May 2019). Trends in Individuals’ Access and Use of Online Medical Records and Technology for Health Needs: 2017-2018. ONC Data Brief, no.48 Office of the National Coordinator for Health Information Technology: Washington DC.
6. Hewitt M, Greenfield S & Stovall E. (November 2005). From cancer patient to cancer survivor: lost in transition. Washington: National Academies Press.
7. Patel V & Johnson C. (April 2018). Individuals’ use of online medical records and technology for health needs. ONC Data Brief, no.40. Office of the National Coordinator for Health Information Technology: Washington DC.
Authors CJ and VP are with the Office of Technology, within the Office of the National Coordinator for Health Information Technology. The data brief was drafted under the direction of Mera Choi, Director of Technical Strategy and Analysis, and Talisha Searcy, Director of the Data Analysis Branch. Author MK is with the National Cancer Institute and contributed to this brief under the approval of the NCI’s Health Communication and Informatics Research Branch in coordination with the ONC.
Johnson C, Krakow M, Patel V. (January 2019). Trends in Individuals’ Access and Use of Online Medical Records and Technology for Health Needs: 2017-2018. ONC Data Brief, no.50. Office of the National Coordinator for Health Information Technology: Washington DC.
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