- Research article
- Open Access
- Open Peer Review
Primary care physicians' use of family history for cancer risk assessment
© Flynn et al; licensee BioMed Central Ltd. 2010
- Received: 16 November 2009
- Accepted: 3 June 2010
- Published: 3 June 2010
Family history (FH) assessment is useful in identifying and managing patients at increased risk for cancer. This study assessed reported FH quality and associations with physician perceptions.
Primary care physicians practicing in two northeastern U.S. states were surveyed (n = 880; 70% response rate). Outcome measures of FH quality were extent of FH taken and ascertaining age at cancer diagnosis for affected family members. Predictors of quality measured in this survey included: perceived advantages and disadvantages of collecting FH information, knowledge of management options, access to supportive resources, and confidence in ability to interpret FH.
Reported collection of information regarding second degree blood relatives and age of diagnosis among affected relatives was low. All hypothesized predictors were associated with measures of FH quality, but not all were consistent independent predictors. Perceived advantages of taking a family history, access to supportive resources, and confidence in ability to identify and manage higher risk patients were independent predictors of both FH quality measures. Perceived disadvantages of taking a family history was independently associated one measure of FH quality. Knowledge of management options was not independently associated with either quality measure.
Modifiable perception and resource factors were independently associated with quality of FH taking in a large and diverse sample of primary care physicians. Improving FH quality for identification of high risk individuals will require multi-faceted interventions.
- Family History
- Primary Care Physician
- Cancer Risk Assessment
- Supportive Resource
- Family History Information
Cancer risk assessment can be used in primary care to identify patients who may benefit from risk management strategies. A family history is a relatively simple and accurate method of stratifying risk for several major cancers [1–6].
Recommendations from national consensus groups support the case for systematic use of family history to assess cancer risk. The U.S. Preventive Services Task Force (USPSTF) statement on colorectal cancer screening considers patients with a first degree relative diagnosed before age 60 to be at increased risk . Characterization of increased risk as moderate or high requires information on second degree relatives. The moderate risk group is recommended for accelerated screening and the higher risk group may be candidates for assessment of hereditary disease . Breast cancer risk stratification recommendations follow a similar pattern . Use of family history information for cancer risk assessment is recommended by other professional organizations [10–12].
Although family histories are collected routinely, gaps that reduce their value for risk assessment have been reported. Data on second degree relatives and age of diagnosis are often missing and data are updated infrequently [2, 13–19]. Barriers to more effective use of family histories have included time costs, low confidence in ability to effectively collect and utilize data, and lack of clear guidelines [4, 20–25].
This study was designed to identify predictors of family history quality among primary care physicians as a basis for developing strategies to improve cancer risk assessment and management. Social Cognitive Theory (SCT) was used as a conceptual framework for developing hypotheses and measures of key variables [26, 27]. This model describes three major types of influence on behavior: intrapersonal factors, such as beliefs about the results of performing a behavior (outcome expectations), and beliefs about ability to perform the behavior (confidence or self-efficacy); perceived environment factors, such as peer norms or access to supportive resources related to the behavior; and behavioral factors such as past behavior and skills needed to perform the behavior.
Hypotheses derived from this conceptual model stated that physicians would be more likely to take higher quality family histories if reporting: higher positive and lower negative beliefs about the value of identifying familial risks; greater knowledge of management options for higher risk patients; higher levels of resources to assist in using family history information; and higher levels of confidence in ability to identify and manage familial cancer risk.
The study was based on data collected through surveys of primary care physicians in the northeastern United States during 2005. Three health care organizations provided lists of physicians practicing general internal medicine, family medicine, and gynecology in urban, suburban, and rural communities. The survey was conducted with up to four mailings; physicians responding or opting-out were not sent additional mailings. Procedures were approved by institutional review boards at the University of Vermont and collaborating organizations.
Predictor and outcome measures were developed using qualitative interviews with 20 physicians  and consultation with an expert panel and other primary care physicians. Measures were refined using principal components factor analyses to confirm that intercorrelated groups of items comprised valid measures ; internal consistency reliability was estimated using Cronbach's alpha. Five theory-based predictors and two outcome variables were assessed. The survey instrument is shown in Additional file 1.
Advantages of Taking Family History. A seven item measure assessed expectations that taking a family history would be advantageous (e.g., "basis for providing preventive guidance to patients"). Four response options for each item ranged from "disagree" (1) to "agree" (4). The internal consistency reliability coefficient was alpha = .72.
Disadvantages of Taking Family History. A seven item measure assessed expectations that taking a family history would be disadvantageous (e.g., "difficult to interpret risk based on family history"). Four response options ranged from "disagree" (1) to "agree" (4). Alpha = .83.
Risk Management Knowledge. A thirteen item measure assessed knowledge of options for managing a patient identified as at risk for cancer because of family history. Seven items described possible management strategies for breast cancer risk based on family history (e.g., "increased frequency of screening"); six similar items focused on familial risk of colon cancer (e.g. "earlier initiation of screening"). Five response options ranged from "unlikely" (1) to "likely" (5). Alpha = .74.
Supportive Resources. A seven item measure assessed perceived levels of support for using family history information to assess risk. Respondents were asked to rate their use of possible resources (e.g., "professional organization guidelines"). Five response options ranged from "never" (1) to "always" (5). Alpha = .74.
Confidence. A four item measure assessed confidence that respondents could identify and manage patients at risk of cancer due to family history. For both breast and colon cancer they were asked to rate confidence that "you can identify a patient who may be at increased risk" and that "you can effectively manage a patient who is at increased risk" based on family history. Eleven response options ranged from "not at all confident" (0) to "completely confident" (10). Alpha = .82.
These predictor variables were moderately correlated with one another in the expected directions, indicating both content validity and the independence of the constructs measured. Advantages of Taking Family History, for example, was negatively correlated with Disadvantages of Taking Family History (Pearson correlation r = -.40) and positively correlated with Risk Management Knowledge (r = .27), Supportive Resources (r = .25), and Confidence (r = .26).
Family History Taking Extent. A five item measure assessed how often respondents included specific first and second degree family members in a family history. Listed relatives included parents, children, siblings, grandparents, and aunts and uncles. Five response options for each item ranged from "never" (1) to "always" (5). Alpha = 0.68.
Age of Diagnosis Determination. A single item assessed the frequency with which a physician collected the age of diagnosis for a family member's disease. The question asked "when you collect family history information, how often do you include age of diagnosis?" Five response options for this item ranged from "never" (1) to "always" (5).
The two outcome variables were moderately and positively correlated (r = .22).
Preliminary analyses examined distributions and assessed impact of respondent characteristics on outcome variables to determine the need to include these in the main analyses . For the hypothesis tests, each potential predictor was entered into a multiple regression analysis for each of the two quality measures, controlling for variables representing geographic location of the physician's practice and specialty. Relative strength of relationships between predictor and outcome variables was assessed by analyses that included all five predictor measures and the two control variables with each of the two quality measures as outcomes.
Physician practice specialties by geographic location.
Physician reported frequency of family history taking by types of family relationships (n = 867)
These outcomes differed slightly but not significantly by practice location. Differences in FH Taking Extent by practice specialty were significant (p = .05) but small with the mean scores for family medicine practitioners at 22.0, gynecology at 21.6, and internal medicine at 21.4. No significant differences by specialty were found for the Age of Diagnosis outcome.
Predictors of family history-taking quality
Results for the Advantages measure showed a mean score of 3.5 (on the four point scale from 1 = disagree to 4 = agree) indicating a high level of primary care physician agreement with the stated advantages of taking a family history; the mean score for the Disadvantages measure was 2.0, indicating a moderate level of physician disagreement with the stated disadvantages of taking a family history. The Management Knowledge measure had a mean score of 3.3 on a 1-5 scale indicating a moderate level of likely use of these options. The Supportive Resources mean score was 2.5 on a 1-5 scale, indicating relatively infrequent use of these resources. The mean Confidence score was 7.1 on a 0-10 scale indicating moderate confidence.
A small difference was found by practice location for Advantages (p = .01) with mean scores for suburban physicians at 3.3, and for rural and suburban physicians at 3.2. More notable differences in predictor scores were found by practice specialty. Knowledge of Treatment Options was higher (p < .01) among gynecology physicians (mean = 3.4) than among internal medicine or family medicine practitioners (3.2). Confidence in identifying and managing patients at higher risk of cancer because of family history, on the other hand, was lower (p < .01) among gynecology physicians (6.7) than among family medicine (7.3) or internal medicine (7.1) practitioners.
Associations between predictors and outcomes
Association of each hypothesized predictor with family history-taking quality indicators (n = 867).
FH Taking Extent
Age of Diagnosis Determination
Relative strength of predictors
Simultaneous tests of association of hypothesized predictors with family history-taking quality indicators (n = 867).
FH Taking Extent
Age of Diagnosis Determination
Salient barriers and facilitators
Mean scores for individual items in selected predictor measures were ranked to identify more specific barriers and facilitators. The most strongly endorsed Advantage items were: "better understand risk of future disease" (mean score of 3.9 on the 1-4 scale); "better rationale for screening modalities" (3.8); "basis to provide preventive guidance to patients" (3.7); and "better address patient's concerns" (3.5). Disadvantage items most likely to elicit agreement were: "patients often have limited knowledge of family history" (mean score of 2.5 on the 1-4 scale); "less important than other office visit tasks" (mean = 2.2); "difficult to interpret risk based on family history" (2.0); and "difficult to communicate risk based on family history" (1.9). The supportive resources utilized most often included: "professional organization guidelines" (mean score of 3.4 on the 1-5 scale); "refer to a specialist" (3.2); "discuss with a specialist" (3.0); "other published guidelines" (3.0); and "on-line resources" (2.9).
This survey of primary care physicians provides information about self-reported family history-taking behaviors, views on using family history for cancer risk assessment and management, and associations between these perceptions and behaviors from a large sample of primary care physicians. The sample was based on comprehensive rosters of physicians in selected locations. The range of community settings and specialties and the high response rates provided an unusually complete and representative portrait of primary care physicians in these areas. Results from this diverse sample of physicians are generally consistent with findings from more focused studies, providing additional confidence in the generalizability of the findings.
Reported family history taking among these physicians was concentrated on first degree relatives and specific diagnoses, but not second degree relatives or age of diagnosis for those affected. Family history data were often collected at new patient visits for periodic health exams, but were not often updated. These results were consistent with interviews of primary care physicians suggesting that family histories often were collected as part of the development of a general understanding of the patient's situation ; systematic use of family history to identify and manage cancer risk was rarely reported [4, 13, 25, 31].
All of the hypothesized physician perceptions were significantly associated with reported quality of family history-taking when entered separately into analyses (Table 3). When all five potential predictors were entered into analyses simultaneously, however, several of these demonstrated independent associations with both outcomes (Table 4), indicating that these variables better explained variation in the outcomes than perception measures which demonstrated associations only when entered separately. Perceived Advantages of taking a family history, perceptions of Supportive Resources to facilitate use of family history information, and Confidence in interpreting and using family history results for management of cancer risk independently predicted both measures of family history taking quality. The consistency and statistical significance of these associations suggested that these results provide useful guidance for design of interventions to improve utilization of this cancer risk assessment strategy. Perceived Disadvantages was a strong independent predictor of FH Taking Extent, but was not independently associated with Age of Diagnosis Determination. Management Knowledge was not independently associated with either outcome.
The results provided an encouraging picture of high receptivity to use of family history for cancer risk assessment. In general, participants tended to agree with statements describing Advantages and disagree with statements describing Disadvantages of taking a family history, consistent with other reports of value placed on the strategy of using family history to identify cancer risk [20–22]. Both of these measures were relatively strong independent predictors of one or another of the two outcome measures. The strength of these associations with the family history quality suggested that small differences in these perceptions could have a large impact on clinical behaviors.
The importance of availability and usability of resources focused on collection and interpretation of family history information is highlighted by the independent association of the Supportive Resources measure with both quality outcome measures. The most frequently utilized among the seven resources listed was professional organization guidelines followed by referral or consultation, other published guidelines, and on-line resources. These results reflected a relatively high regard for guidelines endorsed by respected sources relative to other types of resources. This finding is consistent with needs for more specific guidelines and other readily accessible supportive resources as suggested by other investigators [19–21, 25].
Key issues affecting increased levels of guideline use may include usability of guideline statements and related resources within the context of an office visit [3, 6, 19, 32, 33]. Current guidelines for use of family history in cancer risk assessment are not organized in a consolidated statement that can be easily implemented in primary care practice. Some attempts have been made to integrate the major consensus statements into more usable summaries that directly link family history data to risk assessment and management [5, 34].
Confidence was independently associated with both measures of family history quality as hypothesized. Overall scores indicated moderate levels of confidence, similar to relatively low or moderate levels of confidence identified previously [4, 20–22]. More focused family history resources and systems built on succinct consolidated guideline statements concerning cancer risk assessment and management may increase confidence levels.
The hypothesized Cancer Risk Management Knowledge predictor was not significantly associated with either quality indicator. It is possible that the links between family history information and use of management options for patients at higher risk were not clear for some respondents, despite strong endorsement of the overall rationale. This would be an important gap since expanded risk management opportunity is a primary motivation for the investment of effort required for more systematic family history data collection.
Several important barriers to collection and utilization of family history information emerged. These included patient knowledge of their family history, relative value of family history collection compared to other office visit tasks (possibly an indication of time efficiency concerns), and difficulties of interpreting and communication risk. These are substantial barriers but they can be addressed by new strategies. The rapid adoption of electronic health records in some countries presents new opportunities for development of systems to facilitate family history data collection, risk assessment, and consideration of management options. These new resources may provide for more time-efficient processes and a greater role for patients in collecting and recording family history information.
This study has several limitations. Although results were consistent with causal connections between self-reported perceptions and indicators of family history quality, this was a cross-sectional study testing correlational hypotheses. The outcome measures may not accurately reflect family history-taking behavior, with the most likely bias being reporting of more positive behavior. The modest amount of variance explained indicated the potential importance of variables not measured. Lastly, the conclusions may have limited generalizability as the study surveyed physician practicing in targeted communities of one region in the United States.
These results suggest that family history information could be used more systematically to identify patients who may benefit from cancer risk assessment. Clinical practice of cancer risk assessment could be improved by changes in the quality of routinely collected family history data, focusing on inclusion of first and second degree relatives, age at which a cancer is diagnosed and periodic updating.
Although national organizations endorse use of family history data for this purpose and physicians supported the approach, several issues appeared to impede more complete implementation of this cancer risk management strategy. Efficient collection of family history information may require a better-defined role for patients in providing baseline and updated information as envisioned in the U.S. Surgeon General's initiative . Patient efforts may need to be focused and complemented by more systematic health maintenance protocols for cancer risk assessment. Low levels of use of current resources for interpreting and utilizing family history data suggest a need for development of more efficient and accessible methods designed to integrate with the flow of work in typical office visits [4, 23, 32, 36].
We gratefully acknowledge the assistance of Drs. Mildred Reardon, Thomas Lee, and Christopher W. Shanahan in recruiting study participants. This research was supported by grant R01 CA89521 from the National Cancer Institute.
- Burke W: Taking family history seriously. Ann Intern Med. 2005, 143: 388-389.View ArticlePubMedGoogle Scholar
- Murff HJ, Spigel DR, Syngal S: Does this patient have a family history of cancer? an evidence-based analysis of the accuracy of family cancer history. JAMA. 2004, 292: 1480-1489. 10.1001/jama.292.12.1480.View ArticlePubMedGoogle Scholar
- Qureshi N, Wilson B, Santaguida P, Allanson J, Culebro CR, Brouwers M, Raina P: Collection and Use of Cancer Family History in Primary Care. Evid Rep Technol Assess (AHRQ Publication No. 08-E001). 2007, 159: 1-84.Google Scholar
- Rich EC, Burke W, Heaton CJ, Haga S, Pinsky L, Short MP, Acheson L: Reconsidering the family history in primary care. J Gen Intern Med. 2004, 19: 273-280. 10.1111/j.1525-1497.2004.30401.x.View ArticlePubMedPubMed CentralGoogle Scholar
- Scheuner MT, Wang SJ, Raffel LJ, Larabell SK, Rotter JI: Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood. Am J Med Genet. 1997, 71: 315-324. 10.1002/(SICI)1096-8628(19970822)71:3<315::AID-AJMG12>3.0.CO;2-N.View ArticlePubMedGoogle Scholar
- Yoon PW, Scheuner MT, Khoury MJ: Research priorities for evaluating family history in the prevention of common chronic diseases. Am J Prev Med. 2003, 24: 128-135. 10.1016/S0749-3797(02)00585-8.View ArticlePubMedGoogle Scholar
- U.S. Preventive Services Task Force: Screening for colorectal cancer: U.S. Preventive Services Task Force recommendation statement. Ann Intern Med. 2008, 149: 627-637.View ArticleGoogle Scholar
- Winawer S, Fletcher R, Rex D, the Gastrointestinal Consortium Panel: Colorectal cancer screening and surveillance: clinical guidelines and rationale - update based on new evidence. Gastroenterology. 2003, 124: 544-560. 10.1053/gast.2003.50044.View ArticlePubMedGoogle Scholar
- U.S. Preventive Services Task Force: Screening for breast cancer: recommendations and rationale. Ann Intern Med. 2002, 137: 344-346.View ArticleGoogle Scholar
- American Academy of Family Physicians: Summary of Recommendations for Clinical Preventive Services. [http://www.aafp.org]
- ACOG Committee on Gynecologic Practice: Primary and preventive care - periodic assessments. Obstet Gynecol. 2006, 108: 1615-1622.View ArticleGoogle Scholar
- Smith RA, Cokkinides V, Eyre HJ: Cancer screening in the United States: A review of current guidelines, practices, and prospects. CA Cancer J Clin. 2007, 57: 90-104. 10.3322/canjclin.57.2.90.View ArticlePubMedGoogle Scholar
- Acheson L, Wiesner G, Zyzanski S, Goodwin M, Stange K: Family history taking in community family practice: implications for genetic screening. Genet Med. 2000, 2: 180-185. 10.1097/00125817-200005000-00004.View ArticlePubMedGoogle Scholar
- Grover S, Stoffel EM, Bussone L, Tschoegl E, Syngal S: Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patients. Clin Gastroenterol Hepato. 2004, 2: 813-819. 10.1016/S1542-3565(04)00352-0.View ArticleGoogle Scholar
- Murff HJ, Greevy RA, Syngal S: The comprehensiveness of family cancer history assessments in primary care. Community Genet. 2007, 10: 174-180. 10.1159/000101759.PubMedGoogle Scholar
- Schroy PC, Barrison AF, Ling BS, Wilson S, Geller AC: Family history and colorectal cancer screening: a survey of physician knowledge and practice patterns. Am J Gastroenterol. 2002, 97: 1031-1036. 10.1111/j.1572-0241.2002.05624.x.View ArticlePubMedGoogle Scholar
- Sifri RD, Wender R, Paynter N: Cancer risk assessment from family history: gaps in primary care practice. J Fam Pract. 2002, 51: 856-PubMedGoogle Scholar
- Sweet KM, Bradley TL, Westman JA: Identification and referral of families at high risk for cancer susceptibility. J Clin Oncol. 2002, 20: 528-537. 10.1200/JCO.20.2.528.View ArticlePubMedGoogle Scholar
- Tyler CV, Snyder CW: Cancer risk assessment: examining the family physician's role. J Am Board Fam Med. 2006, 19: 468-477. 10.3122/jabfm.19.5.468.View ArticlePubMedGoogle Scholar
- Emery J, Watson E, Rose P, Andermann A: A systematic review of the literature exploring the role of primary care in genetic services. Fam Pract. 1999, 16: 426-445. 10.1093/fampra/16.4.426.View ArticlePubMedGoogle Scholar
- Fry A, Campbell H, Gudmundsdottir H, Rush R, Porteous M, Gorman D, Cull A: GPs' views on their role in cancer genetics services and current practice. Fam Pract. 1999, 16: 468-474. 10.1093/fampra/16.5.468.View ArticlePubMedGoogle Scholar
- Gramling R, Nash J, Siren K, Eaton C, Culpepper L: Family physician self-efficacy with screening for inherited cancer risk. Ann Fam Med. 2004, 2: 130-132. 10.1370/afm.60.View ArticlePubMedPubMed CentralGoogle Scholar
- Guttmacher AE, Collins FS, Carmona RH: The family history - more important than ever. N Engl J Med. 2004, 351: 2333-2336. 10.1056/NEJMsb042979.View ArticlePubMedGoogle Scholar
- Rose PW, Watson E, Yudkin P, Emery J, Murphy M, Fuller A, Lucassen A: Referral of patients with a family history of breast/ovarian cancer - GPs' knowledge and expectations. Fam Pract. 2001, 18: 487-490. 10.1093/fampra/18.5.487.View ArticlePubMedGoogle Scholar
- Suther S, Goodson P: Barriers to the provision of genetic services by primary care physicians: a systematic review of the literature. Genet Med. 2003, 5: 70-76. 10.1097/01.GIM.0000055201.16487.61.View ArticlePubMedGoogle Scholar
- Bandura A: Social Foundations of Thought and Action. A Social Cognitive Theory. 1986, Englewood Cliffs, N.J.: Prentice-HallGoogle Scholar
- Baranowski T, Perry CL, Parcel GS: How individuals, environments, and health behavior interact: social cognitive theory. Health Behavior and Health Education - Theory, Research, and Practice. Edited by: Glanz K, Lewis FM, Rimer BK. 2002, San Francisco: Jossey-Bass, 153-178. 3Google Scholar
- Wood ME, Stockdale A, Flynn BS: Interviews with primary care physicians regarding taking and interpreting the cancer family history. Fam Pract. 2008, 25: 334-340. 10.1093/fampra/cmn053.View ArticlePubMedPubMed CentralGoogle Scholar
- Nunnally JC: Psychometric Theory. 1978, New York: McGraw-Hill, 2Google Scholar
- SAS Institute Inc: SAS System for Windows, v 8.01 Cary. 2000, North Carolina: SAS Institute IncGoogle Scholar
- Murff HJ, Byrne D, Syngal S: Cancer risk assessment: quality and impact of the family history interview. Am J Prev Med. 2004, 7: 239-245.Google Scholar
- Kelly KM, Sweet K: In search of a familial cancer risk assessment tool. Clin Genet. 2007, 71: 76-83. 10.1111/j.1399-0004.2006.00728.x.View ArticlePubMedGoogle Scholar
- Marcy TW, Skelly J, Shiffman RN, Flynn BS: Facilitating adherence to the tobacco use treatment guideline with computer-mediated support systems: physician and clinic manager perspectives. Prev Med. 2005, 41: 479-487. 10.1016/j.ypmed.2004.11.026.View ArticlePubMedGoogle Scholar
- Hampel H, Sweet K, Westman JA, Offit K, Eng C: Referral for cancer genetics consultation: a review and compilation of risk assessment criteria. J Med Genet. 2004, 41: 81-91. 10.1136/jmg.2003.010918.View ArticlePubMedPubMed CentralGoogle Scholar
- Carmona RH, Wattendorf DJ: Personalizing prevention: the U.S. Surgeon General's Family History Initiative. Am Fam Physician. 2005, 71: 36-PubMedGoogle Scholar
- Emery J, Morris H, Goodchild R, Fanshawe T, Prevost AT, Bobrow M, Kinmonth AL: The GRAIDS Trial: a cluster randomized controlled trial of computer decision support for the management of familial cancer risk in primary care. Br J Cancer. 2007, 97: 486-493. 10.1038/sj.bjc.6603897.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2296/11/45/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.