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Medicine in the United States is undergoing fundamental changes that will continue despite 2016 presidential election results. Changes include consolidation of provider networks, movement from volume- to value-based reimbursement, demands for price and quality transparency, and a shift from focusing solely on individual physician-patient interactions to a broader triple aim focus that incorporates individual patients, population, health, and cost. In this month’s column, Sameer Saini and colleagues suggest that we broaden our view of colorectal cancer screening quality metrics from a colonoscopy-centric focus to a focus on the bottom line: Do we reduce cancer in the population of patients that we serve? When we extend our view to a population level, we use current colonoscopy registries only as internal process controls. A successful health system will develop a mechanism to assess and demonstrate how well the collective team of providers accomplishes the only outcome that matters to patients: preventing colon cancer.
John I. Allen, MD, MBA, AGAF, Special Section Editor
Colorectal cancer (CRC) screening is one of the most valuable services provided by gastroenterologists. The evidence that screening “works” on a population level is undeniable. But not every screening program is equally effective. Data indicate ongoing underuse of screening, particularly in high-risk, vulnerable, and minority communities.1,2 Other data indicate that screening is overused, particularly in low-risk patients and in those with limited life expectancy.3-5 It is also known that endoscopist skill plays an important role in the effectiveness of screening. In short, there is ample room for improvement in the quality of CRC screening, and payers and the public have taken notice. Unsurprisingly, gastroenterologists are often focused on procedural quality indicators, such as adenoma detection and cecal intubation rates.6 These endoscopic quality measures are important indicators of high-quality colonoscopy, but colonoscopy is the common touch point of a much broader system of care that includes other screening tests and other providers (e.g., primary care providers [PCPs], pathologists, and anesthesiologists). Coordinating care across this system is essential for improving the health of patients. As the stewards of digestive health, we owe it to our patients to take a more comprehensive view of CRC screening quality and move beyond colonoscopy alone.
The complex web of care that comprises CRC screening is shown schematically in Figure 1. Appropriate screening begins with selection of suitable screening candidates. In the United States, where most screening is initiated during a clinician encounter, this important task falls primarily on the shoulders of PCPs. It is typically the role of the PCP to assess the two key patient factors that determine screening benefit: CRC risk (using personal and family history) and life expectancy (using age and overall health status). Once a patient has been deemed an appropriate candidate for screening, an acceptable screening test must be selected. Here, patient and practitioner are faced with a menu of options, including fecal occult blood testing (FOBT), colonoscopy, multitarget stool DNA, and computed tomography colonography. For average-risk screening, the ideal test depends primarily on patient preference and local availability.
If a screening test other than colonoscopy is selected, it becomes critical that a positive test is followed by timely and high-quality colonoscopy. High-quality colonoscopy begins with evidence-based preprocedure education and preparation, including appropriate selection of anesthesia services. Once a patient has been well prepared and adequately sedated, an endoscopist must carefully examine the colonic mucosa and completely resect any suspicious polyps. Unless discarded, resected polyps must be reviewed and categorized by a pathologist, including appropriate identification of serrated polyps. Finally, pathology results must be correctly interpreted by the clinician, with evidence-based follow-up recommendations made and effectively communicated to the patient and the referring provider. Additionally, in the short term, delayed gastrointestinal (GI) and non-GI complications of colonoscopy must be recognized and appropriately addressed. In the long term, the rate of interval cancers must be monitored.
Recognizing the importance of CRC screening, GI specialty societies have proposed a variety of quality measures to ensure that patients receive high-quality and high-value colonoscopy. Several of these measures have been adopted by CMS as part of the Physician Quality Reporting System. Non-GI groups, such as the National Center for Quality Assurance and the Ambulatory Surgery Center Association, have also proposed their own CRC screening–related measures.
Despite the proliferation of measures in the domain of CRC screening, current measures fall short in several ways. First, they are largely focused on colonoscopy technical performance, with less attention paid to the important steps that occur before and after colonoscopy. For example, the existing Healthcare Effectiveness Data and Information Set measure for underuse of CRC screening assesses the proportion of patients in a health plan between the ages 50 and 75 who are up to date for CRC screening. This measure is satisfied if a patient completes FOBT, regardless of the result. But FOBT alone is not sufficient to reduce mortality from CRC. Rather, it is imperative that a positive FOBT test be followed by colonoscopy. Numerous studies suggest a quality gap in this critical referral step.7
Yet, outside of selected clinical settings (e.g., the Veterans Affairs Healthcare System), no existing quality measure focuses on colonoscopy completion after positive FOBT. Other examples of important performance gaps beyond colonoscopy technical performance include appropriate use of monitored anesthesia care (data suggest overuse) and appropriate pathology interpretation (data suggest variation in the interpretation of serrated lesions, some of which are associated with increased risk of CRC).
Second, existing measures fail to consider individual patient factors that are known to be predictive of screening benefit, such as life expectancy and personal or familial cancer risk.8
Returning to the Healthcare Effectiveness Data and Information Set measure as an example, this measure relies on age alone to identify patients who are candidates for screening. Yet, it is widely recognized that life expectancy is a critically important factor when considering screening, particularly in older patients. However, existing measures fail to incorporate estimates of life expectancy. As a result, clinicians are encouraged to screen based on age alone. Data suggest that this leads to overuse in older, sicker patients younger than age 75 (the age cutoff suggested by guidelines and incorporated into the Healthcare Effectiveness Data and Information Set measure) and underuse in healthy and unscreened patients older than age 75.9
Furthermore, existing measures fail to systematically consider patient preferences and undervalue shared decision making. Data suggest, for instance, that patients who are offered a “menu” of options for screening rather than a single screening test are more likely to complete a screening test.10
But existing measures do not consider whether a physician assessed a patient’s preferences, or offered more than one screening option. Of course, measuring the quality of decision making is an evolving science that presents challenges and requires creative solutions.11
Finally, existing measures do not capture the collaborative nature of modern health care. For example, most existing measures focus on the performance of gastroenterologists and GI practices. Although such a focus is appropriate for specialty-specific quality improvement efforts, it neglects to capture the important interactions and hand-offs between providers needed for successful completion of screening (and downstream reduction in cancer mortality). As a result, this specialty-focused approach fails to meet the needs of patients, who are increasingly interested in whether the care they receive is improving their health regardless of who provides it. It also fails to meet the needs of payers, who are interested in whether a network of providers is delivering high-value care for its members. Developing measures that capture the collaborative nature of modern health care becomes increasingly important as payers embrace alternative payment models and other value-based reimbursement systems.
Given these challenges with existing measures, we propose the following concepts for consideration as noncolonoscopy quality measures of CRC screening:
1. Appropriateness of referral for CRC screening (PCP): Measures in this domain should incorporate assessment of family history, prior screening history, and/or life expectancy, all of which are predictive of screening benefit and can be extracted from structured electronic health record data.
2. Shared decision making in choosing a CRC screening test (PCP): Currently, measures in this domain are (by necessity) relatively simple, such as assessment of documentation of whether stool testing was offered alongside colonoscopy during a clinic visit.
3. Percentage of individuals with a positive noncolonoscopy CRC screening test who complete a colonoscopy within 6 months (PCP and GI): A measure in this domain can be developed and implemented using existing infrastructure. The Veterans Affairs Healthcare System currently uses such a measure to monitor appropriate follow-up of positive fecal immunochemical tests.
4. Predicted reduction in CRC mortality: This measure, which provides an estimate of the effectiveness and value of a screening program, represents the “bottom line” that is ultimately of interest to both patients and payers. However, composite measures that use projected results require sophisticated statistical approaches and case-mix adjustment. They must also contend with “churn” in the covered population.
Although a more comprehensive view of screening is desirable, operationalizing measure concepts, such as those proposed previously, is challenging for several reasons. First, as we have outlined, CRC screening is truly a “team sport.” The stakeholders in CRC screening include public health, primary care, gastroenterology, colorectal surgery, oncology, anesthesiology, and pathology practitioners. As a result, screening has no natural and obvious steward. Rather, various components of care are adopted by different specialty groups, and this approach leads to unmonitored gaps in care. We believe that gastroenterologists can and should take the lead in developing comprehensive quality measures for CRC screening. Such comprehensive measures will be of value to patients and to payers. Second, assessing quality of care more comprehensively has traditionally been infeasible. For example, incorporating life expectancy into quality measures requires electronic assessment of health status.
Traditionally, such efforts have been hampered by the lack of systematic clinical data collection. However, as meaningful use of electronic health records increases, measures that incorporate such information are likely to become increasingly feasible. Finally, we also need to consider how to make these improvements while avoiding measure proliferation. Proliferation leads to provider fatigue and discourages thoughtful clinical decision making, potentially worsening quality of care. Creative approaches, such as rotating measure sets over time, use of clinical decision support tools, and balancing underuse measures with overuse measures, may be warranted. Additionally, composite measures may prove to be more meaningful and more practical for patients, providers, and payers. Ultimately, a distinction must be made between quality assurance and quality improvement; both are important, but the types of measures and the level of measure sophistication used in each program undoubtedly vary.
In summary, gastroenterologists are uniquely positioned to advocate for high-quality CRC screening that extends beyond simply providing a high-quality colonoscopy. This broader view of quality benefits patients by ensuring that our expertise informs the metrics by which delivery of CRC screening is measured. It also ensures that we hold ourselves and our colleagues to the highest standards across the continuum of care. Additionally, as alternative payment models and value-based contracting are implemented, nonendoscopic screening methods will likely become more commonplace. Advocating for high-quality nonendoscopic screening will help maintain gastroenterologists’ role as the stewards of CRC screening and digestive health. Although operationalizing measure concepts such as those proposed here may be difficult, it is critical if we are to provide the best possible care for our patients.
References
1. Sabatino, S.A., White, M.C., Thompson, T.D., et al. Cancer screening test use – United States, 2013. MMWR Morb Mortal Wkly Rep. 2015;64:464-8.
2. Anderson, A.E., Henry, K.A., Samadder, N.J., et al. Rural vs urban residence affects risk-appropriate colorectal cancer screening. Clin Gastroenterol Hepatol. 2013;11:526-33.
3. Walter, L.C., Lindquist, K., Nugent, S., et al. Impact of age and comorbidity on colorectal cancer screening among older veterans. Ann Intern Med. 2009;150:465-73.
4. Murphy, C.C., Sandler, R.S., Grubber, J.M., et al. Underuse and overuse of colonoscopy for repeat screening and surveillance in the Veterans Health Administration. Clin Gastroenterol Hepatol. 2016;14:436-44.
5. Mittal, S., Lin, Y.-L., Tan, A., et al. Limited life expectancy among a subgroup of Medicare beneficiaries receiving screening colonoscopies. Clin Gastroenterol Hepatol. 2014;12:443-50.e1
6. Allen, J.I. Quality measures for colonoscopy: where should we be in 2015?. Curr Gastroenterol Rep. 2015;17:10.
7. Fisher, D.A., Jeffreys, A., Coffman, C.J., et al. Barriers to full colon evaluation for a positive fecal occult blood test. Cancer Epidemiol Biomark Prev. 2006;15:1232-5.
8. Saini, S.D., van Hees, F., Vijan, S. Smarter screening for cancer: possibilities and challenges of personalization. JAMA. 2014;312:2211-2.
9. Saini, S.D., Vijan, S., Schoenfeld, P., et al. Role of quality measurement in inappropriate use of screening for colorectal cancer: retrospective cohort study. BMJ. 2014;348:g1247.
10. Inadomi, J.M., Vijan, S., Janz, N.K., et al. Adherence to colorectal cancer screening: a randomized clinical trial of competing strategies. Arch Intern Med. 2012;172:575-82.
11. Writing Committee Members, Drozda, J.P., Ferguson, T.B., et al. 2015 ACC/AHA focused update of secondary prevention lipid performance measures: a report of the American College of Cardiology/American Heart Association Task Force on Performance Measures. J Am Coll Cardiol. 2016;67:558-87.
Dr. Saini is a research scientist at the VA Center for Clinical Management Research and an assistant professor of internal medicine at the University of Michigan, Ann Arbor; Dr. Adams is a clinical lecturer in the division of gastroenterology, department of internal medicine, University of Michigan, and a research investigator, VA Center for Clinical Management Research; Dr. Brill is the chief medical officer of Predictive Health, Paradise Valley, Ariz., and a clinical assistant professor of medicine, University of Arizona School of Medicine, Phoenix; Dr. Gupta is codirector of Digestive Health Center, director of interventional endoscopy, and associate professor of medicine in the division of gastroenterology at Loyola University Medical Center; Dr. Naveed is a clinical assistant professor in the department of gastroenterology and hepatology, University of Iowa Hospitals and Clinics; Dr. Rosenberg is at Illinois Gastroenterology Group; and Dr. Gellad is associate professor of medicine at Duke University School of Medicine, Durham, N.C. Dr. Saini’s and Dr. Gellad’s research is funded by Veterans Affairs Health Services Research and Development Career Development Awards (CDA 09-213-2 and CDA 14-158). Dr. Gupta has received research support from Cook Medical, Cosmo Pharmaceuticals, and CDx Diagnostics.
Medicine in the United States is undergoing fundamental changes that will continue despite 2016 presidential election results. Changes include consolidation of provider networks, movement from volume- to value-based reimbursement, demands for price and quality transparency, and a shift from focusing solely on individual physician-patient interactions to a broader triple aim focus that incorporates individual patients, population, health, and cost. In this month’s column, Sameer Saini and colleagues suggest that we broaden our view of colorectal cancer screening quality metrics from a colonoscopy-centric focus to a focus on the bottom line: Do we reduce cancer in the population of patients that we serve? When we extend our view to a population level, we use current colonoscopy registries only as internal process controls. A successful health system will develop a mechanism to assess and demonstrate how well the collective team of providers accomplishes the only outcome that matters to patients: preventing colon cancer.
John I. Allen, MD, MBA, AGAF, Special Section Editor
Colorectal cancer (CRC) screening is one of the most valuable services provided by gastroenterologists. The evidence that screening “works” on a population level is undeniable. But not every screening program is equally effective. Data indicate ongoing underuse of screening, particularly in high-risk, vulnerable, and minority communities.1,2 Other data indicate that screening is overused, particularly in low-risk patients and in those with limited life expectancy.3-5 It is also known that endoscopist skill plays an important role in the effectiveness of screening. In short, there is ample room for improvement in the quality of CRC screening, and payers and the public have taken notice. Unsurprisingly, gastroenterologists are often focused on procedural quality indicators, such as adenoma detection and cecal intubation rates.6 These endoscopic quality measures are important indicators of high-quality colonoscopy, but colonoscopy is the common touch point of a much broader system of care that includes other screening tests and other providers (e.g., primary care providers [PCPs], pathologists, and anesthesiologists). Coordinating care across this system is essential for improving the health of patients. As the stewards of digestive health, we owe it to our patients to take a more comprehensive view of CRC screening quality and move beyond colonoscopy alone.
The complex web of care that comprises CRC screening is shown schematically in Figure 1. Appropriate screening begins with selection of suitable screening candidates. In the United States, where most screening is initiated during a clinician encounter, this important task falls primarily on the shoulders of PCPs. It is typically the role of the PCP to assess the two key patient factors that determine screening benefit: CRC risk (using personal and family history) and life expectancy (using age and overall health status). Once a patient has been deemed an appropriate candidate for screening, an acceptable screening test must be selected. Here, patient and practitioner are faced with a menu of options, including fecal occult blood testing (FOBT), colonoscopy, multitarget stool DNA, and computed tomography colonography. For average-risk screening, the ideal test depends primarily on patient preference and local availability.
If a screening test other than colonoscopy is selected, it becomes critical that a positive test is followed by timely and high-quality colonoscopy. High-quality colonoscopy begins with evidence-based preprocedure education and preparation, including appropriate selection of anesthesia services. Once a patient has been well prepared and adequately sedated, an endoscopist must carefully examine the colonic mucosa and completely resect any suspicious polyps. Unless discarded, resected polyps must be reviewed and categorized by a pathologist, including appropriate identification of serrated polyps. Finally, pathology results must be correctly interpreted by the clinician, with evidence-based follow-up recommendations made and effectively communicated to the patient and the referring provider. Additionally, in the short term, delayed gastrointestinal (GI) and non-GI complications of colonoscopy must be recognized and appropriately addressed. In the long term, the rate of interval cancers must be monitored.
Recognizing the importance of CRC screening, GI specialty societies have proposed a variety of quality measures to ensure that patients receive high-quality and high-value colonoscopy. Several of these measures have been adopted by CMS as part of the Physician Quality Reporting System. Non-GI groups, such as the National Center for Quality Assurance and the Ambulatory Surgery Center Association, have also proposed their own CRC screening–related measures.
Despite the proliferation of measures in the domain of CRC screening, current measures fall short in several ways. First, they are largely focused on colonoscopy technical performance, with less attention paid to the important steps that occur before and after colonoscopy. For example, the existing Healthcare Effectiveness Data and Information Set measure for underuse of CRC screening assesses the proportion of patients in a health plan between the ages 50 and 75 who are up to date for CRC screening. This measure is satisfied if a patient completes FOBT, regardless of the result. But FOBT alone is not sufficient to reduce mortality from CRC. Rather, it is imperative that a positive FOBT test be followed by colonoscopy. Numerous studies suggest a quality gap in this critical referral step.7
Yet, outside of selected clinical settings (e.g., the Veterans Affairs Healthcare System), no existing quality measure focuses on colonoscopy completion after positive FOBT. Other examples of important performance gaps beyond colonoscopy technical performance include appropriate use of monitored anesthesia care (data suggest overuse) and appropriate pathology interpretation (data suggest variation in the interpretation of serrated lesions, some of which are associated with increased risk of CRC).
Second, existing measures fail to consider individual patient factors that are known to be predictive of screening benefit, such as life expectancy and personal or familial cancer risk.8
Returning to the Healthcare Effectiveness Data and Information Set measure as an example, this measure relies on age alone to identify patients who are candidates for screening. Yet, it is widely recognized that life expectancy is a critically important factor when considering screening, particularly in older patients. However, existing measures fail to incorporate estimates of life expectancy. As a result, clinicians are encouraged to screen based on age alone. Data suggest that this leads to overuse in older, sicker patients younger than age 75 (the age cutoff suggested by guidelines and incorporated into the Healthcare Effectiveness Data and Information Set measure) and underuse in healthy and unscreened patients older than age 75.9
Furthermore, existing measures fail to systematically consider patient preferences and undervalue shared decision making. Data suggest, for instance, that patients who are offered a “menu” of options for screening rather than a single screening test are more likely to complete a screening test.10
But existing measures do not consider whether a physician assessed a patient’s preferences, or offered more than one screening option. Of course, measuring the quality of decision making is an evolving science that presents challenges and requires creative solutions.11
Finally, existing measures do not capture the collaborative nature of modern health care. For example, most existing measures focus on the performance of gastroenterologists and GI practices. Although such a focus is appropriate for specialty-specific quality improvement efforts, it neglects to capture the important interactions and hand-offs between providers needed for successful completion of screening (and downstream reduction in cancer mortality). As a result, this specialty-focused approach fails to meet the needs of patients, who are increasingly interested in whether the care they receive is improving their health regardless of who provides it. It also fails to meet the needs of payers, who are interested in whether a network of providers is delivering high-value care for its members. Developing measures that capture the collaborative nature of modern health care becomes increasingly important as payers embrace alternative payment models and other value-based reimbursement systems.
Given these challenges with existing measures, we propose the following concepts for consideration as noncolonoscopy quality measures of CRC screening:
1. Appropriateness of referral for CRC screening (PCP): Measures in this domain should incorporate assessment of family history, prior screening history, and/or life expectancy, all of which are predictive of screening benefit and can be extracted from structured electronic health record data.
2. Shared decision making in choosing a CRC screening test (PCP): Currently, measures in this domain are (by necessity) relatively simple, such as assessment of documentation of whether stool testing was offered alongside colonoscopy during a clinic visit.
3. Percentage of individuals with a positive noncolonoscopy CRC screening test who complete a colonoscopy within 6 months (PCP and GI): A measure in this domain can be developed and implemented using existing infrastructure. The Veterans Affairs Healthcare System currently uses such a measure to monitor appropriate follow-up of positive fecal immunochemical tests.
4. Predicted reduction in CRC mortality: This measure, which provides an estimate of the effectiveness and value of a screening program, represents the “bottom line” that is ultimately of interest to both patients and payers. However, composite measures that use projected results require sophisticated statistical approaches and case-mix adjustment. They must also contend with “churn” in the covered population.
Although a more comprehensive view of screening is desirable, operationalizing measure concepts, such as those proposed previously, is challenging for several reasons. First, as we have outlined, CRC screening is truly a “team sport.” The stakeholders in CRC screening include public health, primary care, gastroenterology, colorectal surgery, oncology, anesthesiology, and pathology practitioners. As a result, screening has no natural and obvious steward. Rather, various components of care are adopted by different specialty groups, and this approach leads to unmonitored gaps in care. We believe that gastroenterologists can and should take the lead in developing comprehensive quality measures for CRC screening. Such comprehensive measures will be of value to patients and to payers. Second, assessing quality of care more comprehensively has traditionally been infeasible. For example, incorporating life expectancy into quality measures requires electronic assessment of health status.
Traditionally, such efforts have been hampered by the lack of systematic clinical data collection. However, as meaningful use of electronic health records increases, measures that incorporate such information are likely to become increasingly feasible. Finally, we also need to consider how to make these improvements while avoiding measure proliferation. Proliferation leads to provider fatigue and discourages thoughtful clinical decision making, potentially worsening quality of care. Creative approaches, such as rotating measure sets over time, use of clinical decision support tools, and balancing underuse measures with overuse measures, may be warranted. Additionally, composite measures may prove to be more meaningful and more practical for patients, providers, and payers. Ultimately, a distinction must be made between quality assurance and quality improvement; both are important, but the types of measures and the level of measure sophistication used in each program undoubtedly vary.
In summary, gastroenterologists are uniquely positioned to advocate for high-quality CRC screening that extends beyond simply providing a high-quality colonoscopy. This broader view of quality benefits patients by ensuring that our expertise informs the metrics by which delivery of CRC screening is measured. It also ensures that we hold ourselves and our colleagues to the highest standards across the continuum of care. Additionally, as alternative payment models and value-based contracting are implemented, nonendoscopic screening methods will likely become more commonplace. Advocating for high-quality nonendoscopic screening will help maintain gastroenterologists’ role as the stewards of CRC screening and digestive health. Although operationalizing measure concepts such as those proposed here may be difficult, it is critical if we are to provide the best possible care for our patients.
References
1. Sabatino, S.A., White, M.C., Thompson, T.D., et al. Cancer screening test use – United States, 2013. MMWR Morb Mortal Wkly Rep. 2015;64:464-8.
2. Anderson, A.E., Henry, K.A., Samadder, N.J., et al. Rural vs urban residence affects risk-appropriate colorectal cancer screening. Clin Gastroenterol Hepatol. 2013;11:526-33.
3. Walter, L.C., Lindquist, K., Nugent, S., et al. Impact of age and comorbidity on colorectal cancer screening among older veterans. Ann Intern Med. 2009;150:465-73.
4. Murphy, C.C., Sandler, R.S., Grubber, J.M., et al. Underuse and overuse of colonoscopy for repeat screening and surveillance in the Veterans Health Administration. Clin Gastroenterol Hepatol. 2016;14:436-44.
5. Mittal, S., Lin, Y.-L., Tan, A., et al. Limited life expectancy among a subgroup of Medicare beneficiaries receiving screening colonoscopies. Clin Gastroenterol Hepatol. 2014;12:443-50.e1
6. Allen, J.I. Quality measures for colonoscopy: where should we be in 2015?. Curr Gastroenterol Rep. 2015;17:10.
7. Fisher, D.A., Jeffreys, A., Coffman, C.J., et al. Barriers to full colon evaluation for a positive fecal occult blood test. Cancer Epidemiol Biomark Prev. 2006;15:1232-5.
8. Saini, S.D., van Hees, F., Vijan, S. Smarter screening for cancer: possibilities and challenges of personalization. JAMA. 2014;312:2211-2.
9. Saini, S.D., Vijan, S., Schoenfeld, P., et al. Role of quality measurement in inappropriate use of screening for colorectal cancer: retrospective cohort study. BMJ. 2014;348:g1247.
10. Inadomi, J.M., Vijan, S., Janz, N.K., et al. Adherence to colorectal cancer screening: a randomized clinical trial of competing strategies. Arch Intern Med. 2012;172:575-82.
11. Writing Committee Members, Drozda, J.P., Ferguson, T.B., et al. 2015 ACC/AHA focused update of secondary prevention lipid performance measures: a report of the American College of Cardiology/American Heart Association Task Force on Performance Measures. J Am Coll Cardiol. 2016;67:558-87.
Dr. Saini is a research scientist at the VA Center for Clinical Management Research and an assistant professor of internal medicine at the University of Michigan, Ann Arbor; Dr. Adams is a clinical lecturer in the division of gastroenterology, department of internal medicine, University of Michigan, and a research investigator, VA Center for Clinical Management Research; Dr. Brill is the chief medical officer of Predictive Health, Paradise Valley, Ariz., and a clinical assistant professor of medicine, University of Arizona School of Medicine, Phoenix; Dr. Gupta is codirector of Digestive Health Center, director of interventional endoscopy, and associate professor of medicine in the division of gastroenterology at Loyola University Medical Center; Dr. Naveed is a clinical assistant professor in the department of gastroenterology and hepatology, University of Iowa Hospitals and Clinics; Dr. Rosenberg is at Illinois Gastroenterology Group; and Dr. Gellad is associate professor of medicine at Duke University School of Medicine, Durham, N.C. Dr. Saini’s and Dr. Gellad’s research is funded by Veterans Affairs Health Services Research and Development Career Development Awards (CDA 09-213-2 and CDA 14-158). Dr. Gupta has received research support from Cook Medical, Cosmo Pharmaceuticals, and CDx Diagnostics.
Medicine in the United States is undergoing fundamental changes that will continue despite 2016 presidential election results. Changes include consolidation of provider networks, movement from volume- to value-based reimbursement, demands for price and quality transparency, and a shift from focusing solely on individual physician-patient interactions to a broader triple aim focus that incorporates individual patients, population, health, and cost. In this month’s column, Sameer Saini and colleagues suggest that we broaden our view of colorectal cancer screening quality metrics from a colonoscopy-centric focus to a focus on the bottom line: Do we reduce cancer in the population of patients that we serve? When we extend our view to a population level, we use current colonoscopy registries only as internal process controls. A successful health system will develop a mechanism to assess and demonstrate how well the collective team of providers accomplishes the only outcome that matters to patients: preventing colon cancer.
John I. Allen, MD, MBA, AGAF, Special Section Editor
Colorectal cancer (CRC) screening is one of the most valuable services provided by gastroenterologists. The evidence that screening “works” on a population level is undeniable. But not every screening program is equally effective. Data indicate ongoing underuse of screening, particularly in high-risk, vulnerable, and minority communities.1,2 Other data indicate that screening is overused, particularly in low-risk patients and in those with limited life expectancy.3-5 It is also known that endoscopist skill plays an important role in the effectiveness of screening. In short, there is ample room for improvement in the quality of CRC screening, and payers and the public have taken notice. Unsurprisingly, gastroenterologists are often focused on procedural quality indicators, such as adenoma detection and cecal intubation rates.6 These endoscopic quality measures are important indicators of high-quality colonoscopy, but colonoscopy is the common touch point of a much broader system of care that includes other screening tests and other providers (e.g., primary care providers [PCPs], pathologists, and anesthesiologists). Coordinating care across this system is essential for improving the health of patients. As the stewards of digestive health, we owe it to our patients to take a more comprehensive view of CRC screening quality and move beyond colonoscopy alone.
The complex web of care that comprises CRC screening is shown schematically in Figure 1. Appropriate screening begins with selection of suitable screening candidates. In the United States, where most screening is initiated during a clinician encounter, this important task falls primarily on the shoulders of PCPs. It is typically the role of the PCP to assess the two key patient factors that determine screening benefit: CRC risk (using personal and family history) and life expectancy (using age and overall health status). Once a patient has been deemed an appropriate candidate for screening, an acceptable screening test must be selected. Here, patient and practitioner are faced with a menu of options, including fecal occult blood testing (FOBT), colonoscopy, multitarget stool DNA, and computed tomography colonography. For average-risk screening, the ideal test depends primarily on patient preference and local availability.
If a screening test other than colonoscopy is selected, it becomes critical that a positive test is followed by timely and high-quality colonoscopy. High-quality colonoscopy begins with evidence-based preprocedure education and preparation, including appropriate selection of anesthesia services. Once a patient has been well prepared and adequately sedated, an endoscopist must carefully examine the colonic mucosa and completely resect any suspicious polyps. Unless discarded, resected polyps must be reviewed and categorized by a pathologist, including appropriate identification of serrated polyps. Finally, pathology results must be correctly interpreted by the clinician, with evidence-based follow-up recommendations made and effectively communicated to the patient and the referring provider. Additionally, in the short term, delayed gastrointestinal (GI) and non-GI complications of colonoscopy must be recognized and appropriately addressed. In the long term, the rate of interval cancers must be monitored.
Recognizing the importance of CRC screening, GI specialty societies have proposed a variety of quality measures to ensure that patients receive high-quality and high-value colonoscopy. Several of these measures have been adopted by CMS as part of the Physician Quality Reporting System. Non-GI groups, such as the National Center for Quality Assurance and the Ambulatory Surgery Center Association, have also proposed their own CRC screening–related measures.
Despite the proliferation of measures in the domain of CRC screening, current measures fall short in several ways. First, they are largely focused on colonoscopy technical performance, with less attention paid to the important steps that occur before and after colonoscopy. For example, the existing Healthcare Effectiveness Data and Information Set measure for underuse of CRC screening assesses the proportion of patients in a health plan between the ages 50 and 75 who are up to date for CRC screening. This measure is satisfied if a patient completes FOBT, regardless of the result. But FOBT alone is not sufficient to reduce mortality from CRC. Rather, it is imperative that a positive FOBT test be followed by colonoscopy. Numerous studies suggest a quality gap in this critical referral step.7
Yet, outside of selected clinical settings (e.g., the Veterans Affairs Healthcare System), no existing quality measure focuses on colonoscopy completion after positive FOBT. Other examples of important performance gaps beyond colonoscopy technical performance include appropriate use of monitored anesthesia care (data suggest overuse) and appropriate pathology interpretation (data suggest variation in the interpretation of serrated lesions, some of which are associated with increased risk of CRC).
Second, existing measures fail to consider individual patient factors that are known to be predictive of screening benefit, such as life expectancy and personal or familial cancer risk.8
Returning to the Healthcare Effectiveness Data and Information Set measure as an example, this measure relies on age alone to identify patients who are candidates for screening. Yet, it is widely recognized that life expectancy is a critically important factor when considering screening, particularly in older patients. However, existing measures fail to incorporate estimates of life expectancy. As a result, clinicians are encouraged to screen based on age alone. Data suggest that this leads to overuse in older, sicker patients younger than age 75 (the age cutoff suggested by guidelines and incorporated into the Healthcare Effectiveness Data and Information Set measure) and underuse in healthy and unscreened patients older than age 75.9
Furthermore, existing measures fail to systematically consider patient preferences and undervalue shared decision making. Data suggest, for instance, that patients who are offered a “menu” of options for screening rather than a single screening test are more likely to complete a screening test.10
But existing measures do not consider whether a physician assessed a patient’s preferences, or offered more than one screening option. Of course, measuring the quality of decision making is an evolving science that presents challenges and requires creative solutions.11
Finally, existing measures do not capture the collaborative nature of modern health care. For example, most existing measures focus on the performance of gastroenterologists and GI practices. Although such a focus is appropriate for specialty-specific quality improvement efforts, it neglects to capture the important interactions and hand-offs between providers needed for successful completion of screening (and downstream reduction in cancer mortality). As a result, this specialty-focused approach fails to meet the needs of patients, who are increasingly interested in whether the care they receive is improving their health regardless of who provides it. It also fails to meet the needs of payers, who are interested in whether a network of providers is delivering high-value care for its members. Developing measures that capture the collaborative nature of modern health care becomes increasingly important as payers embrace alternative payment models and other value-based reimbursement systems.
Given these challenges with existing measures, we propose the following concepts for consideration as noncolonoscopy quality measures of CRC screening:
1. Appropriateness of referral for CRC screening (PCP): Measures in this domain should incorporate assessment of family history, prior screening history, and/or life expectancy, all of which are predictive of screening benefit and can be extracted from structured electronic health record data.
2. Shared decision making in choosing a CRC screening test (PCP): Currently, measures in this domain are (by necessity) relatively simple, such as assessment of documentation of whether stool testing was offered alongside colonoscopy during a clinic visit.
3. Percentage of individuals with a positive noncolonoscopy CRC screening test who complete a colonoscopy within 6 months (PCP and GI): A measure in this domain can be developed and implemented using existing infrastructure. The Veterans Affairs Healthcare System currently uses such a measure to monitor appropriate follow-up of positive fecal immunochemical tests.
4. Predicted reduction in CRC mortality: This measure, which provides an estimate of the effectiveness and value of a screening program, represents the “bottom line” that is ultimately of interest to both patients and payers. However, composite measures that use projected results require sophisticated statistical approaches and case-mix adjustment. They must also contend with “churn” in the covered population.
Although a more comprehensive view of screening is desirable, operationalizing measure concepts, such as those proposed previously, is challenging for several reasons. First, as we have outlined, CRC screening is truly a “team sport.” The stakeholders in CRC screening include public health, primary care, gastroenterology, colorectal surgery, oncology, anesthesiology, and pathology practitioners. As a result, screening has no natural and obvious steward. Rather, various components of care are adopted by different specialty groups, and this approach leads to unmonitored gaps in care. We believe that gastroenterologists can and should take the lead in developing comprehensive quality measures for CRC screening. Such comprehensive measures will be of value to patients and to payers. Second, assessing quality of care more comprehensively has traditionally been infeasible. For example, incorporating life expectancy into quality measures requires electronic assessment of health status.
Traditionally, such efforts have been hampered by the lack of systematic clinical data collection. However, as meaningful use of electronic health records increases, measures that incorporate such information are likely to become increasingly feasible. Finally, we also need to consider how to make these improvements while avoiding measure proliferation. Proliferation leads to provider fatigue and discourages thoughtful clinical decision making, potentially worsening quality of care. Creative approaches, such as rotating measure sets over time, use of clinical decision support tools, and balancing underuse measures with overuse measures, may be warranted. Additionally, composite measures may prove to be more meaningful and more practical for patients, providers, and payers. Ultimately, a distinction must be made between quality assurance and quality improvement; both are important, but the types of measures and the level of measure sophistication used in each program undoubtedly vary.
In summary, gastroenterologists are uniquely positioned to advocate for high-quality CRC screening that extends beyond simply providing a high-quality colonoscopy. This broader view of quality benefits patients by ensuring that our expertise informs the metrics by which delivery of CRC screening is measured. It also ensures that we hold ourselves and our colleagues to the highest standards across the continuum of care. Additionally, as alternative payment models and value-based contracting are implemented, nonendoscopic screening methods will likely become more commonplace. Advocating for high-quality nonendoscopic screening will help maintain gastroenterologists’ role as the stewards of CRC screening and digestive health. Although operationalizing measure concepts such as those proposed here may be difficult, it is critical if we are to provide the best possible care for our patients.
References
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Dr. Saini is a research scientist at the VA Center for Clinical Management Research and an assistant professor of internal medicine at the University of Michigan, Ann Arbor; Dr. Adams is a clinical lecturer in the division of gastroenterology, department of internal medicine, University of Michigan, and a research investigator, VA Center for Clinical Management Research; Dr. Brill is the chief medical officer of Predictive Health, Paradise Valley, Ariz., and a clinical assistant professor of medicine, University of Arizona School of Medicine, Phoenix; Dr. Gupta is codirector of Digestive Health Center, director of interventional endoscopy, and associate professor of medicine in the division of gastroenterology at Loyola University Medical Center; Dr. Naveed is a clinical assistant professor in the department of gastroenterology and hepatology, University of Iowa Hospitals and Clinics; Dr. Rosenberg is at Illinois Gastroenterology Group; and Dr. Gellad is associate professor of medicine at Duke University School of Medicine, Durham, N.C. Dr. Saini’s and Dr. Gellad’s research is funded by Veterans Affairs Health Services Research and Development Career Development Awards (CDA 09-213-2 and CDA 14-158). Dr. Gupta has received research support from Cook Medical, Cosmo Pharmaceuticals, and CDx Diagnostics.