Guideline Title
Screening for peripheral arterial disease.
Bibliographic Source(s)
U.S. Preventive Services Task Force. Screening for peripheral arterial disease: recommendation statement. Am Fam Physician 2006 Feb 1;73(3):497-500. PubMed  |
Guideline Status
This is the current release of the guideline.
This guideline updates a previously published guideline: U.S. Preventive Services Task Force. Guide to clinical preventive services. 2nd ed. Baltimore (MD): Williams & Wilkins; 1996. Chapter 5, Screening for peripheral arterial disease. p. 63-6. [16 references]
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Disease/Condition(s)
Peripheral arterial disease
Guideline Category
Prevention
Screening
Clinical Specialty
Cardiology
Family Practice
Geriatrics
Internal Medicine
Preventive Medicine
Intended Users
Advanced Practice Nurses
Allied Health Personnel
Health Care Providers
Health Plans
Managed Care Organizations
Nurses
Physician Assistants
Physicians
Guideline Objective(s)
- To summarize the U.S. Preventive Services Task Force (USPSTF) recommendations on screening for peripheral arterial disease and the supporting scientific evidence
- To update the 1996 recommendations contained in the Guide to Clinical Preventive Services, Second Edition
Target Population
Asymptomatic adults seen in primary care
Interventions and Practices Considered
Considered but not Recommended
Routine screening for peripheral arterial disease using ankle brachial index, history-taking, questionnaires, or palpation of peripheral pulses
Major Outcomes Considered
- Key Question 1: Does screening for peripheral arterial disease (PAD) lead to reduced morbidity from PAD (including claudication, amputation, impaired ambulation)?
- Key Question 2: What is the yield of screening (e.g., prevalence, sensitivity, specificity) for PAD in primary care practice?
- Key Question 3: What are the harms of screening (e.g., labeling, over-diagnosis, over treatment)?
- Key Question 4: Does treatment of people with screening-detected PAD lead to improvement in the outcomes specified in Question #1 beyond the benefits of treatment at the time of symptoms?
- Key Question 4a: Is there a subgroup of screening-detected PAD patient in whom detection of PAD results in more effective treatment of claudication beyond identification of conventional risk factors alone (e.g., through earlier or more aggressive use of treatments such as aspirin or other anti-platelet agents, lipid-lowering therapy, blood pressure treatment of lifestyle intervention)?
- Key Question 5: What are the harms of earlier treatment for PAD (i.e., side-effects of treatment)?
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Methods Used to Collect/Select the Evidence
Searches of Electronic Databases
Description of Methods Used to Collect/Select the Evidence
Note from the National Guideline Clearinghouse (NGC): A targeted review of the literature was prepared by the Lewin Group for the Agency for Healthcare Research and Quality (AHRQ) for use by the U.S. Preventive Services Task Force (USPSTF) (see the "Companion Documents" field).
Search Strategy
The literature search was guided by an analytic framework developed specifically for peripheral arterial disease (PAD) by the USPSTF. Specifically, this review focused on PAD outcomes and did not examine PAD as a risk factor for coronary heart disease (CHD).
The search strategy included a review of English language articles identified from Pubmed, the Cochrane Library, and the National Guideline Clearinghouse, published between 1994 and 2003. The search excluded letters, editorials, and narrative reviews. Studies of symptomatic (i.e., PAD or intermittent claudication) populations were also excluded from this search.
Abstracts were reviewed to determine which articles addressed the Key Questions. One reviewer examined the abstracts with the instruction to retain all that were clearly in-scope and those with potential or ambiguous relevance. These abstracts were then reviewed by a senior staff member for relevance.
Upon finalizing this report, a subsequent bridge search was conducted of literature published between January 2004 and June 2005. No relevant studies were identified.
Number of Source Documents
- Key question #1: One randomized controlled trial
- Key question #2: No new evidence meeting search criteria was identified.
- Key question #3: No new evidence meeting search criteria was identified.
- Key question #4: One cross-sectional study
- Key question #4a: One fair quality study
- Key question #5: No new evidence meeting search criteria was identified.
Methods Used to Assess the Quality and Strength of the Evidence
Weighting According to a Rating Scheme (Scheme Given)
Rating Scheme for the Strength of the Evidence
The U.S. Preventive Services Task Force (USPSTF) grades the quality of the overall evidence for a service on a 3-point scale (good, fair, poor):
Good
Evidence includes consistent results from well-designed, well-conducted studies in representative populations that directly assess effects on health outcomes.
Fair
Evidence is sufficient to determine effects on health outcomes, but the strength of the evidence is limited by the number, quality, or consistency of the individual studies, generalizability to routine practice, or indirect nature of the evidence on health outcomes.
Poor
Evidence is insufficient to assess the effects on health outcomes because of limited number or power of studies, important flaws in their design or conduct, gaps in the chain of evidence, or lack of information on important health outcomes.
Methods Used to Analyze the Evidence
Systematic Review
Description of the Methods Used to Analyze the Evidence
Methods Used to Formulate the Recommendations
Balance Sheets
Expert Consensus
Description of Methods Used to Formulate the Recommendations
When the overall quality of the evidence is judged to be good or fair, the
U.S. Preventive Services Task Force (USPSTF) proceeds to consider the magnitude
of net benefit to be expected from implementation of the preventive service.
Determining net benefit requires assessing both the magnitude of benefits and
the magnitude of harms and weighing the two.
The USPSTF classifies benefits, harms, and net benefits on a 4-point scale:
"substantial," "moderate," "small," and "zero/negative."
"Outcomes tables" (similar to "balance sheets") are the USPSTF's standard
resource for estimating the magnitude of benefit. These tables, prepared by the
topic teams for use at USPSTF meetings, compare the condition specific outcomes
expected for a hypothetical primary care population with and without use of the
preventive service. These comparisons may be extended to consider only people of
specified age or risk groups or other aspects of implementation. Thus, outcomes
tables allow the USPSTF to examine directly how the preventive service affects
benefits for various groups.
When evidence on harms is available, the topic teams assess its quality in a
manner like that for benefits and include adverse events in the outcomes tables.
When few harms data are available, the USPSTF does not assume that harms are
small or nonexistent. It recognizes a responsibility to consider which harms are
likely and judge their potential frequency and the severity that might ensue
from implementing the service. It uses whatever evidence exists to construct a
general confidence interval on the 4-point scale (e.g., substantial, moderate,
small, and zero/negative).
Value judgments are involved in using the information in an outcomes table to
rate either benefits or harms on the USPSTF's 4-point scale. Value judgments are
also needed to weigh benefits against harms to arrive a rating of net benefit.
In making its determinations of net benefit, the USPSTF strives to consider
what it believes are the general values of most people. It does this with
greater confidence for certain outcomes (e.g., death) about which there is
little disagreement about undesirability, but it recognizes that the degree of
risk people are willing to accept to avert other outcomes (e.g., cataracts) can
vary considerably. When the USPSTF perceives that preferences among individuals
vary greatly, and that these variations are sufficient to make trade-off of
benefits and harms a "close-call," then it will often assign a C recommendation
(see the "Recommendation Rating Scheme" field). This recommendation indicates
the decision is likely to be sensitive to individual patient preferences.
The USPSTF uses its assessment of the evidence and magnitude of net benefit
to make recommendations. The general principles the USPSTF follows in making
recommendations are outlined in Table 5 of the companion document cited below.
The USPSTF liaisons on the topic team compose the first drafts of the
recommendations and rationale statements, which the full panel then reviews and
edits. Recommendations are based on formal voting procedures that include
explicit rules for determining the views of the majority.
From: Harris RP, Helfand M, Woolf SH, Lohr KN, Mulrow, CD, Teutsch SM,
Atkins D. Current methods of the U.S. Preventive Services Task Force: a review
of the process. Methods Work Group, Third U.S. Preventive Services Task Force.
Am J Prev Med 2001 Apr;20(3S):21-35.
Rating Scheme for the Strength of the Recommendations
The U.S. Preventive Services Task Force (USPSTF) grades its recommendations according to one of 5 classifications (A, B, C, D, I) reflecting the strength of evidence and magnitude of net benefit (benefits minus harms):
A
The USPSTF strongly recommends that clinicians provide [the service] to
eligible patients. The USPSTF found good evidence that [the service] improves
important health outcomes and concludes that benefits substantially outweigh
harms.
B
The USPSTF recommends that clinicians provide [this service] to eligible
patients. The USPSTF found at least fair evidence that [the service] improves
important health outcomes and concludes that benefits outweigh harms.
C
The USPSTF makes no recommendation for or against routine provision of [the
service]. The USPSTF found at least fair evidence that [the service] can improve
health outcomes but concludes that the balance of benefits and harms is too
close to justify a general recommendation.
D
The USPSTF recommends against routinely providing [the service] to
asymptomatic patients. The USPSTF found at least fair evidence that [the
service] is ineffective or that harms outweigh benefits.
I
The USPSTF concludes that the evidence is insufficient to recommend for or
against routinely providing [the service]. Evidence that [the service] is
effective is lacking, of poor quality, or conflicting and the balance of
benefits and harms cannot be determined.
Cost Analysis
A formal cost analysis was not performed and published cost analyses were not reviewed.
Method of Guideline Validation
Comparison with Guidelines from Other Groups
External Peer Review
Internal Peer Review
Description of Method of Guideline Validation
Peer Review. Before the U.S. Preventive Services Task Force (USPSTF)
makes its final determinations about recommendations on a given preventive
service, the Evidence-based Practice Center and the Agency for Healthcare
Research and Quality send a draft systematic evidence review to 4 to 6 external
experts and to federal agencies and professional and disease-based health
organizations with interests in the topic. They ask the experts to examine the
review critically for accuracy and completeness and to respond to a series of
specific questions about the document. After assembling these external review
comments and documenting the proposed response to key comments, the topic team
presents this information to the Task Force in memo form. In this way, the Task
Force can consider these external comments and a final version of the systematic
review before it votes on its recommendations about the service. Draft
recommendations are then circulated for comment from reviewers representing
professional societies, voluntary organizations, and Federal agencies. These
comments are discussed before the whole USPSTF before final recommendations are
confirmed.
Recommendation of Others. Recommendations for screening for peripheral arterial disease from the following groups were discussed: the American Diabetes Association (ADA), the American Academy of Family Physicians (AAFP), the American Heart Association (AHA), and the Society for Interventional Radiology (SIR).
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Major Recommendations
The U.S. Preventive Services Task Force (USPSTF) grades its recommendations (A, B, C, D, or I) and the quality of the overall evidence for a service (good, fair, poor). The definitions of these grades can be found at the end of the "Major Recommendations" field.
The USPSTF recommends against routine screening for peripheral arterial disease (PAD). D recommendation
The USPSTF found fair evidence that screening with ankle brachial index can detect adults with asymptomatic PAD. The evidence is also fair that screening for PAD among asymptomatic adults in the general population would have few or no benefits because the prevalence of PAD in this group is low, and because there is little evidence that treatment of PAD at this asymptomatic stage of disease, beyond treatment based on standard cardiovascular risk assessment, improves health outcomes.
The USPSTF found fair evidence that screening asymptomatic adults with the ankle brachial index could lead to some small degree of harm, including false-positive results and unnecessary work-ups. Thus, the USPSTF concludes that, for asymptomatic adults, harms of routine screening for PAD exceed benefits.
Clinical Considerations
- The ankle brachial index, a ratio of Doppler-recorded systolic pressures in the lower and upper extremities, is a simple and accurate noninvasive test for the screening and diagnosis of PAD. The ankle brachial index has demonstrated better accuracy than other methods of screening, including history-taking, questionnaires, and palpation of peripheral pulses. An ankle-brachial index value of less than 0.90 (95% sensitive and specific for angiographic PAD) is strongly associated with limitations in lower extremity functioning and physical activity tolerance.
- Smoking cessation and lipid-lowering agents improve claudication symptoms and lower extremity functioning among patients with symptomatic PAD. Smoking cessation and physical activity training also increase maximal walking distance among men with early PAD. Counseling for smoking cessation, however, should be offered to all patients who smoke, regardless of the presence of PAD. Similarly, physically inactive patients should be counseled to increase their physical activity, regardless of the presence of PAD.
Definitions:
Strength of Recommendations
The USPSTF grades its recommendations according to one of 5 classifications
(A, B, C, D, I) reflecting the strength of evidence and magnitude of net benefit
(benefits minus harms):
A
The USPSTF strongly recommends that clinicians provide [the service] to
eligible patients. The USPSTF found good evidence that [the service] improves
important health outcomes and concludes that benefits substantially outweigh
harms.
B
The USPSTF recommends that clinicians provide [this service] to eligible
patients. The USPSTF found at least fair evidence that [the service] improves
important health outcomes and concludes that benefits outweigh harms.
C
The USPSTF makes no recommendation for or against routine provision of [the
service]. The USPSTF found at least fair evidence that [the service] can improve
health outcomes but concludes that the balance of benefits and harms is too
close to justify a general recommendation.
D
The USPSTF recommends against routinely providing [the service] to
asymptomatic patients. The USPSTF found at least fair evidence that [the
service] is ineffective or that harms outweigh benefits.
I
The USPSTF concludes that the evidence is insufficient to recommend for or
against routinely providing [the service]. Evidence that [the service] is
effective is lacking, of poor quality, or conflicting and the balance of
benefits and harms cannot be determined.
Strength of Evidence
The U.S. Preventive Services Task Force (USPSTF) grades the quality of the overall evidence for a service on a 3-point scale (good, fair, poor):
Good
Evidence includes consistent results from well-designed, well-conducted studies in representative populations that directly assess effects on health outcomes.
Fair
Evidence is sufficient to determine effects on health outcomes, but the strength of the evidence is limited by the number, quality, or consistency of the individual studies, generalizability to routine practice, or indirect nature of the evidence on health outcomes.
Poor
Evidence is insufficient to assess the effects on health outcomes because of limited number or power of studies, important flaws in their design or conduct, gaps in the chain of evidence, or lack of information on important health outcomes.
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Evidence Supporting the Recommendations
Type of Evidence Supporting the Recommendations
The type of evidence supporting the recommendations is identified in the "Major Recommendations" field.
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Benefits/Harms of Implementing the Guideline Recommendations
Potential Benefits
Appropriate screening for peripheral arterial disease
Potential Harms
Potential harms of screening include false-positive results, labeling, and the adverse events associated with an angiographic workup, including contrast-related events, arterial perforations, hematomas, thromboses, and distal embolizations. The harms of treatment include the adverse events associated with medical (antithrombotic medications) and surgical treatments (angioplasty, femoral bypass procedures).
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Qualifying Statements
Recommendations made by the U.S. Preventive Services Task Force are independent of the U.S. Government. They should not be construed as an official position of the Agency for Healthcare Research and Quality or the U.S. Department of Health and Human Services.
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Implementation of the Guideline
Description of Implementation Strategy
The experiences of the first and second U.S. Preventive Services Task Force (USPSTF), as well as that of other evidence-based guideline efforts, have highlighted the importance of identifying effective ways to implement clinical recommendations. Practice guidelines are relatively weak tools for changing clinical practice when used in isolation. To effect change, guidelines must be coupled with strategies to improve their acceptance and feasibility. Such strategies include enlisting the support of local opinion leaders, using reminder systems for clinicians and patients, adopting standing orders, and audit and feedback of information to clinicians about their compliance with recommended practice.
In the case of preventive services guidelines, implementation needs to go beyond traditional dissemination and promotion efforts to recognize the added patient and clinician barriers that affect preventive care. These include clinicians' ambivalence about whether preventive medicine is part of their job, the psychological and practical challenges that patients face in changing behaviors, lack of access to health care or of insurance coverage for preventive services for some patients, competing pressures within the context of shorter office visits, and the lack of organized systems in most practices to ensure the delivery of recommended preventive care.
Dissemination strategies have changed dramatically in this age of electronic information. While recognizing the continuing value of journals and other print formats for dissemination, the Agency for Healthcare Research and Quality will make all U.S. Preventive Services Task Force (USPSTF) products available through its Web site . The combination of electronic access and extensive material in the public domain should make it easier for a broad audience of users to access U.S. Preventive Services Task Force materials and adapt them for their local needs. Online access to U.S. Preventive Services Task Force products also opens up new possibilities for the appearance of the annual, pocket-size Guide to Clinical Preventive Services.
To be successful, approaches for implementing prevention have to be tailored to the local level and deal with the specific barriers at a given site, typically requiring the redesign of systems of care. Such a systems approach to prevention has had notable success in established staff-model health maintenance organizations, by addressing organization of care, emphasizing a philosophy of prevention, and altering the training and incentives for clinicians. Staff-model plans also benefit from integrated information systems that can track the use of needed services and generate automatic reminders aimed at patients and clinicians, some of the most consistently successful interventions. Information systems remain a major challenge for individual clinicians' offices, however, as well as for looser affiliations of practices in network-model managed care and independent practice associations, where data on patient visits, referrals, and test results are not always centralized.
Implementation Tools
Foreign Language Translations
Patient Resources
Tool KitsFor information about availability, see the Availability of Companion Documents and Patient Resources fields below.
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Institute of Medicine (IOM) National Healthcare Quality Report Categories
IOM Care Need
Staying Healthy
IOM Domain
Effectiveness
Patient-centeredness
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Identifying Information and Availability
Bibliographic Source(s)
U.S. Preventive Services Task Force. Screening for peripheral arterial disease: recommendation statement. Am Fam Physician 2006 Feb 1;73(3):497-500. PubMed  |
Adaptation
Not applicable: The guideline was not adapted from another source.
Guideline Developer(s)
U.S. Preventive Services Task Force - Independent Expert Panel
Source(s) of Funding
Agency for Healthcare Research and Quality
Guideline Committee
U.S. Preventive Services Task Force (USPSTF)
Composition of Group That Authored the Guideline
Corresponding Author: Ned Calonge, MD, MPH, Chair, U.S. Preventive Services Task Force (USPSTF), c/o Program Director, USPSTF, Agency for Healthcare Research and Quality
Task Force Members*: Ned Calonge, MD, MPH, Chair, USPSTF (Acting Chief Medical Officer and State Epidemiologist, Colorado Department of Public Health and Environment, Denver, CO); Diana B. Petitti, MD, MPH, Vice-chair, USPSTF (Senior Scientific Advisor for Health Policy and Medicine, Regional Administration, Kaiser Permanente Southern California, Pasadena, CA); Janet D. Allan, PhD, RN, CS, (Dean, School of Nursing, University of Maryland Baltimore, Baltimore, MD); Alfred O. Berg, MD, MPH, (Professor and Chair, Department of Family Medicine, University of Washington, Seattle, WA); Paul S. Frame, MD (Tri-County Family Medicine, Cohocton, NY, and Clinical Professor of Family Medicine, University of Rochester, Rochester, NY); Joxel Garcia, MD, MBA, (Deputy Director, Pan American Health Organization, Washington, DC); Leon Gordis, MD, MPH, DrPH (Professor, Epidemiology Department, Johns Hopkins Bloomberg School of Public Health, Baltimore MD); Kimberly D. Gregory, MD, MPH (Director, Women's Health Services Research and Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, CA); Russell Harris, MD, MPH (Associate Professor of Medicine, Sheps Center for Health Services Research, University of North Carolina School of Medicine, Chapel Hill, NC); Mark S. Johnson, MD, MPH (Professor and Chair, Department of Family Medicine, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, NJ); Jonathan D. Klein, MD, MPH (Associate Professor, Department of Pediatrics, University of Rochester School of Medicine, Rochester, NY); Carol Loveland-Cherry, PhD, RN (Executive Associate Dean, Office of Academic Affairs, University of Michigan School of Nursing, Ann Arbor, MI); Virginia A. Moyer, MD, MPH (Professor, Department of Pediatrics, University of Texas Health Sciences Center, Houston, TX); Judith K. Ockene, PhD (Professor of Medicine and Chief of Division of Preventive and Behavioral Medicine, University of Massachusetts Medical School, Worcester, MA); Albert L. Siu, MD, MSPH (Professor and Chairman, Brookdale Department of Geriatrics and Adult Development, Mount Sinai Medical Center, New York, NY); Steven M. Teutsch, MD, MPH (Executive Director, Outcomes Research and Management, Merck & Company, Inc., West Point, PA); and Barbara P. Yawn, MD, MSc (Director of Research, Olmstead Research Center, Rochester, MN)
*Members of the USPSTF at the time this recommendation was finalized. For a list of current Task Force members, go to www.ahrq.gov/clinic/uspstfab.htm .
Financial Disclosures/Conflicts of Interest
The U.S. Preventive Services Task Force has an explicit policy concerning conflict of interest. All members and evidence-based practice center (EPC) staff disclose at each meeting if they have an important financial conflict for each topic being discussed. Task Force members and EPC staff with conflicts can participate in discussions about evidence, but members abstain from voting on recommendations about the topic in question.
From: Harris RP, Helfand M, Woolf SH, Lohr KN, Mulrow, CD, Teutsch SM, Atkins
D. Current methods of the U.S. Preventive Services Task Force: a review of the
process. Methods Work Group, Third U.S. Preventive Services Task Force. Am J
Prev Med 2001 Apr;20(3S):21-35.
Guideline Status
This is the current release of the guideline.
This guideline updates a previously published guideline: U.S. Preventive Services Task Force. Guide to clinical preventive services. 2nd ed. Baltimore (MD): Williams & Wilkins; 1996. Chapter 5, Screening for peripheral arterial disease. p. 63-6. [16 references]
Availability of Companion Documents
The following are available:
Background Articles:
- Woolf SH, Atkins D. The evolving role of prevention in health care: contributions of the U.S. Preventive Services Task Force. Am J Prev Med 2001 Apr;20(3S):13-20.
- Harris RP, Helfand M, Woolf SH, Lohr KN, Mulrow, CD, Teutsch SM, Atkins D. Current methods of the U.S. Preventive Services Task Force: a review of the process. Methods Work Group, Third U.S. Preventive Services Task Force. Am J Prev Med 2001 Apr;20(3S):21-35.
- Saha S, Hoerger TJ, Pignone MP, Teutsch SM, Helfand M, Mandelblatt JS. The art and science of incorporating cost effectiveness into evidence-based recommendations for clinical preventive services. Cost Work Group of the Third U.S. Preventive Services Task Force. Am J Prev Med 2001 Apr;20(3S):36-43.
Electronic copies: Available from U.S. Preventive Services Task Force (USPSTF) Web site .
The following are also available:
- The guide to clinical preventive services, 2006. Recommendations of the U.S. Preventive Services Task Force. Rockville (MD): Agency for Healthcare Research and Quality (AHRQ), 2006. 228 p. Electronic copies available from the AHRQ Web site
.
- A step-by-step guide to delivering clinical preventive services: a systems approach. Rockville (MD): Agency for Healthcare Research and Quality (AHRQ), 2002 May. 189 p. Electronic copies available from the AHRQ Web site
. See the related QualityTool summary on the Health Care Innovations Exchange Web site .
Print copies: Available from the Agency for Healthcare Research and Quality Publications Clearinghouse. For more information, go to http://www.ahrq.gov/news/pubsix.htm or call 1-800-358-9295 (U.S. only).
The Electronic Preventive Services Selector (ePSS) , available as a PDA application and a web-based tool, is a quick hands-on tool designed to help primary care clinicians identify the screening, counseling, and preventive medication services that are appropriate for their patients. It is based on current recommendations of the USPSTF and can be searched by specific patient characteristics, such as age, sex, and selected behavioral risk factors.
NGC Status
This NGC summary was completed by ECRI on June 10, 2005. The information was verified by the guideline developer on June 17, 2005.
Copyright Statement
Requests regarding copyright should be sent to: Gerri M. Dyer, Electronic Dissemination Advisor, Agency for Healthcare Research and Quality (formerly the Agency for Health Care Policy and Research), Center for Health Information Dissemination, Suite 501, Executive Office Center, 2101 East Jefferson Street, Rockville, MD 20852; Facsimile: 301-594-2286; E-mail: gdyer@ahrq.gov.
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