Final Recommendation Statement
Abdominal Aortic Aneurysm: Screening
December 10, 2019
Recommendations made by the USPSTF 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.
An AAA is typically defined as aortic enlargement with a diameter of 3.0 cm or larger. The prevalence of AAA has declined over the past 2 decades among screened men 65 years or older in various countries such as the United Kingdom, New Zealand, Sweden, and Denmark.1-10 Population-based studies in men older than 60 years have found an AAA prevalence ranging from 1.2% to 3.3%.1-10 The reduction in prevalence is attributed to the decrease in smoking prevalence over time. Previous prevalence rates of AAA reported in population-based screening studies ranged from 1.6% to 7.2% of the general population 60 to 65 years or older.1 The current prevalence of AAA in the United States is unclear because of the low uptake of screening.1 Most AAAs are asymptomatic until they rupture. Although the risk for rupture varies greatly by aneurysm size, the associated risk for death with rupture is as high as 81%.1,11
The USPSTF concludes with moderate certainty that screening for AAA in men aged 65 to 75 years who have ever smoked is of moderate net benefit (Table).
The USPSTF concludes with moderate certainty that screening for AAA in men aged 65 to 75 years who have never smoked is of small net benefit (Table).
The USPSTF concludes that the evidence is insufficient to determine the net benefit of screening for AAA in women aged 65 to 75 years who have ever smoked or have a family history of AAA (Table).
The USPSTF concludes with moderate certainty that the harms of screening for AAA in women aged 65 to 75 years who have never smoked and have no family history of AAA outweigh the benefits (Table).
For more details on the methods the USPSTF uses to determine the net benefit, see the USPSTF Procedure Manual.12
Patient Population Under Consideration
Based on the scope of the evidence review, this recommendation applies to asymptomatic adults 50 years or older. However, the randomized trial evidence focuses almost entirely on men aged 65 to 75 years. In this Recommendation Statement, the recommendations are stratified by “men” and “women,” although the net benefit estimates are driven by biologic sex (ie, male/female) rather than gender identity. Persons should consider their sex at birth to determine which recommendation best applies to them.
Assessment of Risk
Important risk factors for AAA include older age, male sex, smoking, and having a first-degree relative with an AAA.13-16 Other risk factors include a history of other vascular aneurysms, coronary artery disease, cerebrovascular disease, atherosclerosis, hypercholesterolemia, and hypertension.17-19 Factors associated with a reduced risk include African American race, Hispanic ethnicity, Asian ethnicity, and diabetes.13,20-24 Risk factors for AAA rupture include older age, female sex, smoking, and elevated blood pressure.1 Clinicians should consider the presence of comorbid conditions and not offering screening if patients are unable to undergo surgical intervention or have a reduced life expectancy.
Epidemiologic literature commonly defines an “ever smoker” as someone who has smoked 100 or more cigarettes. Indirect evidence shows that smoking is the strongest predictor of AAA prevalence, growth, and rupture rates.1 There is a dose-response relationship, as greater smoking exposure is associated with an increased risk for AAA.1
Family history of AAA in a first-degree relative doubles the risk of developing AAA.25 The risk of developing an AAA is stronger with a female first-degree relative (odds ratio [OR], 4.32) than with a male first-degree relative (OR, 1.61).1,25 However, evidence is lacking on whether persons with family history experience a different natural history or surgical outcomes than those without such a history.1
The primary method of screening for AAA is conventional abdominal duplex ultrasonography.26 Screening with ultrasonography is noninvasive, is simple to perform, has high sensitivity (94%-100%) and specificity (98%-100%) for detecting AAA,1,27-31 and does not expose patients to radiation. Computed tomography is an accurate tool for identifying AAA; however, it is not recommended as a screening method because of the potential for harms from radiation exposure.1 Physical examination has been used in practice but has low sensitivity (39%-68%) and specificity (75%) and is not recommended for screening.32
Evidence is adequate to support 1-time screening for men who have ever smoked. All of the population-based randomized clinical trials (RCTs) of AAA screening used a 1-time screening approach; 7 fair- to good-quality cohort studies and 1 fair-quality case-control study (n = 6785) show that AAA-associated mortality over 5 to 12 years is rare (<3%) in men with initially normal results on ultrasonography (defined as an AAA <3 cm in diameter).1
Treatment of AAA depends on aneurysm size, the risk of rupture, and the risk of operative mortality. Larger size is associated with an increased risk of rupture. The annual risk for rupture is nearly 0% for persons with AAAs between 3.0 and 3.9 cm in diameter, 1% for those with AAAs between 4.0 and 4.9 cm in diameter, and 11% for those with AAAs between 5.0 and 5.9 cm in diameter.1 Surgical repair is standard practice for men with an AAA of 5.5 cm or larger in diameter or an AAA larger than 4.0 cm in diameter that has rapidly increased in size (defined as an increase of 1.0 cm in diameter over a 1-year period). Endovascular aneurysm repair (EVAR) has become the most common approach for elective AAA repair. Open repair is a time-tested, effective treatment for AAA. In the United States, 80% of intact AAA repairs and 52% of ruptured AAA repairs are performed using EVAR.1
The majority of screen-detected AAAs (≥90%) are between 3.0 and 5.5 cm in diameter and thus below the usual threshold for surgery. The current standard of care for patients with stable smaller aneurysms is to maintain ultrasound surveillance at regular intervals because the risk of rupture is small. Recommended surveillance intervals for monitoring the growth of small AAAs vary across guideline groups, and adherence with surveillance guidelines has been reported to be as low as 65%.1 Repairing smaller aneurysms with a lower risk of rupture increases the harms and reduces the benefits of screening.
Suggestions for Practice Regarding the I Statement
Potential Preventable Burden
The estimated prevalence of AAA in women is reportedly less than that in men.1 The Chichester trial reported a prevalence in women that was one-sixth of the prevalence in men (1.3% vs 7.6%), and most AAA-related deaths occurred in women 80 years or older (70% vs <50% in men).33 In women, small AAAs have an increased risk of rupture, and rupture at an older age than in men.1 Studies estimate that one-fourth to one-third of women have an AAA with a diameter below the current 5.5-cm threshold at the time of rupture.1
Operative mortality associated with AAA is higher in women than in men. Women had higher 30-day mortality rates (2.31%) than men (1.37%) after EVAR procedures (OR, 1.67 [95% CI, 1.38-2.04]) and open repair (5.37% vs 2.82%; OR, 1.76 [95% CI, 1.35-2.30]).1,34 Women also experience higher rates of other harms, such as major surgical complications and hospital readmission, after elective open repair or EVAR compared with men.1
Evidence is insufficient to accurately characterize current practice patterns related to screening for AAA in women.
The standard of care for elective repair is that patients with an AAA of 5.5 cm or larger in diameter should be referred for surgical intervention with either open repair or EVAR.1 This recommendation is based on RCTs conducted in men. The AAA size needed for surgical intervention in women may differ. As a result, guidelines from the Society for Vascular Surgery recommend repairing AAAs between 5.0 and 5.4 cm in diameter in women.26 However, concerns about poorer surgical outcomes in women, who have more complex anatomy and smaller blood vessels, have led some to caution against lowering the threshold for surgical intervention in women.1
This recommendation incorporates new evidence and replaces the 2014 USPSTF recommendation.35 It is consistent with the 2014 USPSTF recommendation, which was a B recommendation for 1-time screening for AAA with ultrasonography in asymptomatic men aged 65 to 75 years who have ever smoked, a C recommendation for selective screening in men aged 65 to 75 years who have never smoked, a D recommendation against routine screening in asymptomatic women who have never smoked, and an I statement for women aged 65 to 75 years who have ever smoked.
Scope of Review
The USPSTF commissioned a systematic evidence review to update its 2014 recommendation on screening for AAA. The USPSTF examined evidence regarding the effectiveness of 1-time and repeated screening for AAA, the associated harms of screening, and the benefits and harms of available treatments for small AAAs (3.0-5.4 cm in diameter) identified through screening.
Accuracy of Screening Tests and Risk Assessment
Ultrasonography is the primary method used to screen for AAA in primary care because of its high sensitivity (94%-100%) and specificity (98%-100%).1 It is also noninvasive, is simple to perform, and does not expose patients to radiation.
Benefits of Early Detection and Treatment
Four large, population-based RCTs (n = 134,271) that predominantly enrolled men 65 years or older examined the effectiveness of 1-time screening for AAA: the good-quality Multicenter Aneurysm Screening Study (MASS) (n = 67,800);36 the good-quality Viborg County, Denmark, screening trial (n = 12,639);13 the fair-quality Chichester, United Kingdom, screening trial (n = 15,382);37 and the fair-quality Western Australia screening trial (n = 38,480).38 Reported mean (or median) ages ranged from 67.7 to 72.6 years; the oldest participants were aged 83 years.1 The Western Australia screening trial38 reported outcomes by smoking status in the screened group. The trial was underpowered to detect differences in subpopulations. No comparisons in the unscreened group were reported.1,39 None of the 4 population-based screening RCTs reported family history of AAA in the trial populations.1
The prevalence of AAA in male screening participants ranged from 4.0% to 7.6% across the studies. Most screen-detected AAAs were small (≤4 to 4.5 cm in diameter); 0.3% to 0.6% of screened participants had an AAA measuring 5 cm or larger or 5.5 cm or larger in diameter.1 Two of the population-based screening trials analyzed AAA-associated mortality by age. The Viborg trial found similar risk reduction in AAA-related mortality in screening men aged 64 to 65 years compared with men aged 66 to 73 years.13 The Western Australia trial found no AAA-associated mortality benefit in men aged 65 to 74 years (rate ratio, 0.92 [95% CI, 0.62-1.36]) at 12.8-year follow-up; results were similar to findings for men aged 64 to 83 years.1,38
As noted previously, only the Chichester trial included women (aged 65-80 years). It found a low prevalence of AAA in women (1.3%), and 75% of screen-detected AAAs in women were 3.0 to 3.9 cm in diameter. Rupture rates (0.2% in both groups), AAA-specific mortality (0.06% vs 0.04% in both groups), and all-cause mortality (10.7% vs 10.2%) at 5 years did not statistically significantly differ between the invitation-to-screening and control groups.1,33 The trial was underpowered to draw definitive conclusions about health outcomes in women. Although the risk for rupture at a smaller aneurysm diameter seems to be higher in women than in men,1,40 the overall rupture rate in women is low. In the Chichester trial, more than two-thirds of deaths from AAA occurred in women 80 years or older.1,33
Pooled analysis of AAA-related mortality from the 4 trials showed a statistically significant 35% reduction associated with invitation to screening (Peto OR, 0.65 [95% CI, 0.57-0.74]; I2 = 80%).1 The number needed to screen was 305 men (95% CI, 248-411) to prevent 1 AAA death. The MASS and Viborg trials each found a statistically significant reduction in AAA-related mortality in the groups invited to screening compared with the control groups up to 13 years after screening (hazard ratio [HR], 0.58 [95% CI, 0.49-0.69] and 0.34 [95% CI, 0.20-0.57], respectively).13,36 The Chichester trial reported an HR of less than 1 (HR, 0.89 [95% CI, 0.60-1.32]), but it was not statistically significant.1,37 Pooled analysis of all available trials also showed no effect on all-cause mortality (relative risk, 0.99 [95% CI, 0.98-1.00]; I2 = 0%).1 Of the individual trials, only MASS showed a statistically significant benefit of screening for all-cause mortality at up to 15-year follow-up (HR, 0.97 [95% CI, 0.95-0.99]).1 Invitation to screening was associated with a statistically significant reduced rate of rupture in the pooled analysis of the 4 trials (Peto OR, 0.62 [95% CI, 0.55-0.70]; I2 = 53%).1 The number needed to screen was 246 men (95% CI, 207-311) to prevent 1 AAA rupture. Pooled results of the trials showed a reduction in emergency surgery in the invited-to-screening group (Peto OR, 0.57 [95% CI, 0.48-0.68]; I2 = 27%).1 Screening 1000 men for AAA would decrease the number of emergency operations by 2 (95% CI, 2-2).1
Four trials evaluated early surgical intervention compared with surveillance of smaller aneurysms (4-5.4 cm in diameter).41-44 Two good-quality open repair trials (n = 2226) and 2 fair-quality EVAR trials (n = 1088) showed no differences in all-cause and AAA-related mortality. However, there was a reduction in rupture rate with early open surgery compared with surveillance for small AAAs12,16,37,38 in the Aneurysm Detection and Management (ADAM) Veterans Affairs trial (relative risk, 0.18 [95% CI, 0.04-0.81]) and the UK Small Aneurysm Trial (UKSAT) (relative risk, 0.51 [95% CI, 0.26-0.99]).1,41,42 Individual patient data meta-analysis of the 2 early open vs surveillance trials (ADAM and UKSAT) reported no differences in all-cause mortality effect by sex or age.1,36,37 The UKSAT trial reported no difference in all-cause mortality by smoking status; there were no analyses stratifying by family history or race/ethnicity.1
Seven pharmacotherapy RCTs (n = 1553) of antibiotics, antihypertensive medications (eg, angiotensin-converting enzyme inhibitors, calcium channel blockers, and propranolol), and a mast cell stabilizer showed no significant effect on AAA growth compared with placebo.1
Harms of Screening and Treatment
An individual’s risk for death related to elective surgery for AAA is lower than that related to emergency surgery for aneurysm rupture. However, the increase in the overall rates of detection and surgery in the screening groups still potentially represents a harm. The extent of overdiagnosis and overtreatment is difficult to estimate.
Each of the 4 older screening trials and a more recent population-based screening RCT (n = 18,614), the Viborg Vascular (VIVA) trial, showed an increase in elective operations in the intervention vs control group.1,45 There were approximately 40% more operations in the invitation-to-screen group than in the control group (5 studies; n = 175,085; Peto OR, 1.44 [95% CI, 1.34-1.55]), driven primarily by an increase in elective operations (5 studies; n = 175,085; Peto OR, 1.75 [95% CI, 1.61-1.90]).1 There was no statistically significant difference in 30-day mortality rates between the invited and control groups for either elective or emergency operations at 12- to 15-year follow-up.1
Five studies (n = 2734) reported mixed results on quality-of-life outcomes.1 Overall, there were no substantial differences on quality-of-life measures or anxiety or depression scores at up to 12 months of follow-up between patients who screened positive for an AAA and patients who screened negative or were unscreened.1
Two trials of early open repair vs surveillance (ADAM and UKSAT trials) reported a 50% higher rate of procedures in the early intervention group, with no difference in 30-day operative mortality.1,41,42 Readmission rates at 30 days were similar, and major surgical complications were lower in the early intervention group. Analysis of quality-of-life measures showed mixed results; although there was generally a decline in both groups over time, there were no statistically significant differences between the groups for up to 1 to 2 years. Only the ADAM trial showed higher general health scores in the early repair group in the first 2 years, but this difference did not persist over time.1 One trial reported an increased incidence of impotence in the early repair group at up to 4 years’ follow-up.1
Registry harms data were generally comparable to the findings of the 2 trials, with the exception of reintervention rates, which were higher in the registries than in the ADAM trial.1
Two trials of early EVAR vs surveillance reported approximately 100% more procedures in the early intervention group and similarly rare 30-day operative mortality rates between the groups.1,43,44 In the Comparison of Surveillance vs Aortic Endografting for Small Aneurysm Repair (CAESAR) trial, the early intervention group had a higher percentage of patients with any adverse events (19% vs 5%; P < 0.01), any major morbidity related to repair at 30 days (18% vs 6%; P = 0.01), endoleaks at 1 year (12% vs 2%; P = 0.028), and reintervention (6% vs 0%; P = 0.03) but similar rates of any major morbidity over the trial duration (3.3% vs 2.8%; P = 0.99).1,43 The Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL) trial reported similar rates of adverse events at 30 days (12% vs 10%) and at 1 year (26% vs 35%), as well as reintervention (3.7% vs 4.6%).1,44 Reported complication rates from registry data were generally comparable with rates reported in the above trials for 30-day operative mortality and reintervention.1
Two propranolol trials reported high discontinuation rates related to adverse events (38% and 60% of participants in the propranolol groups withdrew from the trials). Other medications (eg, angiotensin-converting enzyme inhibitors, calcium channel blockers, and antibiotics) seemed well tolerated based on rare trial withdrawals reported from 1 to 2 studies per drug class.1
Response to Public Comment
A draft version of this recommendation statement was posted for public comment on the USPSTF website from June 18 to July 15, 2019. Some comments expressed concerns about the harms of screening. In response, the USPSTF added information about overtreatment as a harm of screening to the Supporting Evidence section and added information about comorbid conditions to the Practice Considerations section. Some comments urged more research in diverse populations. The USPSTF clarified its call for research in the Research Needs and Gaps section. Some comments suggested expanding the populations for whom screening is recommended. The USPSTF did not expand the scope of its recommendation beyond the populations justified by its review of the current evidence and recommends research about the benefits and harms of screening in these groups.
Addressing several key research gaps could help inform the benefit of screening for AAA in US-based populations:1
- Although evidence shows that women who smoke or have a family history are at increased risk for AAA compared with nonsmoking women without a family history, evidence is insufficient that screening this population confers a net benefit. Ideally, appropriately powered RCTs among women with risk factors could answer these critical gaps in the evidence on screening for AAA. In the absence of new trial data, high-quality, well-calibrated modeling studies based on reliable data on the harms and benefits of screening in women who smoke or in men and women with a family history of AAA may be informative.
- Well-conducted cohort studies examining rescreening benefits (including growth rates and health outcomes) are needed for persons who initially screen negative for AAA to determine the benefit and timing of additional screening ultrasonography.
- External validation of risk prediction models that have already been developed will allow policy makers to assess their value for making more individualized screening recommendations.
- Epidemiologic studies on the current prevalence of AAA in the United States, including in subpopulations, would help inform the applicability of older population-based screening trials to the current US population.
- Well-designed studies, RCTs, or registry data on the thresholds for repair of AAA in women may inform the benefits and harms of screening in women, as evidence suggests that AAAs in women may rupture at a smaller size than in men.
- Studies examining systems approaches to improving implementation of evidence-based AAA screening in the United States are needed.
- Studies examining the efficacy of screening and treatment in diverse populations (eg, older adults, women, and racial/ethnic groups) are needed to inform the need for specific recommendations in subpopulations of Americans.
The American College of Cardiology and the American Heart Association jointly recommend 1-time screening for AAA with physical examination and ultrasonography in men aged 65 to 75 years who have ever smoked or in men 60 years or older who are the sibling or offspring of a person with AAA. These organizations do not recommend screening for AAA in men who have never smoked or in women.46 The Society for Vascular Surgery recommends 1-time ultrasonography screening for AAA in all men and women aged 65 to 75 years with a history of tobacco use, men 55 years or older with a family history of AAA, and women 65 years or older who have smoked or have a family history of AAA.47 The American College of Preventive Medicine recommends 1-time screening in men aged 65 to 75 years who have ever smoked; it does not recommend routine screening in women.48
The US Preventive Services Task Force (USPSTF) members include the following individuals: Douglas K. Owens, MD, MS (Veterans Affairs Palo Alto Health Care System, Palo Alto, California, and Stanford University, Stanford, California); Karina W. Davidson, PhD, MASc (Feinstein Institute for Medical Research at Northwell Health, Manhasset, New York); Alex H. Krist, MD, MPH (Fairfax Family Practice Residency, Fairfax, Virginia, and Virginia Commonwealth University, Richmond); Michael J. Barry, MD (Harvard Medical School, Boston, Massachusetts); Michael Cabana, MD, MA, MPH (University of California, San Francisco); Aaron B. Caughey, MD, PhD (Oregon Health & Science University, Portland); Chyke A. Doubeni, MD, MPH (Mayo Clinic, Rochester, MN); John W. Epling Jr, MD, MSEd (Virginia Tech Carilion School of Medicine, Roanoke); Martha Kubik, PhD, RN (Temple University, Philadelphia, Pennsylvania); C. Seth Landefeld, MD (University of Alabama at Birmingham); Carol M. Mangione, MD, MSPH (University of California, Los Angeles); Lori Pbert, PhD (University of Massachusetts Medical School, Worcester); Michael Silverstein, MD, MPH (Boston University, Boston, Massachusetts); Melissa A. Simon, MD, MPH (Northwestern University, Evanston, Illinois); Chien-Wen Tseng, MD, MPH, MSEE (University of Hawaii, Honolulu); John B. Wong, MD (Tufts University School of Medicine, Boston, Massachusetts).
Conflict of Interest Disclosures: Authors followed the policy regarding conflicts of interest described at https://www.uspreventiveservicestaskforce.org/uspstf/about-uspstf/conflict-interest-disclosures. All members of the USPSTF receive travel reimbursement and an honorarium for participating in USPSTF meetings. Dr. Barry reported receiving grants and personal fees from Healthwise, a nonprofit, outside the submitted work. No other disclosures were reported.
Funding/Support: The USPSTF is an independent, voluntary body. The US Congress mandates that the Agency for Healthcare Research and Quality (AHRQ) support the operations of the USPSTF.
Disclaimer: Recommendations made by the USPSTF are independent of the US government. They should not be construed as an official position of AHRQ or the US Department of Health and Human Services.
Additional Information: The USPSTF makes recommendations about the effectiveness of specific preventive care services for patients without obvious related signs or symptoms. It bases its recommendations on the evidence of both the benefits and harms of the service and an assessment of the balance. The USPSTF does not consider the costs of providing a service in this assessment. The USPSTF recognizes that clinical decisions involve more considerations than evidence alone. Clinicians should understand the evidence but individualize decision-making to the specific patient or situation. Similarly, the USPSTF notes that policy and coverage decisions involve considerations in addition to the evidence of clinical benefits and harms.
Copyright Notice: USPSTF recommendations are based on a rigorous review of existing peer-reviewed evidence and are intended to help primary care clinicians and patients decide together whether a preventive service is right for a patient's needs. To encourage widespread discussion, consideration, adoption, and implementation of USPSTF recommendations, AHRQ permits members of the public to reproduce, redistribute, publicly display, and incorporate USPSTF work into other materials provided that it is reproduced without any changes to the work of portions thereof, except as permitted as fair use under the US Copyright Act.
AHRQ and the US Department of Health and Human Services cannot endorse, or appear to endorse, derivative or excerpted materials, and they cannot be held liable for the content or use of adapted products that are incorporated on other Web sites. Any adaptations of these electronic documents and resources must include a disclaimer to this effect. Advertising or implied endorsement for any commercial products or services is strictly prohibited.
This work may not be reproduced, reprinted, or redistributed for a fee, nor may the work be sold for profit or incorporated into a profit-making venture without the express written permission of AHRQ. This work is subject to the restrictions of Section 1140 of the Social Security Act, 42 U.S.C. §320b-10. When parts of a recommendation statement are used or quoted, the USPSTF Web page should be cited as the source.
1. Guirguis-Blake JM, Beil TL, Senger CA, Coppola EL. Primary Care Screening for Abdominal Aortic Aneurysm: Updated Systematic Review for the U.S. Preventive Services Task Force. Evidence Synthesis No. 184. AHRQ Publication No. 19-05253-EF-1. Rockville, MD: Agency for Healthcare Research and Quality; 2019.
2. Guirguis-Blake JM, Beil TL, Senger CA, Coppola EL. Primary care screening for abdominal aortic aneurysm: evidence report and systematic review for the US Preventive Services Task Force. JAMA. 2019;322(22):2219-2238.
3. Svensjö S, Björck M, Gürtelschmid M, Djavani Gidlund K, Hellberg A, Wanhainen A. Low prevalence of abdominal aortic aneurysm among 65-year-old Swedish men indicates a change in the epidemiology of the disease. Circulation. 2011;124(10):1118-23.
4. Benson RA, Poole R, Murray S, Moxey P, Loftus IM. Screening results from a large United Kingdom abdominal aortic aneurysm screening center in the context of optimizing United Kingdom National Abdominal Aortic Aneurysm Screening Programme protocols. J Vasc Surg. 2016;63(2):301-4.
5. Choke E, Vijaynagar B, Thompson J, Nasim A, Bown MJ, Sayers RD. Changing epidemiology of abdominal aortic aneurysms in England and Wales: older and more benign? Circulation. 2012;125(13):1617-25.
6. Anjum A, Powell JT. Is the incidence of abdominal aortic aneurysm declining in the 21st century? Mortality and hospital admissions for England & Wales and Scotland. Eur J Vasc Endovasc Surg. 2012;43(2):161-6.
7. Sandiford P, Mosquera D, Bramley D. Trends in incidence and mortality from abdominal aortic aneurysm in New Zealand. Br J Surg. 2011;98(5):645-51.
8. Wanhainen A, Hultgren R, Linné A, et al; Swedish Aneurysm Screening Study Group (SASS). Outcome of the Swedish Nationwide Abdominal Aortic Aneurysm Screening Program. Circulation. 2016;134(16):1141-8.
9. Johansson M, Zahl PH, Siersma V, Jørgensen KJ, Marklund B, Brodersen J. Benefits and harms of screening men for abdominal aortic aneurysm in Sweden: a registry-based cohort study. Lancet. 2018;391(10138):2441-7.
10. Grøndal N, Søgaard R, Lindholt JS. Baseline prevalence of abdominal aortic aneurysm, peripheral arterial disease and hypertension in men aged 65-74 years from a population screening study (VIVA trial). Br J Surg. 2015;102(8):902-6.
11. Reimerink JJ, van der Laan MJ, Koelemay MJ, Balm R, Legemate DA. Systematic review and meta-analysis of population-based mortality from ruptured abdominal aortic aneurysm. Br J Surg. 2013;100(11):1405-13.
12. U.S. Preventive Services Task Force. Procedure Manual. https://www.uspreventiveservicestaskforce.org/Page/Name/procedure-manual. Published June 2018. Accessed October 15, 2019.
13. Lindholt JS, Juul S, Fasting H, Henneberg EW. Screening for abdominal aortic aneurysms: single centre randomised controlled trial. BMJ. 2005;330(7494):750.
14. Kent KC, Zwolak RM, Egorova NN, et al. Analysis of risk factors for abdominal aortic aneurysm in a cohort of more than 3 million individuals. J Vasc Surg. 2010;52(3):539-48.
15. Wilmink AB, Hubbard CS, Day NE, Quick CR. The incidence of small abdominal aortic aneurysms and the change in normal infrarenal aortic diameter: implications for screening. Eur J Vasc Endovasc Surg. 2001;21(2):165-70.
16. Vardulaki KA, Walker NM, Day NE, Duffy SW, Ashton HA, Scott RA. Quantifying the risks of hypertension, age, sex and smoking in patients with abdominal aortic aneurysm. Br J Surg. 2000;87(2):195-200.
17. van Vlijmen-van Keulen CJ, Pals G, Rauwerda JA. Familial abdominal aortic aneurysm: a systematic review of a genetic background. Eur J Vasc Endovasc Surg. 2002;24(2):105-16.
18. MacSweeney ST, O'Meara M, Alexander C, O'Malley MK, Powell JT, Greenhalgh RM. High prevalence of unsuspected abdominal aortic aneurysm in patients with confirmed symptomatic peripheral or cerebral arterial disease. Br J Surg. 1993;80(5):582-4.
19. Lederle FA, Johnson GR, Wilson SE, et al; The Aneurysm Detection and Management (ADAM) Veterans Affairs Cooperative Study Investigators. Relationship of age, gender, race, and body size to infrarenal aortic diameter. J Vasc Surg. 1997;26(4):595-601.
20. Li X, Zhao G, Zhang J, Duan Z, Xin S. Prevalence and trends of the abdominal aortic aneurysms epidemic in general population--a meta-analysis. PLoS One. 2013;8(12):e81260.
21. De Rango P, Farchioni L, Fiorucci B, Lenti M. Diabetes and abdominal aortic aneurysms. Eur J Vasc Endovasc Surg. 2014;47(3):243-61.
22. Lederle FA, Johnson GR, Wilson SE, et al; Aneurysm Detection and Management Veterans Affairs Cooperative Study Investigators. The aneurysm detection and management study screening program: validation cohort and final results. Arch Intern Med. 2000;160(10):1425-30.
23. Takagi H, Umemoto T; ALICE (All-Literature Investigation of Cardiovascular Evidence) Group. Negative association of diabetes with rupture of abdominal aortic aneurysm. Diab Vasc Dis Res. 2016;13(5):341-7.
24. Xiong J, Wu Z, Chen C, Wei Y, Guo W. Association between diabetes and prevalence and growth rate of abdominal aortic aneurysms: a meta-analysis. Int J Cardiol. 2016;221:484-95.
25. Joergensen TM, Houlind K, Green A, Lindholt JS. Abdominal aortic diameter is increased in males with a family history of abdominal aortic aneurysms: results from the Danish VIVA-trial. Eur J Vasc Endovasc Surg. 2014;48(6):669-675.
26. Chaikof EL, Dalman RL, Eskandari MK, et al. The Society for Vascular Surgery practice guidelines on the care of patients with an abdominal aortic aneurysm. J Vasc Surg. 2018;67(1):2-77.e2
27. Lederle FA, Walker JM, Reinke DB. Selective screening for abdominal aortic aneurysms with physical examination and ultrasound. Arch Intern Med. 1988;148(8):1753-6.
28. Lindholt JS, Vammen S, Juul S, Henneberg EW, Fasting H. The validity of ultrasonographic scanning as screening method for abdominal aortic aneurysm. Eur J Vasc Endovasc Surg. 1999;17(6):472-5.
29. Costantino TG, Bruno EC, Handly N, Dean AJ. Accuracy of emergency medicine ultrasound in the evaluation of abdominal aortic aneurysm. J Emerg Med. 2005;29(4):455-60.
30. Tayal VS, Graf CD, Gibbs MA. Prospective study of accuracy and outcome of emergency ultrasound for abdominal aortic aneurysm over two years. Acad Emerg Med. 2003;10(8):867-71.
31. Rubano E, Mehta N, Caputo W, Paladino L, Sinert R. Systematic review: emergency department bedside ultrasonography for diagnosing suspected abdominal aortic aneurysm. Acad Emerg Med. 2013;20(2):128-38.
32. Lederle FA, Simel DL. The rational clinical examination. Does this patient have abdominal aortic aneurysm? JAMA. 1999;281(1):77-82.
33. Scott RA, Bridgewater SG, Ashton HA. Randomized clinical trial of screening for abdominal aortic aneurysm in women. Br J Surg. 2002;89(3):283-5.
34. Ulug P, Sweeting MJ, von Allmen RS, Thompson SG, Powell JT; SWAN Collaborators. Morphological suitability for endovascular repair, non-intervention rates, and operative mortality in women and men assessed for intact abdominal aortic aneurysm repair: systematic reviews with meta-analysis. Lancet. 2017;389(10088):2482-2491.
35. LeFevre, ML; U.S. Preventive Services Task Force. Screening for abdominal aortic aneurysm: U.S. Preventive Services Task Force recommendation statement. Ann Intern Med. 2014;161(4):281-90.
36. Ashton HA, Buxton MJ, Day NE, et al; Multicentre Aneurysm Screening Study Group. The Multicentre Aneurysm Screening Study (MASS) into the effect of abdominal aortic aneurysm screening on mortality in men: a randomised controlled trial. Lancet. 2002;360(9345):1531-9.
37. Norman PE, Jamrozik K, Lawrence-Brown MM, et al. Population based randomised controlled trial on impact of screening on mortality from abdominal aortic aneurysm. BMJ. 2004;329(7477):1259.
38. Scott RA, Wilson NM, Ashton HA, Kay DN. Influence of screening on the incidence of ruptured abdominal aortic aneurysm: 5-year results of a randomized controlled study. Br J Surg. 1995;82(8):1066-70.
39. McCaul KA, Lawrence-Brown MM, Dickinson JA, Norman, PE. Long-term outcomes of the Western Australian trial of screening for abdominal aortic aneurysms: secondary analysis of a randomized clinical trial. JAMA Intern Med. 2016;176(12):1761-1767.
40. Svensjö S, Björck M, Wanhainen A. Current prevalence of abdominal aortic aneurysm in 70-year-old women. Br J Surg. 2013;100(3):367-72.
41. Lederle FA, Wilson SE, Johnson GR, et al; Aneurysm Detection and Management Veterans Affairs Cooperative Study Group. Immediate repair compared with surveillance of small abdominal aortic aneurysms. N Engl J Med. 2002;346:1437-44.
42. Powell JT, Brady AR, Brown LC, et al; The UK Small Aneurysm Trial Participants. Mortality results for randomised controlled trial of early elective surgery or ultrasonographic surveillance for small abdominal aortic aneurysms. The UK Small Aneurysm Trial Participants. Lancet. 1998;352(9141):1649-1655.
43. Cao P, De Rango P, Verzini F, Parlani G, Romano L, Cieri E; CAESAR Trial Group. Comparison of surveillance versus aortic endografting for small aneurysm repair (CAESAR): results from a randomised trial. Eur J Vasc Endovasc Surg. 2011;41:13-25.
44. Ouriel K, Clair DG, Kent KC, Zarins CK; Positive Impact of Endovascular Options for Treating Aneurysms Early (PIVOTAL) Investigators. Endovascular repair compared with surveillance for patients with small abdominal aortic aneurysms. J Vasc Surg. 2010;51(5):1081-7.
45. Lindholt JS, Søgaard R. Population screening and intervention for vascular disease in Danish men (VIVA): a randomised controlled trial. Lancet. 2017;390(10109):2256-2265.
46. Hirsch AT, Haskal ZJ, Hertzer NR, et al; American Association for Vascular Surgery; Society for Vascular Surgery; Society for Cardiovascular Angiography and Interventions; Society for Vascular Medicine and Biology; Society of Interventional Radiology; ACC/AHA Task Force on Practice Guidelines Writing Committee to Develop Guidelines for the Management of Patients With Peripheral Arterial Disease; American Association of Cardiovascular and Pulmonary Rehabilitation; National Heart, Lung, and Blood Institute; Society for Vascular Nursing; TransAtlantic Inter-Society Consensus; Vascular Disease Foundation. ACC/AHA 2005 Practice Guidelines for the management of patients with peripheral arterial disease (lower extremity, renal, mesenteric, and abdominal aortic): a collaborative report from the American Association for Vascular Surgery/Society for Vascular Surgery, Society for Cardiovascular Angiography and Interventions, Society for Vascular Medicine and Biology, Society of Interventional Radiology, and the ACC/AHA Task Force on Practice Guidelines (Writing Committee to Develop Guidelines for the Management of Patients With Peripheral Arterial Disease): endorsed by the American Association of Cardiovascular and Pulmonary Rehabilitation; National Heart, Lung, and Blood Institute; Society for Vascular Nursing; TransAtlantic Inter-Society Consensus; and Vascular Disease Foundation. Circulation. 2006;113(11):e463-e654.
47. Chaikof EL, Brewster DC, Dalman RL, et al; Society for Vascular Surgery. The care of patients with an abdominal aortic aneurysm: the Society for Vascular Surgery practice guidelines. J Vasc Surg. 2009;50(4 Suppl):S2-S49.
48. Lim LS, Haq N, Mahmood S, Hoeksema L; ACPM Prevention Practice Committee; American College of Preventive Medicine. Atherosclerotic cardiovascular disease screening in adults: American College of Preventive Medicine position statement on preventive practice. Am J Prev Med. 2011;40(3):381.e1-10.
|Ever Smoked||Never Smoked||Ever Smoked or Family History||Never Smoked and No Family History|
|Detection||There is adequate evidence that ultrasonography is a safe and accurate screening test for AA||There is adequate evidence that ultrasonography is a safe and accurate screening test for AA||There is adequate evidence that ultrasonography is a safe and accurate screening test for AA||There is adequate evidence that ultrasonography is a safe and accurate screening test for AA|
|Benefits of early detection and treatment (based on direct or indirect evidence)||There is adequate evidence that 1-time screening for AAA with ultrasonography results in a moderate benefit in men aged 65 to 75 y who have ever smoked||There is adequate evidence that 1-time screening for AAA with ultrasonography results in a small benefit in men aged 65 to 75 y who have never smoked||There is inadequate evidence to conclude whether 1-time screening for AAA with ultrasonography is beneficial in women aged 65 to 75 y who have ever smoked or have a family history of AAA||There is adequate evidence that 1-time screening for AAA with ultrasonography results in no benefit in women who have never smoked and have no family history of AAA|
|Harms of early detection and treatment||There is adequate evidence that the harms associated with 1-time screening for AAA with ultrasonography are small to moderate||There is adequate evidence that the harms associated with 1-time screening for AAA with ultrasonography are small to moderate||There is adequate evidence that the harms associated with 1-time screening for AAA with ultrasonography are small to moderate|
|USPSTF assessment||There is moderate certainty that screening for AAA with ultrasonography in men aged 65 to 75 y who have ever smoked has a moderate net benefit||There is moderate certainty that screening for AAA with ultrasonography in men aged 65 to 75 y who have never smoked has a small net benefit||The benefits and harms of screening for AAA with ultrasonography in women aged 65 to 75 y who have ever smoked or have a family history are uncertain, and the balance of benefits and harms cannot be determined||There is moderate certainty that the harms of screening for AAA with ultrasonography in women who have never smoked and have no family history outweigh the benefits.|
Abbreviations: AAA, abdominal aortic aneurysm; USPSTF, US Preventive Services Task Force.