ARTYKUŁ ORYGINALNY / ORYGINAL ARTICLE |
The prevalence of abdominal aortic aneurysms in the rural/urban population in central Poland — Gniewkowo Aortic Study
Tadeusz L. Dereziński1, Bartosz Fórmankiewicz2, Arkadiusz Migdalski2, Paweł Brazis2, Grzegorz Jakubowski3 , Łukasz Woda2, Arkadiusz Jawień2
1Out-Patient Clinic Esculap, Gniewkowo, Poland
2Clinic of Vascular Surgery and Angiology, Collegium Medicum of Nicolaus Copernicus University, Bydgoszcz, Poland
3Private Radiology Centre, Inowroclaw, Poland
Address for correspondence:
Tadeusz L. Dereziński, MD, PhD, Out-Patient Clinic Esculap, ul. Dworcowa 8c, 88–140 Gniewkowo, Poland, e-mail: tadziude@wp.pl
Received: 04.11.2016 Accepted: 20.03.2017 Available as AoP: 31.03.2017
Abstract Background and aim: Abdominal aortic aneurysm (AAA) is a widening of the aorta below the renal arteries with a diameter equal to or greater than 3 cm. The prevalence of AAA is estimated at 4–8% in men aged 65 years or older and 1–2% among women over 65 years old. Participation in screening programmes has decreased the number of aortic ruptures. Methods: All men aged 60 years and older, and women aged 65 years and older living in the rural/urban commune in central Poland were invited to participate in the study. In total 922 persons (61% of the invited population) entered the study. The men were divided into two groups: 60–64 years old, and 65 years and older. Screening abdomen ultrasound was performed and demographic data was collected. Results: Among the 922 examined persons two (1.01%) AAAs were diagnosed in the group of men 60–64 years of age, three (0.82%) AAAs amongst women ≥ 65 years old, and 33 (9.29%) AAAs were found in the group of men aged 65 years and older. A positive relationship between the presence of AAA and smoking (p = 0.0048), age of men (p = 0.0009), and history of myocardial infarction/acute coronary syndrome (MI/ACS) (p = 0.0079) was found. There was no correlation between the frequency of AAA and diabetes mellitus (p = 0.46), hypertension (p = 0.38), and family history of AAA (p = 0.44). Conclusions: The prevalence of AAA in men aged 65 years and older is seemingly larger than in previously conducted studies, while among men 60–64 years of age and women aged ≥ 65 it is similar. Older age, smoking, and a history of MI/ACS were the most important risk factors of AAA occurrence. Key words: abdominal aortic aneurysm, ultrasonography, prevalence, screening, population studies Kardiol Pol 2017; 75, 7: 705–710 |
INTRODUCTION
Abdominal aortic aneurysm (AAA) is defined as a widening of the aorta below the renal arteries with a diameter greater than 3 cm [1] or exceeding 50% of the normal diameter, measured, for example, above the aneurysm sac [2]. For the purpose of this study the authors adopted the first definition, which has its justification in screening programmes for abdominal aortic aneurysms carried out in other countries where the results have been published. The prevalence of AAA is estimated at 4–8% in men aged 65 years and older and 1–2% of women in this age group [3–5]. AAA is usually asymptomatic, and its first sign may be rupture, which is associated with 59–83% mortality [6].
In the United States ruptured AAA is the 11th most common cause of death [7]. The risks factors associated with AAA are: older age [6], male sex [4], and smoking [7, 8]. Other potential risk factors are: aneurysms of other arteries, chronic heart failure, cerebrovascular disease, atherosclerosis, hypercholesterolaemia, and arterial hypertension [9, 10]. Female gender and diabetes mellitus are so-called “protective” factors in AAA development. In the 1990s, large randomised studies showed that ultrasound screening can reduce risk of AAA rupture in males [9]. The abdomen ultrasound screening test seems to be the standard procedure for the early detection of AAA, which has a high sensitivity (96%) and specificity close to 100% [11–13]. In addition to, the abdomen ultrasound is a non-invasive, simple, and inexpensive test. Since 2007, men in the United States, aged 65–75 years, who have ever smoked are offered a single ultrasound scan examination of the aorta. In the United Kingdom, since 2009, the National Health Service Abdominal Aortic Aneurysm Screening Programme is applicable to 65-year-old men [13]. Recently published data from Western Countries show a decreasing number of AAAs. This may be due to widely incorporated population-based screening strategies [9]. So far, no studies focused on prevalence of AAA have been conducted in Central and Eastern Europe.
METHODS
The study was conducted in a rural/urban Gniewkowo commune in central Poland, in the period from October 2009 to April 2012, and included men aged 60 years and above and women aged 65 years and older. Patients were divided into three groups: men aged 60–64 years (n = 198), men aged 65 years and older (n = 355), and women aged 65 years and older (n = 365). In total, during the study, 922 people were examined. Two research methods were used: 1) the questionnaire method; 2) ultrasound measurement of the diameter of the abdominal aorta. The questionnaire used closed questions and consisted of parts relating to: 1) identification and demographic data; 2) AAA-associated risk factors such as smoking and family history of AAA; and 3) information on the prevalence of diabetes mellitus, arterial hypertension, and myocardial infarction/acute coronary syndrome (MI/ACS). Analysis of the data from the questionnaire determined the relationship between the studied risk factors and the development of AAA. Subsequently the abdominal ultrasonography was performed to assess the abdominal aorta. Ultrasound examination was performed using a convex transducer, and the diameter measurement was made on the abdominal aorta (from renal arteries to the bifurcation). Two measurements were taken into account: the anterior-posterior and transverse. The cut-off value for aneurysm was the diameter ≥ 30 mm. The lists of patients invited to join the study was based on the populations covered by the care of primary care physicians in the municipality. The response rate was 61% of patients (Table 1).
Table 1. Study population
Characteristic/population |
Women: 65 years and older |
Men: 60–64 years |
Men: 65 years and older |
N |
365 |
198 |
355 |
Smoking current or ever |
116 (31.78%) |
122 (61.61%) |
227 (63.94%) |
Family abdominal aortic aneurysm |
3 (0.82%) |
3 (1.51%) |
9 (2.53%) |
Diabetes |
107 (29.31%) |
27 (13.63%) |
53 (14.92%) |
Arterial hypertension |
202 (55.34%) |
94 (47.47%) |
198 (55.77%) |
Acute coronary syndrome/myocardial infarction |
69 (18.90%) |
27 (13.63%) |
76 (21.40%) |
RESULTS
Two aneurysms were found (1.01%) (51 mm and 38 mm) in the group of men aged 60–64 years. Both patients had smoked more than 40 packet-years, suffered from high blood pressure, had no history of acute MI and/or ACS, and did not have diabetes mellitus. In women aged 65 years and over, three aneurysms were found (0.82%) (37 mm, 36 mm, 33 mm), all women smoked more than 30 packet-years and suffered from hypertension, had no history of acute MI/ACS, and did not suffer from diabetes. In men aged 65 years and older 33 (9.29%) AAAs were found in the group of 355 persons, including six (1.7% of the study population) with a diameter ≥ 55 mm, requiring urgent surgical intervention. For this group, the relationship between the occurrence of AAA and smoking currently or in the past and acute MI/ACS; OR = 4.54 (95% CI 1.55–13.22); p = 0.0048 and OR = 2.68 (95% CI 1.26–5.68); p = 0.0079, respectively, was demonstrated. No correlation between occurrence of AAA and smoking was observed in the group with mean age 60–64 years, while among women aged 65 years and older a borderline trend towards association between occurrence of AAA and smoking was found (p = 0.0546). No relationship between the presence of AAA and acute MI/ACS in these two groups was found, while no relationship between the incidence of AAA and diabetes (p = 0.46), hypertension (p = 0.38), and family history of AAA (p = 0.44) was found (Figs. 1, 2).
Figure 1. Relationship of abdominal aortic aneurysm (AAA) to age in men
Figure 2. Abdominal aortic aneurysm (AAA) in men smoking currently or in the past
In the entire study population, 38 cases of AAA were found, for which the following algorithm of the follow-up (depending on the size of the aneurysm) was used:
- — 3.0–4.4 cm: check-up examination once a year;
- — 4.5–5.4 cm: check-up examination every three months;
- — ≥ 5.5 cm: referral to a specialist in vascular surgery and consider surgery (Table 2).
Table 2. Abdominal aortic aneurysm (AAA) in observed population
Diameters of AAA [mm] |
AAA, n (%) |
≥ 55 |
6 (15.8%) |
45–54 |
9 (23.7%) |
30–44 |
23 (60.5%) |
Total (N) |
38 (100%) |
In six men in the group aged 65 years and older, who were diagnosed with AAA larger than 55 mm, the operation was performed urgently within one month from diagnosis. Another eleven people were operated on in the subsequent five years, and eight patients from the observed group died in the period following diagnosis. Four of them died of cancer, one in the course of severe post-infarction heart failure, and two died suddenly — in these cases, no autopsy was performed. Another patient diagnosed at the age of 61 years also died suddenly, probably due to aneurysm rupture. He was diagnosed with lung cancer and was disqualified from surgery due to the severity of the disease (Table 3).
Table 3. Demographic data of patients treated with abdominal aortic aneurysm (AAA) (up to 30 September 2016)
Total number of patients with AAA |
38 (100%) |
Urgent AAA surgery |
6 (15.7%) |
Elective AAA surgery |
11 (28.9%) |
Total number of operated patients with AAA |
17 (44.7%) |
Mortality: |
8 deaths (21%) |
Neoplasma |
4 (10.5%) |
Heart failure |
1 (2.6%) |
Sudden death of unknown origin |
3 (7.9%) |
DISCUSSION
Large scale population-based studies carried out in the 1980s and 1990s showed that AAA occurs in 4.9–8.9% of men over 65 years old, its course is frequently asymptomatic, and sometimes the first symptom of aneurysm is rupture, characterised by roughly 65% mortality [3–5]. The introduction of population-based screening reduced mortality associated with AAA by 45% [14]. A meta-analysis published in January 2014 demonstrated that a one-time screening for AAA in men aged 65 years and older is associated with a decreased incidence of AAA ruptures and mortality associated with the AAA, but has no effect on total mortality [9]. So far, the prevalence of AAA in Poland and Central and Eastern Europe has not been evaluated. The aim of this study was to evaluate the prevalence of AAA in the population of the one of the municipalities in central Poland. The age groups in men have been chosen to compare obtained results with other population-based studies. After finishing the screening programme with the population aged 65 years and over an additional sample with mean age 60–64 years was invited to find the proper cut-off age for the Polish population. In 2010, in a special issue of the ‘European Journal of Vascular and Endovascular Surgery’, the current guidelines for the treatment of AAA were published [15, 16]. According to these guidelines, mortality from AAA can be reduced by almost a half within four years, mostly by reducing the incidence of ruptured aneurysms due to population screening for AAA of older men, in areas where the prevalence is 4% or more (level of evidence 1a, strength of recommendation A). In two studies conducted in the Kuyavian-Pomeranian voivodship in 2012 and 2013, AAA during screening among men aged 65 years and more was found in 5.4% of patients [17, 18]. The data obtained in this study by the authors showed that the prevalence of AAA is a bit higher than the results obtained in the 1990s. In the authors’ opinion, this fact may correspond to a larger number of current or ex-smokers (among men aged 65–75 years they constituted 65.72%, and in the group aged 76 years and more, 59.81% of respondents). According to the recommendations of the European Society of Cardiology, Poland is included in the group of countries at high cardiovascular risk. This is primarily due to a greater percentage of current or past smokers than in Western Europe and a higher prevalence of lipid disorders, arterial hypertension, and acute MI/ACS.
The incidence of MI in the group of 65–75-year-olds was 19.35%, and in the group aged 76 years and more it was 26.16%, which can also influence the results obtained. The study also confirmed a significantly lower incidence of AAA among women aged 65 years and over (0.82% vs. 9.29%, p = 0.00002) compared to that in men, and it was in line with expectations. This may happen due to the large number of diabetic patients in that group (more than 50% of study participants suffered from diabetes and prediabetes) [19]. In the study population, in 38 cases of AAA only one person knew of fact the presence of an aneurysm prior to submission to the test; the others did not have that awareness. Extrapolating data from the population of the examined community, approximately 80,000 unidentified AAAs can be expected among men aged 65 years and over in Poland, and among them almost 15% require surgery urgently.
The study confirmed the desirability of ultrasound screening in the diagnosis of abdominal aortic aneurysms in men over 65 years of age, especially with a history of smoking. Such a procedure should become standard based on the recommendations of the European Society of Vascular Surgery.
The results of this study and the results of studies conducted in the years 2011 and 2012 among men aged 65 years were a contribution to the development of the Programme for Early Diagnosis of abdominal aortic aneurysms, which is intended to include men aged 65 years, who are current/past smokers. This programme was approved by the Health Technology Assessment Agency and has been implemented in Poland.
CONCLUSIONS
The prevalence of AAA in men aged 60–64 years and in women aged 65 years and over was similar to that seen in previously conducted studies in other countries. In men aged 65 years and over it was a little higher. Special attention should be paid in men aged 65 years and over, who are current or past smokers, with a history of myocardial infarction or acute coronary syndrome.
Conflict of interest: none declared
References
- 1. 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, doi: 10.1161/CIRCULATIONAHA.106.174526, indexed in Pubmed: 16549646.
- 2. Johnston KW, Rutherford RB, Tilson MD, et al. Suggested standards for reporting on arterial aneurysms. Subcommittee on Reporting Standards for Arterial Aneurysms, Ad Hoc Committee on Reporting Standards, Society for Vascular Surgery and North American Chapter, International Society for Cardiovascular Surgery. J Vasc Surg. 1991; 13(3): 452–458, indexed in Pubmed: 1999868.
- 3. Scott R, Wilson NM, Ashton HA, et al. 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): 1066–1070, doi: 10.1002/bjs.1800820821.
- 4. Lindholt JS, Juul S, Fasting H, et al. Screening for abdominal aortic aneurysms: single centre randomised controlled trial. BMJ. 2005; 330(7494): 750, doi: 10.1136/bmj.38369.620162.82, indexed in Pubmed: 15757960.
- 5. 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, doi: 10.1136/bmj.38272.478438.55, indexed in Pubmed: 15545293.
- 6. Powell J, Greenhalgh R. Small abdominal aortic aneurysms. N Engl J Med. 2003; 348(19): 1895–1901, doi: 10.1056/nejmcp012641.
- 7. National Center for Injury Prevention and Control. WISQARS leading causes of death reports 1997-2007. Atlanta: Center for Disease Control and Prevention. (http://webappa.cdc.gov/sasweb/ncipc/ leadcaus10.html).
- 8. Lederle FA, Johnson GR, Wilson SE, et al. Prevalence and associations of abdominal aortic aneurysm detected through screening. Aneurysm Detection and Management (ADAM) Veterans Affairs Cooperative Study Group. Ann Intern Med. 1997; 126: 441–449.
- 9. Keisler B, Carter Ch. Abdominal Aortic Aneurysm. Am Fam Physician. 2015; 91: 538–543.
- 10. 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): 539–548, doi: 10.1016/j.jvs.2010.05.090, indexed in Pubmed: 20630687.
- 11. Fleming C, Whitlock EP, Beil TL, et al. Screening for abdominal aortic aneurysm: a best-evidence systematic review for the U.S. Preventive Services Task Force. Ann Intern Med. 2005; 142(3): 203–211, indexed in Pubmed: 15684209.
- 12. Guirguis-Blake JM, Beil TL, Senger CA, et al. Ultrasonography screening for abdominal aortic aneurysms: a systematic evidence review for the U.S. Preventive Services Task Force. Ann Intern Med. 2014; 160(5): 321–329, doi: 10.7326/M13-1844, indexed in Pubmed: 24473919.
- 13. 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): 281–290, doi: 10.7326/M14-1204, indexed in Pubmed: 24957320.
- 14. Takagi H, Goto Sn, Matsui M, et al. A further meta-analysis of population-based screening for abdominal aortic aneurysm. J Vasc Surg. 2010; 52(4): 1103–1108, doi: 10.1016/j.jvs.2010.02.283, indexed in Pubmed: 20541347.
- 15. Primary Care Screening for Abdominal Aortic Aneurysm. A Systematic Evidence Review for the U.S. Preventive Services Task Force Evidence Syntheses, No. 109. http:// www.ncbi.nlm.nih.gov/pubmedhealth/PMH0062922/.
- 16. Moll FL, Powell JT, Fraedrich G, et al. European Society for Vascular Surgery. Management of abdominal aortic aneurysms clinical practice guidelines of the European society for vascu- lar surgery. Eur J Vasc Endovasc Surg. 2011; 41 (Suppl 1): S1–S58, doi: 10.1016/j.ejvs.2010.09.011, indexed in Pubmed: 21215940.
- 17. Jawień A, Fórmankiewicz B, Dereziński T, et al. Preliminary results from the first Polish screening program for abdominal aortic aneurysm in the Kuyavian-Pomeranian Province. Acta Angiol. 2012; 18(1): 9–17.
- 18. Jawien A, Formankiewicz B, Derezinski T, et al. Abdominal aortic aneurysm screening program in Poland. Gefasschirurgie. 2014; 19(6): 545–548, doi: 10.1007/s00772-014-1348-4, indexed in Pubmed: 26120253.
- 19. Dereziński T, Wolf J, Wąsikowska B, et al. Prevalence of hyper- tension and metabolic disturbances in a population-based cohort of postmenopausal women. The Gniewkowo Women Study. Arterial Hypertension. 2015; 19(2): 88–94, doi: 10.5603/ah.2015.0012.
Cite this article as: Dereziński TL, Fórmankiewicz B, Migdalski A, et al. The prevalence of abdominal aortic aneurysms in the rural/urban population in central Poland — Gniewkowo Aortic Study. Kardiol Pol. 2017; 75(7): 705–710, doi: 10.5603/KP.a2017.0071. |