CC BY 4.0 · Aorta (Stamford) 2020; 08(05): 132-140
DOI: 10.1055/s-0040-1715609
Original Research Article

Aortic Thickness: A Forgotten Paradigm in Risk Stratification of Aortic Disease

Ashutosh Hardikar
1   Menzies Institute for Medical Research, University of Tasmania, Australia
2   Department of Cardiothoracic Surgery, Royal Hobart Hospital, Hobart, Australia
,
Robin Harle
3   Department of Radiology, Royal Hobart Hospital, Hobart, Australia
,
Thomas H. Marwick
1   Menzies Institute for Medical Research, University of Tasmania, Australia
4   Baker Heart and Diabetes Institute, Melbourne, Australia
› Author Affiliations
Funding None.
 

Abstract

Background This study aimed at risk-stratifying aortic dilatation using aortic wall thickness (AWT) and comparing methods of AWT assessment.

Methods Demographic, epidemiological, and perioperative data on 72 consecutive aortic surgeries (age = 62 years[standard deviation (SD) = 12] years) performed by a single surgeon were collected from hospital database. Aortic thickness was measured on computed tomography scans, as well as intraoperatively in four quadrants, at the level of aortic sinuses, as well as midascending aorta, using calipers. Aortic wall stress was calculated using standard mathematical formulae.

Results The ascending aorta was 48.2 (SD = 8) mm and the mean thickness at ascending aorta level was 1.9 (SD = 0.3) mm. There was congruence between imaging and intraoperative measurements of thickness, as well as between the radiologist and surgeon. Preoperatively, 16 patients had multiple imaging studies showing an average rate of growth of 1.2 mm per year without significant difference in thickness. The wider the aorta, the thinner was the lateral or convex wall. Aortic stenosis (p = 0.01), lateral to medial wall thickness ratio (p = 0.04), and history of hypertension (p = 0.00), all had protective effect on aortic root stress. The ascending aortic stress was directly affected by age (p = 0.03) and inversely related to lateral to medial wall thickness ratio (p = 0.03).

Conclusion Aortic thickness can be measured preoperatively and easily confirmed intraoperatively. Risk stratification based on both aortic thickness and diameter (stress calculations) would better predict acute aortic events in dilated aortas and define aortic resection criteria more objectively.


#

Introduction

The aortic dilatation associated with bicuspid aortic valves (BAV), pathologic tricuspid aortic valves (TAV), and other aortopathies is clinically relevant due to the risk of acute aortic events. Risks for acute aortic events are governed by genetic predisposition, hemodynamic factors, and morphology. The law of Laplace (Duprey et al[1]), best explained by the Young–Laplace equation, shows wall stress to relate to the internal pressure (P), radius of the aneurysm (R), and aortic wall thickness (AWT;“t”).

Hypertension, wall thinning, and aortic enlargement are the most important factors increasing aortic wall stress and leading to aortic rupture or dissection.[2] Aortic diameter has been the primary measurement in the literature,[3] and guidelines have concentrated only on aortic diameters.[4] Few studies have focused on blood pressure,[5] and very few have considered aortic thickness.[6] Some surgeons have used subjective criteria of friability or tissue quality, or indexing body size to facilitate intraoperative decisionmaking in aortas <45 mm.[7] Some studies have highlighted the possibly catastrophic thinness of aortas.[8] We here present an easy method of aortic thickness measurement and wall stress calculation to objectively prognosticate the risk of future aortic events.


#

Materials and Methods

Study Design

The study was approved under aortic pathology registry by the Tasmanian Human Research and Ethics committee (Reference no.: H0013456). Individual patient consents were obtained to join the registry. Demographic, epidemiological, and perioperative data were collected from a database at the Royal Hobart Hospital (RHH). AWT measurements were obtained on computed tomography (CT) imaging studies in 72 consecutive aortic surgeries by a single surgeon between 2014 and 2018, and interobserver variability was assessed by a specialist radiologist in 10 randomly selected cases. The intraoperative thickness was measured using calipers in four quadrants at the level of the aortic sinuses, as well as the mid-ascending aorta. The measurement was done on-table before sending the specimen for pathology using standard calipers and using a point where one cannot pull the aortic wall out of the calipers as the thickness.[9] The stress in aortic wall was calculated using standard mathematical formula; aortic wall circumferential stress = (P × R) / t; where P is the systolic blood pressure of the aorta while measuring the diameter, R is the radius, and t is the AWT.

In three patients, thickness could not be measured intraoperatively in all four quadrants (aortic dissection cases). Imaging studies were unable to measure the exact thickness in at least one quadrant in seven cases.


#

Epidemiology

Confounding variables which would likely affect aortic thickness including sociodemographic, morphometric (height, weight, and dimensions), hypertension, diabetes, dyslipidemia, vasculopathy, renal disease, smoking history, aortic valve pathology, and medications were entered ([Table 1]). A family history of aortic or cardiovascular disease was recorded if a parent or a sibling was affected.

Table 1

Demographic, clinical, and morphometric characteristics of 72 patients undergoing aortic surgery

Characteristic

Total

Aneurysm

Dissection

p-Value

Number

72

58

14

NA

Demographics:

 Male (n)

58

49

9

0.12

 Age in year (SD)

62.04 (11.6)

61.95 (12.1)

62.40 (9.7)

0.91

Anthropometric:

 Height in cm (SD)

173.87 (8.28)

173.53 (8.31)

175.30 (8.42)

0.55

 Weight in kg (SD)

83.17 (20.6)

85.12 (17.6)

74.8 (30.3)

0.16

 Body surface area in m2 (SD)

1.99 (0.20)

1.99 (0.20)

1.97 (0.22)

0.76

History:

 Hypertension

46

35

11

0.20

 Chronic obstructive pulmonary disease

11

9

2

0.91

 Peripheral vascular disease

5

5

0

0.26

 Diabetes

1

1

0

0.62

 Dyslipidemia

26

23

3

0.20

 Smoker

35

28

7

0.91

Clinical features:

 ≥ Moderate aortic stenosis

27

27

0

0.01

 ≥ Moderate aortic regurgitation

36

28

8

0.14

 Bicuspid aortic valve

31

29

2

0.02

Abbreviation: SD, standard deviation.



#

Surgery

Aortic resection was performed in accordance with the recent guidelines.[10] The indication was primary pathology meeting size criteria or rapid growth in aneurysm size in 26 cases, concomitant surgery in 32 cases, and acute aortic dissection in 14 cases.


#

Intraoperative Measurement

Aortic diameter was measured intraoperatively by measuring the circumference of the aorta and deriving the diameter. Aortic thickness was measured in four quadrants, anterior, posterior, medial, or inner/concave border (toward the pulmonary artery) and lateral or outer/convex border (toward the superior vena cava). Measurements were done at mid-ascending aorta or the aortic root or both, depending on the extent of aortic resection ([Table 2]). A surgical grade Vernier's caliper was used to measure aortic thickness. A note of type of aortic valve and its pathology was made at the same time.

Table 2

Aortic dimensions/measurements at time of surgery

Total (n = 72)

Aneurysm (n = 58)

Dissection (n = 14)

p

Aortic annulus

26.72 (SD = 2.5)

27.20 (SD = 2.4)

24.74 (SD = 1.9)

0.00

Aortic root(the sinus of Valsalva)

44.75 (SD = 9.6)

45.10 (SD = 10.1)

43.36 (SD = 7.3)

0.55

Sinotubular junction

40.58 (SD = 9.6)

40.24 (SD = 9.8)

41.95 (SD = 8.6)

0.55

Ascending aorta

48.19 (SD = 8)

47.45 (SD = 7.7)

51.26 (SD = 8.7)

0.11

Proximal arch

33.68 (SD = 6.7)

33.65 (SD = 6.9)

33.82 (SD = 5.9)

0.93

Left ventricular outflow tract–root angle

12.38 (SD = 5.6)

11.89 (SD = 4.6)

14.40 (SD = 8.3)

0.13

Root–ascending aorta angle

30.27 (SD = 12.2)

29.75 (SD = 12.9)

32.43 (SD = 8.9)

0.46

Aortic valve angle

46.80 (SD = 8.5)

47.15 (SD = 8.8)

45.38 (SD = 7.2)

0.49

Asymmetry index

1.09 (SD = 0.1)

1.09 (SD = 0.1)

1.09 (SD = 0.1)

0.92

Root thickness (mm)

1.88 (SD = 0.36)

1.84 (SD = 0.32)

2.18 (SD = 0.51)

0.05

Ascending aorta thickness (mm)

1.91 (SD = 0.30)

1.88 (SD = 0.28)

2.02 (SD = 0.39)

0.11

Lateral/medial wall ratio aortic root

0.86 (SD = 0.1)

0.86 (SD = 0.1)

0.85 (SD = 0.1)

0.73

Lateral/medial wall ratio ascending aorta

0.86 (SD = 0.1)

0.86 (SD = 0.1)

0.87 (SD = 0.1)

0.60

Aorta root stress (mm Hg)

1,486.72 (SD = 475)

1,529.8 (SD = 476)

1,211.3 (SD = 398)

0.94

Aortic stress (mm Hg)

1,402.68 (SD = 314)

1,404.33 (SD = 331)

1,396.53 (SD = 252)

0.17

Abbreviation: SD, standard deviation.


Note: Values are expressed as mean and standard deviation.



#

Imaging

All 72 patients had a preoperative imaging studies performed in a standard protocol and 21 had more than one study before surgery. Aortic diameters were measured at predetermined levels, and asymmetry index (AI) was derived ([Fig. 1]). Aortic thickness measurements were assessed in four quadrants at the aortic root and mid-ascending aorta level ([Table 2]). Three different angles, namely, aortic valve angle (AVAng), left ventricular outflow tract (LVOT)–root angle (RootAng), and root-aorta angle (AortAng) were measured ([Fig. 1]).

Zoom Image
Fig. 1 Aortic angles and asymmetry index.

#

Interobserver Variability

In a random selection of 10 representative studies, all measurements were obtained twice by primary investigator (A.H.) on separate occasions and repeated by an experienced radiologist (R.H.). The mean measurement was taken and percentage deviation from the mean was used to estimate measurement variability.


#

Statistical Analysis

The statistical analysis was performed using a standard statistical software package (IBM Corp. Released 2017. IBM SPSS Statistics for Macintosh, Version 23.0. Armonk, NY; IBM Corp.). Continuous data are presented as mean (standard deviation [SD]). Correlations among different variables were performed using Pearson's or Spearman's test where appropriate. We also performed univariable and multivariable analyses for the study of association of aortic stress with different parameters. The standardized beta values with confidence intervals and probability values are presented. The inter- and intraobserver agreement for the aortic root measurements was described by kappa statistics. Reproducibility was assessed using Bland–Altman analysis and intraclass correlation coefficient (ICC). We considered an α < 0.05 to be significant.


#
#

Results

Patient Characteristics

The demographic, morphometric parameters along with other variables affecting aortic thickness are given in [Table 1]. The aneurysm and dissection groups were essentially similar except that dissection group had more proportion of females and hypertensive patients (not statistically significant), while aneurysm group patients were more likely to have a bicuspid aortic valve or more than moderate aortic stenosis (p  ≤  0.02).


#

Aortic Wall Thickness

The mean thickness in four quadrants of the aortic root, mid-ascending aorta, or both, along with aortic diameters from annulus, sinuses, sinotubular junction, mid-ascending aorta, and different arch and descending levels along with aortic angles are given in [Table 2]. Average aortic root thickness was different in aneurysm (1.84 (SD = 0.3] mm) and dissection (2.18 [SD = 0.5] mm) groups (p = 0.05). The aortic annuls was also wider in the aneurysm group (27.2 [SD = 2.4] mm) versus the dissection group (24.7 [SD = 1.9] mm). We plotted a ratio of outer/convex to inner/concave wall thickness against the aortic diameter at the level of ascending aorta ([Fig. 2]), which shows that the ratio reduces as the aorta dilates, indicating a preferential thinning of the convexity of the aorta.

Zoom Image
Fig. 2 Relationship of convex/outer to concave/inner wall thickness ratio to aortic diameter in the ascending aorta. Lateral to medial aortic wall thickness ratio reduces as the aorta dilates.

#

Aortic Wall Stress

[Table 3] shows the multivariable regression analysis for aortic wall circumferential stress, derived from operative measurements. Ratio of outer/convex to inner/concave AWT significantly affected the aortic stress at both ascending aorta and root levels (p  ≤  0.05). Furthermore, age correlated with ascending aortic stress (p  ≤  0.05), while hypertension history was associated with lower stress levels in the aortic root (p< 0.001). Aortic stenosis had a significant protective effect on aortic root stress (p = 0.01), while the female sex had some effect as well (beta = 1.83, p = 0.08).

Table 3

Independent associations of aortic wall stress

For aortic root

Model R 2 = 0.58, p = 0.00

Parameter

Beta (CI)

t” value

p-Value

 Height (cm)

−0.25 (−29.1 to 3.5)

−1.6

0.12

 Sex

0.27 (−33.4 to 613.3)

1.83

0.08

 Hypertension history

−0.78 (−920.5 to −436)

−5.73

0.00

 Lateral/medial aortic wall thickness ratio

−0.28 (−2165 to −69.9)

−2.18

0.04

 Aortic valve angle

0.1 (−7.55 to 17.51)

0.81

0.42

 Aortic stenosis

−0.41 (−229 to 36)

−2.81

0.01

 Aortic regurgitation

0.01 (−70 to 135.6)

0.65

0.52

For ascending aorta

Model r 2 = 0.28, p = 0.08

Parameter

Beta (CI)

t” value

p-Value

 Body surface area

0.19 (−123.2 to 750.7)

1.44

0.16

 Age

0.3 ( 1.1 to 17.1)

2.28

0.03

 Hypertension history

−0.12 (−272.8 to 97.4)

−0.95

0.35

 Lateral/medial AWT ratio

−0.35 (−2681 to −121.7)

−2.2

0.03

 Root–ascending aorta angle

−0.29 (−16.7 to 0.56)

−1.88

0.07

 Aortic stenosis

0.0 (−99.5 to 101.9)

0.02

0.98

 Aortic regurgitation

−0.0 (−89.3 to 78.2)

−0.02

0.90

 Sex

−0.22 (−447.2 to 59.7)

−1.5

0.13

[Figure 3] shows the association of aortic wall stress with aortic diameter. While wall stress and diameter are concordant in most patients, a meaningful number of patients have high wall stress despite a small diameter, or low wall stress with a high diameter.

Zoom Image
Fig. 3 Relationship of aortic wall stress to aortic diameter in the ascending aorta. Wall stress increases as the aorta dilates, but the most meaningful observations may be the outliers. AA, ascending aorta.

[Figure 4] shows aortic stress plotted against true lumen diameter in 14 patients with aortic dissection. We measured the true lumen based on a previous article by Neri et al.[11] This measurement was done on-table after we excised the dissected segment, before sending it off to the pathologist. Thirteen of these had true lumen diameter (prior to dissection) of <45 mm. In dissected aortas, we measured AWT of the dissected aorta by putting together the layers after removing any blood clot/thrombus in between the layers. We measured thickness at the mid-ascending aortic level (over the main pulmonary artery) for ascending aorta at all times.

Zoom Image
Fig. 4 Wall stress versus aortic lumen diameter in 14 patients with aortic dissection. In 13 cases, the true lumen diameter was <45 mm and the wall stress was low, emphasizing the role of tissue characteristics or blood pressure surges.

#

Thickness Measurement over Time

The aortic measurements in 21 patients with more than one preoperative imaging studies, including aortic diameters and thickness showed that average growth in the aortic diameter was 1.19 mm per year, but there was no significant change in the AWT.


#

Correlation between Imaging and on-Table Actual Measurements

The kappa values for intraobserver variation was 0.73 while between the surgeon and radiologist, it was 0.62, suggesting substantial agreement. The Bland–Altman plot for comparison of on-table AWT measurement with the CT scan measurements ([Fig. 5]) had coefficient of 0.18 (p = 0.01), showing a weaker agreement.

Zoom Image
Fig. 5 Agreement between intra-operative and computed tomography assessment of aortic wall thickness. AWT, aortic wall thickness; CT, computed tomography; SD, standard deviation.

#
#

Discussion

These results show that preoperative measures of aortic thickness are possible and readily validated by intraoperative measurements. Risk stratification based on both aortic thickness and diameter would better predict aortic events in patients with dilated aortas.

Aortic Thickness

Aortic thickness measurements in the normal population[12] show increasing thickness with age, affected by race and gender. AWT and distensibility are related to cardiovascular risk factors, including hypertension.[13] AWT has also been shown to predict lifetime risk of cardiovascular disease in middle-aged individuals with a low short-term risk of coronary heart disease.[14] In addition to age, gender, and ethnicity, AWT is affected by smoking status, systolic blood pressure, high-density lipoprotein (HDL) and low-density lipoprotein (LDL) cholesterol levels, and fasting blood sugar level.[15] Interestingly, a conclusive relation between increased AWT and coronary artery disease has not been shown.[16] The other associations of AWT are with hypothyroidism,[17] increased cerebrovascular events,[18] and possibly for diagnosis of aortitis.[19]

AWT is a risk factor in aortic dissection.[20] Previous studies using finite element model have predicted that assessment of regional AWT would better predict the dissection risk.[21] The aortic stress in the dissection subgroup (1,386 [SD = 298] mm Hg) trended to be lower than the aneurysm subgroup (1,448 [SD = 351] mm Hg) which indicates that either blood pressure surges are at work,[22] or the dissected aortas were weaker and there are factors beyond the Law of Laplace like aortic strength or elasticity are relevant. AWT has been measured by epiaortic echocardiography and used to calculate mechanical characteristics of the aorta.[23]


#

Measurement of Aortic Wall Thickness

Population-based values of AWT are variable, and probably dependent on imaging modality with an echocardiographic AWT of 2.4 (SD = 0.8) mm,[24] compared with a median value of 1.5 mm by magnetic resonance imaging.[25] This variation has been taken into consideration in mathematical models.[26] Due to this variation in assessment of thickness, it has been recommended that intra vascular ultra sound might be the most accurate in measuring AWT.[27] Our measurements of mean ascending aortic thickness of 1.91 mm and aortic root thickness of 1.88 mm are close to that reported in literature.

In the absence of objective measurements or indices, the traditional intraoperative assessment of the quality and the AWT has been subjective.[28] Although magnetic resonance imaging (MRI) was first used to calculate AWT,[12] CT is more widely available and seems equally effective. Semiautomated analysis of CT aortogram images can be used to identify circumferential variations in AWT.[29] Of the echocardiographic methods, the epiaortic probe appears the most robust. In our study, the CT measurement of AWT slightly overestimated the intraoperative measurement. The intra- and interobserver agreement of CT measures are fair.

The measurement of AWT in pathology specimens[20] is unlikely to be accurate.[30] Even when the postmortem CT scan was done only 20 hours after dissection, the AWT increased in the range of 20 to 25%. We have hence used intraoperative caliper measurements in all our calculations, hoping this measure to be closest to the actual AWT in vivo. AWT is variable along the circumference (some studies separately mention the mean and maximal AWT), and during surgery, a surgeon can inspect and sample the thinnest or most friable area and have an objective assessment of the possible stress generated at that spot for a given blood pressure.

We agree that it is possible that the AWT might change once it is excised, as the aortic wall is no longer under the pressure when normally it was in a cylindrical structure with blood in it. However, we believe that, first of all, the change should be minimal as compared with other studies who have done measurements from specimens fixed in formalin. Second, the change would uniformly affect all the specimen, so any variation should be similar across the board.

For the same reason, we possibly have only a weak correlation (Bland–Altman plot coefficient of 0.18) for comparison of preoperative CT image measurement and intraoperative measurement with calipers.


#

Contributors to Wall Stress

Hypertension and the strength of the aortic wall may contribute to aortic dilatation in aortopathies. Aortic size increases at more than double the rate in hypertensive than normotensive patients after aortic valve replacement (AVR).[31] However, observations of aortic dilatation after AVR are not uniform; Yasuda et al[32] showed that the BAV group were not affected by hemodynamic parameters, whereas the TAV group had increased dilatation for higher diastolic blood pressure and higher fractional shortening. In our study group, a history of hypertension actually had a protective effect on aortic wall stress. Likewise, although Forsell et al[33] showed decreased wall thickness in BAV as compared with TAV, our study showed similar wall thickness in BAV, as well as TAV. Another factor to note is that only 1 of the 72 patients had diabetes. It is possible that diabetes might affect the aortic stiffness and have a protective effect,[34] although the data are small to draw any conclusions.

Aortic morphology is also important. The RootAng was different between the aneurysm and dissection subgroups (but not statistically significant) suggesting a role for hemodynamic forces in the dissection patients. [Fig. 2] illustrates that with increasing aortic diameter, the ratio of outer/convex versus inner/concave wall thickness reduces (p = 0.04), which explains why the convexity of the aorta is more vulnerable to acute aortic events with increasing diameter.


#

Clinical Implications

A comprehensive assessment of the aortic wall stress, based on the aortic diameter and the AWT, taking into account whether the patient is hypertensive or not, would yield a more objective assessment about the decision of aortic surgery in a given patient. To some extent, this mirrors practice by some surgeons. Bauer et al[28] have argued that during reduction aortoplasty, either the effective diameter of the aorta should be reduced to <35 mm or the wall should be supported externally with a Dacron graft. This reduces the effective stress in the aortic wall by either reducing the diameter or increasing the effective thickness. The role of wall thickness may explain the 40% of patients in the International Registry of Acute Aortic Dissection (IRAD) registry with aortic dissections despite a diameter <5 cm.[35] Preoperative assessment by ultrasound, CT, or MRI can be used to predict the variation in the AWT, and further on-table measurement of a sample of the aortic wall may help to inform decisions.


#
#

Limitations

The small numbers in this study are a reflection of the study design that provided consistent measurement of thickness by a single surgeon. The data (especially [Fig. 4]) indicates that either significant blood pressure surges cause acute aortic syndromes,[22] or all aortas are not created equal and even the Law of Laplace might not completely explain the risk of acute aortic events. We utilized intraoperative blood pressures for calculating aortic wall stress, which would be obviously much lower in an anaesthetized patient. We have not actually shown that incorporating AWT enhances the prediction of aortic dissection, we are proposing that it might improve the predictive accuracy.


#

Conclusion

Using aortic diameter alone to quantify the risk of acute aortic events is proven inadequate. Aortic thickness is an important parameter in the assessment of wall stress that can be measured preoperatively and easily confirmed intraoperatively. Risk stratification, based on calculation of aortic wall stress, might help to individualize decision-making.


#
#

Conflict of Interest

The authors declare no conflict of interest related to this article.

Acknowledgment

The authors would like to acknowledge the efforts of Ms. Carmel Fenton in maintaining a database at the Royal Hobart Hospital and assistance of Dr. Mehr Gupta in following -up on these patients.

  • References

  • 1 Duprey A, Khanafer K, Schlicht M, Avril S, Williams D, Berguer R. In vitro characterisation of physiological and maximum elastic modulus of ascending thoracic aortic aneurysms using uniaxial tensile testing. Eur J Vasc Endovasc Surg 2010; 39 (06) 700-707
  • 2 Erbel R, Eggebrecht H. Aortic dimensions and the risk of dissection. Heart 2006; 92 (01) 137-142
  • 3 Coady MARJ, Rizzo JA, Hammond GL. et al. What is the appropriate size criterion for resection of thoracic aortic aneurysms?. J Thorac Cardiovasc Surg 1997; 113 (03) 476-491 , discussion 489–491
  • 4 2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the Diagnosis and Management of Patients with Thoracic Aortic Disease Representative Members; Hiratzka LFCMA, Isselbacher EM. et al. Surgery for Aortic dilatation in Patients with Bicuspid Aortic valves: a statement of clarification from the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation 2016; 133 (07) 680-686
  • 5 Chau KH, Elefteriades JA. Natural history of thoracic aortic aneurysms: size matters, plus moving beyond size. Prog Cardiovasc Dis 2013; 56 (01) 74-80
  • 6 Van Puyvelde J, Verbeken E, Verbrugghe P, Herijgers P, Meuris B. Aortic wall thickness in patients with ascending aortic aneurysm versus acute aortic dissection. Eur J Cardiothorac Surg 2016; 49 (03) 756-762
  • 7 Svensson LG, Adams DH, Bonow RO. et al. Aortic valve and ascending aorta guidelines for management and quality measures: executive summary. Ann Thorac Surg 2013; 95 (04) 1491-1505
  • 8 Elefteriades JA, Sang A, Kuzmik G, Hornick M. Guilt by association: paradigm for detecting a silent killer (thoracic aortic aneurysm). Open Heart 2015; 2 (01) e000169
  • 9 Flack D. Measurement good practice guide no. 40: callipers and micrometers. Accessed July 8, 2020 at: https://docplayer.net/21009990-Good-practice-guide-no-40-callipers-and-micrometers-david-flack-issue-2.html
  • 10 Nishimura RA, Otto CM, Bonow RO. et al; ACC/AHA Task Force Members. 2014 AHA/ACC Guideline for the Management of Patients WithValvular Heart Disease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation 2014; 129 (23) e521-e643
  • 11 Neri E, Barabesi L, Buklas D. et al. Limited role of aortic size in the genesis of acute type A aortic dissection. Eur J Cardiothorac Surg 2005; 28 (06) 857-863
  • 12 Li AEKI, Kamel I, Rando F. et al. Using MRI to assess aortic wall thickness in the multiethnic study of atherosclerosis: distribution by race, sex, and age. Am J Roentgenol 2004; 182 (03) 593-597
  • 13 Malayeri AA, Natori S, Bahrami H. et al. Relation of aortic wall thickness and distensibility to cardiovascular risk factors (from the Multi-Ethnic Study of Atherosclerosis [MESA]). Am J Cardiol 2008; 102 (04) 491-496
  • 14 Gupta S, Berry JD, Ayers CR. et al. Left ventricular hypertrophy, aortic wall thickness, and lifetime predicted risk of cardiovascular disease:the Dallas Heart Study. JACC Cardiovasc Imaging 2010; 3 (06) 605-613
  • 15 Rosero EB, Peshock RM, Khera A, Clagett P, Lo H, Timaran CH. Sex, race, and age distributions of mean aortic wall thickness in a multiethnic population-based sample. J Vasc Surg 2011; 53 (04) 950-957
  • 16 Shakeri A, Hafez Quran F, Javadrashid R, Abdekarimi MH, Ghojazadeh M, AbolghassemiFakhree MB. Correlation between aortic wall thickness and coronary artery disease by 64 slice multidetector computed tomography. J Cardiovasc Thorac Res 2013; 5 (03) 91-95
  • 17 Ittermann T, Lorbeer R, Dörr M. et al. High levels of thyroid-stimulating hormone are associated with aortic wall thickness in the general population. Eur Radiol 2016; 26 (12) 4490-4496
  • 18 Tresoldi S, Di Leo G, Zoffoli E. et al. Association of aortic wall thickness on contrast-enhanced chest CT with major cerebro-cardiac events. Acta Radiol 2014; 55 (09) 1040-1049
  • 19 Slobodin G, Nakhleh A, Rimar D, Wolfson V, Rosner I, Odeh M. Increased aortic wall thickness for the diagnosis of aortitis: a computed tomography-based study. Int J Rheum Dis 2016; 19 (01) 82-86
  • 20 Van Puyvelde J, Verbeken E, Verbrugghe P, Herijgers P, Meuris B. Aortic wall thickness in patients with ascending aortic aneurysm versus acute aortic dissection. Eur J Cardiothorac Surg 2016; 49 (03) 756-762
  • 21 Nathan DP, Xu C, Gorman III JH. et al. Pathogenesis of acute aortic dissection: a finite element stress analysis. Ann Thorac Surg 2011; 91 (02) 458-463
  • 22 Elefteriades JA, Farkas EA. Thoracic aortic aneurysm clinically pertinent controversies and uncertainties. J Am Coll Cardiol 2010; 55 (09) 841-857
  • 23 Koullias G, Modak R, Tranquilli M, Korkolis DP, Barash P, Elefteriades JA. Mechanical deterioration underlies malignant behavior of aneurysmal human ascending aorta. J Thorac Cardiovasc Surg 2005; 130 (03) 677-683
  • 24 Muraru D, Maffessanti F, Kocabay G. et al. Ascending aorta diameters measured by echocardiography using both leading edge-to-leading edge and inner edge-to-inner edge conventions in healthy volunteers. Eur Heart J Cardiovasc Imaging 2014; 15 (04) 415-422
  • 25 Mensel B, Quadrat A, Schneider T. et al. MRI-based determination of reference values of thoracic aortic wall thickness in a general population. Eur Radiol 2014; 24 (09) 2038-2044
  • 26 Scotti CM, Shkolnik AD, Muluk SC, Finol EA. Fluid-structure interaction in abdominal aortic aneurysms: effects of asymmetry and wall thickness. Biomed Eng Online 2005; 4: 64
  • 27 Goldstein SA, Evangelista A, Abbara S. et al. Multimodality imaging of diseases of the thoracic aorta in adults: from the american society of echocardiography and the European association of cardiovascular imaging: endorsed by the society of cardiovascular computed tomography and society for cardiovascular magnetic resonance. J Am Soc Echocardiogr 2015; 28 (02) 119-182
  • 28 Bauer M, Pasic M, Schaffarzyk R. et al. Ann Thorac Surg 2002; 73: 720-724
  • 29 Shang EK, Lai E, Pouch AM. et al. Validation of semiautomated and locally resolved aortic wall thickness measurements from computed tomography. J Vasc Surg 2015; 61 (04) 1034-1040
  • 30 Okuma H, Gonoi W, Ishida M. et al. Greater thickness of the aortic wall on postmortem computed tomography compared with antemortem computed tomography: the first longitudinal study. Int J Legal Med 2014; 128 (06) 987-993
  • 31 Kuralay E, Demirkilic U, Ozal E. et al. Surgical approach to ascending aorta in bicuspid aortic valve. J Card Surg 2003; 18 (02) 173-180
  • 32 Yasuda H, Nakatani S, Stugaard M. et al. Failure to prevent progressive dilation of ascending aorta by aortic valve replacement in patients with bicuspid aortic valve: comparison with tricuspid aortic valve. Circulation 2003; 108 (Suppl. 01) II291-II294
  • 33 Forsell C, Björck HM, Eriksson P, Franco-Cereceda A, Gasser TC. Biomechanical properties of the thoracic aneurysmal wall: differences between bicuspid aortic valve and tricuspid aortic valve patients. Ann Thorac Surg 2014; 98 (01) 65-71
  • 34 Patel K, Zafar MA, Ziganshin BA, Elefteriades JA. Diabetes mellitus: is it protective against aneurysm? A narrative review. Cardiology 2018; 141 (02) 107-122
  • 35 Pape LA, Tsai TT, Isselbacher EM. et al; International Registry of Acute Aortic Dissection (IRAD) Investigators. Aortic diameter >or = 5.5 cm is not a good predictor of type A aortic dissection: observations from the International Registry of Acute Aortic Dissection (IRAD). Circulation 2007; 116 (10) 1120-1127

Address for correspondence

Ashutosh Hardikar, MD
Department of Cardiothoracic Surgery, Royal Hobart Hospital
48 Liverpool Street, Hobart, Australia 7000

Publication History

Received: 15 July 2019

Accepted: 20 June 2020

Article published online:
23 December 2020

© 2020. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA

  • References

  • 1 Duprey A, Khanafer K, Schlicht M, Avril S, Williams D, Berguer R. In vitro characterisation of physiological and maximum elastic modulus of ascending thoracic aortic aneurysms using uniaxial tensile testing. Eur J Vasc Endovasc Surg 2010; 39 (06) 700-707
  • 2 Erbel R, Eggebrecht H. Aortic dimensions and the risk of dissection. Heart 2006; 92 (01) 137-142
  • 3 Coady MARJ, Rizzo JA, Hammond GL. et al. What is the appropriate size criterion for resection of thoracic aortic aneurysms?. J Thorac Cardiovasc Surg 1997; 113 (03) 476-491 , discussion 489–491
  • 4 2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the Diagnosis and Management of Patients with Thoracic Aortic Disease Representative Members; Hiratzka LFCMA, Isselbacher EM. et al. Surgery for Aortic dilatation in Patients with Bicuspid Aortic valves: a statement of clarification from the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation 2016; 133 (07) 680-686
  • 5 Chau KH, Elefteriades JA. Natural history of thoracic aortic aneurysms: size matters, plus moving beyond size. Prog Cardiovasc Dis 2013; 56 (01) 74-80
  • 6 Van Puyvelde J, Verbeken E, Verbrugghe P, Herijgers P, Meuris B. Aortic wall thickness in patients with ascending aortic aneurysm versus acute aortic dissection. Eur J Cardiothorac Surg 2016; 49 (03) 756-762
  • 7 Svensson LG, Adams DH, Bonow RO. et al. Aortic valve and ascending aorta guidelines for management and quality measures: executive summary. Ann Thorac Surg 2013; 95 (04) 1491-1505
  • 8 Elefteriades JA, Sang A, Kuzmik G, Hornick M. Guilt by association: paradigm for detecting a silent killer (thoracic aortic aneurysm). Open Heart 2015; 2 (01) e000169
  • 9 Flack D. Measurement good practice guide no. 40: callipers and micrometers. Accessed July 8, 2020 at: https://docplayer.net/21009990-Good-practice-guide-no-40-callipers-and-micrometers-david-flack-issue-2.html
  • 10 Nishimura RA, Otto CM, Bonow RO. et al; ACC/AHA Task Force Members. 2014 AHA/ACC Guideline for the Management of Patients WithValvular Heart Disease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation 2014; 129 (23) e521-e643
  • 11 Neri E, Barabesi L, Buklas D. et al. Limited role of aortic size in the genesis of acute type A aortic dissection. Eur J Cardiothorac Surg 2005; 28 (06) 857-863
  • 12 Li AEKI, Kamel I, Rando F. et al. Using MRI to assess aortic wall thickness in the multiethnic study of atherosclerosis: distribution by race, sex, and age. Am J Roentgenol 2004; 182 (03) 593-597
  • 13 Malayeri AA, Natori S, Bahrami H. et al. Relation of aortic wall thickness and distensibility to cardiovascular risk factors (from the Multi-Ethnic Study of Atherosclerosis [MESA]). Am J Cardiol 2008; 102 (04) 491-496
  • 14 Gupta S, Berry JD, Ayers CR. et al. Left ventricular hypertrophy, aortic wall thickness, and lifetime predicted risk of cardiovascular disease:the Dallas Heart Study. JACC Cardiovasc Imaging 2010; 3 (06) 605-613
  • 15 Rosero EB, Peshock RM, Khera A, Clagett P, Lo H, Timaran CH. Sex, race, and age distributions of mean aortic wall thickness in a multiethnic population-based sample. J Vasc Surg 2011; 53 (04) 950-957
  • 16 Shakeri A, Hafez Quran F, Javadrashid R, Abdekarimi MH, Ghojazadeh M, AbolghassemiFakhree MB. Correlation between aortic wall thickness and coronary artery disease by 64 slice multidetector computed tomography. J Cardiovasc Thorac Res 2013; 5 (03) 91-95
  • 17 Ittermann T, Lorbeer R, Dörr M. et al. High levels of thyroid-stimulating hormone are associated with aortic wall thickness in the general population. Eur Radiol 2016; 26 (12) 4490-4496
  • 18 Tresoldi S, Di Leo G, Zoffoli E. et al. Association of aortic wall thickness on contrast-enhanced chest CT with major cerebro-cardiac events. Acta Radiol 2014; 55 (09) 1040-1049
  • 19 Slobodin G, Nakhleh A, Rimar D, Wolfson V, Rosner I, Odeh M. Increased aortic wall thickness for the diagnosis of aortitis: a computed tomography-based study. Int J Rheum Dis 2016; 19 (01) 82-86
  • 20 Van Puyvelde J, Verbeken E, Verbrugghe P, Herijgers P, Meuris B. Aortic wall thickness in patients with ascending aortic aneurysm versus acute aortic dissection. Eur J Cardiothorac Surg 2016; 49 (03) 756-762
  • 21 Nathan DP, Xu C, Gorman III JH. et al. Pathogenesis of acute aortic dissection: a finite element stress analysis. Ann Thorac Surg 2011; 91 (02) 458-463
  • 22 Elefteriades JA, Farkas EA. Thoracic aortic aneurysm clinically pertinent controversies and uncertainties. J Am Coll Cardiol 2010; 55 (09) 841-857
  • 23 Koullias G, Modak R, Tranquilli M, Korkolis DP, Barash P, Elefteriades JA. Mechanical deterioration underlies malignant behavior of aneurysmal human ascending aorta. J Thorac Cardiovasc Surg 2005; 130 (03) 677-683
  • 24 Muraru D, Maffessanti F, Kocabay G. et al. Ascending aorta diameters measured by echocardiography using both leading edge-to-leading edge and inner edge-to-inner edge conventions in healthy volunteers. Eur Heart J Cardiovasc Imaging 2014; 15 (04) 415-422
  • 25 Mensel B, Quadrat A, Schneider T. et al. MRI-based determination of reference values of thoracic aortic wall thickness in a general population. Eur Radiol 2014; 24 (09) 2038-2044
  • 26 Scotti CM, Shkolnik AD, Muluk SC, Finol EA. Fluid-structure interaction in abdominal aortic aneurysms: effects of asymmetry and wall thickness. Biomed Eng Online 2005; 4: 64
  • 27 Goldstein SA, Evangelista A, Abbara S. et al. Multimodality imaging of diseases of the thoracic aorta in adults: from the american society of echocardiography and the European association of cardiovascular imaging: endorsed by the society of cardiovascular computed tomography and society for cardiovascular magnetic resonance. J Am Soc Echocardiogr 2015; 28 (02) 119-182
  • 28 Bauer M, Pasic M, Schaffarzyk R. et al. Ann Thorac Surg 2002; 73: 720-724
  • 29 Shang EK, Lai E, Pouch AM. et al. Validation of semiautomated and locally resolved aortic wall thickness measurements from computed tomography. J Vasc Surg 2015; 61 (04) 1034-1040
  • 30 Okuma H, Gonoi W, Ishida M. et al. Greater thickness of the aortic wall on postmortem computed tomography compared with antemortem computed tomography: the first longitudinal study. Int J Legal Med 2014; 128 (06) 987-993
  • 31 Kuralay E, Demirkilic U, Ozal E. et al. Surgical approach to ascending aorta in bicuspid aortic valve. J Card Surg 2003; 18 (02) 173-180
  • 32 Yasuda H, Nakatani S, Stugaard M. et al. Failure to prevent progressive dilation of ascending aorta by aortic valve replacement in patients with bicuspid aortic valve: comparison with tricuspid aortic valve. Circulation 2003; 108 (Suppl. 01) II291-II294
  • 33 Forsell C, Björck HM, Eriksson P, Franco-Cereceda A, Gasser TC. Biomechanical properties of the thoracic aneurysmal wall: differences between bicuspid aortic valve and tricuspid aortic valve patients. Ann Thorac Surg 2014; 98 (01) 65-71
  • 34 Patel K, Zafar MA, Ziganshin BA, Elefteriades JA. Diabetes mellitus: is it protective against aneurysm? A narrative review. Cardiology 2018; 141 (02) 107-122
  • 35 Pape LA, Tsai TT, Isselbacher EM. et al; International Registry of Acute Aortic Dissection (IRAD) Investigators. Aortic diameter >or = 5.5 cm is not a good predictor of type A aortic dissection: observations from the International Registry of Acute Aortic Dissection (IRAD). Circulation 2007; 116 (10) 1120-1127

Zoom Image
Fig. 1 Aortic angles and asymmetry index.
Zoom Image
Fig. 2 Relationship of convex/outer to concave/inner wall thickness ratio to aortic diameter in the ascending aorta. Lateral to medial aortic wall thickness ratio reduces as the aorta dilates.
Zoom Image
Fig. 3 Relationship of aortic wall stress to aortic diameter in the ascending aorta. Wall stress increases as the aorta dilates, but the most meaningful observations may be the outliers. AA, ascending aorta.
Zoom Image
Fig. 4 Wall stress versus aortic lumen diameter in 14 patients with aortic dissection. In 13 cases, the true lumen diameter was <45 mm and the wall stress was low, emphasizing the role of tissue characteristics or blood pressure surges.
Zoom Image
Fig. 5 Agreement between intra-operative and computed tomography assessment of aortic wall thickness. AWT, aortic wall thickness; CT, computed tomography; SD, standard deviation.