This study aims to investigate the prognostic value of incidental aortic valve calcification (AVC), mitral valve calcification (MVC) and mitral annular calcification (MAC) for cardiovascular events and non-rheumatic valve disease in particular on routine diagnostic chest CT.
Methods
The study followed a case-cohort design. 10410 patients undergoing chest CT were followed for a median period of 17 months. Patients referred for cardiovascular disease were excluded. A random sample of 1285 subjects and the subjects who experienced an endpoint were graded for valve calcification by three reviewers. Cox-proportional hazard analysis was performed to evaluate the prognostic value.
Results
515 cardiovascular events were ascertained. Compared with patients with no valve calcification, patients with severe AVC, MVC or MAC had respectively 2.03 (1.48–2.78), 2.08 (1.04–4.19) and 1.53 (1.13–2.08) increased risks of experiencing an event during follow-up. For valve endpoints the hazard ratios were respectively 14.57 (5.19–40.53), 8.78 (2.33–33.13) and 2.43 (1.18–4.98).
Conclusion
Incidental heart valve calcification, detected on routine chest CT is an independent predictor of future cardiovascular events. The study emphasises how incidental imaging findings can contribute to clinical care. It is a step in the process of composing an evidence-based approach in the reporting of incidental subclinical findings.
Abkürzungen
AVC
Aortic Valve Calcification
AVL
Aortic Valve Leaflet
CHD
Coronary Heart Disease
CI
Confidence Interval
CT
Computed Tomography
CVD
Cardiovascular Disease
FOV
Field of View
MAC
Mitral Annular Calcification
MVC
Mitral Valve Calcification
MVL
Mitral Valve Leaflet
PAOD
Peripheral Arterial Obstructive Disease
PROVIDI
Prognostic Value of Unrequested Information in Diagnostic Imaging
Introduction
Multidetector chest Computed Tomography (CT), which is usually performed during the diagnostic work-up of patients suffering from a variety of chest complaints, can yield extensive additional information about the heart, the lungs, the mediastinum, the vertebrae and the large vessels [1]. In the last decade, the image quality of chest Computed Tomography has improved and its usage has thereby increased considerably. A side effect of this intense usage is the frequent occurrence of incidental findings [2‐4]. We define these as imaging characteristics that are incidentally detected and unrelated to the clinical indication leading to the CT referral. Only follow-up studies can determine whether patients can benefit from these incidental findings as such studies uncover which incidental imaging abnormalities have or do not have clinically relevant prognostic value. The latter will serve to reduce redundant additional diagnostic work-up.
Examples of frequently encountered incidental findings are aortic valve calcification (AVC), mitral valve calcification (MVC) and mitral annulus calcification (MAC). These imaging characteristics are considered to be expression of the process of atherosclerosis [5‐7] and have repeatedly been shown to be related to cardiovascular disease (CVD), cardiovascular death and even all-cause mortality [8‐10]. However, in previous literature those image characteristics were mainly scored on transthoracic or transoesophageal echocardiography and to date no follow-up studies are available that have investigated the prognostic value of these aortic abnormalities when incidentally detected on routine chest CT in a clinical care population. Investigating this can provide an additional means of identifying those patients who can benefit from timely preventative measures [11].
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The PROgnostic Value of incidental Information in Diagnostic Imaging (PROVIDI) Study is the first longitudinal study to investigate the prevalence and clinical relevance of incidental, subclinical image characteristics in a cohort consisting of patients with diagnostic chest CT. In this particular study we aimed to examine whether subclinical calcification of the aortic and mitral valve, detected incidentally on routine diagnostic chest CT, can be used by radiologists as independent predictors of the occurrence of CVD and non-rheumatic valve disease in particular. Additionally, we examine whether incidentally detected calcified heart valves have prognostic value beyond the hitherto typically investigated CVD markers: aortic- and/or coronary arteries [12‐16]. This study operates from radiologist’s perspective and only seeks to incorporate information that is readily available in routine radiological setting. No allowance was made for the collection of additional clinical information, such as diabetes and renal failure, which may not routinely be available in such settings.
Materials and methods
PROVIDI
The PROVIDI study employs a case-cohort design [17], in cooperation with 8 participating hospitals in the Netherlands. All patients aged 40 years and older who were referred to one of the participating hospitals with an indication for a chest CT between 2002 and 2005 were included (N = 23,443). Patients diagnosed with primary lung cancer (including mesothelioma) or distant metastatic disease from other types of cancer (excluding haematological malignancies) were excluded, as it is highly unlikely that detection of incidental imaging characteristics will alter clinical decision-making in patients with a very poor prognosis. This resulted in a cohort of 14,366 patients. The PROVIDI study is approved by the Medical Ethics Committee of the Medical Ethics Committee of the University Medical Center Utrecht, as well as the ethical review boards of all other participating centres. Written informed consent was waived for all patients because of the retrospective design of this study. A privacy protocol was implemented to protect patient’s anonymity.
Study subjects and CT protocols
In this study patients with a CT indication directly related to suspected cardiovascular disease were excluded (n = 2303) from the PROVIDI cohort in order to ensure that valve calcification observed was truly incidental. Additionally, a total of 1653 patients from a randomly chosen hospital were excluded, to serve as an external validation sample for future research conducted within PROVIDI. The resulting cohort consisted of 10,410 patients. Consistent with a case-cohort design a random sample—called subcohort—was taken from this cohort immediately after the patients who experienced an outcome event were ascertained to serve as a control. It was sampled so that the resulting sample would be at least 10% [18] of the full cohort and twice as large as the specific group of outcome event under study, with a reasonable margin for error (subcohort, n = 1285). Figure 1 shows a flowchart of the study design and selection of the study population.
Fig. 1
Flowchart of study design. CBS: Dutch central bureau of statistics. LMR: Dutch medical data registration
×
When study subjects had more than one Chest CT examination during follow-up, only the first Chest CT was used. Chest CTs were obtained with 2-, 4-, 8-, 16-, 32- or 64-slice systems from different vendors. All types of contrast enhanced CT protocols were considered eligible as long as the field-of-view (FOV) included the heart and the full length of the thoracic aorta. Slice thickness varied according to the Chest CT indication and corresponding protocol and—due to exclusion of CT examinations performed for a cardiovascular indication—none of the CT studies were ECG gated. Patient characteristics, information on slice thickness and the use of a contrast agent were abstracted from Chest CT reports by a research physician, who also assessed the diagnostic Chest CT indication and classified them as ‘pulmonary disease’, ‘haematological malignancy’, ‘mediastinal disease’, ‘ruled-out pulmonary malignancy’, ‘pulmonary embolism’ or ‘other CT indications’.
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Image characteristics
The CT-findings were scored for valve calcification by three readers: one board certified radiologist with 10 years’ experience and two research physicians with two and three years’ Chest CT experience respectively. All readers were blinded for patient characteristics and outcome status. CT images were stored in DICOM format and read using a commercially available software program (Dicomworks, version 1.3.5). All CTs were analysed in the axial plane; no other reformatted planes were included for analysis. Readings were performed using a standardised score form including information on the type of CT protocol used and the use of contrast agent and imaging quality. This was defined as good: clearly visible, minimal movement artefacts, adequate: Slight blurring and/or movement artefacts, or poor: major defects significantly affecting visibility. These classes reflect the reliability with which the scoring of CT characteristics was possible.
Calcification of the heart valves was anatomically subdivided into calcification of the aortic valve leaflets (AVL), the mitral valve leaflets (MVL) and the mitral annulus. MVL calcification present as linear calcification between the area of the left atrium and ventricle. Mitral Annulus Calcification (0, absent; 1, present) are visible as round or curled spots at the periphery of this horizontal leaflet plane. AVL and MVL calcification was graded as: grade 0, absent; grade 1, mild (one leaflet affected); grade 2, severe (2 or 3 leaflets affected), comparable to other studies [19, 20].
Calcification was also visually assessed in the coronary arteries and the thoracic aorta, as premature calcification in these anatomical regions has already frequently been related to CVD in the literature. Calcification of the aorta was also assessed in the ascending and descending part and in the supra-aortic arteries branching from the aortic arch. An overall aorta score was compiled and graded as absent, mild, moderately, or severe affected aorta. Calcification in the coronaries was scored in a similar fashion. Both aortic and coronary visual grading were partly comparable to a previously described grading of coronary calcification [21]. Tables 1 and 2 provide information about the visual grading and examples of image characteristics are presented in Fig. 2.
Table 1
Definitions used for visual grading of valve calcification on routine diagnostic Chest CT
Grades
Finding
0
1
2
Aortic valve calcification
none
One small calcification or linear calcification of one leaflet
Linear calcification on two or three leaflets
Mitral valve calcification
none
One small calcification or linear calcification of one leaflet
Linear calcification on two leaflets
Annular calcification mitral valve
none
Presence of annular calcification
Table 2
Definitions used for visual grading of coronary and aortic calcification on routine diagnostic Chest CT
Grades
Finding
Absent
Mild
Moderate
Severe
Coronary calcification (LM, LAD, LCX, RCA)a
none
≤5 calcified foci or 1 calcification extending over ≥ 2 slices
>5calcified foci or 2 calcification extending over ≥ 2 slices
>6 calcified foci and ≥ 3 calcification extending over ≥ 2 slices
Aortic and supra aortic calcification
none
≤4 calcified foci or 1 calcification extending over ≥ 3 slices
>4 calcified foci or 2 calcification extending over ≥ 3 slices
calcified aorta covering multiple segments
Note that this table needs to be interpreted as a guideline. Clinical experience of a radiologist is essential to assign points
aLM left main; LAD left anterior descending; LCX left circumflex; RCA right coronary artery
Fig. 2
Image examples. Upper left image shows two affected leaflets of the aortic valve. The upper right shows one calcified leaflet of the aortic valve. The lower left image shows annular calcification of the mitral valve and the lower right image shows an affected leaflet of the mitral valve
×
Scoring was trained under the supervision of an experienced board certified chest radiologist. The reproducibility of visual grading was successfully evaluated in a previous study [22]. Briefly, weighted kappa 0.78, 0.58, 0.56 and 0.87, 0.56, and 0.70 for inter- and intra observer agreement of AVC, MVC and MAC. The weighted kappa’s for inter- and intraobserver agreement were 0.77, 0.91 for the coronaries, 0.72, 0.88 for the aorta and 0.89, 0.96 for the supra aortic calcification respectively.
Follow-up and outcomes
We recorded incident fatal and non-fatal CVD events for a mean of 17 months (max. 48 months). Endpoint status was obtained through linkage of patients with the National Death Registry and the National Registry of Hospital Discharge Diagnoses from January 2002 to December 2005. Database linkage was performed with a validated probabilistic method [23‐26]. In these databases, cause of death and the indications for hospitalisation are coded according to the International Classification of Diseases, 9th and 10th revision (ICD-9, ICD-10) [27]. Correct designation of causes of death has been established within a comparison study with patient medical records [28].
A trained research physician abstracted all valid endpoints from these databases on the basis of ICD codes. Fatal and non-fatal CVD events with an atherosclerotic background were defined by ICD-9 codes as coronary heart disease (CHD) (codes 410–414), heart failure (code 428), peripheral arterial disease (PAOD) (codes 440, 443–444), aortic aneurysm (code 441), cerebrovascular disease (codes 430–438), non-rheumatic valve disease (code 424), or other forms of heart disease (e.g. cardiac dysrythmias, or cardiomyopathy (425, 427)). Only the latter (endpoints with codes 424) were used in the analysis for fatal and non-fatal non-rheumatic valve endpoints. In case of multiple valid endpoints in the same patient, cause of death prevailed over hospital admissions or else the first hospital discharge diagnosis was used.
Data analysis
Descriptive information of patients, imaging characteristics, CT indications and follow-up time were evaluated for patients from the subcohort (random sample from cohort) and patients with cardiovascular disease (cases). We used regression methods implemented in SPSS software (SPSS 14.0, Chicago, IL, USA) to impute missing values (<3% for the scored imaging characteristics). All other analyses were performed with R software, version 6.2.
Cox proportional hazard analysis was used to investigate whether valve calcification can be used as a predictor of CVD events and non-rheumatic valve disease in particular. Apart from crude associations, the hazard ratios were also adjusted for age, sex, indication for CT and type of medical hospital in which the CT was performed (tertiary/secondary). Interaction terms were included in the model to test whether imaging characteristics (valve calcification• section thickness (continuous), calcification • use of contrast agent (yes/no), calcification •imaging quality (bad, moderate, good), calcification • age (continuous) and calcification gender (male/female)) modified the associations. Furthermore, survival curves of the strongest predictors were presented to visually illustrate the effect of the adjusted hazard ratios on the occurrence of CVD. The curves show the observed proportion of patients being free of CVD events during follow-up per stratum of the heart valve score. Finally, a sub-analysis was performed to investigate whether the predictive value of calcified heart valves for future CVD events attenuated when additional commonly used atherosclerotic markers were included in the model. In this analysis, the adjusted hazard ratios were additionally corrected for calcification in aorta and/or coronary arteries.
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All hazard ratios were modified based on robust variance estimates. These adaptations were carried out with the method according to Prentice in which all subcohort members are equally weighted [17]. This method has been shown to resemble most closely estimates from a full-cohort analysis [18].
Results
A total of 121 subjects (44 out of 559 cases (7.9%), and 77 out of 1285 subjects from the subcohort (6.0%)) were excluded from analyses because CTs could not be retrieved from hospital CT databases. Table 3 presents descriptive information on patient and imaging characteristics: The mean age of the patients from the subcohort was 61.5 years and 58% were male. The overall prevalence in the subcohort patients of aortic valve, mitral valve and mitral annular calcification was respectively 27%, 9% and 12%. The proportion of moderately or severely affected coronary arteries was 43% and 31% for the aorta in subcohort patients. A total of 515 patients experienced a cardiovascular event during follow-up (for specification according ICD codes see Appendix). With regard to the cases the proportions of calcified heart valves, coronary arteries and aorta were all higher. Cases were also older (mean: 68 years) and were more often male (65%).
Table 3
Baseline characteristics
General information
Subcohort(n = 1208)
CVD cases(n = 515)
Male, [%]
58
65
Age, y [SD]
61.5 (40–96)
67.9 (40–96)
Follow-up, days [SD]
620 (1–1460)
322 (1–1369)
Academic referral centre, [%]
77
77
Use of contrast agent [%]
68
67
Image quality, [%]
Good
72
74
Moderate
24
24
Bad
3
2
Indication category, [%]
(1)Lung disease
37
47
(3)Haematological malignancies
11
6
(4)Mediastinal abnormalities
11
8
(5)Ruled-out pulmonary malignancya
24
21
(6)Pulmonary emboli
6
8
(8)Other indications
11
10
Thoracic aorta calcification
None
39
18
Mild
30
25
Moderate
19
33
Severe
12
24
Coronary arteries calcification
None
33
12
Mild
24
22
Moderate
25
29
Severe
18
37
Aortic valve calcification, [%]
None
72
53
Calcification on one leaflet
16
20
Calcification on two or three leaflets
11
27
Mitral valve calcification, [%]
None
91
82
Calcification on one leaflet
7
14
Calcification on two leaflets
2
4
Presence of annular calcification mitral valve [%]
12
20
aPulmonary mass, which is proven to be non-malignant
Values are means [SD] or proportions
Table 4 shows that the risk of a CVD event increased with an increase in the stratum of valve calcification. After adjustment for age, sex, CT indication and type of referral centre the hazard ratio for 1 affected aortic valve leaflet was no longer significant (HR 1.18, 95% CI 0.87–1.61). However, with two or three aortic leaflets affected, the risk doubled (HR 2.03, 95% CI 1.48–2.78). When one leaflet of the mitral valve was affected, the risk increased 1.83-fold (95% CI 1.26–2.64) and 2.08-fold (95% CI 1.04–4.19) when two mitral valve leaflets were affected. Annular calcification increased the risk during follow-up with 53% (HR 1.53, 95% CI 1.13–2.08). Figures 3 and 4 visually present the prognostic effect of aortic and mitral valve calcification adjusted for age, sex, imaging indication and referral centre. The proportion of patients with a severely calcified aorta or mitral valve who suffered a CVD event within 3 years was 5.5% and 7%, respectively. Linearly extrapolated to more widely used 10-year risk predictions, these proportions would be 18% and 23%. No statistically significant interactions were found between the valve and annular scores and section thickness (range p = 0.27–0.30), the use of intravenous contrast medium (range p = 0.13–0.27), imaging quality (range p = 0.11–0.92), age (range p = 0.13–0.69) or gender(range p = 0.42–0.90).
Table 4
Risk of any CVD event (n = 515) associated with increasing calcified valve score in clinical care patients undergoing routine diagnostic chest CT
Hazard ratios (95% CI)
Crude
Adjusted modela
Aortic valve calcification
None
1
1
One affected leaflet
1.79 (1.36–2.36)
1.18 (0.87–1.61)
Two or three affected leaflets
3.32 (1.83–4.96)
2.03 (1.48–2.78)
Mitral valve calcification
None
1
1
One affected leaflet
2.66 (1.89–3.75)
1.83 (1.26–2.64)
Two affected leaflets
3.46 (1.82–6.37)
2.08 (1.04–4.19)
Mitral annular calcification
None
1
1
Presence
2.11(1.59–2.81)
1.53 (1.13–2.08)
CVD cardiovascular disease. CI confidence interval
aAdjusted model: hazard ratio’s adjusted for age, sex, imaging indication, referral centre
Fig. 3
Proportion of patients free of cardiovascular events according the aortic valve score adjusted for age, sex, imaging indication, referral centre. The dotted line is included as an example and indicates the proportion of severly affected patients free of cardiovascular events after 3 years of follow-up
Fig. 4
Proportion of patients free of cardiovascular event according the mitral valve score adjusted for age, sex, imaging indication, referral centre. The dotted line is included as an example and indicates the proportion of severely affected patients free of cardiovascular events after 3 years’ follow-up
×
×
Looking specifically at the relationship between incidentally detected valve calcification and the occurrence of non-rheumatic valve disease (n = 43) we could demonstrate strongly increased hazard ratios, yet the pattern of the associations was the same (Table 5). For a moderately affected aortic valve the risk increased 2.40-fold (95% CI 0.78–7.53). When the aortic valve was severely affected the risk increased 14.57-fold (95% CI 5.19–40.53). The corresponding hazard ratios for the mitral valve were respectively 3.84 (95% CI 1.77–8.34) and 8.78 (95% CI 2.33–33.3). The presence of mitral annular calcification increased the risk with a factor 2.43 (95% CI 1.18–4.98). Note however that for lack of power, these associations were not visually presented or further adjusted in the prospective sub-analysis.
Table 5
Risk of non-rheumatic valve disease (n = 43) associated with increasing calcified valve score in clinical care patients undergoing routine diagnostic chest CT
Hazard ratios (95% CI)
Crude
Adjusted modela
Aortic valve calcification
None
1
1
One affected leaflet
2.62 (0.96–7.13)
2.40 (0.78–7.53)
Two or three affected leaflets
16.27 (7.85–33.69)
14.57 (5.19–40.53)
Mitral valve calcification
None
1
1
One affected leaflet
5.17 (2.42–11.0)
3.84 (1.77–8.34)
Two affected leaflets
11.27 (4.02–34.40)
8.78 (2.33–33.13)
Mitral annular calcification
None
1
1
Presence
3.15 (1.62–6.51)
2.43(1.18–4.98)
CVD cardiovascular disease. CI confidence interval
aAdjusted model: hazard ratios adjusted for age, sex, imaging indication, referral centre
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Sub-analysis
When coronary and aortic calcification were included in the models for any CVD event, the hazard ratio for a moderately affected aortic valve decreased to 0.96 (95% CI 0.70–1.32) and for a severely affected aortic valve it decreased to 1.46 (95% CI 1.04–2.06). For the mitral valve these ratios became 1.57 (95% CI 1.08–2.28) and 1.79 (95% CI 0.85–3.76), respectively. The corrected hazard ratio for mitral annular calcification was 1.19 (95%CI 0.86–1.66).
Discussion
In this study, we examined whether calcification of the aortic valve, mitral valve and mitral annulus, incidentally detected on routine diagnostic chest CTs, could be used as predictors for CVD events and non-rheumatic valve abnormalities in particular. Furthermore we investigated whether these image characteristics remained prognostically relevant when they were modelled with commonly used predictive coronary and aortic calcification [14‐16, 29, 30]. We found that, within a 95% confidence range, valve and annular calcification were independent predictors of CVD events. Considering the anatomical basis, the strongest associations were found for future valve abnormalities. A sub-analysis showed that these image characteristics only partly lost their prognostic capacity for CVD when jointly modelled with coronary and aortic calcification. Imaging parameters (slice thickness, use of intravenous contrast agents, or quality of the CT images), age or sex did not significantly modify the associations found for valve calcification in relation to future CVD events. This indicates that additional scoring of valve and annular calcification could provide a valuable contribution to the prediction of CVD events with hitherto commonly used atherosclerotic image characteristics on chest CT.
Millions of diagnostic CT examinations are made every year and their usage is still increasing because of the evolving quality of the CT images and the aging population [31]. An inevitable side-effect of this process is the increased number of incidentally detected subclinical image characteristics. Using this information for prognostic purposes is attractive as it can be freely abstracted from existing imaging data and comes with no extra exposure to ionising radiation. However, longitudinal studies, such as this one, are needed to expose the natural course of these findings and to demonstrate any (or lack of) relationship with future events. Ultimately, such studies can help in composing an evidence based approach to reporting incidental subclinical findings.
The prevalence of valve calcification in our study was 27% for AVC, 9% for MVC and 12% for MAC. These numbers are comparable to other studies, where the prevalence was reported to be 13–31% [9, 10, 19] for AVC, 9% for MVC[20] and 6–14% for MAC [6, 9, 10]. In this study we also demonstrated a relationship between the investigated image characteristics and CVD events. Compared with other studies, which were mainly conducted in asymptomatic elderly populations, our study demonstrates these associations in a clinical care population. Another difference is that we scored incidental valve calcification on a very heterogeneous set of routinely made diagnostic chest CTs, instead of the transthoracic or transoesophageal echocardiography mainly used in other studies. This study demonstrates how incidentally detected CT image characteristics (simply scored with minimal extra reviewing time) can be used in daily clinical care for prognostic purposes. The results provide an additional means of improving the identification of high-risk patients, who can benefit from timely preventative measures [11]
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Table 4 shows that ancillary valve calcification is an independent predictor of CVD events after correction for predictors readily available to radiologists. These results are in keeping with previous literature investigating aortic valve calcifications[32] and provide practical benefits compared with hitherto widely used atherosclerotic imaging characteristics (e.g. aortic and coronary calcification) as valve calcification can be scored very simply and quickly. However we would also like to stress that one image characteristic does not have to exclude another in the prediction of CVD: the sub-analysis showed that the prognostic effect of ancillary valve calcification did not attenuate completely when jointly modelled with coronary and aortic calcification. This could mean that predictions of CVD improve (in terms of accuracy) when those image characteristics are incorporated into one prediction model for CVD events. Note however that future research including other statistical model performance tests should confirm this.
This study has also some potential limitations. No clinical information from patients’ medical records was available, which could have influenced the exclusion of patients already known with cardiovascular disease as we could only exclude patients based on their CT report. However, we excluded approximately 16% of patients from the baseline cohort based on information from CT reports and this is largely in line with the overall prevalence of symptomatic CVD in the general US population of whites (11.2%) [33], indicating that this was unlikely to have affected our study population significantly. Clinical information from medical records might also be used to further adjust the hazard ratios: it is known that chronic conditions such as diabetes, renal dysfunction and metabolic syndrome[34‐37]affect the incidence of both CVD and valve calcifications. Despite its potential effect[38], we did not seek to collect data on ethnicity. However, as this research is aimed at routine radiological care, where information about traditional risk factors is often unavailable, these omissions are representative of routine radiological practice. The additive nature of the ‘radiological red flags’ that may result from the clinical implementation of lessons learnt from this research may cause the identification of at-risk patients whom have already been identified by referring clinicians as being at risk. Such double identification of at risk patients on the basis of gratis (without extra radiation exposure) radiological information would not have any negative consequence for patients themselves and might serve as reinforcement for referring clinicians in cases where patients had already received preventative care (e.g. referring clinicians may verify whether the ‘red-flagged’ patient is receiving optimal preventative care in such instances).
Conclusion
The PROVIDI study provides a new approach to employing freely available and potentially valuable prognostic information extrapolated from routine diagnostic imaging. This particular study showed that ancillary AVC, MVC and MAC, detected on routine care, diagnostic chest CT in a clinical care population, can be used by radiologists to predict cardiovascular events. Ultimately, prognostic information can be implemented in CT reports. Note that the impact of providing this information on risk stratification and following preventative measures should be investigated in another study.
Acknowledgements
The PROVIDI Study Group consists of: J. Laméris (Dept. of Radiology, Academic Medical Center, Amsterdam), C. van Kuijk (Dept. of Radiology, VU University Medical Center Amsterdam), W. ten Hove (Dept. of Radiology, Gelre Hospitals, Apeldoorn), M. Oudkerk (Dept. of Radiology, University Medical Center Groningen), Ay L. Oen(Dept. of Radiology, Elkerliek Hospital, Helmond), J. Wildberger (Dept. of Radiology, Academic Hospital Maastricht), J. van Heesewijk (Dept. of Radiology, St. Antonius Hospital, Nieuwegein), W. Mali (Dept. of Radiology, University Medical Center Utrecht) and Y. van der Graaf (Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht).
We acknowledge the help with data collection and administrative support by Cees Haaring (UMCU), Karin Flobbe (AZM), Mirjam Borg (VUMC), Pascal Verzijl (Antonius), Jan Wolfers (AMC), Peter van Ooijen (UMCG), Willie Donkers (Elkerliek), and Robert Dragt (Gelre).
Funding
This study was funded by a program grant from the Netherlands Organization for Scientific Research-Medical Sciences (NWO-MW) grant 40-00812-98-07-005). The funders had no involvement in the study design, data collection, analysis and interpretation, the writing of the report, or the decision to submit the paper for publication.
Open Access
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
Open AccessThis is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License (https://creativecommons.org/licenses/by-nc/2.0), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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Patients who experienced a fatal or non-fatal cardiovascular event specified according the ICD codes
Disease
Codes
Number (fatal)
Ischemic heart disease
410–414
273 (84)
peripheral arterial disease (PAOD)
440, 443, 444
40 (14)
aortic aneurysm
441
19 (15)
cerebrovascular disease
430–438
59 (27)
non-rheumatic valve disease
424
43 (19)
Other forms of Heart disease (e.g. dysrythmias, heart failure, cardiomyopathy)
425, 427, 428
81 (79)
Total
515 (238)
Please note that in case of multiple valid endpoints in the same patient, cause of death prevailed over hospital admissions or else the first hospital discharge diagnosis was used.
