E. van der Does
Erasmus University Rotterdam
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European Journal of Vascular Surgery | 1994
H.J.C.M. Pleumeekers; Arno W. Hoes; E. van der Does; H. van Urk; D.E. Grobbee
Aneurysms of the abdominal aorta (AAA) are a common cause of death. Ruptured AAA accounts for 1.3% of the deaths in men over 65 years of age. 1 In principle, most of these deaths are preventable because an asymptomatic AAA can be treated surgically. In 1952, Dubost 2 was the first to replace an abdominal aortic aneurysm with a graft. Since then the prognosis of the aneurysm of the abdominal aorta has changed dramatically. Nowadays the elective perioperative mortality is less than 5% 3 and a patient surviving aortic grafting has a life expectancy similar to that of men and women of the same age category. 4 In the case of ruptured AAA only one patient in three reaches the hospital alive. The reported mortality rates for emergency surgery for ruptured AAA vary from 30 to 63%.4-7 Despite the importance of aneurysms of the abdominal aorta, little is known about its prevalence, incidence, risk indicators and prognostic factors. Studies dealing with the epidemiology of AAA have only recently been performed. This may be related to the development of ultrasound diagnosis in the midseventies, a technique which provides an easy, inexpensive and accurate method to detect AAA. In this article the available literature on etiology, diagnosis, prevalence, incidence, risk indicators, and prognosis of AAA is reviewed. The objective of this review is to detect gaps in the knowledge on the epidemiology of the aneurysm of the abdominal aorta and to make suggestions as to the direction of future research in the light of the question as to whether screening of the general population for aneurysms of the abdominal aorta should be advocated. Three theories of the aetiology of AAA have emerged: 13 the genetic theory; the proteolytic enzyme theory; and the trace metal theory. Aneurysms of the abdominal aorta were first thought to be atherosclerotic in origin, s-ll Martin 12 was the first to question this concept, suggesting that atherosclerosis may not be the cause but rather the consequence of aortic degeneration. Sterpetti and co-workers 13 proposed the existence of two types of abdominal aneurysms: the first type associated with atherosclerotic occlusive disease and the other not. In their study of 526 patients undergoing aneurysmal resection, 25% were believed to be non-atherosclerotic. There were significantly more ruptures in this group, compared to the atherosclerotic group. A positive family history of AAA was also reported more frequently in the group of the non-atherosclerotic patients. Other differences between atherosclerotic and non-atherosclerotic patients with AAA suggest a generalised weakness of the aortic wall in the non-atherosclerotic type AAA. This may explain the higher risk of rupture and the increased incidence of false aneurysms after operative repair in these patients. They also appear to have a higher risk of aneurysms at other sites of the arterial tree. The finding that men with a first degree relative with AAA experience a 10-fold increased risk of developing an AAA, 14-2° provides a strong argument for a genetic component. Genetic variation on chromosome 16 in patients with AAA has been reported. 21 This has been related to an increased activity of alpha-2 haptaglobulin leading to an acceleration of the hydrolysis of elastin fibres by elastase.
Journal of Medical Screening | 1998
H.J.C.M. Pleumeekers; Arno W. Hoes; P G H Mulder; E. van der Does; A. Hofman; J S Laméris; Diederick E. Grobbee
Objective To assess the observer variability of ultrasound measurements of the abdominal aorta and to study whether observer variability is influenced by the site of measurement or cardiovascular risk factors. Setting Population based screening programme for abdominal aortic aneurysms. Methods For 135 subjects taking part in a screening programme for abdominal aortic aneurysms, two of the three ultrasonographers measured the distal and proximal ultrasound diameter of the abdominal aorta, using B-mode ultrasound, according to the Rotterdam study scanning protocol. Results The mean difference between two different observers was 0.06 mm (95% CI –0.15 to 0.27) for measurements of the distal aorta and 0.32 mm (95% CI 0.09 to 0.55) for the proximal aorta. Maximal differences between observers for measurements of both the distal and proximal aortic diameter were 4.0 mm. Interobserver variability in the proximal and distal measurements of the abdominal aorta was not related to the level of the major cardiovascular risk indicators. However, interobserver variability in ultrasound measurements of the proximal aorta increased with increasing waist circumference and increasing diameter of the proximal aorta. Conclusion Ultrasonographic readings of the distal and proximal aortic measurements can be interpreted within a range of plus or minus 3 mm. Ultrasound measurements are more accurate for the distal than for the proximal measurement. Definition of the aortic diameter based on a combination of both distal and proximal measurement may be more accurate.
Pharmacy World & Science | 1990
E. van der Does
In this article the growing need and necessity to accomplish a shift from in-patient care towards out-patient care, and the role of the hospital pharmacists after this shift has been accomplished, are discussed. If certain obstacles, which still hamper the development towards home care are overcome, then — given the hospital pharmacists possibilities and limitations — his task in patient care, although important, seems limited. Besides, several other provisions have to be made before the hospital pharmacist comes into the picture. On the other hand, other contributions to health care in general, such as contributions to journals, helping with executing research, information to the public and participation in pharmaceutical consultation groups, have increased and are also important. Although these contributions may already have been realized, they could be more firmly structured, extended and intensified.
American Journal of Epidemiology | 1995
H.J.C.M. Pleumeekers; Arno W. Hoes; E. van der Does; H. van Urk; A. Hofman; P.T.V.M. de Jong; Diederick E. Grobbee
European Heart Journal | 1995
E. W. M. Grijseels; M. J. M. Bouten; Timo Lenderink; J. W. Deckers; Arno W. Hoes; J.A.M. Hartman; E. van der Does; M. L. Simoons
The Lancet | 1991
J. van der Lei; J. H. van Bemmel; E. van der Does; A. J. Man In 'T Veld; Mark A. Musen
Methods of Information in Medicine | 1978
Jacobus Lubsen; Jan Pool; E. van der Does
Methods of Information in Medicine | 2006
Manon M. Kuilboer; M. A. M. van Wijk; Mees Mosseveld; E. van der Does; J. C. de Jongste; Shelley E. Overbeek; Ben Ponsioen; J. van der Lei
Methods of Information in Medicine | 1993
J. van der Lei; E. van der Does; A. J. Man In 'T Veld; Mark A. Musen; J. H. van Bemmel
European Heart Journal | 1996
E. W. M. Grijseels; J. W. Deckers; Arno W. Hoes; Eric Boersma; J.A.M. Hartman; E. van der Does; M. L. Simoons