The Aneurysm Information Project

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    Papers of the Month - May 1998
    
    1. Lipski DA, Ernst CB.  Natural history of the residual infrarenal
    aorta after infrarenal abdominal aortic aneurysm repair.  
    J VascSurg 1998; 27: 805©12.
    
    Brief abstract (adapted from authors)
    
    Methods & Results: 800 translumbar aortograms were reviewed,
    performed on 272 AAA patients, preoperatively and postoperatively. 
    The mean follow up time from the preop study to the most recent
    postop study was 42 months.  Magnification was adjusted by
    normalizing to first lumbar vertebral body height.
    
    The length of the native infrarenal aorta cephalad to the graft
    increased a mean of 3 mm.  However, in a subset of 43% of the
    patients, it elongated >5 mm; and in 24% it elongated >10 mm.  The
    mean dilatation of this segment was 1 mm; but in 21 patients (8%)
    it dilated more than 5 mm.
    
    Conclusion:  A mean period of 42 months after conventional AAA
    repair, the cuff elongates and dilates.  The average increases are
    small, but in a subset of patients the increases are sufficiently
    great to pose "potentially serious implications for endovascular 
    treatment of AAA.
    
    Comment by mdt © As reviewed by the authors and mentioned in the
    discussion section by Dr. Hallett (Mayo Clinic), the concern is
    that after endovascular repair, the aorta may dilate sufficiently
    to pull away from the graft and result in an endoleak.  Dr. Hallett 
    cited a study from Mayo Clinic with a 6 year follow©up, which
    found that 13% of the patients had dilated to 30 mm.  Dr. Hallett
    also raised the interesting question of whether there were any
    clinical characteristics that might predict which patients belong in the 
    subset that will undergo significant dilatation.  This is perhaps
    where the laboratory might come into play, to see if homozygosity for a
    genetic susceptibility allele (J Vasc Surg 1998; 27: 500) or high titer of
    serum antibody against aorta©specific antigenic proteins (Surg Forum
    1997; 48: 401) might have predictive power.
    
    2. Vorp DA, Raghavan ML, Webster MW.  Mechanical wall stress in AAA:
    Influence of diameter and asymmetry.  J Vasc Surg 1998; 278:632©9.
    
    Purpose: To investigate the effect of maximum diameter and asymmetric
    bulge on wall stress, by holding diameter constant while varying shape or
    to hold assymetry constant while varying diameter.
    
    Results: Both diameter and bulge (assymetry) influence distribution of
    wall stress.  The magnitude of peak stress increased nonlinearly with
    increases in either variable.  Interestingly, under some 
    combinations of diameter and bulge, the maximum stress occurred in the
    midsection, and in others it occurred elsewhere.  
    
    Conclusion: The stress within the wall of a AAA (and possibly the
    potential for rupture) are as dependent on shape as they are on
    maximum diameter.
    
    Comment by mdt:  I am not an engineer, but I found this paper interesting.
    As observed by the authors, the prediction of wall stress might become
    useful in the future to help to balance the risk of rupture against the
    risk of elective repair.
    
    3. Vasseur M©A, Haulon S, Beregi JP et al.  Endovascular treatment of
    abdominal aneurysmal aortitis in Behcet's disease.  J Vasc Surg
    1998; 27: 974©6.
    
    Case Report (abstracted):  Open surgical repair of aneurysms in
    Behcet's is difficult, and anastamotic false aneurysms (30©50%) are
    common because of aortic wall fragility.  Accordingly, the authors
    performed an endovascular repair on a 37 y/o patient with the
    disease.  Recovery was uneventful, and at follow©up at 6 months all
    was well.
    
    Comment by mdt: Compliments to the authors.  Another reason for citing
    this paper this month is that it gives me a platform to continue
    discussions of autoimmune mechanisms in aneurysmal diseases.  One of the
    proteins with an important epitope in Behcet's has been identified 
    as a retinal protein related to photoreceptor function.
    We have been interested to note that it
    may share an epitope with an aorta©specific antigenic protein that we have
    implicated in AAA disease.  This observation may explain why uvietis 
    and AAA may be paired in Behcet's.