The Aneurysm Information Project

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    April 1998 - Papers of the Month
    
    1. May J et al (Sydney, Australia).  Concurrent
    comparison of endoluminal versus open repair in the
    treatment of AAAs: Analysis of 303 patients by life table
    method.  J Vasc Surg 1998; 27: 213-21.
    
    Purpose - "...to compare the outcome of consecutive
    patients with AAA treated concurrently by open operation
    (OR) and endoluminal intervention (ER) by the same
    surgeons during a defined interval" (May 92-May 96).
    
    Methods - 303 consecutive patients who underwent elective
    repair; OR in 195 and ER in 108.  "The decision to
    perform ER was based on comorbidities that precluded OP
    (48) and patient choice (60)." 
    
    Results - Peri-operative mortality = 5.6% for OR and 5.6%
    for ER.  "No significant difference was seen in survival
    rate between ER and OR when analyzed by the log-rank
    test."   "The rate of graft failure, however, was
    significanly higher in ER than in OR."
    
    Conclusion - "This study suggests that ER is safe...,
    despite 44% of the ER group being rejected as unfit for
    OR."  ER "results in shorter LOS, shorter length of ICU
    stay, and less blood loss..."  "Patients who opt for
    endoluminal method of repair should be made aware that
    the minimally invasive technique carries the disadvantage
    of a higher failure rate."
    
    
    Comment by mdt:  Well, as that noted vascular surgeon
    John Porter once said, "Live for today."  With more or
    less similar up-front mortality risks, the choice is
    between a shorter hospital stay (with a greater risk of
    long-term complications) and a more difficult post-
    operative period (with fewer chances of problems later).
    
    2. Lobato AC & Leao PP (Sao Paulo, Brazil).  Predictive
    factors for rupture of thoracoabdominal aortic aneurysm. 
    J Vasc Surg  1998; 27: 446-53.
    
    Methods & Results - 31 patients with TAA were followed
    for a median period of 47 months.  Five underwent
    elective repair; 6 died of unrelated causes; 9 ruptured;
    and 11 reached the end of the study without rupture or
    surgery.  
    
    Conclusion - The authors "recommend elective repair for
    a fit patient with asymptomatic TAA with an initial AP
    diameter of 50 mm only when there is an annual growth
    rate of at least 10 mm."  "Patients with an initial AP
    diameter of 60 mm and an annual growth rate of 6 mm
    should undergo surgical treatment..."  "These guidlines
    for elective repair of TAA are based on the results of a
    relatively small series and have to be carefully
    individualized for each patient."
    
    
    Comment by mdt:  Nicely done.  The natural history of AAA
    has been subject to much more extensive analysis than
    TAA.  This study is a step toward better knowledge of the
    TAA.
    
    
    3. Hirose H, et al (Nagasaki, Japan).  Genetic risk
    factor for AAA: HLA-DR2(15), A Japanese study.  J Vasc
    Surg 1998; 27: 500-3.  
    
    Purpose - "These experiments were carried out to
    determine whether the same HLA DR types that have been
    reported to be associated with AAA in a mixed North
    American population are similarly associated with AAA in
    a more homogeneous group of patients in Japan."
    
    Methods and Results - 46 AAA and 50 Control patients;
    DR2(15) detected in 27 patients with AAA and 14 controls
    (p<0.005).
    
    Conclusion - These results suggest that "DR2(15) has an
    important role as a genetic factor for AAA in Japanese
    patients, as previously reported in a mixed North
    American population".
    
    
    Comment by mdt:  Hitoshi Hirose (who goes by "Gene") was
    a student in my laboratory when we reported that DR2
    might be a susceptibility gene for AAA at the NY Academy
    of Sciences Symposium in 1996.  When he returned to
    Japan, he carried out a study of the Japanese population
    referred to the vascular clinic at Nagasaki; and of
    course the senior author of this paper is happy to note
    that one of the same alleles has come up as a risk
    factor.