(Circulation. 1999;99:1280-1283.)
© 1999 American Heart Association, Inc.
Editorial |
From the School of Medicine, University of California, San Diego.
Correspondence to Kirk L. Peterson, MD, Professor of Medicine, Perlman Professor of Clinical Cardiology, University of California, San Diego, School of Medicine, 200 W Arbor Dr, Mail Code 8411, San Diego, CA 92103. E-mail klpeterson@ucsd.edu
Key Words: Editorials pulmonary heart disease echocardiography
Despite nearly 4 decades of creative scientific and clinical scrutiny by physicians and surgeons, worldwide pulmonary thromboembolism remains a dreaded, life-threatening illness.
Natural History Statistics
Older statistics estimate that in the United States, acute
pulmonary thromboembolism afflicts 500 000 to 600 000 persons
annually and is either a primary or secondary cause of death in
150 000 to 200 000 of these individuals.1 2
Extrapolation of a population-based study from data accumulated in 1985
through 1986 in Worcester, Mass, suggests that each year there are
170 000 new cases of clinically recognized venous thromboembolism
treated in short-stay hospitals and 99 000 hospitalizations for
recurrent disease.3 When the disease process was followed
from the time of clinical recognition, the 1-year mortality rate in a
national multicenter project (PIOPED) was reported as
25%, with
2.5% dying from pulmonary embolism itself and most patients
dying from the major diseases that are associated with
pulmonary thromboembolism, including cancer, various
infections, cardiovascular diseases, and other
pulmonary diseases.4 Other studies have reported
that in patients without preexisting cardiac or pulmonary
disease, the 1-year mortality rate ranged from 3% to
9%.5 6 If a massive pulmonary embolism occurs
associated with systemic hypotension, the in-hospital mortality rate is
18%.7 The persistence of pulmonary
hypertension after embolization has been associated with increased
mortality rates; the higher the pulmonary artery pressure, the
lower the survival rate at 5 years.8 Furthermore, it has
been predicted, with admitted imprecision, that 0.01% of patients
develop what is now commonly referred to as chronic pulmonary
thromboembolic pulmonary hypertension.9
Impediments to Investigation of Natural History
Although
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