Study objectives: The aims of this study were: to evaluate the perform
ance of a novel arterial biopsy catheter in obtaining pulmonary endova
scular samples in hypertensive dogs; to compare the results of pulmona
ry endoarterial biopsy in hypertensive vs normotensive dogs; and to as
sess the histologic changes in the hypertensive model, Design and inte
rventions: Thirty-four dogs (27 with normal pulmonary arterial pressur
es and seven with pulmonary hypertension) were catheterized through an
external jugular vein to obtain endovascular biopsy samples from dist
al pulmonary arteries 2 to 3 mm in luminal diameter. To induce pulmona
ry hypertension, seven dogs were given repeated infusions of 0.6- to 0
.9-mm ceramic microspheres into the superior vena cava, Endoarterial s
amples were obtained at pulmonary systolic arterial pressures ranging
from 10 to 110 mm Hg. Measurements and results: Sixty-two biopsy cathe
terization procedures were performed in the 34 dogs. After 12 initial
procedures of technique refinement, endoarterial samples were obtained
in each of the last 50 procedures (21 in normotensive dogs and 29 in
hypertensive dogs). The average number of endovascular biopsy samples
retrieved was 7.1 (range, 2 to 12) from a mean of 8.6 (range, 2 to 15)
biopsy attempts per catheterization (success rate=83%). The average b
iopsy piece measured 1.13 mm in length, 0.33 mm in depth, and up to 1.
0 mm in width. The biopsy success rates and endoarterial sample sizes
were similar in normotensive and hypertensive dogs. Smooth muscle cell
s and endothelial cells were grown fi om the biopsy samples, There wer
e no significant procedural complications, except for one self-limited
hemorrhage. Histologically, samples obtained from dogs with pulmonary
hypertension showed characteristic changes when compared with biopsie
s from normotensive dogs. Conclusion: This new endoarterial biopsy cat
heter was safe and effective when used to obtain pulmonary endoarteria
l samples in dogs with normal and experimentally elevated pulmonary ar
terial pressures. The quality and quantity of the biopsy samples allow
ed identification of pathologic changes.