A B S T R A C T Onset of lung edema is usually associated with increase in the pulmonary transvascular flux of water and proteins. Clinical measurement of these parameters may aid in early diagnosis of pulmonary edema, and allow differentiation between "cardiogenic" and "noncardiogenic" types based on the magnitude of the detected changes. We have previously described a noninvasive method for estimating transvascular protein flux in lung (Gorin, A. B., W. J. Weidner, R. H. Demling, and N. C. Staub. 1978. Noninvasive measurement of pulmonary transvascular protein flux in sheep. J. . Using this method, we measured the net transvascular flux of [ll3mIn]transferrin (mol wt, 76,000) T/2 = 7.0+2.6 h (mean± SD). The pulmonary transvascular flux coefficient, a, was 2.9±1.4 x 10-3 ml/s (mean +SD) in man, slightly greater than that previously measured in sheep (2.7±0.7 x 10-3 ml/s; mean+SD).The pulmonary transcapillary escape rate is twofold greater than the transcapillary escape rate for the vascular bed as a whole, indicating a greater "porosity" of exchanging vessels in the lung than exists for the "average" microvessel in the body. Time taken to reach half-equilibrium concentration of tracer protein in the lung interstitium was quite short, 52+13 min (meantSD).We have shown that measurement of pulmonary transvascular protein flux in man is practical. The coefficient of variation of measurements of a (between subjects) was 0.48, and of measurements of pulmonary transcapillary escape rates was 0.39. In animals, endo- Onset of lung edema is usually associated with increase in the pulmonary transvascular flux of water and proteins. In typical "cardiogenic" pulmonary edema, recruitment of capillary bed results in an increased surface area available for macromolecular flux, whereas an increase in convective forces leads to greater flux per unit surface area (2-4). In "noncardiogenic" pulmonary edema, a "capillary-leak syndrome," with impairment of the normal molecular sieving function of the endothelial membrane, results in veritable "flooding" of the interstitium with oncotically active proteins (5-7). Clinical measurement of transvascular protein flux in lung may aid in early diagnosis of pulmonary edema, and allow differentiation between "cardiogenic" and "noneardiogenic" types based on the magnitude of detected changes.We have previously described a noninvasive method for estimating transvascular protein flux in the lung (8 A scintillation detection unit (probe) externally positioned over the lung must measure input from tracer in both compartments; a venous sample of whole blood (WB) taken simultaneously and counted in a well counter will measure input only from one (IV). By also using a marker restricted to the IV compartment (R) it is possible to partition the probe input by use of the following relationship. the IV compartment at any time, (ti); DWB is the observed count rate for that label in a venous sample drawn at t,; R,v is the externally detected count rate for the restricted label at any time, t1; RWB is th...