Doppler ultrasound measurement of cardiac output in patients with physiologic pacemakers. Effects of left ventricular function and retrograde ventriculoatrial conduction.

Dual-chamber cardiac pacing (DDD) offers obvious theoretical advantages over traditional ventricular demand (VVI) pacing. Nevertheless, no widely agreed upon criteria exist for the selection of patients for physiologic DDD pacemakers compared with the simpler VVI systems. Accordingly, a non-invasive method for measuring cardiac output (Doppler ultrasound) was used to identify candidates for pacing who would derive the greatest hemodynamic benefit from DDD vs VVI pacing. Among 29 patients studied at rest during VVI-mode pacing, the average cardiac output by Doppler ultrasound was 4.3 +/- 0.3 liters/min (mean +/- standard error of the mean). In the DDD mode, the average cardiac output was 5.0 +/- 0.3 liters/min (p less than 0.001). Baseline left ventricular ejection fraction did not identify a group that improved more with DDD pacing. Patients who showed either retrograde ventriculoatrial conduction or described symptoms consistent with the "pacemaker syndrome" during VVI pacing, however, showed greater increases in cardiac output during DDD pacing. In these patients, the mean improvement in cardiac output was 30.4 +/- 8.6% with DDD vs VVI pacing, as opposed to an average increase of only 14.4 +/- 3.4% in the remaining 20 patients (p = 0.02). Thus, Doppler ultrasound can be used to quantitate the change in cardiac output at rest that occurs with DDD vs VVI pacing. The change is independent of the level of left ventricular function but is substantially higher when there is evidence of ventriculoatrial conduction or the pacemaker syndrome.

Physiological pacemakers.

It has long been possible to prevent death from bradycardia by using single-chamber ventricular pacemakers. Important advances in dual-chamber pacemaker technology now make physiological control of cardiac output during pacing almost a reality. These pacemakers have properly timed atrial contraction and rate variability and have significant hemodynamic advantages over ventricular pacemakers. The pathophysiology of bradycardia and the current status of physiological pacemakers are reviewed in this article.

Pathophysiological correlates of thallium-201 myocardial uptake in experimental infarction.

The pathophysiological correlates of thallium-201 (201TI) myocardial uptake were studied in a 24-hour-old closed-chest canine infarct model. Reduction in regional 201Tl uptake correlated well with the magnitude of tissue creatine phosphokinase depletion and microsphere estimates of transmural blood flow. In low flow endocardial regions 201Tl occasionally under-estimated the magnitude of flow reduction. Even slight reductions of 201Tl uptake (less than 0.86 of normal) were associated with histopathological and histochemical evidence of necrosis.

Myocsrdial uptake of technetium-99m stannous pyrophosphate following direct current transthoracic countershock.

The effect of direct current (DC) countershock upon myocardial technetium-99m stannous pyrophosphate (PYP) uptake was studied in 22 dogs. All eight dogs imaged had positive abnormal PYP scintigrams that were usually indistinguishable from experimental infarction. In three animals, additional areas of radionuclide uptake were seen in overlying noncardiac tissue. Left and right ventricular myocardial PYP uptake averaged (+/- SEM) 23 +/- 5 times control and 24 +/- 6 times control, respectively. These activity ratios occurred without reduction in regional myocardial blood flow (RMBF), and were associated with histologic evidence of necrosis. The necrosis was usually epicardial, corresponding to the transmural site of greatest PYP uptake. The magnitude of PYP accumulation and the weight of damaged tissue increased with increasing applied energy. Thus, PYP uptake following DC countershock could result in false-positive interpretation of acute ischemic myocardial infarction. Since RMBF is normal in regions of PYP uptake, the major determinant of radionuclide accumulation is the extent of cellular damage.

Dual radionuclide study of myocardial infarction. Relationships between myocardial uptake of potassium-43, technetium-99m stannous pyrophosphate, regional myocardial blood flow and creatine phosphokinase depletion.

The dual radionuclide myocardial distributions of imaging agents potassium-43 (43K) and technetium-99m stannous pyrophosphate (99mTc-PYP) were studied in a 24-hour closed chest canine infarct preparation. In multiple myocardial biopsies in 20 dogs, tissue levels of both radionuclides were compared to either an index of tissue viability (myocardial creatine phosphokinase [CPK] depletion), or to estimates of regional myocardial blood flow as measured by the microsphere technique. Myocardial 43K uptake in the ischemic and infarcted zone correlated well with both CPK depletion (r = 0.73) and microsphere estimates of relative blood flow. The correlation with microspheres was excellent in the transmural sample (r = 0.93) as well as endocardial (r = 0.97) and epicardial (r = 0.86) portions. On the other hand, 99mTc-PYP myocardial uptake did not correlate with the extent of CPK depletion. Maximal uptake was frequently noted in border zones with only moderate CPK depletion, while lesser degrees of 99mTc-PYP uptake were noted in the central infarct zone where CPK activity was lowest. The relationship of 99mTc-PYP uptake to microsphere regional flow estimates demonstrated that 99mTc-PYP uptake was maximal at flows of 0.3 to 0.4 of normal. At lower flows, 99mTc-PYP uptake fell toward normal levels. A similar relationship was noted between the distributions of 99mTc-PYP and 43K. In relatively high flow border segments (larger than or equal to 0.80 of normal), abnormal 99mTc-PYP uptake of five to six times normal persisted. The transmural distribution of 99mTc-PYP demonstrated that in low flow regions 99mTc-PYP uptake was primarily epicardial, while in the higher flow ischemic periphery of the infarct endocardial uptake predominated. Thus, while there is a direct correlation between cationic 43K myocardial uptake and regional myocardial viability and blood flow, no such direct relationship exists for 99mTc-PYP. This is in part based on the necessity for delivery of the radioactive tracer to the infarct zone.