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DOI 10.1001/archinte.157.5.564

Медицинская библиотека · Archives of internal medicine · 1997

Renal blood flow detection with Doppler ultrasonography in patients with hepatic cirrhosis.

Celebi H, Dönder E, Celiker H

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Аннотация

BACKGROUND

Hepatorenal syndrome, a well-recognized complication of established liver disease, is characterized by early renal vasoconstriction before clinically recognized renal disease. Renal vasoconstriction causes increased renal vascular resistance, which can be detected noninvasively by Doppler ultrasonography.

OBJECTIVE

To detect early renal hemodynamic changes in patients with hepatic cirrhosis who had clinically normal renal functions.

PATIENTS: Twenty patients with hepatic cirrhosis and ascites, 11 patients with hepatic cirrhosis without ascites, and 23 healthy control subjects. All cirrhotic patients had normal serum urea nitrogen and creatinine values.

MAIN OUTCOME MEASURES: Peak systolic, peak diastolic, and mean flow velocities; pulsatile index; resistive index; and peak systolic velocity/peak diastolic velocity ratio as measured by renal Doppler ultrasonography.

RESULTS

Peak diastolic flow velocity was significantly lower in cirrhotic patients with ascites than in cirrhotic patients without ascites and control subjects (P < .02 and P < .004, respectively), but the peak systolic flow velocity/peak diastolic flow velocity ratio (P < .007 and P < .001, respectively), pulsatile index (P < .007 and P < .001, respectively), and resistive index (P < .007 and P < .001, respectively) were significantly higher in cirrhotic patients with ascites than in cirrhotic patients without ascites and controls.

CONCLUSION

Renal Doppler ultrasonography can noninvasively identify a subgroup of nonazotemic patients with hepatic cirrhosis who are at high risk for subsequent development of renal dysfunction and hepatorenal syndrome.

Для цитирования: Celebi H, Dönder E, Celiker H. Renal blood flow detection with Doppler ultrasonography in patients with hepatic cirrhosis.. Archives of internal medicine. 1997. DOI: 10.1001/archinte.157.5.564.

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