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Anesthesia Progress logoLink to Anesthesia Progress
. 1996 Fall;43(4):108–115.

Clinically safe dosage of felypressin for patients with essential hypertension.

K Sunada 1, K Nakamura 1, M Yamashiro 1, M Sumitomo 1, H Furuya 1
PMCID: PMC2148772  PMID: 10323116

Abstract

Hemodynamic changes were evaluated in patients with essential hypertension when felypressin of various concentrations was administered. The parameters studied were systolic pressure, diastolic pressure, heart rate, left ventricular systolic phase, and endocardial viability ratio. Results showed that blood pressure tended to increase, and the value of 1/pre-ejection period2 (PEP2) tended to decrease, upon administration of 3 ml of 2% propitocaine containing 0.06 international units/ml (IU/ml) of felypressin. Significant increase of blood pressure and decrease in 1/PEP2 was noted upon administration of 3 ml of anesthetic solution containing 0.13 IU/ml of felypressin. No ischemic change of the myocardium was detected even with the highest felypressin concentration (3 ml of 2% propitocaine containing 0.25 IU/ml of felypressin). These results suggest that the clinically safe dosage of felypressin for patients with essential hypertension is approximately 0.18 IU. This amount is equivalent to 6 ml of 3% propitocaine with 0.03 IU/ml of felypressin, which is a commercially available local anesthetic for dental use. It seems that the decrease in 1/PEP2 that occurred during blood pressure increase was due to the increase in afterload caused by contraction of the arterioles. Although in the present study no ischemic change was noted, special care should be taken to prevent myocardial ischemia in patients with severe hypertension.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Aochi O., Takeshita S., Kawaguchi C., Goto Y., Yasunaka H. [Fundamental and clinical studies on PLV2 (Octapressin)]. Masui. 1966 May;15(5):436–443. [PubMed] [Google Scholar]
  2. Goldman V., Astrom A., Evers H. The effect of tricyclic antidepressant on the cardiovascular effects of local anaesthetic solutions containing different vasoconstrictors. Anaesthesia. 1971 Jan;26(1):91–91. doi: 10.1111/j.1365-2044.1971.tb04730.x. [DOI] [PubMed] [Google Scholar]
  3. Johnson W. C., Widrich W. C., Ansell J. E., Robbins A. H., Nabseth D. C. Control of bleeding varices by vasopressin: a prospective randomized study. Ann Surg. 1977 Sep;186(3):369–376. doi: 10.1097/00000658-197709000-00015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Kennotsu O., Honna E., Shirai O., Takahashi N. [Effects of intravenous anesthetics on pre-ejection period (PEP) and left ventricular ejection time (LVET). Comparative evaluation of propanidid, ketamine, Ct-1341 and thiamylal]. Masui. 1975 Sep;24(9):860–865. [PubMed] [Google Scholar]
  5. Shimizu R., Iemura M., Fukuda Y., Minobe A. [Clinical study of Octapressin]. Masui. 1967 Mar;16(3):227–236. [PubMed] [Google Scholar]
  6. TSAKIRIS A., BUEHLMANN A. [Experimental research in humans on the effects of vasopressin on the liver blood pressure and portal pressure]. Helv Med Acta. 1961 Sep;28:615–621. [PubMed] [Google Scholar]
  7. Wexler L. F., Pohost G. M. Hemodynamic monitoring: noninvasive techniques. Anesthesiology. 1976 Aug;45(2):156–183. doi: 10.1097/00000542-197608000-00006. [DOI] [PubMed] [Google Scholar]

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