1982
DOI: 10.1097/00132586-198206000-00007
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Effects of Propranolol on the Cardiovascular and Renin-Angiotensin Systems during Hypotension Produced by Sodium Nitroprusside in Humans

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Cited by 5 publications
(5 citation statements)
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“…A number of previous studies have proposed premedication with a β-blocker in combination with SNP during DH for the reduction of reflex tachycardia and rebound hypertension. 8 19 20 However, to the best of our knowledge, no prior studies have investigated the impact of a preoperative oral β-blocker or ACE inhibitor administration on the intraoperative blood loss or achievement of adequate DH when combined with intraoperative NTG as an adjuvant agent under balanced anesthesia.…”
Section: Discussionmentioning
confidence: 99%
“…A number of previous studies have proposed premedication with a β-blocker in combination with SNP during DH for the reduction of reflex tachycardia and rebound hypertension. 8 19 20 However, to the best of our knowledge, no prior studies have investigated the impact of a preoperative oral β-blocker or ACE inhibitor administration on the intraoperative blood loss or achievement of adequate DH when combined with intraoperative NTG as an adjuvant agent under balanced anesthesia.…”
Section: Discussionmentioning
confidence: 99%
“…[18] examined the effects of controlled hypotension induced with SNP with or without propranolol on cardiovascular, pulmonary, and renin-angiotensin system, and concluded that propranolol, when given during SNP hypotension, exhibits an early cardiovascular response manifested as a decrease in cardiac output and heart rate and a delayed action on the kidney resulting in an inhibition of renin release and decrease the amount of SNP.…”
Section: Discussionmentioning
confidence: 99%
“…Among these agents are isoflurane, a potent inhalation anesthetic with vasodilating properties, and propranolol, a p-blocker that decreases baseline sympathetic tone and attenuates the stress response (8). Unlike isoflurane, which has been used as a primary agent for induced hypotension (9), p-blockers available before the release of esmolol had elimination half-lives that were too long for this use and thus served as secondary rather than primary hypotensive agents (8,10,11). Esmolol's elimination half-life of 9 min provides both ease in achieving the desired level of hypotension by regulating the dose and ease in terminating the hypotensive effect after the termination of the infusion.…”
Section: Discussionmentioning
confidence: 99%