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Department of Anesthesiology, Pitié-Salpêtrière Hospital, Paris, France
Correspondence and reprint requests should be addressed to Gilles Godet, MD, Département dAnesthésie-Réanimation, Hôpital Pitié-Salpêtrière, 47-83 Bd de lHôpital, 75013, Paris.
| Abstract |
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Implications: This prospective randomized study demonstrated that more severe hypotensive episodes, requiring vasoconstrictor treatment, occur after induction of general anesthesia in patients chronically treated with AIIA and receiving this drug on the morning before operation, in comparison with those in whom AIIA were discontinued on the day before operation. Recommendations to discontinue these drugs on the day before the surgery may be justified.
| Introduction |
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There are no data concerning AIIA administration in patients scheduled for vascular surgery performed under general anesthesia. The aim of this prospective randomized study was to compare hemodynamics during induction of anesthesia in patients chronically treated with AIIA versus those of patients not receiving this drug on the morning before operation. Our hypothesis is that the incidence and the severity of hypotension during induction of anesthesia are less when AIIA are discontinued on the day before the anesthesia.
| Methods |
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Patients were randomized in 2 groups as follows: Group I, AIIA discontinued on the day before surgery (n = 18); and Group II, AIIA given 1 h before anesthesia (n = 19).
Exclusion criteria were the following: severe heart failure (stages III-IV of the New York Heart Association), severe renal insufficiency (creatinine plasma level more than 200 µmol/L), and patients chronically treated with ACEI.
In all patients, premedication consisted of PO midazolam 5 mg. Patients received their cardiovascular medication on the morning before the operation. A radial catheter was inserted before induction and patients were monitored with continuous ST-T analysis (Marquette, Milwaukee). After a 10 mL/kg crystalloid infusion and breathing a 100% oxygen, patients received sufentanil 0.4 µg/kg, propofol 1.5 mg/kg, and atracurium 0.5 mg/kg IV.
Mechanical ventilation was performed using a mixture of 50% N2O in oxygen. Maintenance of anesthesia consisted of isoflurane administration. Boluses of sufentanil were administered intraoperatively as needed.
Hemodynamic variables were recorded each 1 min, from 10 min before the induction of anesthesia, and during at least the next 30 min. Hemodynamic study ended at incision. During the procedure, systolic blood pressure and heart rate were maintained within 30% of baseline values (defined as the average of three repeated measures on the day before surgery), using IV fluid administration and vasoconstrictors (e.g., ephedrine, phenylephrine, or terlipressin).
Hemodynamic events were defined as follows:
The number and duration of hemodynamic events were collected, and total doses of vasoactive drugs were noted in each group.
After surgery, patients were transferred to our recovery room. Treatments for HT were orally continued in the postoperative period. Hemodynamic events such as HT (more than 130% of control value) were treated with a bolus of nicardipine 1 mg or titrated esmolol when associated with increased HR (more than 85 bpm) or clonidine. Postoperative myocardial ischemia, defined as a ST depression > 1 mm at 60 ms after the J point, was treated with diltiazem, or nitrates in case of poor left ventricular function. Postoperative analgesia included paracetamol administration and morphine administered by patient-controlled analgesia. Postoperative period ended at discharge. Postoperative cardiac complications were defined as follows: congestive heart failure, pulmonary edema, cardiac death, supraventricular arrhythmia, ventricular arrhythmia, new Q-wave or ST-T depression longer than 48 h on twice-daily 12-lead electrocardiogram, associated or not with clinical findings such as circulatory failure with the need for catecholamines, or a decrease in global or regional function on echography, or an increase of cardiac troponin I (cTnI). cTnI was measured at recovery and on the first, second, and third postoperative days, using an immunoenzymofluorometric assay on a Stratus autoanalyzerTM (Dade-Behring, Deerfield, IL). Normal values are 00.5 ng/mL.
Statistical analysis was performed by using NCSS 6.0TM software (Statistical Solutions, Cork, Ireland). Hemodynamic variables were analyzed using analysis of variance and paired-t-test; clinical characteristics of the patients, hemodynamic events, and use of vasoactive drugs were analyzed using paired-t or K2 tests when appropriate, and normality of the variables were checked by using the Kolmogorov-Smirnov test.
| Results |
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Only one patient in each group developed a postoperative complication: one patient in Group I developed it during the postoperative period, a transient new chest pain with ST-T abnormalities on electrocardiogram, but without increased cTnI, necessitating a circumflex angioplasty on postoperative day 3. One patient in Group II developed transient ST-T abnormalities without pain nor increased cTnI on postoperative day 1.
| Discussion |
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Adverse circulatory effects during anesthesia are well known in patients chronically treated with ACEI, leading to the recommendation to discontinue them at least 24 hours before the induction of anesthesia. Similarly, a case of refractory hypotension was reported after the induction of anesthesia in a patient chronically treated with AIIA (5,6).
AIIA acts by binding to specific membrane-bound receptors that are coupled to one of several signal transduction pathways. The AT 1 receptor mediates the major cardiovascular action of the renin angiotensin system. Losartan, the leader in this field, is a selective AT1 receptor antagonist that was demonstrated to be an effective antagonist of many angiotensin II-induced actions and an effective antihypertensive drug in many animal models of HT (10). Clinical studies have confirmed the AIIA action of losartan and suggest that it is as effective in the treatment of essential HT, and congestive heart failure, as ACEI. The key advantage AIIA provide over ACEI is that they may avoid unwanted side effects that are related to bradykinin potentiation with the latter drugs (1013).
Blockade of the renin-angiotensin system increases the blood-pressure decreasing effect of anesthetic induction. A severe hypotensive episode, requiring vasoconstrictor treatment, occurs after the induction of general anesthesia in patients chronically treated with AIIA. Recommendations to discontinue these drugs on the day before the surgery may be justified.
| Conclusion |
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| References |
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