2002, Número 1
<< Anterior Siguiente >>
Rev Mex Anest 2002; 25 (1)
Determinación de la dosis efectiva de Sevofluorano capaz de bloquear la respuesta hipertensiva durante laparoscopia.
Tamariz-Cruz O. , Reza A. , Zaragoza J. , Gaona C. , Ulibarri M. , Perales E
Idioma: Español
Referencias bibliográficas: 19
Paginas: 24-28
Archivo PDF: 123.32 Kb.
RESUMEN
Background: Vasopressin (VP) was recently identified as a major modulator of hypertension during laparoscopy (LAP). We searched for the effective dose (ED) of sevoflurane (S) with and without N2O able to control hemodynamic response (CHR) during LAP.
Material and Methods: The study was developed in five Mexican states, including ASA I patients divided in two groups: G I: S plus 60% N
2O (n=88) and G II: S alone (n=72). Conventional monitoring along BIS was used and basal data were recorder. Blood samples for nor epinephrine (NE) determination were drawn basal, 3´ after endotracheal intubation and 10´ after sustained insufflation (SI) and for VP basal, after hydration and 3´ after SI. The range of S for ED determination was 0.5 to 4% for both groups, as measured in Et concentration. Identification of the ED
50-95 of S for CHR during LAP was done using Waud´s method.
Results: No demographic differences were observed between groups except for gender. ED
50 of S for G I was 1.5 +/- 0.3 and for G II 2.0 +/- 0.32. ED
95 were 2.0 +/- 0.4 and 3.0 +/- 0.27 respectively. No differences in hemodynamic behavior were observed for ED
50 or
95 between groups. Plasma VP levels were significantly lower in N
2O supplemented patients (6.4 vs. 97.3 pg/ml). Adequacy of anesthetic depth was observed in all cases for ED
50-95 .
Discussion: The ED
50-95 of S for CHR during LAP with and without N
2O are described. A different dose of the one described for open procedures is reported. Neuroendocrine behavior is likely to be the explanation for this difference.
REFERENCIAS (EN ESTE ARTÍCULO)
Rademaker BM, Odoom JA, de Wit LT, Kalkman CJ, Brink SA, Ringers J. Haemodynamic effects of pneumoperitoneum for laparoscopic surgery: a comparison of CO2 with N2O insufflation. Eur J Anaesthesiol 1994 Jul;11(4):301.
Schob OM, Allen DC, Benzel E, Curet MJ, Adams MS et al. A comparison of the pathophysiological effects of CO2, N2O and He pneumoperitoneum on ICP. Am J Surg 1996; 172: 248.
Bode RHJr, Lewis KP, Zarich SW, Pierce ET, Roberts M, Kowalchuk GJ, Satwicz PR, Gibbons GW, Hunter JA, Espanola CC, Nesto RW. Cardiac Outcome after peripheral vascular surgery. Comparison of general and regional anesthesia. Anesthesiology 1996; 84: 3-13.
Donald RA, Perry EG, Wittert GA, Chapman M, Livesey JH, Ellis MJ, Evans MJ, Yandle T, Espiner EA. The plasma ACTH, AVP, CRH and catecholamine responses to conventional and laparoscopic cholecystectomy. Clin Endocrinol (Oxf) 1993 Jun;38(6):609-15.
Mann Cl, Boccara G, Pouzeratte Y, Eliet J, Claudine Serradeil-Le Gal C, Christine Vergnes, Daniel G. Bichet, Gilles Guillon, Jean M. Fabre, Pascal Colson. The Relationship Among Carbon Dioxide Pneumoperitoneum, Vasopressin Release, and Hemodynamic Changes. Anesth Analg 1999; 89:278.
Waud DR. On biological assays involving quantal responses. J Pharmacol Exp Ther 1972; 183: 577 - 607.
Cunningham AJ. Anesthetic implications of laparoscopic surgery. Yale J Biol Med 1999 Nov-Dec;71(6):551-78.
Roizen MF, Horrigan RW, Frazer BM. Anesthetic doses blocking adrenergic (stress) and cardiovascular responses to incision – MAC BAR. Anesthesiology 1981; 54: 390 – 8.
Katoh T, Ikeda K. The Effects of Fentanyl on Sevoflurane Requirements for Loss of Consciousness and Skin Incision. Anesthesiology 1998; 88: 18-24.
Daniel M, Weiskopf R, Noorani M, Eger E. Fentanyl Augments the Blockade of Sympathetic Response to Incision (MAC BAR) Produced by Desflurane and Isoflurane. Anesthesiology 1998; 88: 43-9.
Glass PSA. Anesthetic Drug Interactions. An insight into General Anesthesia – Its Mechanisms and Dosing Strategies. Anesthesiology 1998; 88: 5-6.
Walder AD, Aitkenhead AR. Role of vasopressin in the haemodynamic response to laparoscopic cholecystectomy. Br J Anaesth 1997 Mar;78(3):264-6.
Solis Herruzo JA, Castellano G, Larrodera L, Morillas JD, Moreno Sanchez D, Provencio R, Munoz-Yague MT. Plasma arginine vasopressin concentration during laparoscopy. Hepatogastroenterology 1989 Dec;36(6):499-503.
Tamariz-Cruz O, Reza-Albarrán, Perales E, Guevara U, Jáuregui LA and the Multicentric Group for the Study of Anesthesia for Laparoscopy. Determination of the effective dose of sevoflurane able to block haemodynamic response during laparosocopy. XII World Congress of Anaesthesiologist, Book of Abstracts. Montreal, Canada, 2000; p 4.4.37:pp.174.
Abballe C, Camaioni D, Mascaro A, Boccardi M, Evangelista M. Anesthesia for laparoscopic cholecystectomy: the use of nitrous oxide in the anesthetic mixture. G Chir 1993 Dec;14(9):493-5.
Tanaka M, Nishikawa T. Sevoflurane Speeds Recovery of Baroreflex Control of Heart Rate After Minor Surgical Procedures Compared with Isoflurane. Anesth Analg 1999; 89: 284-9.
AndersssonL, Wallin C-J, Sollevi A, Odeberg-Wernerman S. Pneumoperitoneum in healthy humans does not affect central blood volume or cardiac output. Acta Anesthesiol Scand 1999; 43: 809 – 814.
Guo TH, Davies MF, Kingery WS, Patterson AJ, Limbird LE, Maze M. Nitrous Oxide Produces Antinociceptive Response via a2 and/or a2c Adrenoceptor Subtypes in Mice. Anesthesiology 1999; 90:470 – 6.
Barr G, Jakobsson JG, Owall A, Anderson RE. Nitrous Oxide Does not alter BIS: study with nitrous oxide as sole agent and as adjunct to I.V. anaesthesia. Br J Anaesthesiology 1999; 82(6): 827-6.