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嗜铬细胞瘤切除的术前评估与准备 被引量:9

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出处 《实用医学杂志》 CAS 2004年第5期469-472,共4页 The Journal of Practical Medicine
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  • 1[1]Serfas D, Shoback DM, Lorell BH. Phaeochromocytoma and hypertophic cardiomyopathy: apparent suppression of symptoms and noradrenaline secretion by calcium-channel blockade. Lancet, 1987, ii 711-713
  • 2[2]Nanda AS, Feldman AM, Liang CS. Acute reversal of phaeochromocytoma-induced catecholamine cardiomyopathy.Clin Cardiol, 1995, 18:421-423
  • 3[3]Hull CJ. Phaeochromocytoma: diagnosis, pre-operative preparation, and anaesthetic management. Br J Anaesth, 1986, 58:1453-1468
  • 4[4]Gilsanz FJ, Luengo C, Conejero P, et al. Cardiomyopathy and phaeochromocytoma. Anaesthesia, 1983, 38:888-891
  • 5[5]Fripp RR, Lee JC, Downing SE. Inotropic responsiveness of the heart in catecholamine cardiomyopathy. Am Heart J,1981, 101:17-21
  • 6[6]Van Vliet PD, Bruchell HB, Titus JL. Focal myocarditis associated with phaeochromocytoma. N Engl J Med, 1966,274:1102-1108
  • 7[7]Prys-Roberts C. Phaeochromocytoma-recent progress in its management. Br J Anaesth, 2000, 85:44-57

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