期刊
BRITISH JOURNAL OF ANAESTHESIA
卷 100, 期 4, 页码 494-503出版社
OXFORD UNIV PRESS
DOI: 10.1093/bja/aen017
关键词
arterial pressure, drug effects; complications, vasoconstriction; intensive care; oxygen, transport
Background. Terlipressin bolus infusion may reduce cardiac output and global oxygen supply. The present study was designed to determine whether dobutamine may counterbalance the terlipressin-induced depression in mixed-venous oxygen saturation (Sv(O2)) in patients with catecholamine-dependent septic shock. Methods. Prospective, randomized, controlled study performed in a university hospital intensive care unit. Septic shock patients requiring a continuous infusion of norepinephrine (0.9 mg kg(-1) min(-1)) to maintain mean arterial pressure (MAP) at 70 (SD 5) mm Hg were randomly allocated to be treated either with ( i) sole norepinephrine infusion (control, n = 20), (ii) a single dose of terlipressin 1 mg (n = 19), or (iii) a single dose of terlipressin 1 mg followed by dobutamine infusion titrated to reverse the anticipated reduction in Sv(O2) (n = 20). Systemic, pulmonary, and regional haemodynamic variables were obtained at baseline and after 2 and 4 h. Laboratory surrogate markers of organ (dys) function were tested at baseline and after 12 and 24 h. Results. Terlipressin (with and without dobutamine) infusion preserved MAP at 70 ( 5) mm Hg, while allowing to reduce norepinephrine requirements to 0.17 (0.2) and 0.2 ( 0.2) mg kg 21 min(-1), respectively [vs1.4 (0.3) mg kg(-1) min(-1) in controls at 4 h; each P, < 0.001]. The terlipressin-linked decrease in Sv(O2) was reversed by dobutamine at a mean dose of 20 (8) mg kg 21 min(-1) [Sv(O2) at 4 h: 59 (11)% vs 69 (12)%, P = 0.028]. Conclusions. In human catecholamine-dependent septic shock, terlipressin (with and without concomitant dobutamine infusion) increases MAP and markedly reduces norepinephrine requirements. Although no adverse events were noticed in the present study, potential benefits of increasing Sv(O2) after terlipressin bolus infusion need to be weighted against the risk of cardiovascular complications resulting from high-dose dobutamine.
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