1990
DOI: 10.1016/0888-6296(90)90104-n
|View full text |Cite
|
Sign up to set email alerts
|

Effects of aprotinin on blood loss, platelet function, fibrinolysis, complement, and renal function after cardiopulmonary bypass

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

4
34
0
1

Year Published

1992
1992
2011
2011

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 27 publications
(39 citation statements)
references
References 4 publications
4
34
0
1
Order By: Relevance
“…Blauhat et al reported an increase of fractional sodium excretion during the late intraoperative and early postoperative stages, 18 which might reflect incipient renal tubular failure, but they also demonstrated that tubular dysfunction was unremarkable 24 h after the operation. In agreement with their results, we also found that the fractional sodium excretion increased similarly in both groups during the first postoperative day and returned to the preoperative value by 2 days after operation.…”
Section: Discussionmentioning
confidence: 99%
“…Blauhat et al reported an increase of fractional sodium excretion during the late intraoperative and early postoperative stages, 18 which might reflect incipient renal tubular failure, but they also demonstrated that tubular dysfunction was unremarkable 24 h after the operation. In agreement with their results, we also found that the fractional sodium excretion increased similarly in both groups during the first postoperative day and returned to the preoperative value by 2 days after operation.…”
Section: Discussionmentioning
confidence: 99%
“…4346 The only evaluation of renal function in patients receiving high-dose aprotinin also reported no untoward effect on serum electrolytes, osmolarity and creatinine, and creatinine clearance. 47 The only major side effect caused by aprotinin is a hypersensitivity reaction, which is more likely to occur after previous exposure to the drug, and has an overall incidence of approximately 0.1%.13'42 Previous exposure to aprotinin was the only exclusion criterion in a study by Bidstrup et al, presumably on this basis. 46 However, repeated use of aprotinin in a small series of 15 patients by Freeman was not associated with allergic phenomena.…”
Section: Pharmacokinetic Behaviour and Side Effectsmentioning
confidence: 99%
“…Devido ao fato de a meia-vida de eliminação situar-se entre uma e sete horas, o regime recomendado consta de uma dose inicial é de 2 × 10 6 UIK (2.000.000 UIK), outra dose igual na CEC e infusão contínua de 5 × 10 5 UIK.h -1 durante todo o procedimento cirúrgico. Esse regime mostrou, em vários estudos, reduzir a perda de sangue em até 50% e diminuir a necessidade de transfusão de 40% a 80% em intervenção cirúrgica cardíaca com CEC [39][40][41][42] . Além desse, que é o mais adota e estudado, têm sido empregados regimes com doses mais baixas.…”
Section: Aprotininaunclassified
“…Since its elimination half-life is between 1 and 7 hours, the recommended regimen consists of an initial dose of 2 x 10 6 KIU (2,000,000 KIU), followed by the same dose in the CPB, and continuous infusion of 5 x 10 5 KIU.h -1 during surgery. Several studies demonstrated that this regimen reduces blood loss by up to 50% and the need of transfusion in 40% to 80% of the cases of cardiac surgery with CPB [39][40][41][42] . Besides this regimen, the one used more often and that has been studied the most, regimens with lower doses have been used.…”
Section: Aprotininmentioning
confidence: 99%