摘要:

To determine if four commercially available intravenous protamine preparations differed in their ability to bind to human anti-protamine antibody, the sera of seven protamine-insulin-dependent diabetics who had experienced life-threatening reactions to intravenous protamine and whose sera contained a mean of 67.4 μg/ml (range, 16–200 μg/ml) of antiprotamine IgG antibody were evaluated. Each serum was preincubated with buffer and 0.0014 to 1.4 mg/ml of the four protamine preparations before addition to an agarose-based solid-phase radioimmunoassay using125I-radiolabeled staph protein A as the detection protein. In the seven sera, the concentration of soluble protamine inhibiting 50% of protamine antibody (IC50) was determined by interpolating from points above and below 50% inhibition for each protamine preparation. No significant difference was found in the IC50among the four different protamine preparations (P> 0.25; Kruskal-Wallis). The authors concluded that there is no significant difference in the immunoreactivity of the four commercial protamine preparations with human antiprotamine IgG antibody. Thus, there appears to be no advantage in using a particular intravenous protamine preparation based on immunoreactivity with human antiprotamine antibody.

ISSN:0003-3022    

出版商:OVID    

年代:1990

数据来源: OVID

摘要:

Use of pharmacokinetic concepts to predict anesthetic drug concentrations has not had extensive use in clinical anesthetic practice to date. The multiple exponent equations needed to describe iv drug disposition have required computer capability not practical for the operating room. An algorithm is presented that allows the clinician to use information from the pharmacokinetic literature to improve accuracy of drug dosing in the operating room. Implemented on a pocket calculator, this approach does not involve complex mathematics or lengthy computations and allows the clinician to obtain a continuous prediction of the plasma anesthetic concentration during the course of the anesthetic from iv bolus or continuous infusion of anesthetic drugs.

ISSN:0003-3022    

出版商:OVID    

年代:1990

数据来源: OVID

ISSN:0003-3022    

出版商:OVID    

年代:1990

数据来源: OVID

ISSN:0003-3022    

出版商:OVID    

年代:1990

数据来源: OVID

ISSN:0003-3022    

出版商:OVID    

年代:1990

数据来源: OVID

ISSN:0003-3022    

出版商:OVID    

年代:1990

数据来源: OVID

ISSN:0003-3022    

出版商:OVID    

年代:1990

数据来源: OVID

ISSN:0003-3022    

出版商:OVID    

年代:1990

数据来源: OVID

ISSN:0003-3022    

出版商:OVID    

年代:1990

数据来源: OVID

ISSN:0003-3022    

出版商:OVID    

年代:1990

数据来源: OVID