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Patency was preserved with a slow saline infusion (0.9% NaCl).
A butterfly needle was inserted into an antecubital vein, and patency was maintained with a slow saline drip.
Intravenous lines were inserted into a large antecubital vein of one arm for blood sampling between 8 a.m. and 10 a.m. and patency was preserved by a slow saline infusion (0.9% NaCl).
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After infusion of tacrolimus (which is oily), slow saline flushing was applied and adequate tacrolimus diffusion could be confirmed by observation of lightening of the discoloration of cyanotic myocardium and occurrence of mildly oily or shiny appearance of LV surface.
Both venous lines were kept patent by a slow 0.9% NaCl saline drip.
Lines were kept patent by a slow infusion of isotonic saline.
Both intravenous lines are kept patent with a slow infusion of normal saline.
A slow intravenous infusion of saline will be used as needed to keep the sampling line patent.
In order to minimize the potential risk of any thrombo-embolic complications from the pressure wire in the systemic circulation, a 2500 U heparin bolus was administered, followed by a slow infusion of heparinized saline (500 U per 500 mL).
During the first phase that lasted 4 months, patients were enrolled and treated with 2 g of citicoline through a slow intravenous infusion in saline 500 mL for 5 days, to be repeated for 5 more days in the case of nonresponders.
In agreement with previous observations [8], [9], [13], [14], neonatal DEX-treated pups gained weight at a slower rate than saline (SAL -treated ratSAL -treated6 weeks afteratseatment was discontinued (forupe 1).
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