Pulsed arterial infusions. Chemotherapeutic implications
β Scribed by Kenneth C. Wright; Siney Wallace; E. Edmund Kim; Thomas Hynie; Chulsip Charnsagavej; C. Humberto Carrasco; Vincent P. Chuang; Cesare Gianturco
- Book ID
- 101329222
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 489 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
β¦ Synopsis
To simulate the intra-arterial infusion of chemotherapy, ink was infused at a steady rate through a vascular catheter inserted in a transparent tube carrying water at a rate similar to that of arterial blood. The ink ran in one or two discrete streams for 10 to 15 cm before mixing with the water, and there were substantial differences in the concentrations of ink in the water collected from side holes made at various distances from the catheter tip. If the ink was delivered in short pulses, however, it mixed with the water 2 to 3 cm beyond the catheter tip, and the samples collected from the side holes showed similar concentrations of ink. A similar situation may be encountered when chemotherapeutic agents are infused into patients. Therefore, pulsation may produce a more homogeneous drug distribution in the infused tissue. The in vitro data was substantiated in patients by the following: (1) the intra-arterial administration of technetium 99m(99mTc)labeled macroaggregated albumin (MAA) by both steady and pulsed infusions; and (2) changes in the severity of inflammatory skin reactions frequently associated with intra-arterial chemotherapy of the extremities. Improved isotope distribution was noted in 19.3% of the liver and 40% of the extremity studies. Reduced skin reactions were observed in approximately 90% of the extremities receiving pulsed chemotherapeutic infusions.
π SIMILAR VOLUMES
This report reviews the results of trcatnicnt of hepatic malignancies by intra-arterial infusional chemotherapy and hepatic artery ligation. Seventynine patients with liver metastases or primary hepatomas were treated by this technique bctween the years 1970 and 1982. 'The nia.jority of patients had
A short half-life alkylating agent designed for intra-arterial infusion, p-[ 2,3-di (2bromoethylthio) -n-propyloxy]benzoic acid ( C B 1850), was tested against the Walker tumour growing in the hind limb of vats. When administered intravenously C B 1850 was without effect at a dose which produced lOO