Assessing and managing venous irritation associated with vinorelbine tartrate (Navelbine) 1995

C N Rittenberg, and R J Gralla, and T A Rehmeyer
Ochsner Cancer Institute, New Orleans, LA, USA.

OBJECTIVE To determine the effect of duration of infusion time on venous irritation in patients receiving vinorelbine tartrate (Navelbine, Burroughs Wellcome Co., Research Triangle Park, NC) in combination with cisplatin or mitomycin. METHODS Prospective and descriptive. METHODS Five outpatient hematology/oncology units in southern Louisiana and Mississippi. METHODS 96 patients receiving vinorelbine in combination with cisplatin or mitomycin through a peripheral vein. METHODS Nurses completed the Venous Irritation Record (VIR), on which they documented the incidence of irritation reactions on the day of infusion as well as 24 hours and one to two weeks later. METHODS Incidence and severity of venous irritation as well as the duration of administration. RESULTS Significantly lower incidence of venous irritation at 6-10 minute infusion rate was observed (p < 0.05). No difference in incidence was observed when vinorelbine was given with a vesicant (mitomycin) or a nonvesicant (cisplatin) drug. CONCLUSIONS Although venous irritation is a problem associated with peripherally administered vinorelbine, it does not necessitate central line placement. Incidence of this problem can be reduced with a shorter duration of administration. The VIR was feasible, easy to use, and could be adapted for other drugs and other toxicities. The National Cancer Institute Common Toxicity Criteria are not adequate for grading venous irritation reactions. CONCLUSIONS Vinorelbine should be administered in accordance with the manufacturer's recommendations as a 6-10 minute infusion. Determination of this rate came as a result of clinical nursing research. Nurses involved in clinical trials can and should play a role in describing emergent toxicities and investigating methods to prevent or minimize those toxicities.

UI MeSH Term Description Entries
D007262 Infusions, Intravenous The long-term (minutes to hours) administration of a fluid into the vein through venipuncture, either by letting the fluid flow by gravity or by pumping it. Drip Infusions,Intravenous Drip,Intravenous Infusions,Drip Infusion,Drip, Intravenous,Infusion, Drip,Infusion, Intravenous,Infusions, Drip,Intravenous Infusion
D008175 Lung Neoplasms Tumors or cancer of the LUNG. Cancer of Lung,Lung Cancer,Pulmonary Cancer,Pulmonary Neoplasms,Cancer of the Lung,Neoplasms, Lung,Neoplasms, Pulmonary,Cancer, Lung,Cancer, Pulmonary,Cancers, Lung,Cancers, Pulmonary,Lung Cancers,Lung Neoplasm,Neoplasm, Lung,Neoplasm, Pulmonary,Pulmonary Cancers,Pulmonary Neoplasm
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D008937 Mitomycins A group of methylazirinopyrroloindolediones obtained from certain Streptomyces strains. They are very toxic antibiotics used as ANTINEOPLASTIC AGENTS in some solid tumors. PORFIROMYCIN and MITOMYCIN are the most useful members of the group.
D009859 Oncology Nursing A nursing specialty concerned with the care provided to cancer patients. It includes aspects of family functioning through education of both patient and family. Nursing, Oncologic,Oncologic Nursing,Cancer Nursing,Oncological Nursing,Nursing, Cancer,Nursing, Oncological,Nursing, Oncology
D010689 Phlebitis Inflammation of a vein, often a vein in the leg. Phlebitis associated with a blood clot is called (THROMBOPHLEBITIS). Periphlebitis,Periphlebitides,Phlebitides
D011446 Prospective Studies Observation of a population for a sufficient number of persons over a sufficient number of years to generate incidence or mortality rates subsequent to the selection of the study group. Prospective Study,Studies, Prospective,Study, Prospective
D002945 Cisplatin An inorganic and water-soluble platinum complex. After undergoing hydrolysis, it reacts with DNA to produce both intra and interstrand crosslinks. These crosslinks appear to impair replication and transcription of DNA. The cytotoxicity of cisplatin correlates with cellular arrest in the G2 phase of the cell cycle. Platinum Diamminodichloride,cis-Diamminedichloroplatinum(II),cis-Dichlorodiammineplatinum(II),Biocisplatinum,Dichlorodiammineplatinum,NSC-119875,Platidiam,Platino,Platinol,cis-Diamminedichloroplatinum,cis-Platinum,Diamminodichloride, Platinum,cis Diamminedichloroplatinum,cis Platinum
D005260 Female Females

Related Publications

C N Rittenberg, and R J Gralla, and T A Rehmeyer
August 1996, European journal of cancer (Oxford, England : 1990),
C N Rittenberg, and R J Gralla, and T A Rehmeyer
May 1995, Oncology nursing forum,
C N Rittenberg, and R J Gralla, and T A Rehmeyer
June 2005, Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners,
C N Rittenberg, and R J Gralla, and T A Rehmeyer
January 1995, Cancer practice,
C N Rittenberg, and R J Gralla, and T A Rehmeyer
April 2000, Gastroenterologie clinique et biologique,
C N Rittenberg, and R J Gralla, and T A Rehmeyer
April 1995, Seminars in oncology,
C N Rittenberg, and R J Gralla, and T A Rehmeyer
October 1994, Seminars in oncology,
C N Rittenberg, and R J Gralla, and T A Rehmeyer
July 2012, Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer,
C N Rittenberg, and R J Gralla, and T A Rehmeyer
January 1997, Anticancer research,
C N Rittenberg, and R J Gralla, and T A Rehmeyer
February 1991, Onkologie,
Copied contents to your clipboard!