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Granulocyte colony-stimulating factor use in cancer patients

OBJECTIVE: To conduct a retrospective drug utilization evaluation comparing the use of granulocyte colony-stimulating factor (G-CSF) at a university medical center with the American Society of Clinical Oncology (ASCO) CSFs Practice Guidelines. METHODS: Patients who received G-CSF from June 1, 1996,...

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Published in:The Annals of pharmacotherapy 2000-07, Vol.34 (7), p.851-857
Main Authors: Baker, J, McCune, JS, Harvey RD, , 3rd, Bonsignore, C, Lindley, CM
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creator Baker, J
McCune, JS
Harvey RD, , 3rd
Bonsignore, C
Lindley, CM
description OBJECTIVE: To conduct a retrospective drug utilization evaluation comparing the use of granulocyte colony-stimulating factor (G-CSF) at a university medical center with the American Society of Clinical Oncology (ASCO) CSFs Practice Guidelines. METHODS: Patients who received G-CSF from June 1, 1996, to December 31, 1996, were identified through the pharmacy computer system and the medical records were reviewed for a randomly selected sample of 26% of the 289 patients identified. Outpatient, inpatient, and electronic medical records were reviewed for the indication, dosage, day of initiation, day of discontinuation, and absolute neutrophil count (ANC) monitoring plan for each course of G-CSF; these records were subsequently compared with the ASCO guidelines. RESULTS: The use of G-CSF after chemotherapy was evaluated in 51 patients who received a total of 182 courses of G-CSF. The goal of chemotherapy was curative in 61% of courses. Sixty-five percent of G-CSF courses were prescribed for primary prophylaxis. Of these, 74% followed chemotherapy in patients with an expected incidence of febrile neutropenia ≥40% or followed chemotherapy in patients with compromised marrow reserve secondary to extensive prior therapy or in patients older than 60 years. Most of the G-CSF courses (75%) were rounded to the nearest vial size. The areas of greatest departure from the ASCO guidelines included aspects of initiation and discontinuation of G-CSF courses and inadequate documentation of ANC recovery. CONCLUSIONS: These results demonstrate a number of specific opportunites for oncology pharmacists to improve the use of G-CSF in patients receiving chemotherapy. Recommendations were made to the pharmacy and therapeutics committee and medical oncologists to improve compliance with the ASCO guidelines.
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METHODS: Patients who received G-CSF from June 1, 1996, to December 31, 1996, were identified through the pharmacy computer system and the medical records were reviewed for a randomly selected sample of 26% of the 289 patients identified. Outpatient, inpatient, and electronic medical records were reviewed for the indication, dosage, day of initiation, day of discontinuation, and absolute neutrophil count (ANC) monitoring plan for each course of G-CSF; these records were subsequently compared with the ASCO guidelines. RESULTS: The use of G-CSF after chemotherapy was evaluated in 51 patients who received a total of 182 courses of G-CSF. The goal of chemotherapy was curative in 61% of courses. Sixty-five percent of G-CSF courses were prescribed for primary prophylaxis. Of these, 74% followed chemotherapy in patients with an expected incidence of febrile neutropenia ≥40% or followed chemotherapy in patients with compromised marrow reserve secondary to extensive prior therapy or in patients older than 60 years. Most of the G-CSF courses (75%) were rounded to the nearest vial size. The areas of greatest departure from the ASCO guidelines included aspects of initiation and discontinuation of G-CSF courses and inadequate documentation of ANC recovery. CONCLUSIONS: These results demonstrate a number of specific opportunites for oncology pharmacists to improve the use of G-CSF in patients receiving chemotherapy. Recommendations were made to the pharmacy and therapeutics committee and medical oncologists to improve compliance with the ASCO guidelines.</description><identifier>ISSN: 1060-0280</identifier><identifier>EISSN: 1542-6270</identifier><identifier>DOI: 10.1345/aph.19124</identifier><identifier>PMID: 10928394</identifier><identifier>CODEN: APHRER</identifier><language>eng</language><publisher>Cincinnati, OH: Harvey Whitney Books</publisher><subject>Aged ; Antineoplastic Agents - therapeutic use ; Biological and medical sciences ; Cost-Benefit Analysis ; Drug toxicity and drugs side effects treatment ; Drug Utilization Review ; Female ; Granulocyte-Macrophage Colony-Stimulating Factor - administration &amp; dosage ; Granulocyte-Macrophage Colony-Stimulating Factor - therapeutic use ; Guideline Adherence ; Humans ; Leukocyte Count ; Male ; Medical sciences ; Middle Aged ; Monitoring, Physiologic ; Neoplasms - drug therapy ; Neoplasms - immunology ; Neutrophils ; Pharmacists ; Pharmacology. 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ispartof The Annals of pharmacotherapy, 2000-07, Vol.34 (7), p.851-857
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subjects Aged
Antineoplastic Agents - therapeutic use
Biological and medical sciences
Cost-Benefit Analysis
Drug toxicity and drugs side effects treatment
Drug Utilization Review
Female
Granulocyte-Macrophage Colony-Stimulating Factor - administration & dosage
Granulocyte-Macrophage Colony-Stimulating Factor - therapeutic use
Guideline Adherence
Humans
Leukocyte Count
Male
Medical sciences
Middle Aged
Monitoring, Physiologic
Neoplasms - drug therapy
Neoplasms - immunology
Neutrophils
Pharmacists
Pharmacology. Drug treatments
Random Allocation
Retrospective Studies
Toxicity: blood
title Granulocyte colony-stimulating factor use in cancer patients
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