Cost-effective analysis of topical chlorhexidine in hematologic patients at risk for oral mucositis

2015 ◽  
Vol 19 (8) ◽  
pp. 1843-1850 ◽  
Author(s):  
Sharon Elad ◽  
Todd Thierer
2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Jamie A. Bastek ◽  
Holly Langmuir ◽  
Laxmi A. Kondapalli ◽  
Emmanuelle Paré ◽  
Joanna E. Adamczak ◽  
...  

Objectives. Antenatal corticosteroids (ACS) are not routinely administered to patients at risk for delivery between 34 and 36 6/7 weeks. Our objective was to determine whether ACS are cost-effective for late-preterm infants at risk for imminent preterm delivery. We hypothesized that the preferred strategy <36 weeks would include ACS while the preferred strategy ≥36 weeks would not. Methods. We performed decision-analytic and cost-effectiveness analyses to determine whether ACS was cost-effective at 34, 35, and 36 weeks. We conducted a literature review to determine probability, utility, and cost estimates absent of patient-level data. Base-case cost-effectiveness analysis, univariable sensitivity analysis, and Monte Carlo simulation were performed. A threshold of $100,000/QALY was considered cost-effective. Results. The incremental cost-effectiveness ratio favored the administration of a full course of ACS at 34, 35, and 36 weeks ($62,888.25/QALY, $64,425.67/QALY, and $64,793.71/QALY, resp.). A partial course of ACS was not cost-effective. While ACS was the consistently dominant strategy for acute respiratory outcomes, all models were sensitive to changes in variables associated with chronic respiratory disease. Conclusions. Our findings suggest that the administration of ACS to patients at risk of imminent delivery 34-36 weeks could significantly reduce the cost and acute morbidity associated with late-preterm birth.


1999 ◽  
Vol 161 (1) ◽  
pp. 62-65 ◽  
Author(s):  
CRAIG ZIPPE ◽  
LAKSHMI PANDRANGI ◽  
ASHOK AGARWAL

1995 ◽  
Vol 29 (12) ◽  
pp. 1228-1232 ◽  
Author(s):  
Colleen C Harrell ◽  
Sandra S Kline

Objective: To report 6 patients taking oral vitamin K1 (phytonadione) to reduce warfarin's activity. Case Summary: Six patient cases are summarized in which oral vitamin K1 was used to reduce the international normalized ratio (INR) in patients at risk of bleeding. Discussion: The use of oral vitamin K1 to antagonize warfarin's effects is discussed, as well as the benefits of oral vitamin K1 administration and the disadvantages of parenteral vitamin K1 administration. In addition, an extensive literature review of the discovery and clinical development of warfarin and vitamin K1 is described. Conclusions: In patients receiving warfarin therapy who have an increased INR and are at risk of bleeding, oral vitamin K1 therapy may be safer, less painful, and more cost-effective than the traditional parenteral route of administration.


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