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1.
JAMA Ophthalmol ; 132(12): 1476-9, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25188508

ABSTRACT

IMPORTANCE: Quality and safety of eyedrop use for patients treated in a health care setting play a vital role in the delivery of health care. OBJECTIVE: To describe the development of a policy and procedural approach to the use of multidose eyedrops in multiple patients, approved and accepted by The Joint Commission in compliance with preferred practice standards in ophthalmology, the safe handling and administration of multidose eyedrops, and cost benefits of a multidose eyedrop approach. DESIGN, SETTING, AND PATIENTS: Using a policy and procedural approach, we petitioned The Joint Commission for approval and evaluated the cost benefits of implementation of a multidose process for eyedrop administration in patients undergoing surgery and treatment at the Utah Valley Regional Medical Center, Provo. RESULTS: The Joint Commission approved our policy and procedural approach, implemented in April 2012. Cost savings to both patients and the facility were significant. Costs to patients undergoing a single cataract operation were decreased as much as $283.85. Costs to the facility were decreased by $330.91 per cataract case. CONCLUSIONS AND RELEVANCE: Approval of our policy and processes indicates that The Joint Commission validates our policy and its adherence to accepted preferred practice guidelines of safe handling and administration of multidose eyedrops and establishes precedence that may be followed by other eye care facilities and health care organizations in the future. Our policy provides a safe and effective process for administering eyedrop medications to patients as well as controlling excessive health care costs to both patients and health care facilities.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Cataract Extraction , Drug Packaging , Ophthalmic Solutions/administration & dosage , Ophthalmology/standards , Practice Guidelines as Topic/standards , Academies and Institutes/organization & administration , Anti-Bacterial Agents/economics , Cost-Benefit Analysis , Delivery of Health Care , Drug Costs , Health Care Costs , Health Policy , Humans , Ophthalmic Solutions/economics , Ophthalmology/organization & administration , Pharmacy and Therapeutics Committee/standards , Professional Practice/standards , Quality Control , United States
2.
J Occup Environ Med ; 49(4): 453-60, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17426529

ABSTRACT

INTRODUCTION: An employer-based cost-benefit analysis for varenicline versus bupropion was conducted using clinical outcomes from a recently published trial. METHODS: A decision tree model was developed based on the net benefit of treatment to produce a nonsmoker at 1 year. Sensitivity analyses were conducted based on quit rates with placebo and varenicline and the cost of varenicline. RESULTS: Estimated 12-month employer cost savings per non-smoking employee were $540.60 for varenicline, $269.80 for bupropion SR generic, $150.80 for bupropion SR brand, and $81.80 for placebo. Varenicline was more cost beneficial than placebo, which had quit rates of 16.9% or less. The quit rate with varenicline would have to be

Subject(s)
Benzazepines/economics , Bupropion/economics , Employer Health Costs/statistics & numerical data , Health Benefit Plans, Employee , Nicotinic Agonists/economics , Quinoxalines/economics , Smoking Cessation/economics , Smoking Cessation/methods , Absenteeism , Benzazepines/therapeutic use , Bupropion/therapeutic use , Cost Savings/statistics & numerical data , Cost-Benefit Analysis/statistics & numerical data , Decision Trees , Humans , Maintenance , Nicotinic Agonists/therapeutic use , Program Evaluation , Quinoxalines/therapeutic use , Receptors, Nicotinic/drug effects , Time Factors , Varenicline
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