Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 8 de 8
Filter
1.
Clin Infect Dis ; 58(1): 22-8, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24072931

ABSTRACT

BACKGROUND: Previous studies, largely based on chart reviews with small sample sizes, have demonstrated that infectious diseases (ID) specialists positively impact patient outcomes. We investigated how ID specialists impact mortality, utilization, and costs using a large claims dataset. METHODS: We used administrative fee-for-service Medicare claims to identify beneficiaries hospitalized from 2008 to 2009 with at least 1 of 11 infections. There were 101 991 stays with and 170 336 stays without ID interventions. Cohorts were propensity score matched for patient demographics, comorbidities, and hospital characteristics. Regression models compared ID versus non-ID intervention and early versus late ID intervention. Risk-adjusted outcomes included hospital and intensive care unit (ICU) length of stay (LOS), mortality, readmissions, hospital charges, and Medicare payments. RESULTS: The ID intervention cohort demonstrated significantly lower mortality (odds ratio [OR], 0.87; 95% confidence interval [CI], .83 to .91) and readmissions (OR, 0.96; 95% CI, .93 to .99) than the non-ID intervention cohort. Medicare charges and payments were not significantly different; the ID intervention cohort ICU LOS was 3.7% shorter (95% CI, -5.5% to -1.9%). Patients receiving ID intervention within 2 days of admission had significantly lower 30-day mortality and readmission, hospital and ICU length of stay, and Medicare charges and payments compared with patients receiving later ID interventions. CONCLUSIONS: ID interventions are associated with improved patient outcomes. Early ID interventions are also associated with reduced costs for Medicare beneficiaries with select infections.


Subject(s)
Communicable Diseases/epidemiology , Cross Infection/drug therapy , Cross Infection/prevention & control , Health Care Costs , Infection Control/methods , Aged , Aged, 80 and over , Communicable Diseases/mortality , Cross Infection/mortality , Female , Humans , Length of Stay , Male , Middle Aged , Survival Analysis
4.
Clin Infect Dis ; 50(11): e63-8, 2010 Jun 01.
Article in English | MEDLINE | ID: mdl-20420515

ABSTRACT

We describe 3 cases of daptomycin-induced pulmonary toxic effects that are consistent with drug-induced acute eosinophilic pneumonia. Patients presented similarly with dyspnea, cough, hypoxia, and diffuse ground-glass opacities at chest computed tomography. Clinical suspicion for this adverse drug event and cessation of daptomycin until definitive diagnosis can be made is crucial.


Subject(s)
Anti-Bacterial Agents/adverse effects , Daptomycin/adverse effects , Pulmonary Eosinophilia/chemically induced , Pulmonary Eosinophilia/diagnosis , Aged, 80 and over , Humans , Male , Middle Aged , Pulmonary Eosinophilia/pathology , Radiography, Thoracic , Tomography
5.
Crit Care ; 12(5): 233, 2008.
Article in English | MEDLINE | ID: mdl-18983709

ABSTRACT

Antipseudomonal carbapenems have played a useful role in our antimicrobial armamentarium for 20 years. However, a review of their use during that period creates concern that their clinical effectiveness is critically dependent on attainment of an appropriate dosing range. Unfortunately, adequate carbapenem dosing is missed for many reasons, including benefit/risk misconceptions, a narrow therapeutic window for imipenem and meropenem (due to an increased rate of seizures at higher doses), increasingly resistant pathogens requiring higher doses than are typically given, and cost containment issues that may limit their use. To improve the use of carbapenems, several initiatives should be considered: increase awareness about appropriate treatment with carbapenems across hospital departments; determine optimal dosing regimens for settings where multidrug resistant organisms are more likely encountered; use of, or combination with, an alternative antimicrobial agent having more favorable pharmacokinetic, pharmacodynamic, or adverse event profile; and administer a newer carbapenem with lower propensity for resistance development (for example, reduced expression of efflux pumps or greater stability against carbapenemases).


Subject(s)
Anti-Bacterial Agents/adverse effects , Anti-Bacterial Agents/therapeutic use , Carbapenems/adverse effects , Carbapenems/therapeutic use , Pseudomonas Infections/drug therapy , Pseudomonas Infections/economics , Pseudomonas aeruginosa , Animals , Anti-Bacterial Agents/economics , Anti-Bacterial Agents/pharmacology , Carbapenems/economics , Carbapenems/pharmacology , Clinical Trials as Topic/adverse effects , Clinical Trials as Topic/economics , Humans , Pseudomonas aeruginosa/drug effects
6.
Crit Care ; 12 Suppl 4: S4, 2008.
Article in English | MEDLINE | ID: mdl-18495061

ABSTRACT

Resistance rates are increasing among several problematic Gram-negative pathogens that are often responsible for serious nosocomial infections, including Acinetobacter spp., Pseudomonas aeruginosa, and (because of their production of extended-spectrum beta-lactamase) Enterobacteriaceae. The presence of multiresistant strains of these organisms has been associated with prolonged hospital stays, higher health care costs, and increased mortality, particularly when initial antibiotic therapy does not provide coverage of the causative pathogen. Conversely, with high rates of appropriate initial antibiotic therapy, infections caused by multiresistant Gram-negative pathogens do not negatively influence patient outcomes or costs. Taken together, these observations underscore the importance of a 'hit hard and hit fast' approach to treating serious nosocomial infections, particularly when it is suspected that multiresistant pathogens are responsible. They also point to the need for a multidisciplinary effort to combat resistance, which should include improved antimicrobial stewardship, increased resources for infection control, and development of new antimicrobial agents with activity against multiresistant Gram-negative pathogens.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Gram-Negative Bacterial Infections/drug therapy , Anti-Bacterial Agents/economics , Cross Infection/drug therapy , Cross Infection/economics , Drug Resistance, Bacterial , Drug Resistance, Multiple , Gram-Negative Bacteria/drug effects , Gram-Negative Bacterial Infections/economics , Humans , Microbial Sensitivity Tests , Risk Factors
7.
Am J Med ; 118 Suppl 7A: 1S-6S, 2005 Jul.
Article in English | MEDLINE | ID: mdl-15993671

ABSTRACT

In response to the overuse and misuse of antibiotics, leading to increasing bacterial resistance and decreasing development of new antibiotics, the Council for Appropriate and Rational Antibiotic Therapy (CARAT) has developed criteria to guide appropriate and accurate antibiotic selection. The criteria, which are aimed at optimizing antibiotic therapy, include evidence-based results, therapeutic benefits, safety, optimal drug for the optimal duration, and cost-effectiveness.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Bacterial Infections/drug therapy , Drug Utilization/standards , Anti-Bacterial Agents/economics , Anti-Bacterial Agents/pharmacokinetics , Cost-Benefit Analysis , Humans , Patient Selection
8.
J Fam Pract ; Suppl: S15-7, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15938990

ABSTRACT

Identification of risk factors present in the medical history should alert physicians to patients at potentially high risk for drug-induced QT interval prolongation. Careful patient monitoring and treatment adjustment will aid physicians in avoiding the complications of QT interval prolongation.


Subject(s)
Long QT Syndrome/prevention & control , Anti-Arrhythmia Agents/adverse effects , Electrocardiography , Female , Humans , Long QT Syndrome/chemically induced , Long QT Syndrome/diagnosis , Male , Medical History Taking , Risk Assessment/methods , Risk Factors
SELECTION OF CITATIONS
SEARCH DETAIL
...