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1.
AAOHN J ; 54(8): 355-8, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16921866

ABSTRACT

In Washington State, health care workers have the highest rate of compensable back injuries. Washington Hospital Services, a self-insured workers' compensation program, implemented a zero lift program in 31 of its 38 hospitals. Zero lift was defined as replacing manual lifting, transferring, and re-positioning of patients with mechanical lifting or use of other patient assist devices. This program included two trusts, two pools of hospitals that self-insure workers' compensation. The pools are governed by elected boards of trustees from the pool memberships and regulated by the State Department of Labor and Industries. This pretest-posttest descriptive study compared patient-handling injury data prior to program implementation with those after program implementation. Patient-handling injury claims decreased by 43% in the participating hospitals from 2000 to 2004 (i.e., from 3.51 to 2.23). The time lost frequency rate decreased by 50% (i.e., from 1.91 to 1.03).


Subject(s)
Accidents, Occupational/prevention & control , Back Injuries/prevention & control , Hospitals, Rural , Lifting/adverse effects , Occupational Health Services/organization & administration , Accidents, Occupational/statistics & numerical data , Back Injuries/economics , Back Injuries/epidemiology , Back Injuries/etiology , Causality , Cost of Illness , Ergonomics/methods , Hospital Bed Capacity, 100 to 299 , Hospital Bed Capacity, under 100 , Humans , Inservice Training/organization & administration , Insurance Claim Reporting/statistics & numerical data , Mass Screening/organization & administration , Nursing Assessment/organization & administration , Organizational Policy , Personnel, Hospital/education , Program Evaluation , Safety Management/methods , Transportation of Patients/methods , Washington/epidemiology , Workers' Compensation/economics
2.
Bioorg Med Chem Lett ; 15(5): 1315-9, 2005 Mar 01.
Article in English | MEDLINE | ID: mdl-15713378

ABSTRACT

The synthesis and the preliminary expansion of this new class of CDK2 inhibitors are presented. The synthesis was accomplished using a solution-phase protocol amenable to rapid parallel expansion and suitable to be scaled-up in view of possible lead development. Following a medicinal chemistry program aimed at improving cell permeability and selectivity, a series of compounds with nanomolar activity in the biochemical assay and able to efficiently inhibit tumor cell proliferation has been obtained.


Subject(s)
CDC2-CDC28 Kinases/antagonists & inhibitors , Enzyme Inhibitors/classification , Enzyme Inhibitors/pharmacology , Pyrazoles/classification , Pyrazoles/pharmacology , Cell Line, Tumor , Cell Proliferation/drug effects , Crystallization , Crystallography, X-Ray , Cyclin A/antagonists & inhibitors , Cyclin-Dependent Kinase 2 , Enzyme Inhibitors/chemical synthesis , Glycogen Synthase Kinase 3/antagonists & inhibitors , Humans , Models, Molecular , Molecular Structure , Pyrazoles/chemical synthesis , Structure-Activity Relationship
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