Literature DB >> 9060364

Infusion pump adverse events: experience from medical device reports.

S L Brown1, A E Morrison, C M Parmentier, E K Woo, R L Vishnuvajjala.   

Abstract

Infusion pumps are used in the hospital setting, nursing home, and increasingly, in the home. Medical Device Reports to the Food and Drug Administration of adverse events during the use of infusion pumps for a 10-year period are described. Examples of cases reported to the Food and Drug Administration are provided. The problems reported by medical facilities (hospitals, medical centers, hospital pharmacies, or nursing homes) are compared with those that occur in the home or reported by home health care agencies. Overall, there were no differences in the types of adverse events reported by medical facilities when compared with reports from home health care agencies. However, there were differences in the location of use of some of the infusion pumps studied, which could reflect the trend toward home care over the past decade.

Mesh:

Year:  1997        PMID: 9060364

Source DB:  PubMed          Journal:  J Intraven Nurs        ISSN: 0896-5846


  3 in total

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Authors:  M Husch; C Sullivan; D Rooney; C Barnard; M Fotis; J Clarke; G Noskin
Journal:  Qual Saf Health Care       Date:  2005-04

2.  Monitoring device safety in interventional cardiology.

Authors:  Michael E Matheny; Lucila Ohno-Machado; Frederic S Resnic
Journal:  J Am Med Inform Assoc       Date:  2005-12-15       Impact factor: 4.497

3.  Reporting incidents involving the use of advanced medical technologies by nurses in home care: a cross-sectional survey and an analysis of registration data.

Authors:  Ingrid Ten Haken; Somaya Ben Allouch; Wim H van Harten
Journal:  BMJ Qual Saf       Date:  2020-06-16       Impact factor: 7.035

  3 in total

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