Evidence Based Practice and Applied Nursing Research

(UG, C361, XAP1-0219)

 

Evidence Table

A1.QuantitativeArticle:Duthie, E., Favreau, B., & Ruperto, A. (2015, February 4). Quantitative and Qualitative Analysis of Medication Errors. Retrieved February 8, 2019, from https://www.ncbi.nlm.nih.gov/books/NBK20445/.
BackgroundorIntroduction  249 New York State hospitals implemented an experimental mandatory adverse event reporting system that examine hospital policy issues and identify useful interventions for future prevention.
ReviewoftheLiterature  In total, 14 articles were referenced within the publication.  The supporting material related to drug facts and comparisons, human errors, incident reporting, medication error prevention, and hospital guidelines.
Methodology

 

An 11member panel utilized random error reports received by the New York State Department of Health from the 249 participating hospitals.

A committee of multidisciplinary professionals spent 24 months performing a quantitative analysis that examined several variables to include:

  • where in the medication administration process did the error occur?
  • what departments were involved?
  • how often did the same error occur?
  • what medications or medication class was involved?
DataAnalysis A quantitative analysis of numeric data was used to calculate statistics regarding both fatal and non-fatal medication errors received from the 249 participating in the tracking program.  This type of methodology allows for greater objectivity when results are reviewed.  Also, for purposes of developing new hospital policies and procedures, numerical quantitative

data is viewed as credible and more reliable.

Quantitative Conclusions:  The medication error tracking received from the 249 pilot hospitals was successful in meeting the program mandates.  The data collected from fatal or near-fatal errors was instrumental in improving patient safety.  The information compiled will generate educational initiatives to address identified weaknesses.  These initiatives will provide knowledge and skills that proactively implement a safer medication administration system.

Quantitative: Protection and Considerations: The researchers indicate the information compiled originated from each hospital’s risk management department and there was no need to obtain informed consent.  “In quantitative research, ethical standards prevent against such things as the fabrication or falsifying of data and therefore, promote the pursuit of knowledge and truth which is the primary goal of research.” (Duthie, 2015).

Quantitative: Strengths and Limitations:  The data collected provides useful and practical data to the healthcare industry in order to reduce the incidence of medication errors that cause fatal and non-fatal outcomes.  An initial lack of compliance from each reporting institute proved to be a problem with data collection.  However, the New York Patient Occurrence Reporting and Tracking System (NYPORTS) provided reeducation to the staff of each recruited hospital and cooperation was eventually achieved.  It was determined the most common pitfall of medication administration is human error.  Even with a careful, updated tracking system, a deficit in knowledge must be remedied by continuing education.

Quantitative: Evidence Application:  The expectation of this tracking program is to improve patient outcomes.  If implemented, these initiatives will provide healthcare workers the skills and knowledge to proactively prevent medication errors that result in serious harm.

Evidence Table

B1.QualitativeArticle:Duthie, E., Favreau, B., & Ruperto, A. (2015, February 4). Quantitative and Qualitative Analysis of Medication Errors. Retrieved February 8, 2019, from https://www.ncbi.nlm.nih.gov/books/NBK20445/.
Background/Introduction In total, 14 articles were referenced within the publication.  The supporting material related to drug facts and comparisons, human errors, incident reporting, medication error prevention, and hospital guidelines.
ReviewoftheLiterature In total, 14 articles were referenced within the publication.  The supporting material related to drug facts and comparisons, human errors, incident reporting, medication error prevention, and hospital guidelines.
DiscussionofMethodology An 11member panel utilized random error reports received by the New York State Department of Health from the 249 participating hospitals.

A committee of multidisciplinary professionals spent 24 months performing a qualitative analysis that included findings that related to:

  • lessons learned
  • emergent themes
  • corrective counseling or education absent of punitive fixes
DataAnalysis The research panel consisted of multidisciplinary professionals who were experts in medical qualitative analysis.  Upon receipt of the medication error reports, the panel categorized the collected information using a coding system.  Another qualitive approach is the narrative analysis. This is more subjective and allows a “point of view” approach by asking the following questions:

  • what is this about?
  • who?, what?, where?, when?
  • then what happened?
  • so what?

Qualitative Conclusions:  The narrative data used in qualitative analysis appears to be the best source for implementing initiatives that will reduce medication errors.  The data collected from fatal or near-fatal errors was instrumental in improving patient safety.  The information compiled will generate educational initiatives to address identified weaknesses.  These initiatives will provide knowledge and skills that proactively implement a safer medication administration system.

Qualitative: Protection and Considerations:  Qualitative research is centered around the “do no harm” platform.  One aspect of preventing medication errors is imploring the facility to provide staff with continuing education.  In addition, there needs to be a clear, detailed policy for disclosure of information to the patient regarding a medication error.

Qualitative: Strengths and Limitations:  The data collected provides useful and practical data to the healthcare industry in order to reduce the incidence of medication errors that cause fatal and non-fatal outcomes.  An initial lack of compliance from each reporting institute proved to be a problem with data collection.  However, the New York Patient Occurrence Reporting and Tracking System (NYPORTS) provided reeducation to the staff of each recruited hospital and cooperation was eventually achieved.  It was determined the most common pitfall of medication administration is human error.  Even with a careful, updated tracking system, a deficit in knowledge must be remedied by continuing education.

Qualitative: Evidence Application:  The expectation of this tracking program is to improve patient outcomes.  If implemented, these initiatives will provide healthcare workers the skills and knowledge to proactively prevent medication errors that result in serious harm.

 

References

  • Duthie, E., Favreau, B., & Ruperto, A. (2015, February 4). Quantitative and Qualitative Analysis of Medication Errors. Retrieved February 8, 2019, from https://www.ncbi.nlm.nih.gov/books/NBK20445/.

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