A nurse manager on a risk management committee is providing strategies to decrease the number of medical errors at the facility. Which of the following strategies should the nurse include? (Select all that apply.)
Suggest increasing the number of providers who have ICU specialization.
Educate the nursing staff about the benefits of voluntary reporting of medication errors that caused no harm.
Eliminate the use of barcoding for medication administration.
Propose computerized provider order entry.
Recommend overriding the preset limits available on IV smart pumps.
Correct Answer : B,D
Rationale:
A. Suggest increasing the number of providers who have ICU specialization: Having more specialized staff is not a primary or broadly applicable strategy for reducing medical errors across the facility. This action also does not address system-wide risk management concerns.
B. Educate the nursing staff about the benefits of voluntary reporting of medication errors that caused no harm: Encouraging staff to report near-misses or no-harm errors fosters a culture of safety and helps identify system flaws before they lead to harm. This proactive approach allows for analysis and corrective actions without assigning blame.
C. Eliminate the use of barcoding for medication administration: Barcoding improves medication safety by verifying the right patient, drug, dose, time, and route. Eliminating this system would increase the risk of errors and compromise patient safety protocols.
D. Propose computerized provider order entry: CPOE reduces errors related to illegible handwriting, transcription mistakes, and manual entry. It also facilitates real-time clinical decision support and enhances communication between providers and pharmacists.
E. Recommend overriding the preset limits available on IV smart pumps: Preset limits are safety features designed to prevent dosage errors. Overriding them increases the risk of administering incorrect doses and should only occur under exceptional, justified circumstances.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is D
Explanation
Rationale:
A. Increased urine specific gravity: In fluid volume excess, the urine is often dilute due to increased renal perfusion or diuretic use, leading to a decreased specific gravity. An increased specific gravity is more commonly associated with dehydration or fluid volume deficit.
B. Polyuria: While polyuria can occur with certain conditions like diabetes mellitus or diabetes insipidus, it is not a typical finding in heart failure with fluid volume excess. Fluid is often retained rather than excreted in these clients unless diuretics are being administered.
C. Pericardial friction rub: A pericardial friction rub indicates pericarditis, an inflammation of the pericardial sac, and is not a typical manifestation of fluid volume excess in heart failure. It is unrelated to fluid overload.
D. Distended neck veins: Jugular vein distention is a hallmark sign of fluid volume excess and elevated central venous pressure, commonly seen in clients with heart failure. It indicates poor venous return and systemic fluid congestion.
Correct Answer is A
Explanation
Rationale:
A. Review the proposed change against current medication administration guidelines: Before implementing a new practice, the committee must ensure that the change aligns with evidence-based standards and regulatory guidelines. This review helps identify conflicts or risks and confirms that the proposal supports safe, legal, and effective care.
B. Evaluate the results of the change in medication administration practice: Evaluation should occur after the change has been implemented and sufficient data have been collected. Doing this step prematurely would mean there is no outcome data yet to assess.
C. Develop a plan to analyze the data for the new administration practice: While data analysis is crucial, it comes after implementation. Planning how to analyze data is not the immediate next step following the formulation of a proposed change.
D. Implement the proposed change in the facility's medication administration guidelines: Implementation should not occur until the proposal has been reviewed for consistency with current standards and proven to be safe and effective. Jumping to implementation could introduce risk without adequate vetting.
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