CHPOP Practice Test (V1)
Dive into practice questions
Question 1
A nurse on a medical-surgical floor needs to pull a STAT dose of furosemide for a patient in acute fluid overload, but the order has not yet been verified by a pharmacist. Which hospital policy is most compliant with safety standards regarding Automated Dispensing Cabinet (ADC) overrides?
Question 2
A hospital participating in the 340B Drug Pricing Program is audited. An auditor will primarily focus on ensuring that the hospital has NOT committed which of the following actions, which constitutes diversion?
Question 3
The Joint Commission (TJC) places significant emphasis on medication reconciliation during transitions of care. What is the primary operational goal of this process from a patient safety perspective?
Question 4
As part of a hospital’s quality assurance program for sterile compounding, air sampling in the ISO 7 buffer room yields colony-forming unit (CFU) counts that exceed the established action level. What is the most appropriate immediate operational response according to USP <797>?
Answer Key
- Question 1: B. Restricting overrides to a pre-approved list of emergency medications and requiring a clinical justification. (This approach balances the need for rapid access to life-saving medications with the safety net of pharmacist review, representing a best practice endorsed by organizations like ISMP.)
- Question 2: B. Dispensed 340B-purchased drugs to eligible outpatients for prescriptions written by non-eligible providers. (The fundamental rule of the 340B program is to prevent diversion. Dispensing a 340B drug to a patient who does not have an established relationship with a provider at the covered entity is a clear violation.)
- Question 3: B. To create the most accurate and complete list of a patient’s current medications to avoid errors. (The core purpose of medication reconciliation is to prevent adverse drug events by identifying and resolving discrepancies—such as omissions, duplications, or dosing errors—at every transition of care.)
- Question 4: B. Cease all compounding activities in the affected room and initiate an investigation into the cause. (Exceeding action levels indicates a potential loss of microbial control. USP standards require stopping production to investigate the root cause, implement corrective actions, and re-certify the environment before resuming operations.)