• Wrong document? Swap it for free
  • Written by students who passed
  • Immediately available after payment
  • Read online or as PDF
Sell
Where do you study
Your language
Start selling Create your account
Document preview thumbnail
Preview 4 out of 40 pages
Exam (elaborations)

PROPHECY ASSESSMENTS CORE MANDATORY PART II | Attempt Score 100% Solutions Guide | Complete Q&A | Pass Guaranteed - A+ Graded

Document preview thumbnail
Preview 4 out of 40 pages

Achieve a 100% score on your Prophecy Assessments Core Mandatory Part II exam with this complete solutions guide. This A+ Graded resource contains complete questions and verified answers covering all advanced core mandatory content areas including advanced infection prevention (airborne, droplet, contact precautions, emerging infectious diseases, COVID-19 protocols, multi-drug resistant organisms MDROs such as MRSA, VRE, CRE, C. diff), patient safety culture (just culture, high reliability organizations HRO principles, second victim phenomenon), advanced patient rights (capacity vs competency, informed consent elements, refusal of treatment, involuntary holds), workplace safety advanced (active shooter response - run, hide, fight, workplace bullying and lateral violence, incivility reporting), hazardous material advanced (chemotherapy safety, hazardous drug handling, waste segregation), respiratory protection (N95 fit testing, PAPR use, TB screening protocols), advanced body mechanics (mechanical lift equipment, safe patient handling legislation, musculoskeletal injury prevention), advanced emergency response (rapid response team RRT activation criteria, code documentation, debriefing), ethical dilemmas (end-of-life decisions, withdrawal of treatment, DNR/DNI orders, medical futility, organ donation protocols), patient advocacy (reporting unsafe practices, whistleblower protections, quality improvement reporting), advanced incident reporting (root cause analysis RCA, failure mode effects analysis FMEA, disclosure of adverse events to patients), and advanced regulatory compliance (OSHA, CMS conditions of participation, The Joint Commission survey readiness). Each answer includes clear rationales to reinforce advanced core mandatory competency requirements. Perfect for healthcare professionals seeking a perfect score on Prophecy Core Mandatory Part II assessment. With our Pass Guarantee, you can confidently achieve 100% on your core mandatory exam. Download your complete Prophecy Assessments Core Mandatory Part II 100% solutions guide instantly!

Content preview

PROPHECY ASSESSMENTS CORE MANDATORY PART II |
Attempt Score 100% Solutions Guide | Complete Q&A | Pass
Guaranteed - A+ Graded


Aligned with 2026/2027 Joint Commission Hospital Accreditation Standards,
OSHA Advanced Directives, & CMS Emergency Preparedness Final Rule




[Section 1: Advanced Infection Control & Emerging Pathogens
(Questions 1-10)]

Multi-Drug Resistant Organisms (MRSA, VRE, CRE, C. Auris) | Emerging Infectious Diseases
(Mpox, Ebola) | Sterilization vs Disinfection Levels | Airborne Infection Isolation Rooms
(AIIR)




Q1. A patient admitted from a long-term acute care facility (LTAC) with
mechanical ventilation history is being screened for Candida auris colonization
per CDC guidance. Which specimen collection method and anatomical sites are
CORRECT?

A. Single nasal swab from anterior nares only
B. Bilateral axilla and groin composite swab
C. Rectal swab using Copan Transystem dual swab
D. Throat and perirectal swab combination

Correct Answer: B. Bilateral axilla and groin composite swab [CORRECT]

Rationale: CDC recommends using a composite swab of the patient's bilateral axilla and
groin for C. auris colonization screening, with real-time PCR as the preferred testing
method . Option A is incorrect because nasal swabs are used for MRSA screening, not C.
auris. Option C describes the correct method for carbapenemase-producing organism
(CPO) rectal screening, not C. auris. Option D is incorrect because throat swabs are not
recommended for C. auris detection. Prophecy Part II Testing Insight: This question

,tests the critical distinction between MDRO screening protocols—C. auris requires skin
swabs (axilla/groin) while CRE/CPO requires rectal screening. Regulatory Citation:
CDC C. auris Screening Recommendations for Healthcare Facilities (Dec 2025).




Q2. A hospitalized patient with confirmed carbapenem-resistant Enterobacterales
(CRE) infection has completed antibiotic therapy and is clinically improved. The
infection prevention team is evaluating whether contact precautions can be
discontinued. According to current CDC and SHEA guidance, which criteria MUST
be met?

A. Clinical improvement alone with physician documentation
B. Single negative rectal culture 48 hours after antibiotics completed
C. At least 6 months since last positive culture AND 2 consecutive negative rectal swabs
at least 1 week apart while off antibiotics 7-10 days
D. Three negative cultures obtained daily for 3 consecutive days

Correct Answer: C. At least 6 months since last positive culture AND 2 consecutive
negative rectal swabs at least 1 week apart while off antibiotics 7-10 days
[CORRECT]

Rationale: CDC states there is insufficient evidence for firm discontinuation
recommendations, but CRE colonization can be prolonged (>6 months) . SHEA expert
guidance recommends discontinuation only if: ≥6 months elapsed since last positive
culture, patient is off antibiotics 7-10 days, and at least 2 consecutive negative rectal
swabs are obtained ≥1 week apart . Option A is the classic Prophecy trap—clinical
improvement alone is NEVER sufficient for MDRO discontinuation. Option B fails on
multiple criteria (single culture, insufficient timeframe, no antibiotic washout). Option
D's daily testing is not supported by evidence and may yield false negatives due to
intermittent shedding. Prophecy Part II Testing Insight: The exam consistently tests
whether you know that MDRO discontinuation requires microbiologic clearance, not
just clinical improvement. Regulatory Citation: CDC CRE Toolkit; SHEA Expert
Guidance on Duration of Contact Precautions (2017).

,Q3. During terminal cleaning of a patient room previously occupied by a patient
with Candida auris, which disinfectant and contact time combination is REQUIRED
for effective environmental decontamination?

A. Quaternary ammonium compound (QAC) with 1-minute contact time
B. EPA-registered hospital disinfectant with sporicidal claim and 5-minute contact time
C. 70% isopropyl alcohol with 30-second contact time
D. Chlorine bleach solution (1000 ppm) with 1-minute contact time

Correct Answer: B. EPA-registered hospital disinfectant with sporicidal claim and
5-minute contact time [CORRECT]

Rationale: C. auris is resistant to many standard disinfectants including QACs and
alcohol. CDC recommends using an EPA-registered hospital disinfectant effective
against C. auris (List K) with adequate contact time—typically sporicidal agents such as
hydrogen peroxide or bleach solutions with extended contact times . Option A is
incorrect because QACs are ineffective against C. auris. Option C is incorrect because
alcohol has poor efficacy against fungal spores and biofilms. Option D's concentration
and contact time are insufficient; EPA List K products require specific contact times
(often 5 minutes or more). Prophecy Part II Testing Insight: This tests knowledge that
C. auris requires sporicidal-level disinfection, not standard hospital disinfectants.
Regulatory Citation: CDC Environmental Cleaning Guidance for C. auris.




Q4. A patient with suspected Mpox (Clade I) presents to the emergency
department with vesicular lesions and fever. According to CDC isolation
guidelines, which transmission-based precautions are REQUIRED?

A. Standard Precautions only
B. Contact Precautions only
C. Contact Precautions plus Airborne Precautions (N95 respirator)
D. Droplet Precautions plus Contact Precautions

Correct Answer: C. Contact Precautions plus Airborne Precautions (N95
respirator) [CORRECT]

Rationale: Mpox (Clade I) requires both Contact Precautions (gown, gloves) AND
Airborne Precautions (N95 or higher-level respirator) due to potential for airborne

, transmission during procedures that generate aerosols and theoretical risk of
respiratory droplet transmission. Standard Precautions alone (Option A) are insufficient
for suspected Mpox. Contact Precautions only (Option B) misses the airborne
component required for Clade I. Droplet Precautions (Option D) are insufficient as Mpox
requires airborne-level respiratory protection. Prophecy Part II Testing Insight: The
exam tests whether you distinguish between Clade I (more virulent, airborne added)
and Clade II protocols, and whether you default to the highest level of precaution when
uncertain. Regulatory Citation: CDC Mpox Infection Control Guidance (2024-2025
updates).




Q5. Which level of disinfection is REQUIRED for semi-critical items such as
endoscopes, respiratory therapy equipment, and anesthesia breathing circuits?

A. Low-level disinfection (kills most bacteria, some viruses, not mycobacteria or spores)
B. Intermediate-level disinfection (kills mycobacteria, most viruses, not spores)
C. High-level disinfection (kills all microorganisms except high numbers of bacterial
spores)
D. Sterilization (kills all microbial life including bacterial spores)

Correct Answer: C. High-level disinfection (kills all microorganisms except high
numbers of bacterial spores) [CORRECT]

Rationale: Semi-critical items contact mucous membranes or non-intact skin and
require high-level disinfection (HLD) per Spaulding classification. HLD destroys all
microorganisms except high numbers of bacterial endospores. Option A (low-level) is
for non-critical items contacting intact skin. Option B (intermediate-level) is insufficient
for semi-critical items. Option D (sterilization) is required for critical items (surgical
instruments, implants) but is not required for semi-critical items unless specifically
indicated. Prophecy Part II Testing Insight: The exam frequently tests the Spaulding
classification hierarchy—know that semi-critical = HLD, critical = sterilization, non-
critical = low/intermediate level. Regulatory Citation: CDC Guideline for Disinfection
and Sterilization in Healthcare Facilities (2008, reaffirmed 2023).

Document information

Uploaded on
April 27, 2026
Number of pages
40
Written in
2025/2026
Type
Exam (elaborations)
Contains
Questions & answers
£11.27

Wrong document? Swap it for free Within 14 days of purchase and before downloading, you can choose a different document. You can simply spend the amount again.
Written by students who passed
Immediately available after payment
Read online or as PDF

Seller avatar
Reputation scores are based on the amount of documents a seller has sold for a fee and the reviews they have received for those documents. There are three levels: Bronze, Silver and Gold. The better the reputation, the more your can rely on the quality of the sellers work.
NURSEPEARSONVUE
3.4
(32)
Sold
129
Followers
34
Items
1852
Last sold
1 week ago




Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their exams and reviewed by others who've used these revision notes.

Didn't get what you expected? Choose another document

No problem! You can straightaway pick a different document that better suits what you're after.

Pay as you like, start learning straight away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and smashed it. It really can be that simple.”

Alisha Student

Working on your references?

Create accurate citations in APA, MLA and Harvard with our free citation generator.

Working on your references?

Frequently asked questions