CBIC CIC Dumps

Benchmarkingcompares infection rates across healthcare facilities.For accurate benchmarking, case definitions must be standardized and adjusted for patient demographics, severity of illness, and other risk factors.

Why the Other Options Are Incorrect?

A. Data collectors are trained on how to collect data–Training is necessary, but it does notdirectly ensure comparabilitybetween facilities.

B. Collecting data on a small population–A larger sample sizeincreasesaccuracy and reliabilityin benchmarking.

C. Denominator rates selected based on an organizational risk assessment– Risk assessment is important, butstandardized case definitionsare critical for comparison.

CBIC Infection Control Reference

According to APIC,accurate benchmarking relies on using standardized case definitions that account for differences in patient populations​.

The correct answer is A, "Observe all steps for reprocessing," as this is the most important process for the infection preventionist (IP) to review when evaluating a third-party reprocessor for single-use devices. According to the Certification Board of Infection Control and Epidemiology (CBIC) guidelines, the reprocessing of single-use devices (SUDs) by third-party entities must adhere to stringent infection control standards to ensure they are safe for reuse and do not contribute to healthcare-associated infections (HAIs). Observing all steps—such as cleaning, disinfection, sterilization, packaging, and quality control—allows the IP to directly assess compliance with manufacturer instructions, regulatory requirements (e.g., FDA guidelines), and best practices (e.g., AAMI ST91) (CBIC Practice Analysis, 2022, Domain III: Infection Prevention and Control, Competency 3.3 - Ensure safe reprocessing of medical equipment). This hands-on evaluation is critical because any deviation in the reprocessing chain can compromise device sterility and patient safety.

Option B (review the facility's blueprints and policies) provides context about the physical layout and procedural framework, but it is a preliminary step that does not directly verify the reprocessing process’s effectiveness. Option C (ensure air and water cultures are performed regularly) is important for monitoring environmental contamination risks, particularly in sterile processing areas, but it is a supportive measure rather than the primary focus of evaluating the reprocessor’s core activities. Option D (obtain feedback from other IPs who use the reprocessor) offers valuable peer insights, but it is subjective and secondary to direct observation, which provides firsthand evidence of compliance and performance.

The priority on observing reprocessing steps aligns with CBIC’s emphasis on ensuring the safety and efficacy of reprocessed medical devices, a key responsibility for IPs when outsourcing to third-party reprocessors (CBIC Practice Analysis, 2022, Domain III: Infection Prevention and Control, Competency 3.5 - Evaluate the environment for infection risks). This process enables the IP to identify specific weaknesses, validate adherence to standards, and make informed decisions about the reprocessor’s suitability.

To determine the number of employees whoseroconverted(became infected) after aneedlestick exposure, we use the given data:

Total Needlestick Injuries:250

Needlestick Injuries Involving Bloodborne Pathogens:100

Seroconversion Rate:2%

Calculation:

A black text with black numbers AI-generated content may be incorrect.

Why Other Options Are Incorrect:

A. 1:Incorrect calculation;2% of 100 is 2, not 1.

C. 5:Overestimates the actual number of infections.

D. 10:Exceeds the calculated value based on given data.

CBIC Infection Control References:

APIC Text, "Occupational Exposure and Seroconversion Risks"​.

APIC Text, "Bloodborne Pathogens and Needlestick Injury Prevention"​