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Detailed CHFM Study Dumps - Certification CHFM Exam Cost

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Medical Professional Certified Healthcare Facility Manager (CHFM) certification exam Sample Questions (Q76-Q81):

NEW QUESTION # 76
Which of the following would a facility health manager consult to determine the required number of medical gas outlets for a specific location, such as patient rooms or ICU rooms?

A. The Joint Commission Environment of Care (EOC) Standards
B. ADA Guidelines
C. NFPA 101 Life Safety Code
D. FGI Guidelines for the Design and Construction of Hospitals and Outpatient Facilities

Answer: D

Explanation:
The Facility Guidelines Institute (FGI) Guidelines are the authoritative source that specifies requirements for the design and construction of healthcare facilities. Within these guidelines, the number and type of medical gas outlets required in patient care areas such as intensive care units, operating rooms, and patient rooms are detailed. NFPA 99 governs installation and performance standards for medical gas systems, but the quantities of outlets are determined by the FGI Guidelines, which CHFM candidates are expected to know.
Incorrect Options:
A). NFPA 101 Life Safety Code - Addresses fire and life safety, not medical gas outlet quantities.
C). ADA Guidelines - Focus on accessibility, not medical gas systems.
D). The Joint Commission EOC Standards - Require safe use of systems but do not prescribe outlet numbers.
References:
FGI: Guidelines for Design and Construction of Hospitals and Outpatient Facilities - Medical gas outlet requirements per room type.
NFPA 99: Health Care Facilities Code - Technical standards for installation and testing.
CHFM Candidate Handbook - Planning, Design, and Construction domain.

NEW QUESTION # 77

(Base Bid / Alternate A / Alternate B)
Company A: $18,000 / $2,000 / Not available
Company B: $20,000 / $3,000 / Included
Company C: $19,000 / $4,000 / $500
Company D: $19,000 / $4,000 / $1,000
Which company has the LOWEST cost if alternate B is chosen?

A. $19,000 + $1,000 = $20,000.
B. $19,000 + $500 = $19,500.
C. Not available # cannot be selected.
D. $20,000 + Included ($0) = $20,000.

Answer: B

Explanation:
When Alternate B is chosen, total price = Base Bid + price for Alternate B (or zero if "Included").
Lowest total = $19,500 (Company C).
References:
AHA/CHFM Exam Content Outline - Planning, Design, and Construction domain (procurement/bid evaluations and alternates).
ASHE Project Management guidance - Evaluating base bids with alternates.

NEW QUESTION # 78
Which of the following represents the average power consumed by a single-phase electric motor?

A. KVA x PF
B. KVA / PF
C. kW x PF / 1,000
D. amps / PF

Answer: A

Explanation:
For electrical systems, real power (kW) is obtained by multiplying apparent power (kVA) by the power factor (PF):
kW = kVA × PF
This formula gives the average power consumed by a single-phase motor.
C). KVA × PF (Correct): Standard power equation for real power.
A). KVA / PF: Incorrect; dividing by PF would increase kVA, not convert to kW.
B). kW × PF / 1,000: Incorrect; kW already accounts for PF, and the division by 1,000 is irrelevant here.
D). amps / PF: Incomplete and not dimensionally correct.
References:
CHFM Candidate Handbook - Maintenance and Operations domain (electrical fundamentals).
NFPA 70: National Electrical Code (NEC) - Basic power calculation rules.
ASHE/CHFM study materials on motor loads and electrical systems.
________________________________________

NEW QUESTION # 79
A liquid oxygen tank has the chart shown below attached to the side of the tank:

At 107 in. = 234,480 cu. ft. (from chart)
Hospital usage = 15,000 cu. ft./day
How many days of oxygen are left in the tank?

Answer:

Explanation:
(15 days)
Explanation:
Calculation:
234,480 ÷ 15,000 = 15.63 days # # 15 days supply available.
References: NFPA 99, Oxygen Storage and Piping Systems; CHFM Candidate Handbook - Maintenance and Operations domain.

NEW QUESTION # 80
The Safe Medical Device Act of 1990 requires reporting of incidents involving a medical device when which of the following occurs?

A. major breakdown
B. death or injury
C. inappropriate application of the device
D. recall

Answer: B

Explanation:
The Safe Medical Device Act (SMDA) of 1990 requires healthcare facilities to report to the FDA and the manufacturer when a device is suspected of causing or contributing to death or serious injury.
C). death or injury (Correct): Specifically mandated under SMDA.
A). inappropriate application: A usage issue, not a reporting trigger.
B). recall: Issued by the FDA/manufacturer, not the facility's reporting obligation.
D). major breakdown: Requires service but not mandatory reporting.
References:
Safe Medical Device Act of 1990, Public Law 101-629.
FDA Medical Device Reporting (MDR) requirements.
CHFM Candidate Handbook - Compliance domain.
________________________________________

NEW QUESTION # 81
......

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Lou Bell Lou Bell

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