Cheat sheet

CBIC CIC Cheat Sheet

Identification of Infectious Disease Processes

16.3%of exam

Surveillance and Epidemiologic Investigation

16.3%of exam

Preventing/Controlling Transmission

16.3%of exam

Employee/Occupational Health

8.1%of exam

Management, Communication, Education

10.4%of exam

Program and RegulationRisk AssessmentStewardship Core ElementsCost Avoidance

Education and Research

8.9%of exam

Education and ResearchAdult LearningEvidence HierarchyCompetency Validation

Environment of Care

10.4%of exam

Environment of CareACH Clearance TimesConstruction ICRAWater Management

Cleaning, Disinfection, Sterilization

13.3%of exam

Quick Facts

Credential
CIC
Board
CBIC
Items
150 (135 scored)
Time
3 h, two sections
Navigation
Forward only, no flags
Pass
Scaled 700 (300-900)
Pass rate
64% in 2025
Fee
$445 application
Delivery
Prometric / ProProctor
Retake
90 days, max 4/year
Valid
5 years, 40 IPUs
Outline
2021, new Feb 2027

Sensitivity vs Specificity

Sensitivity

  • True positive rate
  • Negative rules out
  • Prevalence independent

Specificity

  • True negative rate
  • Positive rules in
  • Prevalence independent

Catch sick vs confirm sick

Chain of Infection

Infectious agent
Pathogen causing disease
Reservoir
Where the agent lives
Portal of exit
How the agent leaves
Mode of transmission
Contact, droplet, airborne, vehicle
Portal of entry
How it enters host
Susceptible host
Person at risk
Break any link
Transmission stopsKey

Colonization vs Infection

Colonization

  • No tissue invasion
  • No clinical signs
  • Can still transmit

Infection

  • Tissue invasion
  • Host response present
  • Counted as case

Present vs invading

Disease Process Concepts

Colonization
Present, no tissue invasion
Infection
Invasion plus host response
Contamination
Organism on surface only
Pseudo-outbreak
Lab artifact, no illness
Incubation period
Exposure to first symptom
Communicable period
Window of transmissibility
Virulence
Severity of disease produced
Infectivity
Ability to enter, multiply
Pathogenicity
Share of infected sickened

Test Performance Measures

Sensitivity
True positive rate
Specificity
True negative rate
SnNout
Sensitive test rules out
SpPin
Specific test rules in
PPV
Positive means true disease
NPV
Negative means truly well
Prevalence effect
Low prevalence lowers PPV
Diagnostic stewardship
Test only symptomatic patients

Epi Curve Shapes

Spike, plateau, waves

Spike: point sourcePlateau: continuous sourceWaves: propagated spread

Incidence vs Prevalence

Incidence

  • New cases only
  • Population at risk
  • Measures risk

Prevalence

  • New plus existing
  • Point or period
  • Measures burden

Risk vs burden

Surveillance Metric Picker

  1. Measuring new HAI riskIncidence rate(Per 1,000 device days)
  2. Snapshot of burdenPoint prevalence(One day count)
  3. Comparing to national baselineSIR(Observed over predicted)
  4. Judging device useSUR(Device days ratio)
  5. Foodborne cluster on unitAttack rate(Ill over exposed)
  6. Fewer than 1 predictedNo SIR reported(Estimate unstable)
  7. Linking cases to strainMolecular typing(Confirms relatedness)

Epidemiology Measures

Incidence
New cases, population at-risk
Prevalence
All cases, one time
Attack rate
Ill divided by exposed
Device utilization ratio
Device days over patient days
Device-associated rate
Infections per 1,000 device days
SIR
Observed over predicted infections
SUR
Observed over predicted device days
Point prevalence survey
Snapshot on one day
Denominator
Population or days at-risk

NHSN HAI Concepts

CLABSI
Line >2 days, no source
CAUTI
Catheter >2 days plus symptoms
SSI
Infection after operative procedure
SSI window
30 or 90 days
VAC
Sustained oxygenation worsening
IVAC
VAC plus fever, antimicrobial
PVAP
IVAC plus qualifying microbiology
Date of event
First qualifying element appears
Present on admission
Not counted as HAI
LabID event
Lab-based MDRO or C. difficile

Outbreak Investigation Toolkit

Confirm outbreak
Compare against baseline rate
Case definition
Person, place, time, criteria
Line list
One row per case
Epi curve
Cases plotted over time
Point source
Single sharp peak
Continuous source
Plateau while exposure persists
Propagated
Peaks one incubation apart
Analytic study
Case-control or cohort
Molecular typing
Confirms strain relatedness
Control measures
Start before study finishesTrap

Five Moments

Patient, aseptic, fluid, patient, surroundings

1: before touching patient2: before aseptic task3: after fluid risk4: after touching patient5: after touching surroundings

Airborne vs Droplet

Airborne

  • Small particles, long distance
  • N95 respirator
  • Negative pressure room

Droplet

  • Large droplets, short range
  • Surgical mask
  • Normal room, door open

Respirator vs surgical mask

Precaution Picker

  1. Suspected pulmonary tuberculosisAirborne(N95, AIIR, door closed)
  2. MeaslesAirborne(Immune staff preferred)
  3. VaricellaAirborne plus contact(Both, not contact alone)
  4. Disseminated zosterAirborne plus contact(Any immune status)
  5. Localized zoster, immunocompetentStandard(Cover the lesions)
  6. Influenza or pertussisDroplet(Surgical mask on entry)
  7. Neisseria meningitidisDroplet(Not airborne)
  8. Mumps or rubellaDroplet(Not airborne)
  9. C. difficileContact(Soap, water, bleach)
  10. Norovirus outbreakContact(Alcohol rub insufficient)
  11. MRSA, VRE, CREContact(Gown and gloves)
  12. RSV in infantContact(Add droplet if splashing)
  13. Stem cell transplant patientProtective environment(Positive pressure room)

Precaution Categories

Standard
Every patient, every time
Contact
Gown and gloves
Droplet
Surgical mask on entry
Airborne
N95 plus negative-pressure room
Protective environment
Positive pressure, HEPA supply
Layering rule
Transmission-based adds to standard

Doffing Order

Gloves, gown, eyewear, mask last

Dirtiest comes off firstMask outside the roomHand hygiene immediately after

PPE Rules

Donning order
Gown, mask, eyewear, gloves
Doffing order
Gloves, gown, eyewear, mask
Mask removal
Outside the room
Gloves
Never replace hand hygiene
N95
Fit-tested, seal check each use
Gown
Fluid-resistant, single patient use
Eye protection
Goggles or face shield
Patient transport
Patient wears the mask

Hand Hygiene

Moment 1
Before touching a patient
Moment 2
Before clean, aseptic procedure
Moment 3
After body fluid risk
Moment 4
After touching a patient
Moment 5
After touching patient surroundings
Alcohol rub
Preferred, faster, less drying
Soap and water
Visibly soiled, spores, norovirus
Artificial nails
Prohibited in high-risk units

Organism Precaution Map

Tuberculosis
Airborne
Measles
Airborne
Varicella
Airborne plus contact
Disseminated zoster
Airborne plus contact
Localized zoster, immunocompetent
Standard, cover lesions
Influenza
Droplet
Pertussis
Droplet
Neisseria meningitidis
DropletTrap
Mumps, rubella
Droplet
C. difficile
Contact plus soap
Norovirus
Contact
RSV
Contact
MRSA, VRE, CRE
Contact
Scabies, lice
Contact

OSHA Bloodborne Numbers

Standard
29 CFR 1910.1030
Exposure control plan
Reviewed at least annually
Hepatitis B vaccine
Free within 10 working days
Training
At assignment, then annually
Sharps injury log
Employers over 10 employees
Medical records
Employment plus 30 years
Training records
Kept 3 years
Device selection
Frontline worker input required

Exposure Follow-up

HIV PEP
Start hours, take 28 days
HBV, unvaccinated source-positive
HBIG plus vaccine series
HBV timing
Ideally within 24 hours
Hepatitis C
No PEP, test and treat
Anti-HBs immunity
At least 10 mIU/mL
Source testing
Test source, consent permitting
Sharps injury
Wash, report, evaluate promptly

TB Screening Program

Baseline
Risk assessment, symptoms, test
Baseline TST
Two-step when TST used
IGRA
Blood test, one visit
Routine annual testing
No longer recommendedUpdated
Annual education
Required for all personnel
After exposure
Test baseline, 8-10 weeks
Fit test
Before use, then annually

Program and Regulation

Risk assessment
Ranks risks by priority
IPC plan
Goals from ranked risks
CMS Conditions of Participation
Enforceable federal requirement
Joint Commission
Voluntary, may carry deemed status
CDC/HICPAC guidelines
Recommendations, not law
Stewardship core elements
Seven CDC hospital elements
Cost avoidance
Infections prevented times cost
Cost savings
Real budget line reduction
PDSA
Plan, Do, Study, Act

Education vs Competency Validation

Education

  • Transfers knowledge
  • Attendance or post-test
  • Classroom or module

Competency validation

  • Observed performance
  • Defined criteria
  • Return demonstration

Knows vs can do

Education and Research

Andragogy
Adults are self-directed learners
Readiness to learn
Driven by role demands
Education
Knowledge, measured by post-test
Competency validation
Observed return demonstration
Cognitive domain
Knowledge and reasoning
Psychomotor domain
Physical skill performance
Affective domain
Attitudes and values
Evidence hierarchy top
Systematic review of RCTs
Research trigger
Intent to generalize knowledge
Quality improvement
Local, usually no IRB

AIIR vs Protective Environment

AIIR

  • Negative pressure
  • Protects everyone else
  • Infectious patient inside

Protective environment

  • Positive pressure
  • Protects the patient
  • HEPA-filtered supply air

Keep in vs keep out

Environment of Care

AIIR
Negative pressure, door closed
AIIR air changes
12 new, 6 existing
Pressure monitoring
Daily while room occupied
Protective environment
Positive pressure, HEPA supply
ICRA matrix
Activity type by patient risk
Aspergillus risk
Construction dust, immunocompromised patients
Water management
ASHRAE 188 Legionella program
Legionella conditions
Stagnation, tepid water, low residual
Contact time
Surface stays visibly wet
Bleach for C. difficile
1:10 dilution, EPA List K
Regulated medical waste
Pourable, drippable, caked blood

ACH Clearance Times

2 ACH, 99%
138 minutes
6 ACH, 99%
46 minutes
6 ACH, 99.9%
69 minutes
12 ACH, 99%
23 minutes
12 ACH, 99.9%
35 minutes
15 ACH, 99.9%
28 minutes
20 ACH, 99.9%
21 minutes
Use
Wait time after airborne case

Spaulding C-S-N

Critical sterilize, Semicritical high-level, Noncritical low-level

Critical: sterile tissueSemicritical: mucous membranesNoncritical: intact skin

High-level Disinfection vs Sterilization

High-level disinfection

  • Many spores survive
  • Semicritical devices
  • Liquid chemical, minutes

Sterilization

  • All spores killed
  • Critical devices
  • Validated, monitored cycle

Spores survive vs none

Reprocessing Picker

  1. Visibly soiled instrumentClean first(Soil blocks sterilants)
  2. Enters sterile tissueSterilize(Critical item)
  3. Enters the bloodstreamSterilize(Implants, surgical instruments)
  4. Touches mucous membranesHigh-level disinfection(Semicritical item)
  5. Flexible GI endoscopeHigh-level disinfection(Leak test, brush channels)
  6. BronchoscopeHigh-level disinfection(Sterilize when feasible)
  7. Covered vaginal probeHigh-level disinfection(Cover is not enough)
  8. Touches intact skinLow-level disinfection(Noncritical item)
  9. Blood pressure cuffLow-level disinfection(EPA-registered wipe)
  10. Needed immediately, no spareIUSS(Never routine implants)

Spaulding Classification

Critical
Sterile tissue or bloodstream
Critical process
Sterilization required
Semicritical
Contacts mucous membranes
Semicritical process
High-level disinfection minimum
Noncritical
Intact skin only
Noncritical process
Low-level disinfection
Class driver
Intended use, not nameTrap
Cleaning first
Always precedes disinfection, sterilization

BI Spore Match

Steam Geobacillus, dry heat Bacillus

Geobacillus: steam sterilizationGeobacillus: hydrogen peroxideBacillus atrophaeus: dry heatBacillus atrophaeus: ethylene oxide

Biological vs Chemical Indicator

Biological indicator

  • Live resistant spores
  • Proves lethality
  • Releases implant loads

Chemical indicator

  • Color change
  • Proves exposure only
  • Never proves sterility

Killed vs exposed

Disinfection Levels and Agents

High-level
Kills all but many spores
High-level agents
Glutaraldehyde, OPA, peracetic acid
Intermediate-level
Tuberculocidal claim, no spores
Intermediate agents
Alcohol, phenolics, iodophors, chlorine
Low-level
Vegetative bacteria, some viruses
Low-level agents
Quaternary ammonium compounds
Dividing line
Tuberculocidal separates intermediate, low
Sterilization
Kills all microbial life

Sterilization Monitoring

Biological indicator
Only proof of lethality
Steam, hydrogen peroxide
Geobacillus stearothermophilus
Dry heat, ethylene oxide
Bacillus atrophaeus
Chemical indicator
Proves exposure, not sterility
Bowie-Dick
Daily air removal test
Bowie-Dick setup
Empty chamber, first cycle
Gravity steam
121 C, 30 minutes wrapped
Prevacuum steam
132 C, 4 minutes wrapped
IUSS
Emergency only, never implantsTrap
Implant loads
Quarantine until BI result
Event-related sterility
Package integrity, not date

Common Traps

Droplet is not airborne

Meningococcus, pertussis: droplet Tuberculosis, measles: airborne

Varicella needs both

Airborne plus contact Not contact alone

Zoster depends on spread

Localized: standard, cover lesions Disseminated: airborne plus contact

CLABSI day count

Line >2 calendar days Insertion day is day 1

Bacteriuria is not CAUTI

Positive culture alone: bacteriuria CAUTI needs qualifying symptom

IUSS misuse

Not for inventory shortages Not for routine implants

Chemical indicator is not proof

Color change: exposure only Biological indicator proves kill

Pass rate is 64%

CBIC reports 64% (2025) Not the quoted 75%

Alcohol rub is not universal

Spores need soap, water C. difficile, norovirus: wash

Prevalence moves PPV only

Sensitivity fixed by test Low prevalence lowers PPV

No going back

Forward only, no flags Answer before moving on

Last Minute

  1. 1.150 items, 135 scored
  2. 2.Two 90-minute sections, forward only
  3. 3.Pass = scaled 700 (300-900)
  4. 4.Top three domains: 22 items each
  5. 5.Standard precautions apply to everyone
  6. 6.Airborne = TB, measles, varicella
  7. 7.Droplet = flu, pertussis, meningococcus
  8. 8.Contact = MDRO, C. difficile
  9. 9.Critical sterilize; semicritical high-level
  10. 10.Clean before you disinfect
  11. 11.BI proves kill; CI proves exposure
  12. 12.CLABSI needs line >2 days
  13. 13.SIR = observed over predicted
  14. 14.Incidence = risk; prevalence = burden
  15. 15.12 ACH: 35 minutes to 99.9%
  16. 16.Fit test yearly; seal check daily
  17. 17.HBV vaccine within 10 days
  18. 18.Retake after 90 days, max four
  19. 19.Recert: 40 IPUs or retake
  20. 20.New content outline February 2027
Same family resources

Explore More CBIC Infection Prevention Certifications

Continue into nearby exams from the same family. Each card keeps practice questions, study guides, flashcards, videos, and articles in one place.