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The Devil is in the Details: Applying CAUTI and CLABSI Criteria ...

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<strong>The</strong> <strong>Devil</strong> <strong>is</strong> <strong>in</strong> <strong>the</strong> <strong>Details</strong>:<br />

Apply<strong>in</strong>g <strong>CAUTI</strong> <strong>and</strong> <strong>CLABSI</strong><br />

<strong>Criteria</strong> Accurately<br />

Kathy Allen-Bridson RN, BSN, CIC<br />

Bus<strong>in</strong>ess Computer Applications Inc. Contractor to<br />

Div<strong>is</strong>ion of Healthcare Quality Promotion<br />

Centers for D<strong>is</strong>ease Control <strong>and</strong> Prevention<br />

Mercer Conference Center<br />

Nov. 2009


Objectives<br />

1. State <strong>the</strong> Centers for D<strong>is</strong>ease Control<br />

<strong>and</strong> Prevention’s def<strong>in</strong>itions <strong>and</strong> criteria<br />

of Ca<strong>the</strong>ter-associated Ur<strong>in</strong>ary Tract<br />

Infection (<strong>CAUTI</strong>) <strong>and</strong> Central L<strong>in</strong>eassociated<br />

Bloodstream Infection<br />

(<strong>CLABSI</strong>)<br />

2. Correctly identify <strong>CAUTI</strong> <strong>and</strong> <strong>CLABSI</strong> as<br />

applied to case studies<br />

3. State <strong>the</strong> correct method to identify<br />

denom<strong>in</strong>ators for <strong>CAUTI</strong> <strong>and</strong> <strong>CLABSI</strong><br />

rate calculations.


NHSN Website<br />

A Valuable Resource<br />

• NHSN Manual<br />

– <strong>Criteria</strong><br />

– Key Def<strong>in</strong>itions<br />

– Tables of Instructions<br />

• Data <strong>and</strong> Stat<strong>is</strong>tics<br />

– NHSN publ<strong>is</strong>hed reports<br />

• Tra<strong>in</strong><strong>in</strong>gs<br />

• NHSN forms<br />

• Lots more!!!<br />

http://www.cdc.gov/nhsn/<strong>in</strong>dex.html


http://www.cdc.gov/nhsn/PDFs/ICD-9-cmCODEScurrent.pdf


Horan TC, Andrus ML, Dudeck MA. CDC/NHSN surveillance def<strong>in</strong>ition of healthcareassociated<br />

<strong>in</strong>fection <strong>and</strong> criteria for specific types of <strong>in</strong>fections <strong>in</strong> <strong>the</strong> acute care<br />

sett<strong>in</strong>g. Am J Infect Control 2008;36:309-32.<br />

http://www.cdc.gov/ncidod/dhqp/pdf/NNIS/NosInfDef<strong>in</strong>itions.pdf


Cons<strong>is</strong>tency <strong>is</strong> a Must!<br />

• <strong>Criteria</strong> designed to look at a<br />

population at r<strong>is</strong>k<br />

• Identify patients meet<strong>in</strong>g <strong>the</strong><br />

criteria<br />

• Cons<strong>is</strong>tently apply <strong>the</strong> criteria<br />

• Ensures <strong>the</strong> comparability of <strong>the</strong><br />

data- protects your facility <strong>and</strong><br />

o<strong>the</strong>rs


What If My Physician’s<br />

Balk?<br />

• Rem<strong>in</strong>d of surveillance vs. cl<strong>in</strong>ical<br />

def<strong>in</strong>itions<br />

– Diff purposes<br />

– May not be <strong>the</strong> same<br />

– Comments section useful to note<br />

important factors<br />

• Can submit questions to NHSN<br />

mailbox


Healthcare-associated Infection<br />

(HAI)<br />

• A localized or systemic condition result<strong>in</strong>g from an<br />

adverse reaction to <strong>the</strong> presence of an <strong>in</strong>fectious<br />

agent(s) or its tox<strong>in</strong>(s) that<br />

– Occurs <strong>in</strong> a patient <strong>in</strong> a healthcare sett<strong>in</strong>g <strong>and</strong><br />

– Was not present or <strong>in</strong>cubat<strong>in</strong>g at <strong>the</strong> time of<br />

adm<strong>is</strong>sion, unless <strong>the</strong> <strong>in</strong>fection was related<br />

to a previous adm<strong>is</strong>sion<br />

• When <strong>the</strong> sett<strong>in</strong>g <strong>is</strong> a hospital, meets <strong>the</strong> criteria<br />

for a specific <strong>in</strong>fection (body) site as def<strong>in</strong>ed by<br />

CDC<br />

• When <strong>the</strong> sett<strong>in</strong>g <strong>is</strong> a hospital, may also be called<br />

a nosocomial <strong>in</strong>fection


Major & Specific<br />

Infection Types


<strong>CAUTI</strong> <strong>and</strong> <strong>CLABSI</strong> <strong>Criteria</strong><br />

<strong>and</strong> Application


Ca<strong>the</strong>ter-associated Ur<strong>in</strong>ary Tract<br />

Infection (<strong>CAUTI</strong>)


Ca<strong>the</strong>ter-associated Ur<strong>in</strong>ary<br />

Tract Infection (<strong>CAUTI</strong>)<br />

Surveillance<br />

• Most common HAI<br />

• Rates range between<br />

– 16.8% <strong>in</strong> Rehab<br />

– 3.1% <strong>in</strong> Med Surg ICU non-major teach<strong>in</strong>g<br />

facility<br />

• Renewed <strong>in</strong>terest:<br />

– M<strong>and</strong>atory report<strong>in</strong>g<br />

– Denial of CMS reimbursement dollars


Major & Specific Infection<br />

Types- UTI<br />

• Major: Ur<strong>in</strong>ary Tract Infection<br />

(UTI)<br />

• Specific:<br />

– Symptomatic UTI (SUTI)<br />

– Asymptomatic Bacteremic UTI<br />

(ABUTI)<br />

– O<strong>the</strong>r UTI (OUTI)<br />

<strong>CAUTI</strong>= UTI where an <strong>in</strong>dwelll<strong>in</strong>g ur<strong>in</strong>ary ca<strong>the</strong>ter<br />

was <strong>in</strong> place <strong>in</strong> <strong>the</strong> 48 hours prior to <strong>in</strong>fection<br />

onset


<strong>CAUTI</strong><br />

A UTI when an <strong>in</strong>dwelll<strong>in</strong>g ur<strong>in</strong>ary ca<strong>the</strong>ter<br />

was <strong>in</strong> place <strong>in</strong> <strong>the</strong> 48 hours prior to<br />

<strong>in</strong>fection onset<br />

*Note: <strong>The</strong>re <strong>is</strong> no m<strong>in</strong>imum period of time<br />

that <strong>the</strong> ca<strong>the</strong>ter must be <strong>in</strong> place I norder<br />

for <strong>the</strong> UTI to be considered ca<strong>the</strong>terassociated.<br />

*Note: SUTI 1b <strong>and</strong> 2b <strong>and</strong> O<strong>the</strong>r UTI cannot<br />

be ca<strong>the</strong>ter-associated.


Indwell<strong>in</strong>g Ca<strong>the</strong>ter<br />

• A dra<strong>in</strong>age tube that <strong>is</strong> <strong>in</strong>serted<br />

<strong>in</strong>to <strong>the</strong> ur<strong>in</strong>ary bladder through <strong>the</strong><br />

urethra, <strong>is</strong> left <strong>in</strong> place, <strong>and</strong> <strong>is</strong><br />

connected to a closed collection<br />

system; also called a Foley<br />

ca<strong>the</strong>ter; does not <strong>in</strong>clude:<br />

– straight <strong>in</strong> <strong>and</strong> out ca<strong>the</strong>ters<br />

– Suprapubic ca<strong>the</strong>ters<br />

– Nephrostomy tubes


<strong>CAUTI</strong> Denom<strong>in</strong>ator Data<br />

• <strong>CAUTI</strong>s are attributed to patient<br />

location<br />

• # <strong>in</strong>dwell<strong>in</strong>g ur<strong>in</strong>ary ca<strong>the</strong>ter days/<br />

unit<br />

• For ur<strong>in</strong>ary ca<strong>the</strong>ter device<br />

utilization: # patient days/unit


48 Hour Rule<br />

• If a <strong>CAUTI</strong> develops with<strong>in</strong> 48<br />

hours of transfer from one <strong>in</strong>patient<br />

location to ano<strong>the</strong>r <strong>in</strong> <strong>the</strong> same<br />

facility, <strong>the</strong> <strong>in</strong>fection <strong>is</strong> attributed to<br />

<strong>the</strong> transferr<strong>in</strong>g location.<br />

Th<strong>is</strong> rule applies to <strong>CLABSI</strong> surveillance also.


Example of Completed Denom<strong>in</strong>ators<br />

for ICU/O<strong>the</strong>r Locations Form<br />

10000 Nov<br />

2008 MSICU<br />

6<br />

8<br />

6<br />

7<br />

6<br />

8<br />

6<br />

6<br />

4<br />

7<br />

6<br />

6<br />

//<br />

//<br />

151 138


2 Key Questions<br />

• Was an <strong>in</strong>dwell<strong>in</strong>g ca<strong>the</strong>ter <strong>in</strong><br />

place at <strong>the</strong> time of or with<strong>in</strong> 48<br />

hours prior to <strong>the</strong> ur<strong>in</strong>e specimen<br />

collection?<br />

• Is <strong>the</strong> patient 65 years or older?


Symptomatic UTI – 1a & 1b<br />

1 a <strong>and</strong> 1 b


Symptomatic UTI – 2a


Symptomatic UTI – 2b


SUTI for ≤1 year olds –<br />

<strong>Criteria</strong> 3 & 4


SUTI 1a & 2a Ca<strong>the</strong>ter <strong>in</strong><br />

Place Flow Diagram


Asymptomatic Bacteremic UTI<br />

(ABUTI)


Determ<strong>in</strong>es if<br />

age <strong>is</strong> a<br />

factor


Available<br />

selections<br />

based on<br />

Specific<br />

Event<br />

Type


Case 1<br />

• Patient with end stage pancreatic cancer with liver &<br />

bone mets admitted to hospital with advance<br />

directive for comfort care <strong>and</strong> antibiotics only;<br />

peripheral IV <strong>and</strong> nasal cannula <strong>in</strong>serted<br />

• Day 4: patient <strong>is</strong> febrile <strong>and</strong> has suprapubic<br />

tenderness; IV ampicill<strong>in</strong> started after ur<strong>in</strong>e obta<strong>in</strong>ed<br />

for culture<br />

• Day 5: difficulty breath<strong>in</strong>g; CXR=<strong>in</strong>filtrate L lung<br />

base<br />

• Day 6: ur<strong>in</strong>e culture results = 10 5 CFU/ml E coli<br />

• Day 7: WBC/mm 3 = 3400; patchy <strong>in</strong>filtrates <strong>in</strong> both<br />

lung bases; cont<strong>in</strong>ued ep<strong>is</strong>odes of dyspnea; rales<br />

noted <strong>in</strong> LLL<br />

• Day 11: Patient expired


Case 1<br />

• Does th<strong>is</strong> patient have an HAI?<br />

• What type(s)?<br />

• Device associated?


Case 2<br />

• POD 3: 66 y.o. patient <strong>in</strong> <strong>the</strong> ICU with a Foley<br />

ca<strong>the</strong>ter s/p exploratory lap; patient noted to<br />

be febrile (38.9 ) <strong>and</strong> compla<strong>in</strong>ed of diffuse<br />

abdom<strong>in</strong>al pa<strong>in</strong><br />

• WBC <strong>in</strong>creased to 19,000. He had cloudy,<br />

foul-smell<strong>in</strong>g ur<strong>in</strong>e <strong>and</strong> ur<strong>in</strong>alys<strong>is</strong> showed 2+<br />

prote<strong>in</strong>, + nitrite, 2+ leukocyte esterase, wbc –<br />

TNTC, <strong>and</strong> 3+ bacteria. Culture was 10,000<br />

CFU/ml E. coli. <strong>The</strong> abdom<strong>in</strong>al pa<strong>in</strong> seemed<br />

localized to surgical area<br />

Is th<strong>is</strong> a UTI?<br />

If so, what type?<br />

<strong>Criteria</strong>?


Case 3<br />

• 84 year old patient <strong>is</strong> hospitalized with GI bleed<br />

• Day 3: Patient has ca<strong>the</strong>ter <strong>in</strong> place <strong>and</strong> no signs or<br />

symptoms of <strong>in</strong>fection<br />

• Day 9: Patient becomes unresponsive, <strong>is</strong> <strong>in</strong>tubated <strong>and</strong><br />

CBC shows WBC of 15,000. Temp 38.5 C. Patient <strong>is</strong><br />

pan-cultured. Blood culture <strong>and</strong> ur<strong>in</strong>e both grow<br />

Streptococcus pyogenes – ur<strong>in</strong>e >10 5 CFU/ml.<br />

Is th<strong>is</strong> a UTI?<br />

If so, what type?


Case 4<br />

• 3 week old <strong>in</strong>fant born at 27 weeks gestation.<br />

Umbilical ca<strong>the</strong>ter <strong>in</strong> place. HR 100, RR 32,<br />

<strong>and</strong> core temperature ranges between 37.8 C<br />

<strong>and</strong> 36.2 C. Straight cath ur<strong>in</strong>e culture yields<br />

>10 5 CFU/ml Staphylococcus epidermid<strong>is</strong>.<br />

• 1 blood culture sent same day, also positive<br />

for S. epi. No susceptibilities provided.<br />

Is th<strong>is</strong> a UTI?<br />

If so, what type?


Case 4<br />

• What if <strong>the</strong> one blood <strong>and</strong> ur<strong>in</strong>e culture had<br />

been positive for a Micrococcus not<br />

speciated?<br />

Is th<strong>is</strong> now a UTI?<br />

If so, what type?<br />

For you NHSN bra<strong>in</strong>iacs..<strong>is</strong> it<br />

a BSI?


Laboratory Confirmed Bloodstream<br />

Infections


Central L<strong>in</strong>e-associate Bloodstream<br />

Infections (<strong>CLABSI</strong>) Module<br />

• 250,000 <strong>CLABSI</strong>s occur <strong>in</strong> <strong>the</strong><br />

United States each year 1<br />

• Most bloodstream <strong>in</strong>fections are<br />

associated with <strong>the</strong> presence of a<br />

central l<strong>in</strong>e or umbilical ca<strong>the</strong>ter (<strong>in</strong><br />

neonates) at <strong>the</strong> time of or before<br />

<strong>the</strong> onset of <strong>the</strong> <strong>in</strong>fection<br />

• Estimated mortality <strong>is</strong> 12-25% for<br />

each <strong>CLABSI</strong> 1<br />

Cost to <strong>the</strong> healthcare system est. $34,000-$56,000/<strong>CLABSI</strong><br />

$296 mil- $2.3 bil. <strong>in</strong> US/year 2,3,4


Central L<strong>in</strong>e-associated<br />

Bloodstream Infection<br />

(<strong>CLABSI</strong>)<br />

• <strong>CLABSI</strong> surveillance utilizes <strong>the</strong><br />

Major Event Type: BSI<br />

• <strong>CLABSI</strong>= Primary BSI that<br />

develops <strong>in</strong> a patient that had a<br />

central l<strong>in</strong>e with<strong>in</strong> <strong>the</strong> 48 hours<br />

prior to <strong>the</strong> <strong>in</strong>fection onset.<br />

NOTE: <strong>The</strong>re <strong>is</strong> no m<strong>in</strong>imum time period that <strong>the</strong> central l<strong>in</strong>e<br />

must be <strong>in</strong> place <strong>in</strong> order for <strong>the</strong> BSI to be considered central<br />

l<strong>in</strong>e-associated.


48 Hour Rule<br />

• <strong>CLABSI</strong>s are attributed to <strong>the</strong><br />

patient location at <strong>the</strong> onset of <strong>the</strong><br />

BSI<br />

• If <strong>the</strong> BSI develops <strong>in</strong> a patient<br />

with<strong>in</strong> 48 hours of d<strong>is</strong>charge from a<br />

location, <strong>in</strong>dicate <strong>the</strong> d<strong>is</strong>charg<strong>in</strong>g<br />

location on <strong>the</strong> <strong>in</strong>fection report


Def<strong>in</strong>ition: Central L<strong>in</strong>e<br />

A vascular <strong>in</strong>fusion device that term<strong>in</strong>ates at or close<br />

to <strong>the</strong> heart or <strong>in</strong> one of <strong>the</strong> great vessels <strong>and</strong> <strong>is</strong> used<br />

for <strong>in</strong>fusion, withdrawal of blood, or hemodynamic<br />

monitor<strong>in</strong>g.


Def<strong>in</strong>ition: Central L<strong>in</strong>e<br />

<strong>The</strong> follow<strong>in</strong>g are considered great vessels for <strong>the</strong><br />

purpose of report<strong>in</strong>g central l<strong>in</strong>e <strong>in</strong>fections <strong>and</strong><br />

count<strong>in</strong>g central l<strong>in</strong>e days<br />

• Aorta<br />

• Pulmonary artery<br />

• Superior vena cava<br />

• Inferior vena cava<br />

• Barchiocephalic ve<strong>in</strong>s<br />

• Internal jugular ve<strong>in</strong>s<br />

• Subclavian ve<strong>in</strong>s<br />

• External iliac ve<strong>in</strong>s<br />

• Common femoral ve<strong>in</strong>s


Infusion<br />

• Introduction of a solution through a<br />

blood vessel via a ca<strong>the</strong>ter lumen<br />

• Includes:<br />

– Cont<strong>in</strong>uous <strong>in</strong>fusions such as<br />

nutritious fluids or medications, or<br />

– Intermittent <strong>in</strong>fusions such as<br />

flushes or IV antimicrobial<br />

adm<strong>in</strong><strong>is</strong>tration<br />

– Adm<strong>in</strong><strong>is</strong>tration of blood or blood<br />

products <strong>in</strong> <strong>the</strong> case of transfusion<br />

or hemodialys<strong>is</strong>


Note<br />

• Nei<strong>the</strong>r <strong>the</strong> location of <strong>the</strong> <strong>in</strong>sertion site<br />

nor <strong>the</strong> type of device may be used to<br />

determ<strong>in</strong>e if a l<strong>in</strong>e qualifies as a central<br />

l<strong>in</strong>e<br />

• Pacemaker wires <strong>and</strong> o<strong>the</strong>r non-lumened<br />

devices <strong>in</strong>serted <strong>in</strong>to central blood vessels<br />

or <strong>the</strong> heart are not considered central<br />

l<strong>in</strong>es, because fluids are not <strong>in</strong>fused,<br />

pushed, nor withdrawn through such<br />

devices.


Bloodstream Infection<br />

Def<strong>in</strong>itions :<br />

Event Type LCBI:<br />

Criterion 1


LCBI – Criterion 1<br />

Example: Jon Smith had a PICC l<strong>in</strong>e<br />

<strong>in</strong>serted on adm<strong>is</strong>sion (June 1). On<br />

hospital day 4, he became confused<br />

<strong>and</strong> experienced chills. Blood cultures<br />

were drawn which grew E. faecal<strong>is</strong>.<br />

Mr. Smith meets <strong>the</strong> criteria for LCBI<br />

Criterion 1.


LCBI Criterion 2


LCBI Criterion 3


Bloodstream Infection: Event<br />

Type: Cl<strong>in</strong>ical Seps<strong>is</strong>


One or more blood<br />

cultures means that at<br />

least one bottle from a<br />

blood draw <strong>is</strong> reported by<br />

<strong>the</strong> laboratory as hav<strong>in</strong>g<br />

grown organ<strong>is</strong>ms (i.e., <strong>is</strong><br />

a positive blood culture).<br />

Recognized pathogen does<br />

not <strong>in</strong>clude organ<strong>is</strong>ms<br />

considered common sk<strong>in</strong><br />

contam<strong>in</strong>ants. A few of <strong>the</strong><br />

recognized pathogens are<br />

Staph aureus, Enterococcus<br />

spp., E. coli, Pseudomonas<br />

spp., Klebsiella spp., C<strong>and</strong>ida<br />

spp., etc.


<strong>The</strong> phrase “two or more blood cultures (BC)<br />

drawn on separate occasions” means:<br />

1. That blood from at least two blood draws<br />

were collected with<strong>in</strong> two days of each o<strong>the</strong>r,<br />

<strong>and</strong><br />

2. That at least one bottle from each blood draw<br />

<strong>is</strong> reported by <strong>the</strong> laboratory as hav<strong>in</strong>g grown<br />

<strong>the</strong> same common sk<strong>in</strong> contam<strong>in</strong>ant organ<strong>is</strong>m<br />

(i.e., <strong>is</strong> a positive BC)


Determ<strong>in</strong><strong>in</strong>g “sameness”<br />

of two organ<strong>is</strong>ms<br />

If <strong>the</strong> common sk<strong>in</strong> contam<strong>in</strong>ant from one culture <strong>is</strong><br />

identified to both genus <strong>and</strong> species level (e.g., S.<br />

epidermid<strong>is</strong>) <strong>and</strong> <strong>the</strong> companion culture identifies only <strong>the</strong><br />

genus with or without o<strong>the</strong>r attributes (<strong>in</strong> th<strong>is</strong> example,<br />

coagulase-negative staphylococci), <strong>the</strong>n it <strong>is</strong> assumed that<br />

<strong>the</strong> organ<strong>is</strong>ms are <strong>the</strong> same.<br />

Report <strong>the</strong> genus/species to NHSN, i.e., <strong>in</strong> th<strong>is</strong> example,<br />

report S. epidermid<strong>is</strong>. See o<strong>the</strong>r examples below:


Determ<strong>in</strong><strong>in</strong>g “sameness”<br />

of two organ<strong>is</strong>ms<br />

If common sk<strong>in</strong> contam<strong>in</strong>ant<br />

organ<strong>is</strong>ms are speciated (e.g.,<br />

both are B. cereus), but no<br />

antibiograms are done, or <strong>the</strong>y<br />

are done for only one of <strong>the</strong><br />

<strong>is</strong>olates, it <strong>is</strong> assumed that <strong>the</strong><br />

organ<strong>is</strong>ms are <strong>the</strong> same.


Determ<strong>in</strong><strong>in</strong>g “sameness” of<br />

two organ<strong>is</strong>ms (cont.)<br />

If <strong>the</strong> common sk<strong>in</strong> contam<strong>in</strong>ants from <strong>the</strong> cultures<br />

have antibiograms that are different for two or more<br />

antimicrobial agents, it <strong>is</strong> assumed that <strong>the</strong><br />

organ<strong>is</strong>ms are not <strong>the</strong> same.<br />

Examples:


Collect<strong>in</strong>g Blood Culture<br />

Specimens<br />

Ideally, blood specimens for culture should<br />

be obta<strong>in</strong>ed from two to four blood draws<br />

from separate venipuncture sites (e.g., right<br />

<strong>and</strong> left antecubital ve<strong>in</strong>s), not through a<br />

vascular ca<strong>the</strong>ter.<br />

<strong>The</strong>se blood draws should be performed simultaneously or<br />

over a short period of time (i.e., with<strong>in</strong> a few hours).<br />

If your facility does not currently obta<strong>in</strong> specimens us<strong>in</strong>g<br />

th<strong>is</strong> technique, you may still report BSIs us<strong>in</strong>g <strong>the</strong> NHSN<br />

criteria, but you should work with appropriate personnel to<br />

facilitate better specimen collection practices for blood<br />

cultures.


Case 1<br />

• James <strong>is</strong> a 28 year old patient with a central<br />

l<strong>in</strong>e who <strong>is</strong> 3 days post colon surgery on April<br />

1. He spikes a fever <strong>and</strong> has blood cultures<br />

x2 drawn; on April 2, 1 set <strong>is</strong> negative, 1<br />

bottle from <strong>the</strong> second set <strong>is</strong> positive for<br />

Bacillus cereus. H<strong>is</strong> doctor orders antibiotics<br />

<strong>and</strong> notes “postop seps<strong>is</strong>” <strong>in</strong> <strong>the</strong> chart.<br />

How should th<strong>is</strong> be reported?


Case 1<br />

• On April 2 nd , ano<strong>the</strong>r set<br />

of blood cultures are<br />

collected <strong>and</strong> ½ bottles<br />

grow B. cereus.<br />

Susceptibilities of <strong>the</strong> 2<br />

organ<strong>is</strong>ms are shown:<br />

Organ<strong>is</strong>m Azithromyc<strong>in</strong> Cetriaxone Gentamyc<strong>in</strong> Piperacill<strong>in</strong> Vancomyc<strong>in</strong><br />

#1 S R S R S<br />

#2 S S S R S


Case 1<br />

• Is th<strong>is</strong> a BSI?<br />

• If yes, what criteria?<br />

• If yes, what date of<br />

onset?<br />

Organ<strong>is</strong>m Azithromyc<strong>in</strong> Cetriaxone Gentamyc<strong>in</strong> Piperacill<strong>in</strong> Vancomyc<strong>in</strong><br />

#1 S R S R S<br />

#2 S S S R S


Case 1<br />

• What if <strong>the</strong> patient was 3<br />

weeks old?<br />

Organ<strong>is</strong>m Azithromyc<strong>in</strong> Cetriaxone Gentamyc<strong>in</strong> Piperacill<strong>in</strong> Vancomyc<strong>in</strong><br />

#1 S R S R S<br />

#2 S S S R S


Case 2<br />

• A patient with a PICC placed <strong>in</strong> ano<strong>the</strong>r facility has<br />

been <strong>in</strong> our hospital for <strong>the</strong> past week <strong>and</strong> now has<br />

a blood culture grow<strong>in</strong>g Ac<strong>in</strong>etobacter baumanii.<br />

Is th<strong>is</strong> a BSI?<br />

Is th<strong>is</strong> a <strong>CLABSI</strong>?<br />

Should it be attributed to our hospital or to <strong>the</strong><br />

facility that placed <strong>the</strong> PICC?


Case 2<br />

• What if <strong>the</strong> patient also has an <strong>in</strong>crease <strong>in</strong><br />

h<strong>is</strong> sputum, <strong>and</strong> developed rales, a fever<br />

of 38 C <strong>and</strong> has two chest xrays with<br />

<strong>in</strong>creased consolidation <strong>in</strong> h<strong>is</strong> right lower<br />

lobe, <strong>in</strong> <strong>the</strong> two days before h<strong>is</strong> blood<br />

culture?<br />

Is th<strong>is</strong> a BSI?<br />

Why or why not?


An 81 year old patient was <strong>in</strong> MICU for a week with a<br />

central l<strong>in</strong>e <strong>in</strong> place <strong>the</strong> entire time. Just prior to<br />

d<strong>is</strong>charge from <strong>the</strong> MICU to a medical ward, <strong>the</strong> l<strong>in</strong>e was<br />

pulled. With<strong>in</strong> 36 hours, she became d<strong>is</strong>oriented <strong>and</strong><br />

hypotensive. Blood cultures x 2 were drawn <strong>and</strong> 3 of 4<br />

bottles grew Micrococci <strong>and</strong> coagulase-negative<br />

staphylococci.<br />

Is th<strong>is</strong> a BSI?<br />

Is th<strong>is</strong> a <strong>CLABSI</strong>?<br />

<strong>Criteria</strong>?<br />

Case 3


Location of attribution?<br />

Case 3<br />

Organ<strong>is</strong>m(s)?


Case 4<br />

• Patient admitted to MICU on 1/21 due to GI bleed<br />

• L subclavian l<strong>in</strong>e placed on 1/22<br />

• 1/28 patient spikes fever (102.1 F); blood specimen for<br />

culture drawn through <strong>the</strong> l<strong>in</strong>e x 1; l<strong>in</strong>e removed <strong>and</strong> tip<br />

sent for culture<br />

• 1/3 blood <strong>and</strong> tip culture positive for coagulase-negative<br />

staphylococci<br />

Is th<strong>is</strong> a <strong>CLABSI</strong>?


Case 5<br />

• 85-year old female admitted from an<br />

extended care facility. Recent onset<br />

confusion <strong>and</strong> ur<strong>in</strong>ary <strong>in</strong>cont<strong>in</strong>ence.<br />

Started on antibiotics.<br />

PMH: Hypertension, recent CVA, Insul<strong>in</strong>dependant<br />

diabetic<br />

• Day 1: Temp 37.5 C, pan cultured<br />

(blood, ur<strong>in</strong>e, sputum). Foley ca<strong>the</strong>ter<br />

<strong>in</strong>serted. Blood sugar 198. PICC l<strong>in</strong>e<br />

<strong>in</strong>serted. Admitted to ICU.


Case 5<br />

• Day 3: All cultures negative, antibiotics<br />

D/Cd. Blood sugar rema<strong>in</strong>s unstable.<br />

• Day 6: Temp 39.5 . Noted to have<br />

suprapubic tenderness <strong>and</strong> shak<strong>in</strong>g<br />

chills. Pan cultures repeated, antibiotics<br />

restarted, CXR clear. PICC d/c <strong>and</strong> tip<br />

cultured.<br />

• Day 8: Ur<strong>in</strong>e culture ≥10 5 MRSA. Blood<br />

culture 2 of 3 <strong>and</strong> PICC tip positive for<br />

MRSA.


Case 5<br />

• Day 10: Improv<strong>in</strong>g ur<strong>in</strong>e clear transferred back to<br />

long-term care on antibiotics.<br />

• Does th<strong>is</strong> patient have a HAI UTI?<br />

• If so, what type?<br />

• Does <strong>the</strong> patient have a bacteremia?<br />

• If so, what type?


Case 6<br />

• 8/14- A 41 year old female presents to <strong>the</strong><br />

Emergency Room <strong>in</strong> diabetic coma <strong>and</strong> with<br />

anemia. She has a subclavian ca<strong>the</strong>ter<br />

<strong>in</strong>serted <strong>in</strong> <strong>the</strong> Emergency Room. <strong>The</strong> next<br />

day, <strong>in</strong> <strong>the</strong> ICU, she has a midl<strong>in</strong>e central<br />

ca<strong>the</strong>ter <strong>in</strong>serted for blood transfusions. 8/21-<br />

she develops fever to 39 C, <strong>and</strong> shak<strong>in</strong>g chills.<br />

2 sets of blood cultures sent.<br />

• 8/15- blood cultures positive for Pseudomonas<br />

aerg<strong>in</strong>osa. Nei<strong>the</strong>r <strong>in</strong>sertion site shows<br />

<strong>in</strong>flammation <strong>and</strong> <strong>the</strong>re <strong>is</strong> no o<strong>the</strong>r<br />

documented <strong>in</strong>fection


• Is <strong>the</strong>re a BSI?<br />

Case 6<br />

• If so, what type?<br />

• <strong>Criteria</strong>?<br />

• If so, which l<strong>in</strong>e should <strong>the</strong> BSI be<br />

attributed to?


Case 6<br />

• What unit should be <strong>in</strong>dicated for<br />

<strong>the</strong> Location of Device Insertion<br />

field?


Case 7<br />

• Day 1: One-day-old tw<strong>in</strong> male <strong>in</strong>fant admitted<br />

<strong>and</strong> emergently transferred to Neonatal<br />

Intensive Care Unit. Vented <strong>in</strong> <strong>is</strong>olette dur<strong>in</strong>g<br />

transport. Peripheral IV <strong>in</strong> scalp, IV fluid at<br />

1cc/hr with Prost<strong>in</strong> (0.05mcg/kg/m<strong>in</strong>) started<br />

prior to transport, <strong>and</strong> umbilical ca<strong>the</strong>ter<br />

<strong>in</strong>serted upon adm<strong>is</strong>sion to NICU.<br />

• Neonatal H<strong>is</strong>tory: Gestational age-term<br />

<strong>in</strong>fant, birth wt. 1810 grams, Apgars 8 & 9.<br />

A cardiac echocardiogram showed<br />

transposition of <strong>the</strong> great vessels of <strong>the</strong><br />

heart.


Case 7<br />

• Day 3: Repair of Patent Ductus Arteriosus <strong>and</strong> Atrial<br />

Septal Defect performed; later that day <strong>the</strong> umbilical<br />

ca<strong>the</strong>ter site was noted to be slightly red.<br />

• Day 4: umbilical ca<strong>the</strong>ter site rema<strong>in</strong>ed slightly red<br />

<strong>and</strong> a low grade temperature developed.<br />

• Day 5: <strong>the</strong> umbilical l<strong>in</strong>e was pulled, 1 blood culture<br />

was drawn <strong>and</strong> <strong>the</strong> umbilical ca<strong>the</strong>ter tip was sent for<br />

culture.<br />

• Day 6: cont<strong>in</strong>ued elevated temp of 38.1 <strong>and</strong><br />

antibiotics were started.<br />

• Day 7: <strong>the</strong> culture <strong>and</strong> umbilical ca<strong>the</strong>ter tip were<br />

both positive for Aerococcus sp. Antibiotics adjusted<br />

as needed for coverage. Patient cl<strong>in</strong>ically improv<strong>in</strong>g.


Case 7<br />

• Does th<strong>is</strong> patient have an HAI?<br />

• If so, what type?<br />

• <strong>Criteria</strong><br />

• What if both cultures were positive for<br />

Staphylococcus aureus?


Case 8<br />

• Baby girl Jones <strong>is</strong> born at 35<br />

weeks <strong>and</strong> weighs 1200 grams at<br />

birth. An <strong>in</strong>fusion l<strong>in</strong>e <strong>is</strong> placed<br />

<strong>in</strong>to her umbilical ve<strong>in</strong> after<br />

adm<strong>is</strong>sion to <strong>the</strong> NICU. 2 days<br />

after birth, her core temperature<br />

drops to 35° C, she <strong>is</strong> diagnosed<br />

with seps<strong>is</strong> <strong>and</strong> started on<br />

antibiotics. A s<strong>in</strong>gle blood culture<br />

<strong>is</strong> drawn <strong>and</strong> returns positive for<br />

C<strong>and</strong>ida albicans 2 days later.


Case 8<br />

• Is <strong>the</strong> criteria for a lab confirmed<br />

bloodstream <strong>in</strong>fection met?<br />

• If her blood culture had been<br />

negative, would <strong>the</strong> criteria for<br />

cl<strong>in</strong>ical seps<strong>is</strong> be met?<br />

• What would be assigned as a<br />

pathogen?


Case 8<br />

• What criteria would be met if blood<br />

cultures had been drawn on Day 2<br />

<strong>and</strong> Day 3 <strong>and</strong> both were positive<br />

for S. epidermid<strong>is</strong> with <strong>the</strong> same<br />

antibiogram?


Case 9<br />

• 6/4-49 year old diabetic patient admitted <strong>in</strong><br />

diabetic coma. Patient with left foot with pa<strong>in</strong>ful<br />

swollen, red <strong>and</strong> warm to touch, but without<br />

dra<strong>in</strong>age. Subclavian l<strong>in</strong>e <strong>in</strong>serted <strong>in</strong> E.R. Patient<br />

admitted to MICU. Temp 37.8 C. Antibiotics<br />

begun for “cellulit<strong>is</strong>”<br />

• 6/6 Temp 38.2 C. Hypotension. Blood cultures x 2<br />

sets collected.<br />

• 6/7 Staph aureus cultured from blood x2.<br />

Does th<strong>is</strong> patient have an BSI?<br />

Primary or secondary?<br />

What <strong>is</strong> <strong>the</strong><br />

primary <strong>in</strong>fection?


Case 9


Collect<strong>in</strong>g Summary Data<br />

• NHSN Protocol for <strong>the</strong> collection of<br />

device-associated <strong>in</strong>fection<br />

denom<strong>in</strong>ators:<br />

– Patient Days: at <strong>the</strong> same time<br />

every day count <strong>the</strong> number of<br />

patients on <strong>the</strong> unit<br />

– Device Days: at <strong>the</strong> same time<br />

every day, count <strong>the</strong> number of<br />

patients with one or more devices<br />

(pt with >2 gets counted as 1)


Collect<strong>in</strong>g Summary Data<br />

• Data collected differs accord<strong>in</strong>g to<br />

location<br />

• <strong>CLABSI</strong>:<br />

– SCAs:<br />

• # pts.with permanent central l<strong>in</strong>es<br />

• # pts with temp central l<strong>in</strong>es<br />

• Pts with both count only temp l<strong>in</strong>e<br />

– NICUs: stratified by birthweight<br />

• # pts with central l<strong>in</strong>e<br />

• # pts with umbilical l<strong>in</strong>e<br />

• Pts with both count only umbilical l<strong>in</strong>e


Collect<strong>in</strong>g ICU/O<strong>the</strong>r<br />

Summary Data


Collect<strong>in</strong>g SCA Summary<br />

Data


Collect<strong>in</strong>g NICU Summary<br />

Data


Collect<strong>in</strong>g Summary Data<br />

• MICU – collect<strong>in</strong>g patient days <strong>and</strong><br />

device days on June 8 at noon<br />

Patient ADT Vascular Ur<strong>in</strong>ary Respiratory<br />

101 Smith Home @ 9 am PICC home w/<br />

pt<br />

Indwell<strong>in</strong>g foley<br />

to DD<br />

102 Wash<strong>in</strong>gton Day 3 Peripheral IV Bedpan – cath<br />

spec to lab<br />

103 Doe Adm 10 am IJ CL <strong>in</strong>serted<br />

at 2 pm<br />

104 -----<br />

105 Chen Day 2 Swan Ganz<br />

<strong>and</strong><br />

PICC<br />

106 Jones Day 8 Subclavian CL<br />

cont<br />

107 Gonzales D/C to nurs<strong>in</strong>g<br />

home @ 4 pm<br />

Peripheral l<strong>in</strong>e<br />

d/c at 1 pm<br />

Void<strong>in</strong>g<br />

Suprapubic to<br />

direct dra<strong>in</strong>age<br />

Indwell<strong>in</strong>g foley<br />

to DD<br />

Incont<strong>in</strong>ent<br />

O2 @2L/m<strong>in</strong><br />

cont<br />

IPPB q 6 hours<br />

O2 @ 2L/m<strong>in</strong><br />

prn<br />

Intubated/vent<br />

Trach / vent<br />

Suctioned prn


Collect<strong>in</strong>g Summary Data<br />

How many patient days<br />

are counted for th<strong>is</strong><br />

MICU on June 8?<br />

A. 7<br />

B. 6<br />

C. 5<br />

D. 4<br />

E. 3<br />

Patient<br />

ADT<br />

101 Smith Home @ 9 am<br />

102 Wash<strong>in</strong>gton Day 3<br />

103 Doe Adm 10 am<br />

104 -----<br />

105 Chen Day 2<br />

106 Jones Day 8<br />

107 Gonzales D/C to nurs<strong>in</strong>g<br />

home @ 4 pm


Collect<strong>in</strong>g Summary Data<br />

How many central l<strong>in</strong>e<br />

days?<br />

A. 6<br />

B. 5<br />

C. 3<br />

D. 2<br />

E. 0<br />

Patient ADT Vascular<br />

101 Smith Home @ 9 am PICC home w/<br />

pt<br />

102 Wash<strong>in</strong>gton Day 3 Peripheral IV<br />

103 Doe Adm 10 am IJ CL <strong>in</strong>serted at<br />

2 pm<br />

104 -----<br />

105 Chen Day 2 Swan Ganz <strong>and</strong><br />

PICC<br />

106 Jones Day 8 Subclavian CL<br />

cont<br />

107 Gonzales D/C to nurs<strong>in</strong>g<br />

home @ 4 pm<br />

Peripheral l<strong>in</strong>e<br />

d/c at 1 pm


Collect<strong>in</strong>g Summary Data<br />

How many <strong>in</strong>dwell<strong>in</strong>g<br />

ca<strong>the</strong>ter days?<br />

A. 6<br />

B. 5<br />

C. 4<br />

D. 3<br />

E. 2<br />

F. 1<br />

Patient ADT Ur<strong>in</strong>ary<br />

101 Smith Home @ 9 am Indwell<strong>in</strong>g foley<br />

to DD<br />

102 Wash<strong>in</strong>gton Day 3 Bedpan – cath<br />

spec to lab<br />

103 Doe Adm 10 am Void<strong>in</strong>g<br />

104 -----<br />

105 Chen Day 2 Suprapubic to<br />

direct dra<strong>in</strong>age<br />

106 Jones Day 8 Indwell<strong>in</strong>g foley<br />

to DD<br />

107 Gonzales D/C to nurs<strong>in</strong>g<br />

home @ 4 pm<br />

Incont<strong>in</strong>ent


References<br />

• AJIC: American Journal of<br />

Infection Control, Volume 36, Issue<br />

5, Pages 309-332, June 2008,<br />

Authors:Teresa C. Horan; Mary<br />

Andrus; Margaret A. Dudeck.<br />

www.ajicjournal.org/article/S0196-<br />

6553(08)00167.../abstract


Co-organized by:<br />

Save <strong>the</strong> Date<br />

Fifth Decennial<br />

International Conference on<br />

Healthcare-Associated<br />

Infections<br />

March 18-22, 2010<br />

Hyatt Regency Atlanta<br />

Atlanta, Georgia<br />

www.decennial2010.com


nhsn@cdc.gov

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