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NHSN Surveillance Case
Studies
Rachel Cathey, MPH, CIC
Healthcare-Associated Infections Epidemiologist
April 25, 2019
Central Line-Associated Bloodstream Infections
Key Terms and Definitions
Present on Admission (POA) vs.
Healthcare-Associated Infection (HAI)
Hospital DayDate of Event
AssignmentClassification
2 days before admit Hospital Day 1
POA1 day before admit Hospital Day 1
1 Hospital Day 1
2 Hospital Day 2
3 Hospital Day 3
HAI4 Hospital Day 4
5 Hospital Day 5
Infection Window Period (IWP)
7 day period in which all site-specific
infection criteria must be met
Infe
cti
ou
s W
ind
ow
Pe
rio
d
3 days
before
Date of first positive diagnostic test that is used as an element
of the site-specific criterion
OR
In the absence of a diagnostic test, use the date of the first
documented localized sign or symptom that is used as an
element of the site-specific criterion
3 days
after
Repeat Infection Timeframe (RIT)
• 14-day timeframe during which no new infections of the same type are reported
• Applies to POA and HAI determination
• DOE is Day 1 of the 14-day RIT
• If criteria for the same type of infection are met and the date of event is within the 14-day RIT, a new event is not identified or reported
• Additional pathogens identified are added to the event
• RIT does not carry over from one admission to another
Example: Miss Lady
• June 3 – Miss Lady was admitted to the ICU
• June 4 – A blood culture was collected that resulted in E. coli
• June 10 – A subsequent blood culture resulted in K. pneumonia
• The June 4 culture is found to be a primary BSI
Should the June 10th
specimen be reported as a
new event?a. Yes
b. No
• June 3 – admitted to ICU
• June 4 – BC+ E. coli
• June 10 – BC+ K. pneumonia
Hospital
DayDate First Diagnostic Test IWP POA RIT Notes
-2 6/1
I
W
P
P
O
A
-1 6/2
1 6/3 Admitted
2 6/4 Blood cx: E. coli
R
I
T
3 6/5
4 6/6
5 6/7
6 6/8
7 6/9
8 6/10 Blood cx: K. pneumonia
9 6/11
10 6/12
11 6/13
12 6/14
13 6/15
14 6/16
15 6/17
16 6/18
17 6/19
LCBI 1 Criterion
• Patient of any age has a recognized
pathogen identified from one or more blood
specimens by a culture or non-culture based
microbiologic testing method
AND
• Organism(s) identified in blood is not related
to an infection at another site
DOE: date of the blood specimen collection identifying an
organism in the blood; no symptom required
Example: Mr. Shannon
• June 3 – Mr. Shannon was admitted to CCU after having a heart attack
• June 4 – A central line was placed
• June 7 – A blood culture was collected because he became confused and was having chills
– Culture resulted Serratia marcescens (a recognized pathogen)
• No other source of infection was identified
Is this an LCBI 1?
a. Yes
b. No
Hospital Day Date DOE IWP Notes
1 6/3 Admitted
2 6/4 Central Line inserted, CCU
3 6/5
4 6/6
5 6/7 Blood culture: S. marcescens
6 6/8
7 6/9
8 6/10
9 6/11
10 6/12
• June 3 – admitted to CCU
• June 4 – central line placed
• June 7 – BC+ S. marcescens
LCBI 2 Criterion
• Any age patient have at least one: fever (>38.0◦C), chills, or hypotension
AND
• Organism(s) identified in blood is not related to an infection at another site
AND
• The same NHSN common commensal is identified from two or more blood specimens drawn on separate occasions by a culture or non-culture based microbiologic testing method
LCBI 2 Criterion
• All elements must occur within the 7-day IWP
– Collection date of the positive blood specimen
– 3 days before
– 3 days after
• The two matching CC specimens represent a single element for use in meeting the criteria and the collection date of the first is used to determine the BSI IWP
• At least one element (fever, chills, or hypotension) is required to meet LCBI 2
Date of Event (DOE)
• First date an element that is used to
meet the LCBI 2 or 3 criteria (symptom
or the first of 2 cultures with matching
CC) occurs within the BSI IWP
ExampleDate Element IWP Notes
6/3
6/4
6/5 Fever > 38.0◦F LCBI 2 DOE
6/6
6/7 Blood culture: S. epidermidis (1 of 2) Date of 1st diagnostic test
6/8 Blood culture: S. epidermidis (2 of 2)
6/9
6/10
6/11
6/12
ExampleDate Element IWP Notes
6/3
6/4
6/5
6/6
6/7 Blood culture: S. epidermidis (1 of 2)Date of 1st diagnostic test;
DOE
6/8 Blood culture: S. epidermidis (2 of 2)
6/9
6/10 Fever > 38.0◦F
6/11
6/12
Ms. Lady (LCBI 2 Scenario)
• June 3 – Ms. Lady was admitted to the oncology ward and a central line was placed
• June 4 – She developed a fever (102◦F)
• June 6 – Blood culture was collected that grew S. epidermidis
• June 7 – Repeat blood culture collected grew S. epidermidis
• No other source of infection was identified
What is Ms. Lady’s Date of
Event?
a. 6/6
b. 6/4
c. 6/7
• June 3 – admitted; CL placed
• June 4 – fever (102◦F)
• June 6 – Positive blood culture
• June 7 – matching repeat blood
culture
Is it POA or HAI?
a. POA
b. HAIHospital Day Date First Diagnostic Test IWP POA Notes
-2 6/1
P
O
A
-1 6/2
1 6/3
I
W
P
Admitted
2 6/4 Fever 102F
3 6/5
4 6/6 Blood cx – S. epidermidis
5 6/7 Blood cx – S. epidermidis
6 6/8
7 6/9
8 6/10
• June 3 – admitted; CL placed
• June 4 – fever (102◦F)
• June 6 – Positive blood cultures
• June 7 – matching repeat blood
cultures
LCBI 3 Criterion
A patient ≤ 1 year of age have at least one: fever (>38.0◦C), apnea, hypothermia (<36.0 ◦C), or bradycardia
AND
Organism(s) identified in blood is not related to an infection at another site
AND
The same NHSN common commensal is identified from two or more blood specimens drawn on separate occasions by a culture or non-culture based microbiologic testing method
LCBI 3 Criterion
• LCBI 1 and 2 can be used for this population
• All elements must occur within the 7-day IWP– Collection date of the positive blood specimen
– 3 days before
– 3 days after
• The two matching CC specimens represent a single element for use in meeting the criteria and the collection date of the first is used to determine the BSI IWP
• At least one element (fever, hypothermia, apnea, or bradycardia) is required to meet LCBI 3
Date of Event (DOE)
• First date an element that is used to
meet the LCBI 2 or 3 criteria (symptom
or the first of 2 cultures with matching
common commensal) occurs within the
BSI IWP
– Symptom required
Baby Girl (LCBI 3 Scenario)
• March 1 – 4 mo. old baby girl was
admitted; afebrile with no symptoms of an
infection
• March 2 – She developed a fever and
periods of bradycardia; 2 blood cultures
were collected – one specimen grew
Micrococcus spp. (a common commensal)
and the other had no growth
What criteria does baby girl
meet?
a. LCBI 2
b. LCBI 3
c. This is a trick question – she doesn’t
meet criteria
Baby Boy (LCBI 3 Scenario)
• June 5 – baby boy was admitted to the NICU
• June 7 – central line is placed
• June 8 – new onset of apnea
• June 9 – he developed a low grade fever and 2 sets of blood cultures were drawn separately both growing Streptococcus viridans
• No other source of infection identified
What criteria does baby boy
meet?
a. LCBI 2
b. LCBI 3
Explanation
Hospital Day Date First Diagnostic Test IWP DOE Notes
1 6/5 Admitted
2 6/6
I
W
P
3 6/7 CL inserted
4 6/8 DOE Apnea onset
5 6/9 Blood cx: S. viridans x2
6 6/10
7 6/11
8 6/12
+BC sets the IWPDOE because
apnea is the first
element met
Central LineAn intravascular catheter that terminates at or close to the heart OR in one of the great vessels which is used for infusion, withdrawal of blood, or hemodynamic monitoring
Types of Central Lines
• Temporary: a non-tunneled, non-implanted catheter
• Permanent: a tunneled catheter or implanted catheter (including port)
• Umbilical catheter: inserted through the umbilical artery or vein in a neonate
NOT Central Lines
• Arterial catheters
• Arteriovenous fistula
• Arteriovenous graft
• Atrial catheters
• Extracorporeal membrane oxygenation
• Hemodialysis reliable outflow dialysis catheter
• Intra-aortic balloon pump
• Peripheral IV or midline
• Ventricular Assist Device
Central Line Access
The performance of any of the following activities during the current inpatient admission:
• Line placement
• Use of (entering the line with a needle or needless device) any central line for:
– Infusion
– Withdrawal of blood
• Use for hemodynamic monitoring
Eligible Central Line
• Has been in place > 2 consecutive
calendar days following the first access
of the CL in an inpatient location during
the current admission
• Eligible for CLABSI events until the day
after removal from the body or patient
discharge, whichever comes first
Central Line-Associated BSI
(CLABSI)
A laboratory-confirmed bloodstream
infection where the eligible BSI organism
is identified and an eligible central line is
present on the LCBI DOE or the day
before
Examples of Associating the Use of Central
Lines to BSI Events
Date April 1 April 2 April 3 April 4 April 5 April 6 April 7
Patient A:
Port Status
Port in Port in Port in Port in Port in Port in Port in
Accessed No No Yes Yes Yes Yes Yes
Eligible for
CLABSI
event?
No
-
No
-
No
CL Day 1
No
CL Day 2
Yes
CL Day 3
Yes
CL Day 4
Yes
CL Day 5
Date April 1 April 2 April 3 April 4 April 5 April 6 April 7
Patient B:
CL Status
CL in CL in CL in CL in CL in /
CL out
No device No device
Accessed No No Yes Yes Removed No No
Eligible for
CLABSI
event?
No
-
No
-
No
CL Day 1
No
CL Day 2
Yes
CL Day 3
Yes
-
No
-
Examples of Associating the Use of Central
Lines to BSI Events
Date April 1 April 2 April 3 April 4 April 5 April 6 April 7
Patient C:
CL Status
CL in CL in CL in /
CL out
CL in CL in CL in /
CL out
No device
Accessed Yes Yes Removed Placed Yes Removed -
Eligible for
CLABSI
event?
Yes
CL Day 3
Yes
CL Day 4
Yes
CL Day 5
Yes
CL Day 6
Yes
CL Day 7
Yes
CL Day 8
Yes
-
Date April 1 April 2 April 3 April 4 April 5 April 6 April 7
Patient D:
CL Status
No device CL in CL in CL in CL in CL in CL in
Accessed - Placed Yes Yes Yes Yes Yes
Eligible for
CLABSI
event?
-
-
No
CL Day 1
No
CL Day 2
Yes
CL Day 3
Yes
CL Day 4
Yes
CL Day 5
Yes
CL Day 6
*Admitted on March 30 with central line in place
Examples of Associating the Use of Central
Lines to BSI Events
Date April 1 April 2 April 3 April 4 April 5 April 6 April 7
Patient E:
CL Status
CL in CL in CL in /
CL out
No device CL in CL in CL in
Accessed Yes Yes Removed - Placed Yes Yes
Eligible for
CLABSI
event?
Yes
CL Day 3
Yes
CL Day 4
Yes
CL Day 5
Yes No
CL Day 1
No
CL Day 2
Yes
CL Day 3
*Admitted on March 30 with central line in place
Counting Denominator Days
• Count begins on the first day of CL (of any type) is present in an inpatient unit– Day of placement (during current admission)
– Day of admission (if patient is admitted with a CL in place)
• Count only one device day for each day that patient has at least one CL in place, regardless of how many CLs the patient has in place on the same day
• Continue counting until: – Device is removed
– Patient is discharged
Examples of Denominator Day Counts
Date April 1 April 2 April 3 April 4 April 5 April 6 April 7
Patient A: Inpatient
Location ICU
CL inserted
ICU CL
in
ICU CL
in
ICU CL
in
ICU CL
in
ICU CL
in
ICU CL
in
Denominator
Day Counts
Day 1 Day 2 Day 3 Day 4 Day 5 Day 6 Day 7
Date April 1 April 2 April 3 April 4 April 5 April 6 April 7
Patient B: ED CL in
place at time
of admission
Admitted
to ICU
CL in
ICU CL
in
ICU CL
in
ICU CL
in
ICU CL
in
ICU CL
in
Denominator
Day Counts
- Day 1 Day 2 Day 3 Day 4 Day 5 Day 6
Examples of Denominator Day Counts
Date April 1 April 2 April 3 April 4 April 5 April 6 April 7
Patient C: Inpatient
Location ICU
Pt. admitted
with non-
accessed
port
ICU Port
not
accessed
ICU Port
not
accessed
ICU Port
accessed
ICU Port
accessed
ICU Port
accessed
ICU Port
accessed
Denominator
Day Counts
Day 1 Day 2 Day 3 Day 4 Day 5 Day 6 Day 7
BREATHE… WE’RE HALFWAY
THERE!
HAI CASE STUDY 1
Ms. Polly Microbial
Ms. Polly Microbial
• 2/4: 32yo admitted to the ED with fever (102F) and abdominal pain. Patient has a port in place at time of admission. Past medical history includes cervical cancer.
• 2/5: Admitted to oncology floor and port is flushed
• 2/6: Patient complains of pain at the port site and insertion site is red.
• 2/8: blood cultures collected; positive for Candida albicans (a recognized pathogen)
• No other source of infection is identified
Question 1
What criteria did Ms. Polly meet?
a. LCBI 2
b. LCBI 1
c. Ms. Polly did not meet any criteria• 2/4: Admitted to the ED with fever (102F) and
abdominal pain.
• 2/5: Admitted to oncology floor and port is
flushed
• 2/6: Complains of pain at the port site and
insertion site is red
• 2/8: blood cultures collected; positive for
Candida albicans
Question 2
What is the date of event?
a. 2/5
b. 2/6
c. 2/8• 2/4: Admitted to the ED with fever (102F) and
abdominal pain.
• 2/5: Admitted to oncology floor and port is
flushed
• 2/6: Complains of pain at the port site and
insertion site is red
• 2/8: blood cultures collected; positive for
Candida albicans
Question 3
Is this a POA or HAI?
a. POA
b. HAIDate
Hospital
DayDOE Classification Notes
2/5 1 POA Admitted;
port flushed
2/6 2 POA
2/7 3 HAI
2/8 4 Blood
culture +
HAI
2/9 5 HAI
2/10 6 HAI
HAI CASE STUDY 2
Mr. Dude
Mr. Dude
• 2/11 – 55yo male admitted to the ED with rectal bleeding. Peripheral IV line placed. Past medical history shows end-stage renal disease (ESRD) and diabetes. He has a permanent HD catheter in place. Last HD performed, 2/10.
• 2/12 – Admitted to Renal floor
• 2/13 – Patient refused HD
• 2/14 – Patient consented to HD. HD performed.
• 2/17 – Fever 102◦F; Blood cultures collected – Pseudomonas putida x 1 (a recognized pathogen)
• 2/18 – HD central line removed.
• 2/19 – New HD central line replaced
No site-specific infection identified
Question 1
What criteria did Mr. Dude
meet?
a. LCBI 2
b. LCBI 1
c. Mr. Dude is fine.
Pseudomonas putida
doesn’t mean anything.
• 2/11 – admitted to the ED;
Peripheral IV line placed; has a
permanent HD catheter in
place. Last HD performed, 2/10.
• 2/12 – admitted to Renal floor
• 2/13 – Pt. refused HD
• 2/14 – Pt. consented to HD; HD
performed
• 2/17 – Fever 102◦F; blood
cultures collected; positive for
Pseudomonas putida
• 2/18 – HD CL removed.
• 2/19 – New HD CL replaced in
RIJ
Question 2
Is this a POA or HAI
event?
a. POA
b. HAI
• 2/11 – admitted to the ED;
Peripheral IV line placed; has a
permanent HD catheter in
place. Last HD performed, 2/10.
• 2/12 – admitted to Renal floor
• 2/13 – Pt. refused HD
• 2/14 – Pt. consented to HD; HD
performed
• 2/17 – Fever 102◦F; blood
cultures collected; positive for
Pseudomonas putida
• 2/18 – HD CL removed.
• 2/19 – New HD CL replaced in
RIJ
Question 3
Is this event central line
associated?
a. Yes
b. No
c. No event was
identified
• 2/11 – admitted to the ED;
Peripheral IV line placed; has a
permanent HD catheter in
place. Last HD performed, 2/10.
• 2/12 – admitted to Renal floor
• 2/13 – Pt. refused HD
• 2/14 – Pt. consented to HD; HD
performed
• 2/17 – Fever 102◦F; blood
cultures collected; positive for
Pseudomonas putida
• 2/18 – HD CL removed.
• 2/19 – New HD CL replaced in
RIJ
Question 4
What is the date of
event?
a. 2/16
b. 2/17
c. 2/18
d. I already told you…
he is FINE.
• 2/11 – admitted to the ED;
Peripheral IV line placed; has a
permanent HD catheter in
place. Last HD performed, 2/10.
• 2/12 – admitted to Renal floor
• 2/13 – Pt. refused HD
• 2/14 – Pt. consented to HD; HD
performed
• 2/17 – Fever 102◦F; blood
cultures collected; positive for
Pseudomonas putida
• 2/18 – HD CL removed.
• 2/19 – New HD CL replaced in
RIJ
Hospital
DayDate First Diagnostic Test IWP DOE RIT
HAI/POA
ClassificationNotes
1 2/11POA
Admitted to ED
2 2/12 Admitted to Renal Floor
3 2/13
HAI
Refused HD
4 2/14
I
W
P
Consented HD; HD performed
5 2/15
6 2/16
7 2/17 Blood cx – P. putida DOE
R
I
T
Fever 102◦F
8 2/18 HD central line removed
9 2/19 New HD central line replaced in RIJ
10 2/20
11 2/21
12 2/22
13 2/23
14 2/24
15 2/25
16 2/26
17 2/27
18 2/28
19 3/1
20 3/2
21 3/3
HAI CASE STUDY 3
January 1, 2018 (HD 1)
• 23yo male with paraplegia secondary to T1 transverse myelitis is admitted to inpatient ward
• Implanted port and suprapubic catheter are POA
• Unaccessed port is scheduled for removal on 1/3/18 due to history of recurrent polymicrobialbacteremias
• Late November 2017 – BSI treated with 4-week course of antibiotics completed on 12/31/17– Blood cultures positive for Candida albicans,
Chryseobacterium indolegenes, and Enterococcus faecalis
January 3, 2018, 12:23a.m. (HD 3)
• Patient complains of ‘itching at port insertion site’
• Port insertion site is red, warm, and tender
• Port is accessed for the first time during this admission to collect blood cultures– One set collected from port
– One set collected from peripheral venipuncture
• Port is de-accessed after collection and scheduled removal is postponed pending culture results
• Peripheral IV is placed for temporary access
January 4, 2018 (HD 4)
• Blood cultures from 1/3/18 are
preliminarily resulted as no growth
• Port is removed
January 5, 2018 (HD 5)
• Patient pulls out IV
• PICC is inserted at 1:30pm
• Chart shows “Patient continues to be non-compliant with medical care. The nurse witnessed tampering with PICC line.”
• Low-grade fever 99.8◦F is noted at 8:00pm
January 6, 2018 (HD 6)
• 11:00am – patient complains of pain, severity 10/10, 15mg oxycodone is given. Patient is requesting to leave the unit to smoke with visitors.
• 11:20am – nurse disconnected CL and caps; patient leaves unit to smoke
• 12:40pm – patient returns to unit slurring words and unable to open eyes– Marked change in level of consciousness (LOC) since
leaving
– Safety cap is missing from the secondary port
– CL is un-clamped
January 6, 2018 (continued)
• 1:30pm – physician assesses patient
and concludes that condition is
inconsistent with current narcotic order
and previous response to ordered pain
medications
• Physician orders discontinuation of
PICC and all narcotics
• 5:15pm – PICC is removed
January 7, 2018 (HD 7)
• Fever spikes to 101.2oF
• Two sets of blood cultures are collected,
and one bottle from each set is positive
for Staphylococcus hominis, Klebsiella
oxytoca, and Enterococcus faecium
• The blood cultures collected on January
3rd are still showing no growth
Question
On January 7th, how many CL days have occurred to determine if the BSI is a CLABSI?
a. 6 CL days
b. 4 CL days
c. 2 CL days
d. 0, the BSI is not CL associated
Jan. 1 Jan. 2 Jan. 3 Jan. 4 Jan. 5 Jan. 6 Jan. 7
CL
Unaccessed
Port POA
Unaccessed
port
Port
accessed
then de-
accessed
Port removed RUA PICC
placed
RUA PICC
removed
Blood
Specimen
BC x2
No growth
+BC x2
K. oxytoca,
E. faecium,
S. hominis
Eligible Central Line
• Has been in place > 2 consecutive
calendar days following the first access
of the CL in an inpatient location during
the current admission
• Eligible for CLABSI events until the day
after removal from the body or patient
discharge, whichever comes first
ExplanationJan. 1 Jan. 2 Jan. 3 Jan. 4 Jan. 5 Jan. 6 Jan. 7
CL
Unaccessed
Port POA
Unaccessed
port
Port
accessed
then de-
accessed
Port removed RUA PICC
placed
RUA PICC
removed
Blood
Specimen
BC x2
No growth
+BC x2
K. oxytoca,
E. faecium,
S. hominis
• 1/3/18: The port is accessed and then de-accessed. This is CL day 1 for CLABSI attribution.
• 1/4/18: The port is removed, but has been present for some portion of the calendar day. Because the port was
accessed during the current admission, it continues to count towards central-line attribution until the day after
removal from the body or the day after patient discharge. This is CL day 2 for CLABSI attribution.
• 1/5/18: A PICC is placed (during current admission). Because a full calendar day did not pass without a CL in
place between device removal and placement of the new device, CL day count for device attribution continues
uninterrupted. The device is now an eligible CL (eligible for CLABSI event) as this is CL day 3 for CLABSI
attribution.
• 1/6/18: The PICC is removed but has been present for some portion of the calendar day. This is CL day 4 for
CLABSI attribution.
• 1/7/18: No CL is in place for any part of this calendar day, therefore, no device day for denominator data is
counted.
Question
What is the correct determination for the positive blood specimens collected on January 7th and how should the field for CL be completed?
a. LCBI 1; CL=No due to self injection DOE 1/7
b. LCBI 1; CL=Y (CLABSI) DOE 1/7
c. LCBI 2; CL=No due to self injection DOE 1/5
d. LCBI 2; CL=Y (CLABSI) DOE 1/5
e. No LCBI because patient is non-compliant and tampering with line
Jan. 1 Jan. 2 Jan. 3 Jan. 4 Jan. 5 Jan. 6 Jan. 7
CL
Unaccessed
Port POA
Unaccessed
port
Port
accessed
then de-
accessed
Port removed RUA PICC
placed
RUA PICC
removed
Blood
Specimen
BC x2
No growth
+BC x2
K. oxytoca,
E. faecium,
S. hominis
Explanation: LCBI and DOE
• LCBI 1 criteria met on 1/7 with +BC (DOE) and BSI is attributed to the eligible CL (CLABSI)– E. faecium and K. oxytoca are recognized pathogens
– No other site-specific source of infection is identified that the BSI can be attributed as secondary ---- primary BSI is identified
• DOE for LCBI 1 is always the collection date of the first positive blood specimen
Jan. 1 Jan. 2 Jan. 3 Jan. 4 Jan. 5 Jan. 6 Jan. 7
CL
Unaccessed
Port POA
Unaccessed
port
Port
accessed
then de-
accessed
Port removed RUA PICC
placed
RUA PICC
removed
Blood
Specimen
BC x2
No growth
+BC x2
K. oxytoca,
E. faecium,
S. hominis
Explanation: CL=Y (CLABSI)
• Device became an eligible CL on CL day 3 (1/5)
because it was in place >2 consecutive calendar days
and is still in place on the BSI DOE or the day before
• The BSI DOE occurs the day after removal of an eligible
CL, therefore, a CLABSI is identified and reported
• Documentation does not meet the patient injection
exclusion, therefore, ‘CL=No’ cannot be reported
Jan. 1 Jan. 2 Jan. 3 Jan. 4 Jan. 5 Jan. 6 Jan. 7
CL
Unaccessed
Port POA
Unaccessed
port
Port
accessed
then de-
accessed
Port removed RUA PICC
placed
RUA PICC
removed
Blood
Specimen
BC x2
No growth
+BC x2
K. oxytoca,
E. faecium,
S. hominis
Question
But wait… on 1/7 he had a fever and
matching blood cultures for S. hominis.
Shouldn’t this be reported as LCBI 2?
a. Yes
b. No
c. I don’t know Rachel, you’re confusing
me
Explanation: LCBI 2
• LCBI 2 criteria met on 1/7 with fever spike and common commensal– Fever spikes to 101.2oF
– Organism not related to an infection at another site
– S. hominis is a matching common commensal from +BC x2
• Since both LCBI 1 and LCBI 2 are met → LCBI 1 is reported
Jan. 1 Jan. 2 Jan. 3 Jan. 4 Jan. 5 Jan. 6 Jan. 7
CL
Unaccessed
Port POA
Unaccessed
port
Port
accessed
then de-
accessed
Port removed RUA PICC
placed
RUA PICC
removed
Blood
Specimen
BC x2
No growth
+BC x2
K. oxytoca,
E. faecium,
S. hominis
Reporting LCBI 1 and 2
• If a patient meets both LCBI 1 and LCBI
2 criteria, always report LCBI 1
• Enter the recognized pathogen as
pathogen #1 and the common
commensal as pathogen #2
January 8, 2018 (HD 8)
• Left upper arm (LUA) PICC is placed for
treatment of polymicrobial bacteremia
• Repeat blood cultures are collected
• Patient has personal sitter assigned
January 9, 2018 (HD 9)
• Blood cultures from 1/8 are positive for
Enterococcus faecium and
Pseudomonas aeruginosa
January 11, 2018 (HD 11)
• Progress notes state:
– Patient continues with non-compliant
behavior
– Likely represents on-going contamination
of CL from patient injecting illicit drugs
– In the patient’s best interest to discontinue
the CL and change to oral antibiotics
– Left upper arm PICC removed at 2:40 p.m.
January 13, 2018 (HD 13)
• Repeat blood cultures are collected and
all are negative for growth
• Progress note states: “PICC removed
January 11th, recent blood cultures
clear”
QuestionHow many device days should be reported for this patient for the January CL summary denominator data?
a. 6 device days
b. 8 device days
c. 9 device days
d. 10 device days
Jan. 1 Jan. 2 Jan. 3 Jan. 4 Jan. 5 Jan. 6 Jan. 7 Jan. 8 Jan. 9 Jan. 10 Jan. 11
CL
Unaccessed
Port POA
Unaccessed
port
Port
accessed
then de-
accessed
Port
removed
RUA
PICC
placed
RUA
PICC
removed
LUA
PICC
placed
LUA
PICC
LUA
PICC
LUA
PICC
removed
CL d
ay
for
CLA
BS
I
dete
rmin
ation CL day 1 CL day 2 CL day
3; CL is
eligible
CL day
4;
CLABSI
event
eligible
Remains
CLABSI
event
eligible
CL day 1 CL day 2 CL day 3 CL day 4
Devic
eday
for
denom
inato
r
data
CL day 1 CL day 2 CL day 3 CL day 4 CL day 5 CL day 6 - CL day 7 CL day 8 CL day 9 CL day
10
Explanation
• Business rule changed in 2017 for how denominator summary data is counted
– Pre-existing CL weren’t included in denominator counts until the day the line was first accessed during inpatient admission
• NHSN changed the rule so that it is now consistent with other device-associated events (UTI’s and VAE’s)
• Effective January 1, 2018
Counting Denominator Days
• Count begins on the first day of CL (of any type) is present in an inpatient unit– Day of placement (during current admission)
– Day of admission (if patient is admitted with a CL in place)
• Count only one device day for each day that patient has at least one CL in place, regardless of how many CLs the patient has in place on the same day
• Continue counting until: – Device is removed
– Patient is discharged
Explanation
Jan. 1 Jan. 2 Jan. 3 Jan. 4 Jan. 5 Jan. 6 Jan. 7 Jan. 8 Jan. 9 Jan. 10 Jan. 11
CL
Unaccessed
Port POA
Unaccessed
port
Port
accessed
then de-
accessed
Port
removed
RUA
PICC
placed
RUA
PICC
removed
LUA
PICC
placed
LUA
PICC
LUA
PICC
LUA
PICC
removed
CL d
ay
for
CLA
BS
I
dete
rmin
ation CL day 1 CL day 2 CL day
3; CL is
eligible
CL day
4;
CLABSI
event
eligible
Remains
CLABSI
event
eligible
CL day 1 CL day 2 CL day 3 CL day 4
Devic
eday
for
denom
inato
r
data
CL day 1 CL day 2 CL day 3 CL day 4 CL day 5 CL day 6 - CL day 7 CL day 8 CL day 9 CL day
10
Question
Which of these documented notes would meet criteria for use of the patient self-injection exclusion, assuming LCBI criteria are met and documentation is within the BSI infection window period (IWP)?
Note: The NHSN BSI protocol states: “A BSI meeting LCBI criteria that is accompanied by documentation of observed or suspected patient injection into the vascular access line, within the BSI Infection Window Period, will be considered an LCBI but not a CLABSI for NHSN reporting purposes”.
1. “Patient is manipulating his CL by scratching around it aggressively and interfering with line maintenance by refusing care”.
2. Patient is very non-compliant with medical care…have witnessed patient tampering with PICC line
3. At 11am, patient complaining of pain 10/10, 15mg oxy given per MAR... Patient left floor at 11:20am to smoke…Patient back on unit at 12:40 pm… slurring words with difficulty keeping eyes open…Safety cap was missing and the line was un-clamped.
4. Changed to PO antibiotics due to misuse and contamination of intravascular line
5. Patient infection likely represents contamination of CL from patient using the line to inject unknown substance …CL removed and recent blood cultures are clear”.
Explanation
• Exclusion is very specific to “injection”
• BSI meeting LCBI criteria must have documentation of observed or suspected patient injection into the vascular access line, within the BSI IWP, to be considered an LCBI and not a CLABSI
• Documentation must state that the patient was “observed injecting” or “suspected of injecting” the device
• Does not meet exclusion:– Manipulating or tampering with the line (biting, picking
at, sucking on, etc.)
– Descriptions that suggest behavior
1. “Patient is manipulating his CL by scratching around it aggressively and interfering with line maintenance by refusing care”.
2. Patient is very non-compliant with medical care…have witnessed patient tampering with PICC line
3. At 11am, patient complaining of pain 10/10, 15mg oxy given per MAR... Patient left floor at 11:20am to smoke…Patient back on unit at 12:40 p.m…slurring words with difficulty keeping eyes open…Safety cap was missing and the line was un-clamped.
4. Changed to PO antibiotics due to misuse and contamination of intravascular line
5. Patient infection likely represents contamination of CL from patient using the line to inject unknown substance …CL removed and recent blood cultures are clear”.
✔
Note on Exclusions
CLABSI Exclusion Exclusion
Field
Marked
Yes or No
Central
Line Field
Marked
Yes or No
Exclusion
Reporting
Requirement
in 2019
Exclusion
Reporting
Requirement
in 2020
Epidermolysis Bullosa (EB) Y N Optional Required
Munchausen’s syndrome by proxy
(MSBP)
Y N Optional Required
Patient self-injection Y N Optional Required
Pus at vascular site Y N Optional Required
Group B Streptococcus BSI- 1st 6
days of life
Y N Optional Required
ERC Updates
TB & LTBI Reporting
TB Reporting
• All TB cases and suspects are reportable within 24 hours of diagnosis
• Anyone starting on RIPE therapy is considered a TB suspect and must be reported
• Submit Report of TB in NBS
• Can be found on tb.in.gov under Information for Health Professionals
Reporting TB in NBS
• Submit a morbidity report for TB
• Attach current Report of TB form• Don’t need to complete variables
• Add supporting documentation
• Immediately viewable by LHDs and ISDH
• Please do not mail/fax report of TB to ISDH
LTBI Reporting
• Latent TB infection (LTBI) has been reportable in Indiana since December 2015
• Only those with a diagnosis of LTBI by a provider are reportable
• Positive reactors are reportable in Marion County
• Patients can receive LTBI treatment free through LHDs
Reporting LTBI in NBS
• Open an LTBI Investigation within NBS
• Attach supporting documentation under Supplemental Info tab
• Please don’t submit a TB morbidity report for LTBI
• Change investigation status to closed when outcome is reached
Isolation of Infectious TB Patients
Infectious TB patients must be in negative air pressure isolation until:
• Three consecutive AFB smear negative sputa obtained at least eight hours apart with one being an early morning specimen
• Are clinically improving
• Are known to be medically evaluated
• Have completed two weeks of an adequate antituberculosis therapy per Centers for Disease Control and Prevention guidelines
Discharge of TB Patients410 IAC 1-2.5-141 Tuberculosis; specific control measures
Prior to discharge of a tuberculosis case or suspect case, the local health department shall make plans, in writing, for continuation of medical follow-up,
ensuring adherence to therapy and isolation unless the case or suspect case meets the criteria in this subdivision and is deemed to be noninfectious.
Plans shall be developed in cooperation with the treating physician and the patient and must be in
accordance with this rule.
Measles & Mumps
Measles
Measles
• New FAQ guide for healthcare providers
– Signs and symptoms
– Risk factors
– Immunization recommendations
– What to do if you suspect measles
– Testing and interpretation of results
– Infection prevention
– When to give PEP for non-symptomatic contacts
https://www.in.gov/isdh/25456.htm
Measles/Mumps
IU Mumps
• 20 confirmed cases, as of 4/22/19
• Majority of cases are epi-linked to a fraternity
• Third dose recommendation– Gives boost for one month, return to baseline
immunity after a year
– Takes up to two weeks for immunity after MMR vaccine
• Recommendations– Self-isolate 5 days after onset of parotid swelling
– Discourage sharing of drinks, smoking devices, and utensils
November 20-21, 2019
Marriott East, Indianapolis
2019 Indiana Infectious Disease
Summit: United in Prevention,
Response, and Service
Summit Objectives
• Understand trends and responses to
current and emerging infectious diseases
• Discuss the implementation of
epidemiology preparedness to prevent and
mitigate infectious disease
• List three new partnerships to enhance
infectious disease prevention and
response
Summit will include…
• Keynote speaker - Jay C. Butler, MD (CAPT,USPHS,RET) CDC Deputy Director for Infectious Diseases
• Panel discussions
• Break-out sessions– Infectious disease epidemiology
– Public health preparedness
– Outbreak response
– Emerging infectious diseases and prevention
– Cross-sector collaboration
– Laboratory methods, research and best practices
– Social determinants of health
– Non-traditional partnerships
Call for Presentations
• Call for presentations will be sent out on May 25th to:– Past ID Summit participants
– LHD’s and Indiana state partners
– Other State Health Departments
– Professional organizations listservs (APIC )
– ERC Weekly Digest
Submission Deadline: June 28, 2019
Notification of Acceptance/Denial: July 26, 2019
Break Out Sessions
• Speakers identified by the planning
committee
• Must be in alignment with the ID
Summit objectives and preference given
to those submissions following the
suggested topic guidance
Contact Information
Rachel Cathey, MPH, CIC
Healthcare-Associated Infections Epidemiologist
Infectious Disease Epidemiology
Epidemiology Resource Center
Indiana State Department of Health
Work: 317-234-2805
Email: [email protected]