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Changes in CDC CLABSI Definition January 2013 Version Chris Mansell Clinical Microbiologist, Waikato Hospital

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Changes in CDC CLABSI DefinitionJanuary 2013 Version

Chris MansellClinical Microbiologist, Waikato Hospital

NZ CLAB Collaborative

Insertion Bundle Maintenance Bundle Surveillance

CDC definitions

CDC CLABSI Event definitions 4pschttp://www.cdc.gov/nhsn/pdfs/pscmanual/4psc_clabscurrent.pdf

Problems with CLAB Surveillance Definitions

Types of diagnosis– Biological aetiology– Clinical working diagnosis

– Surveillance• Quality improvement• Audit• Political

Value of Surveillance Definition

• Feedback metric for assessing effectiveness of changes in practice– An integral part of current quality

improvement methodology

• Incentive to implement good practice– Reinforces process changes as being

“patient and outcomes oriented” rather than “bureaucratic”.

Recognised factors devaluing the surveillance definition

• Sample collection and surveillance effort• Subjective interpretation

– Self reporting– Potential cases diverted to “Hospital Acquired

Infection at another site”• PNU1

• Capture of cases after patient discharge• Publication of “Time since last CLAB” and rates

– League tables– Celebrations– Unrealistic expectations

Refinement of Definitions for Central Venous Line Infection

Doubts ICHE 2010 31 1286

2008 VICNISS

CDC HAI 2008AJIC 2008 36 309

Meta analysis of definitionsCID 2011 53 697Connecticut audit

AJIC 2010 38 832

Victorian AuditICHE 2009 30 1045

NHSN review CID 2012 55 364

CDC CLABSI HAI and org list Jan 2013

CDC CLABSI June 2011VICNISS

Org list

June 2011

Jan 2013 CDC CLABSI • 17 pages - No Table of Contents

• Sections– Introduction– Settings– Requirements– Definitions– Tables

• 1. Lab Confirmed BSI Criteria• 2. Examples of how to report organisms• 3. Mucosal Barrier Injury LCBI Enterobacteriaceae• 4. Examples for MCI-LCBI

– Numerator data– Data analyses– Appendix 1. Secondary BSI guide

• 4 scenarios• Definition of matching organism• Notes• Reporting instructions

HAI

Primary BSI

Date of event

Central line

Infusion

Umbilical catheter

Temporary central line

Permanent central line

CLABSI

Location of attribution

Transfer rule

Jan 2013 CDC CLABSI • 17 pages - No Table of Contents

• Sections– Introduction– Settings– Requirements– Definitions– Tables

• 1. Lab Confirmed BSI Criteria• 2. Examples of how to report organisms• 3. Mucosal Barrier Injury LCBI Enterobacteriaceae• 4. Examples for MBI-LCBI

– Numerator data– Data analyses– Appendix 1. Secondary BSI guide

• 4 scenarios• Definition of matching organism• Notes• Reporting Instructions

HAI

Primary BSI

Date of event

Central line

Infusion

Umbilical catheter

Temporary central line

Permanent central line

CLABSI

Location of attribution

Transfer rule

CLABSI definition

LCBI CL or UC > 2 cal days

CLABSI

Secondary BSI

• Do these over ride CLABSI ?• What is primary vs secondary BSI ?

Primary LCBI CL or UC > 2 cal days

CLABSI

Secondary LCBI

Meets criteria for a site specific HAI

Not a CLAB

CDC HAI definitions 17pschttp://www.cdc.gov/nhsn/PDFs/pscManual/17pscNosInfDef_current.pdf

Jan 2013 CDC CLABSI • 17 pages - No Table of Contents

• Sections– Introduction– Settings– Requirements– Definitions– Tables

• 1. Lab Confirmed BSI Criteria• 2. Examples of how to report organisms• 3. Mucosal Barrier Injury LCBI Enterobacteriaceae• 4. Examples for MBI-LCBI

– Numerator data– Data analyses– Appendix 1. Secondary BSI guide

• 4 scenarios• Definition of matching organism• Notes• Reporting Instructions

HAI

Primary BSI

Date of event

Central line

Infusion

Umbilical catheter

Temporary central line

Permanent central line

CLABSI

Location of attribution

Transfer rule

See next slide for details

Table 1. Laboratory Confirmed Bloodstream Infection Criteria

LCBI Criterion

LCBI 1

LCBI 2

timeframe measured in calendar days

List of 431 common commensals and 2000 total organisms

LCBI 3

MBI-LCBI criterion

MBI-LCBI 1 “intestinal organisms”

MCI-LCBI 2 “viridans group streptococci”

MCI-LCBI 3 “viridans group streptococci”

Comments

Clarifications• Location of attribution

– Date when last element occurred– Contractors– Wards which don’t have overnight patients

• Separate occasions for blood cultures• “No other organism isolated”• Graft vs Host Disease• Catheter tip cultures are not used• Unspeciated organisms

– More examples provided• “Special Care Areas/Oncology”• Standardised Infection Ratio

– New references included• Appendix 1 Secondary BSI guide

– More, expanded, slightly changed example cases– Blood and site specific cultures don’t have to be collected on the same day

• Reporting instructions– Don’t report secondary BSI for

• VASC• PNU1• VAC• IVAC

Jan 2013 CDC CLABSI • 17 pages - No Table of Contents

• Sections– Introduction– Settings– Requirements– Definitions– Tables

• 1. Lab Confirmed BSI Criteria• 2. Examples of how to report organisms• 3. Mucosal Barrier Injury LCBI Enterobacteriaceae• 4. Examples for MBI-LCBI

– Numerator data– Data analyses– Appendix 1. Secondary BSI guide

• 4 scenarios• Definition of matching organism• Notes• Reporting Instructions

HAI

Primary BSI

Date of event

Central line

Infusion

Umbilical catheter

Temporary central line

Permanent central line

CLABSI

Location of attribution

Transfer rule

Secondary BSI Guide

VASC

No culture required

PNU1No culture required

VAC & IVAC

Nested Criteria

• VAC = deterioration

• IVAC = Temp/WBC and Antibiotic treatment

No culture required