Preventing Surgical Site Infections...

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Preventing Surgical Site Infections (SSI) Preventing Surgical Site Infections (SSI)

Transcript of Preventing Surgical Site Infections...

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Preventing Surgical Site Infections (SSI)Preventing Surgical Site Infections (SSI)

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Learning Objectives:

• Discuss risk factors for surgical site infections in healthcare settings.

• Review current strategies and emerging guidelines for SSI prevention.

• Discuss challenges in monitoring and preventing SSIs.p g

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SSI Surveillance: Definitions and Methods

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Wh f SSI d i ?Why focus on SSI detection?• Growing patient safety focus on preventing healthcare‐

associated infections, including surgical site infections• Accurate tracking of infections is an essential foundation for 

preventionprevention• Increasing number of states that require mandatory reporting 

of SSI following select proceduresV li it d SSI ill d t il bl f b l t• Very limited SSI surveillance data available for ambulatory surgery

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Why perform surveillance?Why perform surveillance?

• Identify clustersIdentify clusters

• Determine baseline risks

• Evaluate prevention measures• Evaluate prevention measures

• Compare to others

• Identify risk factors• Identify risk factors 

• Satisfy regulators

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A Reliable and Useful Surveillance Program Requires . . .

• Meaningful definitions of infection that are...

• Consistently appliedConsistently applied...

• To the entire population at risk...

• Without too much effort• Without too much effort

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Why is it hard?

• Problematic definitions

• Resource intensiveResource intensive

• Much of the action occurs after hospitalization endshospitalization ends

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NHSN NSQIP STS

Which infections

Superficial, deep, organ/space

Superficial, deep, organ/space

Deep/organ

spaceg / p g / p

Surveillance period

30 days (no implant) or 1 year (implant)

30 days 30 days

year (implant)

Risk ASA, wound Many Many adjustment class, duration

in risk modelvariables in risk model

variables in risk model

What’s reported

SSI rates, observed/ expected

Observed/ expected

Observed/ expected

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Defining Surgical Site Infections

Superficial incisional(skin or subcutaneous tissue)

• Infection ≤30 days after procedure and at least 1 of the following:

– Purulent drainage from superficial incision– Organisms isolated aseptically– At least 1: pain/tenderness swelling rednessAt least 1: pain/tenderness, swelling, redness,

heat AND superficial incision deliberately opened by surgeon unless culture-negative

– SSI diagnosed by surgeon or attending physician– SSI diagnosed by surgeon or attending physician

Horan TC et al Infect Control Hosp

10

Horan TC et al. Infect Control Hosp Epidemiol. 1992;13:606–608.

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Defining Surgical Site Infections (cont.)g g ( )– Deep incisional– (deep soft tissue at incision site)– Infection ≤30 days after procedure (no implant) or ≤1 year (with implant) plus at least 1 of the following:

– Purulent drainage from deep incision but not fromPurulent drainage from deep incision but not from organ/space

– Spontaneous dehiscence or surgical opening of deep incision unless culture-negative AND at leastdeep incision unless culture-negative AND at least 1: fever or pain or tenderness

– Abscess or other evidence of infection involving deep incisiondeep incision

– SSI diagnosed by surgeon or attending physician

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Horan TC et al. Infect Control Hosp Epidemiol. 1992;13:606–608.

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Defining Surgical Site Infections (cont.)

Organ/space(any site other than incision)( y )• Infection ≤30 days after procedure (no implant) or ≤1 year (with implant) plus at least 1 of the following:

Purulent drainage from a drain placed through a– Purulent drainage from a drain placed through a stab wound into organ/space

– Organisms isolated from aseptically obtained culture of fluid or tissueculture of fluid or tissue

– Abscess or other evidence of infection involving the organ/space found by histopathologic examination X ray or reoperationexamination, X-ray, or reoperation

– SSI diagnosed by surgeon or attending physician

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Horan TC et al. Infect Control Hosp Epidemiol. 1992;13:606–608.

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Data sources used for surveillance

• Microbiology data

• Operative reports• Operative reports

• Readmissions following surgery

• Inpatient antibiotic data

• Discharge diagnosis codesg g

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NHSN risk adjustment (previous)• 3 equally weighted variables:

– American Society of Anesthesiologists (ASA) f 3score of 3

– Wound classification of either contaminated or dirt /infe teddirty/infected

– Length of surgery >75th percentile for the specific operationspecific operation

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NHSN Risk Adjustment (future)• Measurement System: CDC National Healthcare Safety Network (NHSN)

• Baseline Period: 2006‐2008

• Current (CY 2009): SIR = 0.95 = 3,930 / 4,144 SSIs

– 5% reduction from baseline

– 946 facilities reporting;  416,341 procedures reportedSCIP Procedure No. of SSIs Validated Parameters for Risk Model

Abdominal aortic aneurysm repair 30 duration of procedure, wound class

Coronary artery bypass graft 1,644 age, ASA, duration of procedure, gender, med school affiliation, age gender (interaction)gender (interaction)

Cardiac surgery 229 age, duration of procedure, emergency (y/n)

Colon surgery 1,825 age, ASA, duration, endoscope, med school affiliation, hospital bed size, wound class

Hip prosthesis 1,183 total/partial/revision, age, anesthesia, ASA, duration of procedure, med school affiliation, hospital bed size, trauma (y/n)

Abdominal hysterectomy 389 age, ASA, duration of procedure, hospital bed size

Knee prosthesis 1,108 age, ASA, duration of procedure, gender, med school affiliation, hospital bed size trauma (y/n) bed size, trauma (y/n)

Peripheral vascular bypass surgery 176 age, ASA, duration of procedure, med school affiliation

Rectal surgery 38 duration of procedure, gender, hospital bed size

Vaginal hysterectomy 122 age, duration of procedure

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Courtesy of S Fridkin, CDC

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Standardized Infection Ratio (SIR)Standardized Infection Ratio (SIR)

SIR = Observed number of infections/Expected number of i f tiinfections

Not significantly different from benchmark if “1.0” falls between the lower and upper 95% confidence intervalspp

Hospital A with CABG SIR of 1.6 (95% CI of 0.8, 1.9): not significantly different

Hospital B with CABG SIR of 1.6 (95% CI of 1.2, 1.8): significantly higher SSI rate 

Hospital C with CABG SIR of 0 8 (95% CI of 0 5 0 9):Hospital C with CABG SIR of 0.8 (95% CI of 0.5, 0.9): significantly lower SSI rate

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CMS Inpatient Prospective PaymentCMS Inpatient Prospective Payment System 2011: HAI reporting requirements

• Jan 2011: report CLABSI among ICU and NICU patients

• Jan 2012: SSI rates for some procedures– Coronary artery bypass graft?

– Other cardiac surgery?

– Hip or knee arthroplasty?

– Colorectal surgery?

– Hysterectomy?

V l ?

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– Vascular surgery?

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SSI surveillance outside of the inpatientSSI surveillance outside of the inpatient hospital setting

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M th d f t di hMethods for post‐discharge surveillance

• “Standard” infection prevention surveillance

• Prospective surveillance with post‐discharge• Prospective surveillance with post‐discharge follow‐up

• Self‐reporting by patients and surgeonsSelf reporting by patients and surgeons

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Li it f h it l b d SSILimits of hospital based SSI surveillance

•Many procedures have no post‐op hospital stay.

Percent infected

•Most infections are identified after discharge.

2

2.5 Postdischarge

1

1.5 Predischarge

0

0.5

5,572 procedures. Sands, JID 1996

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Limits of hospital based SSI surveillance

•The majority never returned to the hospital

Percent infected

returned to the hospital.

•These SSIs caused 4‐5 additional ambulatory 

2

2.5Post/unknown

Post/knownencounters.

1

1.5

2 Post/known

Predischarge

0

0.5

15,572 procedures. Sands, JID 1996

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0

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Post discharge SSI surveillancePost‐discharge SSI surveillance

90100

•Surgeons’ questionnaires miss most infections

•Most infections reported by607080

•Most infections reported by surgeons aren’t postoperative SSIs 

304050Sens

01020

Surgeons

0 20 40 60 80 100

5 572 d S d JID 1996 S d JID 1999 179 434

Predictive value

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5,572 procedures. Sands, JID 1996; Sands JID 1999;179:434

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Post‐discharge SSI surveillancePost discharge SSI surveillance

•Surgeons’ questionnaires miss  90

100

g qmost infections

•Most infections reported by ’t t ti

60

70

80

S

HMO data

surgeons aren’t postoperative SSIs

•Patients do just as poorly 20

30

40

50Sens

Patientsj p y

•Administrative data are much more accurate 0

10

20

0 20 40 60 80 100

Surgeons

Predictive value

5 572 d S d JID 1996 S d JID 1999 179 434

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5,572 procedures. Sands, JID 1996; Sands JID 1999;179:434

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Alt ti ill th dAlternative surveillance methods:Using claims‐based SSI indicators

Developed claims‐based indicators of CABG SSI to identify hospitals with high SSI rates*

Applied algorithms to 2005 Medicare claims to rank hospitals into deciles of post‐CABG SSI risk

N i l lid i f i d b d il National validation of cases in top and bottom decile

*Platt R et al. Using automated health plan data to assess infection risk from coronary artery g p y ybypass surgery. Emerg Infect Dis 2002;8(12):143-41.

Huang SS et al. Developing algorithms for healthcare insurers to systematically monitor SSI rates. BMC Med Res Methodol 2007;7:20

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Predictors of 60‐day CABG SSI Risky

Odds Ratio(Confidence Interval) P‐value

CABG Performed in Bottom vs. Top Decile Hospital

2.7 (2.2, 3.3) <0.0001

Age 0.0006

65 74 1 065‐74 1.0

75‐84 0.6 (0.4, 1.0)

85+ 0.7 (0.5, 0.8)

Female 1.7 (1.4, 2.1) <0.0001

Open vs. Minimally Invasive 1.0 (0.8, 1.2) 0.8

Comorbidity Score (Romano) <0.0001

0 1.0

1‐4 1.4 (0.9, 2.2)

5+ 2.5 (1.6, 4.0)

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Huang SS, et al. SHEA Annual Meeting (San Diego), 2009

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Concl sions (H an SS et al)Conclusions (Huang SS, et al)

• Claims‐based algorithm can be used to rank US ghospitals by CABG SSI risk for Medicare patients

• There is a 3‐fold risk of SSIs between top and bottom d il h it ldecile hospitals

• Claims enables adjustment for host‐based predictors of SSI such as gender age and comorbiditiesof SSI, such as gender, age, and comorbidities

• Medicare could use this algorithm to identify outlier hospitals for targeted review and assessment of actual p gSSI risk

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Ambulatory Surgery:Ambulatory Surgery: The next surveillance frontier

• “Ambulatory surgery” =• Ambulatory surgery  = surgical episode where the patient requires hospital 

Proportion of surgical procedures that are ambulatory surgery

care for <24 hours and no overnight stay.

• Accounts for an increasing60%

80%

Accounts for an increasing proportion of surgeries in the U.S.

0%

20%

40%

• Little data about the risk of infectious complications

0%1980 1990 2005

National Center for Health Statistics. Health, United States 2007. Hyattsville, MD 2008.

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National Center for Health Statistics. Health, United States 2007. Hyattsville, MD 2008.

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Preventing surgical site infections

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http://www shea online org/about/compendium cfm

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http://www.shea‐online.org/about/compendium.cfm

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Basic PracticesBasic Practices• Perform SSI surveillance for targeted procedures

• Provide ongoing feedback to surgical and perioperative personnel and leadership

k f d d i h• Make use of automated data to increase the efficiency of surveillance

Ph d tPharmacy data

Diagnosis codes

b l dMicrobiology data

OR information

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Basic Practices

• Administer antimicrobial prophylaxis in accordance with evidence‐based standardsaccordance with evidence based standards and guidelines

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Perioperative antimicrobial prophylaxis

What is perioperative antimicrobial prophylaxis?

– A brief course of an antimicrobial agent initiated just before an operation begins (i.e., before contamination occurs)

’ fWhat’s the purpose of prophylaxis?

– To reduce the microbial burden of intraoperative t i ti i d t t thcontamination in order to prevent the occurrence 

of surgical site infections.

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Which surgical procedures benefitWhich surgical procedures benefit from prophylaxis?

High risk for infection

• Procedure related risks OR• Procedure‐related risks OR

• Patient risk factors

P d i l i h i i l Procedures involving prosthetic implants

Potential severe sequelae from SSI

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R l ti b fit f ti i bi lRelative benefit from antimicrobial prophylaxis

Operation Prophylaxis (%) Placebo (%)Colon 4‐12 24‐48Other (mixed) GI 4‐6 15‐29Vascular 1‐4 7‐17Cardiac 3‐9 44‐49Hysterectomy 1‐16 18‐38Craniotomy 0.5‐3 4‐12Spinal operation 2.2 5.9Total joint repl 0.5‐1 2‐9Brst & hernia ops 3.5 5.2

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S i l C I t P j t (SCIP)Surgical Care Improvement Project (SCIP) recommendations

– Choice of antimicrobial agent

– Start time within 1 hour of incision (2 hrs forStart time within 1 hour of incision (2 hrs for vancomycin and fluoroquinolones)

– Discontinuation within 24 hours (48 hours for (cardiac surgery)

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How should prophylaxis be used?How should prophylaxis be used?

• Use an agent that is safe, inexpensive and g pwith an antimicrobial spectrum that is appropriate.

Procedures where skin colonizers (e.g., Staphylococcus aureus) are the most 

th ticommon pathogens, use an anti‐staphylococcal agent: cefazolin 

Keep spectrum as narrow as possibleKeep spectrum as narrow as possible

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Updated Perioperative Antimicrobial Prophylaxis Guidelines

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How should prophylaxis be used?How should prophylaxis be used?

• Need inhibitory levels in serum and tissues when contamination occurs and maintain therapeutic levels throughout the operation.

Initiate prophylaxis before incision

Adjust dosing to be appropriate for patient weight 

Consider repeat intraoperative doses for l dlong procedures

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Timing of antimicrobial prophylaxis

• Prophylactic antimicrobials should be started within one hour prior to surgical incision (two hours allowed for vancomycin or quinolones)

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Timing of prophylaxis and risk of surgical site infectionsite infection

6 Classen, et al. NEJM 326:281, 1992

4

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(%)

3

4

ctio

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ate

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2

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c

0>2 2 1 1 2 3 4 5 6 7 8 9 10 >10

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Hours before Hours after IncisionIncision

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How should prophylaxis be used?How should prophylaxis be used?

• End prophylaxis within 24 hours after completion of p p y psurgery (48 hours for cardiac surgery)

No evidence to support extending prophylaxis for devices (e.g., drains, chest tubes, pacing wires) 

Little evidence to support use of antimicrobial prophylaxis after incision closure

Extended prophylaxis may promote antimicrobial resistance

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Provide protocolsProvide protocols• Design standard protocols based on surgery typeg p g y yp

Minimize reliance on individual physician memory

• Include guidance for common exceptionsg p

Penicillin/cephalosporin allergy

• Use your own formulary to narrow choicesUse your own formulary to narrow choices

Makes protocol easier and saves costs

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Provide a clear process

• Identify owners clearly: who starts it and who documents it

T k d f h bi d• Take advantage of habits and patterns

Dose of antibiotic started at a point that makes sense and is eas to remembermakes sense and is easy to remember

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Provide a clear process• Verify that the antibiotic has been started before theVerify that the antibiotic has been started before the incision

Final check at pre‐procedural briefing or time‐outp p g

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August 2, 2011 46Version 1.0 Copyright © SHEA, March 2011 

http://www.who.int/patientsafety/safesurgery/en/

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Haynes AB, et al. A surgical safety checklist to reduce morbidity and mortality in a global population NEJM 2009; 360: 491-9

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mortality in a global population. NEJM 2009; 360: 491-9

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Basic PracticesBasic Practices

• Do not remove hair at the operative site unless theDo not remove hair at the operative site unless the presence of hair will interfere with the operation; do not use razors

ll f h i i iRemove all razors from the perioperative suite

Provide mechanical clippers with replaceable heads.

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Shaving Clipping and SSIShaving, Clipping and SSI

% Infected

22.5

11.5

2

00.5

1

0Shave Clip Neither

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Cruse. Arch Surg 1973; 107: 206

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Basic PracticesBasic Practices

• Control blood glucose levels during the• Control blood glucose levels during the immediate postoperative period for patients undergoing cardiac surgeryg g g y

Set clear goals: glucose <200 mg/dL measured at 6:00 AM on postoperative days 1 and 2

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Other basic prevention practices

• Implement policies and practices that meet regulatory and accreditation requirements and are aligned with evidence‐based standards (e.g., HICPAC guidelines)

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Intrinsic modifiable risksIntrinsic modifiable risks

• Reduce hemoglobin A1c to <7% A‐II

• Smoking cessation >30 days prior to surgery A‐II

Anderson DJ, Kaye KS, et al. Infect Control Hosp Epidemiol 2008; 29:S51-S61

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Extrinsic risks: Pre operativeExtrinsic risks: Pre‐operative

T t i ti i f ti t t it• Treat pre‐existing infections at remote sites prior to surgery A‐II

Anderson DJ, Kaye KS, et al. Infect Control Hosp Epidemiol 2008; 29:S51-S61

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Extrinsic risks: Peri‐operativeExtrinsic risks: Peri‐operative

• Surgical scrub or alcohol‐based surgical hand• Surgical scrub or alcohol‐based surgical hand antiseptic agent A‐II

• Skin preparation at the operative site A‐IISkin preparation at the operative site A II

• Optimize surgeon technique A‐III

• Adhere to principles of operating room asepsis A‐III• Adhere to principles of operating room asepsis A‐III

Anderson DJ, Kaye KS, et al. Infect Control Hosp Epidemiol 2008; 29:S51-S61

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Extrinsic risks: PerioperativeExtrinsic risks: Perioperative

• Follow facility guidelines for OR construction y gand ventilation C‐I

• Minimize traffic B‐II

• Optimize sterilization of equipment; minimize use of flash sterilization B‐I

• Optimize environmental cleaning B‐III

Anderson DJ, Kaye KS, et al. Infect Control Hosp Epidemiol 2008; 29:S51-S61

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Unresolved issuesUnresolved issues

• Pre‐operative Staphylococcus aureus screening• Pre‐operative Staphylococcus aureus screening and decolonization

• Maintain normothermiaMaintain normothermia

• Maintain oxygenation

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D CHG b hi d i lDo CHG bathing and intranasal mupirocin prevent SSIs?

• Theoretical benefit:

N l S i l b l i d t• Nasal S. aureus carriers may also be colonized at extra‐nasal sites

• Combining CHG bathing and intranasal• Combining CHG bathing and intranasal mupirocin may eradicate nares and skin S. aureus colonizationaureus colonization

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CHG b thi l i in• Randomized, double‐blinded, placebo‐controlled 

CHG bathing plus mupirocinp

multicenter study of 6,771 patients in the Netherlands (Bode NEJM 2010)

• Mainly surgical patients

• Rapid screening for MSSA/MRSA on admission 

• Carriers randomized to mupirocin/CHG soap vs. placebo/bland soap x 5 days 

Bode LGM, et al. NEJM 2010;362:9-17

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Bode et al (continued)Bode, et al (continued)

• Results: CHG bathing/mupirocin group had significantly• Results: CHG bathing/mupirocin group had significantly lower SSI rates than the placebo group

Localization of infection Mupiroc-CHG

Placebo RR (95% CI)

Deep surgical site 4 (0.9) 16 (4.4)

0.21 (0.07-0.62)

S fi i l i l 7 (1 6) 13 0 45 (0 18 1 11)Superficial surgical site

7 (1.6) 13 (3.5)

0.45 (0.18-1.11)

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Bode LGM, et al. NEJM 2010;362:9-17

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B d l ( i d)

• Conclusions: Rapid preoperative identification of S aureus

Bode, et al (continued)

• Conclusions: Rapid preoperative identification of S. aureuscarriers followed by 5 days of intranasal mupirocin plus CHG bathing reduced S. aureus SSIs by ~60%

• Caveat: No MRSA carriers or mupirocin resistance were found, patients with expected stay of <4 days were excluded

Bode LGM et al NEJM 2010;362:9-17

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Bode LGM, et al. NEJM 2010;362:9 17

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Why not use pre‐operative mupirocin for ALLWhy not use pre operative mupirocin for ALLsurgical patients?

Prevent S. aureusPrevent S. aureusSSIsSSIs for some

patients

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Why not use pre‐operative mupirocin for ALLy p p psurgical patients?

MupirocinMupirocin resistancePrevent S. aureus MupirocinMupirocin resistance

Costs and logistics

Prevent S. aureusSSIsSSIs for some

patients

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Possible implementation strategies• Target patients known to be S. aureus nasal carriers (MSSA and MRSA)

Possible implementation strategies

carriers (MSSA and MRSA)

Most likely to benefit from decolonization

Reduce the risk of promoting mupirocinReduce the risk of promoting mupirocin resistance by focusing on this subgroup

• Target patients scheduled for high risk non‐generalTarget patients scheduled for high risk, non general surgery 

Orthopedic surgery involving implantsOrthopedic surgery involving implants

Cardiac surgery

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P SSIProcess measures: SSI• Compliance with antimicrobial prophylaxis guidelinesCh i f i i bi lChoice of antimicrobial agent Start time within 1 hour of incision (2 hrs for vancomycin and fluoroquinolones)

Discontinuation within 24 hours (48 hours for cardiac surgery)

• Compliance with hair removal guidelines• Compliance with hair removal guidelines• Compliance with perioperative glucose control guidelines• Look for documentation of the number of procedures in 

compliance / number of observations x 100

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Outcome Measures: SSIOutcome Measures: SSI

• Perform SSI surveillance Identify high‐risk, high‐volume operative procedures to target

Use NHSN definitions

Risk adjustment per NHSN

Benchmark against NHSN rates using SIRs

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ResourcesResources• Anderson DJ, Kaye KS, et al. Strategies to prevent surgical site 

infections in acute care hospitals. Infect Control Hosp Epidemiol2008; 29:S51‐61. http://www.shea‐online.org/about/compendium.cfm

• National Healthcare Safety Network (NHSN) webpage Available atNational Healthcare Safety Network (NHSN) webpage. Available at http://www.cdc.gov/nhsn/index.html

• Bratzler DW, Hunt DR. The surgical infection prevention and surgical i t j t N ti l i iti ti t icare improvement projects: National initiatives to improve 

outcomes for patients having surgery. Clin Infect Dis 2006; 43:322‐330.

• Mangram AJ, Horan TC, et al. Guideline for prevention of surgical site infections, 1999. Hospital Infection Control Practices Advisory Committee. Infect Control Hosp Epidemiol 1999; 20:250‐278.

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