SlideShare ist ein Scribd-Unternehmen logo
1 von 42
MDRO (Multiple drug-resistant organisms) How they relate to patients in the healthcare setting UT Southwestern University Hospitals: Infection Control Department
Multi-drug resistant organisms (MDRO’s) have increased in prevalence in US hospitals over the last three decades These organisms have important implications for patient safety Options for treating patients with these infections are often extremely limited MDRO infections are associated with increased lengths of stay, costs, and mortality Background
Methicillin Resistant Staphylococcus aureus (MRSA) was first isolated in the United States in 1968.  In the early 1990s, MRSA accounted for 20%-25% of Staphylococcus aureus isolates from hospitalized patients.  By 2003, MRSA accounted for >50% of S. aureus isolates from patients in ICUs. A similar rise in prevalence has occurred with Vancomycin Resistant Enterococcus (VRE) . From 1990 to 1997, the prevalence of VRE in Enterococcus isolates from hospitalized patients increased from <1% to approximately 15% .  By 2003 VRE accounted for 28.5 % of Enterococcus isolates in ICUs. History of MDRO’s
Methicillin-Resistant Staphylococcus aureus (MRSA) Vancomycin-Resistant Enterococcus species     (VRE) Multidrug-Resistant (MDR) Acinetobacter species. Multidrug-Resistant (MDR) Klebsiella species, Enterobacter species, and Escherichia coli. Resistant Organisms include:
To be defined as an MDRO the organism must meet these criteria: MRSA: S. aureus tests resistant to Oxacillin VRE: Enterococcus species tests resistant to Vancomycin. MDRO-Acinetobacter species: Resistant to all agents tested within at least 3 antimicrobial classes, including B-lactams, carbapenems, aminoglycosides and fluoroquinolones  Specific definitions
Resistant Bacteria Mutations XX Resistance Gene Transfer New Resistant Bacteria Emergence of Antimicrobial Resistance Susceptible Bacteria Bacteria have evolved to evade antimicrobial drugs through chromosomal mutations & acquisition of resistance genes via conjugation, transposition, or transformation
Resistant StrainsRare Antimicrobial  Exposure x Resistant Strains  Dominant x x x x x x x x x x x Selection for antimicrobial-resistant Strains Once resistant strains of bacteria are present in a population, exposure to antimicrobial drugs favors their survival.
Methicillin Methicillin-resistant S. aureus (MRSA) [1970s] Vancomycin [1997] [1990s] [ ???? ] Vancomycin-resistant Vancomycin Vancomycin- resistant S. aureus enterococci (VRE) intermediate- resistant S. aureus (VISA) Penicillin Penicillin-resistant S.aureus [1950s] S. aureus Introduction of every new class of antimicrobial drug is followed by emergence of resistance
B-lactams: includes ampicillin/sulbactam, piperacillin/tazobactam, cefepime, ceftazidime Carbapenems: includes imipenam, meropenem and doripenam Aminoglycosides: includes amikacin, gentamycin, tobramycin Fluoroquinolones: includes ciprofloxacin, levofloxacin Drug classes:
Staphylococcus aureus commonly found on skin, in eyes, upper respiratory track, mouth, and GU system developed resistance to many Antibiotics including Methicillin (oxacillin) to create the particular strain, MRSA MRSA  Is found anywhere Staphylococcus aureus is commonly found may colonize the patient  or cause active infections is a public health concern because there are few drugs left to treat serious MRSA infections. Vancomycin is the current drug of choice for serious infections. Other antimicrobial agents would include: Daptomycin and Linezolid. A high percentage of wound infections are caused by MRSA. Reservoirs for MRSA in the hospital include infected or colonized patients with HCW being the link for nosocomial spread of the infection. The main mode of transmission is via hands of HCW. Other reservoirs include contaminated equipment and other items in the environment Methicillin-Resistant Staphylococcus aureus (MRSA)Fact Sheet
The emergence of new epidemic strains of MRSA in the community, (CA-MRSA) among patients without established MRSA risk factors, may present new challenges to MRSA control in healthcare settings. Historically, genetic analyses of MRSA isolated from patients in hospitals worldwide revealed a relatively small number of MRSA strains have the unique qualities to facilitate transmission from patient to patient. To date, most MRSA strains isolated from patients with CA-MRSA infections have been microbiologically distinct from those endemic in healthcare settings, suggesting some of these strains may have arisen de novo in the community via the acquisition of the mecA gene from Methicillin Susceptible Staph aureus. CA-MRSA infection commonly presents as relatively minor skin and soft tissue infections, but severe invasive disease and mortalities have been described in children and adults.  Community-associated MRSA
When a patient is identified as having an infection or colonization with an MDRO: Place the patient in Contact Precautions  Enter the isolation information into EPIC Staff will be alerted of isolation status upon subsequent admissions into the hospital Monitoring of MDRO’s
Infection control monitors MDRO incidence and transmission and provides data monthly and quarterly to the units Monitoring of MDRO’s
Removing Patients From Isolation Follow-up screenings MUST be negative:	 Original site of infection  				 + Nasal if previously MRSA positive  			           or Rectal if previously VRE positive Once the C. Diff positive patient is discharged, the isolation is removed automatically Notify Infection Control to Remove Isolation Status from EPIC
Once MDROs are introduced into a healthcare setting, transmission and persistence of the resistant strain is determined by the: availability of vulnerable patients selective pressure exerted by antimicrobial use. the number of patients already colonized with an MDRO the impact of implementation and adherence to prevention efforts Patients vulnerable to colonization and infection include: those with severe disease those with compromised host defenses from underlying medical conditions recent surgery indwelling medical devices (e.g., urinary catheters or endotracheal tubes) Hospitalized patients have more risk factors than non-hospitalized patients, and have the highest infection rates.
Hands are the culprits There is ample epidemiologic evidence to suggest MDROs are carried from one person to another via the hands of HCW.  Hands are easily contaminated during the process of care-giving or from contact with environmental surfaces in close proximity to the patient.  Without adherence to published recommendations for hand hygiene and glove use HCW are more likely to transmit MDROs to patients.  Strategies to increase and monitor adherence are important components of MDRO control programs.
Standard Precautions are a group of infection prevention practices which apply to all patients, regardless of suspected or confirmed infection status. They are in effect for all patients, all the time. These include the use of: * Hand hygiene Gloves Gown Mask Eye protection, or face shield *depending on the anticipated exposure; and safe injection practices. Equipment or items in the patient environment likely to have been contaminated with body fluids must be handled in a  manner to prevent transmission of infectious agents.
	While good hand hygiene remains the most important method to prevent the transmission of any organism on the hands of HCW, the addition of Contact Precautions can break the chain of infection by preventing the organisms from being carried from one room to another on inanimate objects (foamites). Contact Precautions
Touching the PATIENT isn’t the only way to become contaminated with an MDRO!
Contact Isolation Precautions Place green Contact Isolation sign on the room door Any PERSON entering the room wears gloves and gown, no matter the reason for entering the room or for how long. This includes all staff and visitors.
Contact Isolation Precautions Remove Personal Protective Equipment and perform hand hygiene BEFORE leaving the room. Equipment from a Contact Precautions room should be disinfected before being used for the care of another patient .
Contact Isolation Precautions Sign
Stop Sign for Clostridium difficile Contact Precautions + Use ONLY soap & water to wash hands
Droplet Isolation Precautions Sign
Airborne Isolation Precautions Sign
12 Steps to Prevent Antimicrobial Resistance: Hospitalized Adults
Prevent Infection: Get the catheters out Fact:Catheters and other invasive devices are the #1 exogenous cause of hospital-onset infections. Actions: ,[object Object]
Use the correct catheter
Use proper insertion & catheter-care protocols
Remove catheters when not essential  ,[object Object]
The Infection Control Team Doramarie Arocha David Townson Gwen Way
Use Antimicrobials WiselyTreat infection, not colonization Fact:A major cause of antimicrobial overuse is treatment of colonization.  Actions: ,[object Object]
Treat bacteremia, not the catheter tip or hub
Treat urinary tract infection, not the indwelling catheter ,[object Object]
Know when to say “no” to vanco Fact:  Vancomycin overuse promotes emergence, selection, and spread of resistant pathogens. Actions: Treat infection, not contaminants or colonization  Fever in a patient with an intravenous catheter is not a routine indication for vancomycin
Use Antimicrobials Wisely When to stop antimicrobial treatment Fact:Failure to stop unnecessary antimicrobial treatment contributes to overuse and resistance. Actions: ,[object Object]
When cultures are negative and infection is unlikely
When infection is not diagnosed,[object Object]
Contain infectious body fluids	(use approved airborne/droplet/contact isolation precautions) ,[object Object],[object Object]
Prevent Transmission: Contain your contagion Patients from Long Term Acute Care Facilities (LTAC) have a higher incidence of being colonized with an MDRO Isolate immediately upon arrival, no questions asked! Follow MDRO Reduction Protocol Notify Infection Control
[object Object]
Dallas

Weitere ähnliche Inhalte

Was ist angesagt?

Hospital acquired infection presentation
Hospital acquired infection presentationHospital acquired infection presentation
Hospital acquired infection presentationlzeltzer
 
Surveillance of healthcare associated infections
Surveillance of healthcare associated infectionsSurveillance of healthcare associated infections
Surveillance of healthcare associated infectionsTHL
 
Mdro pct & non clinical final-January
Mdro pct & non clinical final-JanuaryMdro pct & non clinical final-January
Mdro pct & non clinical final-Januarycapstonerx
 
HOSPITAL-ACQUIRED INFECTION.pptx
HOSPITAL-ACQUIRED INFECTION.pptxHOSPITAL-ACQUIRED INFECTION.pptx
HOSPITAL-ACQUIRED INFECTION.pptxRinkupatel55
 
Multi drug resistant organisims
Multi drug resistant organisimsMulti drug resistant organisims
Multi drug resistant organisimsJayant Balani
 
Challenges in healthcare and infection control
Challenges in healthcare and infection controlChallenges in healthcare and infection control
Challenges in healthcare and infection controlLee Oi Wah
 
Hospital infection control(Indicators)
Hospital infection control(Indicators)Hospital infection control(Indicators)
Hospital infection control(Indicators)Jayant Balani
 
The Superbug MRSA !!
The Superbug MRSA !!The Superbug MRSA !!
The Superbug MRSA !!Aruna M Das
 
Prevention of Catheter Associated Urinary Tract Infection ( CAUTI ) [compatib...
Prevention of Catheter Associated Urinary Tract Infection ( CAUTI ) [compatib...Prevention of Catheter Associated Urinary Tract Infection ( CAUTI ) [compatib...
Prevention of Catheter Associated Urinary Tract Infection ( CAUTI ) [compatib...drnahla
 
Cauti.dr rudrika
Cauti.dr rudrikaCauti.dr rudrika
Cauti.dr rudrikarudrika
 
Hospital Acquired Infections
Hospital Acquired InfectionsHospital Acquired Infections
Hospital Acquired InfectionsSathish Kumar
 
Hospital Infection Control Guidelines-LECTURE (4).pptx
Hospital Infection Control Guidelines-LECTURE (4).pptxHospital Infection Control Guidelines-LECTURE (4).pptx
Hospital Infection Control Guidelines-LECTURE (4).pptxemmanueladdo39
 
Catheter Associated Urinary Tract Infections (CAUTI)
Catheter Associated Urinary Tract Infections (CAUTI)Catheter Associated Urinary Tract Infections (CAUTI)
Catheter Associated Urinary Tract Infections (CAUTI)Ujjwal Shah
 

Was ist angesagt? (20)

Hospital acquired infection presentation
Hospital acquired infection presentationHospital acquired infection presentation
Hospital acquired infection presentation
 
Surveillance of healthcare associated infections
Surveillance of healthcare associated infectionsSurveillance of healthcare associated infections
Surveillance of healthcare associated infections
 
Mdro pct & non clinical final-January
Mdro pct & non clinical final-JanuaryMdro pct & non clinical final-January
Mdro pct & non clinical final-January
 
HOSPITAL-ACQUIRED INFECTION.pptx
HOSPITAL-ACQUIRED INFECTION.pptxHOSPITAL-ACQUIRED INFECTION.pptx
HOSPITAL-ACQUIRED INFECTION.pptx
 
Mrsa ppt
Mrsa pptMrsa ppt
Mrsa ppt
 
Antimicrobial stewardship
Antimicrobial stewardshipAntimicrobial stewardship
Antimicrobial stewardship
 
Multi drug resistant organisims
Multi drug resistant organisimsMulti drug resistant organisims
Multi drug resistant organisims
 
Challenges in healthcare and infection control
Challenges in healthcare and infection controlChallenges in healthcare and infection control
Challenges in healthcare and infection control
 
Hospital infection control(Indicators)
Hospital infection control(Indicators)Hospital infection control(Indicators)
Hospital infection control(Indicators)
 
Catheter Associated Urinary Tract Infection (CAUTI)
Catheter Associated Urinary Tract Infection (CAUTI)Catheter Associated Urinary Tract Infection (CAUTI)
Catheter Associated Urinary Tract Infection (CAUTI)
 
The Superbug MRSA !!
The Superbug MRSA !!The Superbug MRSA !!
The Superbug MRSA !!
 
Prevention of Catheter Associated Urinary Tract Infection ( CAUTI ) [compatib...
Prevention of Catheter Associated Urinary Tract Infection ( CAUTI ) [compatib...Prevention of Catheter Associated Urinary Tract Infection ( CAUTI ) [compatib...
Prevention of Catheter Associated Urinary Tract Infection ( CAUTI ) [compatib...
 
Hospital Acquired Infection
Hospital Acquired Infection Hospital Acquired Infection
Hospital Acquired Infection
 
Cauti.dr rudrika
Cauti.dr rudrikaCauti.dr rudrika
Cauti.dr rudrika
 
CLABSI
CLABSICLABSI
CLABSI
 
Stop Cauti
Stop CautiStop Cauti
Stop Cauti
 
Hospital Acquired Infections
Hospital Acquired InfectionsHospital Acquired Infections
Hospital Acquired Infections
 
Antimicrobial Stewardship
Antimicrobial StewardshipAntimicrobial Stewardship
Antimicrobial Stewardship
 
Hospital Infection Control Guidelines-LECTURE (4).pptx
Hospital Infection Control Guidelines-LECTURE (4).pptxHospital Infection Control Guidelines-LECTURE (4).pptx
Hospital Infection Control Guidelines-LECTURE (4).pptx
 
Catheter Associated Urinary Tract Infections (CAUTI)
Catheter Associated Urinary Tract Infections (CAUTI)Catheter Associated Urinary Tract Infections (CAUTI)
Catheter Associated Urinary Tract Infections (CAUTI)
 

Andere mochten auch

Monitoring mdro in healthcare
Monitoring mdro in healthcareMonitoring mdro in healthcare
Monitoring mdro in healthcarePathKind Labs
 
Antimicrobial stewardship(asp)and mdr
Antimicrobial stewardship(asp)and mdrAntimicrobial stewardship(asp)and mdr
Antimicrobial stewardship(asp)and mdrDel Del
 
Internet & Medicine 2.0
Internet & Medicine 2.0Internet & Medicine 2.0
Internet & Medicine 2.0Anuj Sharma
 
Multi drug resistance molecular pathogenesis
Multi drug resistance   molecular pathogenesisMulti drug resistance   molecular pathogenesis
Multi drug resistance molecular pathogenesisAlagar Suresh
 

Andere mochten auch (6)

Monitoring mdro in healthcare
Monitoring mdro in healthcareMonitoring mdro in healthcare
Monitoring mdro in healthcare
 
Antimicrobial stewardship(asp)and mdr
Antimicrobial stewardship(asp)and mdrAntimicrobial stewardship(asp)and mdr
Antimicrobial stewardship(asp)and mdr
 
MDR , XDR
MDR , XDRMDR , XDR
MDR , XDR
 
Internet & Medicine 2.0
Internet & Medicine 2.0Internet & Medicine 2.0
Internet & Medicine 2.0
 
Multi drug resistance
Multi drug resistanceMulti drug resistance
Multi drug resistance
 
Multi drug resistance molecular pathogenesis
Multi drug resistance   molecular pathogenesisMulti drug resistance   molecular pathogenesis
Multi drug resistance molecular pathogenesis
 

Ähnlich wie Mdro infection controlnursing final version 11.17.09 1

Hospital acquired infections
Hospital acquired infectionsHospital acquired infections
Hospital acquired infectionsGiven Sishekano
 
Inf control for hcw 2012
Inf control for hcw 2012Inf control for hcw 2012
Inf control for hcw 2012Lee Oi Wah
 
Antimicrobial Resistance in Intensive Care Unit
Antimicrobial Resistance in Intensive Care UnitAntimicrobial Resistance in Intensive Care Unit
Antimicrobial Resistance in Intensive Care Unitmansoor masjedi
 
Prevention of Infection
Prevention of InfectionPrevention of Infection
Prevention of Infectionshabeel pn
 
Campaign to prevent antimicrobial resistance
Campaign to prevent antimicrobial resistanceCampaign to prevent antimicrobial resistance
Campaign to prevent antimicrobial resistanceguest3008cc
 
Capstone project multidrug resistant microorganisms
Capstone project multidrug resistant microorganismsCapstone project multidrug resistant microorganisms
Capstone project multidrug resistant microorganismsLaurie Crane
 
3. prophylactic use of Anti-microbial agents
3. prophylactic use of Anti-microbial agents3. prophylactic use of Anti-microbial agents
3. prophylactic use of Anti-microbial agentsJagirPatel3
 
Hospital Associated Infection ( Updated 2022 )
Hospital Associated Infection ( Updated 2022 ) Hospital Associated Infection ( Updated 2022 )
Hospital Associated Infection ( Updated 2022 ) Yashasvi Verma
 
ALERT ORGANISM SURVEILLANCE.pptx
ALERT ORGANISM SURVEILLANCE.pptxALERT ORGANISM SURVEILLANCE.pptx
ALERT ORGANISM SURVEILLANCE.pptxssuser60557c
 
Infection control orientation
Infection control orientationInfection control orientation
Infection control orientationsubauday
 
Hospital Acquired Infection
Hospital Acquired InfectionHospital Acquired Infection
Hospital Acquired InfectionRana Shankor Roy
 

Ähnlich wie Mdro infection controlnursing final version 11.17.09 1 (20)

Infection control in icu
Infection control in icuInfection control in icu
Infection control in icu
 
Hospital acquired infections
Hospital acquired infectionsHospital acquired infections
Hospital acquired infections
 
Inf control for hcw 2012
Inf control for hcw 2012Inf control for hcw 2012
Inf control for hcw 2012
 
Antimicrobial Resistance in Intensive Care Unit
Antimicrobial Resistance in Intensive Care UnitAntimicrobial Resistance in Intensive Care Unit
Antimicrobial Resistance in Intensive Care Unit
 
Prevention of Infection
Prevention of InfectionPrevention of Infection
Prevention of Infection
 
Campaign to prevent antimicrobial resistance
Campaign to prevent antimicrobial resistanceCampaign to prevent antimicrobial resistance
Campaign to prevent antimicrobial resistance
 
CDC12Step.ppt
CDC12Step.pptCDC12Step.ppt
CDC12Step.ppt
 
MRSA AN UPDATE
MRSA  AN UPDATE MRSA  AN UPDATE
MRSA AN UPDATE
 
Capstone project multidrug resistant microorganisms
Capstone project multidrug resistant microorganismsCapstone project multidrug resistant microorganisms
Capstone project multidrug resistant microorganisms
 
Infection control sandra
Infection control sandraInfection control sandra
Infection control sandra
 
3. prophylactic use of Anti-microbial agents
3. prophylactic use of Anti-microbial agents3. prophylactic use of Anti-microbial agents
3. prophylactic use of Anti-microbial agents
 
Infection control
Infection controlInfection control
Infection control
 
Nosocomial infections
Nosocomial infectionsNosocomial infections
Nosocomial infections
 
Hospital Associated Infection ( Updated 2022 )
Hospital Associated Infection ( Updated 2022 ) Hospital Associated Infection ( Updated 2022 )
Hospital Associated Infection ( Updated 2022 )
 
ALERT ORGANISM SURVEILLANCE.pptx
ALERT ORGANISM SURVEILLANCE.pptxALERT ORGANISM SURVEILLANCE.pptx
ALERT ORGANISM SURVEILLANCE.pptx
 
Infection control orientation
Infection control orientationInfection control orientation
Infection control orientation
 
Hospital Acquired Infection
Hospital Acquired InfectionHospital Acquired Infection
Hospital Acquired Infection
 
New precaution manual new version june 2010
New precaution manual   new version june 2010New precaution manual   new version june 2010
New precaution manual new version june 2010
 
AMR.pptx
AMR.pptxAMR.pptx
AMR.pptx
 
INFECTION AND CHALLENGES AHEAD BY Dr.T.V.Rao MD
INFECTION AND CHALLENGES AHEAD BY Dr.T.V.Rao MDINFECTION AND CHALLENGES AHEAD BY Dr.T.V.Rao MD
INFECTION AND CHALLENGES AHEAD BY Dr.T.V.Rao MD
 

Mehr von capstonerx

Annual ed personal prep for disaster alerts10 10
Annual ed personal prep for disaster alerts10 10Annual ed personal prep for disaster alerts10 10
Annual ed personal prep for disaster alerts10 10capstonerx
 
Annual ed dvt.pe.vte10 10
Annual ed dvt.pe.vte10 10Annual ed dvt.pe.vte10 10
Annual ed dvt.pe.vte10 10capstonerx
 
Annual ed restraint and seclusion.10 10
Annual ed restraint and seclusion.10 10Annual ed restraint and seclusion.10 10
Annual ed restraint and seclusion.10 10capstonerx
 
Annual ed pt fam views of restraints.10-10
Annual ed pt fam views of restraints.10-10Annual ed pt fam views of restraints.10-10
Annual ed pt fam views of restraints.10-10capstonerx
 
Annual ed being your best.7 10
Annual ed being your best.7 10Annual ed being your best.7 10
Annual ed being your best.7 10capstonerx
 
Annual ed recognition of abuse.neglect.09 10
Annual ed recognition of abuse.neglect.09 10Annual ed recognition of abuse.neglect.09 10
Annual ed recognition of abuse.neglect.09 10capstonerx
 
Annual ed core measures.09 10
Annual ed core measures.09 10Annual ed core measures.09 10
Annual ed core measures.09 10capstonerx
 
Annual ed pain mgt.clin staff.09.10
Annual ed pain mgt.clin staff.09.10Annual ed pain mgt.clin staff.09.10
Annual ed pain mgt.clin staff.09.10capstonerx
 
2010 cv annual ed central line care
2010 cv annual ed central line care2010 cv annual ed central line care
2010 cv annual ed central line carecapstonerx
 
Annual ed pain mgt nonclinical staff.09.10
Annual ed pain mgt nonclinical staff.09.10Annual ed pain mgt nonclinical staff.09.10
Annual ed pain mgt nonclinical staff.09.10capstonerx
 
Annual ed never events and poa.7 10
Annual ed never events and poa.7 10Annual ed never events and poa.7 10
Annual ed never events and poa.7 10capstonerx
 
Annual ed workplace violence.07.10
Annual ed workplace violence.07.10Annual ed workplace violence.07.10
Annual ed workplace violence.07.10capstonerx
 
Annual ed transplant awareness6 2010
Annual ed transplant awareness6 2010Annual ed transplant awareness6 2010
Annual ed transplant awareness6 2010capstonerx
 
Annual ed infection control.09
Annual ed infection control.09Annual ed infection control.09
Annual ed infection control.09capstonerx
 
Annual ed patient satisfaction6 2010
Annual ed patient satisfaction6 2010Annual ed patient satisfaction6 2010
Annual ed patient satisfaction6 2010capstonerx
 
Annual ed transplant awareness6 2010
Annual ed transplant awareness6 2010Annual ed transplant awareness6 2010
Annual ed transplant awareness6 2010capstonerx
 
Annual ed infection control.09
Annual ed infection control.09Annual ed infection control.09
Annual ed infection control.09capstonerx
 
Annual ed patient satisfaction6 2010
Annual ed patient satisfaction6 2010Annual ed patient satisfaction6 2010
Annual ed patient satisfaction6 2010capstonerx
 
Annual ed performance improvement.4 2010
Annual ed performance improvement.4 2010Annual ed performance improvement.4 2010
Annual ed performance improvement.4 2010capstonerx
 
Annual ed mission vision4 2010
Annual ed mission vision4 2010Annual ed mission vision4 2010
Annual ed mission vision4 2010capstonerx
 

Mehr von capstonerx (20)

Annual ed personal prep for disaster alerts10 10
Annual ed personal prep for disaster alerts10 10Annual ed personal prep for disaster alerts10 10
Annual ed personal prep for disaster alerts10 10
 
Annual ed dvt.pe.vte10 10
Annual ed dvt.pe.vte10 10Annual ed dvt.pe.vte10 10
Annual ed dvt.pe.vte10 10
 
Annual ed restraint and seclusion.10 10
Annual ed restraint and seclusion.10 10Annual ed restraint and seclusion.10 10
Annual ed restraint and seclusion.10 10
 
Annual ed pt fam views of restraints.10-10
Annual ed pt fam views of restraints.10-10Annual ed pt fam views of restraints.10-10
Annual ed pt fam views of restraints.10-10
 
Annual ed being your best.7 10
Annual ed being your best.7 10Annual ed being your best.7 10
Annual ed being your best.7 10
 
Annual ed recognition of abuse.neglect.09 10
Annual ed recognition of abuse.neglect.09 10Annual ed recognition of abuse.neglect.09 10
Annual ed recognition of abuse.neglect.09 10
 
Annual ed core measures.09 10
Annual ed core measures.09 10Annual ed core measures.09 10
Annual ed core measures.09 10
 
Annual ed pain mgt.clin staff.09.10
Annual ed pain mgt.clin staff.09.10Annual ed pain mgt.clin staff.09.10
Annual ed pain mgt.clin staff.09.10
 
2010 cv annual ed central line care
2010 cv annual ed central line care2010 cv annual ed central line care
2010 cv annual ed central line care
 
Annual ed pain mgt nonclinical staff.09.10
Annual ed pain mgt nonclinical staff.09.10Annual ed pain mgt nonclinical staff.09.10
Annual ed pain mgt nonclinical staff.09.10
 
Annual ed never events and poa.7 10
Annual ed never events and poa.7 10Annual ed never events and poa.7 10
Annual ed never events and poa.7 10
 
Annual ed workplace violence.07.10
Annual ed workplace violence.07.10Annual ed workplace violence.07.10
Annual ed workplace violence.07.10
 
Annual ed transplant awareness6 2010
Annual ed transplant awareness6 2010Annual ed transplant awareness6 2010
Annual ed transplant awareness6 2010
 
Annual ed infection control.09
Annual ed infection control.09Annual ed infection control.09
Annual ed infection control.09
 
Annual ed patient satisfaction6 2010
Annual ed patient satisfaction6 2010Annual ed patient satisfaction6 2010
Annual ed patient satisfaction6 2010
 
Annual ed transplant awareness6 2010
Annual ed transplant awareness6 2010Annual ed transplant awareness6 2010
Annual ed transplant awareness6 2010
 
Annual ed infection control.09
Annual ed infection control.09Annual ed infection control.09
Annual ed infection control.09
 
Annual ed patient satisfaction6 2010
Annual ed patient satisfaction6 2010Annual ed patient satisfaction6 2010
Annual ed patient satisfaction6 2010
 
Annual ed performance improvement.4 2010
Annual ed performance improvement.4 2010Annual ed performance improvement.4 2010
Annual ed performance improvement.4 2010
 
Annual ed mission vision4 2010
Annual ed mission vision4 2010Annual ed mission vision4 2010
Annual ed mission vision4 2010
 

Mdro infection controlnursing final version 11.17.09 1

  • 1. MDRO (Multiple drug-resistant organisms) How they relate to patients in the healthcare setting UT Southwestern University Hospitals: Infection Control Department
  • 2. Multi-drug resistant organisms (MDRO’s) have increased in prevalence in US hospitals over the last three decades These organisms have important implications for patient safety Options for treating patients with these infections are often extremely limited MDRO infections are associated with increased lengths of stay, costs, and mortality Background
  • 3. Methicillin Resistant Staphylococcus aureus (MRSA) was first isolated in the United States in 1968. In the early 1990s, MRSA accounted for 20%-25% of Staphylococcus aureus isolates from hospitalized patients. By 2003, MRSA accounted for >50% of S. aureus isolates from patients in ICUs. A similar rise in prevalence has occurred with Vancomycin Resistant Enterococcus (VRE) . From 1990 to 1997, the prevalence of VRE in Enterococcus isolates from hospitalized patients increased from <1% to approximately 15% . By 2003 VRE accounted for 28.5 % of Enterococcus isolates in ICUs. History of MDRO’s
  • 4. Methicillin-Resistant Staphylococcus aureus (MRSA) Vancomycin-Resistant Enterococcus species (VRE) Multidrug-Resistant (MDR) Acinetobacter species. Multidrug-Resistant (MDR) Klebsiella species, Enterobacter species, and Escherichia coli. Resistant Organisms include:
  • 5. To be defined as an MDRO the organism must meet these criteria: MRSA: S. aureus tests resistant to Oxacillin VRE: Enterococcus species tests resistant to Vancomycin. MDRO-Acinetobacter species: Resistant to all agents tested within at least 3 antimicrobial classes, including B-lactams, carbapenems, aminoglycosides and fluoroquinolones Specific definitions
  • 6. Resistant Bacteria Mutations XX Resistance Gene Transfer New Resistant Bacteria Emergence of Antimicrobial Resistance Susceptible Bacteria Bacteria have evolved to evade antimicrobial drugs through chromosomal mutations & acquisition of resistance genes via conjugation, transposition, or transformation
  • 7. Resistant StrainsRare Antimicrobial Exposure x Resistant Strains Dominant x x x x x x x x x x x Selection for antimicrobial-resistant Strains Once resistant strains of bacteria are present in a population, exposure to antimicrobial drugs favors their survival.
  • 8. Methicillin Methicillin-resistant S. aureus (MRSA) [1970s] Vancomycin [1997] [1990s] [ ???? ] Vancomycin-resistant Vancomycin Vancomycin- resistant S. aureus enterococci (VRE) intermediate- resistant S. aureus (VISA) Penicillin Penicillin-resistant S.aureus [1950s] S. aureus Introduction of every new class of antimicrobial drug is followed by emergence of resistance
  • 9. B-lactams: includes ampicillin/sulbactam, piperacillin/tazobactam, cefepime, ceftazidime Carbapenems: includes imipenam, meropenem and doripenam Aminoglycosides: includes amikacin, gentamycin, tobramycin Fluoroquinolones: includes ciprofloxacin, levofloxacin Drug classes:
  • 10. Staphylococcus aureus commonly found on skin, in eyes, upper respiratory track, mouth, and GU system developed resistance to many Antibiotics including Methicillin (oxacillin) to create the particular strain, MRSA MRSA Is found anywhere Staphylococcus aureus is commonly found may colonize the patient or cause active infections is a public health concern because there are few drugs left to treat serious MRSA infections. Vancomycin is the current drug of choice for serious infections. Other antimicrobial agents would include: Daptomycin and Linezolid. A high percentage of wound infections are caused by MRSA. Reservoirs for MRSA in the hospital include infected or colonized patients with HCW being the link for nosocomial spread of the infection. The main mode of transmission is via hands of HCW. Other reservoirs include contaminated equipment and other items in the environment Methicillin-Resistant Staphylococcus aureus (MRSA)Fact Sheet
  • 11. The emergence of new epidemic strains of MRSA in the community, (CA-MRSA) among patients without established MRSA risk factors, may present new challenges to MRSA control in healthcare settings. Historically, genetic analyses of MRSA isolated from patients in hospitals worldwide revealed a relatively small number of MRSA strains have the unique qualities to facilitate transmission from patient to patient. To date, most MRSA strains isolated from patients with CA-MRSA infections have been microbiologically distinct from those endemic in healthcare settings, suggesting some of these strains may have arisen de novo in the community via the acquisition of the mecA gene from Methicillin Susceptible Staph aureus. CA-MRSA infection commonly presents as relatively minor skin and soft tissue infections, but severe invasive disease and mortalities have been described in children and adults. Community-associated MRSA
  • 12. When a patient is identified as having an infection or colonization with an MDRO: Place the patient in Contact Precautions Enter the isolation information into EPIC Staff will be alerted of isolation status upon subsequent admissions into the hospital Monitoring of MDRO’s
  • 13. Infection control monitors MDRO incidence and transmission and provides data monthly and quarterly to the units Monitoring of MDRO’s
  • 14. Removing Patients From Isolation Follow-up screenings MUST be negative: Original site of infection + Nasal if previously MRSA positive or Rectal if previously VRE positive Once the C. Diff positive patient is discharged, the isolation is removed automatically Notify Infection Control to Remove Isolation Status from EPIC
  • 15. Once MDROs are introduced into a healthcare setting, transmission and persistence of the resistant strain is determined by the: availability of vulnerable patients selective pressure exerted by antimicrobial use. the number of patients already colonized with an MDRO the impact of implementation and adherence to prevention efforts Patients vulnerable to colonization and infection include: those with severe disease those with compromised host defenses from underlying medical conditions recent surgery indwelling medical devices (e.g., urinary catheters or endotracheal tubes) Hospitalized patients have more risk factors than non-hospitalized patients, and have the highest infection rates.
  • 16. Hands are the culprits There is ample epidemiologic evidence to suggest MDROs are carried from one person to another via the hands of HCW. Hands are easily contaminated during the process of care-giving or from contact with environmental surfaces in close proximity to the patient. Without adherence to published recommendations for hand hygiene and glove use HCW are more likely to transmit MDROs to patients. Strategies to increase and monitor adherence are important components of MDRO control programs.
  • 17. Standard Precautions are a group of infection prevention practices which apply to all patients, regardless of suspected or confirmed infection status. They are in effect for all patients, all the time. These include the use of: * Hand hygiene Gloves Gown Mask Eye protection, or face shield *depending on the anticipated exposure; and safe injection practices. Equipment or items in the patient environment likely to have been contaminated with body fluids must be handled in a manner to prevent transmission of infectious agents.
  • 18. While good hand hygiene remains the most important method to prevent the transmission of any organism on the hands of HCW, the addition of Contact Precautions can break the chain of infection by preventing the organisms from being carried from one room to another on inanimate objects (foamites). Contact Precautions
  • 19. Touching the PATIENT isn’t the only way to become contaminated with an MDRO!
  • 20. Contact Isolation Precautions Place green Contact Isolation sign on the room door Any PERSON entering the room wears gloves and gown, no matter the reason for entering the room or for how long. This includes all staff and visitors.
  • 21. Contact Isolation Precautions Remove Personal Protective Equipment and perform hand hygiene BEFORE leaving the room. Equipment from a Contact Precautions room should be disinfected before being used for the care of another patient .
  • 23. Stop Sign for Clostridium difficile Contact Precautions + Use ONLY soap & water to wash hands
  • 26. 12 Steps to Prevent Antimicrobial Resistance: Hospitalized Adults
  • 27.
  • 28. Use the correct catheter
  • 29. Use proper insertion & catheter-care protocols
  • 30.
  • 31. The Infection Control Team Doramarie Arocha David Townson Gwen Way
  • 32.
  • 33. Treat bacteremia, not the catheter tip or hub
  • 34.
  • 35. Know when to say “no” to vanco Fact: Vancomycin overuse promotes emergence, selection, and spread of resistant pathogens. Actions: Treat infection, not contaminants or colonization Fever in a patient with an intravenous catheter is not a routine indication for vancomycin
  • 36.
  • 37. When cultures are negative and infection is unlikely
  • 38.
  • 39.
  • 40. Prevent Transmission: Contain your contagion Patients from Long Term Acute Care Facilities (LTAC) have a higher incidence of being colonized with an MDRO Isolate immediately upon arrival, no questions asked! Follow MDRO Reduction Protocol Notify Infection Control
  • 41.
  • 44. Plano
  • 48. Multiple Locations in Dallas and Fort Worth
  • 60. Baylor Specialty HospitalMulti-Drug Resistant Organism Reduction (MDRO) Protocol: Known LTACs
  • 61. Multi-Drug Resistant Organism (MDRO) Reduction Screening Protocol
  • 62.
  • 63.
  • 64. Transport the labeled specimen to the lab WITHIN 1 HOUR.
  • 65. Label the swab with the patient’s preprinted label in the presence of the patient, in the patient’s room
  • 68. Transport the labeled specimen to the lab WITHIN 1 HOUR.Push the end of the swab firmly to ensure that the swab is inserted into the end of the transport tube. Ensure that the swab tip is in contact with the moistened pledget. Secure the transport tube cap. Label the swab with the patient’s preprinted label in the presence of the patient, in the patient’s room Remove and discard gloves
  • 69.
  • 72.