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MRSA. Initially emerged in the 1960'sMajor pathogen by 1980Currently 30% of Staph aureus in hospitals is Methicillin-resistantCommunity carriage is 4-10% and growing.. Classical Risk Factors for MRSA. Prior antibioticsPenicillinsCephalosporinsaminoglycosidesProlonged hospitalization (nursin
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1. MRSA: A Doctors Nightmare? John Verstraete D.O.
Mid-America Infectious Disease Consultants
2. MRSA Initially emerged in the 1960s
Major pathogen by 1980
Currently 30% of Staph aureus in hospitals is Methicillin-resistant
Community carriage is 4-10% and growing.
3. Classical Risk Factors for MRSA Prior antibiotics
Penicillins
Cephalosporins
aminoglycosides
Prolonged hospitalization (nursing homes)
Underlying disease (COPD)
Advanced age
Invasive procedures
4. Community Acquired MRSA Often do not fall into the classical risk groups
Several other antibiotic options often still show sensitivity
Involved healthy individuals
Spider bite?
5. Transmission of MRSA Patients are commonly colonized in the nares or respiratory tract or on their skin
Transmission is typically by direct contact with colonized or infected persons
6. Microbiology of MRSA Caused by changes in penicillin binding proteins
Generally resistant to all B-lactam antibiotics
May be resistant to TMP/Sulfa, Tetracyclines, Quinolones
Vancomycin resistance has been reported (VISA, GISA)
7. Clinical Manifestations of MRSA Infection
Skin/soft tissue infection
Pneumonia
Endocarditis
Bone infection
Line infection
8. CA-MRSA Recurrent skin infections
9. Colonization of the Newborn
Uterus and contents are normally sterile and remain so until just before birth.
Breaking of fetal membrane exposes the infant; all subsequent handling and feeding continue to introduce what will be later become normal flora.
10. Resident Flora Includes bacteria, fungi, protozoa, viruses and arthropods
Most areas of the body in contact with the outside environment harbor resident microbes; large intestine has the highest numbers of bacteria.
Internal organs and tissues and fluids are microbe-free.
Bacterial flora benefit host by preventing overgrowth of harmful microbes microbial antagonism.
11. Staphylococcus aureus Gram-positive bacterium that frequently colonizes the nose and skin of healthy persons
Leading cause of skin & soft tissue infections (SSTI)
Abscesses (boils), furuncles, and cellulitis
12. Methicillin-resistant Staphylococcus aureus (MRSA) Resistant to all beta-lactam antibiotics
Note: methicillin no longer used clinically or in lablook for oxacillin or nafcillin resistance
Increasingly important cause of healthcare-associated infections since the 1960s
For 20 yrs, MRSA infections mostly associated with healthcare settings
13. Here we have plotted theprevalenceo MRSA, MR CNS and VRE reported from
nosocomial infections. These pathogens account for over half of the bloodstream
infections among ICU patients. In 1999 the prevalence of MRSA has broken the 50%
mark for ICU patients, and VRE has reached 25%.Here we have plotted theprevalenceo MRSA, MR CNS and VRE reported from
nosocomial infections. These pathogens account for over half of the bloodstream
infections among ICU patients. In 1999 the prevalence of MRSA has broken the 50%
mark for ICU patients, and VRE has reached 25%.
14. Emergence of MRSA in the Community 1990s: Strains of MRSA distinct from those already established in healthcare settings (HA-MRSA) emerged worldwide as a cause of infection among otherwise healthy adults and children in the community (CA-MRSA)
Genetic characteristics of these strains suggested they originated in the community, and did not spread from hospitals
15. Original Case Definition for CA-MRSA A positive culture for MRSA within 48 hours of admission
No history of hospitalization, surgery, residence in a long-term care facility, or dialysis within the prior year
No indwelling or percutaneous medical devices
No history of MRSA infection or colonization
16. Distinctions Between CA-MRSA and HA-MRSA Now Blurring Strain characteristics (genotypes & susceptibility profiles) are becoming less closely linked to epidemiologic case classifications (CA-MRSA vs. HA-MRSA)
Movement of community strains into healthcare settings
Emerging resistance to non-beta-lactam agents in community strains
17. MRSA Was the Most Commonly Identified Cause of Purulent SSTIs Among Adult ED Patients
18. Factors Facilitating MRSA Transmission (5 Cs)
Contact
Crowding
Contaminated items
Compromised skin integrity
Cleanliness (lack thereof)
19. Persons at Risk for CA-MRSA
Household contacts of patient with proven CA-MRSA
Day-care center contacts of hospitalized patients with MRSA infection
Incarcerated persons
Soldiers
Men who have sex with men
Drug users
Athletes
Students
Children
20. Persons at Risk for CA-MRSA (cont.)
Pacific Islanders
Native Americans
Persons with a previous CA-MRSA infection
21. Its Everywhere
22. Clinical Considerations SSTI MRSA Obtain material for culture
I&D should be routine for all purulent skin lesions
No data to suggest molecular typing or toxin-testing should guide management
23. Clinical Management of SSTI MRSA Incision & drainage is the mainstay
Antimicrobial therapy sometimes prudent
Use susceptibility data to guide treatment
Avoid fluoroquinolones & macrolides
Nasal culture not typically beneficial
Patient education is critical!
Maintain adequate follow-up
24. Empiric Antibiotic: Considerations Severity & rapidity of progression, or cellulitis
Signs and symptoms of systemic illness
Patient co-morbidities or immune suppression
e.g., diabetes mellitus, neoplastic disease, HIV infection
Extremes of patient age
Location of the abscess
area difficult to drain or associated with septic phlebitis of major vessels (e.g., central face)
Lack of response to initial treatment with I & D alone
25. Options for Outpatient Rx of MRSA SSTIs
26. Infection Control in the Clinic(open or draining SSTI) Wear gloves when providing care for patients
Remove gloves before leaving the patient's room and wash hands or use alcohol-based hand sanitizer immediately.
Do not touch potentially contaminated environmental surfaces or items in the patient's room after glove removal and hand washing, to avoid transfer of microorganisms to other patients and environments.
27. Infection Control in the Clinic(open or draining SSTI) cont. Wear a gown (if there will be substantial contact with the patients wound)
Remove the gown before leaving the examination room
Limit the movement and transport of the patient
Ensure that patient-care items and potentially contaminated surfaces are cleaned and disinfected after use.
Avoid wearing ties
Clean stethoscope after each patient
28. Key Prevention Messages for Patients and their Close Contacts Keep wounds that are draining covered with clean, dry, bandages
Clean hands regularly with soap and water or alcohol-based hand gel (if hands are not visibly soiled). Always clean hands immediately after touching infected skin or any item that has come in direct contact with a draining wound
Maintain good general hygiene with regular bathing
Do not share items that may become contaminated with wound drainage, such as towels, clothing, bedding, bar soap, razors, and athletic equipment that touches the skin
29. Key Prevention Messages for Patients and their Close Contacts (cont.) Launder clothing that has come in contact with wound drainage after each use and dry thoroughly.
If you are not able to keep your wound covered with a clean, dry bandage at all times, do not participate in activities where you have skin to skin contact with other persons (such as athletic activities) until your wound is healed.
Clean equipment and other environmental surfaces with which multiple individuals have bare skin contact with an over the counter detergent/disinfectant that specifies Staphylococcus aureus on the product label and is suitable for the type of surface being cleaned.
Isolation is not practical
30. Case 1 87 y.o. white male presents with complaints of a wound on his foot
PMH COPD DM
MEDS Albuterol Inhaler prn, Insulin, Multi- vitamin
Allergies PCN-rash
SH- remote tobacco, denies ETOH, lives in a Nursing home
FH- positive for DM in mother
Temp 102.5 120 28 140/90 88%
31. Case 1 cont. Gen A & O x 3
HEENT- PERRLA, EOMI
Neck- supple, No LAD, No JVD
H-tacky
L- CTA
Abd- Soft NT ND
Ext- Marked erythema of Left foot with ulceration
WBC-13,000 with an increased number of PMNs
32. An infected ulceration plantar to the fifth metatarsal head. This ulceration could be probed to the bone, and a deep space infection was present. The patient was taken to surgery to drain the underlying abscess.
33. Foot infection. Radiographs of the foot demonstrate the development of osteomyelitis. The cuboid, anterior portion of the calcaneus, base of the fifth metatarsal, and base of the fourth metatarsal were all involved and required debridement.
34. Foot infection. Lateral view of foot demonstrating osteomyelitis
35. Most Likely Infecting bacteria
Staph aureus
Strept
Gram Negatives (Pseudomonas)
Anerobes
36. Due to pts allergy pt was started on IV
Cefepime
37. Despite minimal improvement, on day 3 it was noted that patients culture was positive for MRSA. Patient was immediately changed to Vancomycin.
38. Pt was transferred to the skilled unit to complete 6 weeks of IV vancomycin.
39. Diabetic Foot Infection Prevelance
An estimated 15% of people with diabetes in the United States will develop a foot ulcer that may have a potentially serious complication
Microbiology
The predominant pathogens in DFI are aerobic gram positive cocci
Gram negative rods, and anaerobes.
?MRSA
40. Treatment of MRSA Vancomycin is the drug of choice
Zyvox (Linezolid) IV or oral an alternative
Synercid (Quinupristin/Dalfopristin) IV only
Cubicin (Daptomycin) is another IV alternative (Doesnt cover pulmonary infections)
Mild MRSA infections
TMP/Sulfa
Tetracyclines
Rifampin
Quinolones
Removal of foreign bodies
41. Case 2 JB is a previously healthy 49 year old white male
He cut his foot on a clean piece of aluminum that he was installing around a window frame of his house in late April
He received local wound care only and the wound appeared to heal and crust over
Approximately 1 week later, the wound began to develop erythema, swelling, & pain;
Ffevers or chills
42. Case Presentation The wound later spontaneously opened and purulent material began to drain from it
The swelling and erythema began to spread up the leg
There was increased pain with movement of the leg or with ambulation
Pt. presented to a local ED
43. Case Presentation Afebrile upon presentation (T=98.9)
ESR 77; CRP 29.99, WBC=11,000
Plain films ? marked soft tissue swelling but no evidence of osteo, fracture, or foreign body
Pt was admitted.
Seen by podiatry and thought to have an abscess
Underwent I & D; cultures submitted
44. Case Presentation Treated with cefazolin, elevation, W?D dressings, with a slow response
Culture data then forthcoming
ID consult was obtained
45. Culture Results
46. Infectious Disease Conclusions Foot soft tissue infection/abscess secondary to MRSA no evidence of bony involvement S/P I&D
Cefazolin was changed to vancomycin with cont. tx for 2 weeks
Of interest was that the infection was community-acquired. Pt had no risk factors for MRSA nor did any of his immediate family.
47. Resistant Gram Positive Organisms Whos Winning?
48. Case presentation 33 y/o male nurse admitted to the hospital because of fever and increasing pain in the right leg
On physical exam he appeared toxic and there was erythema over the medial malleolus
Patient believed he had been bitten by a spider
The next day the leg doubled in size, he is lethargic and c/o severe pain.
50. Differential diagnosis Staph or strep Grp A Strept cellulitis
Necrotizing fasciitis
Clostridial myonecrosis
Synergistic necrotizing cellulitis
Vibrio vulnificus
Capnocytophaga canimorsus (DF-2)
51. MRSA Hospital-acquired Infections
52. Pathogenesis MRSA colonization can lead to infection
Increased colonization seen in the elderly, and debilitated patients
Increased colonization also seen in:
-Hospital workers - Dialysis pts
-Newborns -IVDA pts
-Pts with dermatitis - IDDM pts
-Previous exposure to ABXs
53. Modes of Transmission Principle mode of spread is pt. to pt. via transiently colonized HANDS of hospital personnel
Acquired from direct pt. contact or handling
contaminated equipment (stethoscopes, thermometers)
Airborne transmission ?
Chronic-care facilities are the major reservoir
54. Virulence MRSA strains are NOT more virulent than MSSA
MRSA strains are NOT less virulent than MSSA
MRSA strains are NOT more contagious
Increase risk of infection:
Long-term colonization
Underlying host factors
Increasing disability
55. Treatment of MRSA Vancomycin is drug of choice
If vancomycin allergic, TMP/SMX + rifampin, clindamycin, doxycycline, linezolid, synercid, daptomycin
Vancomycin is ineffective in eradicating the carrier state
56. Guidelines for Infection Control Identify the pts and place on contact isolation
HANDWASHING ;Change gloves between patients!!!
Alcohol hand rub liquid
Keep BP cuff, stethoscopes, etc. in pts room
Do not transfer instruments from pt to pt unless disinfect between pts i.e. scissors
57. Preventing Antimicrobial Resistance in Hospitals Prevent Infection Use Antimicrobials Wisely
1. Seek expert input
2. Get the catheters out 3. Know you antibiogram
Eradicate Infection
4. Obtain cultures 5. Know when to say no to Vanco
6. Treat to cure 7. Less is best
8. Dont treat colonization
9. Quit when you are ahead
58. Use Antimicrobials Wisely Less is often best
Target the pathogen and only the pathogen
Use/switch ASAP to an effective narrow spectrum regimen
59. Dont treat pseudobacteremias Coag-negative staphylococci
Patient risk factors?
Prosthetic devices?
Check # positive / # ordered
Compare antibiograms/ fingerprints
60. Use Antimicrobials Wisely Dont treat colonization
Treat pneumonia, not the endotracheal tube
Treat urinary tract infection, not the Foley catheter
Treat bacteremia, not the catheter tip
Treat the bone infection, not the skin flora
61. Use Antimicrobials Wisely Quit when you are ahead
Stop antimicrobials
When infection is not diagnosed
When infection is unlikely
When cultures are negative
62. Prevent Transmission Isolate the pathogen
Use standard infection control precautions
Contain infectious body fluids
Airborne/droplet/contact precautions
When in doubt use common sense
63. Prudence use of Antibiotics Antibiotics exert tremendous selection pressure for organisms to develop resistance
64. Zyvox
Bactrim
Doxycycline
Clindamycin (Risk for C-diff)
Levaquin? Oral Options for MRSA
65. Decolonization? Effectiveness in preventing disease not clear
Resistance is a concern
May be reasonable to administer (after optimizing basic strategies):
Patient with recurrent infections
Ongoing transmission in a closely-associated cohort (e.g., household)
Appropriate regimens (agents and schedules) not established for community settings