Skin and Soft Tissue Infections Flashcards

1
Q

What is the most common pathogen in skin abscesses?

A

S. aureus (75%)

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2
Q

What ate the main kinds of skin abscesses?

A
  • nodules, carbuncles and furuncles
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3
Q

What is a nodule?

A
  • painful and red in the dermis and deeper structures
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4
Q

What is a furuncles?

A
  • boils in the hair follicle

- inflammatory nodule with overlying pustule collection in the dermis and the deeper structures

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5
Q

What are carbuncles?

A
  • collection of furuncles
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6
Q

Where are skin abscesses usually located?

A
  • on the back of the neck, face and axillae
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7
Q

What is the difference between an abscess and cellulitis?

A

Abscess - kind of like a pocket

Cellulitis - goes into the structure of the fat and the hair glands

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8
Q

Where does an abscess usually start?

A
  • typically in the hair follicle
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9
Q

What is the general approach to treating skin abscesses?

A
  • drainage plus/minus heat compresses by 30 minutes, 3-4 times daily for small lesions, or surgical incision and drainage for larger lesions
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10
Q

When is antimicrobial therapy needed to treat a skin abscess?

A
  • for abscesses larger than 2 cms, multiple lesions, extensive cellulites, systemic signs of infection, indwelling medical device or immunocompromised
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11
Q

What are the 2 most common antibiotics for treating skin abscesses?

A

Cloxacillin

Cephalexin

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12
Q

What is the alternative therapy for treating skin abscess in a severe beta lactam allergy?

A

clindamycin

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13
Q

What is the risk of using Clindamycin to treat a skin abscess?

A

increasing resistance in S. aureus

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14
Q

What are the risk factors for a MRSA infection?

A
  • MRSA colonization, close contact with MRSA infection, previous antimicrobials or S aureus infection particularly is treatment failure with regimen that lacked MRSA coverage
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15
Q

In what facilities are hospital acquired MRSA infections generally spread?

A
  • medical procedures
  • dialysis
  • hospitalization
  • long term care facilities
  • higher antimicrobial resistance rates than CA strains
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16
Q

What antibiotics are MRSA resistant to? What causes this resistance

A
  • penicillins
  • cephalosporins
  • carbapenams

– alterations in the penicillin binding protein causes this resistance to occur

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17
Q

How can S. aureus get into the body?

A
  • natural bug on the skin- if a patient is immunocompromised or in the case of a cut it can get into the skin
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18
Q

What medications are used to treat community acquired skin and soft tissue infections?

A
  • Clindamycin (if macrolide resistant there will be an increased risk of inducible clindamycin resistance developing during therapy)
  • Doxycycline
  • TMP-SMX
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19
Q

Explain an approach to managing patients with recurrent furuncles or carbuncles?

A
  • S. aureus colonized (positive nasal swabs) - mupirocin 2% applied 2-3 time daily for 5 days every month
  • decolonize their nose as a way to get rid of the staph where it is colonized. This can get rid of the skin and staph infections and these patients are susceptible to
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20
Q

Describe the characteristics and most common pathogens of impetigo?

A
  • highest incidence in children 2-5 years old

- superficial infection of epidermis, 90% non-bullous, 10% bullous

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21
Q

What bacteria are potentially in non-bullous impetigo?

A

S aureus and S pyogenes

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22
Q

What bacteria are potentially in bullous impetigo?

A

S aureus

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23
Q

Gram positive cocci in clumps are _____

A

Staph aureus

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24
Q

Gram positive cocci in a chain are _____

A

Strep pyogenes

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25
Q

Is antimicrobial therapy always indicated?

A
  • moderate to severe non-bullous, and bullous infection
  • mild, non-bullous infections often resolve spontaneously within weeks, however antimicrobial therapy reduces transmission, hastens symptoms and progression, prevents complications
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26
Q

Where is strep. viridans usually found?

A

in the mouth and in endocarditis

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27
Q

What factors influence the selection of topical antimicrobial therapy?

A
  • non-bullous infections with limited area and number of lesions and low risk of complications
  • mupirocin 2% applied bid for 5 days - mono carboxylic acid inhibits RNA synthesis, more effective than the alternatives
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28
Q

What are the anti-staph antibiotics used to treat impetigo?

A
  • cloxacillin, cephalexin (these are anti-staph - clindamycin in the case of severe beta lactic allergies)
  • – duration of 7 days
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29
Q

What are the po antimicrobial options for pathogen-directed therapy?
(MSSA)

A

cloxacillin and cephalexin

Clindamycin in the case of severe beta lactic allergies

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30
Q

What are the po antimicrobial options for pathogen directed therapy? (MRSA)

A

Clindamycin and doxycycline or TMP-SMX

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31
Q

What are the po antimicrobial options for pathogen directed therapy to treat S. pyogenies?

A

Pen V or Amoxicillin

Clindamycin in the case of a severe beta lactam allergy

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32
Q

Doxycycline does not cover ______ infections

A

Strept. pyogenes

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33
Q

Who can you not give doxycycline to? Why?

A
  • You cannot give doxy to pregnant women and children- it affects the bone and teeth formation
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34
Q

What is the main side effect associated with TMP-SMX?

A

-severe allergy or sensitivity reactions

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35
Q

Describe cellulitis

A
  • diffuse, superficial skin infection of epidermis and dermis that can extend to cutaneous lymphatics and SC fat; erysipelas synonymous with cellulitis, with various definitions but generally superficial involving upper dermis or lower superficial lymphatics with more delineated borders
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36
Q

What bug is the most common in cellulitis?

A
  • S pyogenes and other beta hemolytic streptococcus including Group B, C, F or G, or less common S aureus (typically associated with purulence abscess, wound, trauma)
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37
Q

What is the clinical presentation of cellulitis?

A
  • appearance can include orange-peel-like, vesicles, bullae, petechiae or ecchymoses, phlebitis or lymphangitis (streaking)
  • local pain, erythema, warmth, deem with systemic sings of infection (fever, chills and malaise)
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38
Q

What are the risk factors for cellulitis?

A
  • skin disruption (abrasion, insect bite, ulcer, wound, trauma, IVDU), inflammation (eczema, radiation)
  • advanced age, obesity
  • diabetes mellitus, immunocompromised
  • peripheral vascular disease, lymphatic obstruction
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39
Q

What are the important adjuvant, non-pharm measures for treating cellulitis?

A
  • immobilization
  • elevation
  • cool and warm dressing
40
Q

Why would we use rifampin to treat a staphylococcal infection?

A
  • used in combination with other medications because on its own it can lead to resistance
  • we use rifampin to treat some STAPH infections but only in combination with other antibiotics
  • also use in the case of prosthetic join replacement
41
Q

What enzyme does rifampin induce?

A
  • Cyp P450
42
Q

What is the interaction between TMPSMX and spironolactone?

A
  • affects the renal elimination of potassium so it will increase the K in the body
  • doxy does not have this interaction with spironolactone
43
Q

What factors are considered in selecting po vs IV antimicrobials for treating cellulitis?

A
  • severity of cellulitis based on location, area and progression
  • systemic signs of infections (fever, chills, confusion)
  • po tolerability
44
Q

What is the drug indicated for treating a mild cellulitis infection with S. pyogenes? (po)

A

Pen V
Amov
[Clinda]
— TMPSMX and Doxy both lack strept coverage so therefore clinda is our drug

45
Q

What are the medications that are used for severe cellulitis with suspected pyogenes and/or MSSA?

A
  • cloxacillin
  • cephazolin, cephalexin
    [clinda]
46
Q

You can never give _____ and ______ with an MSSA infection? (do not want to miss the chance that the patient is infected with staph)

A

penicillin and amoxicillin

47
Q

What antibiotic (IV) us used to treat severe cellulitis in outpatient IV programs?

A
  • ceftriaxone (can be given OD)
48
Q

What are the drugs that could be used in treating moderate cellulitis for treating suspected s.pyogenes and/or MRSA?

A
  • clindamycin
  • doxy + (pen and amox)
  • TMP-SMX + (pen and amox)
49
Q

What are the risk factors for MRSA?

A
  • MRSA colonization, close contact with MRSA infection, previous antimicrobials or S.aureus infection particularly if treatment failure with regimen that lacked MRSA coverage
50
Q

What is used for severe cellulitis with suspected S.pyogenes and/or MRSA?

A
  • vancomycin (this is the drug of choice)

[linezolid (also po) or daptomycin]

51
Q

What are the potential disadvantages of using Levo or Moxi?

A
  • quinolines should never be used for a SSTI
  • less effective than the alternative due to unreliable strept and staph activity from intrinsic or acquired resistance during therapy
  • unnecessarily broad Gram negative coverage
  • increasing resistance and significant cover regarding collateral resistance
52
Q

Why might a cellulitis infection get worse after you start antibiotics?

A
  • if the patient receives appropriate therapy and the bacteria break open - release all of the toxins that were inside of the cells so you can notice that the site of infection may not get better in 2 days and might actually get worse
  • should notice that fever and fatigue are better however
53
Q

What is the typical response and duration of therapy for uncomplicated cellulitis?

A

Response: clinical improvement within 24-48 hours, visible improvement may be delayed for 72 hours
Duration: 5 days (for 14 days for severe infection, slow response, immunocompromised)

54
Q

Describe type 1 necrotizing cellulitis

A
  • Type 1 (80%) associated with surgery or trauma; polymicrobial mixed infection with GP, GN and anaerobes
55
Q

Describe type 2 necrotizing cellulitis

A
  • Type 2 (streptococcal gangrene, flesh eating bacteria) caused by virulent S.pyogenes, very rapid progression with severe systemic signs of infection including septic shock
56
Q

Describe type 3 necrotizing cellulitis

A

Type 3 (clostridial gas gangrene- C.perfringens, myonecrosis- C.septicum) associated with surgery or trauma, very rapid progression with gas production and myonecrosis

57
Q

What is used as empirical broad-spectrum antimicrobial therapy for necrotizing cellulitis?

A
  • pip-tazo or meropenum + vanco + clinda
58
Q

S.pyogenes is treated with what?

A
  • PenG and clinda and IVIG for toxic shock
59
Q

Clostridium is treated with what?

A
  • PenG and clinda and IVIG for toxic shock
60
Q

Aeromonas hydrophila (fresh water) is treated with what?

A
  • TMPSMX or Cipro and Ceftriaxone for Doxy
61
Q

Vibrio vulnificus (sea water) is treated with what?

A
  • ceftriaxone and doxy/cipro
62
Q

Why do we want to save carbapenems for last resort?

A
  • broadest antibiotics that we have - carbapenams are the last line of antibiotics and we want to save these antibiotics for when we absolutely need them- we are very worried about resistance
63
Q

Clindamycin is a _____ inhibitor?

A
  • ribosomal- therefore it is inhibiting the synthesis of proteins in the body
  • – macrolides and tetracyclones are also ribosomal inhibitors of protein synthesis
64
Q

What bugs are typically present in a dog or cat bite wounds?

A
  • pasteurella multocida. steptococcus or S.aureus, fusobacteria, prevotella, porphyromonas, bacteroides spp
65
Q

P. multocida is typically susceptible to Pen, Doxy, FQ, TMPSMA and is resistant to what?

A
  • Clinda
66
Q

How many days before do you give antibiotics prophylactically for animal bite wounds?

A
  • 3-5 days before to prevent infection of high risk wounds from a moderate to severe bite, on face, on hands involving joins, significant edema or immunocompromised
67
Q

What is the duration of therapy when treating a bite wound that is already infected?

A

5 to 10 days

68
Q

What is the first line antibiotic for treating an animal bit wound?

A
  • amoxi-clav 875/125 mg q12h, children 20 mg/kg
69
Q

What are the alternatives that are used to treat animal bite wounds?

A
  1. Doxy + (clinda or metro)
  2. Cipro/levo/moxy) + (clinda or metro)
  3. TMPSMX + (clinda or metro)
  4. Macrolide/azolide (if susceptible pasteurella) +clinda
  5. Macrolide/azolide (susceptible pasteurella) + clinda
70
Q

What is used in the case of a severe animal bite infection?

A
  • pip-tazo
  • ceftriax + metro
  • cipro/levo/moxi and clinda/or metro
71
Q

Why can you not use doxy in pregnancy or children?

A
  • has effects on the bones or calcification of the teeth
72
Q

Why can you not use cipro and quinolones in pregnancy?

A
  • tendon issues
73
Q

Why can you not used TMPSMA in pregnancy?

A
  • displaced bilirubin and can cause babies to be born with jaundice
74
Q

What bacteria is cat scratch disease caused by??

A

bartonella henselae

75
Q

What does cat scratch disease appear as?

A
  • presents as papule or pustule with lymphadenopathy within 3-30 days
76
Q

What is cat scratch disease treated with?

A
  • azithromycin 500mg then 1 250mg q24h for 4 days
77
Q

What bacteria are commonly found in human bite wounds?

A
  • B hemolytic streptococcus in over 80%, eikenella corrodens in 30%, then S. aureus and oral anaerobes
78
Q

E. corrodens is susceptible to what antibiotics?

A
  • penicillins, doxy, TMPSMX, and is resistant to clinda and metronidazole
79
Q

How long does antimicrobial treatment for human bite infections last?

A

7-14 days or 4-6 weeks for septic arthritis

first line is amoxi-clav

80
Q

What are the alternatives used to treat human bite wounds?

A
  • doxy + (clinda or metro)
  • cipro/levo/moxi + clinda or metro
  • TMPSMX + clinda or metro
81
Q

What diabetes related factors increase the risk of diabetic foot ulcers and infections?

A
  • angiopathy with peripheral vascular disease and schema
  • neuropathy with sensory, motor and autonomic dysfunction
  • immune dysfunction
82
Q

What are the adjuvant (non-antimicrobial) measures for treating diabetic foot ulcers?

A
  • glycemic control
  • wound care including debridement, dressing changes
  • pressure relief, off-loading, elevation
83
Q

What ar the clinical features of a diabetic foot infection?

A
  • erythema, swelling (edema), warmth and purulent discharge

- little to no pain or systemic signs of infection in >50%

84
Q

What is the classification of a mild diabetic foot infection?

A
  • superficial skin with erythema <2 cm, swelling, heat or pain; no systemic signs of infection
85
Q

What is the classification of a moderate diabetic foot infection?

A
  • deep localized with erythema >2 cm, abscess, fasciitis, septic arthritis or osteomyelitis, no systemic signs of infection
86
Q

What is the classification of a severe diabetic foot infection?

A
  • significant systemic signs of infection, eg. tachycardia, tachypnea, leukocytosis, hypotension
87
Q

Describe the most common pathogens in DFIs?

A
  • superficial, acute cellulitis and/or infected ulcer not treated with antimicrobials in the previous month - strept and staph
88
Q

What is the most common pathogen in a deep, chronic infected ulcer and treated with antimicrobials int he previous month?

A
  • mixed polymicrobial with gram positive aerobes, gram negative aerobes and anaerobes in 25-40%
89
Q

What are the common complications of DFIs?

A
  • spread to joints or bone

- amputation in 10-20% of cases at one year and 25-50% at 5 years

90
Q

What factors are considered in using antimicrobials in treating DFIs?

A
  • infected wound vs colonized ulcer
  • adequate wound debridement and care
  • severity of infection and clinical status
  • bone involvement
  • risk factors for antimicrobial resistance: chronic infections, repeat antimicrobial exposure, low antimicrobial concentrations at the infection site, MDR pathogens that limit options for antimicrobial therapy
91
Q

What antibiotics are used for a mild DFI with suspected gram positive?

A
  • cloxacillin (plus/minus doxy or TMPSMX)
  • cephalexin (plus/minus doxy or TMPSMX)
    [clindamycin]
92
Q

What antibiotics are use for moderate acute or chronic infection with suspected mixed, polymicrobial?

A
  • amoxi-clav (plus doxy or TMPSMX)

[clindamycin plus cipro/levo/moxi]

93
Q

Clindamycin has _____ coverage

A

anerobic

94
Q

What other Ab has anaerobic coverage?

A
  • metronidazole

- moxifloxacin also has some anaerobic coverage

95
Q

What is used in a severe, chronic infection that is mixed polymicrobial?

A
  • piptazo
  • meropenum
  • cefriaxone+ metro
  • ceftazidime + metro
96
Q

What factors do you consider when choosing a dose for an antibiotic?

A
  • severity
  • limiting toxicity
  • body weight
  • kidney function
  • generation into the bone or the CSF to limit the growth of bacteria in these cases