Bacteremia Flashcards

1
Q

What pathogen is the leading cause of community-acquired and hospital-acquired bacteremia?

A

staphylococcus aureus
(also streptococcus spp or enterococcus spp)
Patients with SAB can develop numerous potential complications
Mortality rates ∼20-40% (higher with MRSA compared to MSSA)

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2
Q

Treatment failure in staphylococcus aureus

A

Treatment failure is relatively common in SAB, especially if due to MRSA
* Death within 30 days following treatment
* Persistent bacteremia > 10 days after initiation of appropriate therapy (some recommend shorter duration of persistence)
* Recurrence of bacteremia within 60 days of discontinuing treatment

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3
Q

What is the clinical approach to SAB? - history and physical exam

A

What is the source of the bacteremia?
Question patients carefully regarding potential entry sites
* Skin/skin structure infection, any breaks in the skin
* Presence of indwelling IV catheters; orthopedic hardware; cardiac devices (remove if medically possible)
Question patients regarding symptoms that may reflect metastatic infection (occurs in up to 30% of cases)
* Bone or joint pain; back pain may suggest vertebral osteomyelitis, discitis, and/or epidural abscess
* Protracted fever, night sweats, murmur, heart failure – suggestive of infective endocarditis
* Abdominal pain, especially LUQ pain – may reflect splenic infarction (due to embolic phenomenal [endocarditis?])
* CVA tenderness – may reflect renal infarction or psoas abscess
* Headache, difficulty breathing – septic emboli

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4
Q

What is the clinical approach to SAB? - physical exam

A

Serial bedside examinations to detect complications that may develop after initial evaluation
* Metastatic seeding may occur within the first few days of hospitalization but may not be clinically apparent
for several weeks
* 39% of patients with vertebral osteomyelitis and 57% of patients with epidural abscess had the diagnosis on admission
INFECTIOUS DISEASES CONSULTATION
* Do it, even if not mandatory!
* ID consults associated with decreased mortality, fewer relapses, and decreased readmission rates
Repeat blood cultures q48-72h to document clearance

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5
Q

What are peripheral manifestations of endocarditis?

A

osler’s nodes, janeway lesions, splinter hemorrhages, petechiae, roth spots

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6
Q

What are osler’s nodes?

A

Purplish or erythematous subcutaneous papules or nodules that appear on the pads of the fingers and toes (painful and tender)

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7
Q

What are janeway lesions?

A
  • Hemorrhagic, painless plaques on palms of hands or
    soles of feet
  • Embolic in origin
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8
Q

What are splinter hemorrhages?

A

Thin, linear hemorrhages under the nail beds of fingers or toes

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9
Q

What is petechiae?

A
  • Small, erythematous, painless hemorrhagic lesions on anterior trunk, conjunctivae, buccal mucosa, and palate
  • Result from either local vasculitis or emboli
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10
Q

What are roth spots?

A

Oval, pale, retinal lesions surrounded by hemorrhage

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11
Q

What is the diagnostic evaluation in SAB?

A
  • Blood cultures – always clinically significant regardless of number of positive blood cultures
  • Repeat blood cultures (2 sets) q48-72h until negative
  • Echocardiography – all patients with SAB!!
  • Transthoracic echocardiography (TTE) performed FIRST
  • Transesophageal echocardiography (TEE) usually performed after TTE (preferred for MRSA bacteremia): All patients with community-acquired SAB; may not be needed for hospital-acquired SAB; More sensitive that TTE for identifying vegetation size/location; Better for identifying intracardiac abscesses and valve perforation; Most sensitive when performed 5-7 days after onset of bacteremia; May repeat if negative but highly clinical suspicion of IE
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12
Q

What if urine cultures are positive for staph aureus?

A
  • S. aureus is NOT a common organism in UTIs.
  • Prevalence of S. aureus bacteriuria in patients with SAB is 8-40%
  • Associated with increased mortality
  • Translocation of S. aureus from blood to urine due to hematogenous seeding and development of microabscesses
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13
Q

Catheter and prosthetic device management

A
  • S. aureus has many virulence factors that allow the organism to colonize and infect metal, plastic surfaces, catheters, and other prosthetic devices; may be infected without any clinical signs/symptoms of infection.
  • Consider all IV catheters and prosthetic devices to be infected in patients with SAB until infection ruled out: Attempt to remove all prosthetic devices; if not, significant increase in risk of relapse; If unable to remove, may add rifampin and may need long-term suppressive therapy
  • Catheter management: Short term catheters–remove ASAP; Long-term catheters–remove unless major contraindication; Replace catheters when blood cultures negative for 48-72 hours
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14
Q

What is the empiric treatment of S. aureus bacteremia?

A
  • Prompt source control and antimicrobial therapy
  • Empirically cover MSSA and MRSA (rapid diagnostics): Vancomycin or Daptomycin
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15
Q

What is the treatment of MRSA bacteremia?

A
  • Vancomycin
  • Daptomycin: May be used in patients with septic pulmonary emboli
  • Addition of gentamicin or rifampin to vancomycin is not recommended
  • Limited data with ceftaroline
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16
Q

What is the treatment of MSSA bacteremia?

A

nafcillin, oxacillin, or cefazolin

17
Q

When would you use combination therapy for MRSA bacteremia?

A

It may be reasonable to employ combination therapy with a PBP-1 active β-lactam or ceftaroline with vancomycin or daptomycin early in MRSA bacteremia treatment course, especially in patients at highest risk of treatment failure and death.

18
Q

What is the duration of treatment for uncomplicated SAB?

A

14 days of IV therapy from 1st negative blood culture

19
Q

What is the duration of treatment for complicated SAB?

20
Q

What is the duration of treatment for complicated SAB with metastatic infection?

21
Q

Bacteremia due to other gram-positive cocci: streptococci

A
  • Treatment duration:14 days (IV→PO)
  • S.pyogenes, S.agalactiae–penicillin IV (q4h or CI)→high dose amoxicillin PO * S.pneumoniae–ceftriaxone or penicillin (if susceptible)
22
Q

Bacteremia due to other gram-positive cocci: enterococci

A
  • Treatment duration: 7 days
  • E.faecalis: Ampicillin (majority are susceptible); if amp-R or β-lactam allergy – vancomycin or daptomycin
  • E.faecium: If vanA and vanB negative – vancomycin; If vanA or vanB positive (VRE) – daptomycin, linezolid
23
Q

What is the treatment of uncomplicated gram-negative bacteremia?

A

treatment duration: 7 days (total days of therapy, not from 1st day of negative blood cultures, do not always have to repeat blood cultures like in S. aureus!)
* IV → PO when clinically improved and able to take PO: PO–frequently TMP/SMZ, FQ, or β-lactam

24
Q

What is the treatment duration of uncomplicated gram-negative bacteremia?

A

Take home point: Longer is not always better. 7 days of therapy had comparable outcomes as compared to 14 days in patients with uncomplicated gram-negative bacteremia

25
Q

What is the treatment duration for enterobacteriaceae bacteremia?

A

Take home point: Longer duration of therapy is not always better.
less than 10 days

26
Q

What is the antibiotic therapy duration for P. aeruginosa bacteremia?

A

short course (median 9 days)

27
Q

Clinical pearls + key takeaways

A
  • Mandatory repeat blood cultures q48-72h until negative for S. aureus, usually not needed for other bacteremia
  • Empiric therapy for MRSA: Vancomycin (AUC-guided dosing) or Daptomycin (higher dose in severe infections)
  • MSSA treatment: Beta-lactams (nafcillin, oxacillin, cefazolin) are superior to vancomycin
  • Shorter treatment durations (7-10 days) are effective for most cases of bacteremia including uncomplicated Gram- negative bacteremia