Sepsis Flashcards
(33 cards)
Risk Factors for Sepsis :
- ___ admission or previous hospitalization
- ___ infection
- B ___
- what kind of pneumonia?
- Severe acute ___ from covid 19
- What age ?
- I
- C
- D and O
ICU
nosocomial
bacteremia
CAP
respiratory syndrome
Age >= 65 yrs old
Immunosuppression
cancer
diabetes and obesity
Clinical criteria for diagnosis of sepsis?
Clinical criteria for septic shock?
Infection PLUS Increase in SOFA score by >=2
Hypotension requiring vasopressors to maintain MAP >= 65 mmHg AND Serum lactate >18 mg/dL (>2mmol/L) despite adequate fluid resuscitation
What are the SOFA criterias?
- AMS
- MAP
- PaO2/FiO2
- Scr or bili
- Plts
- AMS (GCS<15)
- MAP < 70
- PaO2/FiO2 < 400
- Scr or Bili >=1.2
- Plts < 150
If your pt comes in with suspected infection you could also use the SIRS score and NEWS score to assess if they probably have sepsis :
- How many points does a pt need for SIRS and what are the criteria?
- HOw many points does pt need for NEWS and what are the criteria?
However, the ultimate decision to deciding whether ur patient has sepsis is?
- SIRS >=2
-Temp >38 or <36
-HR >90
-RR >20
-WBC > 12 or <4 - NEWS >= 3 or 5
-AMS
-Temp >38 or <36
-SBP <=110 , HR >90 or <=50
-RR>20, O2 sat <96% - A SOFA score of >=2
Diagosis :
You need to do what if sepsis is suspected?
Send your cultures ___ starting antibiotics
CULTURE IMMEDIATELY
BEFORE
Diagnosis and monitoring :
For infection what should u monitor? (5)
Organ (dys) function ? (4)
Infection : Cultures/sensitivities, temp + vitals, CBC w/differntial, PCT, Xray, ultrasound, CT, MRI
chemistry (SCr, LFTs) , lactate, blood gas, coags
Goal : identify and control source within how many hours of diagnosis?
Non Drug therapies ? (5)
Consider risk vs benefit by assessing ?
6-12 hrs
Remove infected catheters/lines, change foley catheters, debride soft tissue/wound infections, drain abscesses, surgery
Bleeding, organ injury complications
If Shock is present and or sepsis is definite/probable when should you administer antimicrobials ?
If shock is absent, and sepsis is POSSIBLE but not definite, what should u do?
immediately, within 1 hr
Rapid assessment of infectious vs noninfectious causes of acute illness
and administer antimicrobials within 3 hrs if concern for infection persists
- Initiate IV within ??
- Furthermore, initiate empiric, broad spectrum therapy with ?
- 1 hr of diagnosis
- > =1 agents active against the likely pathogen
For the following sources, what are the likely bugs?
- CAP
- HAP
- Bacteremia
- Abdominal infection
- UTI
- SSTI
- Meningitis
- Strep pneumo, atypicals
- MRSA, pseudomonas
- Staph aureus, strep, enterobacter , pseudomonas, candida
- e coli and bacteroides
- e coli
- strep, MSSA, MRSA
- Strep pneumo, N meningitidis, listeria
Empiric Regimen should cover? (3)
Monotherapy may be adequate with the following agents ? (4)
-What kind of infusions should be used?
COnsider double coverage for? (4)
- GRam neg & gram pos, +/- MRSA, +/- anaerobes
- 3rd or 4th gen cephalosporins, beta lactam combo agents (zosyn), quinolones, carbapenems
-Use prolonged infusions
-septic shock or
-neutropenic at high risk for mdr bugs
-MDR pseudomonas or GNR
Risk factors for MDR organisms?
1. Proven __ or ___ w/resistant organisms in the prior year
- local ___ of resistant orgs
- ___ or ___ associated
- WHat kind of abx in 90 days?
- selective ____
- Traveling to ??
- ____ within 90 days
- infection , colonization
- prevalence
- hospital, health care associated
- broad spectrum
- digestive decontamination
- highly endemic country within 90 days
- hospitalization abroad
Empiric Monotherapy - Cephalosporins
- what are the 3 regimens?
- Advantages?
- limitations such as less ___, no ___ coverage, and strong inducers of ?
- What are the holes in spectrum? (3)
- ceftazidime 1 gm IV q8
-cefotaxime 1.5 gm IV q12
-cefepime 1-2 gm IV q 8-12 - Broad spectrum with low toxicity
-greater gram neg activity +/- pseudo coverage - active against gram pos orgs, entercoccus , ESBL
- Enterococcus, anaerobes, MRSA
Empiric Monotherapy Beta Lactam Combos
- 2 regimens
- Advnatages (3)
- Limitations (1)
- Holes in spectrum? (3)
- Ticarcillin/clavulanate (Timentin) 3.1 gm IV q 4-6
-Zosyn 3.375 gm IV q 6-8 - Greater gram neg activity, including pseudo.
-includes gram + organisms +/- anaerobes
-well tolerated - Susceptible to gram + and - bacteria with Beta lactamase
- MRSA, VRE, ESBL orgs
Empiric Monother - Carbapenems
- list 3 regimens
- What are the AE’s? (4)
- Advantages ? (3)
- Holes in spectrum? (6)
- Meropenem 0.5-1 gm IV q8
- imipenem 0.5-1 gm IV q6-8h
-doripenem 0.5 gm IV q8 - N/V/D, HA, Rash, Seizures
- Broad spectrum of activity, greater cell wall penetration and PBP affinity , stable against beta lactamases (but also induces)
- MRSA, VRE, CoNS, C diff, stenotrophomonas, atypicals
Empiric Gram + Therapy
-Cover gram + for which pt’s with sepsis?
-Consider adding MRSA coverage when??
-Discontinue if what?
-Not recc as empiric ___
-ALL PATIENTS
- Prior history of MRSA infection or colonization
- Recent IV antibiotics
- History of recurrent skin infections or chronic wounds
- Presence of invasive devices, hemodialysis
- Recent hospital admissions or high severity of illness
If gram + orgs are ruled out
MONOtherapy
Empiric ANTI-Fungal Therapy
-Is this reccomended ?
-Consider in high risk or refractory pt’s such as?
For anti fungal therapy regimen see chart
NO
-Prior fungal colonization and infection
* Prior exposure to prophylactic or therapeutic antifungals
* Immunosuppressed or neutropenic
* Prolonged LOS, devices/lines, TPN
* GI perforation or leakage, recent abdominal surgery
See chart for empiric abx regimen for HAP or Immunocomp
-CAP or immunocomp
Best Drugs (good suscpetibility) for Pseudomonas? (2)
Which cephalosporins?
Other 2?
Which AG’s?
Which fluoroquinolones?
When should u use double coverage? and what do u add in this case?
- Cefepime
- Piperacillin with or w/o Tazo
- Cefepime or ceftazidime
- Carbapenem, aztreonam
- Amikacin > Tobra> Genta
- Cipro >= Levo, but NOT moxi !
- Critically ill or neutropenic pt’s, add Aminoglycoside for empiric antipseudo coverage unless ur beta lactam is REALLY good (>85% S)
Review allergies to penicillin chart
See chart
For vancomycin : What 4 components should u monitor?
For Beta Lactams : what 4 components should u monitor?
For infection : What 6 components should u monitor?
- Renal function daily
- levels (DAte and time)
- PK and AUC
- Total days
- Renal function daily
- CLcr daily
- dose
- total days
- cultures, sensitivities
- temp q 6 hrs
- wbc daily
- lactate daily
- BP, HR, BG q 6 hrs
- sx’s
How often should u reassess therapy for de-escalation ?
Whats the timeline for narrowing down abx tx?
Whats the tx duration ?
For each of the PCT values for sepsis follow up, state what u should do with abx tx :
- <0.25
- 0.25 - 0.49 or drop by >80%
- > = 0.5 ng/mL and decr by <80%
- > = 0.5 ng/mL and incr or not decreasing
daily
<= 3-5 days
5-14 days (based on clin response and u should dc abx if NO infectious cause)
- cessation strongly encouraged (if pt is clinically unstable, consider continuing therapy )
- Cessation encouraged (if pt is clinically unstable, consider continuing therapy )
- Cessation DIScouraged (consider expanding coverage and diagnostic eval)
- Cessation STRONGLY discouraged (consider expanding coverage and diagnostic eval)
Bacteremia -Tx duration :
- Uncomplicated
- how long from 1st neg blood culture?
Criteria (Must meet all)
-Removable ___
-No ___
-No ___ devices
-Negative ____
-Fever resolved within ?
-No evidence of ?
- Complicated
-Tx course?
-The following are deemed complicated
E,O,S,I,P,C,M
- 7-14 days
-focus of infection
-endocarditis
-indwelling
-blood cultures after 2-4 days on IV Abx
-72 hrs after initiating IV Abx
-Metastatic staphylococcal infxn
- longer tx course
- Endocarditis
- Osteomyelitis
- Septic arthritis
- Infected hardware
- Prosthetic joint infection
- Cardiac device infection
- Meningitis (some cases)
Septic Shock Hemodynamics :
What happens to preload, afterload, and contractility ?
What drugs can you use to fix these three aspects?
Preload decreases
afterload decreases
Contractility increases to makeup for these decreases but sometimes when ur heart is tired of contracting it will decr contractility
to increaase preload –> IV fluids
to increase AFTERload –> PRessors
to Fix contractility use inotropes