Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
127 Cards in this Set
- Front
- Back
What are goals for fluid therapy?
|
central venous pressure 8-12mmHg, MAP greater than or equal to 65mmHg, urine output greater than or equal to 0.5mL/kg/h, central venous or mixed venous oxygen saturation greater than or equal to 70%
|
|
Which vasopressors are mainly used?
|
NE and DA
|
|
Why disadvantage from epinephrine?
|
tachycardia, disadvantageous effects on splanchnic circulation
|
|
Why disadvantage from phenylephrine?
|
decrease stroke volume
|
|
Can low dose DA improve renal function?
|
no support
|
|
What is first choice for inotropic therapy?
|
dobutamine, increases cardiac output combined with NE
|
|
What is goal for glucose control?
|
<150mg/dL
|
|
When is drotrecogin used?
|
pts at high risk of death: APACHE II > 25, sepsis induced multiple organ failure, septic shock, sepsis induced ARDS
|
|
What is used for DVT prophylaxis in sepsis?
|
low dose unfractionated heparin or LMW heparin
|
|
What is used for stress ulcer prophylaxis?
|
H2 antagonist more effective than sucralfate
|
|
When is a lumbar puncture indicated?
|
mental alteration, severe HA, seizure, assuming there are no focal cranial lesions identified by CT
|
|
What urinary antigen is tested for in outbreak?
|
Legionella serogroup 1
|
|
When should tx for sepsis be started?
|
within the first hour of recognition of severe sepsis after cultures
|
|
What pathophysiologic changes in sepsis?
|
high creatinine clearance in pts with normal creatinine from increased renal preload
Vd increase from leaky capillaries and altered protein binding clearance of antimicrobial agent is decreased prolonging the t1/2 of antimicrobial |
|
What is empiric tx in noneutropenic pt with UTI?
|
FQ
|
|
What is most common cause of community acquired pneumonia?
|
S. pneumoniae
|
|
What are the "respiratory" FQ?
|
levofloxacin, moxifloxacin, gemifloxacin
|
|
What coverage do the "respiratory" FQ have?
|
pen resistant pneumococci, aerobic gram negative bacteria, Legionella pneumophila, Mycoplasma pneumoniae, Chlamydia pneumoniae
|
|
Which is least tolerated: clarithromycin, azithromycin, and erythromycin?
|
erythromycin
|
|
What are major pathogens in nosocomial pneumonia?
|
enteric gram negative (Enterobacter or Klebsiella) and P. aeruginosa are major ones
also S. aureus |
|
What is tx if P. aeruginosa is suspected?
|
short course AG (5 days) added to antipseudomonal pen or third or fourth gen ceph
|
|
What is used if AG is undesirable for antipseudomonal?
|
antipseudomonal FQ - cipro, or levo
|
|
What is preferred if pneumonia caused by MRSA?
|
linezolid preferred over vanc because of poor penetration of vanc into lungs
|
|
table 123-4 pg1949
|
1949
|
|
What is tx for intraabdominal infection?
|
surgical intervention
broad spectrum (B lactamase inhibitor combo like pip/tazo or ticar/clav carbapenems (imipenem and meropenem) used in tx resistant pathogens including Enterobacteriaceae and P. aeruginosa |
|
What agents does imipenem cover?
|
more potent against gram positive bacteria
|
|
What agents does meropenem cover?
|
gram negative rods
|
|
What is metronidazole used for?
|
infections caused by anaerobes: Bacteroides, Prevotella, Porphyromonas
|
|
What is concern with skin and skin structure infections?
|
growing resistance to macrolide among S. pyogenes
|
|
What is tx for S. pyogenes skin and skin structure infection?
|
clindamycin or penicillin
|
|
What is tx for MRSA in community acquired skin and skin structure infection?
|
vanc, daptomycin, and linezolid
|
|
When should antimicrobial regimen be reassessed?
|
after 48-72 hours based on microbiological and clinical data
|
|
When is combo therapy preferred?
|
Pseudomonas and neutropenic pts with severe sepsis or septic shock
|
|
What is tx for invasive candidiasis?
|
amphotericin B, azole antifungals, chinocandin antifungal, combo fluconazole plus amphotericin B
|
|
What is advantage of new lipid ampho B?
|
less nephrotoxic, increased daily dose, high tissue concentrations in reticuloendothelial organs (lungs, liver, and spleen), decreased infusion associated SE
|
|
When is new ampho B used over old ampho B?
|
intolerant of or have infection refractory to old ampho B
|
|
What is often resistant to fluconazole?
|
C. albicans in HIV and immunocompetent
C. glabrata has reduced susceptibility |
|
Which azole antifungal can be used in fluconazole resistant Candida?
|
voriconazole
|
|
What is Caspofungin used against?
|
Candida, Aspergillus
|
|
How does casponfungin compare to ampho B?
|
equally effective but better tolerated for invasive candidiasis
|
|
What are echinocandins?
|
caspofungin, micafungin, anidulafungin
|
|
What should empiric tx for fungal be?
|
ampho B or caspofungin
|
|
What is associated with the highest rate of inappropriate initial tx?
|
fungal bloodstream infections
|
|
What is empirical tx for nosocomial blood stream fungal infection?
|
fluconazole
|
|
What is duration of antimicrobial therapy in sepsis?
|
7-10 days
|
|
What is duration of antifungal therapy in sepsis?
|
10-14 days
|
|
When can pt start PO meds?
|
hemodynamically stable, afebrile for 48-72 hrs, normalizing WBC cound, able to take PO meds
|
|
How long is tx in neutropenic pt?
|
until pt is no longer neutropenic and has been afebrile for 72hrs
|
|
What is cardiac output and systemic vascular resistance in septic shock?
|
high cardiac output and low systemic vascular resistance
|
|
What causes hypotension in sepsis?
|
low systemic vascular resistance and abnormal distribution of blood flow in the microcirculation, resulting in compromised tissue perfusion
|
|
What are categories of hemodynamic support?
|
fluid, vasopressor, and inotropic therapy
|
|
Why do septic pts have enormous fluid requirement?
|
peripheral vasodilation and capillary leakage
|
|
What is best tx for hypotension in sepsis?
|
rapid fluid resuscitation
|
|
How often does fluid alone reverse hypotension in sepsis?
|
50%
|
|
What is goal of fluid therapy?
|
maximize cardiac output by increasing left ventricular preload which restores tissue perfusion
|
|
Which crystalloids are used in fluid therapy?
|
isotonic: NS and LR
|
|
How much isotonic fluid does a pt typically require in first 24 hrs?
|
up to 10L
|
|
What % of crystalloids remain in the intravascular space?
|
25%
|
|
Which colloids are used in fluid therapy?
|
5% albumin and 6% hetastarch
|
|
What is advantage of colloids?
|
more rapid restoration of intravascular volume because they produce greater intravascular volume expansion per quantity of volume infused
produce less peripheral edema |
|
When should colloid and blood products be used?
|
if there is significant blood loss associated with sepsis or if severe preexisting anemia
|
|
What clinical outcome differences between crystalloid and colloid?
|
none
|
|
How much more volume is needed for crystalloid vs colloid?
|
2-4x
|
|
When is colloid preferred over crystalloid?
|
with serum albumin less than 2g/dL
|
|
What are major complications with fluid resuscitation?
|
pulmonary edema and systemic edema
can also cause hypoxemia from aggressive volume expansion and increase in pulmonary capillary pressure leading to increase in lung water |
|
Does colloids or crystalloids cause more pulmonary edema?
|
no difference
|
|
When are vasopressor and inotropic agents used in sepsis?
|
when fluid resuscitation doesn't provide adequate arterial pressure and organ perfusion
|
|
What are the inotropic agents?
|
dopamine and dobutamine
|
|
When should vasopressor be considered?
|
when SBP is less than 900mmHg or MAP is lower than 60-65mmHg after adequate left ventricular preload and inotrope therapy
|
|
What complications caused by inotropes or vasopressors?
|
tachycardia and myocardial ischemia and infarction from change in myocardial oxygen consumption in pts with coexisting coronary disease
|
|
What can be used to restore MAP without impairing stroke volume?
|
catecholamine infusion trated gradually
|
|
What is first choice vasopressor?
|
NE
|
|
What is MOA of NE?
|
potent alpha adrenergic agent with less pronounced beta adrenergic activity
increases MAP from vasoconstrictive effects on peripheral vascular beds |
|
How does normal dose of NE affect heart rate and cardiac index?
|
little change
|
|
Is NE or DA more potent in refractory septic shock?
|
NE
|
|
Does NE have effect on renal blood flow and cardiac output?
|
demonstrates NE induced renal blood flow as well as urine and cardiac output
|
|
Does NE or DA cause more increase in arterial BP?
|
NE
|
|
Does NE, DA, or EPI have a higher rate of survival?
|
NE
|
|
What is MOA of DA?
|
alpha and beta adrenergic agent with DA activity, increases MAP and cardiac output (from increase in stroke volume and HR)
|
|
What is advantage of DA?
|
combined vasopressor and inotropic effects
useful in pts with hypotension and compromised systolic function |
|
What is disadvantage of DA?
|
cause more tachycardia and more arrhythmogenic
|
|
Does DA maintain renal perfusion?
|
no
|
|
What is MOA of dobutamine?
|
beta adrenergic inotropic agent
|
|
When is dobutamine preferred drug?
|
for improvement of cardiac output and oxygen delivery, particularly in early sepsis before significant peripheral vasodilation
|
|
When should dobutamine be considered?
|
severe sepsis with adequate filling pressures and BP but low cardiac index
|
|
What is advantage of using a vasopressor and inotrope?
|
can maintain MAP and cardiac output
|
|
What is MOA of phenylephrine?
|
selective alpha 1 agonist
|
|
How is onset of phenylephrine?
|
rapid
|
|
How is duration of phenylephrine?
|
short
|
|
What are the primary effects from phenylephrine?
|
vascular effects
|
|
Which vasopressor/inotrope is least likely to cause tachycardia?
|
phenylephrine
|
|
When is phenylephrine useful?
|
when tachycardia limits use of other vasopressors
|
|
What effect does phenylephrine have on cardiac or renal function?
|
none
|
|
What is MOA of epinephrine?
|
nonspecific alpha and beta adrenergic agonist
|
|
What is action of phenylephrine?
|
increase BP modestly in fluid resuscitated pts
|
|
What is action of EPI?
|
increasing CI and producing significant peripheral vasoconstriction
|
|
What AE from EPI?
|
propensity to increase lactate level and impair blood flow to splanchnic system
|
|
When should EPI be used?
|
pts who fail to respond to traditional therapies for increasing BP
|
|
What is action of endogenous vasopressin in hypotension?
|
maintain arterial BP, direct vasoconstrictor without inotropic or chronotropic effects
|
|
How or vasopressin levels in septic shock?
|
deficient
|
|
What is action of vasopressin?
|
low dose produces significant increase in MAP in septic shock, and can d/c other vasopressors
|
|
What SE from high dose of vasopressin?
|
myocardial ischemia, significant decrease in CO, cardiac arrest
|
|
When is vasopressin usually used?
|
in pts requiring high dose vasopressors
|
|
What is preferred agent after fluids for increasing BP?
|
NE
|
|
What is used for refractory hypotension?
|
EPI
|
|
Which vasopressors/inotropes cause more tachycardia?
|
dopamine and epinephrine
|
|
What is used in pt with low CI and adequate MAP?
|
dobutamine first line, dopamine can also be used
|
|
table 123-5 pg 1952
|
1952
|
|
What are the goals in the first 6hrs of therapy?
|
central venous pressure of 8-12mmHg, MAP 65 or more, urine output of 0.5mL/kg/h or more, central venous or mixed venous oxygen saturation of 70% or more
|
|
What is goal for RBC transfusions?
|
HCT 30% or more
|
|
What is oxygen saturation goal?
|
greater than 90%
|
|
What is goal blood glucose in sepsis?
|
less than 150mg/dL
|
|
What is role of insulin in sepsis?
|
control blood glucose
reduced rate of death from multiple organ failure among pts with sepsis regardless of presence of diabetes prior to sepsis |
|
Is routine use of corticosteroids in sepsis recommended?
|
no
|
|
When are corticosteroids used?
|
severe septic shock
pts with adrenal insufficiency, requiring high dose or increasing vasopressor therapy within the first 8 hours of septic shock |
|
Which CS are used and duration?
|
fludrocortisone and hydrocortisone for 7 days in 3-4 divided doses
|
|
Was there a benefit for CS in pts without adrenal insufficiency?
|
no
|
|
What is used for DVT prophylaxis?
|
low dose unfractionated heparin or LMW heparin
|
|
When should DVT prophylaxis be used?
|
genreal ICU pts, including sepsis pt
|
|
What should be used for stress ulcer prophylaxis in sepsis?
|
PPI and H2 antagonists
|
|
What immunotherapeutic is used to treat inflammatory process initiated during sepsis?
|
recombinant human activated protein C (rhAPC; drotrecogin alfa)
|
|
What is drotrecogin alfa?
|
an endogenous anticoagulant with antiinflammatory properties
|
|
What is action of drotrecogin alfa?
|
promotes fibrinolysis and associated antiinflammatory mechanisms
|
|
What is a major risk with rhAPC?
|
hemorrhage
|
|
When is rhAPC recommended?
|
pts at high risk of death, APACHE II score of 25 or more, sepsis induced multiple organ failure, septic shock, or sepsis induced ARDS with no CI for bleeding risk
|
|
Why is rhAPC used less in elederly?
|
bleeding, high drug cost, clinician's tendency to tx elderly less aggressively
|
|
Why is rhAPC not used if APACHE II is less than 25?
|
no difference in 28 day mortality and increased risk of bleeding
|