Monitoring Flashcards
1
Q
What is the definition of intraabdominal hypertension?
A
sustained or repeated pathologic elevation of IAP of >12 mm Hg
2
Q
What is abdominal compartment syndrome?
A
sustained increase in intraabdominal pressure of >20 mm Hg that is associated w/ new organ dysfunction/failure
3
Q
approximately how many ICU patients (people) have abdominal hypertension?
A
32-50%
4
Q
How many human ICU patients have intraabdominal hypertension severe enough to be classified as having abdominal compartment syndrome?
A
14% of the patients who have intraabdominal hypertension
5
Q
What are 4 conditions that are associated with increased risk of intraabdominal hypertension in people?
A
- diminished abdominal wall compliance
- increased intraluminal content
- increased abdominal content
- capillary leak syndrome
6
Q
T/F: in human studies it is determined that a physical exam is a reliable tool to evaluate intraabdominal pressure?
A
false
7
Q
Briefly describe the method for determining intraabdominal pressure
A
U. bladder method is gold standard
- Urethral catheter placed- tip just inside trigone
- sterile urine collection system hooked up to 2 three way stop cocks
- water manometer attached to upright stopcock port
- 35 or 60 ml syringe of 0.9% NaCl attached to distal stopcock
- bladder emptied
- 0.5 to 1 ml/kg (max 25 ml/patient) NaCl instilled
- system zeroed to midline, stopcock closed to fluid source, and pressure is read
8
Q
What is normal intraabdominal pressure in a dog? A cat?
A
0-5 cm H2O dogs
6-11 cm H2O cats
9
Q
What are some hemodynamic effects of increased intraabdominal pressure?
A
Initially increased CVP & RA/pulmonary pressure; then decreased cardiac output; can falsely increase CVP
10
Q
Name some renal effects of intraabdominal hypertension
A
decreased GFR and urine output, oliguria/anuria when IAH >25 cm H2O
11
Q
Name some pulmonary and thoracic effects of IAH
A
Decreased pulmonary compliance, decreased chest wall compliance, more severe lung injury
12
Q
What type of ventilator setting is recommended in patients with IAH?
A
volume controlled
13
Q
Name CNS effects of IAH
A
increased intracranial pressure
14
Q
Name visceral effects of IAH
A
hDecreased hepatic, portal, intestinal and gastric blood flow; decreased lymphatic drainage, increased intestinal permeability, possible increased bacteremia from gut
15
Q
Name systemic/hormonal effects of IAH
A
Increase in ADH, elevated plasma renin activity, increased aldosterone levels, increased epi and norepi, rise in IL1B, IL6, TNFalpha, MODS, thrombotic disease, impairment of wound healing
16
Q
What is the recommended course of action if your patient has an IAP of 10-20 cm H2O?
A
ensure normovolemia, pursue underlying cause
17
Q
What should you do if your patient has an IAP of 20-35 cm H2O?
A
volume resuscitate if necessary; perform diagnostics to identify cause, consider decompression
18
Q
Recommendation if patient’s IAP is >35 cm H2O?
A
decompression via paracentesis or surgical explore is strongly recommended; consider managing patient as open abdomen
19
Q
What percent of the original fluid volume that enters the nephron will be excreted as urine?
A
Less than 1%
20
Q
Between what MAP is auto regulation maintained?
A
Between 80 and 180 mmHg
This means that renal blood flow and therefore GFR is maintained
21
Q
What is the lowest normal urine output value reported for dogs?
A
0.27 ml/kg/hr
22
Q
What is the difference between absolute and relative oliguria?
A
Absolute oliguria refers to a UOP less than 1 ml/kg/hr in a hydrated, well-perfused patient.
Relative oliguria refers to a UOP between 1 and 2 ml/kg/hr in a patient receiving IV fluids
23
Q
Name some common conditions that can cause pre-renal oliguria
A
Severe dehydration, hypovolemia, hemorrhage, cardiac failure, SIRS, sepsis
24
Q
A urine sodium of less than what value is consistent with the action of aldosterone? (in the absence of diuretic administration or intrinsic renal disease)
A
Urine Na of less than 20 mEq/L
25
A urine sodium level of what value supports a diagnosis of syndrome of inappropriate ADH?
Serum hyponatremia with urine Na of more than 40 mEq/L
26
Name 10 causes of pre-renal polyuria
Increased intake (polydipsia, fluid administration)
Drugs (diuretics, alpha 2 agonists, K agonists, alcohols, glucocorticoids, anticonvulsants)
Hormonal conditions (cushings, addisons, DI, hyperthyroidism, cerebral salt wasting syndrome)
Electrolyte abnormalities (hypokalemia, hypercalcemia)
Osmotic conditions (DM, salt ingestion or administration, glycols)
E. coli endotoxin
Liver disease
27
what is special about a swan-ganz catheter in comparison to other pulmonary arterial catheters?
it has a sensor 4 cm distal to the tip that allows temp measurement
28
what type of PAC can measure blood oxygenation?
oximetry thermodilution catheter
29
what are most thermodilution catheters (besides swan-ganz) made of? why?
polyurethane, it softens at body temperature
30
how big should the catheter introducer sheath be for a PAC?
at least 1 size larger than the catheter itself (i.e. a 6-6.5 fr introducer for a 5 fr catheter)
31
describe the 2 different ports and what they are used to measure in a PAC designed for thermodilution method of cardiac output
proximal port- CVP port; measures RA or CV pressure; used for fluid boluses
distal port-central lumen; measures PA pressure and PCWP; samples mixed venous blood
32
what is the K constant of the steward-hamilton equiation?
computation constant that is manually entered into computer that adjusts for amt of thermal signal during each measurement, volume of catheter dead space, and specific heat/volume/gravity of the injectate used
33
briefly describe the technique for CO measurement using a PAC
1.5 ml/kg of saline of known temp injected into proximal port; the thermistor probe on distal end of PAC measures change in blood temp and calculates CO based on AUC of temperature; the bolus should be given as quickly as possible to minimize changes in temperature
34
what does PCWP estimate?
LV preload (LV end diastolic pressure)
35
in which patients might PCWP not be accurate as an estimate for LV preload?
pulmonary hypertension, mitral regurgitation, decreased ventricular compliance; patients on PPV
36
why might RV end diastolic volume be useful as an estimate of volume status?
if patients are on PPV with PEEP or other scenarios in which PCWP may not be accurate for indicating LV end diastolic pressure
37
what is required of the patient/ECG to measure RVEDV?
catheter must be synced to ECG; R-R interval must be regular
38
besides PCWP and RA pressure and CO, what other measurements/diagnostics can be made using PAC?
pulmonary angiography, calculate systemic vascular resistance, pulmonary vascular resistance
39
t/f- a recent meta analysis of PAC monitoring showed no increased morbidity but no benefit?
true
40
patients with which type of shock may benefit the most from PAC measurement?
cardiogenic; the other types of shock showed uncertain benefit in 1 study
41
briefly describe placement of a PAC (without flow directed placement)
clip/prep wide area of skin; place sterile drapes and use sterile gown/gloves/mask/cap; sedation of patient with benzo/opioid; local with lidocaine; skin incision over vessel; placement of introducer sheath into external jugular vein via cutdown or seldinger technique; premeasure to cardiac structures; wrap the neck up; make sure the balloon is good; flush all ports with hep NaCl before placing
42
describe flow-directed placement of a PAC
attach the distal port of catheter to a calibrated pressure transducer and connection to a monitor; monitor pressure tracing as catheter is introduced into jugular vein; once the catheter is in the RA the balloon can be inflated with ~1.5 ml of air; make sure the balloon is always deflated before withdrawing catheter to prevent valvular damage and knotting of catheter
43
t/f- the balloon of a PAC should always be deflated after PCWP measurement?
true; to avoid unnecessary obstruction of blood flow
44
what might be seen on the ECG if the PAC is contacting the RV wall?
ventricular arrhythmias
45
List the normal systolic/mean pressures for different chambers of PAC placement? For use for flow-directed placement
RA- systolic 4-6 mm Hg, diastolic 0-4 mm Hg, mean 2-5 mm Hg
RV- mean 15-30 mm Hg, diastolic 0-4 mm Hg
PA- diastolic 5-15 mm Hg (no longer has diastolic pressure at 0 b/c pulmonic valve), mean 8-20 mm Hg
PCWP- mean 5-12 mm Hg
46
what is the max length of PCWP measurement before deflating the balloon?
2 resp cycles or 10-15 seconds
47
what should you do if you try to fill the air in the ballooon to measure PCWP and you are unable to get the full 1.5 ml into the balloon?
balloon should be deflated and catheter backed out out until PCWP is noted with full inflation of 1.5 ml of air
48
pros/cons of fluoroscopy for PAC placement?
pros- may increase speed, can quickly identify misplacement
| cons-special equipment, generation of radiation
49
complications of PAC placement?
wire/catheter embolus, carotid artery rupture, cardiac arrhythmias, knotting, cardiac tamponade, tricuspid valve damage, hemothorax, pneumothorax, pulmonary artery rupture
50
alternatives to PAC placement for cardiac output monitoring?
LiDCO, PulseCO, transesophageal echo, lithium chloride
51
what is the equation for MAP? MAP= ???
MAP=CO X SVR
52
t/f- normal blood pressure does not necessarily mean adequate blood flow?
true
53
what other monitoring techniques, besides arterial BP, can be useful into patient blood flow and tissue perfusion?
serial PE, cardiac output, blood lactate, central venous hemoglobin, direct imaging of microcirculation
54
in which clinical scenarios may ABP be the most useful?
- patients in shock with hypotension or CV collapse
- patients on vasopressors
- titration of medications for afterload reduction in patients with CHF
- patients receiving meds for severe hypertension
- patients on ventilator
- patients with high anesthetic risk
55
advantages of noninvasive/indirect BP monitoring?
inexpensive, less technically challenging, don't require arterial catheterization
56
what is the major limitation to noninvasive BP monitoring?
less accurate in dogs and cats, whether awake or anesthetized; espec true in hypotensive/hypothermic or small patients
57
which factors can affect accuracy of noninvasive BP ?
cuff size, technique, operator error
58
pro/con to oscillometric BP monitoring?
pro- provides more information (systolic, diastolic and MAP)
| con- less reliable in cats and small dogs compared to doppler or invasive methods
59
benefits of invasive BP monitoring?
- "hands off", allowing tech to spend more time doing other things
- beat to beat monitoring
- less stress to patient, less patient handling
- arterial cath allows for easy ABG sampling
60
risks of invasive BP monitoring?
technically challenging to place arterial cath, expensive equipment necessary, errors can occur
61
complications assoc with arterial catheterization?
hematoma, bleeding, infection, arterial thrombosis, tissue ischemia, hemorrhage if transducer disconnected
62
t/f- dorsal pedal artery is more accurate than femoral or coccygeal for invasive BP monitoring?
false- they are all similar
63
briefly describe the procedure for arterial catheterization
aseptically prepare area
+/- 2% lidocaine over artery
palpate artery and advance catheter
use only small movements, as lumen is smaller than vein
secure catheter with tape and protective wrap
label it ART LINE
64
briefly describe set-up of pressure transducer and monitoring system
pressure transducer attached via line to pressurized 500 ml or 1L bag of 0.9% NaCl (contains heparin 1-2 U/ml)
inflate pressure bag to 250-300 mm Hg
flush heparinized NaCl through system to prime tubing, make sure no air bubbles present
at other end of transducer, noncompliant tubing will be attached that is attached to art line
zero the transducer; set to level of right atrium if CVP desired; set to level of catheter if peripheral pressures desired
open tubing to patient and waveform should appear
65
In a spontaneously breathing patient, what changes in CVP will you see with respiration?
CVP will decrease during inspiration
CVP will increase during expiration
66
In what phase of respiration should the CVP reading be taken?
End-expiration if the patient is breathing normally.
If pronounced abdominal effort, measurement should be taken at the beginning of the expiratory phase
67
Describe how to take an intermittent CVP measurement
1. Connect the three-way stopcock to the manometer, to the saline-filled syringe, and to the fluid tubing.
2. Orient the three-way stopcock valve so that it is closed to the manometer and open to the tubing and fluid-filled syringe.
Then, prime (fill) the stopcock and fluid tubing with 0.9% NaCl from the syringe. Connect the fluid tubing to the central
venous catheter. If a multilumen catheter is being used, connect the tubing to the central lumen.
3. Orient the stopcock valve so that it is closed to the patient’s central venous catheter and open between the manometer
and the fluid-filled syringe. Using the 20-mL syringe, fill the manometer with 0.9% NaCl to a level that is approximately
10–20 cm H2O greater than the patient’s expected CVP. Do not allow the manometer to overflow while filling.
4. Locate the 0 cm H2O mark and position the manometer so that it is level with the zero reference
point (the patient’s right atrium).
5. Close the stopcock valve toward the syringe, which will open a fluid column between the manometer and the patient.
6. When the measurements have been completed, turn the stopcock off to the manometer and disconnect the pressure tubing from the central venous catheter.
68
What tasks should be performed to maintain a continuous CVP system?
• Flush q4h
• Re-zero transducer at least q12h
• Change flush solution and tubing q48h
• Ensure there are no air bubbles in the fluid line at anytime.
• Periodically inspect and reinflate the pressure bag to300 mm Hg as necessary, and verify the heparinized saline
bag is not empty.
69
True or false:
| Right atrial pressure is a major determinant of right ventricular end-diastolic pressure
TRUE
70
When are right atrial and right ventricular pressures equal?
When the tricuspid valve is open and pressures have equilibrated at the end of ventricular diastole
71
How is right ventricular end-diastolic pressure related to preload?
65%Right ventricular end-diastolic pressure is in turn related to right ventricular end-diastolic volume, which determines end-diastolic myocardial wall stretch, or preload.
72
What percent of the systemic blood volume is contained within the venous system?
65%
73
True or False:
In the presence of normal cardiac function, patients with a low CVP are more likely to respond to volume than patients with a normal or high CVP
TRUE
74
If a patient with a CVP of greater than 10 mmHg responds well to a fluid bolus, what might be causing the elevated CVP?
Elevated intra-thoracic pressure
| Elevated intra-abdominal pressure
75
If a patient has a rising CVP with worsening tissue perfusion, what might be occurring?
Declining cardiac function
76
What are the possible causes of a flat line CVP waveform?
Occlusion of the catheter, stopcock, or fluid line
Small patient
Air bubble of leak in the system
77
What are the possible causes of a lack of CVP on the monitor?
Monitor settings are incorrect
Transducer not zeroed
Transducer cable is broken
78
What are the possible causes of a higher than expected CVP reading?
Elevated intra-thoracic or intra-abdominal pressure
Catheter is clamped or occluded
Transducer below the right atrium
Defective transducer
79
What are the possible causes of a lower than expected CVP reading?
Transducer is above the right atrium
Defective transducer
80
What are the possible causes of a "noisy" CVP waveform?
Patient movement
Panting
Catheter tip within the heart
Arrhythmia
81
What are the possible causes of a sudden change in CVP?
Hemodynamic instability
Transducer position relative to zero reference point has changed
82
complications associated with under-resuscitation during shock?
organ dysfunction, prolonged O2 deprivation
83
complications assoc with over-resuscitation during shock?
abdominal compartment syndrome, pulmonary edema, dilutional coagulopathy, exacerbation of cerebral edema, ARDS
84
research has shown microcirculatory hypoperfusion in what % of severely injured human patients despite normalization of traditional perfusion parameters (HR, MAP, UOP)
85%
85
untreated compensatory shock and occult shock are assoc with what in critically ill humans?
MODS, increased morbidity/mortality
86
list the theoretical pathogeneses for occult hypoperfusion related MODS
direct damage from ischemia, reperfusion injury, overwhelming SIRS, compensatory anti-inflammatory response syndrome (CARS), irreversible cellular dysfunction; ischemia activates endothelial adhesion molecules, platelet activating factor, coagulation system (causes breakdown of glycocalyx and increased vascular permeability)
87
Why/how can hypoxia lead to cell swelling, apoptosis or necrosis?
it interferes with ATP dependent processes such as active electrolyte pumping; causes cessation of cellular metabolilsm
88
what is the result of increased leukocyte adhesion to endothelium and release of cytokines and ROS in response to overwhelming inflammation
increased chemotaxis, endothelial damage, vascular permeability
89
what % of the total circulating volume do the venous capacitance vessels make up
75% normally
90
how is the venous system adversely affected during SIRS
can became less able to constrict in response to sympathetic signalling
91
what is the appropriate physiologic response to shock (re: the sympathetic nervous system)
first, B adrenergic stimulation enhances CO, oxygen delivery, chronotropy, inotropy
then alpha receptors cause vasoconstriction which shunts blood to vital organs
92
besides regional hypoxia, what other adverse effects can damage the microcirculation?
TNFalpha, endothelial swelling, alterations in NO, interstitial edema, increased RBC aggregation/adhesiveness, increased blood viscocity, activated platelets causing capillary obstruction
93
list SIRS diseases that can affect microcirculation
polytrauma, necrotizing pancreatiis, hemorrhagic shock, heat stroke, IMHA, ITP, MUE, HGE, neoplasia, ARDS, hepatic lipidosis
94
list diseases that can cause severe sepsis and affect microcirculation
peritonitis, pyothorax, pneumonia, pyometra, urosepsis, GI translocation, parvo, endocarditis, hepatic abscess
95
list diseases that cause ischemia-reperfusion injury which affects the microcirculation
GDV, aortic thrombus, PTE, reexpansion pulmonary injury, post CPR
96
list causes of anaphylaxis, which can affect microcirculation
bee envenomation, antivenin, drug rxn, transfusion rxn, insects, vaccine rxn
97
what is the "no reflow" phenomenon
nonfunctional microcirculatory bed despite resuscitation efforts
98
list upstream hemodynamic parameters
CVP, PAOP, MAP, CO, HR, PaO2, RVEDVI
99
list downstream hemodynamic parameters
UOP, blood lactate, lactate clearance, BD, VO2, O2ER, NIRS, O2/CO2 tissue monitoring
100
is downstream or upstream more sensitive for detecting underlying physiologic disturbances?
downstream
101
in what types of conditions is lactate produced
under anaerobic conditions when pyruvate isn't used for oxidative phosphorylation
102
what enzyme converts pyruvate-->lactate
lactate dehydrogenase
103
t/f- lactate dehydrogenase is present in all tissues except brain?
false; all tissues
104
why does lactate result in acidosis?
lactate production results in hydrogen ion production from ATP hydrolysis and reduction of NAD->NADH
105
in what type of cell is pyruvate normally converted to lactate?
erythrocytes
106
what 3 organs receive lactate in order to be oxidized, transaminated or converted back to pyruvate?
heart, kidneys, liver
107
what might help differentiate type A from type B hyperlactatemia
lactate to pyruvate ratio
108
mechanism of hyperlactatemia in states of increased glycolysis?
glycolysis occurs faster than pyruvate oxidation-->excessive pyruvate-->more lactate
109
what things stimulate glycolysis?
dextrose infusion, alkalosis, sepsis, endogenous or exogenous catecholamines
110
possible pathophys of hyperlactatemia in sepsis?
decreased DO2, microcirculatory shunting, exotoxin mediated impairment of pyruvate dehydrogenase, mitochond dysfunction, hypermetabolism from inflammation, hepatic dysfunction
111
in what way may increased lactate may be adaptive/protective? in what organs specifically?
heart/brain- may preserve glucose for energy production in O2 poor tissues
