This thread for people who are interested in CRRT and critical care 😓🤦🏽♂️
Basics about RRT;
Convection: It depends on Hydrostatic pressure (HP)
Diffusion: it depends on solutes gradients
Filtration (Convection): blood from the Pt goes through the filter, In the filter with the effect of HP plasma, small, and medium size molecules get filtered by the HP effect, then the blood goes back to the patient and the filtered fluid and molecules goes to the effluent bag
Diffusion; blood from the Pt to the filter, In the same time there is another fluid called the Dialysate goes in the opposite way of the filter around the blood which the solutes start the exchange according to the gradient difference and then go out to the effluent bag
IHD, SLED, CVVHD (needs dialysate)
CVVH, SCUF (needs Pressure only)
CVVHDF (needs pressure and dialysate)
Common used mode: CVVHDF
To start Pt on CRRT after reviewing the indications, you need to think about the
• Mode (SLED, SCUF, CVVHD, CVVHF, CVVHDF)
• CRRT Dialyzer membrane,
• type of anticoagulation (None, Heparin, citrate) ,
• substitution fluid
• CRRT dose
CVVHDF can has Pre-filter, post-filter or pre and post filter replacement fluid
When we think about CVVHDF we need to think about (Blood flow, Replacement fluid, and Dialysate)
CRRT dose;
20-25 ml/kg/hr (Qd+Qr) 🤯 you can increase according to the metabolic needs
For example 100 kg patient his [CVVHDF post-filter] dose will be 2000-2500 (Qr + Qd) how can we apply that?
1000 ml/hr for Qd
1000 ml/hr for Qr
Qb ml/min = > 2.5 x Qd
Qb ml/min = > 5 x Qr (post filter)
Qb ml/min = > 6 x Qr (pre filter)
In this pt Qb = > 83 ml/min
What’s about the machine pumps limits
Blood Pump 10-450 ml/min
Dialysis and Replacement fluid pump: 0-133 ml/min
What’s about anticoagulation?
You can use Citrate Pre-filter or Systemic Heparin.
If you will use Citrate Pre-filter do not use Pre-filter Qr.
Citrate rate 2 x Qb
Let us take an example;
75 kg Pt who requires CRRT 2/2 resistant metabolic acidosis.
CRRT dose; 75 x 20 = 1500 ml/hr
CVVHD-Post Filter
Qr 750
Qd 750
Qb = 5 x Qr (ml/min) (5 x 12.5)
Qb = > 62 ml/min let’s us say 100
And then re-evaluate according to your metabolic needs
What’s about if I want to add citrate ?
As we said Citrate 2 x Qb
Qb is 100 ml/min
Citrate 100 x 2 = 200 ml/hr
Then the final dose will be
Qb 100 ml/min
Citrate 200 ml/hr
Dialysate 750 ml/hr
Qr post filter 550
Citrate works by binding to the Ionized Ca in the blood before it reach the filter which it will make it more thin to prevent filter clothing (complications; It needs Ca replacement, and it increases the risk of Citrate toxicity;
What’s the difference between Pre and Post filter ?
The benefit of pre-filter replacement fluid is diluting the blood which it makes it less clotting risk but less clearance, But the post filter replacement fluid it’s more risk of filter clotting but more clearance.
What’s about volume removal, it’s mainly driven by the nurse. The nurse will count the fluid in per hr and accordingly you can set up the ultrafiltration rate to reach your goal
For example if your target is 1000 negative in 24 hrs, and your patient on multiple drips and she/he takes total of 300 ml/hr in. Then you set the UF rate 350 ml/hr then your Pt will have 50 ml negative every hr.
Things you need to watch on CRRT;
• Acsess site
• Pump Alarms
• Filtration fraction
• and TMP
Keep Filtration fraction (FF) < 20% and TMP < 300 to avoid early filter clothing
FF = In none CRRT Pt = GFR/RPF
FF = total UFR/Qb x 100%
This topic is very important, and controversial. Intermediate high risk PE is tough, as the mortality benefits evidence of CDT compared to AC alone its not strong, Therefore, I believe PERT is very helpful.
A large meta-analysis showed the mortality of Submassive (Intermediate high risk) PE is 2.8% and other study showed the mortality ranges from 1.8-10%.
We are dealing with Pts in the red circle 🔴 (before shock but more than low risk)
Evidence showed patients in intermediate high risk PE they might be in normotensive shock 20-40% of these patient can have low cardiac index < 1.8
How do you titrate your PEEP in moderate to severe ARDS Patients?
2004 alveoli trial
DOI: 10.1056/NEJMoa032193
549 Pts.
TV ~ 6 ml/kg
Pplat (24-27)
Low PEEP 8.3±3.2 cmh2o (death 24.9%)
High PEEP 13.2±3.5 cmh2o (death 27.5%)
Result= no significant difference between high or low PEEP
2008 ~ LOVS trial
JAMA. 2008;299(6):637-645
983 PTs
TV ~ 6 ml/kg
CG: Pplat<30, low PEEP mortality 40.4%
IG: Pplat <40, high PEEP ~ mortality 36.4%
The high PEEP group had lower rates of refractory hypoxemia (4.6% vs 10.2%)
COPD is a Heterogenous lung condition characterized by chronic resp symptoms due to abnormalities in the airway (bronchitis, bronchiolitis, emphysema) that cause persistent airflow obstruction
(2018 def in the pic)
65 yo/f with PMH of recently diagnosed SCLC s/p chemotherapy last session 1 month before presentation who was presented to the ER due to worsening SOA, Cough and after evaluation found to be tachypnic and tachycardiac
CXR showed mild enlargement of the cardiac shadow, obliteration of the right CP angle and bilateral central reticular pattern suggestive of pulmonary edema. Right mediport.
Another Pt with HFrEF < 20%, and AKI on GDMT and 40 mg Lasix BID on PE he has Bil LE 2+ edema, no respiratory distress. Would you just increase his Lasix or work on improving his LV contractility, afterload with keeping the same preload control?
🤯🤯 The plan was written (stop Lasix for 2 days and then re-evaluate) their rational is the patient is clinically dry and his creatinine is up?!!!!!!!!😓 these images was taken while Pt on Debutamin