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EXTRACORPOREALA
RENALA
IRA
Scaderea brusca şi potenţial reversibila a funcţiei renale
AKI
LA CONFERITA ACUTE KIDNEY INJURY NETWORK (AMSTERDAM-2005) S-A RECOMANDAT UTILIZAREA TERMENULUI DE LEZIUNE RENALA ACUTA
(ACUTE KIDNEY INJURY – AKI), ÎN DETRIMENTU IRA, REZERVATA CAZURILOR CELE MAI GRAVE ALE AKI
DE CE CRRT?
Indeparteaza cantitati importante Mimeaza indeaproape functia
de apa si produsi de excretie, in renale fiziologica
timp
Restabileste si mentine
echilibrul electrolitic si acido-
bazic
Difuzie
Convectie Difuzie +
Ultrafiltrare
Convectie
Pompa de efluent
creeaza o presiune
negativa tragand Blood In
ultrafiltratul prin filtru (from patient)
Fluid Volume
Reduction
Blood Out
to waste (to patient)
S ● edem pulmonar
● rezistenta la diuretice(fara uremie sau dezechilibre acido-bazice importante
C
U
F
B.Filipoiu, Smart Medical Solutions
DIFUZIA
to waste
V
V
H
D B.Filipoiu, Smart Medical Solutions
CONVECTIA
to waste Blood In
(from patient)
Repl.
Solution
Blood Out
(to patient)
C ●dezechilibrul acido-bazic
●dezechilibrul electrolitic (cu sau fara exces de lichid)
V
V
H
B.Filipoiu, Smart Medical Solutions
C Indicata in SIRS, MSOF, ARF, sepsis, rabdomioloza,etc
V
V
H
D
F B.Filipoiu, Smart Medical Solutions
DIFUZIE vs. CONVECTIE
Acidoza
Hipertermie (>39,5ºC)
metabolica
Azotemia ARDS
Hiperpotasemie Sepsis
(K >6.5 mmol/L)
Edemul cerebral
Disnatremia severa progresiva
(Na >180 or 115 mmol/L)
Rabdomioliza
2. INITIEREA CRRT
5.1.1: Initiate RRT emergently when life-threatening changes in fluid, electrolyte, and acid-base balance exist. (Not Graded)
5.1.2: Consider the broader clinical context, the presence of conditions that can be modified with RRT, and trends of laborato ry tests—rather than
single BUN and creatinine thresholds alone—when making the decision to start RRT. (Not Graded)
3. SEVRAREA DE CRRT
5.2.1: Discontinue RRT when it is no longer required, either because intrinsic kidney function has recovered to the point that it is
adequate to meet patient needs, or because RRT is no longer consistent with the goals of care. (Not Graded)
5.3.2: For patients without an increased bleeding risk or impaired coagulation and not already receiving effective systemic anticoagulation, we
suggest the following:
5.3.2.2: For anticoagulation in CRRT, we suggest using regional citrate anticoagulation rather than heparin in patients who do not have
contraindications for citrate. (2B)
5. DOZE IN CRRT
5.8.4: We recommend delivering an effluent volume of 20–25ml/kg/h for CRRT in AKI (1A). This will usually require a higher prescription
of effluent volume. (Not Graded)
In conclusion, there are now consistent data from two large multicenter trials (Hannover Dialysis Outcome Stud, ARFTN study, etc)showing
no benefits of increasing CRRT doses in AKI patients above effluent flows of 20–25ml/kg/h. In clinical practice, in order to achieve a
delivered dose of 20–25ml/kg/h, it is generally necessary to prescribe in the range of 25–30ml/kg/h, and to minimize interruptions in
CRRT.
Evidente clinice:
Ronco et al, 2000 (using post-dilution hemofiltration) and Saudan et al, 2006 found that lower doses around 20 -
25ml/kg/h were inferior to higher effluent flows of around 35 to 45 mL/kg/h in terms of survival (15 to 20%
reduction in mortality)
Two other studies by Bouman et al, 2002 (48 vs 20 mL/kg/h) and Tolwani et al, 2008 (20 vs 35 ml/kg/hr) however
found no difference in survival with higher effluent rates
The VA/HIH Acute renal failure Trial Network or ATN study in NEJM 2008 In-hospital mortality through day 60 was
51.2% among patients undergoing intensive therapy and 48.0% among those undergoing less -intensive therapy In the
more intensive arm IHD and or SLED were used six times per week and CVVHDF at an effluent flow rate of 35
mL/kg/h
The RENAL study by the ANZICS CTG in NEJM 2009 compared 25 v 40 mL/kg/). No difference in mortality
between the two groups at 90 days, a higher incidence of hypophosphatemia in the higher dose group.
- - - -+ - -+ +
- - + - + Hep a
- -
+
- -+
+
Heparin - -+ rin
-- + - -+ + - -+ +
- - + - + +
in
+
-
ar
- Polyethyleneimine -
p
He
+ +
(PEI)
AN69 AN69 ST AN69 ST
membrana membrana membrana
• PROPRIETATILE ADSORBANTE:
ADSORBTIA ENDOTOXINELOR: MEMBRANA PEI RETINE ENDOTOXINELE (INCARCATE
ELECTRIC NEGATIV)
ADSORBTIA CYTOKINELOR: MEMBRANA CU STRUCTURA “DE BURETE” ADSOARBE
CONCENTRATII MARI DE CITOKINE B. Filipoiu, Smart Medical Solutions
sa nu induca
sangerari
sa aiba T ½
scurt usor de
monitorizat
sa previna
infundarea sa aiba
filtrului antidot
actiune limitata
fara efecte la nivelul
sistemice circuitului
extracorporeal
ANTICOAGULAREA CU HEPARINA
• FUNCTIONEAZA PRIN ACTIVAREA ANTITROMBINEI
III→INHIBAREA FACT. IX SI FACT. X
• DOZA RECOMADATA :
BOLUS: 20-40UI/KGC
RATA CONTINUA: 10-20UI/KGC/H
Infuzia solutiei cu citrat pe linia arteriala a circuitului extraorporeal determina formarea unui complex
care, prin saderea concentratiei de calciu ionizat (F IV) in sange, impiedica procesul de
coagulare
INLOCUITOR
PRISMASOL 2/ PHOXILIUM
DOZE IN CRRT
(ANTICOAGULANT:HEPARINA)
CVVHDF-35ML/KG/H
EX.:PAC 70 KG
Inlocuitor=875 ml/h
Filter P + Return P
TMP = ------------------------- - Effluent P POZ
POZ
2
SAU
NEG
Rata de ultrafiltrare
• FF%=
Fluxul de sange (1- Hct)
RATA DE ULTRAFILTRARE=FLUXUL DE INLOCUITOR+ ELIMINARE LICHID PACIENT
Q B(1-Htc) Q UF
Doza UFR= X
Q B(1-Htc)+Qpre BW