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Transcript of Tomáš Zaoral1, Michal Hladík1, Jana Zapletalová2 1Pediatric intensive care unit, Department of...
![Page 1: Tomáš Zaoral1, Michal Hladík1, Jana Zapletalová2 1Pediatric intensive care unit, Department of Pediatrics,Faculty of Medicine, University Hospital Ostrava.](https://reader036.fdocuments.in/reader036/viewer/2022082517/56649f0d5503460f94c21ed4/html5/thumbnails/1.jpg)
COMPARISON OF CITRATE WITH HEPARIN
IN PEDIATRIC CONTINUOUS VENOVENOUS HAEMODIALYSIS
(CVVHD) Tomáš Zaoral1, Michal Hladík1, Jana Zapletalová2 1Pediatric intensive care unit, Department of Pediatrics,Faculty of Medicine, University Hospital Ostrava 2The Department of Medical Biophysics, Faculty of Medicine, University hospital Olomouc
8th International Conference onPediatric Continuous Renal Replacement
Therapy (PCRRT)16-18 July 2015, London, UK
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8th pCRRT Conference ,16-18 July 2015, London TZ
Single center prospective crossover study January 2009 – December 2014
SettingPediatric intensive care unit, Department of
Pediatrics, University Hospital Ostrava, Czech republic
ObjectiveTo compare circuit lifetimes during CVVHD in
children with heparin and citrate Approved by the Ethics Committee, parental
consent was obtained before recruitment
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Single center prospective crossover study January 2009 – December 2014
All children indicated for CVVHD were eligible to participate
Age: 0 – 18yearsAll children were on ventilator and sedatedEach child received a maximum of 4 circuits with
anticoagulants in the following order: heparin, citrate, heparin, citrate (HACG-heparin, citrate –CACG )
The maximum length of one circuit 72 hCircuit life ended when TMP was ≥250mmHg
for≥60 min Circuits failed for other reasons were censored8th pCRRT Conference ,16-18 July 2015,
London TZ
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8th pCRRT Conference ,16-18 July 2015, London TZ
Single center prospective crossover study January 2009 – December 2014
Exclusion criteria:liver failure, high risk of bleeding or
posttraumatic bleeding, thrombocytopenia (below 50 × 109/L)
8 children excluded: 1x LF, 1x ↓PLT, 6x bleeding or high risk of bl.
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8th pCRRT Conference ,16-18 July 2015, London TZ
Single center prospective crossover study January 2009 – December 2014
71 children started Premature termination 8children 3x surgery, 3x CT, 2x hemorrhage 63 children received at least 24h of CVVHD (age 89.24±62.9 months, weight 30.37±20.62 kg)Of the 63 children included, 8 received only 2
circuits (1x HACG and 1x CACG), 55 received all four circuits
(2x HACG and 2x CACG) we analyzed a total of 118 pairs of HACG and CACG
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8th pCRRT Conference ,16-18 July 2015, London TZ
Single center prospective crossover study January 2009 – December 2014
Indication for CVVHD: 37 children (58.7%) with oliguria and >10%
fluid overload (pRIFLE )21 children (33.3%) with elevated creatinin
(pRIFLE)5 children (7.9%) with poisoning
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8th pCRRT Conference ,16-18 July 2015, London TZ
METHODS
All circuits rinsed with heparin 10.000IU/5L NSHACG: bolus of 30 IU, than 10 IU/kg/h ivTarget APTT 1,5 – 2 of the normal rangeCACG: 4% trisodium citrate (136 mmol/L) and
CaCl2 (500 mmol/L)Basic setting: citrat 4.0 mmol/L Ca
1,7mmol/LiCa ++ the target range of 0.25-0.35 mmol/L
iCa++ in the patient’s blood (1.1 – 1.3 mmol/L)
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8th pCRRT Conference ,16-18 July 2015, London TZ
METHODS
Postfilter iCa++ checked q 1h, 6h and 12hAfter target was achieved q 12h
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CVVHD Citrate protocol in our UNIT INITIAL SETTING :
8th pCRRT Conference ,16-18 July 2015, London TZ
Weight CVCBlood
flow rate ml/min
4% Citrateflow rate
ml/hrCaCl 10%
ml/hr
Dialysate flow rate
ml/hrHemofilter
/ m2
Over 30kg11-12FrArrow 100 160 10 2000 AV 1000S/1,8
15 - 25kg
8-12FrMedcomp
proVencare 80 140 8 1500 AV600S/1,4
10 - 15kg
8FrMedcomp
proVencare 60-70 120 5 1000 AV400S/0,75
3 - 10kg6,5 - 8Fr
proVencare 50-60 100 4 800
AV400S/0,75Ultraflux AV
ped./0,2
≤ 3kg 6,5Fr vas.surg. ≥ 40 80 3 - 4 600Ultraflux AV
ped./0,2
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8th pCRRT Conference ,16-18 July 2015, London TZ
DIALYSIS SOLUTION
Nammol/L
Clmmol/L
Mgmmol/L
Kmmol/L
Ca mmol/L
HCO3mmol/L
Glucoseg/L
Ph Osmolaritymosmol/L
Ci-Ca dialysateFresenius MC
CITRATE133 116.5 0.75 2-4 0 20 1 7.4 277.8
multiBicFresenius MC
HEPARIN140 109 - 113 0.5 0 - 4 1.5 35 1 7.2 300
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Characteristic pts enrolled in the studyAll group Survivors Not survivors
PNumber of pts 63 42 (66,7%) 21 (33,3%)
Gender: M/F35/28
(55,6% / 44,4%)22/20
(52,4% / 47,6%)13/8
(61,9% / 38,1%)0,473
Age (months) 84.0 (1w – 204) 88.46 (4 -204) 81.42 (1w - 192) 0,770
Weight (kg) 26,5 (2,8-82) 26,0 (3,3-82) 26,5 (2,8-65) 0,625
CVC: VJI/SC/VF41/14/8
(65%/22%/13%)29/9/4
(69%/21%/10%)12/5/4
(57%/24%/19%)0,528
FO >10%(fluid overload)
39 (61,9%) 23 (54,8%) 16 (76,2%) 0,099
Creatinine (umol/l) 259,9(76-570,2) 271,4(80,4-611,7) 249,3(89,3 -480) 0,672
Urea (mmol/l) 58,8 (19,3-132) 56,4 (19,3-131,6) 58,8 (21,8-120,5) 0,678
PRISM III 19 (13-46) 16 (13-26) 24 (16-46) < 0,0001
MODS 23 (36,5%) 5 (11,9%) 18 (85,7%) < 0,0001
8th pCRRT Conference ,16-18 July 2015, London TZ
All values represent the number (%) or the mean (range); CVC–central venous catheter; VJI - internal jugular vein; SC - subclavian vein; VF – femoral vein; FO – fluid overload; %FO = ((CRRT initiation weight – ICU admission weight) / ICU admission weight) x 100; PRISM III – pediatric risk of mortality; MODS- multiorgan dysfunction syndrome
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8th pCRRT Conference ,16-18 July 2015, London TZ
DIAGNOSIS
Sepsis
Septic
shoc
k
Traum
a, M
ODS
Burn
s
Mal
ignan
cy
Dru
g in
toxica
tion AK
I
HUS
Cardi
ac d
isea
se
Pulmon
ary fa
ilure
0
2
4
6
8
10
12
14
16
1816
No of pts
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Total duration of CVVHD
(hrs)9381
Duration of CVVHD (hrs)
4219 (HACG) 5162(CACG)
One circuit duration (hrs)
36(18-56)*HACG 41(22-72)*CACG
BFR(ml/kg/min) 90 (40-180)
Dialysateml/kg/hr
60,34 (22,2-121,4)
Heparin dose (IU/kg/hr)
15 (9,6 - 23,3)
8th pCRRT Conference ,16-18 July 2015, London TZ
Data are presented as median (min – max) CACG – citrate anticoagulation, HACG - heparin anticoagulation, BFR – blood flow rate , CVVHD – continuous venovenous hemodialysis, NSS –not statistically significant
Citrate Heparin
P
APTT sec50,3(40,3 -
74,9)65,4(21,3-
81,7) < 0,0001
Na
(mmol/l) 140(135-147) 142(137-147)
< 0,0001
iCa
(mmol/l)1,13(0,87-
1,31)1,12(0,99-
1,24)NSS
pH7,41(7,38-
7,48)7,40(7,37-
7,44) < 0,0001
HCO3
(mmol/l)25,20(22,9-
28,7)24,45(23,1-
26,2)< 0,0001
BE (mmol/l)0,8(-1,2 -(+)5,5)
0,20(-0,9-(+)1,9) < 0,0001
p 0,0001
Parameters for CVVHD Circuit parameters 6h after initiation CVVHD
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8th pCRRT Conference ,16-18 July 2015, London TZ
Indication Number (%) total=113
Restoration of diuresis 38 (33.6)
Alarms 12 (10.6)
Clotting: TMP ≥250 mmHg
54 (47.8)
CVC 2 (1.76)
Death 1 (0.88)
CT scan/Surgery 6 ( 5.3)
CACG (%) total=59
HACG (%) total=59
HypoCa: < 0.9 mmol/L 4 (6.77) 0 (0)
HyperCa: > 1.25 mmol/L 2 (3.4) 0 (0)
HypoNa: Na < 130 mmol/L 0 (0) 0 (0)
HyperNa: Na > 145 mmol/L 4 (6.77) 1 (1.7%)
HypoMg: Mg < 0.70 mmol/L 0 (0)
pH < 7.36 or BE< - 3 1 (0.88) 0 (0)
pH >7.46 or BE> +3 4 (6.77) 0 (0)
Reasons for terminating circuits Metabolic and electrolytes imbalances q.6h
118 circuits were evaluated, 5 circuits achieved the maximum 72-h duration; 113 circuits ended before 72 h; CVVHD – continuous venovenous hemodialysis; TMP –transmembrane pressure; CVC–central venous catheter; CT-computed tomography
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8th pCRRT Conference ,16-18 July 2015, London TZ
RESULTS
The total mean circuit lifetime 39.75±10.73
Median lifetime for HACG (36.0 h, CI: 35.4 – 36.6) was shorter than for CACG (41.0 h, CI: 37.6 – 44.4 p< 0.0001)
Total mortality was 33.33%, ≤ 5KG was 75%
Dialysis dose was not SS higher in the citrate
group (60.34 vs. 53.27mL/kg/h p= 1.28)
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8th pCRRT Conference ,16-18 July 2015, London TZ
ConclusionCitrate lifetimes were shorter for heparin than for
citrateCircuit lifetime was significantly correlated to pt age, weight and blood flow rateMortality was similar to the other studiesMortality was significantly correlated to MODS,
PRISM III but not to FO over 10%Metabolic, electrolyte imbalances was readily resolvedCitrate was feasible and safe even for infants and
newborns