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Albumin ~clinical indication

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Albumin ~clinical indication Speaker: 2003/2/10 Mechanism of action/Effect Blood volume expander 70 to 80% of the colloid oncotic pressure of plasma. – PowerPoint PPT presentation

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Title: Albumin ~clinical indication


1
Albumin clinical indication
  • Speaker???
  • 2003/2/10

2
Mechanism of action/Effect
  • Blood volume expander70 to 80 of the colloid
    oncotic pressure of plasma.
  • AntihyperbilirubinemicAlbumin is a transport
    protein that reversibly binds both endogenous and
    exogenous substances including bilirubin fatty
    acids, hormones, enzymes, drugs, dyes, and trace
    metals

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Indications
7
General Consideration
  • The benefit of administration of albumin to
    seriously ill patients is currently
    controversial.

8
  • A meta-analysis of randomized, controlled
    clinical studies of albumin use revealed excess
    mortality of approximately 6 (i.e., 1 excess
    death per 17 treated patients)
  • combined groups of patients with hypovolemia,
    burns, or hypoproteinemia who received albumin
    either instead of or in addition to crystalloid
    solutions. Also, for each of these patient
    subgroups, the risk of death in the
    albumin-treated group was higher than in the
    comparison group.
  • BMJ 1998 317 235-40.

9
????
  • (1) ?????????????
  • A.??????????????????????1000 mL????????????,???(he
    matocrit)gt30,????(hemoglobin)gt10
    gm/dL,?????????,???????????,?dextran?hydroxyethyls
    tarch?polyvinylpyrolidone??????????,???????,??????
    ?50 gm(86/1/1)?
  • B. 70???????????????????????,???????????,?????????
    ???,???????50 gm?

10
  • (2) ??????????????????????
  • A.????????? 2.5 gm/dL
  • a.  ????(???????????)???????25gm?
  • b. ?????(?????????????),???????25 gm?
  • c. ??????
  • d. ????

11
  • B.????????? 3.0 gm/dL
  • a.   ???????????????,??????
  • b.  ??????
  • c.   ?????(gt40)
  • C.?????????????,??? 37.5 gm?

12
Accepted
  • Hypovolemia (treatment)
  • Hypoproteinemia (treatment)
  • ------lt25 g/l, and edema
  • Med J Aust 1992 157 340-3
  • Hyperbilirubinemia, neonatal (treatment)
  • Respiratory distress syndrome, adult (ARDS)
    (treatment adjunct)
  • Cardiopulmonary bypass (treatment adjunct)

13
Accepted
  • Ascites (treatment adjunct)1
  • Nephrotic syndrome, acute (treatment adjunct)
  • .Hemodialysis--susceptible to shock and
    hypotension
  • Pancreatitis (treatment adjunct)
    orIntra-abdominal infections (treatment adjunct)
  • Liver failure, acute (treatment adjunct)

14
Accepted
  • Red blood cell resuspension
  • Plasmapheresis

15
Unaccepted
  • Chronic cirrhosis or nephrosis
  • Malnutrition
  • Given in excessive amounts, albumin may increase
    the catabolism of endogenous albumin.
  • DICP 1984 18
    202-12.
  • Surg Gynecol Obstet 1986 163 359-62.

16
Contraindication
  • 1.allergy
  • 2.heart failure
  • 3.severe anemia

17
BMJ 1998317235-240
  • Human albumin administration in critically ill
    patients systematic review of randomised
    controlled trials

18
  • A systematic review of cohort studies meeting
    specified criteria estimated that for each 2.5
    g/l decrement in serum albumin concentration the
    risk of death increases by between 24 and 56.
  • J Clin Epidemiol 199750693703.

19
Results
  • For each patient category the risk of death in
    the albumin treated group was higher than in the
    comparison group.
  • For hypovolaemia the relative risk of death after
    albumin administration was 1.46 (95 confidence
    interval 0.97 to 2.22),
  • For burns the relative risk was 2.40 (1.11 to
    5.19), and for hypoalbuminaemia it was 1.69 (1.07
    to 2.67).

20
Result
  • Pooled relative risk of death with albumin
    administration was 1.68 (1.26 to 2.23).
  • Pooled difference in the risk of death with
    albumin was 6 (95 confidence interval 3 to 9)
    with a fixed effects model.

21
Conclusions
  • There is no evidence that albumin administration
    reduces mortality in critically ill patients with
    hypovolaemia, burns, or hypoalbuminaemia and a
    strong suggestion that it may increase mortality.
  • These data suggest that use of human albumin in
    critically ill patients should be urgently
    reviewed and that it should not be used outside
    the context of rigorously conducted, randomised
    controlled trials.

22
A plausible mechanism
  • Furthermore, albumin has been shown to distribute
    across the capillary membrane, a process that is
    accelerated in critically ill patients
  • . It has been suggested that increased leakage of
    albumin into the extravascular spaces might
    reduce the oncotic pressure difference across the
    capillary wall, making oedema more likely.

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A plausible mechanism
  • Is there by which human albumin might increase
    mortality?
  • Albumin is used in hypovolaemia and
    hypoalbuminaemia because it is believed to be
    effective in replacing volume and supporting
    colloid oncotic pressure.
  • However, albuminis also believed to have
    anticoagulant properties, inhibiting platelet
    aggregation and enhancing the inhibition of
  • factor Xa by antithrombin III. Such anticoagulant
  • activity might be detrimental in critically ill
    patients, particularly those with haemorrhagic
    hypovolaemia.
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