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Letters to the Editor

Indian Pediatrics 2005; 42:845-846

Reply


Thanks for giving this opportunity to clarify some doubts that the readers have about composition of various colloids, and fluid therapy of septic shock.

1. The composition of various colloids that are available commercially is shown in Table I(1). It may be seen that all the available colloids are "colloids in saline" solutions.

There is no justification for use of fresh frozen plasma as a volume expander because of high risk of disease transmission associated with it(2). Dextrans are inappropriate for volume expansion in children because of high incidence of adverse effects. Albumin, and hydroxyethyl starches are very expensive. Moreover, there is no clear-cut advantage of albumin over crystalloids despite several metanalysis and randomized trials in adults. Hence we selected gelatin polymer (Haemaccel®) for this study. It has a long track record of safety and efficacy in adults, which is borne out of case-series involving thousands of patient(3). Haemaccel® (Gelatin Polymer in Saline) is one of the least expensive colloid solutions available, and has good water binding capacity and reasonable duration of action. It also has lesser side effects as compared to dextran.

		
TABLE I

Characteristics of Various Colloids.
  Albumin Haemaccel Hetastarch Pentastarch Dextran 40
Mw (kDa)
69
35
450
200
40
Sodium  (mmol/L)
130-160
145
154
154
154
Potassium (mmol/L)
1
5.1
0
0
0
Duration of action (Hrs)
6
3-4
>8
6-8
3-4
Water binding
 (Ml H2O/g colloid)
18
41.7
20
30
37

2. In septic shock, infection triggers endogenous mediators, which in turn injure the capillary endothelium and other organs. Vascular injury leads to mal-distribution of circulation with vasodilatation and pooling of blood (arterial and venous) and capillary leaks leading to loss of intravascular fluid to interstitial space ("third spacing"). The major physiologic aberration, therefore, in septic shock is hypovolemia and reduced pre-load. Myocardial dysfunction is next important physiologic aberration, responsible for poor tissue perfusion. Vasoactive and inotropic drugs are used as soon as intravascular volume is restored. Many of our patients did receive inotropes. It should however, be appreciated that after completion of initial resuscitation the fluid leak from intravascular compartment to interstitial space (‘third-space loss’) does not stop immediately. Moreover, a significant proportion of administered fluid continues to move out of intravascular space. It has been shown that only about 20% of administered saline stays in intravascular compartment by the end of two hours(4). The capillary leak may take several hours, sometime days, before it is reversed. In such patients, therefore, the continuing management of intravascular volume requires replacement of ongoing’ ‘third space loss’. Usually, this is achieved by administration of maintenance fluids at a higher infusion rate but some patients need fluid bolus because of continuing rapid ‘third space loss’.

Sunit Singhi,
Professor and Incharge,
Pediatric Emergency and
Intensive Care Units,
PGIMER,
Chandigarh, India.

 

References

 

1. Huskisson L. Intravenous volume replacement: which fluid and why? Arch Dis Child 1992; 67: 649-653.

2. National Institute of Health. Fresh frozen plasma indications and risk. JAMA 1985; 253: 551-355.

3. Boon P. Clinical use of polygelatin. Dev Biol Stand 1981; 48: 193-197.

4. Ernest D, Belzberg AS, Dodek PM. Distribution of normal saline and 5% albumin infusions in septic patients. Crit Care Med 1999; 27: 46-50.

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