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Indian Pediatr 2010;47: 789-790 |
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Intravenous Adrenaline for Shock in Neonates |
Ruchi Rai and DK Singh
From Department of Pediatrics, SN Children Hospital, MLN Medical
College, Allahabad, UP, India.
Correspondence to: Dr Ruchi Rai, Assistant Professor, S N
Children Hospital, Church Lane, Allahabad,
U.P. 211 002, India.
Email: [email protected]
Received: May 13, 2009;
Initial review: July 13, 2009;
Accepted: September 25, 2009.
Published online: 2010, January 15.
PII: S097475590900332-2
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Abstract
Dopamine and dobutamine have been widely used to
treat shock with variable success in newborns. In this retrospective
data analysis, we report on the use of adrenaline in 20 neonates with
birth asphyxia and shock that was refractory to dopamine and dobutamine.
We concluded that adrenaline is a safe and effective drug that can be
used as an add-on therapy to dopamine and/or dobutamine in newborns with
shock secondary to birth asphyxia.
Keywords: Adrenaline, Birth asphyxia, Neonate, Refractory
shock.
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Dopamine
and dobutamine are widely used to treat shock in newborns. However, clear
cut consensus is lacking regarding the use of adrenaline in neonatal
shock. We present the outcome of 20 newborns in whom adrenaline was used
for the treatment of shock refractory to dopamine and dobutamine.
Methods
This was a retrospective study conducted at a teaching
hospital in which data of all the newborns admitted over a period of 18
month from August 2007 to December 2008 was screened. Data of neonates
with perinatal asphyxia (Apgar score <7 at 5min) with shock within 24 hrs
of birth, which was refractory to fluid resuscitation, dopamine and
dobutamine administration was analyzed. Twenty such newborns were
identified.
All these babies had received standard management of
shock at our unit, which included care under a radiant warmer with
constant oxygen saturation monitoring, and fluid delivered by a syringe
infusion pump. All babies were initially given a fluid challenge of 10 mL/kg
as central venous pressure (CVP) monitoring was not possible. Fluid
refractory shock was managed by dopamine infusion which was rapidly
increased to a maximum of 20 µg/kg/min followed by dobutamine (upto a
maximum dose of 20 µg/kg/min), through an umbilical venous catheter. The
blood pressure (BP) was measured non invasively using an appropriate sized
cuff and urine output was monitored. Non responders received adrenaline
through a separate infusion starting with a dose of 0.3 µg/kg/min,
increased rapidly as needed (maximum 1.5 µg/kg/min).
The primary outcome measure was improvement in mean
arterial blood pressure (MAP) and the ultimate survival of the patient.
Results
Of the 20 patients who fulfilled our inclusion
criteria, 15 (75%) were outborn and 10 (50%) were full term. Adrenaline
infusion was given for a mean duration of 53±29 h in 14 survivors (Table
I). The rise of MAP by at least 20% was seen in the 17 (85%)
patients while the patient was on maximum adrenaline infusion. The total
duration of hospital stay ranged from 10-25 d in the survivors.
Tachycardia was the only side effect encountered in 6 (33%) patients,
which responded to a reduction in the dose of dopamine infusion.
TABLE I
Patient Characteristics and Outcome
Birth- |
Gestation |
*Age |
Duration of |
Outcome |
weight |
(weeks) |
(h) |
adrenaline |
|
(kg) |
|
|
infusion(h) |
|
1.4 |
30 |
24 |
36 |
Died† |
1.6 |
38 |
22 |
24 |
Discharge |
1.8 |
34 |
26 |
96 |
Died |
2.5 |
38 |
20 |
36 |
Discharge |
2.7 |
37 |
24 |
36 |
Discharge |
1.2 |
32 |
30 |
48 |
Died† |
2.1 |
36 |
25 |
48 |
Died |
2.2 |
38 |
20 |
90 |
Discharge |
2.3 |
39 |
32 |
72 |
Discharge |
2.7 |
38 |
30 |
24 |
Died† |
1.5 |
30 |
28 |
72 |
Discharge |
1.8 |
37 |
30 |
18 |
Discharge |
2.2 |
38 |
26 |
90 |
Discharge |
3.4 |
39 |
29 |
70 |
Discharge |
1.5 |
32 |
26 |
68 |
Discharge |
1.8 |
34 |
26 |
108 |
Discharge |
1.6 |
32 |
24 |
40 |
Discharge |
1.3 |
34 |
28 |
12 |
Died |
1.6 |
34 |
30 |
48 |
Discharge |
2.6 |
37 |
29 |
20 |
Discharge |
*Age at start of adrenaline infusion; †patients who died at least 4 days after stopping all ionotropes.
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Six neonates died; 3 out of these died at least 4 days
after stopping all ionotropic support indicating that they had actually
recovered from shock but succumbed to other complications of the illness.
Rest of the three patients died while on adrenaline.
Discussion
Adrenaline increases the myocardial contractility and
peripheral vascular resistance by acting on both
a
and b
receptors(1). It is not used as a first line agent for shock but can be
used as an adjunct. Studies regarding the use of adrenaline in newborns
with shock have been inconclusive(2). Daga, et al.(3) showed that
adrenaline is useful in neonates with septic shock. Adrenaline is an
effective ionotrope which increases BP and decreases blood lactate levels
in other age groups as well(4). There have been concerns regarding rise in
peripheral vascular resistance and decrease in cardiac output and tissue
perfusion, hypertension, tachycardia and tissue necrosis with
extravasation of infusate.
A major lacunae of the present study is its
retrospective nature and absence of a control group. All the 20 newborns
whom we analyzed had shock which was refractory to the routine management.
Adrenaline infusion was effective in two-third babies and out of the 6
neonates who ultimately died, it was found to be effective in at least 3
newborns as they recovered from shock although they succumbed to other
complications. No significant side effects were encountered apart from
tachycardia. Adrenaline was found to be safe and effective and a very
useful ionotrope, which is easily available and is cheap and therefore may
be used as an add-on ionotrope. Controlled studies are needed to validate
our experience.
Contributors: RR designed the manuscript and
collected and analyzed the data. DKS critically reviewed the manuscript
and searched the literature.
Funding: None.
Competing interests: None stated.
What This Study Adds?
• Adrenaline is an effective ionotrope in refractory shock in
newborns with perinatal asphyxia.
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References
1. Phillipos EZ, Barrington KJ, Robertson MA. Dopamine
versus epinephrine for ionotropic support in the neonate: A randomized
double blinded controlled trial. Pediatr Res 1996; 39: 238A.
2. Paradisis M, Osborn DA. Adrenaline for prevention of
morbidity and mortality in preterm infants with cardiovascular compromise.
Cochrane Database System Rev 2004; 1. CD003958.
3. Daga SR, Gosavi DV, Verma B. Adrenaline for septic
shock in newborns. Indian Pediatr 2000; 37: 799-800.
4. Moran JL, O’Fathartaigh MS, Peisach AR, Chapman MJ, Leppard P.
Epinephrine as an ionotropic agent in septic shock: a dose profile
analysis. Crit Care Med 1993; 21: 70-77.
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