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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 29, No 6, November/December 2018

384

AFRICA

surgery were not identified. It was also difficult to compare

results with the literature because of vast differences within the

patient population.

Similar to data in a study by Jobes

et al

.,

21

our documentation

of amount of blood products transfused by both the anaesthetists

and perfusionists were in units and not in millilitres.

In our study, patients were categorised according to the

RACHS category, as it signifies complexity of the congenital

cardiac lesion and surgery.

20

There was an increasing progression

of transfused blood products across the RACHS categories.

Patients in RACHS category 4 had a higher transfusion rate for

RPC, platelets and cryoprecipitate than the other groups. These

patients were younger and had prolonged CPB and AOX times.

Studies by Kipps

et al.

9

and Szekely

et al

.

6

also demonstrated this

association with increased rates of transfusion of blood products.

No FFP was transfused in RACH category 4 patients, with

a preference being shown for cryoprecipitate, which contains

concentrated clotting factors in a small volume.

5

This allowed

for haemostasis to be achieved without the complication of fluid

overload in these patients.

Bloodless paediatric cardiac surgery has been performed

successfully with the use of miniature circuits.

13,14,18,22

At our

institution, miniature CPB circuits were not utilised at the time

of the audit. Perhaps this was the reason for only 1.9% of cardiac

surgical cases having bloodless surgery in our study. Miniature

circuits have also resulted in a decrease in volume of RPC

transfusion without an increase in morbidity or mortality rates.

23

Studies by Redlin

et al.

24

and Miyaji

et al

.

18

showed higher

rates of bloodless cardiac surgery (48%) on patients below 16

kg in weight, and 64% on patients less than 7 kg. A one-year

retrospective study by Durandy

et al

.

25

reported 61% of patients

between 6 and 15 kg having undergone bloodless cardiac surgery.

The blood products mostly transfused were RPC and FFP,

with perfusionists mainly transfusing RPC and anaesthetists

transfusing RPC, FFP, cryoprecipitate and platelets. The reason

for this might be that the perfusionists primed the CPB circuit

with RPC to prevent haemodilution associated with large-

volume CPB circuits.

22

As a result, the haemoglobin levels

were not significantly different across the RACHS categories

throughout the peri-operative period.

There was an overall decrease in haemoglobin from

pre-operative levels on initiation of CPB, and an increase to

>

10 g/dl on arrival in ICU. A similar peri-operative haemoglobin

pattern was seen in the blood transfusion group of the cohort

study by Redlin

et al.

24

This demonstrates the appropriate use of

RPC in the maintenance of haemoglobin levels.

The anaesthetists empirically transfused FFP, cryoprecipitate

and platelets at the end of CPB to manage bleeding. Only

activated clotting time was used as a point-of-care test, which

did not give information about the state of the other components

of the coagulation system. A recent cohort by Machovec

et al

.

26

in infant cardiac surgery showed decreased transfusion exposure

with the use of a haemostasis-management system compared to

using activated clotting time.

It has become common practice to use intra-operative point-

of-care tests to assess the coagulation status of patients before

transfusion of blood products, as well as blood-management

programmes in paediatric cardiac surgery.

23,27

This practice has

resulted in decreased units of blood products transfused when

used in conjunction with algorithms.

26-29

Testing of fibrinogen

and platelet function during rewarming resulted in decreased

cryoprecipitate transfusion post CPB in a cohort by Machovec

et al

.

29

Although there were no blood-usage protocols at our

institution, the mean haemoglobin level on CPB of 8.3 (1.5) g/dl

was attained, which is comparable with haemoglobin trigger

levels of 7–8 g/dl observed in other studies.

24,25

Even though

transfusion triggers are set, transfusion of blood products should

be individualised to the clinical condition of the patient.

4,30

In this study, an expected statistically significant difference

was shown in CPB and AOX times across RACHS categories.

There was a statistically significant correlation between FFP

units transfused with CPB time, and RPC units transfused.

Jenkins

et al.

20

had concluded that a high RACHS category,

signifying the complexity of the surgery, was associated with

long CPB time, which increased the risk for transfusion of

blood products. A study by Redlin

et al

.

24

revealed a significant

association between transfusion amount and CPB time (OR

=

1.02, 95% CI

=

1.01–1.03,

p

0.0001). Another study by Salvin

et al

.

31

showed that patients with increased CPB and AOX times

were transfused more blood products postoperatively.

In the current study, when secondary analysis was conducted

by categorising data according to body weight, there was no

significant difference with median FFP transfusion between the

weight categories. There was a statistically significant difference

in transfusion of RPC, cryoprecipitate and platelets between

the weight groups. Studies have shown that low body weight

is associated with an increased transfusion amount of blood

products.

9,32

There are no protocols on conservation strategies at our

institution, but the majority of patients utilised some form

of blood-conservation strategy, singly or in combination. The

Table 10.

Post hoc

Dunn’s test of use of blood products

between weight categories

Products

RPC

Cryoprecipitate

Platelets

Weight categories

<

6 kg 6–15 kg

<

6 kg 6–15 kg

<

6 kg 6–15 kg

6–15 kg

0.096

0.049*

0.019*

>

15 kg

0.002* 0.002* 0.004* 0.043* 0.099 0.097

*

p

<

0.05; RPC, red packed cells.

Table 8. Peri-operative haemoglobins across the RACHS categories

Haemoglobin (g/dl) RACHS 1 RACHS 2 RACHS 3 RACHS 4

p

-value

Pre-operative

12.6 (1.3) 14.7 (3.6) 14.3 (3.6) 11.1 (2.6)

0.16

Initial CPB

8.5 (1.4)

9.1 (1.8)

9.3 (1.5)

8.9 (2.6)

0.61

Lowest CPB

8.3 (1.4)

8.3 (1.6)

8.5 (1.2)

7.2 (1.2)

0.42

Last CPB

8.9 (1.3)

9.4 (1.3)

9.7 (1.2) 10.3 (1.4)

0.33

Initial ICU

12.5 (1.3) 12.1 (2.1) 11.8 (1.9) 11.2 (1.8)

0.72

CPB, cardiopulmonary bypass; ICU, intensive care unit; RACHS, risk-adjusted

classification for congenital heart surgery.

Table 9. Median units of blood products transfused, by body weight

Products

Weight

<

6 kg

(

n

=

11)

Weight 6

15 kg

(

n

=

52)

Weight

>

15 kg

(

n

=

42)

Kruskal

Wallis

p

-value

RPC

1 (1–2)

1 (1–1)

1 (0–1)

0.001*

FFP

0 (0–0)

0 (0–1)

1 (0–1)

0.087

Platelets

1 (0–1)

0 (0–0)

0 (0–1)

0.038*

Cryoprecipitate 0 (0–1)

0 (0–0)

0 (0–0)

0.009*

*

p

<

0.05; RPC, red packed cells; FFP, fresh frozen plasma.