Basic Science
Human brain weighs about 1,500 g and uses 15% of
the total metabolic energy. This demand can be supplied
by an average blood flow of 50 mL (3 mLO2) per 100 g
of brain tissue per min. The mechanism of blood flow
changes (with the adjustment of cerebral vascular resistance) according to the metabolic need is called
autoregulation, and this safety feature can maintain
adequate blood flow in a wide range of perfusion
pressures (mean: 50 to 130 mmHg).[3] Autoregulation
may be lost in deep hypothermia, resulting in a
"luxury" perfusion of the brain with a risk of increased
intracerebral pressures and cerebral edema.[4]
Animal studies
The porcine model was mostly used to address
the issues related to the aforementioned variables.
Halstead et al.[5] reported that alpha-stat management
for ACP provided more effective metabolic suppression
and better preservation of cerebral autoregulation than
pH-stat. In another study, these authors also suggested
that selective cerebral perfusion (20°C) at 50 mmHg
provided neuroprotection superior to those at higher
pressures.[6] In a study comparing hypothermic ACP with low (20%) and high (30%) hematocrit groups, both
groups had equivalent cerebral metabolic suppression,
while the low hematocrit group had higher cerebral
blood flow which may be injurious possibly due to an
embolic load.[7]
Clinical studies
Pressure, flow, temperature
Clinical applications of ACP at moderate
hypothermia with different variations in flow,
pressure, and temperature have been reported. Some
of them are summarized in Table 1.[8-14] Accordingly,
in series with warmer temperatures, the flow and
pressure were kept higher.
Table 1: Some of the clinical applications of antegrade cerebral perfusion at moderate hypothermia
In most of the studies, the flow rates of ACP are the same for unilateral or bilateral applications. One should consider these flow rates as the total blood supply to the brain delivered either one or more sources.
Unilateral versus bilateral ACP
There are numerous clinical studies and metaanalyses
comparing the outcomes of unilateral and
bilateral ACP.[12-16] They found similar mortality
and neurological event rates. However, the outcome
measures such as mortality and stroke are multifactorial, particularly in the setting of emergent operations for
acute dissections and cannot be attributed to the type
of ACP implementation. In general, the preference of
bilateral application has been based upon factors, such
as predicted long periods of ACP (>40 to 50 min),
decrease in near infrared spectroscopy (NIRS) values,
and incomplete circle of Willis.[13,16]
Cannulation sites
The right subclavian, innominate, carotid and
brachial arteries have been used for cannulation
either directly or through a side graft.[8-14,17-19] The
advantages and risks are briefly shown in Table 2.
Arch grafts, either straight or multibranched, can be
cannulated either directly or through a side arm for
ACP.
Table 2: Cannulation sites for antegrade cerebral perfusion
Left subclavian artery perfusion/occlusion-when?
The left subclavian artery can be kept cross-clamped
during ACP to prevent back-bleeding or to monitor
left radial artery pressure as an indirect indicator of
sufficient cerebral cross-perfusion.[11] In cases of an
occluded right vertebral artery, dominant left vertebral
artery or lack of adequate intracranial communication,
additional left subclavian artery perfusion can be used,
as described by Kazui[10]
Lower body ischemia
In a comparison of two groups of 92 patients
with ACP and lower body ischemia of more than 60 min, the rate of paraplegia was 18% at a body
temperature of 25 to 28°C, while it was 0% at 20 to
24°C.[20] Although the difference was not statistically
significant, it raises concern about spinal cord
ischemia at higher temperatures. Distal perfusion
during aortic arch surgery has been shown to reduce
the incidence of end-organ complications, particularly
in more extensive and time-consuming procedures.[21]
Etz et al.[22] reported that ACP without distal aortic
perfusion longer than 90 min at 28°C was associated
with an increased risk of paraplegia in a pig model.
Therefore, it is reasonable to perfuse the distal aorta
by constructing the descending aortic anastomosis at
an earlier stage of a prolonged ACP.
Our current ACP application
We use the right subclavian artery for unilateral
ACP with a flow of 10 mL/kg/min at 24°C to maintain
a pressure of 50 mmHg. If bilateral ACP is required,
we perfuse the left carotid artery using the cardioplegia
pump head and a balloon-tipped catheter (Figure 1).
In conclusion, there are limited number of animal studies and numerous relatively large retrospective case series and a few meta-analyses investigating the safe limits of ACP. Some of these studies are covered in this article to give recommendations for safe implementation of ACP (Table 3). Since the results with the current applications are quite satisfactory, there may be no urgent need for a prospective, randomized trial to obtain solid evidence in the near future. Acknowledgement The author thanks Merve Evren, PhD for her professional illustration.
Table 3: Suggested ACP variables at different temperatures based on current clinical applications
Declaration of conflicting interests
The authors declared no conflicts of interest with respect to
the authorship and/or publication of this article.
Funding
The authors received no financial support for the research
and/or authorship of this article.
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