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Anestesia Neuroassiale. Tutta l'Anatomia
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Looking at the patient's back with an
epidural anesthesia needle using
the median approach, what structures do we
cross? This exercise,
the needle passes through the skin and the
subcutaneous tissue, the supraspinous ligament,
then the interspinous ligament, the
yellow ligaments, and finally it must stop
in the
epidural space. Now we do this same
exercise but for spinal or
subarachnoid anesthesia. Again looking at the
patient's back, always using
the median approach, with a
spinal anesthesia needle. What structures do we
cross? The needle will pass through the skin,
the subcutaneous tissue, the
supraspinous ligament, and the interspinous ligament,
as before, the yellow ligament, the
epidural space, the duera mater, the
subdural space, the arachnid. Once past the arachnoid,
we are in the liquor
of the
subarachnoid space. When the tip of the needle
passes from the epidural space to the
subarachnoid space, crossing the
dual sac, therefore the duera and the arachnoid, the
transition can be described with a
click. The Pop click sensation is quite famous.
passing the
duera mater and the arachnoid the click is the
sensation that lets the anesthesiologists
know when to stop advancing
the needle and check for
CSF reflux But there are other
interesting sensations associated with the advancement of
the spinal needle through the
Uti tissues the supraspinous ligament gives a
strident sensation Some say
Crunch crunchy the
supraspinous ligament joins the posterior tips of
the adjacent spinous processes up to L3
L4 above the fourth
lumbar vertebra the fibers of the
supraspinous ligament are replaced by fibers
of the latissimus dorsi muscle the
interspinous ligaments the interspinous ligaments
connect the adjacent spinous processes
they extend from the supraspinous ligament
posteriorly to the ligaments flavum
anteriorly from the haptic point of view
the passage through the interspinous ligament
does not give rise to any particular sensations the
yellow ligaments the yellow ligaments
run between the lower margin of
one vertebral plate and the
upper margin of the underlying plate they are
rectangular in shape and Serrano the
spaces between one vertebral plate and
the other demarcating the
vertebral canal posteriorly i The yellow ligaments
may fuse in the midline but this
is not always the case and for this reason,
using a median approach to
spinal anesthesia, one cannot always
rely on the yellow ligament
as a perceptible resistance to the advancement of the or we
advancement of the or we
move to the epidural space
to identify the epidural space
freehand and with an epidural anesthesia needle,
two techniques can be used:
the loss of resistance and the
hanging drop. Despite the growing
interest in ultrasound-guided neuroaxial procedures,
the loss of
resistance technique is based on the different
density of the tissues when the needle passes
from the ligaments to the epidural space. The
most common and most used technique is the
syringe filled with a few milliliters
of saline solution. This resistance opposes a
certain resistance if the tip of the
epidural needle is engaged in the ligaments. This
resistance dissipates
suddenly when the needle enters the
epidural space. The hanging drop technique
is instead based on the
subatmospheric pressure of the epidural space
which is more pronounced and reliable
in the cervical and thoracic regions
than in the lumbar segments. A drop
of saline solution is placed in the
cone of the needle once it has entered the epidural space. this is
engaged in the ligaments the needle is
advanced and the entry into the
epidural space is signaled by the aspiration
of the drop in the transparent cone D lake
the epidural space in my imagination has
long been a cylinder of
continuous tissue of
uniform thickness that completely wrapped the
dura mater in reality the epidural fat
in the vertebral canal is organized in
discrete portions located at the
posterior and lateral level the
epidural fat does not adhere to the other
structures of the vertebral canal except at the
level of its vascular pedicles which
at the posterior level are on the
midline after the epidural space
the meninges begin for the meninges We
help ourselves with this image by looking at the
patient's back the first meninges we
encounter is the Dur mater here in
red the Dur mater has a thickness of about
about
0.35 mm and is made up of about 80
concentric laminae of collagen fibers
organized in all
spatial directions here I have only put three layers but you
have to imagine at least 80 it is
a relatively
permeable structure And since it is much thicker than the
other meninges the The dura mater has
long been considered the most
important obstacle to the diffusion of drugs
between the epidural space and the
central nervous system cerebrospinal fluid. However, it is the
very thin arachnoid membrane that
offers the most resistance to the diffusion
of drugs through the
spinal meninges, with a thickness of only 50-60
microns. The arachnoid is much thinner than
the dura mater but has
much more pronounced barrier properties due to the
lack of intercellular space between the
arachnoid cells, which are firmly connected to each
other by tight junctions and
desmosomes. The entire thickness of the
arachnoid layer is in blue. The black dots
indicate the plasma membrane of the
arachnoid cells. Looking at the
patient's back, after the dura mater but before
the arachnoid, there is nothing in
contradiction with the classic description
of the subdural space as a space.
Therefore, studies have shown that
between the dura mater and the arachnoid there is a
solid but delicate tissue
composed of specialized neuroglial cells.
Neuroglial cells
are also called dural border cells.
These elongated
and fusiform cells are fragile and
The weak cohesive forces between the
neuroglia cells and the lack of
collagen fibers facilitate
the widening of a fissure giving
the impression of a subdural space.
Therefore, the classic concept of a
subdural space is an iatrogenic artifact. The
subdural space is a potential space
that becomes real only after the
involuntary injection of fluid into its
structure with the destruction of the
weak intercellular junctions between the
neuroglia cells which allows the
injected fluids to accumulate in the
subdural space. The dimensions of the
acquired subdural space are
proportional to the volume of fluid
injected, smaller with the typical volumes
used with spinal anesthesia and
larger with the high volumes used with
with
epidural analgesia. This is for the arachnid towards the
dura on the other side towards the
subarachnoid space. The arachnoid sends thread
-like offshoots towards the surface
of the pia mater this creates the
spiderweb appearance which then gives it its name The name
of arachnoid The dura mater and the
arachnoid together form the
spinal dural sac They delimit the
spinal subarachnoid space filled with
spinal cerebrospinal fluid in which
the spinal cord is suspended and floats The
spinal cord is soaked In the cerebrospinal fluid it is
covered by the third and final meninx
The pia mater The pia mater is intimately
associated with the surface of the
spinal parenchyma Deep to the pia mater is
the glial limitans and beyond
this the glia and the neurons of the
spinal cord How an
epidural or peridural anesthesia works To date the only
experimentally demonstrated mechanism
that explains the movement of drugs between
the epidural space and spinal cerebrospinal fluid is
simple diffusion
through the spinal meninges The drugs you
inject into the epidural space
must pass through the dura mater and
the arachnid Disperse in the cerebrospinal fluid
Pass through the pia mater and reach the
spinal cord with
spinal anesthesia The drugs there inject
directly into the
subarachnoid space Since they are already there in the liquor, they
have to travel much less distance and
significantly smaller doses are needed. If the
drug we use is a
local anesthetic, its targets are the axons
of the white matter of both the
nerve roots and the spinal cord. If the
drug is an opioid, it must diffuse
through the white matter and
reach the gray matter 1-2 mm
from the spinal surface to reach
its biophase, which are the neurons of
lamina 2. The gelatinous substance of the
dorsal horns of the spinal cord and the
neurons of the dorsal root ganglia.
And that's all. I hope
you enjoyed this video and that it can be
helpful. If you haven't already done so, I
invite you to subscribe to my
YouTube channel and the podcast, the anesthetist. See you soon.
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