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Cerebrospinal Fluid Dynamics - Leaks and Communicating Hydrocephalus, Dr. Jeffrey Scott Pannell (6-1-23)

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Hello and welcome to Noon Conference,

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hosted by M R I Online Noon Conference connects the global radiology

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is an opportunity to learn alongside top radiologists from around the world.

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You can also sign up for a free trial of our premium membership to get access to

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hundreds of case based micro-learning courses across all key radiology

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subspecialties. Today we are honored to welcome Dr.

0:39

Jeffrey Scott Pinnell for a lecture on cerebral spinal fluid dynamics,

0:44

leaks, and communicating hydrocephalus. Dr.

0:47

Pinnell is a board certified endovascular surgeon and interventional

0:51

neuroradiologist and director of Neuro interventional surgery in the Department

0:55

of Neurological Surgery at uc, San Diego Health. Dr.

0:59

Pinnell specializes in the minimally invasive catheter-based treatment of blood

1:02

vessel disorders that can lead to hemorrhagic or ischemic strokes and treatment

1:07

of pain disorders of the spine and severs spinal fluid leaks,

1:11

as well as diagnostic neuroradiology.

1:13

We're thrilled he's here today to share his expertise with the radiology

1:16

community. At the end of the lecture, please join Dr.

1:19

Pinnell in a q and a session where he will address questions you may have on

1:23

today's topic.

1:24

Please remember to use a q and a feature to submit your questions so we can get

1:28

to as many before our time is up. With that,

1:30

we're ready to begin today's lecture. Dr. Pinnell, please take it from here.

1:34

Thank you for that wonderful introduction.

1:36

I appreciate you all being here with me this morning.

1:39

Lemme just get my screen situated here really fast and we'll get going.

1:45

So, um, we are gonna be talking about, um,

1:47

surface spinal fluid mechanics and disorders of C S F flow dynamics.

1:51

We're primarily gonna be focusing on spinal C S F leaks and

1:55

communicating hydrocephalus, although I may show other cases just to, uh,

1:59

present basically a counterpoint, um, and, and part of the differential.

2:03

So I have some modest consultancies that primarily pertain to my vascular

2:07

practice. I don't have any conflicts pertaining to, um,

2:11

the treatment of C S F leaks or C s F flow disorders.

2:15

In this presentation,

2:16

I'm gonna provide you guys with an overview of the presentation,

2:18

etiologies and findings and spontaneous intracranial hypotension and

2:21

hydrocephalus.

2:22

And I'm gonna discuss the role of m MRI and screening and assessment of

2:25

intracranial hypotension and hydrocephalus. Um, just to kind of get started, um,

2:30

just kind of review C SF flow. I think most everybody knows this,

2:33

but it's good to review it. Um,

2:35

predominantly most of the ceal spinal fluid is produced in the lateral

2:39

ventricles by the cho plexus. Um,

2:41

large concentrations of the cord plexus are located within the atria of the

2:46

lateral ventricles here posteriorly. Um,

2:48

that is basically secreted and flows through the, um,

2:52

framing of Monroe into the third ventricle. And then from the third ventricle,

2:56

it flows through the cerebral aqueduct into the fourth ventricle.

2:59

And then from the fourth ventricle,

3:00

the surface spinal fluid flows out the fara of e lusca and the Fara of magdi at

3:05

the base of the brainstem.

3:06

And then it flows up and down the spinal column aided by the pulsations of the

3:11

brain. Um, once it is produced, eventually it is reabsorbed. We make and, uh,

3:15

reabsorb about 500 milliliters a day. Um,

3:18

just to go back one slide and show you a couple of other little findings.

3:21

These little areas of T2 hyperintensity within the skull near the

3:26

venous sinuses are called oid granulations.

3:28

That's where the cerebral spinal fluid is reabsorbed.

3:31

So essentially the cerebral spinal fluid is made within the ventricular system,

3:34

excreted flows over the surface of the brain and spinal cord,

3:37

and then eventually is reabsorbed in the arachnoid granulations.

3:41

So let's start with spontaneous intracranial hypotension. Um,

3:45

it's basically just a decrease in hydrostatic pressure that results in a

3:48

postural headache. Most ti most of the time patients will denote that they, um,

3:52

have a headache that gets worse after about 10 or 15 minutes of sitting up gets

3:56

better after lying down for a similar period of time.

3:59

It can result from a C S F leak, excess reabsorption, or excess production.

4:05

Um, and essentially spontaneous leaks can occur in the spine due to aural tear,

4:10

um, or degenerative spondylosis or even just dact,

4:13

tasia resulting in potentially a c SF venous fistula, which we'll cover later.

4:17

Um,

4:18

spontaneous skull base leaks can be due to an osseous de hyphens or an cephalic

4:22

seal, um,

4:23

and most frequently occurs in the temporal bone and it's usually associated with

4:27

oea, uh, or rhinorrhea.

4:28

And sometimes there are also associated perinasal sinuses, ef perinasal,

4:32

sinus effusions, um, particularly the,

4:34

the math to an air cells will fill up when it's the temporal bone. Again,

4:37

we're gonna primarily be focusing on spinal CSF leaks today.

4:42

Typically, um, the patients again present with postural headache.

4:45

A lot of 'em will, uh, complain of nausea, vomiting, neck pain,

4:47

visual disturbances, and essentially, um,

4:50

cranial lower cranial nerve issues like tinnitus and,

4:53

and vertigo and things like that. Um,

4:56

generally clinically you're gonna note that their opening pressure when you do

5:00

an LP is usually less than six centimeters of water. Um,

5:03

ideally this would be done in the lateral decubitus position to get the most

5:06

accurate pressure possible. Um, and essentially, um,

5:10

if they have a skull base leak,

5:11

they should have some history of clear OEA or rhinorrhea. If it's,

5:14

if it's the skull base that we're talking about, um,

5:17

most of them will have pacu, menal thickening and some degree of brain sag,

5:20

if not, um, full-blown tonsil or ectopia. Um, and then, um,

5:24

most of them will also have some degree of pituitary engorgement or, um,

5:27

decreased, uh, um, width of the super cellar cistern.

5:30

A lot of them will also have venous sinus distension.

5:33

Some of them will actually even have full-blown subdural collections and

5:36

superficial cirrhosis. Sometimes the ventricles can even start to look slit,

5:39

like very rarely when you have a very high flow CS leak.

5:42

People can have a full minute course where they actually develop cerebral edema

5:45

and,

5:46

and go into a coma and require a very rapid treatment and correction of this

5:49

problem. Um, initially the way that I normally screen a patient, um,

5:54

that comes into my clinic is I get an m r I of the brain with contrast, uh,

5:58

or with, and without contrast, I should say,

6:00

and we get thin section cts in the temporal bone and or MAC space,

6:03

depending on whether or not they complain of ear stuffiness or rhinorrhea oea or

6:08

if they have fluid behind their eardrum. For instance, when I examine them,

6:11

if there's no dehiscence on the ct,

6:13

then I do a full spine survey with flow compensated fiesta images and fat

6:17

saturated two T2 weighted images. Um,

6:20

and essentially at that point I make a decision between doing a more rapidly

6:25

acquired myelogram or doing a pressure augmented myelogram. And really it's,

6:29

it's more of an imaging, um, uh, acuity,

6:32

like how quick is the contrast gonna leak from the fecal sac?

6:35

And MRI is pivotal in deciding what the next step is. Basically,

6:39

if I'm seeing a pseudo ine where there's an actual, uh,

6:43

collection of fluid outside of the dura, normally those,

6:46

those leaks actually happen very quickly and the communications is very rapid.

6:49

Whereas if I'm seeing perineural sts,

6:51

it's usually more of a slower communication,

6:53

either a CSF venous fistula or a small type two leak. In those cases,

6:57

I'm gonna opt more for pressure augmentation and lateral decubitus positioning,

7:00

which we'll get into a little bit later. Um, if I think it's a skull base leak,

7:04

again, I'll do a nuclear medicine cystogram,

7:06

but that's not really gonna be the focus of the lecture day.

7:07

But that's normally what I would do.

7:08

I do a nuclear medicine syn agram if I think there's a dehiscence and just

7:12

confirm it and make sure that we're not just dealing with sinus disease. And,

7:14

and, um, a patient who has, uh, con commitment C S F hypotension,

7:20

um, one of the things that comes up often is, uh, uh, the burn score.

7:24

So the burn score is actually a screening score scale that we can do for

7:27

patients based on their m r and their are minor criteria and major

7:32

criteria for CSF hypotension or spinal CSF leaks. Um,

7:36

engorgement of the sinuses, pacu, menal enhancement and super cell cistern. Um,

7:41

uh,

7:41

flattening or or CLO closure of the super cell cistern down to less than four

7:45

millimeters, um, is a major criteria.

7:47

So you're talking about two points for each of those in the minor criteria or

7:51

having, um, a subdural collection,

7:53

a prep pontine cistern distance of less than five millimeters or a mammolo

7:56

pontine distance of less than 6.5.

7:58

So this burn score can kind of help put you put the patients into risk

8:01

categories. If their score is less than two, we,

8:04

we generally consider them low risk intermediates between two and four,

8:07

and then greater than five, uh, points on the burn scale, uh,

8:10

is the highest risk, obviously for a spontaneous C S F leak,

8:13

and in most cases they are spinal leaks. Um, patients who have, uh,

8:18

cranial leaks generally don't have as many of these elements on the burn score

8:22

particularly, they don't tend to have the brains bag component of it and their,

8:26

their PACU enhancement can be more focal surrounding wherever the leak is as

8:31

opposed to being more diffuse. And that's,

8:32

that's not an uncommon finding when it's a cranial C S F leak.

8:35

So this is a patient with a typical spinal C S F leak.

8:38

We can see that they have, um, uh,

8:40

diffuse pacu menal enhancement and thickening. They have subdural collections.

8:45

Their pituitary is engorged, their straight sinus is engorged. Um,

8:50

their super cell cistern is very, very narrow, much less than four millimeters.

8:54

It'd be very difficult to even measure because the,

8:56

the size of the pituitary theonine distance or prep pontine cistern wit is very

9:01

narrow as well. You can al you, you almost can't even measure it.

9:03

And then the mammolo pontine distance is almost completely closed as well.

9:08

In addition to that, we have an acquired pular ectopia.

9:10

So this is a patient who has a, basically a nine on the burn score.

9:14

There's really, there's there they have, they cover every single point.

9:16

So this patient is extremely high risk for, uh,

9:19

spontaneous intracranial hypertension.

9:21

This is what we would consider a positive screen on M r MRI for spontaneous

9:24

intracranial hyper hypertension.

9:26

They're basically four main types of spinal leaks that we deal with.

9:29

There's the ventral type one leak, which is the most common.

9:32

It's a high flow leak.

9:34

There usually is a ventral pseudomeningocele and it's often related to a

9:37

herniated disc or disc osteophyte complex, uh,

9:41

particularly at the cervical th thoracic junction in those cases.

9:44

And it causes this very long longitudinal epidural collection,

9:48

usually in the ventral, um, epidural space.

9:51

Lateral dal tears are type two leaks tend to be a little slower than type one s.

9:55

Um, they may or may not be associated with an epidural collection,

9:58

but if there is an epidural collection there that you can visualize on m r i,

10:01

those will almost always be more difficult to localize accurately.

10:04

So you have to image more quickly as opposed to doing pressure augmentation.

10:07

So the epidural collection is, is a very important finding to find on mri.

10:12

If you find an epidural collection,

10:13

your myelogram or your myelogram imaging must be much quicker to catch that

10:17

first drop of contrast that goes through the dural defect is particularly if the

10:22

epidural collection is very extensive because those epidural collections can

10:25

parallel the fecal sac and they can almost blend in with a fecal sac on

10:28

myelography.

10:29

And it can be very difficult to see where that leak is if you don't catch that

10:32

first little, um, uh,

10:33

drop of contrast that leaks out of the fecal sac into the,

10:37

the pseudomeningocele. Um,

10:39

it's often related to either a lateral disc herniation or a facet osteophyte,

10:43

and sometimes there can be a small perineural cyst, um, that, uh,

10:47

is facilitating this leak. It is different from the type four leak,

10:50

which I'm gonna talk about in a minute,

10:51

and that it's closer to the margin of the fecal sac.

10:54

So it would be basically within the spinal canal,

10:57

whereas a type four leak is actually a dehiscence of the nerve root sleeve and

11:01

contrast leaking along the nerve without any associated degenerative changes.

11:04

A type three leak is not really an open leak,

11:07

but rather a fistulization of the cerebral spinal fluid space with

11:11

the venous system. So, and it's usually a radicular vein in the neural frame,

11:15

and again, they're slower. Um, and it's also dynamic due to venous washed out.

11:19

So it's,

11:19

it's more difficult to detect these slower type three and type four leaks.

11:23

These are just some illustrations of the things that I was describing,

11:26

but I'll show you some pictures a little bit later on that are of clinical, uh,

11:29

clinical images. But essentially you, you see, you have a,

11:32

a small disc herniation here,

11:33

and then there's aural tear and a collection in the ventral epidural space in

11:37

this patient. This is a type one or ventral, uh, CSF leak.

11:39

This is a type two or lateral CSF leak.

11:41

Presumably this patient would've had a small disc herniation or DIY

11:46

complex out here that resulted in this small tear that's on the margin of the

11:50

fecal sac near potentially a perineural cyst. And, and I'll, again,

11:53

I'll show you a case of this a little bit later on,

11:55

or a couple of cases of this. Um, again, a c SF venous fistula usually is, is,

11:59

is, um, uh, associated with dact to the point where you have a,

12:03

a small perineural cyst or,

12:04

or a perineural cyst that actually visualizes with the venous complex. And,

12:09

and then in those cases, again, the vein watches out.

12:11

So it can be really difficult to detect these. Um, and then lastly,

12:15

type four s are more lateral leaks along the nerve root sleeve where you

12:19

actually have dehiscence of the nerve root sleeve and, um,

12:21

the contrast leaks along the nerve itself. So categorizing them,

12:26

like I said earlier, alluded to earlier into high and low flow is what the,

12:29

the main role of MRI is.

12:31

The other secondary role of MRI is to get a general region because digital

12:35

subtraction myelography, uh,

12:37

and rapid CT myelography for these high flow leaks is kind of the mainstay of

12:41

evaluation.

12:42

You really only get a very short temporal period to detect these leaks.

12:46

So you have to be in the right area, um,

12:48

because you're gonna be injecting only a finite amount of contrast and you only

12:51

inject three grams of contrast into the fecal ack.

12:53

And when you do a digital subtraction image,

12:55

you really only get two shots at seeing the leak.

12:57

So you really need to know about where it is cause you're a detector for your,

13:00

um, your digital subtraction is only gonna be about 20 centimeters,

13:03

so you're not gonna cover the whole spine and,

13:04

and a digital subtraction monogram. Um, so if you can,

13:07

if you can see a pseudomonal that's tracking along the fecal sac,

13:11

you can get a general region where the leak is probably at,

13:13

and then you can focus on that region when you're doing either a DSM or rapidly

13:16

acquired CT igram, which I'll, I'll go through that a little bit later as well.

13:19

They most frequently occur at either the cervical,

13:22

thoracic or thac lumbar junction. The ventral epidural space, and again,

13:25

it's usually caused by DYS, herniation or dico complex, um,

13:28

they vocally leak directly into the epidural space in the acute setting,

13:32

but they're rarely caught in the acute setting because clinicians usually don't

13:35

pick up, uh,

13:36

on c SF leaks in the acute setting unless there's some inciting event like

13:39

trauma. Um, so oftentimes when they present,

13:42

they already have a chronic pseudo low flow leaks. Um,

13:46

both acutely and chronically do tend to persistently leak into the epidural

13:50

space and rarely form chronic pseudomeningocele.

13:53

Type two s occasionally will do that,

13:54

and it does make them harder to detect the exact location,

13:57

but it's easier to detect that there is a C S F leak because a pseudomonal is

14:01

easier to see than basically a focal pinpoint leak into the epidural space

14:05

without a pseudo seal. Um, they typically occur in the lower thoracic region,

14:09

either laterally or posteriorly, uh,

14:11

and they're often associated with a perineural cyst or diverticulum, um,

14:16

and or osteophytes associated with the facet joints. So those are the,

14:19

the different types of leaks, and again,

14:20

categorizing into high and low flow based on the presence of a pseudomonal or a

14:25

perineural cyst is critical for the next steps for those patients. So with that,

14:29

I'm gonna move on to, um, localization of these leaks. Um, again,

14:33

detectability and accuracy, uh,

14:35

of localization is highly dependent upon the rate of,

14:38

of the leak as well as the consistency. Um,

14:40

and the associated extend of the pseudomeningocele,

14:42

the pseudo and enil is very focal, then it's, it's not really a big problem.

14:46

You, you know, about where the leak is, but if it's a really long one,

14:48

it extends along most of the spine, then you really have to be a lot more, uh,

14:52

judicious in your imaging and and image very quickly. If it's a high flow leak.

14:55

Again, high flow acute leaks are easy to detect,

14:58

but clinicians usually don't pick up on them until they're later on in their

15:01

course. The patients don't even suspect it usually. Um, and then, uh,

15:04

chronic leaks, um, that are high flow or easier to detect presence, meaning we,

15:09

we know where they are,

15:10

but accurately localizing them can be extremely difficult just because the

15:14

pseudomeningocele again, can be very extensive. Um,

15:16

both acute and chronic slow C S F leaks as well as intermittent leaks are

15:20

difficult to detect and localize because these patients often have more than one

15:24

abnormality of their fecal sac. They'll have multiple perineural fists,

15:27

so you have to look at multiple different regions and,

15:30

and narrowing it down a little bit can help a lot. Um, so again, um,

15:34

the high flow leaks are typically the type type ones and the type twos. Um,

15:38

low flow leaks, type twos three or fours can be kind of slower, low flow leaks.

15:43

Um, I normally do a screening MRI on, on both of them,

15:47

again to evaluate pseudo and inel and those type two and type one leaks.

15:50

And then looking for peroneal cysts, uh, in the type two s through four s. Um,

15:54

and then if I'm dealing with a high flow leak or suspected high flow leak based

15:57

on the detection of a pseudo and inel,

15:59

then I'm gonna do either a very fast pressure neutral CT mammogram.

16:03

What that means is that I'm gonna put the patient on a bolster in ct,

16:06

do the spinal tap there, and actually put the contrast in,

16:09

pull the bolster out and scan immediately with a large field of view.

16:12

So I can see the contrast as it flows up and I can see the in, uh, the,

16:15

the exact moment or the exact location of the leak without filling the entire

16:19

pseudo and inel and obscuring my my focal area of dehiscence. Um,

16:23

you can also do digital subtraction myography.

16:25

The benefit to digital subtraction is that you can actively watch the contrast

16:29

flow up and, and see where it's leaking from the downside to it.

16:33

Particularly in heavier patients, it can be really difficult to,

16:35

to accurately localize the leak because there there's only, um, uh,

16:39

only so much penetration you can get, um, through the shoulders,

16:43

particularly at the cervical thoracic junction.

16:45

And a lot of these leaks are at the cervical thoracic junction.

16:47

So you can have problems with the shoulders even on oblate, um,

16:51

seeing exactly where it is, particularly on a heavier patient.

16:53

So on heavier patients I tend to lean towards, uh,

16:55

a fast pressure neutral CT milligram. Um, whereas on,

16:59

on thinner patients I tend to go more for digital subtraction myelography and

17:02

watch the contrast come up for slow flow leaks. Um, again,

17:06

I do the screening MRI and I'm looking for, again, perineural cyst. Um,

17:10

and I will normally put them in the lateral recu disposition of the side that's

17:14

most suspicious to me and either do, uh, a pressure augmented, um,

17:17

CT myelogram with plus or minus some delayed imaging and doing everything in ct.

17:22

Or I'll do a digital subtraction and do the same thing.

17:24

Basically I'll watch it with pressure augmentation over time, um, and,

17:28

and look for, um, uh, those slower leaks. Um,

17:31

you can also do contrast enhanced mri my myography with or without pressure

17:35

augmentation. You can basically inject galine in the fecal site,

17:38

which is also a useful tool. And I, I'll go over that in a minute and how,

17:41

how I do it. Um, you can also do nuclear medicine sonography,

17:44

but I I find that to be of limited value unless you're dealing with fairly large

17:48

perineural cyst. If they're very large and there're, there're multiples, um,

17:52

nuclear medicine actually can be very useful, um, for those cases.

17:56

But for smaller cysts it can be really,

17:58

really difficult cause they kind of blend into the fecal sac on nuclear medicine

18:01

stenography. But in patients with massive delicia like,

18:04

like those with marfa syndrome, things like that,

18:06

nuclear medicine can be helpful when it can detect it. Um,

18:10

so let's start with the ultrafast, uh, pressure neutral CT myelography. Um,

18:14

it does have a significant advantage and again,

18:16

those high flow leaks over conventional delayed myelogram cuz you can get that

18:19

pinpoint accuracy of the,

18:20

of the exact location of leak when you have a large complex pseudo and inusal

18:24

that otherwise might be obs might obscure the actual location of the leak. Um,

18:29

we perform at start to finish at U C S D and CT with both the LP and the

18:33

myelogram on the, in, on the same table.

18:35

The head is lowered right after the contrast inject is injected. Normally,

18:38

I I perform the CT fairly quickly after, um, I do use, uh,

18:43

a smart prepped to actually detect when it's getting into the region and then

18:46

it, it triggers and it'll scan the entire region of interest basically. Um, uh,

18:51

and this is just sort of the, the, uh, extensive details.

18:54

I'm not gonna read all of this to you,

18:56

but I tend to use a coaxial system to do the puncture so that I make a smaller

19:00

puncture. I use a 25 gauge for the dural puncture.

19:02

The reason you can get away for get away with this is because you're infusing

19:06

the entire contrast bolus in the, in the luo sacral spine with the patient's,

19:10

um, uh, head elevated.

19:12

So you can infuse the entire thing at whatever rate you want.

19:14

You don't have to infuse it as quickly as you would for A D S M. Um,

19:18

and normally I use omnipaque two 40 for these higher flow leaks. You'll see I,

19:22

I I talk about using a denser contrast, omni pick 300 for those. Uh,

19:26

for those slower leaks it is a little bit more helpful,

19:28

but normally I use two 40 for these, um,

19:30

higher flow leaks and normally I remove the needle before I even get ready to

19:34

scan. I usually remove the bolster and then again do a single slice, um,

19:38

and trigger a smart prep to, to actually, um, do the scan.

19:41

It typically takes about 15 seconds for the contrast to reach the CS sponge.

19:45

So if you just wanna trigger it based on pine,

19:47

you could do it after about 15 seconds, you'll probably catch most of them. Uh,

19:51

and generally I only perform a a, a region where I'm,

19:54

I have concern based on the M r mri, like just the region of the,

19:57

the pseudo and a seal that I'm concerned about. Um, and if no leak is detected,

20:02

I will often roll them into the prone position and immediately repeat the scan

20:05

and just take a look and see if there's anything else that I'm missing.

20:08

So I'm gonna present a case here so you can see the utility of this and,

20:12

and you can hopefully understand what I'm talking about a little bit better and

20:14

it can reinforce this concept.

20:15

So this is a 32 year old female with postural headaches and this patient has a

20:19

pretty obvious type one leak.

20:21

So it doesn't require a flow compensated FIEs or anything special to see that

20:25

this patient has a fairly decent size pseudomeningocele in the ventral epidural

20:29

space at the thac lumbar junction associated with, um, this, uh,

20:33

small disc herniation. Uh, and, um, essentially right below the, the, uh,

20:38

thesis six, uh, level. So in this case, um,

20:42

the pseudomona in seal is big enough that you might not get an accurate

20:45

localization because you're looking at four or five levels.

20:48

So you do need to scan the entire thing, uh,

20:50

and catch the exact moment that the contrast leaks out.

20:53

So this is an example of, uh, of me doing this ultrafast, uh,

20:58

pressure, pressure neutral CT myelogram. I'm doing basically my, uh,

21:01

lumbar puncture. Uh,

21:03

and I I tend to do it in either the lateral to cubitus or prone position and

21:06

I'll put 'em on a bolster and then I'll roll 'em and drop their head and then do

21:10

the smart prep.

21:10

But basically this is the initial immediate CT mammogram showing this tiny

21:16

pinpoint dural tear right at the C6 level, um, just inferior to the C 56 disc.

21:21

This shows that same patient in a delayed image,

21:24

you can see the entire pseudo inic seals filled.

21:26

So you can't see that the leak is exactly right here and you're probably

21:29

thinking in your mind what does it matter if if,

21:32

if you localize it exactly here versus over here?

21:35

It matters for the surgeon based on which way they're gonna approach cuz they're

21:37

gonna approach anteriorly most likely, and they're, in this case,

21:40

they're gonna a approach from the, from the, uh,

21:42

from the right side as opposed to the left. Um, and you can also, um, you can,

21:46

you can also, uh,

21:47

imagine that once you start to look at this in reconstructions,

21:51

it's gonna be a lot harder to see. So I'm gonna demonstrate that. Um,

21:54

but this is the mag view of that. You can see this is the,

21:56

the focal area where the leak occurred.

21:58

This is the delayed conventional myelogram where the leak, the,

22:01

the actual tear the durrin blends in basically with the entire pseudomonal.

22:06

This is the, uh, a level slightly lower around the T1 level.

22:10

So you can see the pseudomeningocele hasn't even filled yet on this ultra fast

22:13

myelogram, whereas on a conventional myelogram, the pseudomeningocele is filled.

22:16

And I just wanna really drive this point home by showing you the,

22:19

the recons of this patient. So when you look at the reconstructions,

22:23

you can see on the conventional myelogram here on the left,

22:25

the entire pseudomeningocele is filled. So you,

22:27

you can't see where the leak is there, there's no way in this blended sort of,

22:31

uh, homogenous, uh, appearing collection in the ventral epidural spaces.

22:34

You're gonna know exactly where the hole is. Um, but on the ultra fast, um,

22:39

myelogram here on the right where we scan immediately after the injection,

22:42

you can see the pseudomeningocele is not even filled yet.

22:45

We just had this tiny little pinpoint focus of extravasation contrast right

22:48

below the C 56 disc, and that's exactly where the leak was.

22:51

The surgeon did actually a full corpectomy in this patient and did find the leak

22:55

and did repair it, basically. Um,

22:58

and it was a very focal pinpoint link that they just oversold and the patient's

23:01

doing well now. So, but that illustrates the, the, the, um,

23:04

the value of localization, um, based upon, uh,

23:07

those ultrafast CT mammograms.

23:09

And without having the m r I beforehand to actually know where the pseudo men

23:13

inusal was and where to focus, it would be a lot harder for me to detect, um,

23:17

exactly where the leak is because I would miss the exact point of where it's

23:20

leaking. Because you can't just scan the entire spine. You have to,

23:22

you have to focus on one area and you have to kind of know ahead of time about

23:26

where the leak is. Um, with that we can move on to pressure.

23:29

Augmented CT myography.

23:31

It has a temporal advantage over conventional myelography and detective slow CSF

23:35

leaks.

23:35

You can perform it entirely in CT or you can split it between fluoroscopy and

23:39

ct. Um, when I do that, I tend to do a DSM in, in, um, uh,

23:43

in fluoroscopy and actually do that first and then I'll send the CT and use the

23:47

CT as sort of my delayed image. Um,

23:49

I usually raise the pressure with a manometer and I, I, I utilize,

23:52

utilize both contrast and Elliot B solution. Um,

23:55

I put them in the lateral decubitus position on the side of most interests.

23:58

So the side with the most suspicious looking, um, uh, perineural,

24:02

cyt on the M R I, I'll put 'em on that side.

24:04

So if the left side's most suspicious,

24:06

I'll put 'em left side down or left lateral decubitus, uh,

24:08

prep their skin and essentially I'll access 'em with a 22 gauge needle in this

24:12

case because I wanna be able to get a really accurate pressure.

24:14

So I need to get some flow of C S F back and forth to kind of get an idea of

24:18

what the pressure is dynamically as I'm injecting additional, um, solution. Um,

24:22

but normally I inject 10 mls of Omni 300, and if I'm doing it under ct,

24:27

I just put 'em on a bolster N CT with the, the bolster underneath their hips,

24:30

uh, which is in contradistinction to what we were talking about earlier. The,

24:33

the rapid CT mammogram we're injecting and everything with their head elevated.

24:37

I would normally have the bolster with those rapid cases with the,

24:39

the bolster under their shoulders. In this case,

24:40

I'm gonna put the bolster under their hips so that the contrast goes ahead and

24:43

flows basically all the way up the spine. And as you,

24:47

you might imagine if they're on their side,

24:49

what tends to happen is that contrast just sort of runs into and drips into each

24:54

one of those perineural cysts almost like the, the, um, uh,

24:58

reservoirs in an ice cube tray.

25:00

And then after I finish dripping the contrast into all of these,

25:04

the next thing that I will do is I will raise their pressure withs.

25:07

You can also use some, uh, um, normal saline. I mean, it,

25:11

it's a little bit more painful for them, but you can use it. Um,

25:14

it causes kind of a pressure sensation for some patients. Um,

25:17

but basically I raise their pressure to between 30 and 35 centimeters of water.

25:21

Some people just wait, some people just, um, uh, essentially, um, uh,

25:26

raise their pressure until their headache is gone. I, I,

25:28

I raise it to 35 to give me my, my best chance of seeing it. Um,

25:32

and then I complete the scan and that position,

25:34

and then the delayed scan is usually performed an hour later.

25:37

So this is a patient who had both a conventional myelogram in the past and had a

25:42

pressure augmented myelogram with us. Um,

25:44

and you can see basically they had a suspicious looking perineural cyst at T

25:48

nine. Um, but which one of these is the one that's leaking it,

25:51

it is really difficult to tell. In this case. After pressure augmentation,

25:54

we could see that it was clearly, um, the one here on the right that is leaking.

25:58

So pretty straightforward to see, um, on the pressure augmented mammogram,

26:02

whereas a conventional mammogram, we could not see it at all.

26:04

And without kind of having the, the, um,

26:07

the M r MRI beforehand to show us where the perineural CSTs were, we,

26:10

we didn't even know where to focus. So, but this is really,

26:12

really helpful and I,

26:13

I can kind of show you some more of these lateral decubitus images as well, um,

26:17

as we go on. But th that was the, that was the final result after doing a D S M.

26:22

Um, this is the patient with a type four CSF leak.

26:25

So you can see basically we've got contrast all along this, uh,

26:28

T1 nerve root extending, um, into the intercostal space.

26:31

So very similar situation.

26:34

Both of these patients actually just underwent blood patches, uh,

26:37

foraminal blood patches and did fine, didn't have any more symptoms of,

26:41

of CSF leak. Um, but without doing these, um, uh, um, uh,

26:45

more specialized, uh, pressure augmented myelograms,

26:48

I would not have seen these C S F leaks. Um,

26:51

with that we can move on to contrast enhanced Mr. Myelography. It usually, um,

26:56

it, it involves an off-label injection of gatum and the fecal sac.

27:00

It has a temple advantage over, uh, um, over, uh, um,

27:05

uh, CT myelography and slow and intermittent leaks and over many other forms of

27:09

myelography.

27:10

Normally I perform the injection and the fluoroscopy suite and I usually make

27:13

sure that I'm in the fecal sac, uh, by injection of, uh, iodinated contrast. Um,

27:18

and then, um, I normally will raise the,

27:21

raise the pressure again using a manometer and lap solution.

27:24

We do a delayed MRI to allow time for the CSF leak to happen. Um,

27:29

uh, in general, um, I do it the same way that I, I do the, uh,

27:34

ultrafast, uh, pressure augmented, um, or not, sorry,

27:37

ultra fast CT myography in, in that I use a discogram set,

27:40

I use the coaxial set with a 20 gauge needle and a 25 gauge puncture needle so

27:45

that I'm making the smallest hole in the fecal sac possible. Um, and in general,

27:49

I just, I give it a little bit more time. The problem is,

27:51

is you're giving 'em so much delay time if you puncture them with a larger

27:54

needle than a 25, it, it,

27:56

it is painful to raise the pressure with a 25 gauge needle,

27:59

but it's worth it in this case cuz you're giving 'em so much time to leak. Um,

28:02

a larger needle can make a pretty impressive leak into the C S F or into the

28:06

epidural space, um, if you use a larger needle to do the lp.

28:09

So I do use a smaller needle for this and I use 0.3 MLS of, of gadolinium, uh,

28:13

and essentially, uh, dilute it, uh, to a total volume of three mls,

28:17

either with Elliot Bs or with autonomous csf,

28:19

and then inject it directly back into their fecal sac. Um,

28:22

and then we do fat sat, T1 and mri. So this is a patient who had, um,

28:27

a postural headache, 64 year old lady, and essentially she had perioral cys.

28:31

They were pretty suspicious on ct, but we really didn't see anything.

28:33

It looked like it was leaking. Um, and then i, I did do, uh, a fat sat,

28:38

um, T1 after injecting gadolinium,

28:40

and we did see a tiny leak from the one on the right here. Ultimately, um,

28:44

she did end up undergoing blood patch for this type four, um, leak and, and,

28:49

you know, did well, didn't need any additional treatments after that. Um,

28:51

here's another similar example except this is actually a type two leak.

28:55

So this patient underwent R Myography as well. Um,

28:58

she did have a suspicious looking nerve root on the, on the Fiesta imaging.

29:03

There was just some irregularity, uh, of the, uh, nerve root sleeve itself,

29:07

and then a small sort of collection outside the nerve root sleeve.

29:10

And then we injected glan, we could see a, a small leak into that, um,

29:14

into that area. And then when we did the digital subtraction myelogram,

29:16

it was clearly extravasated from the fecal sac around the T 11 nerve route here

29:20

on the, uh, on the right side. So this patient again, underwent blood patch,

29:25

did well, didn't need any additional treatments. Um, but that I'll, I'll move,

29:28

move on to digital subtraction. Myography, uh, again,

29:31

digital subtraction myelography is really heavily reliant upon MRI ahead of time

29:35

to kind of know whether we're dealing with a high flow or a low flow leak.

29:38

And as we'll put them either in the prone position if it's a high flow leak or a

29:43

lateral decubitus position. If it's a, uh, a slower leak, I,

29:49

I usually use as you need to inject very quickly, uh,

29:52

because the patient's either gonna be under general anesthesia with a breath

29:54

hold or you're gonna be having them hold their breath and injecting quickly and

29:57

watching the contrast flow up with a mask, uh, or with, uh, a negative roadmap,

30:01

either one. Um, I normally use omni two 40 again for those high flow leaks,

30:06

but I use 300 for the slow flow leaks just to get a little bit better

30:09

visualization. Um,

30:10

and then you can raise their pressure with Elliot BS if it's one of those slower

30:13

flow leaks. Um, but again, the position is critical.

30:16

So if they have perineural cyst on the m I put 'em in the lateral to Cuba

30:20

position in the most su the sort of focus on the most suspicious regions on the

30:23

mri. And then if they have a high flow leak or a, um,

30:27

a pseudo enga seal detected on mri,

30:29

then I focus on that area and I put them in the prone position. Um,

30:32

usually cause the, the, the pseudomonal is, uh, in the, um,

30:36

in the ventral epidural space. That being said,

30:38

sometimes PDO cells are lateral with type two leaks,

30:40

so sometimes we'll put 'em in the, uh, lateral decubitus position, uh, if,

30:44

even if it is a high flow leak,

30:45

if we believe it's one of those lateral type two leaks. Um,

30:48

so this is the patient who had previously undergone a, um, uh, fat sat,

30:53

uh, t2, M R i and it showed basically, uh,

30:57

extensive stranding in the epi within the epidural space in a small ventral

31:01

epidural collection, which we can see here in the lumbar spine.

31:05

This happened after an LP at an outside hospital. And, um,

31:10

essentially we weren't sure where the leak was.

31:12

I think the natural presumption is that it's at the clinical level where the

31:16

lumbar puncture was performed,

31:17

but she had numerous blood patches at L four five and it just did not resolve,

31:21

she continued to have severe postural headaches. Um,

31:25

and ultimately we did do a digital subtraction myelogram with her in the prone

31:29

position. And here's the injection.

31:30

You can see basically here's your initial injection,

31:32

you're just filling the fecal fact. Um, just so you guys are aware,

31:35

this is the S one level, L five, L four, L three, and then this is L two.

31:39

And then we see a little bit of contrast extravasation at L two three, uh,

31:43

on the initial, uh, or, or the second image here. And then on the third image,

31:47

we can see it clearly flowing backwards into the pseudo seal.

31:50

So the puncture clearly occurred much higher than you would suspect based on

31:54

where it should be clinically.

31:55

So it should have been clinically where I put the needle at L four five,

31:58

but it was actually closer to L two three and this was born out in surgery.

32:01

This patient had undergone so many blood patches,

32:04

she just skipped straight the surgery. Dr. Sh I think Dr.

32:06

Shain did the surgery on this patient. And, um, ultimately the,

32:09

the leak was right at two three,

32:10

right where we localized it on the digital subtraction myelogram.

32:13

And he repaired it without any, uh,

32:14

issues and she did well and has had no issues since. Um,

32:18

here's another patient with a type one leak. Sometimes they do present this way.

32:22

This is 74 year old guy with hemorrhagic bilateral subdural collections.

32:25

And the presumption is that this is obviously, uh, gonna be a, uh,

32:29

a subdural hematoma. But this patient had no real, um,

32:33

symptoms referable to the subdural. A patient didn't have any focal deficits.

32:38

He did report a several year history of tinnitus and strange postural headaches

32:42

and he was a very high performance tennis player despite being 74 and a lot of

32:47

twisting, bending when you, when you play tennis.

32:49

And he had a lot of degenerative changes in his spine.

32:52

So our spider senses were tingling with this larger collections.

32:55

And you can see he had the couple of discs here in his cervical spine.

32:58

So the presumption is gonna be that the leak must be up here, right?

33:01

It has to be, it can't be anywhere else.

33:04

This is just a standard TT weighted saal, M R i.

33:06

But this is gonna show you the value of a flow compensated fiesta.

33:09

So the flow compensated fiesta.

33:11

So actually that the epidural collection was down here behind the t1, uh,

33:15

vertebral body.

33:15

And this helped us really focus when we did the digital subtraction myelogram.

33:18

As I had alluded to earlier, when you get around the cervical thoracic junction,

33:21

it gets a little bit dicey with digital subtraction. But this is the T1,

33:25

T2 vertebral bodies that I had marked, um, here.

33:27

And basically the leak did occur right where we predicted it,

33:29

it was going to occur.

33:30

So we have a split in the dura here on the digital subtraction myelogram,

33:33

exactly where we saw the, uh,

33:35

the small epidural collection on the flow compensated Fiesta mri. Ultimately,

33:40

I did again do a blood patch on this patient and he did really, really well.

33:43

The subdurals completely resolved, um, within just a few weeks. So, um,

33:47

presumably we were correct, uh, in, in all of these assumptions, um,

33:50

based upon the mri. So the M R MRI was, uh, you know,

33:53

o obviously extremely helpful in this case. Um, with that, that's,

33:57

that's all I have to say about CSF leaks for now, but I,

33:59

I'm gonna look at the chat really quick before we move to hydrocephalus just to

34:03

see if, uh, anybody's asked any really important burning questions.

34:15

These look all like form responses. I don't see any real questions yet,

34:19

so I'm gonna go ahead and move on then to hydrocephalus. Um, as promised,

34:24

I am gonna show, um, a,

34:26

an obstructive case to start just cuz I don't want people to miss, um,

34:29

obstructive hydro thinking. They're dealing with NPH and,

34:32

and we're gonna get to NPH eventually. But this patient was sent to the,

34:35

the first patient that, that, that I'm gonna show you was sent to me with, uh,

34:38

concern for NPH H and, um, it, it was not nph, but at any rate,

34:43

obstructive hydrocephalus is just an increase in intraventricular volume of C

34:46

sf, um,

34:47

due to impaired drainage of c SF from the lateral ventricles resulting in an

34:51

increase in intraventricular intracranial pressure. So in other words,

34:54

the c SF is being produced normally in the ventricles,

34:56

it just can't get out of the ventricles to be absorbed by the erect

34:58

granulations, which are along the surface of the brain or,

35:01

or along the surface of the skull. And dura near the,

35:03

the venous sis as we talked about earlier, normally presents with headaches,

35:05

visual disturbances, cranial neuropathies, poor balance, ga disturbance,

35:09

sleepiness and seizures. Um, etiologies can include, um,

35:12

aqueduct stenosis adhesions due to prior infection or hemorrhage. Um,

35:17

particularly basler meningitis or prior subarachnoid hemorrhage can do this kind

35:21

of thing can also come from extrinsic compression or entrapment due to a tumor

35:25

like, uh, you know, quadri, genital plate cistern kind of lesion, pineal lesion,

35:29

those sort of things can obstruct the aqueduct. Um,

35:32

there are congenital webs that, that occur in the aqueduct that can cause this,

35:36

um, imaging findings usually, um, include a significant enlargement,

35:40

the lateral in the third ventricle, um,

35:42

without the sort of normal flow artifacts that you see, uh, you know,

35:45

through the, the, the cerebral aqueduct and the fourth.

35:47

And usually the fourth is, is quite a bit smaller than you'd expect to be,

35:51

but you have to keep in mind the fourth is kind of confined by the posterior

35:54

fosus, so it's not gonna get that big to begin with.

35:56

So it might not be that sensitive of the screening, uh,

35:58

evaluation for obstructive hydrocephalus. But one of the things it is,

36:01

is if you see Boeing of that recess of the third ventricle right above the optic

36:05

chiasm or right behind the optic chiasm. And then if you see Boeing, um, uh,

36:09

superiorly of the, um, uh, of the corpus coum, uh,

36:12

that's usually indication that you're dealing with probably obstructive

36:15

hydrocephalus and it can be treated with either a VP shunt or an endoscopic

36:18

third ventriculostomy. So this is a patient who was sent to me with, um,

36:22

gait disturbances and cognitive issues and they,

36:25

they told me that they thought it was MPH and I looked at the patient, he,

36:29

he just, he did not strike me as being someone with MPH cuz he was just really,

36:33

really sharp, um, despite having some minor, you know, issues with,

36:38

um, word finding and, and, and other things. Um, so at,

36:42

at this point my spider sense was tingling,

36:43

so I sent him for a C S F flow study.

36:46

So the C S F flow study we do here at U C S D includes a sagittal fiesta just to

36:51

kind of get a lay of the land beforehand.

36:52

And as you can see immediately we can see that he has an aqueduct web and

36:56

there's dilation of the cerebral aqueduct. There's Boeing of the callosum,

37:00

there's Boeing of the recess of the third ventricle, um, right,

37:02

right behind the optic chim. So all these things are suggestive that,

37:05

that he has obstructive hydrocephalus due to an aqueduct web. Um,

37:08

at this point I stopped them from doing our traditional flow study,

37:12

which is an axial flow study through the aquatory measure,

37:14

basically the velocity and the, the, um, the,

37:17

the rate of flow through the aqueduct. In this case, I asked them just to do,

37:21

um, a, uh, uh, a flow through the, uh, through the frame of magnum,

37:26

the Statal plane with five, 10,

37:27

and 15 banks and just to kind of look and see if there's any flow through the

37:31

aqueduct. Um, there's no flow through the aqueduct on this patient.

37:33

As you can see, there's only, um,

37:35

movement of C S F in the pre pontine cistern and maybe through the frame of

37:39

Magen, a little bit out of the fourth ventricle,

37:41

probably due to just two and fro flow from pulsation of the cerebellum most

37:44

likely. Um, but you know,

37:47

I I think one of the things you have to keep in mind is you wanna set your vex

37:50

on the lower end for something like this,

37:52

because presumably if you have aqueduct stenosis,

37:55

you're gonna have a lower flow rate if it's significant. So you need to,

37:57

you need to bump your vex lower and just make sure, um,

38:01

that it's not more than 10 or 15% above what you think the velocity's gonna be

38:05

through there, which is, it's gonna be pretty slow presumably if it,

38:08

if there's that bad of aqueduct stenosis. Um,

38:10

so that's what we ended up doing in this case. And,

38:12

and I sent this patient for an ET T V and after the ET T V all of his symptoms

38:16

resolved and his ventricles returned to normal thyazide and he didn't have any

38:18

issues. But again, don't,

38:20

don't go down the rabbit hole of NPH until you've at least seen a Saal Fiesta on

38:24

these patients. With that, we're, we're gonna move to the what you came to see,

38:27

which is normal pressure hydrocephalus.

38:28

It usually affects older adults in the sixth and seventh decades of their life.

38:33

Um,

38:33

it results from an increased production of C S F volume without obstruction or,

38:37

or, or elevated pressures.

38:39

Presents with gait disturbances and cognitive decline and incontinence in some

38:43

cases. Um,

38:44

some of the etiologies are speculated to involve sort of changes in compliance

38:48

of the brain that result in kind of compression of the peri ventricular white

38:51

matter and result in emia um, imaging usually demonstrates enlargement,

38:55

the lateral and third ventricles out of proportion of the degree of volume loss

38:59

with some resultant reduction in the, um, uh, colossal angle.

39:02

So you get basically this acute colossal angle at the level,

39:05

the posterior comme.

39:06

One thing to keep in mind though is that this colossal angle is not specific

39:11

nph, I've heard people say, oh,

39:13

it must be NPH cause the colossal angle is narrow. That's not true. It just,

39:17

it's,

39:17

it's a way of determining whether you're dealing with hydrocephalus or just

39:20

plain old volume loss.

39:22

So if you measure the cosal angle and it's narrower than 80 degree, uh,

39:25

80 degrees, um, uh, and, uh, the patient essentially, uh,

39:30

has, you know,

39:31

findings that are concerning for NPH H and they don't have ACR ductal stenosis,

39:35

then probably is NPH h but at that point, you're really just distinguishing mph,

39:40

or sorry, you're just distinguishing hydrocephalus from volume loss.

39:42

You're not dis you're not really making the diagnosis of mph,

39:45

you're just suggesting that there's some form of communicating hydrocephalus at

39:48

that point. Um,

39:50

hyperdynamic flow through the cerebral aqueduct is often present in most of

39:53

these cases, but the diagnostic criteria for this is still pretty controversial.

39:57

Um, a lot of the, the work on, um, C S F flow dynamics was done here by,

40:02

um, a former chair. His name was Bill Bradley,

40:05

and I was actually here when we did the updated studies on our GE machine.

40:09

But originally all this was done on a Siemens, uh, m r MRI machine, uh, with 10,

40:14

20 and 30, uh, van um, velocities or van van, um, settings.

40:19

Um, and essentially what they found was, uh,

40:21

stroke volume of greater than 42 microliters was, um,

40:25

correlated with a higher probability of shunt responsive nph.

40:29

And then the same thing was found on the GE flow sequence, but,

40:32

but only for greater than a hundred microliters. Um, that being said,

40:36

these were small numbers of patients that we took and, um,

40:40

I think with that low of an in number, you have to be a little bit skeptical.

40:43

Same thing for the flow rate of 24 milliliters per minute. Um, that,

40:47

that also could indicate nph.

40:49

The way I think about it though is that the gold standard is still temporary

40:52

aversion of C S F to actually, um, see if the patient's symptoms resolved.

40:56

So if you do a high volume LP or a three day lumbar drain trial and they,

40:59

they improve, then you know, they, they probably do have nph.

41:04

I look at the, um, the,

41:05

the flow study as sort of an adjunct to help me make a decision in those

41:09

patients where we have some equivocal issues. So things that can cause your,

41:14

your, um, uh, gold standard temporary C S F diversion to be somewhat,

41:19

um, uh,

41:20

more dodgy or difficult to trust is patients who've been immobilized for a long

41:24

time and can't walk. So you can't really do a get up and go test,

41:27

you have to rely on their M M S E, uh, or their MOCA test, um, after diversion.

41:32

And honestly, those things can be a little bit variable from day to day,

41:35

even with just normal dementia patients.

41:36

So they could just be having a good day.

41:39

And I think that the C S F flow study can really help in those categories.

41:42

It can also, you know, help with screening too if you,

41:45

if you're not really sure you're dealing with NPH and um,

41:48

you just wanna see if there's hyperdynamic flow and it kind of push you in that

41:51

direction, it can be helpful to do that. Um, but I, I think in the end,

41:55

you're still gonna have to, to,

41:56

to do an LP or a lumbar drain to be 100% certain if that's what you're dealing

42:00

with before you shunt the patient. And again,

42:02

it's treated by either a VP or LP shunt. I, I tend to like, um,

42:06

VP shunts for these patients because the LP shunts just not as easily controlled

42:09

and as, as older patients often do,

42:12

these patients usually have con commit volume loss, and if you do an LP shunt,

42:15

it's harder to control it and you can easily over drain these people with an LP

42:19

shunt and they can end up with subdural collections and or, or subdural HROs,

42:23

you can end up with a a different problem going forward.

42:25

So this is an 82 year old female that that came to me with, uh,

42:29

concern for mph and basically she had progressive gait disturbances, uh, and,

42:34

uh, memory issues. And as you can see, her ventricles are enlarged. Um, and,

42:39

and it is a little bit out of proportion of the degree of her volume loss

42:42

overall. Um,

42:43

you can see she does not have any aqueduct stenosis in her colossal angle is

42:46

narrow suggesting hydrocephalus rather than just volume loss in this case. Um,

42:50

so we did do a, uh, a flow study, um, and essentially the, the first thing,

42:55

I always look at these aile flow studies,

42:57

I wanna see at least that there's two and fro flow through the aqueduct on the

43:00

initial image acquisition. So I wanna see, um, you know, basically the, the,

43:05

the bright flow jet and then the reverse flow jet giving me sort of a dark

43:09

signal as it as it goes backwards. Um, and essentially you're gonna have, um,

43:13

forward flow and backwards flow.

43:15

The stroke volume is actually the flow in one direction,

43:18

not the flow in both direction. So, um,

43:21

the stroke volume in this patient is around, uh,

43:24

or just a little over a hundred microliters.

43:26

It's very common to see patients have slightly more forward flow than

43:31

backwards flow because they're making C S F. So you presume that, you know,

43:34

they're secreting some out of the brain to go to the arachnoid granulations and

43:38

be reabsorbed. So having a slightly higher forward volume is, is typical,

43:42

but if there's a big discrepancy between forward and backward volume,

43:46

I tend to not really believe the stroke volume. So this is a, a,

43:50

a case where technically the stroke volume was telling us that this patient

43:53

probably had nph. Um, the flow volume was not that impressive,

43:57

though it was only six mls per minute. Um, whereas, you know,

44:00

24 has been more closely correlated with, with patients who have nph.

44:05

That being said, you know,

44:06

we felt very strongly about this patient potentially having mph and we did do,

44:10

uh, a, a high volume LP and this patient recovered dramatically and,

44:13

and did very, very well with a shunt. Um, so it just goes to show you the, the,

44:17

the, the, the, um, flow study may not always give you the answer. Um,

44:21

it really is meant to mostly predict shunt responsiveness rather than really

44:25

diagnosed mph. Um, with that we can move on to intracranial, or sorry,

44:30

idiopathic intracranial hypertension or pseudotumor cerebro,

44:33

however you wanna say it,

44:34

and that that's along the same spectrum as venous sinus or or venous outflow

44:38

obstruction, jugular venous obstruction also like from, uh,

44:41

either cranial cervical instability or, um, uh, uh,

44:45

basically venous eagle syndrome if they have elongated styl processes. Um,

44:50

idiopathic intracranial hypertension though typically affects younger,

44:53

more obese females in the kinda the 20 to 40 age range. Um, and again,

44:57

risk factors, obesity, retinoids, like vitamin A overdose, um, uh, you know,

45:02

things like that, venous obstruction contributes to it. Uh,

45:05

in some cases hyper hypoparathyroidism hearing deficiency,

45:09

cushings hormone supplementation and tetracycline can also be risk factors for,

45:13

um, idiopathic intracranial hypertension. Um,

45:16

typically there's an increase in intracranial pressure and opening pressure when

45:20

you do an LP without really an increase in or without a significant increase in

45:24

ventricular volume,

45:25

may typically will present with PA edema and or double vision palsy.

45:29

A lot of 'em do have tinnitus and headaches as well.

45:32

And the imaging findings typically include sort of slit like ventricles and

45:36

empty cell dilated optic nerve sheaths. Uh,

45:39

and typically there's some degree of diffuse sinus narrowing. Um,

45:43

focal venous sinus narrowing, jugular venous stenosis and or, um,

45:47

cerebral venous sinus thrombosis may potentiate or mimic IH in certain select

45:51

cases. Whether it's a mimic or a potentiator is really more, um, uh,

45:57

a judgment call based upon the patient's phenotype.

45:59

So if you're dealing with a thin person who you know,

46:01

has a very low B M I and they have very severe venous stenosis,

46:05

then it's more mimicking I h whereas if you're dealing with someone who's closer

46:09

to the phenotype that you expect for i h then a focal venous sinus stenosis may

46:13

be potentiating it and making it worse and they could benefit from

46:16

revascularization, but typically you'd have to do venous pressure measurements,

46:20

which I'll, I'll go through that in just a minute.

46:21

But the typical treatments would invo involve, involve weight loss diamox, um,

46:26

VP shunting or LP shunting. And, and they, they both,

46:29

they respond to both of those. Again, VP shunts are easier to control,

46:32

but it's harder to put in a VP shun on one of these patients because the,

46:35

the ventricles are more slit like, um,

46:37

you can do venous stenting as I alluded to in select cases. Um,

46:41

this is one of those select cases.

46:43

This is a 46 year old lady who came to me with edema. Um,

46:46

her b m I was on the higher side, but it wasn't really that suspicious. I mean,

46:50

and she didn't really look that big to me. I mean, I'm, I'm from the south.

46:53

I mean she seemed like normal kind of, I mean, so I was like, I don't really,

46:57

I don't, my spider sense was tingling.

46:59

This is more of a venous sinus problem on her. Um,

47:02

but you can see in this patient she does have slit like ventricles. Um,

47:05

she does have, um, dilation of the optic nerve sheath.

47:07

It's easier to see on the right side here. Um,

47:10

she also has a partially empty cell,

47:12

and what we can see is that she has basically diffused sinus narrowing with a

47:16

little bit of superimposed narrowing at the sigmoid transverse junction

47:19

bilateral, which is a common location for arachnoid granulations.

47:22

And that's usually the, the, um,

47:24

con commitment contributing factor in these patients.

47:27

She did have a high opening pressure, I believe it was, um,

47:30

in the mid to high thirties, if I'm remembering right. Um,

47:33

so we did an M R V on this patient,

47:34

and you can see she does have some degree of diffuse sinus airing with some

47:37

distension of the cortical veins. Uh, and then she has actually, um,

47:41

focal arachnoid granulations at both sigmoid transverse junction, um,

47:44

causing superimposed, um, uh, um, uh, stenosis,

47:48

but still because of her b m i being a little on the higher side, we,

47:51

we would have to call this more potentiator as opposed to a, a mimicker.

47:55

And in this case, she definitely needs venous sinus pressure measurements,

47:57

which is what we did.

47:58

We catheterized the venous sinuses all the way across the toula,

48:01

usually from one jugular, and essentially measured the pressures on a pullback.

48:04

Um, she had a six to one gradient with an absolute gradient of 21 millimeters

48:09

mercury, which is very high. Um, anybody with a,

48:12

a gradient of greater than three to one or eight millimeters,

48:14

mercury usually predicts, uh, sh uh, stent responsiveness or,

48:17

or revascularization responsiveness.

48:19

So she ultimately did undergo stenting and didn't require anything else

48:22

required. No more dialogue pressures dropped to normal, uh,

48:26

PA edema resolved everything, um, resolved, and she,

48:29

she's doing well with no headaches. Now at this point. Um,

48:31

I usually treat these patients just like arterial stents. I put 'em on aspirin,

48:34

Plavix for three months, and then after that, just lifelong baby aspirin. And I,

48:38

knock on wood, I haven't had any patients who've had, um,

48:41

significant repeat narrowing. I,

48:42

I typically just for those who are interventionalists, I, I, um, I,

48:46

I typically use, um, the silver biliary stent. I mean, it's just,

48:50

it's really easy to open. And if you have trouble getting there,

48:52

I normally just use our stroke catheters to get a guide up there.

48:55

So I'll use like, um, you know, like a,

48:58

a neuron max guide catheter or B M X 96, and then I'll put like, um,

49:02

either a, uh, red 62 or 68 through it, and then some sort of, you know,

49:07

microcatheter wire. And I, I typically use the road runner wire though,

49:11

but once you get the neuron max into the head, um, it,

49:14

it's very easy to deploy one of these tenents if you, if you,

49:16

if that's what your goal is. So, um,

49:18

but the stroke catheter system is basically just used to get the guide there and

49:21

then the road runner exchange wire will, will easily take the, uh,

49:24

silver stent into position if that's, if that's what needs to happen. Um,

49:29

so this is that same patient after, um, uh, a few months.

49:32

We did an r v prior to taking her off the aspirin PLAs, you can see the stents.

49:35

Why it be patin? It's harder to see the signal through the stent, um,

49:38

because obviously the stent, um, obscures MRI a little bit, but it,

49:41

it's a pretty good, uh, result overall.

49:43

And you can see the stent appears patent, uh, also on the, on the, um,

49:48

uh, the, uh, 2D time and flight. But, um,

49:51

I think that one thing that is a little bit easier if you do a a ctb rim,

49:55

you can see it a little bit easier, but I tend not to like to do, uh,

49:58

ionizing radiation in these younger patients and,

50:00

and give 'em contrast if I don't have to. So I,

50:02

I typically start with an R v and if I'm not,

50:04

if I'm not worried based on the r v and the symptoms,

50:06

I usually just stop at that point. But then I'm,

50:09

I'm gonna move to Keri malformations, which are,

50:11

are more cranio cervical obstructions, um, and can result in hydrocephalus.

50:14

So we, we'll talk about those and then we'll, we'll conclude and I'll,

50:17

I'll take a look at the questions and answers again and see if there's anything

50:20

that I can help people understand a little better or answer any more, you know,

50:24

um, philosophical questions if, if those arise. Um,

50:27

so keary malformations are congenital lesions that are usually associated with a

50:30

small posterior fossa. Type one s are the most common.

50:32

There's usually tons utopia and the tons usually, um,

50:36

as they herniate through the frame of magnum take on like a peg like appearance.

50:39

And that doesn't always happen. But that's, that's what we're looking for,

50:42

sort of a peg like appearance, um, is the classic keary two s are, um,

50:46

displacement of the cerebellar tonsils and the brain stem through the frame of

50:50

magnum with usually a luo sacral pseudo or luo sacro myelo meninge.

50:54

And then type three s are similar to keary two s with either a high cervical or

50:58

occipital myelo meninge.

50:59

And they're typically associated with both hydrocephalus and, um, sargo hydro.

51:03

My Ilia, um, imaging can demonstrate, um, crowding the frame of magnum again,

51:07

like with those peg light, um, uh,

51:10

cerebellar tonsils that you can see a searing sometimes, um, low line conus,

51:14

especially with the Q R E two, um,

51:16

because of the myelo steel and the tethering of the cord. Um,

51:19

the ventricles can be enlarged in some cases if they,

51:21

if they have hydrocephalus. And you can also see, um,

51:23

decreased C S F flow around the frame magnum and brainstem C SF flow studies on

51:28

m r I can be very helpful in determining which patients are really symptomatic

51:31

due to their curi and, and help guide surgical management. Um,

51:35

this was a 29 year old lady with severe headaches that were triggered by

51:38

coughing. Um, and you know, I,

51:41

I was asked to render an opinion on this case because the tonsils really weren't

51:44

peg, like they really weren't lying that low,

51:46

but there was some crowding in the frame of magnum and you,

51:48

you can see they're a little bit low here.

51:49

They're about seven millimeters below the frame of magnum.

51:52

But the patient had a pretty large snx. Um,

51:54

what was interesting about this patient is,

51:56

is she didn't really have any cord signs of any kind,

51:58

which I was kind of shocked at.

51:59

She just had these headaches that were just terrible,

52:02

that were triggered by coughing and sneezing. So I was like,

52:05

this is not a main reason I was asked to render pain.

52:08

Cause someone thought there could be maybe a CSF leak. This is acquired Kia.

52:11

And I was like, ah, I don't think so. Um,

52:13

we did a contrast enhanced brain r i and there there was no secondary signs. Um,

52:17

but in, in the end, this patient did undergo a flow study.

52:20

So this is the Saal Fiesta from that flow study.

52:22

You can see there's crowding the frame of magnum with very little room around

52:25

the brainstem, and there was literally no flow through the frame magnum on the,

52:29

on the sagittal flow study here. Um, and, and again, at this point we,

52:32

we turned our veins very low just in case, um, that we were missing something.

52:36

But we,

52:36

we saw basically no flow through the frame of Magna at that point we decided

52:40

she, she needs decompression. So she got a suboccipital, cranny neuroplasty,

52:44

and um, a few months later the steerings is completely gone.

52:48

So it, it, that had to be what the problem was,

52:51

even though the tonsils weren't peg, like, I mean, and I,

52:53

I show that because the, we, we do fixate on that peg like tonsil thing.

52:56

And I think the flow study can really help you decide if,

52:59

if it is a significant Kiara or not, if you don't see those peg like tonsils.

53:03

Okay. Um, with that, I'm gonna check the questions and answers again, da da da.

53:09

What is the cause of subdural effusion and hypotension? Um,

53:14

that's a good question.

53:15

So presumably there's actually negative pressure in the

53:20

subarachnoid space so that it's actually exerting sort of like a vacuum on the

53:24

PACU meninges to the point where it's actually pulling basically the dura and

53:28

causing the subdural effusions to occur. So that's,

53:31

that's what we believe is happening basically,

53:33

and that's what we believe is causing the enhancement as well.

53:36

It's causing inflammation.

53:37

Do you stent vocal venous sinus stenosis? The patient only have tinnitus. Ooh,

53:43

that's a really good one. So, um,

53:46

I will often do their full workup. I'll do their lp, see what their pressure is,

53:51

and if their pressure is very high to the point where I'm worried about them,

53:56

um, then I will often offer them the, the, um,

54:00

venous sinus pressure measurements and I do all this awake. So I'll,

54:04

I'll basically do an lp. I'll tell 'em, Hey, your pressure's 30, you just,

54:07

you're lucky that you don't have pa edema. Um,

54:09

let's go ahead and do venous sinus pressure measurements if you're okay with it.

54:12

And I'll just flip 'em over and do the venous access. And just quickly,

54:15

you know, I, I use a very small microcatheter,

54:17

so I don't even give 'em that much heparin, so it's safe to do 'em the same day.

54:20

I give 'em like 1500 to Heparin and I just throw in like a five French, um,

54:23

diagnostic catheter, like usually a Bernstein or vert or something.

54:26

And then I'll throw like a prowler select plus through, and then I'll just,

54:29

I'll measure the pressures all the way across. I mean,

54:31

it takes like 10 minutes of added time. And then in, in most cases,

54:34

like if the pressure gradient is there,

54:36

I'll just tell 'em it's there and then we'll have a big conversation in clinic.

54:39

But I can tell you I've never personally stented anyone who just had tinnitus.

54:44

I've stented someone who had tinnitus and bad headaches,

54:47

but never just tinnitus. Okay. Next question.

54:51

What is the,

54:53

what is the specific sign in imaging studies for NPH H and not any

54:57

kind of hydrocephalus? Ooh. Um,

55:02

I don't think there really is a specific sign for MPH and imaging, um,

55:07

that collosal angle, um, that we were, that we were talking about.

55:12

Um, really just predicts, you know, atrophy versus hydro.

55:16

I don't think there is an imaging specific finding.

55:18

It's just a general gestalt that there is, um, enlargement of ventricles.

55:22

It's out of proportion of the degree of overall volume loft.

55:24

And that causal angle is narrow to the point where we suspect hydrocephalus.

55:28

It really is a clinical diagnosis.

55:29

And that's what I fall back on anytime someone tries to push me on, uh, on mph.

55:34

That's generally, um, what I do.

55:36

So someone's asking what the stroke volume cutoff, is there any role, uh, oh,

55:41

sorry, this thing's, man, I'm getting a lot of questions real quick.

55:44

So the cutoff that I use is a hundred cause we have GE machines.

55:47

What is your opinion about complex kiari um

55:52

com? What, um, I'm not sure I understand what they're asking about Complex Kia,

55:57

r e Um, maybe, uh, maybe they could ask another question,

56:01

but maybe define what they're asking exactly. Um, and then, um,

56:06

in which side or C SF Venus officials more frequently and in what level? Ooh,

56:10

that's a good question. Um,

56:13

I find them to be more common actually on the, uh,

56:19

right side of the patient and more common at the thac lumbar junction.

56:24

And I think the reason that that happens is because the pressure actually,

56:29

yeah, it, I think it's just because the pressure is a little bit lower. I mean,

56:33

there's less interference with fistula effor cause you're closer to the ivc,

56:37

closer to the, uh, uh, also closer to the, uh, AGAs hemi AGA system,

56:42

et cetera. Um, let's see. What about agen of the transverse sinus? Oh,

56:46

that's a good question. So, um, agen of the transverse sinus,

56:50

I've never seen bilateral,

56:52

I've seen it unilateral in the setting of a a a a contralateral stenosis.

56:57

And in those cases, those,

56:58

a lot of those patients do end up benefiting from a stent. Um, but yeah,

57:02

agensis is a good thing to think about when you're,

57:04

when you're talking about stenosis.

57:05

So that's where the gradients come in when you're actually measuring the

57:08

pressure gradients, you, you need to make sure it's significant. Um, man,

57:11

these are, these are really good questions. They're coming so fast though.

57:13

I don't know if I'm gonna be able to answer 'em. Let's see here. Um,

57:17

regarding follow up hydrocephalus,

57:19

is there any objective score that can be used?

57:23

I assume they mean for nph H Um, no,

57:27

there's not really an objective score that, that I've used. Um,

57:31

I'm not aware of one. Um, that being said, um,

57:34

somebody's saying Crocker k r ad scale, I've not used that. I just,

57:39

I look at the colossal angle and it oh, KIARI 1.5. Yes. Um,

57:43

very nice presentation. I think that,

57:45

I think that's most of the questions actually.

57:48

How can we determine normal pressure hydrocephalus in the background of

57:51

generalized atrophy? Oh, that, that,

57:53

that's actually gets back to the colossal angle. So that,

57:55

that's a good question too. I mean,

57:57

that coastal angle tells us basically that it's probably more likely hydro and

58:01

not just generalized atrophy,

58:03

because the normal coastal angle is actually usually greater than a hundred.

58:07

If it's less than 80, it's more likely to be, um, mph.

58:10

But I don't use any other scoring system because I don't think anything's

58:14

reliable. I, I just as a gestalt I look at it,

58:17

if the ventricles are bigger than I would expect for the degree of volume loss,

58:20

then I just measure the colossal angle. If it's positive,

58:23

then I just say this is suggested to MPH in the appropriate clinical setting.

58:26

And then the, the neurologist evaluates the patient and they say, yes,

58:28

it looks like mph, then they send 'em back to me.

58:31

Then I end up doing the LP or a three day float of, of a three day, uh, uh,

58:36

lumbar drain trial. And if it's positive, then they go to shunt occasionally,

58:39

like I said, I'll use, uh, I'll do a flow study and, and just see if, um, if,

58:43

if, if it jives with my, um, with my flow diversion, uh, or sorry,

58:47

my temporary flow diversion, particularly if they're immobilized and they,

58:49

they can't walk. Um, let's see. Do you use CT and Mr.

58:53

Milo in the same setting? How much Mr.

58:58

Max contrast can be used? Okay,

58:59

so I personally never use more than 0.5 intrathecal

59:04

gadolinium. I usually stick to 0.3 as far as I'm aware,

59:08

there's no f d a approval for that. I normally just, uh,

59:11

tell 'em it's off label and actually put it in the consent that this is

59:14

off-label. Um, and that's, that's usually what I will do. Um,

59:18

do use the MPH scale from Scandinavian. Now I don't use that NPH scale. Um,

59:23

let's see about intracranial hypertension.

59:27

What do you think is the most reliable MRI finding? Ooh, um, honestly,

59:32

optic disc cupping and, and optic nerve sheath. Um,

59:36

dilation I think is probably most reliable in intracranial hypertension.

59:39

I see empty sellers all the time and it means nothing. Um,

59:44

the other thing that's pretty reliable is diffuse sinus narrowing in the

59:48

appropriate clinical setting. Along with those, um,

59:51

with those findings within the opting nerve, she,

59:53

so if you have diffuse sinus narrowing, um, particularly, um,

59:56

along the SP sidel sinus as it transitions into the transverse sinuses,

59:59

if you have narrowing right there,

60:01

a lot of those patients have have NPH now patient 50 female CSF

60:06

leak history of direct head trauma last 20 years.

60:11

What suitable imaging needed? So from noses? Oh, okay.

60:16

Um,

60:17

so I normally do a super thin section max face to see if I can see a dehiscence.

60:21

And then I actually go to nuclear medicine pretty quickly.

60:24

And when I do the nuclear medicine scan for those patients that I'm looking for,

60:28

uh, C S F rhino, I actually raise their pressure substantially.

60:31

I take 'em to 35 centimeters of water with Elliot B pollution, um, right before,

60:35

sorry, right after I inject the nuclear medicine tracer.

60:38

So first thing I do is I do my lp,

60:40

I confirm I'm in intrathecal with a little bit of, um, uh, iodinated contrast,

60:44

then I inject the radio tracer, then I inject a lot of Elliot bees,

60:47

or you can inject saline and get 'em up to 35 just intermittently monitoring.

60:51

Also, you, you kind of tolerate to their,

60:52

that you kind of titrate with their tolerance. Some people won't get to 35. Um,

60:57

if you can get 'em to 30, even 25, that makes a difference.

60:59

But if you leave 'em with a, a c SF hypertension, uh, or,

61:03

or even a normal pressure, you might not elicit the leak. So I,

61:05

I typically try to get 'em around 30 if I can, um, even for that. And then,

61:09

then I normally have my EMTs packed the nose with pledges right before and we

61:13

actually count the pledges. Um,

61:15

you can also do thin section T2 s through the anterior skull base and try and

61:20

see if you can see the C S F leak. Um,

61:22

there are some cases where you can see that hiss it a little bit better on thin

61:26

section, um, T2 cube or Fiesta Imaging, um, compared to,

61:32

um, uh, compared to just, uh, a plain, um,

61:37

maxillofacial ct. But that being said, seeing the desistance,

61:39

you're relying upon seeing a tiny, usually a sci,

61:43

a tiny ence seal basically is what you're looking for.

61:45

How to differentiate small perineural cyst from SPH leaks on plain

61:50

skin. You can't, um, it's impossible if the patient doesn't have, um,

61:54

if patient has a prior MRI of the brain and they don't have a, um,

61:58

they they do not have a positive burn scale score and they don't have symptoms

62:03

of CSF leak, then it, it clearly is just a normal peroneal cyst.

62:06

But if they have signs of CSF leak on MRI and or clinical,

62:10

then you just have to report that there are perineural cyst in all these

62:13

locations. Um, and in general, if you've already done, um,

62:18

that you could, you could ask your tech, you know,

62:20

to go ahead and try and do a fat sat t2,

62:23

but that's gonna add a lot of time to your scan.

62:25

The fat SAT T2 is really useful.

62:27

If you go back or if you remember back earlier when I was showing a fat sat T2

62:30

of that young, uh, lady who had had the lumbar puncture,

62:33

you could see stranding in the epidural space. So basically on,

62:37

on the fat sat T2 around a perineural cyt,

62:39

you can see stranding in the epidural, uh,

62:41

epidural fat when there's a positive D S F leak and that,

62:44

that can help you kind of focus on one perineural cyst. I,

62:47

I think that probably is what you're asking, basically a fat sat t2,

62:50

but on a standard scan you can't tell if a perineural cyst is,

62:53

is gonna be a leak or not.

62:54

You need the fat sat T2 at minimum to be able to tell if it's,

62:58

if it's really suspicious threshold for stroke volume to be

63:03

CSF flow study. Uh,

63:08

I'm not sure what this, I, again,

63:10

I go back to the a hundred microliters for GE or 42 microliters for Siemens. Um,

63:14

but I still rely ultimately on, on a, um, on a temporary float, uh,

63:18

temporary float aversion meaning like a, um, a lumbar puncture or a, uh, or a,

63:23

um, a lumbar drain restricted diffusion and optic nerve head and pseudotumor.

63:27

Yeah, that is,

63:28

that is actually a finding that we see not infrequently or optic disc cupping

63:31

or, or restricted diffusion. That does happen for sure. Um, let's see.

63:38

Is there any significance using needle gauge size when doing seal? Yes,

63:41

there is significance. So, um, when you're doing a high flow,

63:45

when you're looking for a high flow leak, um,

63:47

somebody asks a question about what size gauge needle to use.

63:50

So if you're doing a high flow leak,

63:51

you need to be able to inject the contrast really quickly if you're doing a dsm.

63:54

So I use a 20 gauge needle to be able to inject it quickly. Um, that being said,

63:58

if you're doing a high flow leak in ct,

64:00

presumably you got the head up for a while and you're actually injecting slowly.

64:05

The, the sort of, the distinction is, is that in, uh, in A D S M,

64:10

the patient can't be moved. So in A D S M you already have the head down,

64:14

so you have to inject quickly and wait for it to flow up.

64:16

Whereas in CT you can inject the entire volume and drop the head.

64:20

You can't drop the head and do a DSM as easily. Um, you, it's,

64:24

it's theoretically possible if your table moves really,

64:26

really quickly for you to drop the head and quickly subtract and then before the

64:30

contrast runs in. Um,

64:32

but I tend to use the smallest gauge needle I can for the low flow leaks because

64:36

I don't want my puncture to obscure the leak basically.

64:40

So I try to use the smallest thing I can. Um, the, the,

64:43

the good compromise though is the gerdy set. So the,

64:46

there's a gerdy set out there that I think has a 20 gauge coaxial.

64:49

It's about an inch and a half long and then a 22 gauge ping cam that goes

64:54

through it. Um, I've had a lot of luck with those. So, um,

64:57

for those sort of leaks where I'm not sure if it's high flow or not,

65:00

if I think it may be a type two lateral leak and it may be kind of high flow,

65:03

um, then I'll use that gerdy set. It's a good compromise.

65:05

But when I think it's a low flow leak,

65:06

I tend to use a 25 basically a discogram set, more or less. Um,

65:12

why should we need to use diagnostic lp? Oh,

65:14

what needle should we use for diagnostic LPs? Um, I, I tend, like I said,

65:19

I tend to use that gerdy set for a diagnostic LP if I'm worried about C S F

65:23

leaks. Um, if I'm not worried about C S F leaks,

65:26

I'm trying to do a very quick, um,

65:29

assessment of whether or not someone has nph. I tend to use a bigger needle, uh,

65:34

cause I don't wanna sit there all day. So I,

65:35

I tend to use a 20 gauge needle and I have this 33 inch one meter

65:40

tubing that I hooked to the 20 gauge needle and I actually raised the head of

65:43

the bed up and I actually dropped the tubing down lower. And um,

65:47

generally I can finish a high volume LP in about 15 minutes. So,

65:52

um, our epidural C s F leak surgical emergencies, like hemorrhages,

65:56

they can be if they're really fast. So if an epidural leak is extremely fast,

66:01

um, to the point where the patient's comatose it can be an emergency. Um,

66:05

I've run into those situations where I don't even have time to localize 'em and

66:08

I tell you exactly what I do.

66:09

Usually the epidural space is so engorged because of the leak and it's so

66:14

soupy for lack of a better way of saying it.

66:16

And you can put almost anything into the epidural space.

66:18

So I'll take a vascular forefront sheath and actually just use like a toy

66:21

needle, uh, and get my toy needle into the epidural space.

66:24

I take a really steep angle into it and then once I get in there,

66:27

I'll put like either an oh three five or a nitrix wire into the epidural space

66:31

and I'll put either a four French radial or, or just a small four French, um,

66:35

vascular sheath into the epidural space. And then I'll put like a vert,

66:38

a four French Burt or a four French Bernstein catheter over an oh three five

66:41

wire. And I will run a catheter all the way up the dorsal epidural space to the

66:46

cervical thoracic junction and I will patch them with a hundred,

66:48

125 ccs of blood.

66:50

Generally injecting about two to four ccs per level titrated into the patient's

66:54

ability to tolerate it. Um, but that's how I deal with,

66:57

with emergent leaks like where I don't really have time to localize it like the

66:59

patient's comatose. I I need to do something fast,

67:02

so I'll put in a catheter and just inject a lot of blood. Uh,

67:05

what is the anticoagulation policy for venous stent and follow up?

67:08

So I normally will give them aspirin and Plavix for three months.

67:12

I do check levels for those. Um,

67:14

so I check P t y 12 level and Aspirin Verify now,

67:18

and I send out full blood platelet aggregation for a D p and um,

67:22

and for the AA level, um, because they're more reliable,

67:25

but they're a 24 hours send out lab for us.

67:27

So if the PT y 12 level is less than 1 94 and the aspirin's less than five 50,

67:32

I normally feel comfortable proceeding. Um, and then I'll wait for the,

67:35

the final numbers, but generally I like them to to be below 50%, um,

67:40

when I'm, when I'm putting in a venous stent on the a d P activation. Um,

67:44

and then for aa I like them to be about the same below 50%.

67:49

What is flow compensated fiesta for the spine? Um,

67:54

oh, so basically, um, essentially we,

67:58

we put on EKG leads and we're actually timing the patient's heart and we're

68:03

compensating for flow based on when their heart beats.

68:05

Cuz when their heart beats their brain pulsates essentially, I mean, and we're,

68:09

we're actually compensating for essentially when their heart beats and when the,

68:13

when the, when the CSF is moving. So it's almost like gating, I mean, and,

68:17

and you can do it that way. Um, another way there,

68:20

there are a couple other ways to do it, but I'm not a physicist full, full, um,

68:22

full disclosure, there are other ways to do flow compensated fiesta,

68:25

but you can gate based on the heartbeat. Um, and then there are,

68:28

there are a couple other ways to do it, but in in general, um,

68:30

flow compensated fiesta is helpful because it removes a lot of different

68:35

artifacts.

68:35

Fiesta itself removes truncation and then the flow compensation removes the flow

68:39

artifacts so that you can see those epidural collections much more easily.

68:42

But you can either, you can either, uh, gate to the cardiac cycle, uh,

68:45

or there's a couple other tricks. And again, I'm, I'm not a, I'm not a,

68:49

I'm not a, uh, a physicist side. I don't know all of the, the tricks to that,

68:53

but I have a very good physicist here and they,

68:55

they do really nice low compensated fiesta for us. And uh, and that's,

68:59

that's how I see a lot of my CS athletes. Okay.

69:02

Looks like we have all of our questions and answers, um, done. Um,

69:07

I really appreciate everyone sticking around to the very end and I,

69:10

I hope this was helpful.

69:11

I know it's a lot of information to throw at y'all at once and it, it's,

69:14

it's as comprehensive as I can get about the specific topics that I'm talking

69:18

about in this amount of time.

69:20

Yeah. Dr. Pinnell, thank you so much for that lecture.

69:22

Thank you so much for answering all of those questions and for everyone else in

69:26

the audience for asking such great questions. We really appreciate it.

69:30

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Report

Faculty

Jeffrey Scott Pannell, MD

Director of Neurointerventional Surgery

University of California San Diego

Tags

Neuroradiology