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Antibiotic Review | Mnemonics And Proven Ways To Memorize For Your Exam!

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0:00

All right, so antibiotic review. Um,

0:02

this is going to be like a triple

0:04

distilled antibiotic review. I basically

0:06

took and went through all the

0:08

antibiotics and I pretty much just kept

0:10

all of the bare necessities that you

0:11

need to know for your boards, for your

0:13

exams, and things like that. I'm not

0:14

going to cover every single detail. I'm

0:16

not going to cover every single

0:17

antibiotic, but I'm going to go over the

0:19

main ones, the ones that you really need

0:20

to know for your exams, and the things

0:22

that you need to really be familiar

0:23

with. Um, so let's go ahead and get

0:25

started with that. I wanted to thank

0:26

everybody for the support, the really

0:28

nice comments, everything. Um, as

0:30

always, thank you so much for that. I

0:31

appreciate that more than you know. Um,

0:33

so let's go ahead and get started with

0:34

antibiotics. Um, so we're going to first

0:36

start with the betalactam. So that's

0:38

penicellin, sephilisporins, carbopenams,

0:40

monobact. Um, makes sense to start with

0:43

the OG antibiotic and that's

0:44

penicillans. Um, there's a lot of

0:46

different subtypes of penicellin. Um, we

0:48

basically had to evolve as bacteria

0:50

became resistant. So I'll break down

0:52

each individual one and kind of progress

0:53

as we did um, in real time with the

0:56

penicellin. So let's start with plain

0:57

penicellin. the original. So we have

0:59

penicellin G, penicellin V or also known

1:02

as penicellin VK. Uh V is PO. So it's by

1:05

mouth and then penicellin G comes in

1:08

both an IV and an IM and intramuscular

1:10

form. So what is penicellin cover? Well,

1:12

it covers Graham positive really well.

1:15

It has really good grandpositive

1:16

coverage. But the problem is it's been

1:18

around for so long that it doesn't cover

1:20

a lot of things that much anymore. Um

1:23

there's just been a lot of time for it

1:25

to build resistance. a lot of the

1:26

organisms are resistant against it now,

1:29

but there's still a few things that it's

1:30

really good at. So, what is it still

1:32

good at? What are the high yield

1:33

indications that you need to know? Now,

1:35

again, with these indications, I'm not

1:36

going to list every single thing. That's

1:38

ridiculous. You'd never be able to

1:39

memorize them all. I'm going to focus on

1:41

the main things, the things that always

1:42

seem to come up on the board. So, for

1:44

penicellin G and penicellin V, that's

1:46

going to be syphilis. That one's huge.

1:48

If you don't remember any of the other

1:49

ones, I'd remember that. Uh, strep

1:51

fingitis, dental infections, roheatic

1:53

fever. Of course, rheumatic fever is

1:54

caused by strep, so it makes sense that

1:56

it would cover that. So, those are your

1:57

your first lines for your penicillins.

2:00

Um, so first line for strep, that's why

2:02

I said we also see it indicated for

2:03

rheumatic fever. Um, can be used for

2:05

dental infections. It does cover most of

2:07

your oral um anorobes, but the high

2:09

yield one, like I said, that's syphilis.

2:11

That's the one they always ask you about

2:12

on exams. Um, that's one we use

2:14

penicellin G, of course. So, that's the

2:16

injectable. Um, and just an FYI in

2:18

regards to strep feritis coverage. So in

2:21

real life when you're actually

2:22

practicing and you're prescribing while

2:24

penicellin V is a first line for strep

2:27

it works well you're really not going to

2:29

prescribe it very often because in

2:31

children specifically moxicylin is used

2:34

much more often it's more palatable it

2:36

tastes better they have the bubble gum

2:37

amoxicylin penicellin V does not taste

2:40

good and then the other thing is

2:41

amoxicylin has twice daily dosing where

2:44

penicellin VK sometimes can be up to

2:45

four times a day so in real life you're

2:48

probably going to prescribe amoxicylin

2:49

but know on the boards on the exams that

2:52

um you may have to pick penicellin V for

2:54

your for your strep treatment as your

2:55

first line but amoxicylin works just as

2:56

well um all right so let's progress on

2:59

here so penicellin was our first

3:01

antibiotic but eventually bacteria

3:03

started to evolve it and resisted

3:05

penicellin by producing something called

3:06

penicillinase so we had to go back to

3:08

the drawing board we had to come up with

3:10

a semi a semiynthetic penicellin and

3:12

that was called penicyinase resistant

3:15

also known as antistafloakal

3:17

penicillins so um What penicellinace is,

3:21

it's an enzyme that's produced by the

3:22

bacteria that basically destroys the

3:24

betalactam ring of penicellin which

3:26

makes it ineffective. So the meds in

3:28

this class are napsylan, oxicylin,

3:30

dicloroxicylin. Back in the day, this

3:32

list also included methasylin. It's how

3:34

we came up with the name MRSA.

3:35

Methasylan resistant stafforius. We

3:37

don't use meth methylin anymore. Just

3:39

has a really poor side effect profile

3:41

and these meds work better. So methasyl

3:43

is how we came up with MRSA. It's in

3:44

this class, but we just don't use it

3:45

anymore in practice. So what do your

3:48

penicellinase resistant um penicillans

3:50

work well at grandpositive it's going to

3:53

be your um MSSA your high yield

3:55

indication is going to be your methylin

3:57

sensitive uh staff ora so that's what

4:00

you're going to use it for so whether

4:01

it's bacteria osteomiitis cellulitis

4:03

endocarditis if it's from M MSSA um

4:07

these are generally going to be your

4:08

drug of choice these meds basically

4:10

exist to treat staff that's why we made

4:13

them that's what they're good at it's

4:14

the only indication I would know for

4:16

them napsylan oxicylin dicloroxicylin

4:19

staff MSSA does not cover MRSA it's not

4:22

good for MRSA but it's good for your

4:23

methasylan sensitive staff orius so when

4:26

you think of your napsylan oxycilin

4:28

dicloicin just think of staff coverage

4:30

that's all you should be focusing on for

4:32

these drugs that's why we made it and

4:34

that's what they're really good at all

4:35

right so we created penicellin we

4:37

covered strep and staff so most of our

4:40

gram positive organisms but the last two

4:42

generations we just talked about they

4:44

didn't really cover gram negatives they

4:46

had very poor gram negative coverage. So

4:48

we had to come up with something that

4:50

did. We had to create a penicellin that

4:51

also covered our gram negatives. So we

4:53

developed what's known as

4:54

amopenicillans. You'll definitely

4:56

recognize these. They were created for

4:58

that specific reason to fight gram

5:00

negative infection. So our amopenicans

5:02

are going to be all the am prefixes

5:04

amoxicilin ampillin. Um if you ever

5:07

forget which one is oral, which one is

5:09

parental, um parental of course means

5:11

non-oral root ivim. Um remember

5:14

amoxicillin the third letter is an O

5:16

which stands for oral and ampein the

5:18

third letter is P which stands for

5:20

parental. So because your parental is

5:21

your IVIM your moxicylin is your oral

5:24

just in case you forgot that you

5:25

probably already know that. Um now what

5:26

do these cover? Like I said before they

5:28

cover our gram positives but they also

5:30

cover our gram negative organisms. We

5:32

broadened our spectrum. So our amino

5:34

penicillins brought in our coverage with

5:36

penicellin. Now we have the ability to

5:37

fight gram negative as well as the gram

5:40

positives. So what are some of the high

5:41

yield indications for the

5:43

amopenicillans? They're going to be

5:45

acute otitis media, strep feritis and

5:47

lististeria. So those are the three big

5:49

ones I'd know for your amopenicans. Um

5:52

otitis media, strep lististeria. There's

5:54

some other less high yield indications.

5:56

Uh remember is one of the meds that we

5:58

use to treat H pylori. Remember in

6:00

triple therapy you have chloriththramy

6:02

and oxycylin PPI. Um it's another option

6:04

in Lyme disease. Doxy is generally

6:06

preferred though unless the patient's

6:07

pregnant or a young child. Some caveats

6:09

I'll discuss when we get to the

6:11

tetracycans. But generally when you're

6:13

thinking of your amino penicillins be

6:14

thinking otitis media strep and

6:17

lististeria. Those are the ones you need

6:18

to know. All right. So this subclass of

6:21

penicellin worked well. We picked up

6:23

some gram negative coverage in addition

6:24

to our gram positives. But the problem

6:26

was this class was susceptible to

6:28

betalacttoase. So betalacttomase are

6:31

enzymes produced by bacteria that break

6:33

open the betalactim ring in inactivating

6:35

the betalactam antibiotic. So what we

6:37

had to do was we had to find a way to

6:39

take these antibiotics and help them

6:41

resist that betalacttoase. So what we

6:44

did was we came up with the

6:46

betalacttoase inhibitor penicellin. So

6:49

we take the same antibiotics we just

6:51

went over a moxicylin ail and we added a

6:54

betalacttoase inhibitor which prevents

6:55

the betalacttoase from eating the

6:57

betalactim ring and destroying the

6:59

antibiotic. You can think of it as a

7:00

shield for the antibiotic and that's

7:02

exactly what I used to think of. So I

7:03

used to think of you have amoxicylin

7:06

here same amoxicylin antibiotic but you

7:09

just gave him a shield you give him

7:10

clavilani which is his shield to protect

7:13

against those betalacttomy so it doesn't

7:15

break it down so whether it's amoxicylin

7:18

um or um ampeoin we just give them a

7:21

shield so betalacttoase so the shield

7:23

for amoxicylin is the clavulonate or

7:24

clavulonic acid and that combo is known

7:27

as augmentin and then with ain we gave

7:29

it soulback soulactam is it shield and

7:31

then we have unisonin which is known as

7:33

So moxicylin clavulonate that's

7:34

augmentin and then ampein sulactum

7:36

municin we're taking the same

7:37

antibiotics we just talked about in the

7:39

imopenic but we gave them a shield to

7:41

help them broaden their coverage and

7:43

help them protect against some other

7:44

things. So they cover gram positive gram

7:47

negative like we went over but the key

7:49

here is they picked up really good

7:51

anorobic coverage with these

7:52

betalacttoase inhibitors which allowed

7:54

them to fight some bugs we haven't

7:56

really talked about before. So what are

7:58

the high yield indications for these

8:00

betalacttoase inhibitors panicillans? So

8:02

we now have coverage for our acute

8:04

sinocitis. So moxylclav is going to be

8:06

your first line for sinocitis. Um animal

8:08

bites as well as human bites. Moxylclav

8:11

is first line. And then aspiration

8:13

pneumonia. So first line for aspiration

8:15

pneumonia because if you remember

8:17

aspiration pneumonia most commonly

8:19

caused by anorobes which I talked about

8:21

we picked up coverage for and that's why

8:23

this class is a good choice. Um also be

8:26

aware moxylclav can be used as a first

8:29

line for acutoitis media as an

8:30

alternative to amoxicylin in some

8:32

specific cases in adults few other

8:34

things um but I wouldn't worry about

8:36

that too much for this those are the

8:37

main ones that I remember hearing about

8:39

and those are the ones that I would

8:40

remember for this class all right so we

8:42

have all of these different types of

8:44

penicellin we've covered a bunch of

8:45

different things a wide variety of

8:47

organisms but what about sudamonus we

8:49

haven't talked about sudamonus none of

8:50

these have really covered sudamonus yet

8:53

so where do our anti anti-seudonal

8:55

penicillins come in. Well, that's what

8:56

they're antiudetamonopal penicillins.

8:58

So, these are broadspectctrum

9:00

antibiotics. You're not going to use

9:01

this on your average patient. The key

9:03

here is their coverage of sudamonus. And

9:05

what we have is we have pipaso,

9:07

pipperyl, tasobactim, and take our

9:09

silent clabulate. So, they cover most

9:12

organisms. They're going to cover your

9:13

gram negatives. They're going to cover

9:15

your gram positives. Um, they're going

9:17

to cover sudamonus anorobes. um which is

9:20

really pseudomonus is really the the key

9:22

the one the reason they're used most

9:24

commonly. Um it's really easy to focus

9:26

easier to focus on what they don't cover

9:28

because they cover almost everything

9:29

else. Um they're not going to cover MRSA

9:31

and they're not going to cover your

9:32

atypicals like mopplasma.

9:35

They're just really good at everything

9:36

else though. Um there's not really a

9:39

specific high yield indication I would

9:41

say to know for these. Just be aware

9:42

particularly when sudamonis is suspected

9:45

like in hospitalacquired pneumonia. This

9:47

class is going to be utilized

9:48

particularly with pipaso because that

9:50

has the best coverage of sudamonus. They

9:52

also can be used in really severe soft

9:54

tissue infections in tradinal

9:56

infections. Um so those are your

9:58

anti-seudonal penicillins. Remember um

10:00

pipasil because that's the one you'll

10:02

hear most commonly about which is also

10:04

known as zosin. You'll hear about that

10:06

when you're on your hospital rotations

10:07

and things like that. It's more for your

10:09

really sick patients. Again, it's not

10:10

going to be used in your everyday

10:12

run-of-the-mill infection. Um, all

10:14

right. So, let's go over some general

10:15

adverse drug reactions for the

10:17

penicellin class as a whole, there's a

10:19

few things I think you should know

10:20

about. So, first, hypersensitivity

10:22

reactions. Of all the drug classes we're

10:25

going to talk about, penicellin is the

10:26

class most associated with

10:28

hypersensitivity reactions. Um, another

10:31

one is your hematlogic reaction. So,

10:33

whether it's thrombocytoenia,

10:34

neutropenia, immune mediated hemolytic

10:37

anemia, it's all possible in the

10:38

betalactim class in general, but

10:40

particularly in the penicellin

10:42

antibiotics. And then finally, GI. So

10:44

this is really non-specific because all

10:46

of the antibiotic classes can cause GI

10:48

problems. But in the penicellin class,

10:50

there's a couple main culprits to look

10:52

out for. That's ampeinil and amoxicylin.

10:54

They're well known for causing diarrhea,

10:56

but particularly augmented, which

10:59

remember is the combo of amoxicilonate.

11:01

This penicellin has the highest

11:03

incidence of diarrhea of all the

11:04

penicillins. And I would advise you in

11:07

real life when you're prescribing if you

11:08

can give somebody emoxicylin rather than

11:11

augmentin the emoxy cloud combo please

11:13

do because augmentin just has a really

11:16

high incidence of diarrhea. So it's not

11:18

great for your patients if you don't

11:20

have to give it. So just keep that in

11:21

mind. Um again GI is really non-specific

11:23

for antibiotics but for penicillins

11:26

remember your moxicylin and pacillin

11:27

specifically augmenting that combo. All

11:30

right so that's penicillans. Those are

11:31

the main things I think you should know.

11:33

Let's move on to a class that seems to

11:35

give a lot of people problems and it's

11:37

the sephilisporins. Uh it always seems

11:39

to come up and there's a few things that

11:41

you really need to know for it. So this

11:43

is where some of your pneummonics come

11:44

in that I that I created that I think

11:46

are going to help you. So before we

11:47

start with the sephilosporins, I wanted

11:49

to review an easy way to remember uh the

11:52

coverage for sephilosporins. So

11:54

particularly your gram negative versus

11:56

gram positive coverage. So as the

11:58

sephisporn generations go on from first

12:01

to second to third to fourth generation

12:03

they lose gram positive coverage and

12:05

they gr they gain gram negative

12:07

coverage. Now it's not 100% accurate in

12:09

every case. There's some exceptions but

12:11

a general rule with the sephilosporins

12:13

is as the generations go on from first

12:15

to fourth they lose gram positive and

12:18

they gain gram negative. So in general,

12:19

first generation's really good at gram

12:22

covering gram positive, not so good at

12:24

gram negative. And fourth generation uh

12:26

has really good gram negative but not so

12:28

good gram positive. Fifth generation

12:30

doesn't really follow these rules. Is

12:32

really good at both gram positive, gram

12:34

negative. Um particularly really great

12:36

gram positive. Um but generally first to

12:38

fourth you're going to see um decreasing

12:42

gram positive and increasing gram

12:43

negative. Um so as the sephisporins like

12:46

I wrote out here go on from first to

12:47

second to third to fourth they lose gram

12:49

positive and gain gram negative that

12:51

seems so simple and it seems like oh

12:53

I'll definitely remember that on the

12:54

exam but you have so many things to

12:56

remember and I remember even like having

12:58

an exam question and being like wait is

13:00

it is the first better at gram negative

13:02

or gram positive so I have a really

13:03

simple way to remember that so all you

13:05

think of is the podium you know with the

13:07

Olympics you have your first place

13:08

second place third place etc. This helps

13:11

you remember when you get in first place

13:13

on the podium, you are super positive.

13:16

You're super happy, super positive. And

13:18

that's your first generation. So that

13:19

helps you remember first place. First

13:21

generation Sephlesporins, super

13:23

positive. Covers positives really well.

13:26

As the generations go on, as the places

13:28

go on, when you're like in second place,

13:30

you're still pretty positive, but you're

13:32

a little bit more negative. And then

13:33

third place, you're pretty negative at

13:35

this point. You're not very positive at

13:37

all. So, that helped me remember. Um,

13:39

when you think about that, you're like,

13:40

"Wait, is first better at positive or

13:42

negative?" Just think about it. When

13:43

you're in first place, are you positive

13:45

or you're negative? You're super

13:46

positive. When you're all the way in

13:48

third place, you're pretty negative at

13:49

that point. That's cuz your third gen's

13:51

covered negative much better and you're

13:53

much less positive. So, hopefully that

13:54

helps you remember. It helped me. Um,

13:56

let's move on to our first generation

13:58

and get started. So, first generation

14:00

sephilisporns, we have sephyllexin, also

14:02

known as Kelex is the brand name. That's

14:04

going to be your PO version. And then we

14:06

have sephazolin that's ansef and that's

14:08

going to be your IV version of the

14:09

firstgens. So what do you need to know

14:11

for these? As I said before, these are

14:13

going to have really great gram positive

14:15

coverage. Um staff strep it's going to

14:17

cover really well. So your skin

14:18

infections really um it does have some

14:21

mild gram negative coverage but it's

14:23

mainly u gram negative like for ecoli

14:26

proteus kleella but the main use for

14:28

your firstgens. What they do best is

14:30

gram positive organisms. Remember you're

14:32

in first place on the podium. You're

14:33

super positive. you got first place.

14:35

Now, high yield indications, there's two

14:37

that you need to know. Um, skin

14:39

infections and surgical prophylaxis. So,

14:42

skin infections, MSSA, methasylan

14:45

sensitive staff orius. So, all of your

14:47

skin infe all your skin infections

14:49

involving staff feliculitis, parinchia,

14:52

etc. MSSA be thinking of your firstgens,

14:55

particularly sephilis, uh, sephylexin,

14:57

which is your pommed. And then surgical

15:00

prophylaxis, that's going to be

15:01

sephosolin, which is known as anseph. So

15:04

when you do your surgical rotate

15:05

rotations, you're going to hear this all

15:06

the time be before every surgery.

15:08

They're going to say two grams of ANSF

15:10

on board. It's basically the most

15:11

commonly used antibiotic for surgical

15:13

prophylaxis. And I feel like that's

15:15

really the only thing you should

15:16

memorize is these two things. Those are

15:18

the main things for your first gent. All

15:20

right, so let's move on to our second

15:21

generation. That is going to be the main

15:24

ones are going to be sephoxitin,

15:26

sephiroxim, sephylchlore, and sephot10.

15:29

So how the heck do you remember that? I

15:31

mean there's so many different

15:32

sephilosporins. So, the way that I used

15:34

to remember that is I thought of this. I

15:36

thought of your second generations. I

15:39

thought of um two furry fox drinking tea

15:43

on the floor. So, two, you have two of

15:46

these foxes. That helps you remember

15:47

your second generation sephilosporin.

15:49

Furry, they're furry. That helps you

15:51

remember your se furoxim fox.

15:55

Sephoxitin. Drinking tea. Sephotan

15:59

on the floor. Sephylchlore which f l o

16:02

r. So you say sephyl kind of sounds like

16:04

floor. So two furry fox drinking tea on

16:06

the floor. Two second generation furry

16:09

sephoroxim fox sephoxitin drinking tea.

16:13

Sephotan on the floor. They're drinking

16:16

tea on the floor. And that's sepho um

16:17

that's sephyliclore. So that helps me

16:20

remember the second generation

16:21

sephilosporins. All right. What are they

16:23

good at? So they have um gram positive

16:27

coverage but weaker compared to firstg

16:29

gen and they have gram negative coverage

16:31

but broader compared to the um first

16:34

generations and they they pick up some

16:37

coverage for entrobacttor niceria and

16:39

the gram negative but then they have

16:40

anorobic coverage. So this is really

16:42

important. So firstgens had better gram

16:44

positive coverage your third gen as I'll

16:46

go over next have better gram negative

16:48

coverage. So the second genens are kind

16:50

of like the forgotten middle child. But

16:51

the key for the second genens is their

16:53

anorobic coverage with sephoxitin and

16:55

sephotin. This is particularly good for

16:59

your pelvic infections, some of your

17:01

intraabdominal infections. And this is

17:03

what you're normally going to see them

17:04

tested on. That's really what I'd focus

17:06

on because like I said, they're not

17:09

great as as the first are firstgens as

17:11

gram positive. There's not as good as

17:13

the third gen for gram negatives. So

17:14

they're kind of in between, but what

17:16

they have unique about them is their

17:17

anorobic coverage, and that's what

17:18

you're going to see come up. Um so they

17:20

do have some indications for covering

17:22

UTI, respiratory infections, Lyme

17:24

disease, second uh line to dooxy, but

17:26

for the sake of the exam, what you need

17:28

to focus on is your intraabdominal and

17:30

your pelvic infections involving anobes

17:32

like bactaroides. That's what you're

17:34

going to see when you um see these

17:35

covered. You're going to see your

17:36

intraabdominal and your pelvic

17:38

infections. Sephotan and sephoxitin are

17:40

really good for P for pelvic

17:42

inflammatory disease. There is some

17:44

resistance being seen with uh sephot10

17:47

for uh bergillis. So for your

17:49

intraabdominal infections, infections

17:51

might not be the best choice anymore,

17:53

but overall they're really good for P.

17:54

And in general, this is what you're

17:55

going to see them tested on. Um, your

17:57

intraabdominal, your pelvic infection.

17:59

So that's what I would know for your

18:00

second generation. All right, let's move

18:02

on to our third generation

18:04

sephilosporins. That's going to be uh

18:06

seph trioxone, sephotaxine, and

18:09

septacidine. There's some others in this

18:12

class uh like sephodoxine, but really

18:14

these are the three that ever really

18:16

ever seem to come up. These are the ones

18:17

that I would focus on. So how do you

18:19

remember these? How do you remember

18:20

those three for the third generation? I

18:22

remember this sentence. You can try seph

18:24

trioxone and also try helps you remember

18:27

third generation. Taxing sepho taxim me

18:31

but you won't get a dime. Septazadime.

18:33

So you can try seph trioxone try third

18:35

gen. Taxing me sephoaxim but you won't

18:38

get a dime. Septazadime. That helped me

18:40

remember the ones the main ones you need

18:42

to know for this class. They have

18:43

excellent gram negative covers. That's

18:45

the main thing including sudamonus with

18:47

septacazidem

18:49

um grand positive coverage overall is

18:51

decreased. Some antibiotics in this

18:53

class like sept septazidem have

18:55

virtually no grandpositive coverage at

18:57

all. Um your third gen is mainly about

18:59

your gram negatives and sudamonus um but

19:02

only with septazidm. That's important.

19:04

Remember septacidm has pseudomonus

19:07

coverage and I have another pneummonic

19:08

for that. So the way that I used to

19:10

remember that is if you sue me you won't

19:12

get a dime. So, septazadime only third

19:15

gen to cover sue doonus. I know that's

19:17

not how it's spelled, but that's how

19:19

it's pronounced. That helps you

19:20

remember. If you sue me, you won't get a

19:22

dime. Septazadime only third gen to

19:24

cover sueonus. All right. So, what are

19:26

your high yield indications for your

19:28

thirdgens? So, there's a few things that

19:30

always seem to come up. Gyneakal

19:32

infections, sept trioxone, um menitis.

19:35

So third generation sephilisporins like

19:37

sephotaxim seph trioxone are the

19:40

betalactims of choice in the empiric

19:41

treatment of menitis generally they're

19:43

going to be combined with other

19:44

antibiotics but those will definitely be

19:46

used and then community acquired

19:48

pneumonia hospitalized um are you're

19:50

going to use some of your third

19:51

generations for that so those are the

19:53

main things that I think you need to

19:54

know for your third gen sephilisporins

19:55

let's move into the last two which are a

19:58

lot easier there's not as much to know

20:00

um so fourth generation there's only one

20:02

you have to know sephop nice and easy

20:04

that's the only fourth generation

20:06

sephilisbborne. Now what does your

20:08

sephopime cover? What does your fourth

20:09

generation cover? It's basically gram

20:11

negative. Main thing here to know is

20:13

pseudamonus. Very limited gram positive

20:16

coverage. It does have some coverage of

20:17

MSSA. Um but sudamonus that's the key to

20:20

remember. Like I said you get some gram

20:22

negative some gram positive mainly for

20:24

staff but specifically remember

20:26

sudamonus. That's the main thing you

20:27

need to know if you're fourth gen. Um,

20:29

so there's not a lot to know about

20:30

sephop basically that it's a fourth

20:32

generation sephilisbborne and then it

20:34

has good coverage against pseudomonus.

20:35

That's all I'd remember. But how do you

20:37

remember that? So the way that you

20:38

remember that is sephop instead of

20:41

remembering sephopime remember

20:43

sephforime.

20:44

So sephorpe helps you remember it's a

20:47

fourth generation sephilospor and then

20:49

sephorpime helps you remember sudomonus

20:52

which has four syllables. So that's all

20:55

I remember for sephop. So instead of

20:57

sephop remember sephorpime fourth

20:59

generation sephilisbborne covers

21:01

pseudomonus four syllables and that's it

21:04

that's your fourth generation

21:05

sephilasbborne. Um let's move on to

21:07

fifth generation which is also very

21:09

simple because you basically just have

21:11

septarene. It's another easy one. That's

21:13

really the only one that you need to

21:15

know. Um because that's the only fifth

21:16

generation we have in the US. Outside of

21:18

the US there's another fifth gen

21:19

sephosporin called sephtober. Don't

21:22

worry about that one. Seerlene is really

21:24

all you need to know about. The only

21:26

thing you really need to know about it

21:27

is that it covers MRSA. It's the only

21:30

sephilisporin that does. That's the

21:32

primary use for this drug. MRSA that's

21:34

really it. So, how do you remember that?

21:37

Okay. So, septaralene instead of

21:40

remembering septarlene add an s here.

21:42

You see sepharolene just add an s in

21:44

there. You have searene.

21:46

So, what do you need to know about

21:48

sepharene? So, seph starline is all

21:52

about the stars. So, remember this. So

21:54

septarene sepharene a star has five

21:58

sides. One 2 3 four five. That helps you

22:01

remember this is your fifth generation

22:03

sephilosporin. What else do you need to

22:05

know about the stars? Well, when you

22:06

look out into the stars, what's the

22:08

closest planet nearby that you can see

22:10

out in the stars? It's Mars. Well, what

22:12

is Mars rearranged? MRSA. When you spell

22:15

MRSA, M RSA, that's just Mars

22:18

rearranged. You put this A right here,

22:19

you have Mars. So remember sepharlene

22:22

just think of seph starline the stars

22:25

and you think a star has five sides

22:26

fifth generation sephless born you think

22:28

when you look out into the stars you see

22:30

Mars what is Mars MRSA rearranged this

22:33

has this is the only sephilis born that

22:34

has merca coverage so that's it that's

22:36

all you need to know for your fifth

22:37

generation sephless borins all right

22:39

let's keep moving along so monoactam

22:42

monobactam is an easy one there's only

22:43

one medication in this med uh this class

22:46

and that's triionamm what does this

22:48

triionam do it covers gram negatives

22:50

including sudamonus. That's basically

22:52

all it does. It covers your gram

22:54

negative aerobes. Has no gram positive

22:57

coverage. So obviously doesn't cover

22:59

MRSA, doesn't cover your anorobes. It's

23:01

just gram negatives. Pseudamonus is the

23:03

main thing you need to know here. The

23:04

problem is with estrion is that um

23:07

there's a lot of resistance in most

23:10

institutions against pseudomonus

23:11

coverage. So normally you need to

23:13

utilize empiric double coverage with

23:15

your estrion with your monoactam.

23:17

There's really only one thing you need

23:19

to know about as trionam and that is

23:22

that it has no cross reactivity with

23:24

other betalactum antibiotics you can

23:26

give if they have a penicellin or

23:28

sephilosporin allergy that's the main

23:29

thing this is really the only thing that

23:32

this drug as far as exams exists for if

23:35

you see as tranam they're just asking

23:37

you a question that says a patient has a

23:39

pen penicellin allergy and which one of

23:42

these are you going to give and they're

23:43

going to list a bunch of penicillins and

23:45

sephilosporins and estrinam's going to

23:47

be on there. That's why that question is

23:49

there. It literally exists for exam

23:50

purposes just for that. So the only FYI

23:55

I'll give you with that which you

23:56

probably don't need to remember for the

23:57

exam because I don't think they're going

23:59

to be that evil. But so it's safe in

24:01

penicellin allergy, it's safe in

24:02

sephilosporin allergy, but there is an

24:04

exception septacidine because they share

24:07

a similar side chain. Um like I said, I

24:10

don't think they're going to be cruel

24:10

and do this to you in a question. But

24:12

it's just important to know that real

24:13

life estrriam you can give with a

24:14

sephilisporn or penicellin allergy

24:16

except septacazidem because it is um it

24:20

does have a similar side chain. Um and

24:22

as we know septazidm is a third

24:24

generation sephilisporin. How do you

24:26

know that? Because remember if you try

24:28

taxing me you won't get a dime. So try

24:30

third generation dime septazadime. All

24:32

right. Okay. The other thing to know

24:35

about it, I would say not as important

24:36

as that as the cross reactivity, but it

24:39

can be used in patients with renal

24:40

insufficiency. It doesn't cause any

24:42

renal toxicity. So that's another side

24:44

thing to know about it. All right, so

24:46

that's your monobactim. Let's move on to

24:47

our carbopenms and then wrap up our um

24:51

betalactims. So carbopen, what's

24:53

included in this class? Immipenum,

24:55

salastine, muropenum, and ertopenim. So

24:58

just an FYI, immipen, you see it's the

25:00

only one that has an additional

25:01

medication. Um that's because it can

25:04

never be administered alone. It always

25:06

gets combined with salastin. The reason

25:08

is because if you give it by itself, it

25:10

actually gets inactivated by the

25:11

proximal renal tubules and it leads to

25:13

necrosis of the proximal tubule. So

25:15

you'll always see this carropenum

25:17

combined with uh salastin. So that's

25:19

just a little thing to know about it. So

25:21

what do car cover carropen cover? Almost

25:24

everything. They're extremely

25:25

broadspectctrum antibiotics. So they're

25:28

going to cover your gram positive.

25:29

They're going to cover your gram

25:30

negatives, including your ESBL

25:32

organisms, which is your extended um

25:34

spectrum betalacttomases. They're going

25:36

to cover sudamonus. They're going to

25:37

cover your anorobes. Um they're really

25:41

going to cover almost everything. It's

25:43

easier just to remember what they don't

25:45

cover. And that's really just MRSA and

25:47

your atypicals. Otherwise, you can

25:48

pretty much use these for anything else.

25:50

And that's why in practice, you won't

25:53

because really broadspectctrum drugs

25:55

like these should rarely be used because

25:56

they breed resistance. They're basically

25:58

just reserved for severe infections

26:00

where you don't know what the bug is

26:02

yet. The person's on their way out and

26:03

you just kind of have to throw

26:04

everything at them. Now, I put sudamonus

26:07

up there and I put a little asterisk.

26:08

That's because there is one exception to

26:11

that. Eradipenum is the only drug in

26:13

this class that does not cover

26:14

sudamonus. So, the way that you remember

26:17

that if they give you a question and

26:19

they say patient has blah blah blah

26:21

infection with sudamonus, which one of

26:23

these are you going to use? And they

26:24

give you a bunch of carbopenums. um or

26:26

they say which is the only one that you

26:28

wouldn't want to use. If you see

26:29

erdipenum that's the only one that does

26:31

not cover sudamonus the way that I used

26:33

to remember that it's the only drug in

26:35

the class that has an E. So I just

26:37

remember that E stood for exception to

26:39

the rule that rule being all carbopenoms

26:41

cover sudamonus because it does not. So

26:43

that is what you need to remember. Now,

26:46

the um what I'm going to say as far as

26:50

like the the ADRs, the adverse drug

26:52

reactions is there's really only one

26:54

thing that I would remember and that's

26:55

that these drugs can lower the seizure

26:57

threshold. This is particularly

26:59

important with your immipenum. Um and

27:01

they can cause CNS toxicities. Outside

27:03

of that, I wouldn't really remember too

27:05

much else about them. Just remember

27:07

they're super broadsp spectrum antibi

27:09

antibiotics and remember that exception

27:11

to that rule with erdependent. All

27:12

right, so that's the end of the

27:14

betalactams that covered penicellin,

27:16

syphilisporins, carbopenms, monobactams.

27:18

So those are some of your big heavy

27:20

hitters for your exams. You'll get a lot

27:21

of questions based off of those, but

27:22

let's keep on moving for some other

27:24

important ones. Let's move on to our

27:26

amoglycosides. So that's going to

27:27

include genttoycin, tobery, amicasin,

27:31

neomy, and streptoyc. So what do these

27:34

cover? Basically just gram negatives

27:36

including pseudomonus. They have little

27:38

to no gram positive coverage, no

27:40

anorobic coverage. They're basically

27:42

just gram negative. Now, there's not

27:44

really any high yield indications I'd

27:46

memorize for your amoglycosides. There's

27:48

very few instances where you'd use

27:50

monotherapies for with systemic

27:52

aminoglycosides. There's really just two

27:54

and it's tarmia and plague. So, those

27:56

aren't exactly high yield diseases. Um,

27:58

you also can use it for its synergistic

28:00

effect with other drugs in endocarditis.

28:02

But overall, the highest yield thing

28:04

about amoglycosides isn't their

28:06

indications, it's their ADRs. I remember

28:08

getting asked about clinical rotations

28:10

about this on exam questions. It's the

28:12

most important thing I would remember

28:13

about your amoglycosides. And there's

28:15

two things that you need to know. They

28:17

can be autototoxic. So amoglycoside

28:19

induced autotoxicity can result in

28:21

either vestibular or coclear damage. And

28:24

they can be nephrotoxic. So 10 to 20% of

28:26

patients can experience some degree of

28:28

nephrotoxicity.

28:30

In most cases though, amoglycide

28:32

nephrotoxicity is reversible, which is

28:34

good. All right. So with your

28:36

amoglycosides, there's really two things

28:38

that you need to know. You need to know

28:40

that they basically just cover gram

28:41

negatives including sudamonus. And you

28:44

need to know those ADRs. They're really

28:45

important. So how do you remember that?

28:47

Well, all medications with amoglycide

28:49

end in cin. Tobbery, amasin, neomy, they

28:53

all end in cin. I know there's other

28:55

drugs in other classes that also end in

28:57

cin, but you're just going to kind of

28:58

have to remember this for the

29:00

pneummonic. So they all end in cin. What

29:02

does cin stand for? So CIN and

29:04

amoglycosides you need to remember is

29:06

that coverage includes negatives because

29:08

remember they only include negatives um

29:10

gram negatives and then CIN stands for

29:13

crushes incis and nephrons. So incis of

29:16

course one of your auditory oicles that

29:17

helps you remember it gets crushed

29:19

leading to autotoxicity and nephrons of

29:21

course your functional unit of the

29:23

kidney helps you remember

29:24

nephrotoxicity. So amoglycosides just

29:27

remember they all end in CIN. CIN stands

29:29

for coverage includes negatives because

29:30

they only really cover gram negatives

29:32

and then that also stands for crushes

29:34

incis and nephrons. That helps you

29:35

remember the autotoxicity and the

29:37

nephrotoxicity because that's really all

29:39

you need to know about your amoglycides.

29:41

All right, moving right along to our

29:42

tetracyc. So tetracycans is going to

29:45

include doxycyc tetracyc minyc. So

29:48

there's a few different meds in the

29:49

tetracyc class, but it doesn't matter

29:51

because this is the doxycyc show. Most

29:54

things that you're going to need to know

29:55

about tetracycans is going to be about

29:57

doxy. So make that your focus.

29:59

Tetracycans basically just remember

30:01

doxycyc. What do they cover a lot? So

30:04

they cover your gram negatives, they

30:05

cover your gram positives including

30:07

MRSA. Um they cover your atypicals and

30:09

then they cover your weird stuff. So

30:11

weird stuff, what's that? Well, anytime

30:13

you have some odd organism, some unusual

30:15

pathogen, you should be thinking about

30:17

using a tetracycline. Uh so vibrio,

30:20

brucillaa, q fever, anthrax, lyme

30:22

disease, they're all covered by tetra

30:24

tetracycans, usually doxy, of course. Um

30:27

what are some of your high yield

30:28

indications? So again this is just going

30:30

to be focused on doxycycline. Um there's

30:32

not a lot of high yield indications for

30:35

minocyc and tetracyc. Minocyc is really

30:38

just used for acne. So high yield

30:40

indications are all going to be about

30:41

doxy. So what does doxy cover? Covers

30:43

three things really well. These are your

30:45

first line indications. So chlamydia,

30:47

rocky mountain spotted fever and Lyme

30:49

disease. So chlamyia doxy is now your

30:52

first line for chlamydia. It used to be

30:55

a zithroyc but due to superior efficacy

30:58

with doxy compared to a zithro the

31:00

guidelines have changed and now it's

31:01

going to be doxy 100 milligrams b 7 days

31:04

for firstline treatment. You may still

31:06

give a zithroycin to some patients

31:08

especially your non-compliant patients

31:10

because the nice thing about a

31:12

zithramycin is it's a onetime dose. You

31:14

give them one gram of a zithro and

31:16

they're done. But the problem is it

31:18

doesn't cover it as well as doxy. But

31:19

really first line, the right uh answer

31:21

choice on a question is going to be

31:23

doxy. Also covers Rocky Mountain spotted

31:26

fever. First line pretty much all

31:27

patients are going to get doxy for Rocky

31:29

Mountain spotted fever. Even in young

31:31

children, um just a heads up about Rocky

31:34

Mountain spotted fever treatment in

31:35

pregnancy. Chlorenol used to be first

31:38

line for your pregnant patients, but now

31:40

even that's being replaced by doxy if

31:42

you look at the updated guidelines. So

31:44

Rocky Mountain spotted fever pretty much

31:46

doxy all the way. Lyme disease. So first

31:49

line for your non-pregant adults, your

31:50

older children with Lyme disease,

31:52

they're always going to get doxy. Kids

31:53

under eight, the guidelines are kind of

31:55

muddy. Uh you're going to be taught that

31:57

less than eight, you normally give them

31:58

a moxicillin over eight doxy. I'd

32:01

probably learn it that way for the

32:02

boards, but the guidelines again, it's

32:04

it's changing. It really depends on the

32:06

stage of the infection the child has. If

32:08

it's just cutaneous disease, normally

32:09

you'll give them a moxicillin, but if

32:11

there's any signs of neurologic

32:12

involvement, then you're going to use

32:13

doxy because it covers it better. Um,

32:15

and actually the American Academy of

32:17

Pediatrics supports the use of doxy for

32:19

children under eight as long as it's

32:21

administered less than 21 days, which it

32:23

is for Lyme disease. Anyways, I know

32:25

that made kind of confusing. Overall,

32:27

when you see tetracycans, think

32:29

particularly doxy, you're going to be

32:31

covering chlamydia, rocky mountain

32:32

spotted fever, and Lyme disease first

32:34

line. So, how do you remember that? This

32:37

is the way that you remember that. So, I

32:39

used to remember when you're sitting on

32:41

a dock by the sea, dock sea cycling,

32:45

eating clams and Rocky Mountain spotted

32:47

oy Rocky Mountain um oysters with a

32:50

squeeze of lime. So, you're sitting on a

32:52

dock by the sea. Dock sea cycling.

32:55

Eating clams helps you remember

32:56

chlamydia and Rocky Mountain oysters.

32:58

Rocky Mountain oysters are not oysters

33:00

if you want to look that up, but it

33:02

helps the pneummonic work. Um that helps

33:04

you remember Rocky Mountain spotted

33:05

fever with a squeeze of lime. So that's

33:07

Lyme disease. So that helps you

33:08

remember. Doc C, sitting by a ducks by

33:11

the sea. It's your first line treatment

33:12

for chlamydia. You're eating clams,

33:14

Rocky Mountain spotted fever, you're

33:15

eating Rocky Mountain oysters, and Lyme

33:17

disease. And that's your lime squeezed

33:19

over the top. So that helps you remember

33:20

all of the high yield indications for

33:22

your doxycyc. All right, what are the

33:24

adverse drug reactions that you need to

33:26

know? There's a few that are pretty high

33:27

yield here. First one is teeth

33:29

discoloration and the fact that it can

33:31

also inhibit bone growth in children. So

33:33

tetraycling antibiotics have been

33:35

associated with permanent tooth

33:36

discoloration in children under 8 years

33:38

old if used repetitively or for

33:40

prolonged courses. This does not happen

33:42

in adults. Um tetracycans also may

33:45

deposit in the bone and affect growth.

33:47

And this is why we're cautious about

33:49

using this class in young children. Um

33:51

they also have impaired absorption when

33:53

taken with certain minerals and acids uh

33:55

like aluminum, calcium, iron, magnesium.

33:58

So certain vitamins or dairy products

33:59

when taken at the same time as a

34:01

tetracycline can chilate with the

34:04

antibiotic and impair its absorption. So

34:05

just be careful. Make sure you tell your

34:07

patients about when they're taking this

34:08

medication to avoid certain supplements

34:10

and acids etc. And then finally

34:13

photosensitivity. So there's other

34:15

classes that can cause photosensitivity

34:17

reactions but it seems to come up most

34:18

commonly in questions about tetracycans.

34:20

So the effect can range from a red rash

34:22

to blistering on exposed areas of the

34:25

sun. Um, so you just want to warn your

34:27

patients about this as well. All right,

34:28

so that's our tetracycans. Let's move on

34:31

to our fluoricquinolones. So the first

34:33

thing to know about this class is you're

34:35

generally going to avoid using it in

34:37

your run-of-the-mill infection. So if

34:39

you have like a rhinocyusitis,

34:40

uncomplicated UTI, the risks outweigh

34:44

the benefits. So keep that in mind when

34:45

you're practicing. You're not going to

34:46

give cypro for a simple UTI when you can

34:49

just as easily give nitrofurantoin.

34:51

So save this for your more complicated

34:53

infections. So the CL the medications in

34:55

this class are going to be cyproloxicin,

34:58

levofluxisonin, and moxy fluxicin. Those

35:00

are the three that you need to know.

35:02

Let's start with moxy. So moxyfluxin is

35:05

what's known as your quote unquote

35:07

respiratory fluoroquinolone. It's not an

35:09

official term, but that's the term

35:11

that's most commonly used. Um, a lot of

35:13

people know this one as far as well as

35:15

levofluxisonin as your respiratory

35:17

fluorocquinolone. So moxy in addition to

35:20

levofluxisonin they're considered

35:21

respiratory fluorocquin quinolones um

35:24

and the reason is because they're both

35:26

both active against your most common

35:29

respiratory pathogens including strep

35:31

numo um h influenza moracella

35:34

threw a little accidental there um and

35:36

that's why we call them unofficially our

35:38

respiratory fluoricquinolones now moxy

35:41

in particular has our best gram positive

35:44

coverage also our best anorob coverage

35:46

also has really good coverage of our

35:48

atypicals. Um it's really the only of

35:51

all the fluoroquinolones that has decent

35:53

anorobic coverage and because of this it

35:56

can be used for some intra abdominal

35:58

infections although it's somewhat

35:59

limited due to some resistance among the

36:02

bactaroides species. So it's not the

36:03

best option. Um it can also be used as

36:06

an alternative to amplanin soactim and

36:08

aspiration pneumonia. So be aware that

36:11

moxy unlike the other fluoricquinolones

36:14

actually has some anorobic coverage. So

36:15

you may see that come up in a question.

36:17

Um, I'd say of the three

36:18

fluoroquinolones, this is probably going

36:20

to be the one you're asked about least.

36:22

Um, most questions from my experience

36:24

come uh about cypro and levofluxisonin.

36:27

And again, if you're asked anything

36:28

about moxy, it's probably going to be

36:30

related to its coverage of anorobes. All

36:33

right, so levofluxisonin,

36:34

this is another respiratory

36:36

fluoricquinolone as we just went over

36:37

with moxy. The same reasons. The big

36:40

difference between moxy and

36:41

levofluxisonin though is that

36:42

levofluxisonin also has some activity in

36:45

the urinary tract. It can be used as an

36:47

alternative to cyproloxisin in some

36:50

cases for pyo nephritis your complicated

36:52

UTI where Moxy cannot. Moxy has

36:55

virtually no urine activity. Um it has

36:58

good gram positive coverage. It has good

37:00

coverage of atypicals. So levofluxisin

37:03

as far as coverage it's kind of in the

37:04

middle here. Moxy has the best gram

37:06

negative. Cypro's got the the best gram

37:09

uh I'm sorry. Moxy has the best gram

37:10

positive. Cypro has the best gram

37:12

negative. Levloxin is kind of hanging

37:15

somewhere out in the middle, but it does

37:16

have really good strep numo coverage,

37:19

better than moxy actually, which is why

37:21

it can be used as monotherapy in

37:23

community acquired pneumonia, although

37:25

we try not to use it for pneumonia to

37:26

prevent fluorocquinolone resistance

37:28

among the respiratory pathogens. Um, and

37:31

like I went over before, levofluxisonin

37:33

also does have similar coverage as seen

37:35

in cyproloxisin for your UTI,

37:37

complicated UTI, etc. So, they can be

37:39

used interchangeably. So, that's

37:41

levofluxisonin. Let's move on to cypro.

37:43

So the main thing to know about cypro is

37:45

that it is not a respiratory

37:46

fluoroquinolone. It is a urinary

37:48

fluoricquinolone. So it's first line for

37:50

pyonfritis your complicated UTI.

37:53

Cyprolaxisin is the only fluoroquinolone

37:55

in it that has a P in it. So as soon as

37:58

I see cypro with a P in it that the

38:00

other ones don't have um it always makes

38:02

me think of your PEP stuff. So

38:04

pyonritis, UTI, prostatitis, and your

38:07

older males. Um, a lot of people think

38:10

the reason we don't use cypro for some

38:12

of the respiratory tract infections like

38:14

pneumonia is because it doesn't

38:16

penetrate the lungs, but that's actually

38:18

not the case. So, cypro has lesser

38:21

activity against your grandpositive

38:22

organisms in particular strep numo and

38:25

that's the reason why we don't use it

38:27

for most respiratory infections. Reserve

38:29

that for moxy and levofluxin which have

38:31

great grandpositive coverage. So it's

38:33

not that cypro doesn't penetrate the

38:35

lungs, it's just that it doesn't cover

38:37

our um our respiratory organisms. Um so

38:41

overall the main thing to know about

38:42

cypro is is has your best gram negative

38:45

coverage of the fluoroquinolones

38:47

including um sudamonus the best

38:49

sudamonus coverage. So remember for your

38:51

fluorocquinolones moxy is going to have

38:53

your best gram positive and it's also

38:55

the only one with really good anorobic

38:56

coverage. Cypro has your best gram

38:58

negative coverage including sudamonus

39:00

and then levoflaxisin is kind of in the

39:02

middle but it has really good strep numo

39:03

coverage. So what are your high yield

39:05

indications for your fluorocquinolones?

39:07

That's going to be pyonfritis with cypro

39:09

and levofluxisonin. complicated UTI

39:12

cypro and levofluxisonin uncomplicated

39:15

of course you're sticking to bactrum or

39:17

nitrofarorin which is macroid um

39:19

prostatitis um cyproloxis and

39:22

levofluxisonin can be used as empiric

39:24

therapy in your older patients younger

39:25

patients of course you're covering more

39:27

for um chlamydia and gorrhea but

39:29

prostatitis and your older patients you

39:31

can use cypron levofluxisonin and then

39:33

community acquired pneumonia so

39:35

levofluxisonin moxifyin these can be

39:37

used as monotherapy but generally

39:39

they're going to be reserved for your

39:40

patients with co-orbidities, older

39:42

patients, etc. All right, ADRs, there

39:44

are some high yield one with the

39:45

fluoroquinolones. So, um, they have a

39:49

bunch of adverse drug reactions that are

39:50

possible. GI, of course, being the most

39:52

common as in most antibiotics, but I'm

39:54

going to focus on the ones that always

39:55

seem to come up in the exam questions,

39:57

the more unique ones, and really there's

39:58

three. So, the first really big one is

40:00

your QT prolongation. So,

40:02

fluoroquinolones can prolong the QT

40:04

interval potentially leading to uh to

40:07

torsads. So we avoid this class in

40:09

patients taking QT prolonging drugs or

40:12

patients with long QT syndromes or any

40:14

other risk factors for arhythmia. So

40:16

that's the first big one for

40:16

fluorocquinolones, QT prolongation.

40:19

Second one is tendinopathy or tendon

40:21

rupture. So fluoroquinolones can cause

40:23

tendinopathy and tendon rupture. Um the

40:25

most common site is going to be the

40:26

Achilles tendon. So always be careful to

40:29

tell your patients avoid vigorous

40:31

exercise while on the medication and

40:33

have them alert you of any signs of

40:34

tendinopathy, pain, swelling, etc. And

40:36

then finally, an interesting one, but

40:38

one that I actually had on an exam

40:40

question is that they can precipitate

40:42

mythenic crises. So, um,

40:45

fluorocquinolones actually have a

40:47

blackbox warning for use in patients

40:49

with myastinia graphis because they can,

40:51

uh, cause neuromuscular blocking

40:53

activity which can precipitate a

40:55

myiathenic crisis. So remember that for

40:57

real life and your exam questions. It's

40:59

an important thing to know. All right.

41:00

So that's your fluoricquinolones. Let's

41:02

move on to our macrolytes. So that's

41:03

going to be uh a zithroyc,

41:05

chloriththramy, or ariththramycin. So

41:07

these are really good well-rounded

41:09

drugs. They cover a lot of different

41:11

things. They cover your gram negatives,

41:12

your gram positives, your atypicals. Um

41:14

class has pretty broad spectrum of

41:16

activity. Um particularly with your

41:19

atypicals, the zithroyc is going to have

41:21

your best atypical coverage. That's

41:23

going to be your drug of course uh drug

41:25

of choice for your atypicals. Now let's

41:27

go over some of your high yield

41:29

indications. Um, first one is going to

41:31

be chlamydia with an asterisk because I

41:34

talked about this before. This used to

41:35

be your first line for treatment of

41:38

chlamydia. But new evidence, like I

41:40

said, is showing that microbial efficacy

41:42

of doxy superior. So most guidelines are

41:45

going to say doxy is going to be your

41:46

first line, but a zithroycin is still a

41:48

good second line option and you still

41:50

need to be aware of it. Another high

41:51

yield indication is going to be your

41:53

MAC. So your microacterium avium

41:55

complex, a zithroyc chloriththroyc. So

41:58

macrolyze are your cornerstone of

42:00

antimicrobial back uh therapy for MAC

42:03

treatment and prophylaxis and your HIV

42:05

patients with MAC. Um it's usually going

42:07

to be combined with rafampen or aambutl.

42:09

But remember macrolytes are always going

42:11

to be used in patients with MAC. So just

42:13

remember when you're treating MAC, use a

42:16

macrolyide.

42:17

So macrolytes treating MAC. It helps you

42:21

remember that. Okay. [laughter]

42:23

Um community acquired pneumonia. So

42:25

zithramycin chloriththramycin both your

42:28

typical organisms like strep numo as

42:30

well as your atypicals like myopplasma

42:32

pneumonia macrolytes are going to be

42:34

your first line options particularly a

42:37

zithro for your atypicals like your

42:39

plasma gastroparesis is another one this

42:42

is really just with um particularly with

42:44

ariththramycin so ariththramycin

42:46

increases gastric motility and it can be

42:48

used as another option in addition to uh

42:50

metylopramide which is normally your

42:52

first line agent but be aware of uh

42:54

riiththramy as well. And then another

42:57

one that you may see come up is your

42:59

COPD uh COPD bacterial exacerbations. Um

43:02

so in chronic bronchitis uh with your

43:05

bacterial exacerbations, macrolyze will

43:08

commonly be used as your first line to

43:09

treat. Um and in selected patients with

43:12

severe COPD with frequent exacerbations,

43:14

macrolytes can actually be used

43:16

prophylactically to prevent

43:17

exacerbations. Now your ADRs, there's a

43:20

few ones that you need to know. Again,

43:22

this is going to be another one that can

43:23

cause QT prolongation. So, all

43:25

macrolytes have been associated with QT

43:27

interval prolongation. So, before giving

43:29

one of these meds, make sure that the

43:30

patient's not at risk for torsads,

43:31

taking any other meds that can prolong

43:33

the QT interval. They do have some

43:35

pretty prominent GI side effects. And I

43:37

know I've said this is non-specific, but

43:39

with your macrolytes, um, of course they

43:42

can have their run of run-of-the-mill

43:43

diarrhea, abdominal pain, but they also

43:45

have the possibility of hpatotoxicity

43:47

with a zithro and even acute

43:49

choleistatic hepatitis with

43:52

ariththroycin. So be aware of those as

43:54

well. And then your cytochrome P450

43:56

inhibition. So you have to look out for

43:58

drug interactions with other drugs they

43:59

may be taking like statins, warfare and

44:01

dioxin. This can um change the

44:04

absorption of these medications. All

44:06

right. So we are going to move on to our

44:08

last class that I feel is important for

44:10

you to know and that's venkco. So

44:11

venkcomy venkcomy covers your

44:14

grandpositive MRSA. That's what you

44:17

really need to know about venkcomy. MRSA

44:20

um it's really not used for a lot as far

44:22

as your high yield indications. Uh

44:24

there's really just two things that you

44:26

need to know. Um MRSA of course like I

44:28

said that's a big one. Veno and MRSA are

44:31

synonymous. As soon as you hear Venko

44:32

right away you should be thinking MRSA.

44:34

The other high yield indication is for

44:37

um for CIFF. So venkco is almost always

44:40

given introvenously. We don't usually

44:42

give venkco p because it has very poor

44:45

GI absorption. But the exception is when

44:48

we're treating ciff. We don't need venko

44:50

to get absorbed systemically to treat

44:51

ciff. We need it to just stay in the GI

44:53

tract and actually not get absorbed. And

44:55

that's why p vanco because of its poor

44:58

GI absorption is actually an asset when

45:00

treating ciff. So with venkco it's the

45:02

really the only time you're going to

45:03

give venkco p it's to treat ciff

45:06

otherwise merca you're going to give it

45:07

IV. So those are really the two main

45:09

high yield indications. I really

45:11

wouldn't worry about anything else. See

45:12

m be thinking either ma or ciff. This

45:15

does have some high yield ADRs though

45:17

some high yield adverse drug reactions.

45:19

First one is going to be red man

45:21

syndrome. So it's not really called red

45:22

man syndrome anymore. It's called

45:24

venkcomy infused infusion reaction

45:26

associated with rash. So, let's just

45:29

keep calling it red man syndrome. So,

45:31

this is something unique with venkco.

45:33

Um, and like most unique things, it's

45:35

often tested on. Basically, if you

45:37

infuse venko too quickly, you get this

45:39

confluent or blotchy rash that covers

45:42

the trunk, the extremities, the head,

45:43

the neck. Um, and you avoid this just by

45:46

infusing it slowly. So, that's red man

45:48

syndrome. Can be caused venko infused

45:50

too quickly. The other one is

45:52

autotoxicity.

45:53

So, this is more common in your older

45:55

patients. generally considered to be

45:57

reversible in most most cases and then

45:59

nephrotoxicity is also possible. So

46:02

venko can be nephrotoxic leading to

46:04

acute kidney injury. Um it's more common

46:06

when it's co-administered with other

46:07

nephrotoxic agents like loop diuretics,

46:09

IV contrast die, empoteras B, etc. So

46:13

Veno has a few high yield ADRs and it

46:16

has a a couple high yield indications.

46:18

So how do you remember them on the exam

46:20

in addition to the other 10,000 things

46:22

you need to know about antibiotics?

46:24

Well, the way that you remember that is

46:26

as soon as you think vancomy, I want you

46:28

to think of a pimped out van with chrome

46:30

rims. So chrome spelled C R O M. So

46:34

pimped out van with chrome rims. As soon

46:35

as you see vancomy, so you think of this

46:38

van here, vancomy with these pimped out

46:41

rims, these chrome rims. So pimped out

46:44

van vancomy with chrome CRM rims. And

46:47

chrome stands for CIFF. That is one of

46:50

your first indications for this

46:52

medication. Of course, that's going to

46:53

be PO. Um, the R is going to stand for

46:55

red man syndrome and renal toxicity,

46:58

your nephrotoxicity. The O in chrome

47:00

stands for autotoxicity. And then the M

47:03

stands for MRSA. So, if you remember, as

47:05

soon as you see venkcomy, think of a van

47:07

with chrome pimped out rims. And that

47:09

helps you remember CIFF, red man

47:10

syndrome, renal toxicity, autotoxicity,

47:12

and MRSA. And you can remember the main

47:14

things that you need to know about

47:15

venkcomy.

47:17

All right, let's wrap this up with five

47:19

quick high yield questions. See what you

47:20

remember. So first one, a patient with a

47:22

penicellin allergy can safely be given

47:25

which class or medication of betalactam

47:28

antibiotics with no risk of cross

47:30

reactivity. So that's going to be as

47:32

trienam your monobactam class. Um so

47:35

betalactam that has no cross reactivity

47:37

with penicellin or sephilosporins. The

47:40

exception of course remember that

47:41

septazidm that we discussed earlier.

47:43

Question two. Patient being treated for

47:45

MRSA with IV antibiotics begins to

47:47

develop a red rash across his head,

47:49

neck, thorax, and extremities as the IV

47:52

antibiotic is being administered. Which

47:54

antibiotic is this patient likely

47:56

receiving? Hopefully remember that

47:57

because we just went over that. It's

47:58

going to be venkcomy. So, we're treating

48:00

MRSA. There's really only a number of

48:01

meds uh to begin with for treatment of

48:03

MRSA. Then we see he's developing a rash

48:06

as the IV antibiotic is administered,

48:08

which we know can be caused by venkcomy.

48:10

Um if the medication is administered too

48:12

quickly they may develop that red man

48:14

syndrome that confluent or blotchy rash

48:16

spread throughout the body. Question

48:18

three which is the only medication in

48:20

the carbopenum class that does not cover

48:22

pseudomonus. So that is going to be

48:25

erdipenum. Remember it's the only

48:26

carbopenum that starts with an e? That's

48:28

because it's your exception to the rule

48:30

that all carbopen cover sudamonus

48:32

because erupenum does not. Question

48:35

four, which medication is the first line

48:37

for chlamydia, Rocky Mountain spotted

48:39

fever, and Lyme disease? That is going

48:41

to be doxycyc. So don't forget sitting

48:44

on a dock by the sea, doxycycan. Eating

48:47

clams, chlamydia, rocky mountain

48:48

oysters, Rocky Mountain spotted fever

48:50

with a squeeze of lime, lyme disease.

48:52

All right, question five, last one.

48:54

Which fifth generation sephilisporin has

48:57

coverage against MRSA? So that is going

48:59

to be septarolene. Remember your seph

49:02

starline star has five sides fifth

49:05

generation. What's up in the stars Mars

49:07

which is just the letters in MRSA

49:09

rearranged. All right, so that is

49:11

antibiotics. I hope that was helpful and

49:13

please let me know if it is or if

49:14

there's any suggestions or anything you

49:16

want me to cover coming up in the next

49:17

few weeks. I'm probably going to be

49:19

starting uh neurology pretty soon. Um

49:21

thank you as always for your support. I

49:23

really do appreciate it and good luck on

49:25

your pants, your panoro ears and good

49:28

luck in PA

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