Monday, May 28, 2018

Complications of massive blood transfusion


Hii everyone! 

Massive blood transfusion is defined as

Complications from massive transfusion include :
1) Hypothermia
2) Hypocalcemia - because citrate present in transfused blood is a calcium chelator, it decreases the available calcium.
3) Acidosis - as citrate is acidic in nature.
4) Hyperkalemia - as Hydrogen ions are present in excess due to acidosis, it is compensated by H+ loss in urine and K+ is regained back into blood. So this causes hyperkalemia.
5) Hypokalemia - in stored blood, the Na+-K+ pump is less functioning,  so there is decrease in intracellular K+ in stored blood.  But after blood transfusion, the Na+ K+  pump again starts functioning and increases intracellular K+, this leads to decrease in the available K+ outside the cell causing hypokalemia.
6) Dilutional coagulopathy - massive blood transfusion leads to dilution of clotting factors . It later manifests as DIC-like leading to multiorgan failure and death.

Thanks for reading.

Madhuri.

Complications of blood transfusion

Hii everyone!
This post is about the complications from a single blood transfusion.

1) The most common complication is febrile nonhemolytic tranfusion reaction(FNHTR). -- this occurs due to anti-HLA antibodies in the recipient which kills WBCs leading to release of interleukins and cytokines which are pyrogens. So the treatment is antipyretics.
2) Urticaria - it is due to IgE antibodies in plasma. So we give antihistamines to control it.
3) Hemolytic transfusion reaction - due to antibodies against RBCs. This is rare.  It may occasionally occur due to clinical errors in pretranfusion tests.
4) Infections - bacterial infection due to faulty storage, hepatitis, HIV, malaria.
5) Air embolism
6) Thrombophlebitis
7) Transfusion- related acute lung injury - usually occurs within 6 hrs after transfusion.

Hope this helps.

Madhuri

MCQ mnemonics series: Genital tuberculosis most common site

#Obs_Gyn
Question:
Most common site of genital tuberculosis is?
(A) Fallopian tubes
(B) Uterus
(C) Ovary
(D) Fimbriae
________
Answer:

MCQ mnemonics series: Fusion inhibitors

#Pharmacology
# Antiretroviral drugs
Question
-
*Fusion inhibitor approved for use in HIV is*
a. Enfuvirtide
b. Atazanavir
c. Cobicistat
d. Rilpivirine
-
Answer:

MCQ mnemonics series: Naturally occurring anticancer drugs

#Pharmacology
#Anticancer Drug

Question
-
*All of the following are naturally occurring anticancer drugs except*
a. Irinotecan 
b. Paclitaxel
c. Etoposide
d. Chlorambucil
-
Answer

MCQ mnemonics series by Dr. Shubham Patidar

Hello Awesomites! :D

I am starting a new series for post graduate medical entrance examination. I'll be solving frequently asked confusing difficult MCQ by simple tricks, tips and mnemonics.

In every post MCQ along with authentic answer and mnemonic will be given!

Friday, May 25, 2018

Hematology Diagrams

Hello Awesomites! :D

I made these diagrams during my exams.
I kept in mind the details of cells.
Hope it will help.



-Upasana Y. :)

Thursday, May 24, 2018

Referred Pain

The pain sensation produced in some parts of the body is felt in other structures away from the place of development. This is called referred pain According to dermatome rule,
  • Pain is referred (transferred) to a structure.
  • This structure is developed from the same Dermatome from which pain producing structure is developed.
I know! It’s confusing *_*
Let me make it easy for you, There is a pain in your heart and this pain is transferred to your left arm.
How is this happening •_• This is because the heart and inner aspect of the left arm is developed from the same dermatome. Now, you must be thinking, what about other areas of the body!
  1. Pain in testis is referred to the abdomen.
  2. Pain in the ovary is referred to the umbilicus.
  3. Pain in the diaphragm is referred to the right shoulder.
  4. Renal pain is referred to loin.
Thought question: Do you know about any other areas? Comment me with your answers! 
I wonder, can acidity cause referred pain?

- Written by Anisha Valli

Wednesday, May 23, 2018

Time management tips for USMLE exams

The USMLE exams are really long and tiring but they are like parts of a big puzzle and each part does play an important role in the journey to become a doctor in the US.

This post will focus on some time management and test-taking skills that are helpful to each test-taker. I hope you enjoy reading

Before your exam:

1- It is advisable to do a simulation of the exam. Do 7 or 8 uworld blocks- with breaks in between - or 2 consecutive NBMEs or UWSAs. This way, you ll be familiar when you start to lose your concentration or feel hungry and when you will need a longer break between the blocks.

2- This is optional, but for some people, doing the practice test in the prometric greatly reduces the tension of the exam day. If you are very tensed, schedule a practice test in your prometric and live the experience. This is also considered a test drive and by doing this, you ll know exactly where the prometric is :)

The night before the exam:

1- Sleep well. You need each synapse in your brain to work perfectly :D your memory and logic will be tested tomorrow. Your brain should be ready for that.

2- Try your best to sleep without taking any meds, if u have to, make sure that this time is not the first time you try them.

Exam morning:

1- Arrive early to the prometric, 30-40 mins earlier than your exam starting time. You'll sign some papers and pass a simple security check.

2- Wear comfortable clothes with less pockets and shorter sleeves. You ll be asked to show your pockets and roll your sleeves each time you go out for a break and each time you back into the exam hall.

Blocks and breaks:

1- Skip the tutorial
By doing this, you ll have a complete one hour break instead of a 45 minutes one. The tutorial will show you the software which is a replica of Uworldso save your time and use these 15 precious minutes.

2-Pre-schedule breaks according to the previous simulation
Enter the exam with a plan in mind about using your breaks. Will you take a small break after each block? Will you do 3 blocks with breaks then 2 without? Choose what best suits you based on what you felt during the simulation that you did. For example, you might have felt hungry after your 3rd block, so you may need a longer break in the real exam after your 3rd block.

2- Eating, drinking and using the restroom
Use your breaks wisely. Eat small things/snacks in breaks to avoid hypoglycemia during the exam and eat a small sandwich/breakfast before the exam to have some energy to start.
Don’t forget to "visit" the restroom in your breaks. You are not allowed to go to the restroom during a block, if you urgently need to do that, this will be labelled as “an irregular behavior” and it will be reported to ECFMG.

3- Staying in the exam hall
You don’t have to leave the hall during your break. If you wanna take a fast 5 minutes break, you can simply stay where you are, close your eyes, relax your mind and continue your exam when you feel ready

While solving blocks:

1- Reading the question/the last line first
 Always read the last line first in all USMLE exams, some questions are answered only by reading this last line! Especially in pharmacology questions, you may have a question stem which is 12 lines long then you ll read: What is the mechanism of action of …..? This will help you to save some valuable seconds.
As a rule, read last line first then go back and read the question normally.

2- Highlight any abnormalities
When you read a question, highlight the age,sex and where the patient was admitted; ER, outpatient. Also highlight any abnormality like hemodynamic instability….chest pain...etc.
Your eyes will focus on these findings and will try to associate them to reach a diagnosis.

3- Omit distractors
With time, this becomes a skill in the USMLE world, you realize that many sentences are just fillers to distract you. For example, a myocardial infarction in a 70-year old male, a person who smokes only occasionally or who drinks on weekends.

4- Resist the urge to re-re-read, simply mark and go on
Read the question and apply the hints mentioned above. If you don’t know the answer yet, read the highlighted parts again, if you still don’t know the answer or you are not 100% sure of it, pick the one you feel it is the right one, mark the question and move to the next question. You may get back to this question only when you finish answering all other questions.

5- Leave abstracts and drug ads till the end
This applies for Step 2 CK and Step 3 exams. Abstracts and drug ads are very lengthy and they may take a lot of time in addition to the fact that many statistically insignificant data is thrown here and there. When you see an abstract or a drug ad, choose any answer then move on and go back only when you finish all other questions. It’s illogical to spend 10 minutes on 2 drug ad questions and miss 7 questions at the end of the block!

6- Don’t leave unanswered questions
Even if you don’t have any clue about a question when you read it, choose an answer, mark it and go on. Having a 20% possibility to answer the question right (supposing a question has 5 choices) is better than having nothing. This will also save some much needed seconds, because if you read a hard question then skip answering it, after reading another 20 questions, you' ll have to re-read the hard one.

In general, don’t change your first answer, your first hunch is most probably the right one. Change your answer only if you are sure that the one that you chose is wrong.

Test taking skills are very important and play a vital role in your journey

Good luck to everyone :) USMLE exams are tough but manageable, just tell yourself: I WILL DO IT :)


And that’s it :)
Murad

Tuesday, May 22, 2018

Interglobular Dentin


  • Sometimes mineralisation of Dentin begins in small globular areas that fail to fuse into the homogeneous mass. 
  • It results in Zones of Hypomineralisation between globules. 
  • Most commonly found in Circumpulpal Dentin which is present below the Mantle Dentin. 


In other words, in poorly formed teeth, due to deficiency of vitamin D or exposure to fluoride, it leads to defect in mineralization i.e. loss of globular dentin.

Note: Defect is not because of improper matrix formation.

Thought Question: Dentinal tubules pass uninterruptedly through Globular Dentin. Why? Comment your answers!

- Written by Anisha Valli

Saturday, May 19, 2018

Leech therapy for venous congestion

Today, I came to know that leeches are a well-recognized treatment for congested tissue :O

When this image was sent to me, I thought it was an infestation. After reading about it though, it was clarified that the leech was put deliberately by the plastic surgeons to treat venous congestion (hirudotherapy). 

Authors' diary: Life support


Tuesday, May 15, 2018

AML and ALL differentiating features.


Hello awesomeites !

Today let us find out the difference between AML and ALL on the basis of cell morphology, cytochemistry and immunophenotyping.

So, Acute Leukemia is the presence of blasts >=20% either in peripheral blood or bone marrow.

Myeloblasts in AML and Lymphoblasts in ALL are the two main types

Cell morphology:

Myeloblasts:  The characteristic feature is the presence of Auer rods with moderate amount of cytoplasm and cytoplasmic granules and multiple nucleoli
Lymphoblasts:  They have a scanty cytoplasm no granules and nucleoli are not present
Many a times differentiating the two on morphological basis isn’t feasible. So we take the help of cytochemistry.

Cytochemistry:

Myeloblasts:  are myeloperoxidase(MPO) and Sudan black B (SBB) positive
                         Monoblasts which are a part of the myeloid lineage are nonspecific esterase (NSE) positive
Lymphoblasts:  are periodic acid Schiff (PAS) positive
MPO stains the enzyme within the azurophilic granules and is the most specific while SBB stains the lipid membrane of the azurophilic granules and is most sensitive for myeloid differentiation .
Even after this if we aren’t able to differentiate then we take the help of immunophenotyping

 
Immunophenotyping:

It is performed by flow cytometry.
The sample either bone marrow or peripheral blood is stained with antibodies and the cells are allowed to fall freely in a single file across a beam of laser (this is the over simplified version of it :P).
The laser used is Blue laser of wavelength 488nm. When the laser beam hits the cells some of it gets scattered to the sides and is known as the side scatter which is a measure if the granularity of the cells. While the rest of the beams travel in the same line without deviation and is called as the forward scatter and is a measure of the size of the cells.
Neutrophils are the cells with the highest side scatter.
Staining of the cells with antibodies helps in subtyping acute leukemias on the basis of CD markers.

Here is a list of CD markers on varies cells of myeloid and lymphoid lineage

B cell markers:
CD19: present on all B cells
CD10: immature B cells
CD20: mature B cells

T cell markers:
CD3: present on all T cells
CD4 CD8 CD2 CD5 CD7 are some of the other markers present on various T cells

Myeloid markers: CD13 CD33 CD117

Stem cell markers: CD34

Monocyte markers: CD14 CD64

NK cell markers: CD16 CD56
CD45 is present on all leucocytes a.k.a pan leucocyte marker 


That’s all for now, hope this helps in better understanding of AML and ALL!
Keep calm and keep studying!
Stay awesome!
-          Ashish G. Gokhale