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Showing posts from October, 2019

Tying things together: Sutures

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Q: Can someone explain the types of sutures used in surgery? There are so many materials and uses but which ones should I really remember? A: I’ll divide the answer into two sections, one introducing the basic terms and terminology that we need to know to understand the suture lingo and the other section will involve using that terminology in a cool kidney transplant. Section 1: Introducing Sutures Sutures can be classified into absorbable and non-absorbable sutures: As the name suggests absorbable sutures are absorbed i.e broken down by the body by enzymatic degradation and hydrolysis and, the time taken to absorb depends on the suture material. For eg: vicryl takes around 2 weeks to breakdown in the body whereas the PDS takes around 8-9 weeks. Non-absorbable sutures do not get absorbed and therefore are either left in the body or are removed later if they are placed on the skin surface. Some things to keep in mind are: 1. Knowing the diameter/thickness/

To Pee or not to Pee?: The Edema Dilemma

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Q: How do cardiac, renal and hepatic edema differ with respect to diuretics given and why? Looks like Urine trouble. Guess what…We've got your back. Let's start by breaking down the  pathophysiology of edema in these conditions which would then help us understand the rationale of administering a diuretic. A) Cardiac Edema: The edema in heart failure is due to a :  A) Pump failure causing a mechanical backing up of fluid  B) Cardiovascular response to poor perfusion causing activation of the renin-angiotensin system (RAAS): Angiotensin II causes vasoconstriction of both afferent and efferent renal arterioles and stimulates release of aldosterone from the adrenal gland. With this background in mind, we’ll come back to your specific question. Mild congestive heart failure is initially managed with a thiazide diuretic. However, loop diuretics (e.g., furosemide, torsemide, or bumetanide) are the principal drugs used in acute exacerbations.  Loop diuretics inhibi

Oscitation, Synchronous Diaphragmatic Flutters & Gingival Algesia

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We've come across a lot of questions that could be answered by a few lines, so we've decided to couple them into one big answer. Here we go! Q1: Why do my eyes tear up while I yawn? A: The most popular answer to this involves the stretching of lacrimal glands, tear ducts and the punctum associated with the eyes when the facial muscles stretch during an episode of yawning. Additional Trivia: New research shows that yawning could be a physiological response to increased brain temperatures!  (Source : Gallup AC, Eldakar OT. The thermoregulatory theory of yawning: what we know from over 5 years of research.  Front Neurosci . 2013;6:188. Published 2013 Jan 2. doi:10.3389/fnins.2012.00188) Q2: Why do hiccups happen and does water really stop them? A: Hiccups are transient episodic involuntary myoclonic jerks of the diaphragm , often in response to a stimulus arising from the esophagus. (through the vagus nerve) Esophageal stimulation, often due to excessiv

Never Break the Chain

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Q: ' If PCR amplifies DNA how do you know if the sequence you're seeing is original number or amplified? For example is AAGGT the sequence n u got AAGGTAAGGTAAGGT how do I know what's the original?' A:  The three essential steps in a PCR (Polymerase Chain Reaction) are: 1)  Denaturation: 'Melting' of DNA into single strands a higher temperatures 2)  Annealing: Addition of Complementary DNA Primers at lower temperatures 3)  Elongation: Replication of DNA by DNA polymerase The processes of denaturation, annealing and elongation constitute a single cycle. Multiple cycles are required to amplify the DNA target to millions of copies.  Now while we're calculating the amount of DNA present in a sample, we retrace to the original number of copies using certain formulae. The formula used to calculate the number of DNA copies formed after a given number of cycles is  2 n , where n is the number of cycles.   Thus, a reaction set for 50 cycles