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R.RAMAKRISHNAN.D.Pharm
Regist No:2701810002
Pathophysiology & Pharmacotherapeutics-III
B.Pharm(Practice)
Final Year 2019-2020
VM College of Pharmacy
Salem,Tamil nadu
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Acute tubular necrosis is kidney injury characterized
by acute tubular cell injury and dysfunction.
Common causes are hypotension causing renal
hypoperfusion and nephrotoxic drugs. The condition is
asymptomatic unless it causes renal failure
The diagnosis is suspected when azotemia develops
after a hypotensive event, severe sepsis, or drug
exposure and is distinguished from prerenal azotemia
by laboratory testing and response to volume
expansion.
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Hypotension (ischemic ATN, common)
Nephrotoxins (common)
Sepsis (common)
Major surgery
Third-degree burns covering > 15% of BSA
Disorders resulting in other endogenous toxins, such
as tumor lysis or multiple myeloma (uncommon)
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Massive volume loss, particularly in patients with
septic or hemorrhagic shock or pancreatitis or in
patients who have had serious surgery, increases the
risk of ischemic ATN.
ATN is more likely to develop in patients with the
following:
Baseline creatinine clearance < 47 mL/min
Diabetes mellitus
Preexisting hypovolemia or poor renal perfusion
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ATN is usually asymptomatic but may cause symptoms or signs
of acute renal failure, typically oliguria .
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Renal (kidney) cortical necrosis is death of the tissue
in the outer part of kidney (cortex) that results from
blockage of the small arteries that supply blood to
the cortex and that causes acute kidney failure.
Usually the cause is a major, catastrophic disorder
that decreases blood pressure.
Symptoms may include dark urine, decreased urine
volume, fever, and pain in the side of the body.
Sometimes an imaging test or tissue analysis (biopsy)
is done to confirm the diagnosis.
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Renal cortical necrosis can occur at any age. About
10% of the cases occur in infants and children..
The next most common cause is a bacterial infection
of the bloodstream (sepsis).
In children, renal cortical necrosis may follow severe
infection, severe dehydration, shock, or the
hemolytic-uremic syndrome.
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In adults, sepsis causes one third of all cases of renal
cortical necrosis.
Other causes in adults include rejection of a
transplanted kidney, burns, inflammation of the
pancreas, injury, use of certain drugs, and poisoning
from certain chemicals.
The diagnosis is often confirmed with an imaging
test such as computed tomography (CT)
angiography.
Kidney biopsy can give doctors the most accurate
diagnostic information, but a biopsy involves
removing kidney tissue and may be unnecessary if
the diagnosis is evident.
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Renal papillary necrosis is a disorder of the kidneys
in which all or part of renal papillae die.
The renal papillae is the area where the openings of
the collecting ducts enter the kidney.
Necrosis (tissue death) of the renal papillae may
make the kidney unable to concentrate the urine
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Conditions causing this condition:
Diabetic Nephropathy
Kidney infection
Kidney transplant rejection
Urinary tract obstruction
Sickle cell anemia is a common cause of renal papillary
necrosis.
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Symptoms may include:
Back pain or flank pain
Bloody urine
Cloudy urine
Dark, rust-colored, or brown urine
Tissue in the urine
Chills
Incontinence
Increased urinary frequency or urgency
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An examination may reveal tenderness when
touching the body over the affected kidney.
There may be a history of chronic or recurrent urinary
tract infections. There may be signs of obstructive
uropathy or renal failure.
A urinalysis may show dead tissue in the urine.
An IVP may show obstruction or tissue .
There is no specific treatment for renal papillary
necrosis. Treatment depends on the underlying cause.
If the underlying cause can be controlled, it may go
away on its own.
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