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qwelly [4]
2 years ago
6

The emt should assess for hypoglycemia in small children with a severe illness or injury because:_____.

Medicine
1 answer:
kiruha [24]2 years ago
5 0

The emt should assess for hypoglycemia in small children with a severe illness or injury because: children cannot store excess glucose as effectively as adults.

<h3>Hypoglycemia </h3>

Blood sugar (glucose) levels that are below the normal range are known as hypoglycemia. Your body mostly uses glucose as fuel.

Diabetes medication frequently has an impact on hypoglycemia. But even in those without diabetes, other medications and a wide range of, frequently undiagnosed diseases can result in low blood sugar.

Treatment must start right away for hypoglycemia. A fasting blood sugar of 70 milligrams per deciliter or lower should be taken as a warning sign for many people. Nevertheless, your figures may vary. Request information from your doctor.

With the aid of a high-sugar food or beverage or by taking medicine, you must swiftly bring your blood sugar levels back into the normal range. Finding and addressing the source of hypoglycemia is necessary for long-term treatment.

Learn more about hypoglycemia here:

brainly.com/question/14757163

#SPJ4

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Answer:

Apply ice right away to reduce swelling. Wrap the ice in cloth. ...

Use ice for the first 3 days. After 3 days, either heat or ice may be helpful if you still have pain.

Rest the pulled muscle for at least a day. ...

Try not to use a strained muscle while it is still painful.

Use an ice pack or slush bath of ice and water for 15 to 20 minutes each time and repeat every two to three hours while you're awake for the first few days after the injury. Compression. To help stop swelling, compress the area with an elastic bandage until the swelling stops.

4 0
3 years ago
82 is what in units from an insulin syringe
shusha [124]

Answer:

82 is 82 units which is equal to 0.82 ml

5 0
3 years ago
What causes galactosemia ?
svetoff [14.1K]

Answer: Mutations in the GALT, GALK1, and GALE genes cause galactosemia.

Explanation: Galactosemia is a disorder that affects how the body processes a simple sugar called galactose. A small amount of galactose is present in many foods. It is primarily part of a larger sugar called lactose, which is found in all dairy products and many baby formulas. The signs and symptoms of galactosemia result from an inability to use galactose to produce energy.Classic galactosemia, also known as type I, is the most common and most severe form of the condition. If infants with classic galactosemia are not treated promptly with a low-galactose diet, life-threatening complications appear within a few days after birth. Affected infants typically develop feeding difficulties, a lack of energy (lethargy), a failure to gain weight and grow as expected (failure to thrive), yellowing of the skin and whites of the eyes (jaundice), liver damage, and abnormal bleeding. Other serious complications of this condition can include overwhelming bacterial infections (sepsis) and shock. Affected children are also at increased risk of delayed development, clouding of the lens of the eye (cataract), speech difficulties, and intellectual disability. Females with classic galactosemia may develop reproductive problems caused by an early loss of function of the ovaries (premature ovarian insufficiency). Galactosemia type II (also called galactokinase deficiency) and type III (also called galactose epimerase deficiency) cause different patterns of signs and symptoms. Galactosemia type II causes fewer medical problems than the classic type. Affected infants develop cataracts but otherwise experience few long-term complications. The signs and symptoms of galactosemia type III vary from mild to severe and can include cataracts, delayed growth and development, intellectual disability, liver disease, and kidney problems.

6 0
3 years ago
Read 2 more answers
A client has been diagnosed with polycystic kidney disease. On assessment of the client, the nurse will observe for which as the
IrinaVladis [17]

Answer:

The correct answer is option C

FLANK PAIN AND HEMATURIA

A client has been diagnosed with polycystic kidney disease. On assessment of the client, the nurse will observe for FLANK PAIN AND HEMATURIA as the most common manifestation of this disorder

Explanation: Polycystic kidney disease is an inherited disease of the kidney caused by abnormal gene mutation, it is characterised by clusters of non cancerous sacs containing water-like fluids (cysts) in the kidney.

Symptoms of polycystic kidney disease includes back or side pain,swollen abdomen,excessive tiredness (fatigue), blood in the urine and high blood pressure.

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5 0
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Refers to the transfer of genes from donor to recipient microorganisms, where the recipient strain shows a change in genetic mak
koban [17]

The mechanism by which genes are transferred from a donor to a recipient microorganism is called TRANSDUCTION. After transduction, the genetic makeup of the recipient cell is different.

Transduction refers to the genetic recombination mechanism by which bacteria can transfer fragments of DNA by using bacteria-infecting viruses called bacteriophages.

During transduction, a bacterial cell interacts by a conjugal bridge through which fragments of DNA are transferred to a suitable (host) recipient cell.

This mechanism (transduction) changes the genome of the host cells by generating genetic recombinants when the bacteriophages initiate a new cycle of infection.

Learn more in:

brainly.com/question/3411854

8 0
2 years ago
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