The client need more explanation from the nurse regarding the contraindications of chewing, crushing, or ingesting Nitroglycerin sublingual pills. The tablet should be dissolved by placing it beneath the tongue or in the space between the cheek and gum.
<h3>What key elements would the nurse emphasize while teaching the client how to use nitroglycerin to treat angina?</h3>
Adults: At the first indication of an angina attack, insert 1 tablet under the tongue or in the space between the cheek and gum. Use 1 pill as needed, up to 15 minutes at a time, every 5 minutes. Take no more than three tablets in a 15-minute period. Use 1 tablet 5 to 10 minutes prior to the activity to prevent angina from stress or exertion.
<h3>When administering nitroglycerin, what should be observed?</h3>
Any nitroglycerin-treated patient who experiences hypotension should have a trial IV fluid delivery. Fluid administration to patients with any form of heart failure is subject to standard safety procedures, including monitoring of blood pressure and lung sounds.
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The insurance issue is the one that is ethically wrong. Placing a patient above another simply because of a personal relationship and not because of health issues is wrong and an abuse of power.
Answer:
"How many minutes after meals should I take the levothyroxine dose?"
Explanation:
Levothyroxine is a synthetic hormone that is prescribed for patients with deficiency in the production of thyroxine, a hormone released by the thyroid gland. It is important that this medication is only used with prescription and medical monitoring, where the correct way to take the medication will be shown, solving the problem and decreasing the chances of side effects.
One of the main instructions on the intake of levothyroxine is that it should be taken when the patient has not yet eaten and is on an empty stomach. In this case, a patient who wishes to take the medicine after meals demonstrates the need for additional teaching about the medicine.
Answer:
The right side of the body
Explanation:
Skin-fold assessment are generally taken on the right side of the body
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.
