Answer:
The duration of the effect of Warfarin is prolonged for 2 to 5 days, while the effect of enoxaparin can be maintained for a maximum of 24 hours. The provider probably switched to Enoxaparin to better control the anticoagulant effect.
Explanation:
Warfarin (Coumadin) is an orally administered anticoagulant that indirectly interferes with the action of vitamin K-dependent coagulation factors II, VII, IV and X. The effect as an anticoagulant can begin after 8 hours of administration, reaching a maximum effect in 72 hours, and an effect that can last up to five days.
Enoxaparin (Lovenox) is an anticoagulant administered subcutaneously, whose effect is to inhibit the activity of coagulation factor Xa. Its effect is rapid after administration, and its half-life is relatively short —about 4 to 6 hours— so that the effect can remain for no more than 24 hours.
When a provider switchs the indication of warfarin to enoxaparin, it is to achieve better control of anticoagulation, use it for a limited time or without affecting other mechanisms of blood coagulation.
Select all that apply.
Which of the following statements are true about the genetic disease phenylketonuria?
It is not tested for until a person has symptoms later in life.
Untreated phenylketonuria can lead to brain damage.
Phenylketonuria is effectively treated with gene therapy.
It requires lifelong treatment.
Prenatal surgery is used to treat it.
Answer:
Untreated phenylketonuria can lead to brain damage.
It requires lifelong treatment.
Explanation:
The statements that are true about the genetic disease phenylketonuria are:
-Untreated phenylketonuria can lead to brain damage.
-It requires lifelong treatment.
What is Phenylketonuria?
Phenylketonuria (PKU) is a rare genetic disorder that affects the metabolism of the amino acid phenylalanine. People with PKU are unable to properly break down phenylalanine, an amino acid found in many protein-rich foods, as a result, the amino acid and its by-product, phenylpyruvic acid (PPA) builds up to harmful levels in the body, leading to intellectual disability, behavioral problems, and other serious health problems. PKU is caused by a mutation in the gene that codes for the enzyme phenylalanine hydroxylase (PAH), which normally converts phenylalanine to tyrosine.
The disorder is inherited in an autosomal recessive pattern, which means that a person must inherit two copies of the mutated gene, one from each parent, to develop the condition. PKU is usually diagnosed soon after birth by newborn screening, it is not typically tested for until a person has symptoms later in life. The treatment for PKU is a low phenylalanine diet, it requires lifelong treatment.
Learn more about Phenylketonuria, here:
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What is the purpose of medical ethics?
It is recommended that women of childbearing age take folic acid daily for prevention of a. neural tube defects. b. hydrocephalus. c. cerebral palsy. d. seizure disorders.
Answer:
A
Explanation:
to help prevent neural tube defects (NTDs). NTDs are major birth defects of the baby's brain (anencephaly) and spine (spina bifida).
The game starts when one person serves from anywhere behind the __________.
Group of answer choices
back row
sideline
baseline
anywhere
Answer:
baseline
Explanation:
l think hope that helps
5. LSD is produced from ergot, a fungus that is found on some plants and grasses.
True
False
Answer:
That would be true.
Explanation:
On what does the World Health Organization base its standards?
research
first–hand observations
what other organizations are doing
solutions that make the most money
Answer:
Its research
Explanation:
I got it right in edge