Week 3 Misc Flashcards

1
Q

What route is medication delivered, when being given IM?

A

Parenteral route

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2
Q

What are the fastest acting routes of medication administration?

A

IV and IO

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3
Q

What may worsen uptake rate of medications given IM?

A
  • Dehydration
  • Poor perfusion
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4
Q

What medications can be given IM within the AP scope of practice?

A

Adrenaline 1:1000 - Anaphylaxis
Glucagon - Hypoglycemia
Hydrocortisone - Addisonian crisis
Naloxone - Opiod overdose with reduced GCS

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5
Q

What are the 3 common sites for IM injection?

A
  • Deltoid muscle
  • Vastus Lateralis
  • Gluteal medius
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6
Q

Where is the Deltoid injection site?

A
  • In the middle of the triangle, that is 3cm away from the acromion
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7
Q

Where is the IM injection site within the gluteal medius?

A

In the lateral upper quadrant, below the illiac crest

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8
Q

Where is the Vastus lateralis IM injection land marks?

A
  • Greater tracanter
  • Lateral condoyle
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9
Q

What does site selection depend on?

A
  • Avoiding sites with adverse features
  • Accessibility of the site
  • Desired flow rate
  • Muscle conditions
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10
Q

What equipment is required for an IM infection?

A
  • Alcohol wipe
  • Drawing up needles
  • 23 guage IM needle
  • Ampule guard
  • Appropriate sized syringe
  • Combi stop
  • medication
  • Guaze
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11
Q

What are the preparation checks before delivering an IM medication?

A
  • Explain the procedure
  • Gain informed consent
  • Check medication
  • Record batch number and expiry
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11
Q

What indicates the weaker area of an ampoule?

A
  • A dot on the neck of the vile
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12
Q

Why is it important to aspirate prior to delivering medication?

A
  • To check for bleeding, to ensure it is going into muscle and not a blood vessel.
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13
Q

What rate should an IM injection be given?

A

1ml per 10 seconds

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14
Q

How long after delivery should the needle be withdrawn from the site?

A

10 seconds

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15
Q

After a needle stick exposure what needs to be done?

A
  • Bleed site
  • Wash site
  • Cover with sterile dressing
  • Speak to TL
  • Document on EPRF
  • DATIX
16
Q

What is effected by sickle cell disease?

A
  • The haemoglobin in red blood cells, they stick together to make a crescent shape.
  • This reduces the ability to carry oxygen
17
Q

How long do Sickle cells last for?

A

10-20 days

18
Q

What occurs when a PT goes into crisis?

A

The sickle cells clump in the blood vessles, causing pain.

19
Q

If both parents are sickle cell carriers, what is the % chance the child will suffer with sickle cell disease?

A

25%

20
Q

When is sickle cell disease often detected?

A
  • At birth/ During pregnancy
21
Q

How long can a sickle cell crisis last?

A

Up to 7 days

22
Q

What are the signs and symptoms of sickle cell crisis?

A
  • Stroke,
  • Difficulty in breathing
  • Chest pain
  • Fatigue
  • Weakness
  • Headache
  • Dehydration
  • Priaprism,
  • Pyrexia
  • Hypoxia
23
Q

What s the leading cause of death in sickle cell patients?

A
  • Acute chest syndrome
24
Q

If someone with sickle cell is presenting with acute chest syndrome, what signs are the likely to present with?

A
  • Typical cardiac symptoms
  • Crackles at the base of the lungs.