Blood Transfusion/Antiviral Drugs Flashcards

1
Q

blood transfusion therapy

A

the TRANSFUSING of WHOLE BLOOD or BLOOD COMPONENTS through IV

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2
Q

why do we utilize BT THERAPY?

A

many different reasons;
- in general – want to REPLACE LOST COMPONENTS OF THE BLOOD
ex. trama/serious injury
ex. surgical procedures
ex. illnesses - anemia, leukemia, kidney dx

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3
Q

what are some BLOOD TRANSFUSION PRODUCTS?

A
  • WHOLE BLOOD
  • RBC/WBC/PLATELETS
  • PLASMA
  • ALBUMIN
  • GAMMA GLOBULIN
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4
Q

standard transfusion

A

transfusion with a compatible blood donor

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5
Q

autologous transfusions

A

where BLOOD IS COLLECTED for ANTICIPATION of FUTURE TRANSFUSIONS
- designated use only for the sole client
- can donate up to 6 WEEKS PRIOR to surgery

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6
Q

intraoperative blood salvage

A

saving of LOST STERILE BLOOD during a procedure by a filter machine - able to transfuse during operation or post-op

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7
Q

what are the TWO BIOMARKERS that are used to ensure safety during a BLOOD TRANSFUSION?

A
  • ABO FACTOR
  • RhD FACTOR

*we can CROSSMATCH for ABO COMPATIBILITY, but NOT for ANTIGENS

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8
Q

Rh Factor

A
  • can be either PRESENT or ABSENT
  • if Rh-NEG; means patient is BORN WITHOUT the Rh ANTIGEN
  • can only develop ANTIBODIES once SENSITIZIED
  • if in contact with RH+ BLOOD; can cause RXN.
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9
Q

what are the BLOOD TYPES?

A

A+/A-
B+/B-
AB+/AB-
O+/O-

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10
Q

abo factor

A

classification of BLOOD TYPES that are classifed by the types of ANTIGENS within the RBC and ANTIBODIES within the plasma

antigens - triggers an IMMUNE response when FOREIGN

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11
Q

group A

A
  • has the A antigen
  • plasma; anti-B antibody
    will attack B antigen
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12
Q

group B

A
  • has the B antigen
  • plasma; anti-A antibody
    will attack A antigen
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13
Q

group AB

A
  • has both A & B antigen
  • plasma; DOES NOT have any anti-A or B antibodies
    will not attack anyone!
    is considered the UNIVERSAL RECIPIENT (AB+)
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14
Q

group O

A
  • does NOT have any A or B antigens
  • but DOES HAVE both ANTI-A and ANTI-B ANTIBODIES

considered the UNIVERSAL DONOR due to not having any ANTIGENS, however, can only receive O type BLOOD due to having both antibodies

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15
Q

what must be done BEFORE administering BLOOD?

A
  • always make sure YOU HAVE THE CORRECT PATIENT, BLOOD, and ORDER
  • recording BASELINE VITAL SIGNS; assessing needle GAUGE (around 18-19) **checking if the patient is afebrile
  • need to only use NS with BLOOD / proper Y-TUBING
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16
Q

how long do you have to START THE BLOOD TRANSFUSION?

A
  • must give blood within 30 MINUTES OF RECEIVING
  • must have a 2-RN check ready to proceed
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17
Q

what is the TYPICAL STARTING RATE of a BLOOD TRANSFUSION?

A
  • around 2 mL/min (120 mL/hr) for the FIRST 15 MINUTES - must STAY BY BEDSIDE
  • rate is increased after
  • blood bag; around 250-300 cc
  • can only TRANSFUSE NO MORE THAN 4 HOURS
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18
Q

when do we check ROUTINE VITAL SIGNS during BLOOD TRANSFUSIONS?

A
  • 5 minutes from start
  • 15 min mark
  • 30 min mark
  • 1 hour until end
  • 1 hour AFTER
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19
Q

what do we NEVER administer with BLOOD?

A
  • dextrose **hemolysis
  • medications
  • in general do not want to mix anything with blood; only allowed NS for priming etc…
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20
Q

allergic reaction

A
  • flushing, SOB, hives, pruritus
  • sensitivity to the plasma protein antibody
21
Q

febrile or non-hemolyic reaction

A

causes sudden chills, fever, headache, anxiety
- greater hypersensitivity to donor white cells or platelets
- often onset within 2 hours of starting

22
Q

hemolytic reaction

A

the INFUSION OF INCOMPATIBLE BLOOD PRODUCTS
- chills, tachycardia, hypotension, flushing, hematuria
- can be LIFE-THREATENING , can cause DIC (disseminated intravascular coagulation)

23
Q

what happens if there is a BLOOD TRANSFUSION REACTION?

A
  • Always STOP THE TRANSFUSION FIRST!!
  • administer IV LINE - NS
  • observe S & S; can place in fowlers/O2 therapy is SOB
  • emergency drugs - antihistamines, fluids, steroids
  • MUST SAVE EVERYTHING! - contact provider ASAP
24
Q

describe VIRUSES

A
  • there are particles that work by INFECTING and REPLICATING INSIDE OF THE CELLS
  • they can only do so when INSIDE OF THE CELL
25
Q

virion

A

type of a MATURE VIRUS that has a GENOME + CAPSID + ENVELOPE

the CAPSID - protects and transports viral genetic information; RNA

26
Q

what are the FOUR MAIN ENTRY ROUTES for viruses?

A
  1. INHALATION - RESP
  2. INGESTION - GI
  3. TRANSPLACENTALLY - MOM - INFANT
  4. INOCULATION - SKIN/MM
27
Q

inoculation route - viruses

A
  • SEXUAL CONTACT
  • BLOOD
  • NEEDLE SHARING
  • ORGAN TRANSPLANTS
  • BITES
28
Q

describe ANTIVIRAL DRUGS

A

work by either KILLING or SUPPRESSING VIRUSES by destroying VIRIONS or INHIBITING their skill of replicating

  • most of these drugs are SYNTHETIC COMPOUNDS - mostly INHIBIT VIRAL REPLICATION vs. direct destruction
  • can interfere with VIRAL NUCLEIC ACID SYNTHESIS
  • why? - similar to viruses, they only work by ENTERING INTO A HOST CELL (must enter by FUSION)
29
Q

antiviral (NON-HIV) drugs; MOA, indications etc…?

A

MOA;
work by BLOCKING POLYMERASE ENZYME

  • enzyme is important for the SYNTHESIS OF VIRAL GENOMES; causes IMPAIRED VIRAL REPLICATION

indications;
treatment for HSV, VARICELLA-ZOSTER, cytomegalovirus CMV, HEP B & C

contraindications;
severe allergies

30
Q

HIV

A

virus affecting the body’s IMMUNE SYSTEM; destroys WBC (CD4/T cells)

  • can develop AIDS; risk for serious infections or cancer **known as END-STAGE HIV INFECTION
31
Q

what are the STAGES OF HIV

A

STAGE I - acute HIV INFECTION
- chills, fevers, muscle aches

STAGE II - CHRONIC HIV INFECTION
- treatment/drug therapy, blood exams

STAGE III - AIDS
increase of opportunistic infections; continued decrease of WBC cells

32
Q

what are our ANTIVIRAL (NON-HIV) DRUGS? (8)

A
  • AMANTADINE*
  • RIMANTADINE
  • ACYCLOVIR*
  • ENTECAVIR
  • GANCICLOVIR
  • OSELTAMIVIR/ZANAMIVIR
  • RIBAVIRIN
  • SOFOSBUVIR
33
Q

amantadine

A
  • only used against INFLUENZA A VIRUSES
    ; also used for PARKINSONS
  • can be used in CHILDREN
  • only used ORALLY
  • can cause DRY MOUTH, URINARY RETENTION, or CONSTIPATION
34
Q

rimantadine

A
  • has a LONGER HALF-LIFE vs. amantadine
  • has LESS ADVERSE EFFECTS
  • similar to AMANTADINE in indications
  • only used ORALLY
35
Q

acyclovir

A
  • used to SUPPRESS REPLICATION of HSV 1 & 2 & VSV
  • can be used orally, topically, or through injection (want to infuse slowly through IV–over 1 hour)
  • IS SAFE DURING PREGNANCY**
  • delays synthesis of VIRAL DNA

adverse effects;
can cause NEUROLOGIC TOXICITY–want to lower doses for pt. in dialysis

36
Q

entecavir

A
  • treats HEP B INFECTIONS
  • is given ORALLY; doses 0.5 - 1 mg/day for min. of 12 months
  • does have BLACK BOX WARNINGS;
    can cause SEVERE EXACERBATIONS - HEP B, LACTIC ACIDOSIS, HEPATOMEGALY, HIV RESISTANCE

adverse effects;
- INCREASED LIVER FUNCTION TESTS
- headaches, rashes, hematuria, increased creatinine

37
Q

ganciclovir

A
  • treats CMV INFECTIONS and PREVENTION of CMV disease in high-risk pts. (who are getting organ transplants)
  • given IV or ORAL
  • must assess for BONE MARROW SUPPRESSION - dose-limiting toxicity
38
Q

oseltamivir/zanamivir

A
  • are NEURAMINIDASE INHIBITORS - enables VIRIONS to ESCAPE from the infected cells/spread throughout body

indications

  • INFLUENZA VIRUS TYPE A and B

adverse effects;
- N/V, diarrhea, nausea, sinusitis

*oral form (oselt) / *powder form (zanamivir)

39
Q

ribavirin

A

MOA;
interferes with RNA & DNA SYNTHESIS

indications;
used to treat HEP C or SMV

**is a CATEGORY X DRUG - TETATOGENIC

40
Q

sofosbuvir

A
  • is the FIRST-IN-CLASS RNA POLYMERASE INHIBITOR
  • helps to treat CHRONIC HEP C **often combined with RIBAVIRIN

interactions

  • STRONG CYP3A4 INDUCERS
  • RIFAMPIN
  • ST. JOHN’s WORT
    **PREGNANCY CATEGORY X DRUG
41
Q

describe HIV TRANSMISSION

A
  • needs OPEN SURFACE CONTACT and is spread through BODY FLUIDS that contain the VIRUS
  • ex. BLOOD, SEMEN, VAGINAL FLUID, BREAST MILK

SUBTYPES;
- HIV-1**more common
- HIV-2

42
Q

ANTI-VIRAL (HIV) DRUGS; MOA, indications etc…

A

MOA;
work by SUPPRESSING the VIRAL REPLICATION PROCESS

indications;
active HIV INFECTION or some to treat HEP B

adverse effects;
- bone demineralization
- osteoporosis (reduced calcium)

43
Q

what are our HIV DRUGS? (10)

A
  • ENFUVIRTIDE
  • INDINAVIR
  • NEVIRAPINE
  • RALTEGRAVIR
  • TENOFOVIR
  • ZIDOVUDINE
  • MARAVIROC (SELZENTRY)
  • RALTEGRAVIR
  • TENOFOVIR ALAFENAMIDE (VEMLIDY)
  • ZIDOVUDINE (RETROVIR)
44
Q

enfuvirtide

A
  • type of FUSION INHIBITOR; suppresses fusion process & replication
  • is quite expensive/inconvenient dosing
45
Q

indinavir

A
  • type of PROTEASE INHIBITOR
  • can cause KIDNEY STONES in around 4% of PATIENTS
  • recommendation; increased LIQUIDS
46
Q

nevirapine

A
  • type of NON-NUCLEOTIDE REVERSE TRANSCRIPTASE INHIBITOR **important enzyme that allows viral rna to change to DNA
  • often is WELL TOLERATED
  • only taken ORALLY
47
Q

raltegravir

A
  • stops HIV REPLICATION; prevents insertion of VIRAL DNA into the human cell – type of INTEGRASE INHIBITOR

indications;
- patients with MULTIDRUG RESISTANCE/ACTIVE REPLICATION

adverse effects;
- myopathy
- immune reconstitution syndrome

contraindications;
- LACTATION, PRE-TERM NEONATES etc…

48
Q

tenofovir

A

indicated for HIV and HEP B–allows to SLOW ITS PROGRESSION by preventing INSERTION OF VIRAL DNA
- is a NRTI (NUCLEOTIDE REVERSE TRANSCRIPTASE INHIBITOR)
- has been having INCREASED RESISTANCE

adv. effects;
- LIVER/KIDNEY FXN, LACTIC ACIDOSIS, TACHYC. DARK URINE

49
Q

zidovudine

A

the first anti-viral drug for HIV
- not typically used now; can cause severe adverse reactions
- was often given to INFECTED PREGNANT WOMEN/NEWBORN BABIES
- adverse effect; BONE MARROW SUPPRESSION