Blood borne viruses Flashcards

1
Q

how are BBVs spread

A

by blood/bodily fluids including semen, vaginal secretions and breast milk

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2
Q

name the three main BBVs

A

hep B and C

HIV

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3
Q

give examples of professions in which there is contact with bodily fluids and as such risk of BBV transmission

A
health care
emergency services
lab work
mortuary
prisons
hairdresser/beautician
plumbing
tattoing/piercing
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4
Q

describe the common course of Hep B infection

A

acute infection for 1-3 months

then 1/20 of those people will be affected by a chronic infection defined as >6 months duration

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5
Q

what are the complications of hep b

A

cirrhosis

liver cancer

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6
Q

how is hep b treated

A
antiviral (tenofovir or entecavir)
or immunomodulator (interferon alpha)
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7
Q

what is the most common reason for hepatitis C infection

A

drug use

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8
Q

how long does the acute infection last for

A

up to 6 months

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9
Q

what proportion of people infected with hep c remain chronically infected

A

75 percent

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10
Q

how many genotypes of hep c are there and which are the most curable with antiviral medication

A

genotypes 1,2,3

genotypes 1 - 50 percent will be cured with medication

genotypes 2,3- 80 percent are cured with medications

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11
Q

what are the long term complications of hep c

A

cirrhosis and liver cancer

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12
Q

What proportion of people infected with HIV are unaware

A

1 in 4

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13
Q

what is the commonest route of infection in the uk of HIV

A

sexual intercours

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14
Q

what affects the chances of infection transmission

A

viral load is proportional to chance of infection

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15
Q

how is HIV treated

A

HAART

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16
Q

what is the typical course of HIV infection

A

seroconvesion illness two to six weeks following infection (avg 15 days) - flu like illness
asymptomatic for up to 10 years
Symptomatic is characterised by opportunistic infections and certain cancers = AIDS

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17
Q

describe the current nice guidelines for referring/treating infertile couples

A

Offer couple further clinical assessment afte 1 yr of not conceiving
Offer earlier if:
female older than 36
known pathology e.g. vasectomy, tubal blockage
apparently no chance of pregnancy with expectant management

offer IVF treatment after 2 yrs for unexplained infertility

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18
Q

Under which aspect of the nice guidelines of treatment of BBV patients fit under`

A

‘apparently no chance of pregnancy with expectant managment’ –>as such can be offered treatment straight away

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19
Q

What investigations are typically done prior to IVF

A
day 21 progesterone
rubella immunity 
chalmydia
gonorhea
TV/BV/candida/syphillus
FSH/LH/E2
Testosterone, SHBG, FAI
prolactin
HSG/hycosy/laparoscopy and HTB to check tubal patency
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20
Q

what abnormality is more common in HIV pts

A

hydrosalpinx (4o percent of HIV positive patients)

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21
Q

what abnormalities in sperm are seen in HIV pts

A

lower sperm motility
semen parameters not significantly different where detectable/undetectable viral load
significant correlation between CD4 count and sperm count and progressive motility
no correlation between CD4 count and sperm morphology

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22
Q

what affect does haart have on sperm parameters

A

lowers sperm count, lower motility and higher percentage abnormal forms

23
Q

how is the risks of BBV transmission minimised in the ACU

A

hep B immunisation to staff
USS probe decontaminated
theatre
gametes/embryos handles and stored separately to non BBV

24
Q

give the advantages of IUI in these patients

A

less invasive than ivf

cheaper

25
what are the disadvantages of IUI
need good sperm parameters low success rate cycle will be cancelled if more than three follicles more than 14mm (risk of multiple pregnancy)
26
what is the success rate of IUI
13 percent per transfer per treatment cycle
27
how is sperm prep done for BBV patients
Integral part of IUI +/- superovulation / IVF / ICSI 1. Density gradient preparation by centrifugation through viscous media (usually 40% / 80%) Puresperm used clinically (Colloidal silica suspension in isotonic salt solution) 2. Pellet washed 3. Followed by swim-up 4. Test for VL
28
what is the difference between HIV virus RNA present in semen vs blood
generally levels are lower in semen (10 times lower)
29
what is done to the sperm to reduce risk of transmission of HIV
sperm washing
30
what percentage of men with undetectable viral load using HAART had virus detected in their semen pre and/or post sperm wash
9.7 percent
31
what is the best indicator for reducing (if not elimating0 risk of transmission of HOV
reducing or elimating viral load
32
when is sperm washing primarily used
IUI
33
what services are offered in ninewells
sperm washing + IUI IVF/ICSI don't do : TUPSI, PrEP
34
how often is peginterferon alpha taken for hep b
weekly injection for 12 months
35
what further steps must be taken in case of patients with hep b
immunise seronegative partner | consider deferring ART to see if acute infection clears
36
what blood result indicated current hep b infection (acute or chonic)
HBsAg | Anti-HBc positive
37
what blood results indicate a previous infection but the person is now immune
Anti HBc and Anti HBs positive
38
what blood results indicate a vaccinated person
antiHBs positive
39
how are patients with hep c treated
refer to hepatologist pegylated inferferon and ribavirin will take 24/48 weeks to erradicate depending on serotype no current immunisation but sexual transmission risk is low
40
how long should a pregnancy be avoided after hep c treatment
6 mths
41
what are the treatment options of a HIV positive male
``` if no HAART/detectable VL: sperm washing then IU/IVF/ICSI HIV test for female 4/52 post treatment DI adoption ``` if HAART/undetectable VL for more than 6mths: options as above TUPSI - monthly HIV test for female partner consider PrEP
42
what is the risk of HIV transmission be receptive vaginal intercourse per exposure
0.1 percent recepive anal intercourse is 10x higher and insertive vaginal or anal intercourse is much lower
43
So what would be the avg HIV transmission risk over a course of TUPSI
3 percent (taking into account 5 exposures per cycle and average of 6 cycles to conceive)
44
what is the dangers of having seroconversion illness in pregnancy
high risk of in utero transmission to fetus
45
what is PreP
post exposure prophylaxis
46
when should prep be started
within 72 hours of risk
47
how long is a course of prep
28 days
48
what are the negatives of Prep and why is it not widely used
may create viral resistance toxicity cost
49
when may prep be useful
in reducing HIV transmission in high risk people: MSM, sero discordant couples, high risk women/men however still only used experimentally or in the special circumstance of conception
50
how is a HIV positive female treated
if not on treatment: self insemination if HAART: self insemination can consider TUPSI if VL undetectable for more than 6 months and normal fertility screen - monthly test for male partener if no conception at 6/12 refer to ACU for IVF/ICSI
51
what is the problem with HIV positive male and female and why can they not have UPSI?
theoretical risk of HIV superinfection however not reported in cohort studies
52
is TUPSI acceptable in HIV positive male and female
yes
53
when can TUPSI not be used in cases where the male and female is HIV +
if either partner has a detectable drug resistant virus if female- recommend self insemination if male- offer sperm washing