baseline tests to consider for persons being seen for ...€¦ · hiv ag/ab testing at 6 weeks...
TRANSCRIPT
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VISI
T AI
DSET
C.O
RG
November 2019
Sexu
ally
tran
smitt
ed G
C/CT
and
tric
hom
onas
in
fect
ions
: all
med
s ad
min
iste
red
on s
ite b
y pr
ovid
er4 -
azi
thro
myc
in l
gram
PO
x l
& c
eftri
axon
e 25
0 m
g IM
x l
& (i
f ris
k of
vag
initi
s) m
etro
nida
zole
2
gram
s PO
x l.
HIV
prop
hyla
xis:
TDF
/FTC
300
/200
mg
(Tru
vada
®) +
do
lute
grav
ir 50
mg
(Tiv
icay
®) –
1 ta
b ea
ch P
O d
aily
x
28 d
ays.
If w
ithin
the
first
trim
este
r of p
regn
ancy
(p
ost-L
MP
or b
y ul
traso
und
datin
g) O
R m
ay b
ecom
e pr
egna
nt w
ithin
the
next
28
days
, pre
scrib
e TD
F/FT
C 30
0/20
0mg
(Tru
vada
®) 1
tab
PO d
aily
+
ralte
grav
ir 40
0mg
(Isen
tress
®) 1
tab
PO tw
ice
a da
y x
28 d
ays.
7,8 A
dmin
iste
r firs
t dos
e on
site
as
soon
as
poss
ible
afte
r rap
id H
IV n
egat
ive
stat
us o
btai
ned3 o
r no
n-ra
pid
HIV
test
sen
t. TD
F/FT
C (T
ruva
da®) s
houl
d no
t be
used
for t
hose
with
est
imat
ed C
rCl l
ess
than
60
mL/
min
; an
alte
rnat
ive
regi
men
mus
t be
used
in th
ose
circ
umst
ance
s.Em
erge
ncy
cont
race
ptio
n: fo
r per
sons
at r
isk
of p
regn
ancy
with
a n
egat
ive
preg
nanc
y te
st. I
f pre
scrib
ed d
olut
egra
vir,
coun
sel o
n ne
ed fo
r pre
gnan
cy
prev
entio
n w
hile
on
nPEP
.Ad
min
iste
r 1 d
ose
of h
epat
itis
B va
ccin
e (w
ithou
t hep
atiti
s B
imm
une
glob
ulin
) to
per
sons
not
pre
viou
sly
vacc
inat
ed o
r inc
ompl
etel
y va
ccin
ated
. If t
he e
xpos
ure
sour
ce is
ava
ilabl
e fo
r tes
ting
& is
HBs
Ag
posi
tive,
unv
acci
nate
d nP
EP p
atie
nts
shou
ld
rece
ive
both
hep
atiti
s B
vacc
ine
& h
epat
itis
B im
mun
e gl
obul
in d
urin
g th
e in
itial
eva
luat
ion.
Fo
llow
-up
dose
(s) s
houl
d be
adm
inis
tere
d as
per
vac
cine
pac
kage
inse
rt. P
revi
ousl
y va
ccin
ated
exp
osed
per
sons
who
did
not
re
ceiv
e po
stva
ccin
atio
n te
stin
g sh
ould
re
ceiv
e a
sing
le v
acci
ne b
oost
er d
ose.
Fo
r tho
se 9
-45
year
s in
clus
ivel
y, o
ffer
first
HPV
vac
cina
tion
dose
if n
ot a
dequ
atel
y va
ccin
ated
pre
viou
sly.9
BASE
LIN
E TE
STS
TO C
ON
SID
ER F
OR
PERS
ON
S BE
ING
SEE
N F
OR
NO
NO
CC
UPA
TIO
NA
L PO
ST-
EXPO
SURE
PRO
PHYL
AX
IS (
nPEP
):Go
norr
hea
& c
hlam
ydia
(GC
/CT)
1 - s
wab
s of
all
site
s of
sex
ual c
onta
ct in
clud
ing
orop
hary
ngea
l, re
ctal
, and
gen
ital:
urin
e te
stin
g m
ay b
e co
nsid
ered
in p
lace
of
geni
tal t
estin
g
Rapi
d HI
V Ag
/Ab
test
ing2,
3
Urin
e pr
egna
ncy
test
for p
erso
ns a
t ris
k of
pre
gnan
cy
Rout
ine
bloo
dwor
k in
ass
essi
ng re
nal &
live
r fun
ctio
n (s
erum
cre
atin
ine,
ALT
, AS
T: e
stim
ated
cre
atin
ine
clea
ranc
e)
Syph
ilis
Sero
logy
: RPR
Hepa
titis
B v
irus
surf
ace
antig
en (H
BsAg
) for
thos
e w
ith k
now
n or
pro
babl
e pr
ior
HBV
infe
ctio
n10
For p
erso
ns a
t ris
k of
pre
gnan
cy w
ith a
neg
ativ
e
preg
nanc
y te
st, o
ffer e
mer
genc
y co
ntra
cept
ion.
For a
ll po
st-s
exua
l exp
osur
es (o
ral,
vagi
nal,
rect
al e
xpos
ures
), of
fer
on-s
ite tr
eatm
ent f
or G
C/CT
, & fo
r tric
hom
onas
(whe
n ris
k of
vag
initi
s).
INIT
IAL
TREA
TMEN
T, P
ATI
ENT
EDU
CA
TIO
N/
CO
UN
SELI
NG
& F
OLL
OW
-UP
VIS
ITS:
Fo
llow
-up
mus
t be
sche
dule
d at
72
hour
s &
4 w
eeks
afte
r ini
tiatin
g nP
EPPo
ssib
le d
rug
side
effe
cts:
naus
ea, G
I ups
et, h
eada
che,
mya
lgia
sPo
ssib
le d
rug
inte
ract
ions
: ant
acid
s, ca
lciu
m, i
ron
supp
lem
ents
Stre
ss a
dher
ence
impo
rtanc
e to
nPE
P re
gim
en fo
r 28
days
with
out i
nter
rupt
ion
PrEP
6 ini
tiatio
n im
med
iate
ly a
fter fi
nish
ing
28-d
ay n
PEP
pres
crip
tion
for t
hose
with
on
goin
g ris
kSy
phili
s se
rolo
gy a
t 4-6
wee
ksHI
V Ag
/Ab
test
ing
at 6
wee
ks &
3 m
onth
s af
ter i
nitia
l non
-reac
tive
test
HBV
& H
CV s
erol
ogy
test
ing
at 6
mon
ths
afte
r ini
tial n
on-re
activ
e te
st
1l F
or p
ost-s
exua
l ass
ault
patie
nts,
the
need
for S
TI te
stin
g sh
ould
be
cons
ider
ed.
12 P
refe
rabl
y a
rapi
d 4t
h ge
nera
tion
(Ag/
Ab) t
est s
houl
d be
don
e, b
ut if
not
ava
ilabl
e, n
on-ra
pid
HIV
test
ing
shou
ld b
e do
ne. I
f non
-rapi
d te
stin
g is
don
e, S
TART
nPE
P im
med
iate
ly &
arra
nge
follo
w-u
p in
l-2
days
for
HIV
resu
lts.
13 If
the
HIV
test
is re
activ
e/po
sitiv
e, th
e pe
rson
sho
uld
NO
T be
giv
en n
PEP,
but
be
prov
ided
sup
porti
ve
coun
selin
g &
con
nect
ed to
an
HIV
prim
ary
care
or s
peci
alty
car
e (ID
) pro
vide
r im
med
iate
ly (b
efor
e be
ing
disc
harg
ed).
14 C
eftri
axon
e is
the
reco
mm
ende
d tre
atm
ent f
or G
C &
sho
uld
not b
e su
bstit
uted
with
ano
ther
ant
ibio
tic
unle
ss th
ere
are
clea
r con
train
dica
tions
for i
ts u
se. I
f con
train
dica
ted,
refe
r to
CDC
2015
STD
Tre
atm
ent
guid
elin
es fo
r alte
rnat
ive:
http
s://w
ww.
cdc.
gov/
std/
tg20
15/g
onor
rhea
.htm
15 A
ll pe
rson
s of
fere
d nP
EP s
houl
d be
pre
scrib
ed a
28-
day
cour
se o
f a 3
-dru
g AR
V re
gim
en.
16 P
re-e
xpos
ure
prop
hyla
xis
(PrE
P): c
onta
ct th
e Cl
inic
ian
Cons
ulta
tion
Cent
er a
t 1-8
88-4
48-7
737
for
clin
icia
n-to
-clin
icia
n ad
vice
.17
Add
ition
al in
form
atio
n on
the
use
of d
olut
egra
vir i
n pr
egna
ncy
can
be fo
und
at: h
ttps:
//ww
w.gs
ksou
rce.
com
/pha
rma/
cont
ent/d
am/G
laxo
Smith
Klin
e/US
/en/
Pres
crib
ing_
Info
rmat
ion/
Tivi
cay/
pdf/
TIVI
CAY-
PI-P
IL.P
DF
18 R
alte
grav
ir (Is
entre
ss®),
to b
e do
sed
400
mg
PO tw
ice
a da
y, a
nd N
OT
Isen
tress
HD
® 6
00 m
g PO
twic
e a
day,
for n
PEP.
19 E
xpan
ded
use
of G
arda
sil:
http
s://w
ww.
fda.
gov/
New
sEve
nts/
New
sroo
m/P
ress
Anno
unce
men
ts/
ucm
6227
15.h
tm
10 S
ever
e ac
ute
exac
erba
tions
of H
BV h
ave
been
repo
rted
in H
BV-in
fect
ed p
eopl
e w
ho h
ave
disc
ontin
ued
Truv
ada®
): h
ttp://
ww
w.gi
lead
.com
/~/m
edia
/File
s/pd
fs/m
edic
ines
/hiv
/truv
ada/
truva
da_p
i.pdf
Cont
act u
s at
info
@ai
dset
c.or
g fo
r mor
e re
sour
ces,
que
stio
ns o
r fee
dbac
k.
IF R
API
D H
IV T
ESTI
NG
RES
ULT
IS “
NEG
ATI
VE”
(NO
N-R
EAC
TIV
E)2 ,
OFF
ER n
PEP
AN
D:
Additional Information• Healthcare providers should evaluate persons rapidly for nPEP
when care is sought ≤72 hours after an exposure that presents a substantial risk for HIV acquisition. The decision to recommend nPEP should not be influenced by the geographic location of the assualt/expoure.
• nPEP is not recommended when care is sought >72 hours after potential exposure.
• Regimens are available for children, and persons with decreased renal function.
• A case-by-case determination about nPEP is recommended when the HIV infection status of the source of the body fluids is unknown and the reported exposure presents a substantial risk for transmission if the source did have HIV infection.
• Follow-up for people receiving nPEP is important and should be provided by or in consultation with a clinician experienced in managing nPEP. Providers who do not have access to a clinician expereinced in providing nPEP follow-up should make linkages with community providers with this experience or contact the Clinician Consultation Center PEPline at (888)448-4911 for assistance http://nccc.ucsf.edu/.
When the source is knownto have HIV
Source ofunknownHIV status
Sourceknown
to have HIV
Nov
embe
r 201
9
nPEP is not recommended when care is sought >72 hours after exposure. If >72 hours after exposure, consult with an expert or contact the Clinician Consultation Center PEPline.