63
1 Lisa Villarroel, MD MPH Medical Director, Division of Public Health Preparedness Arizona Department of Health Services Disclosures: None

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Page 1: Syphilis Roadshow 03.17.18 PC VERSION - …c.ymcdn.com/sites/ syphilis images neurosyphilis can occur at primary secondary tertiary early latent late latent review of ophthal,, 2008

1

Lisa Villarroel, MD MPH

Medical Director, Division of Public Health Preparedness

Arizona Department of Health Services

Disclosures:

None

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2

Fitzgerald TJ, Cleveland P, Johnson RC et al: Scanning electron microscopy of Treponema pallidum (Nichols strain) attached to cultured mammalian cells. J Bacteriol 130:1333, 1977.

PRIMARY

CDC Library

PRIMARY

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3

CDC PHIL 16750

PRIMARY

CDC PHIL 12578 

PRIMARY SECONDARY

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4

CDC Library 

PRIMARY SECONDARY

CDC Picture Cards

PRIMARY SECONDARY

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5

CDC Library 

PRIMARY SECONDARY

PRIMARY SECONDARYEARLY

LATENT

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6

PRIMARY SECONDARYEARLY

LATENTLATE

LATENT

PRIMARY SECONDARYEARLY

LATENTLATE

LATENT

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7

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

CDC clinical slides

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

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8

NEUROSYPHILIS CAN OCCUR AT

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

TRANSMISSION TO THE FETUS CAN OCCUR AT ….

NEUROSYPHILIS CAN OCCUR AT

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9

CDC clinical slides

TRANSMISSION TO THE FETUS CAN OCCUR AT ….

CDC PHIL 16750

TRANSMISSION TO THE FETUS CAN OCCUR AT ….

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10

TRANSMISSION TO THE FETUS CAN OCCUR AT ….

TRANSMISSION TO THE FETUS CAN OCCUR AT ….

NEUROSYPHILIS CAN OCCUR AT

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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11

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

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12

Credit: National Archives.

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

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13

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

TRANSMISSION TO THE FETUS CAN OCCUR AT ….

NEUROSYPHILIS CAN OCCUR AT

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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14

RA

TE

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15

MEN WHO HAVE SEX WITH MEN

MEN WHO HAVE SEX WITH WOMEN

PRIMARY & SECONDARY SYPHILIS CASES

MEN WHO HAVE SEX WITH MEN

WOMEN

MEN WHO HAVE SEX WITH WOMEN

PRIMARY & SECONDARY SYPHILIS CASES

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16

ARIZONA

U.S.

2007 2010 2013 2016

PRIMARY & SECONDARY SYPHILIS RATE / 100,000

2012 2013 2014 2015 2016

PRIMARY & SECONDARY SYPHILIS CASES IN ARIZONA

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17

2012 2013 2014 2015 2016

BLACK (24)

AMERICAN INDIAN

HISPANIC

WHITE

ASIAN (4.5)

PRIMARY & SECONDARY SYPHILIS RATE / 100,000

0

10

20

2012 2013 2014 2015 20160

15

30ARIZONA

CASE RATE

U.S. CASE RATE

CONGENITAL SYPHILIS CASES & RATES / 100,00

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18

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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19

SYMPTOM RECOGNITION

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

PRIMARY

SYMPTOM RECOGNITION

SECONDARY TERTIARYEARLYLATENT

LATELATENT

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20

PRIMARY

SYMPTOM RECOGNITION

SECONDARY TERTIARYEARLYLATENT

LATELATENT

CDC Syphilis Images

PRIMARY

SYMPTOM RECOGNITION

SECONDARY TERTIARYEARLYLATENT

LATELATENT

Joe Engelman, SF City Clinic

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21

SYMPTOM RECOGNITION

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

SYMPTOM RECOGNITION

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

CDC Syphilis Images

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22

SYMPTOM RECOGNITION

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

CDC Syphilis Images

NEUROSYPHILIS CAN OCCUR AT

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

Review of Ophthal,, 2008 

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23

NEUROSYPHILIS CAN OCCUR AT

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

Review of Ophthal,, 2008 

SCREEN

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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25

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

LABORATORY TESTING

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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26

NONTREPONEMAL TESTS

RPR, VDRL

TREPONEMAL TESTS

TPPA, FTA-ABS

CIA, EIA (NEW)

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

YEARSWEEKS

TIME POST-INFECTIONTIME OF

INFECTION

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27

TREPONEMAL TESTS(TPPA, FTA-ABS)

WEEKS

TIME POST-INFECTIONTIME OF

INFECTION

YEARS

NONTREPONEMAL TESTS(RPR, VDRL)

TREPONEMAL TESTS(TPPA, FTA-ABS)

WEEKS

TIME POST-INFECTIONTIME OF

INFECTION

YEARS

UNTREATED

TREATED

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28

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

NONTREPONEMAL TESTS

RPR, VDRL

FOLLOWS RESPONSE TO TREATMENT

1:1 1:2 1:4 1:8 1:16 1:32 1:64 1:128 1:256 1:512 1:1024

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1:1 1:2 1:4 1:8 1:16 1:32 1:64 1:128 1:256 1:512 1:1024

2-FOLD CHANGE

1:1 1:2 1:4 1:8 1:16 1:32 1:64 1:128 1:256 1:512 1:1024

2-FOLD CHANGE

4-FOLD CHANGE [SIGNIFICANT]

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30

NONTREPONEMAL TESTS

RPR, VDRL

FOLLOWS RESPONSE TO TREATMENT

CAN VARY DAILY

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

NONTREPONEMAL TESTS

RPR, VDRL

FOLLOWS RESPONSE TO TREATMENT

CAN VARY DAILY

ARE FALSE POSITIVES

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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31

NONTREPONEMAL TESTS

RPR, VDRL

FOLLOWS RESPONSE TO TREATMENT

CAN VARY DAILY

ARE FALSE POSITIVES

ARE RARE FALSE NEGATIVES

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

TREPONEMAL TESTS

TPPA, FTA-ABS, CIA/EIA

.

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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32

TREPONEMAL TESTS

TPPA, FTA-ABS, CIA/EIA

.GOOD, EARLY PERFORMANCE

REACTIVITY PERSISTS OVER TIME

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

TREPONEMAL TESTS

TPPA, FTA-ABS, CIA/EIA

.GOOD, EARLY PERFORMANCE

REACTIVITY PERSISTS OVER TIME

LESS FALSE POSITIVES (FTA, EIA MAIN PROBLEM)

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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33

NONTREPONEMAL TESTS

RPR, VDRL

TREPONEMAL TESTS

TPPA, FTA-ABS, CIA/EIA

.

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

NONTREPONEMAL TESTS

RPR, VDRL

TREPONEMAL TESTS

TPPA, FTA-ABS, CIA/EIA

.

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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34

Am J OB and GYN, April 2017

TRADITIONAL

NONTREPONEMAL (RPR)

Am J OB and GYN, April 2017

TRADITIONAL

NONTREPONEMAL (RPR)

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Am J OB and GYN, April 2017

TRADITIONAL

NONTREPONEMAL (RPR)

TREPONEMAL

Am J OB and GYN, April 2017

TRADITIONAL

NONTREPONEMAL (RPR)

TREPONEMAL

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36

Am J OB and GYN, April 2017

TRADITIONAL

NONTREPONEMAL (RPR)

TREPONEMAL

TREPONEMAL (EIA/CIA)

REVERSE

Am J OB and GYN, April 2017

TRADITIONAL

NONTREPONEMAL (RPR)

TREPONEMAL

TREPONEMAL (EIA/CIA)

REVERSE

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37

Am J OB and GYN, April 2017

TRADITIONAL

NONTREPONEMAL (RPR)

TREPONEMAL

TREPONEMAL (EIA/CIA)

NONTREPONEMAL (RPR)

REVERSE

Am J OB and GYN, April 2017

TRADITIONAL REVERSE

NONTREPONEMAL (RPR)

TREPONEMAL

TREPONEMAL (EIA/CIA)

NONTREPONEMAL (RPR)

TREPONEMAL (TPPA)

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Am J OB and GYN, April 2017

TRADITIONAL REVERSE

NONTREPONEMAL (RPR)

TREPONEMAL

TREPONEMAL (EIA/CIA)

NONTREPONEMAL (RPR)

TREPONEMAL (TPPA)

Am J OB and GYN, April 2017

TRADITIONAL REVERSE

NONTREPONEMAL (RPR)

TREPONEMAL

TREPONEMAL (EIA/CIA)

NONTREPONEMAL (RPR)

TREPONEMAL (TPPA)

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Am J OB and GYN, April 2017

TRADITIONAL REVERSE

NONTREPONEMAL (RPR)

TREPONEMAL

TREPONEMAL (EIA/CIA)

NONTREPONEMAL (RPR)

TREPONEMAL (TPPA)

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

STAGING

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SYMPTOMS = PRIMARY / SECONDARY STAGES

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

NO SYMPTOMS = LATENT STAGES

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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NO SYMPTOMS = LATENT STAGES

EARLY IF IN PAST YEAR

NEG SYPHILIS SEROLOGY

KNOWN CONTACT TO EARLY CASE OF SYPHILIS

HISTORY OF SYMPTOMS

SUSTAINED 4x INCREASE

ONLY POSSIBLE EXPOSURE

LATE IF IN PAST YEAR

(NONE OF THOSE)

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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42

SYMPTOM RECOGNITION

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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43

SYMPTOM RECOGNITION

EMPIRICALLY TREAT

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

SYMPTOM RECOGNITION

PARTNERS WITHIN 90 DAYS

EMPIRICALLYTREAT

EMPIRICALLY TREAT

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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44

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

GET HISTORY

TREATMENT NEEDED?

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45

SYMPTOM RECOGNITION

PARTNERS WITHIN 90 DAYS

EMPIRICALLYTREAT

EMPIRICALLY TREAT

PRIMARY SECONDARY

GET HISTORY

TERTIARYEARLYLATENT

LATELATENT

TREATMENT NEEDED?

BENZATHINE PENICILLIN G 2.4 MILLION UNITS IM

x 1, ONCE

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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46

BENZATHINE PENICILLIN G 2.4 MILLION UNITS IM

x 1, ONCE

BENZATHINE PENICILLIN G 2.4 MILLION UNITS IM

x 3, Q WEEK

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

DAY OF TREATMENT CHECKLIST

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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47

GET A TITER (REALLY).

DAY OF TREATMENT CHECKLIST

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

GET A TITER (REALLY).

DAY OF TREATMENT CHECKLIST

DAY OF INITIAL LAB TEST DAY OF TREATMENT DAY OF FOLLOW UP

RPR 1:256 RPR 1:256RPR 1:1024

[NOT CHECKED]

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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GET A TITER (REALLY).

WARN ABOUT JARISCH-HERXHEIMER.

DAY OF TREATMENT CHECKLIST

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

GET A TITER (REALLY).

WARN ABOUT JARISCH-HERXHEIMER.

COUNSEL NO SEX x 1 WEEK.

DAY OF TREATMENT CHECKLIST

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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GET A TITER (REALLY).

WARN ABOUT JARISCH-HERXHEIMER.

COUNSEL NO SEX x 1 WEEK.

ADVISE THAT ALL PARTNERS BE EVALUATED.

DAY OF TREATMENT CHECKLIST

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

GET A TITER (REALLY).

WARN ABOUT JARISCH-HERXHEIMER.

COUNSEL NO SEX x 1 WEEK.

ADVISE THAT ALL PARTNERS BE EVALUATED.

CONFIRM HAS BEEN TESTED FOR HIV.

DAY OF TREATMENT CHECKLIST

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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50

GET A TITER (REALLY).

WARN ABOUT JARISCH-HERXHEIMER.

COUNSEL NO SEX x 1 WEEK.

ADVISE THAT ALL PARTNERS BE EVALUATED.

CONFIRM HAS BEEN TESTED FOR HIV.

ESTABLISH FOLLOW-UP EXPECTATIONS.

DAY OF TREATMENT CHECKLIST

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

FOLLOW UP

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FOLLOW UP

SEROLOGIC TESTS ~Q6 MONTHS.

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

HIV (-) HIV (+)

PRIMARY / SECONDARY SYPHILIS

6, 12 MONTHS

3, 6, 9, 12, 24 MONTHS

EARLY LATENT / LATE LATENT SYPHILIS

6, 12, 24MONTHS

6, 12, 18, 24MONTHS

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

FOLLOW UP

SEROLOGIC TESTS ~Q6 MONTHS.

TREATMENT RESPONSE: 4X TITER DECLINE BY 12 (P/S) OR 24 MO.

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SEROLOGIC TESTS ~Q6 MONTHS.

TREATMENT RESPONSE: 4X TITER DECLINE BY 12 (P/S) OR 24 MO.

SUSPECTED TREATMENT FAILURE OR REINFECTION IF:

4-FOLD INCREASE IN TITERS

OR NEWLY SYMPTOMATIC

OR TITERS DON’T DECLINE

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

FOLLOW UP

SEROLOGIC TESTS ~Q6 MONTHS.

TREATMENT RESPONSE: 4X TITER DECLINE BY 12 (P/S) OR 24 MO.

SUSPECTED TREATMENT FAILURE OR REINFECTION IF:

4-FOLD INCREASE IN TITERS

OR NEWLY SYMPTOMATIC

OR TITERS DON’T DECLINE

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

FOLLOW UP

NEW HIV TEST? LP for CSF VDRL

? RETREAT (BICILLIN x3)

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53

PRIMARY SECONDARY TERTIARYEARLYLATENT

LATELATENT

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DATA

DATA PARTNERS

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DATA PARTNERS POLICY

DATA PARTNERS POLICY ANSWERS

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DATA PARTNERS POLICY ANSWERS

DATA PARTNERS POLICY ANSWERS

CALL PUBLIC HEALTH

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.

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

.

PRIMARY SECONDARY TERTIARYEARLY

LATENTLATE

LATENT

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[email protected]

Joseph EngelmanKristen Herrick

Susan RobinsonStephanie Cohen

Laura DaltonPaul Bloomquist

CAPTCRoxanne Ereth

Rebecca ScrantonTymeckia KendallDon Herrington

ACKNOWLEDGEMENTS

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EXTRA SLIDES

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Rac Syphilis in Pregnancy OB GYN

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STAGE STARTS LASTS (untreated) Other sxs Infectivity

Primary 10d‐12 weeks after inoculation (median time 21 d)

1‐6 weeks • Papule‐>Chancre• Nontender regional adenopathy

• Infectious by direct contact or blood

Secondary • 2‐8 weeks after chancre heals or

• 4‐8 weeks after onset of chancre

• can overlap with 1ary

“Several weeks” • symmetric, bilateral rash• mucous patches/condyloma lata• fever, headache, pharyngitis• hepatitis, osteitis, 

glomerulonephritis• meningitis/ocular/oto‐

• Infectious by direct contact (when mucosal lesions present) or blood 

Early Latent After resolution of 2ary symptoms

• Until 1 year after inoculation

• can alternate with2ary

• Neurologic: meningitis, ocular, oto‐, meningovascular (strokes)

• Infectious by direct contact (when mucosal lesions present) or blood

Late Latent 1 year after inoculation Until treatment or development of late symptomatic disease

• Infectious by blood

Late Symptomatic

15‐25 years after inoculation

Until treatment  • General paresis (CNS parenchyma)

• Tabes dorsalis (posterior columns: sensory/proprio)

• Cardiac (aortitis, infarction)• Late benign (gummatous)

Ghanem. CNS Neuroscience & Therapeutics 2010;6(5): e157-68

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“Know syphilis in all its manifestations and relations, and all other things clinical will be added unto you.” – William Osler, 1909

“Syphilis… remains the despair of the statistician.” -- William Osler, 1917

“When it comes to syphilis, suspect your grandmother” – William Osler

“The souls of infants born only to die or suffer, cry out against the infamy of uncured syphilis.” – (well known venereal syphilologist)

“With our present appropriations, Federal and State and private, we might just as well try to empty the Pacific Ocean with a teaspoon.” – Dr. OC Wenger, 1926