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An HIV Post-Exposure Prophylaxis
          Pilot Program
  Implemented in Public Health
     Settings in Los Angeles
     Jennifer N Sayles, MD, MPH, Gary P García,
     MPH, Rosemary C Veniegas, PhD, Robert K
    Bolan, MD, Wilbert C Jordan, MD, and Raphael
                J Landovitz, MD, MsC
Estimated
          Population
                                         HIV/AIDS Cases
            9,848,011                             61,700


   Overall, Race/Ethnicity
13.3%                0.5%        8.8%



   30.1%
                                   47.3%



          HIV/AIDS Cases
           3.0%           1.0%
                                                             Black
                            21.0%                            Latino
     35.0%
                                                             White
                               40.0%                         Asian/PI
                                                             NA/AI
Data Source: U.S. Department of Commerce, 2010; Los Angeles County Department of Public Health, HIV
Surveillance, 2010
A Case for nPEP?
A 26 year old man presents to an outpatient clinic,
reporting that the night before last (36 hours ago) he
had receptive anal intercourse without the use of a
condom with a new male partner, who he just
learned from a mutual acquaintance is infected with
the Human Immunodeficiency Virus (HIV). The
patient is known to the clinic and has had several
negative HIV tests (most recently 6 months ago), and
he recently lost his job and health insurance. He
wants to know if there is anything he can do to help
prevent transmission of HIV from this recent
exposure.
                                                         3
Approach to HIV Prevention




Coates, Lancet, 2008
OAPP
     LAC
                               PPC
     STD


                                     Commission
Providers         P-QUAD               on HIV



    Behavior/SA
    Specialists               CBO/CHCs

                  Academics

                                                  5
The nPEP Pilot: Comprehensive
    Biomedical HIV Prevention for LAC
•   2 demonstration sites; 28 days of ART
•   IRB and FDA regulatory oversight
•   Structured Protocol and Manual of Procedures
•   Demonstration site preparation and training
•   Safety labs and serial HIV and STI testing
•   Sexual/substance use risk-reduction counseling
•   Planned transition to Public Health Service Model
nPEP Logic Model
nPEP Pilot Components
                                        Baseline         Week 2 Visit          Week 4-6 Visit   Week 12 Visit   Week 24
                                         (Day 0)         (Day 10-14)                                             Visit
ART Dispensed                              X                  X
HIV ELISAc                                 X                                        X                X            X
Urine GC/CT                                X                   Xb                   Xb               Xb           Xb
Rectal GC/CT
Pharynx GC
Serum RPR                                   X                                                        X
Urine HCGa                                  X                  Xb                   Xb               Xb           Xb
HBsAg                                       X
CB, Cr, LFTs,                               X                  Xb
HIV Viral Load
HIV Genotype
Stored Plasmad                              X                                        X               X            X
Adherence Cnsl                              X                  X
Drug and Alc Assess                         X
Risk Assess                                 X                                       X                X            X
Risk Red (Standard)                         X                  X                    Xb               Xb           Xb
Referral to Behavioral                      X
Programming (Expanded)

 aFemales    of childbearing potential only
 bIfclinical signs and symptoms direct, not routine
 cPositive or indeterminate rapid HIV ELISA testing will be confirmed with a

 serum Western Blot
 dPlasma will be drawn and stored at indicated time points. If HIV

 seroconversion occurs, these samples will be run for HIV RNA (viral load)
 and genotyping
Inclusion Criteria
1. 18 yrs of age and ability to provide consent
2. High-risk exposure (unprotected or with failed condom):
   •   Receptive/Insertive anal intercourse
   •   Receptive/Insertive vaginal intercourse
   •   Receptive oral intercourse w/ejaculation with HIV+ source
   •   Sharing intravascular injection drug works
3. High-risk source (one or more):
   •   Known HIV+, MSM, MSM/W, IDU, CSW, sexual perpetrator,
       history of incarceration, from an endemic country (prevalence
       >1%), partner of one of the above
4. Exposure within 72-hrs of presentation
5. Not known to be HIV+
6. No countermanding concomitant medications or allergies
Medication Regimens
Standard ART Regimen for high-risk
  exposures:
   • Truvada
   • Combivir – for intolerance to Truvada

Expanded ART Regimen:
  • For highest-risk exposures or suspected
    source drug resistance; added to the
    above medication administration
  • Kaletra or Raltegravir
Preliminary Findings
Presentation data as of July 1, 2011
   • Screened 303, Enrolled 283
   • Data to follow N=163 (151 at Site 1, 12 at Site 2)
   • N=38 had already initiated PEP at another
     location (ED, Primary Care, HIV clinic)
Site 1: LAGLC – Los Angeles Gay and Lesbian Ctr
   • Screened 271, enrolled 260
Site 2: OASIS
   • Screened 32, enrolled 23
nPEP Sites, HIV/STI Clusters, 2009
 Legend
         nPEP sites
 HIV/STI Disease Clusters
 HIV Cases, 2009
         1.3%
         6.6%
         9.2%
         18.4%
         46.3%
         Los Angeles County Boundary




                                           LAGLC




Source: Semi-Annual Surveillance Report,
2008, HIV Epidemiology Program
 Data Source: HIV Testing Services Data,           Oasis Clinic
 CY2009; Zip Codes with <100 tests not
 included in analysis
Demographics: Gender and Age
         (N = 163)
Demographics : Sexual Orientation and
      Race/Ethnicity (N=163)
Demographics: Health Insurance and
       Education (N=163)
Enrollment Risk Exposure (N=163)
      (multiple category reply)
Baseline Sexual Risk Behavior
URAI / UIAI Acts by Status of Partner
  URAI last 30 Days    UIAI last 30 days



            N=48                   N=54


    N=143               N=124
Medication Adherence by
         Visual Analog Scale


                                   X
2 Week Clinical Evaluation
   •Mean self-reported adherence 96.90% (SD 12.81)
   •Range 7-100%

4 Week Clinical Evaluation
   •Mean self-reported adherence 96.57% (SD 11.32)
   •Range 0-100%
Follow up Rates: Clinical Evaluations
              *N=163
Baseline    Day 14    Week 4-6     Week 12     Week 24
163/163    146/163     131/163      98/161      62/161
(100%)      (90%)       (80%)       (61%)       (39%)


*As of July 1, 2011:
2 Significant Adverse Events: both continued treatment




                                                         20
Time Interval: Exposure to First Dose
                 *N=151
             Mean: 36.33 hrs (SD 19.17)
             Range: 2 – 71.7 hrs




* N=12 missing
Time Interval: Exposure to First Dose
               *N=151
     Mean: 36.33 hrs (SD 19.17)
     Range: 2 – 71.7 hrs




                                  N=44 (27%)
                                  < 24 hrs

                                  N=8 (5%)
                                  < 8 hrs


 * N=12 missing
Seroconversions N=4
PID         Date              Exposure           Time to       Med           STIs           Repeat
       Seroconversion                              PEP     Adherence                      Exposures
          identified                                       Self-Report                    Self-Report
1016      12-week          URAI and UIAI          64hrs      100%            None            None
                             w/recently
                        seroconverted Source

1064      12-week          URAI and UIAI          41hrs      100%           + GC at          Yes
                             w/recently                                     baseline
                        seroconverted Source

1101      12-week       UIAI with known HIV+      26hrs       95%            None            Yes
                           Source; Source
                            reported to be
                        undetectable on meds


1155      12-week       RAI with failed condom    62hrs      100%        Positive RPR 3      Yes
                        w/known HIV+ Source                                  month
nPEP Pilot: Summary
• Demonstrated feasible implementation of nPEP
  in clinical care settings for high risk population
• Real life example of how to develop and
  implement comprehensive biomedical and
  behavioral HIV prevention interventions
• Cost of ART is significant and can be an
  obstacle to scaling up service delivery
• Education for primary care (non HIV specialty)
  needed to support providers to deliver nPEP
  more broadly
Next Steps: Sustained nPEP Program
Public health program premised on the findings from
  pilot with few modifications:
• 2 drug regimen (Truvada) except in cases of
  documented drug resistance from source patient
  (3rd drug Raltegravir/Kaletra)
• Integrated hepatitis screening and vaccination
• Streamlined data reporting
• PEP coordinator to do follow up visits
• Full 28 day ART dispensed at intake
• Integrated risk-reduction counseling via OAPP
  funded behavioral programs
Acknowledgements
• Gilead Sciences       • LA County OAPP
  – Jim Rooney             – Mario Perez
  – Alexia Exarchos     • LA County STD
• Abbott Laboratories     Program
  – Ashwaq Hermes          – Sarah Guerry
  – Judith Kruse           – Peter Kerndt
• Merck Laboratories    • LAC Public Health Lab
  – Kathleen Bailey        – Debbie Emlien
  – Michael Harbour        – Ramiro Garate
• GSK/Viiv
  – Gary Pakes          • LAGLC Site Staff
  – Sue Pippin          • OASIS Clinic Site Staff
Contact Information
       Jennifer N. Sayles, MD, MPH
               Medical Director
    Office of AIDS Programs and Policy
600 South Commonwealth Avenue, 10th Floor
    Los Angeles, California 90005-4001
          Phone: (213) 351-8264
      E-mail: jsayles@ph.lacounty.gov




                                            27

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An HIV Post-Exposure Prophylaxis Pilot Program Implemented in Public Health Settings in Los Angeles

  • 1. An HIV Post-Exposure Prophylaxis Pilot Program Implemented in Public Health Settings in Los Angeles Jennifer N Sayles, MD, MPH, Gary P García, MPH, Rosemary C Veniegas, PhD, Robert K Bolan, MD, Wilbert C Jordan, MD, and Raphael J Landovitz, MD, MsC
  • 2. Estimated Population HIV/AIDS Cases 9,848,011 61,700 Overall, Race/Ethnicity 13.3% 0.5% 8.8% 30.1% 47.3% HIV/AIDS Cases 3.0% 1.0% Black 21.0% Latino 35.0% White 40.0% Asian/PI NA/AI Data Source: U.S. Department of Commerce, 2010; Los Angeles County Department of Public Health, HIV Surveillance, 2010
  • 3. A Case for nPEP? A 26 year old man presents to an outpatient clinic, reporting that the night before last (36 hours ago) he had receptive anal intercourse without the use of a condom with a new male partner, who he just learned from a mutual acquaintance is infected with the Human Immunodeficiency Virus (HIV). The patient is known to the clinic and has had several negative HIV tests (most recently 6 months ago), and he recently lost his job and health insurance. He wants to know if there is anything he can do to help prevent transmission of HIV from this recent exposure. 3
  • 4. Approach to HIV Prevention Coates, Lancet, 2008
  • 5. OAPP LAC PPC STD Commission Providers P-QUAD on HIV Behavior/SA Specialists CBO/CHCs Academics 5
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  • 7. The nPEP Pilot: Comprehensive Biomedical HIV Prevention for LAC • 2 demonstration sites; 28 days of ART • IRB and FDA regulatory oversight • Structured Protocol and Manual of Procedures • Demonstration site preparation and training • Safety labs and serial HIV and STI testing • Sexual/substance use risk-reduction counseling • Planned transition to Public Health Service Model
  • 9. nPEP Pilot Components Baseline Week 2 Visit Week 4-6 Visit Week 12 Visit Week 24 (Day 0) (Day 10-14) Visit ART Dispensed X X HIV ELISAc X X X X Urine GC/CT X Xb Xb Xb Xb Rectal GC/CT Pharynx GC Serum RPR X X Urine HCGa X Xb Xb Xb Xb HBsAg X CB, Cr, LFTs, X Xb HIV Viral Load HIV Genotype Stored Plasmad X X X X Adherence Cnsl X X Drug and Alc Assess X Risk Assess X X X X Risk Red (Standard) X X Xb Xb Xb Referral to Behavioral X Programming (Expanded) aFemales of childbearing potential only bIfclinical signs and symptoms direct, not routine cPositive or indeterminate rapid HIV ELISA testing will be confirmed with a serum Western Blot dPlasma will be drawn and stored at indicated time points. If HIV seroconversion occurs, these samples will be run for HIV RNA (viral load) and genotyping
  • 10. Inclusion Criteria 1. 18 yrs of age and ability to provide consent 2. High-risk exposure (unprotected or with failed condom): • Receptive/Insertive anal intercourse • Receptive/Insertive vaginal intercourse • Receptive oral intercourse w/ejaculation with HIV+ source • Sharing intravascular injection drug works 3. High-risk source (one or more): • Known HIV+, MSM, MSM/W, IDU, CSW, sexual perpetrator, history of incarceration, from an endemic country (prevalence >1%), partner of one of the above 4. Exposure within 72-hrs of presentation 5. Not known to be HIV+ 6. No countermanding concomitant medications or allergies
  • 11. Medication Regimens Standard ART Regimen for high-risk exposures: • Truvada • Combivir – for intolerance to Truvada Expanded ART Regimen: • For highest-risk exposures or suspected source drug resistance; added to the above medication administration • Kaletra or Raltegravir
  • 12. Preliminary Findings Presentation data as of July 1, 2011 • Screened 303, Enrolled 283 • Data to follow N=163 (151 at Site 1, 12 at Site 2) • N=38 had already initiated PEP at another location (ED, Primary Care, HIV clinic) Site 1: LAGLC – Los Angeles Gay and Lesbian Ctr • Screened 271, enrolled 260 Site 2: OASIS • Screened 32, enrolled 23
  • 13. nPEP Sites, HIV/STI Clusters, 2009 Legend nPEP sites HIV/STI Disease Clusters HIV Cases, 2009 1.3% 6.6% 9.2% 18.4% 46.3% Los Angeles County Boundary LAGLC Source: Semi-Annual Surveillance Report, 2008, HIV Epidemiology Program Data Source: HIV Testing Services Data, Oasis Clinic CY2009; Zip Codes with <100 tests not included in analysis
  • 14. Demographics: Gender and Age (N = 163)
  • 15. Demographics : Sexual Orientation and Race/Ethnicity (N=163)
  • 16. Demographics: Health Insurance and Education (N=163)
  • 17. Enrollment Risk Exposure (N=163) (multiple category reply)
  • 18. Baseline Sexual Risk Behavior URAI / UIAI Acts by Status of Partner URAI last 30 Days UIAI last 30 days N=48 N=54 N=143 N=124
  • 19. Medication Adherence by Visual Analog Scale X 2 Week Clinical Evaluation •Mean self-reported adherence 96.90% (SD 12.81) •Range 7-100% 4 Week Clinical Evaluation •Mean self-reported adherence 96.57% (SD 11.32) •Range 0-100%
  • 20. Follow up Rates: Clinical Evaluations *N=163 Baseline Day 14 Week 4-6 Week 12 Week 24 163/163 146/163 131/163 98/161 62/161 (100%) (90%) (80%) (61%) (39%) *As of July 1, 2011: 2 Significant Adverse Events: both continued treatment 20
  • 21. Time Interval: Exposure to First Dose *N=151 Mean: 36.33 hrs (SD 19.17) Range: 2 – 71.7 hrs * N=12 missing
  • 22. Time Interval: Exposure to First Dose *N=151 Mean: 36.33 hrs (SD 19.17) Range: 2 – 71.7 hrs N=44 (27%) < 24 hrs N=8 (5%) < 8 hrs * N=12 missing
  • 23. Seroconversions N=4 PID Date Exposure Time to Med STIs Repeat Seroconversion PEP Adherence Exposures identified Self-Report Self-Report 1016 12-week URAI and UIAI 64hrs 100% None None w/recently seroconverted Source 1064 12-week URAI and UIAI 41hrs 100% + GC at Yes w/recently baseline seroconverted Source 1101 12-week UIAI with known HIV+ 26hrs 95% None Yes Source; Source reported to be undetectable on meds 1155 12-week RAI with failed condom 62hrs 100% Positive RPR 3 Yes w/known HIV+ Source month
  • 24. nPEP Pilot: Summary • Demonstrated feasible implementation of nPEP in clinical care settings for high risk population • Real life example of how to develop and implement comprehensive biomedical and behavioral HIV prevention interventions • Cost of ART is significant and can be an obstacle to scaling up service delivery • Education for primary care (non HIV specialty) needed to support providers to deliver nPEP more broadly
  • 25. Next Steps: Sustained nPEP Program Public health program premised on the findings from pilot with few modifications: • 2 drug regimen (Truvada) except in cases of documented drug resistance from source patient (3rd drug Raltegravir/Kaletra) • Integrated hepatitis screening and vaccination • Streamlined data reporting • PEP coordinator to do follow up visits • Full 28 day ART dispensed at intake • Integrated risk-reduction counseling via OAPP funded behavioral programs
  • 26. Acknowledgements • Gilead Sciences • LA County OAPP – Jim Rooney – Mario Perez – Alexia Exarchos • LA County STD • Abbott Laboratories Program – Ashwaq Hermes – Sarah Guerry – Judith Kruse – Peter Kerndt • Merck Laboratories • LAC Public Health Lab – Kathleen Bailey – Debbie Emlien – Michael Harbour – Ramiro Garate • GSK/Viiv – Gary Pakes • LAGLC Site Staff – Sue Pippin • OASIS Clinic Site Staff
  • 27. Contact Information Jennifer N. Sayles, MD, MPH Medical Director Office of AIDS Programs and Policy 600 South Commonwealth Avenue, 10th Floor Los Angeles, California 90005-4001 Phone: (213) 351-8264 E-mail: jsayles@ph.lacounty.gov 27