the challenge and consequences of late diagnosis and late initiation of art
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The challenge and consequences of late diagnosis and late initiation of ART. Brenda Crabtree MD HIV/AIDS Clinic, Department of Infectious Diseases Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán Mexico City, MEXICO. - PowerPoint PPT PresentationTRANSCRIPT
THE CHALLENGE AND CONSEQUENCES OF LATE DIAGNOSIS AND LATEINITIATION OF ART
BRENDA CRABTREE MDHIV/AIDS CLINIC, DEPARTMENT OF INFECTIOUS DISEASES
INSTITUTO NACIONAL DE CIENCIAS MÉDICAS Y NUTRICIÓN SALVADOR ZUBIRÁN
MEXICO CITY, MEXICO
THE CHALLENGE AND CONSEQUENCES OF LATE DIAGNOSIS AND LATE INITIATION OF ART
Poznansky 1995
“Subjects who are HIV positive and present late are a challenge to the control of the
spread of HIV infection…”
Poznansky MC, et al. HIV positive patients first presenting with an AIDS defining illness: characteristics and survival. Br Med J 1995. 311, 156–158.
DHHS, March 29, 2012WHO, April 2012
WHAT DO WE MEAN BY LATE?MANY DEFINITIONS
Fisher M. Curr. Opin. Infect. Dis 2008. 21, 1–3. Wong K-H, et al, AIDS Patient Care STDs 2003; 7, 461–469. Smith RD, et al, AIDS 2010; 24(13), 2109–2115.Fleishman JA, et al, Med. Care 2010; 48(12), 1071–1079 . Waters and Sabin, Expert Rev Anti Infect Ther. 2011; 9(10), 877-889.
Late testing Subjects who first present:
• <50 or <200 CD4 cells/mm3 • +/- AIDS defining event at, or within, a period of time
(3, 6 or 12 months) • Europe <350 CD4 cells/mm3
Delayed engagement to care
Late HAART Initiators
The choice of definition will clearly have an impact on the apparent prevalence of this condition:Prevalence in developed countries:
• 10–55% where a threshold of <50 cells/mm3
• 23–65% where a threshold of <200 cells/mm3
• 54–63% where a threshold of <350 cells/mm3
Higher in studies in which AIDS defining events are included
Worse scenario in developing countries (24 to 77%)
HOW FREQUENT ARE WE LATE?
The UK Collaborative HIV cohort (CHIC) Steering Committee. AIDS 2010; 24, 723–727. Wolbers M, et al, HIV Med 2008. 9(6), 397–405. Fisher M. Curr. Opin. Infect. Dis 2008. 21, 1–3. Waters and Sabin, Expert Rev Anti Infect Ther. 2011; 9(10), 877-889. Althoff KN, Clin Infect Dis 2010; 50(11), 1512–1520. Crabtree-Ramírez, CCASAnet et al; PLOS ONE; May 2011,6(5): e20272
% OF PATIENTS WITH BASELINE CD4 <200, SELECTED COUNTRIES
Mónica Alonso González, HIV & STI Regional Project: Panamerican Health Organization, April 2012
Late HAART initiation (77%): • Late testers (55%): recent diagnosis (<6 mo before initiating HAART) • Late presenters (45%): diagnosis (> 6 mo before initiating HAART )
• Many of these, were also late testers
PREVALENCE IN LATIN AMERICA AND THE CARIBBEAN
Crabtree-Ramírez, CCASAnet et al; PLOS ONE; May 2011,6(5): e20272
Risk factors:• Lack of self perception of risk
• Heterosexuals, elderly population
• Vulnerable population• Immigrant, IVDU, less educated, minority populations
• Social and individual factors• Stigma and discrimination
WHO ARE AT RISK OF BEING LATE?
McDonald AM, Aust NZ Public Health 2003; 27:608-13.CDC. MMWR 2003;32:581–586.Krentz HB, HIV Med 2004; 5:93–8.Nogueda MJ, et al, IAS 2011, Rome, Italy Abstract CDD203Crabtree-Ramírez, CCASAnet et al; PLOS ONE; 2011,6(5): e20272
Fisher M. Curr. Opin. Infect. Dis 2008. 21, 1–3. Girardi Eet al. J Acquir Immune Syndr 2004; 36:951-9.Brannstrom J, et al. Int J STD AIDS 2005; 16:702-706.Sullivan AK, BMJ 2005; 330:1301-1302.Delpierre C, et al. Int J STD AIDS 2007; 18:312-317Castilla J, et al. AIDS 2002; 16:1945–1951.
TRENDS ALONG TIME OF LATE PRESENTERS
In addition, small reduction in the prevalence of late presenters along time…
1. Lundgren J; el at; COHERE; THAB0303, AIDS 2012 2. Egger, IeDEA, Paper 100, CROI 2012, Seattle, USA
1 2
WHAT ARE THE CONSEQUENCES OF STARTING LATE?
Adapted from: Waters and Sabin, Expert Rev Anti Infect Ther. 2011; 9(10), 877-889
Higher risk of mortality in the 1st yearART CC and ART LINC, Lancet 2006; 367: 817–24
Reduced chance of viral supressionWaters L, HIV Med 2011 12(5), 289–298.
Increased risk of hospitalizationSabin CA, AIDS 2004; 18:2145–2151
More potential drug-drug interactionRockstroh JK, Antivir. Ther 2010.15 (S1), 25-30
More likely to have IRISBarber D, Nature Rev 2011 vol 10: 150
Increased risk of non-AIDS eventsReekie, AIDS. 2011;25(18):2259-68
Increased risk of neurocognitive impairment
Ellis RJ, AIDS 2011;25(14):1747-51
Potentially increased risk of HIV transmission
Cohen MS, N Engl J Med. 2011;365(6):493-505
Higher direct cost of careRY Chen, et al; Clin Infect Dis 2006
Short Term Long Term
Consequences: Mozambique
Micek et al JAIDS 2009
23,430 Tested for HIV
7,005 Tested HIV positive (30%)
1,506 Eligible for ART Initiation (49%)
3,956 Enrolled HIV care <30 days (57%)
3,049 (43%) not enrolled in care
3,046 CD4 test ,30 days after enrollment (77%)
910 (23%) No CD4 test drawn
471 Initiated ART <90 days after CD4 test (31%)
1,035 (69%) did not initiate ART
317 Adherent to ART for 6 months (83%)
65 (14%) LTFU after ART
9%
CHALLENGES AND CONSEQUENCES
HIVDiagnosis
Linkageto
Care
HAART
Initiation
HAART
Adherence
Clinical and virologic Outcome
Retention
Challenges Consequences
Adapted from: Ulett KB, et al, AIDS Patient Care STDs 2009; 23(1): 41- 49
CHALLENGES AND CONSEQUENCES
HIVDiagnosis
Challenges
• Improve testing in the general population
• Avoid missing opportunities of testing
• Identify and eliminate barriers for testing
• Innovative strategies • “hot spots”• incentive use• self-testing
HIVDiagnosis
TUPDC304 TUPE 187 TUPE183 TUPE185
CHALLENGES AND CONSEQUENCES
Linkageto
Care
Challenges
Linkageto
Care
• Access to care services
• Proper information
• Be as effective as possible • CD4 count • comorbidities
• Identify people at risk to LTFU
• Active tracing
• Decrease administrative barriers
WEPE137WEAE0203 WEAE0301
CHALLENGES AND CONSEQUENCES
Linkageto
Care
Challenges
Linkageto
Care
• Access to care services
• Proper information
• Be as effective as possible • CD4 count • comorbidities
• Identify people at risk to LTFU
• Active tracing
• Decrease administrative barriers
S T I G M A
CONCLUSIONS
• Late diagnosis and presentation to care is a significant
barrier that limits the benefit of HAART• Early mortality and morbidity• Transmission of infection
• There is a need for establish the prevalence and risk
factors for late HAART initiation in different regions
• Diagnose HIV infection earlier by: widespread testing,
reaching vulnerable populations, identify and fight
stigma
• Innovative Strategies to improve linkage to care and
retention should be evaluated and implemented
• CD4 at point of care
• Addressing LTFU in every step with aggressive
mechanisms for linkage or reengagement to care
• Active tracing: text message, home visits, etc.
CONCLUSIONS II
ACKNOWLEDGEMENTS
Juan Sierra-Madero
Carlos del Río
Francisco Belaunzarán
Stefano Bertozzi
Yanink Caro-Vega
Alicia Piñeirúa
Medical Staff of HIV/AIDS Clinic, INNSZ
ID Department, INNSZ
All CCASAnet Team