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Paediatric ARV's at McCord

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Paediatric ARV's at McCord. Background to the Programme. Baseline ... HAART effective and sustainable in paediatrics in resource limited settings ... – PowerPoint PPT presentation

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Title: Paediatric ARV's at McCord


1
Paediatric ARV's at McCord
  • Background to the Programme
  • Baseline Characteristics of the Cohort
  • Outcomes for first 151 children

2
  • State subsidised hospital
  • July 2004 PEPFAR funding
  • Team of part time paediatrician,2 generalist
    doctors,social worker,intern psychologist and
    counsellors.

3
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4
Process of Care
  • All HIV positive children assessed clinically
  • Not eligible for ARV's-3monthly follow up
  • Eligible for ARV's
  • 3 training sessions
  • Baseline bloods
  • CXR
  • Investigations to exclude TB

5
Eligibility for ART
  • National Guidelines
  • WHO Stage 3 or 4
  • CD4 lt 20 if child lt18 months
  • CD4 lt15 if child lt 18 months

6
  • No clinical problems-HAART at training 3
  • TB at baseline-HAART delayed
  • Monthly visits

7
  • Numerous reports confirming efficacy of HAART in
    adults
  • Very few published studies in paeds in Africa
  • Small cohorts in Senegal and Cote d'Ivoire
    suggest good outcomes achievable.

8
Audit of our first 151 patients
  • Anand Reddi and Sarah Leeper
  • All children initiating HAART at Sinikithemba
    31/08/03-31/10/05
  • Chart Review
  • Hospital electronic data base

9
  • 151 Children
  • 13 Deaths
  • 0 Lost to follow up
  • Median follow up time 8 months

10
Baseline Charateristics
  • 51 (77) female
  • Median age 5,7 years at initiation(range 4 months
    to 15,4 years
  • 70 WHO Stage 3 or 4
  • 97 Severelyimmunocompromised
  • 52 weight lt 5th centile
  • 33 TB at baseline

11
TB Diagnosis
  • Positive Tb contacts
  • Suggestive CXR/Persistent CXR changes
  • Mantoux
  • Symptoms
  • Sputum/gastric washings
  • US abdomen/LP/lymph node biopsy

12

1 These patients received PMTCT outside of
McCord Hospitals PMTCT program
13
Primary caregivers
  • 1-3 primary caregivers identified for each child
  • 52 at least 1 HIV positive primary caregiver
  • 38 at least 1 primary caregiver in care at
    Sinikithemba

14
n14
n25
n14
n15
n19
n12
n38
n26
n36
n19
n36
n36
15
n151 n100 n61
n11 n6
16
How does this compare?
  • Comparable immunologically and in anthropometry
  • Very high levels of viral suppression
  • ?Adherence
  • ?Differences in subtype
  • Further investigation needed

17
Mortality
  • 8.6 compares favourably
  • All 13 in first 5 months
  • None related to adverse events
  • Significant hazard ratios
  • WHO stage 4
  • Weight lt 5th centile
  • Baseline Tb
  • Baseline pneumonia
  • Baseline chronic gastro
  • Age/orphanhood/Hb /CD4 not predictive
  • Primary caregiver HIV positive PROTECTIVE

18
Regimen Durability
  • 134 (89) still on first line
  • 15 (9.9) on second line
  • 1 on third line
  • 1 on fourth line

19
17 Regimen Changes
  • 2 adverse events
  • 6 initiation/completion of Tb treatment
  • 2 kaletra efavirenz
  • 7 treatment failures

20
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21
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22
Limitations
  • Possible information bias in chart review
  • Possible patient selection bias towards patients
    with greater financial resources

23
Conclusion
  • HAART effective and sustainable in paediatrics in
    resource limited settings
  • Children respond very favourably
    immunologically/virologically/clinically and with
    less side effects than adults
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