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Transcript of 1 Guidance on Cotrimoxazole Prophylactic Therapy for HIV Exposed/Infected Children HAIVN Harvard...
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Guidance on Cotrimoxazole Prophylactic Therapy for
HIV Exposed/Infected Children
HAIVNHarvard Medical School AIDS
Initiative in Vietnam
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By the end of this session, participants should be able to: Explain indications of Cotrimoxazole
Prophylactic Therapy (CPT) for HIV-exposed and HIV-infected children
Describe clinical and testing follow up while taking CTX Prophylactic Therapy
Can explain when stop taking CTX Prophylactic Therapy
Learning Objectives
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Introduction
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Anti-retrovirus treatment could prevent OIs
Some medications (mainly CTX) have been proved that they could prevent OIs
Counseling people who provide care for infected children: • Food hygiene • Good nutrition• Regular check up
OI Prophylactic Therapies
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Primary prophylaxis: Giving medication
to prevent an OI from occurring in the first place
Secondary prophylaxis: Giving medication
after an OI is treated to prevent it from recurring
Also known as maintenance therapy
Two Types of OI Prophylaxis
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Cotrimoxazole (CTX): Combination of sulfamethoxazole
and trimethoprim Broad-spectrum antibiotics for gram
positive and negative bacteria, fungi and protozoa
Cotrimoxazole prophylaxis: Overview (1)
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CTX prophylaxis: A part of a standardized Care and
Treatment Package for HIV/AIDS patients
High effective, simple, and economical intervention
Need to be maintained until having evidence of immunological recovery.
Cotrimoxazole prophylaxis: Overview (2)
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Prevents:• PCP (Pneumocystis jiroveci pneumonia)• Cerebral toxoplasmosis
Reduces the occurrence of:• Pneumonia due to streptococcus
pneumoniae, Nocardia, Haemophilus Influenzae, S. aureus, gram-negative bacilli
• Diarrheas due to Salmonella, Isospoiaris and protozoa
• Malaria
Cotrimoxazole prophylaxis: Overview (3)
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PCP is the most common OI in infants and young children • Mortality associated with PCP in infants
is as high as 40% despite treatment CPT is highly effective at preventing
PCP • CPT has been shown to reduce mortality
in infants and children
CTX prophylaxis for PCP
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High Rate of PCP in Infants Age 2-8 Months
Age in Months
Nu
mb
er o
f C
ases
0
0
50
100
150
200
250
300
350
400
450
2 4 6 8 10 12 14 16 18 20 22 24
Other AIDS-defining conditions
Pneumocystis carinii pneumonia
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Indications and Dosefor Cotrimoxazole Prophylaxis
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Prevent OIs: PCP Cerebral toxoplasmosis Some diarrheas Pneumonia due to bacterium
Objective of CTX prophylaxis
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All HIV-exposed infants/children:
Starting at 4–6 weeks of age and Continued until HIV infection is
excluded
Indications for Primary Cotrimoxazole Prophylaxis
Hướng dẫn Quốc gia về Chẩn đoán và Điều trị HIV/AIDS. Bộ Y tế, Việt Nam, 2011.
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HIV-confirmed children
< 24 months
old•All children regardless of symptoms or CD4 count
24-60 months
old
•Clinical stages 2, 3, 4 regardless of CD4 count or
•CD4 ≤ 25% or CD4 ≤ 750 cells/ml regardless of
clinical stage
≥ 5years old
•Clinical stages 1, 2 with CD4 ≤ 350 cells/ml
•Clinical stages 2, 3, and 4 if CD4 unavailable or
•Clinical stages 3, 4 regardless of CD4 count
Indications for Primary Cotrimoxazole Prophylaxis (2)
National Guidelines for the Diagnosis and Treatment of HIV/AIDS. Ministry of Health, Vietnam. 2011.
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Exposed/infected children who acquired: PCP Cerebral toxoplasmosis
Indications for Secondary Cotrimoxazole Prophylaxis
Hướng dẫn Quốc gia về Chẩn đoán và Điều trị HIV/AIDS. Bộ Y tế, Việt Nam, 2011.
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Thành phần
Trimethoprim (TMP) andSulfamethoxazole (SMX)
Dosing 5 mg TMP/kg/day once a day
Formulations
Liquid 8mg TMP/40mg SMXper 1ml
Tablet
80mg TMP/400mg SMX(480mg tablet)
Or
160mg TMP/800mg SMX(960mg tablet)
CTX Prophylaxis: dosing
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Nausea, vomiting Rash can occur during first 1-2 weeks Severe side effects:
• Anemia• Granulocytopenia• Hypersensitivity reaction• Hepatotoxicity
Cotrimoxazole Side Effects (1)
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Need to counsel for care givers and children:• Side effects• How to manage• Check up immediately when suspected
signs of severe side effect occur Do complete blood count, liver
enzymes measuring when anemia or hepatotoxicity is suspected
Cotrimoxazole Side Effects (2)
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Divided into 4 groups Topics of discussion:
• Group 1: manifestations/symptoms of rash at grade 1 and how to manage
• Group 2: manifestations/symptoms of rash at grade 2 and how to manage
• Group 3: manifestations/symptoms of rash at grade 3 and how to manage
• Group 4: manifestations/symptoms of rash at grade 4 and how to manage
Time: 10 minutes
Group Discussion
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Grade Clinical description Management
Grade 1(mild)
Erythema -Continue CPT with careful follow up.-Provide symptomatic treatment and anti-histamine
Grade 2(moderate)
Diffuse maculopapular rash, dry desquamation
Grade 3(severe)
Bulla, mucosal ulceration - Hospitalization with supportive treatment- CTX should be permanently discontinued
Grade 4(very
severe)
Exfoliative dermatitis, Steven Johnson syndrome or erythema multiforms, moist desquamation
Rash due to CTX and management
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There are no adequate data on CTX desensitization in children
Other medications need to be noticed and may be overlapping drug toxicity: • EFV • NVP • Isoniazid…
Rash due to CTX and management
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Indication: allergy to CTX Dose:
• 2mg/kg/day, once a day or• 4mg/kg/time, once a week
Note: • Less effect than CTX in terms of PCP
prevention• Can not prevent Toxoplasma
Alternative Therapy: Dapson
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Indication of discontinuing CPT
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Discontinuing CPT for HIV-exposed Children
Stop CTX prophylaxis when HIV infection has been definitively excluded
Infants <18 months Children >18 months
Confirmed negative HIV virological test and antibody
test
6 weeks after complete cessation of breastfeeding
Confirmed negative HIV antibody test
6 weeks after complete cessation of breastfeeding
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Discontinuing CPT forHIV-infected Children (While on ARV)
National Guidelines for the Diagnosis and Treatment of HIV/AIDS. Ministry of Health, Vietnam. 2009.
0-24 months old Do not discontinue
24-60 months old
Discontinue when:
CD4 count > 25% for at least 6 months
5 years old
Discontinue when:
CD4 count > 200 for at least 6 months
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Case Study
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CPT is highly effective for prevention of PCP in infants and children
All HIV-exposed infants should receive CPT starting at 4–6 weeks of age
Follow up closely CTX side effects and manage them timely
Indication of discontinuing CPT:• Exposed infants: HIV infection has been
definitively excluded • Infected infants/children: after ARV treatment and
CD4 higher the threshold as MOH required for each age group for 6 months continuously.
Key Points
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Thank you!
Questions?