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Pediatric HIV
Clinical Features and
Investigations
Dr Shivanjan Goyal
Guide:- Dr Kanu Takam
Introduction
• As per WHO according to Global HIV Programme people living with HIV an estimated
population is around 39 million at the end of 2022.
• 1.5 million are children (0 to 14yrs ) .
• Since 2010 , the number of people acquiring HIV has been reduced by 38% .
• It has been seen 58% rapid decline in new HIV infections among children due to stepped
up efforts to prevent mother to child transmission of HIV.
Etiology
It is caused by HIV 1 and HIV 2 virus belonging to Reterovirade family and lentivirus
genus , which includes cytopathic viruses causing diverse disease in several animal
species .
Mode of transmission
1. Vertical Transmission
2. Postpartum/Breast feeding
3. Blood products
4. Sexual :- during child abuse / adolescence age group
5. Unsafe needles
Pathophysiology:-
1. Selective tropism for CD4+ molecular receptors :- Uses gp120 envelope protein to bind
CD4+ T cell
2. Internalisation :- For entering into cell membrane it uses CCR(Chemokine coreceptor)
3. Uncoating & Viral DNA formation :-
After entering into T cell cytoplasm
Viral RNA converted to DNA by reverse transcriptase enzyme
ss DNA converted to form ds DNA by DNA polymerase enzyme
This viral DNA then undergoes several mutations
4.Viral Integration :-
Viral DNA in cytoplasm
Enters into nucleus of host T cell using enzyme integrase At this stage it is called as
Provirus
5.Viral Replication:- HIV provirus transcripts for Viral RNA , using tat gene Viral particle
multiplies
6.Latent period and Immune attack:- May remain inactive in infected T-cell for long time
period and immune system get activated and try to eliminate virus
7.CD4+ T cell destruction:- virus particle inside T cell forms buds it get detaches from host
cell and causes cell damage.
8. Viral dissemination
9.Impact if HIV infection on other immune cells
Case Definition: HIV Infection in Adults and children 18 months or older:
Positive HIV antibody testing (rapid or laboratory-based enzyme immunoassay)
confirmed by a second HIV antibody test (rapid or laboratory-based enzyme
immunoassay) relying on different antigens or of different operating
characteristics. and /or; Positive virological test for HIV or its components (HIV-
RNA or HIV- DNA or ultrasensitive HIV p24 antigen) confirmed by a second
virological test obtained from a separate determination.
Case Definition:-Children younger than 18 months: Positive virological test
for HIV or its components (HIV-RNA or HIV- DNA or ultrasensitive HIV p24
antigen) confirmed by a second virological test obtained from a separate
determination taken more than four weeks after birth. Note: Positive antibody
testing is not recommended for definitive or confirmatory diagnosis of HIV
infection in children until 18 months of age.
INVESTIGATIONS AND DIAGNOSIS
FOR CLINICALLY SYMPTOMATIC INDIVIDUALS
1) A patient who is clinically symptomatic and suspected to have hiv infection is referred to ICTC
for confirmation of the diagnosis.
2)In this case the blood sample is tested twice using kits with either different antigens or
principles.
3)The patient is declared hiv negative if the first test is negative
4)In case the first test is positive then a second assay is done.
5)In cases of indeterminate results testing is repeated at 14-28 days with new sample.
ASSAY 2
INTERPRETATION
A1
A1 +
A2
A1+ A2+
REPORT POSITIVE
A1+A2-
A3
A1+ A2- A3+
INDETERMINATE
A1+A2-A3-
REPORT
NEGATIVE
A1-
For clinically asymptomatic individuals
1) Confirmation of HIV diagnosis in asymptomatic patients is done at ICTC using three different rapid test of
three
different antigens.
2)The individual is considered hiv negative if first test is negative and positive when all three tests shows
positive result
3)For intdeterminate results testing should be performed 14 -28 days later as shown.
4) All HIV testing should follow five essential C’S – Consent, Confidentiality , Counselling , Correct test results
and immediate correction to services for hiv prevention.
ASSAY 2
INTERPRETATION
A1
A1+
A2
A1+A2+
A3
A3+
REPORT POSITIVE
A3-
INDETERMINATE
A1+A2-
A3
A3+
INDETERMINATE
A3-
HIGH RISK
CONSIDER
INDETERMINATE
LOW RISK
CONSIDER
NEGATIVE
A1-
REPORT
NEGATIVE
WHO Clinical staging of HIV for infants and children with
established HIV infection
Clinical Stage 1:-
Asymptomatic
Persistent generalized lymphadenopathy
Clinical Stage 2:-
Unexplained persistent hepatosplenomegaly
Papular pruritic eruptions
Extensive wart virus infections
Extensive molluscum contagiosum
Recurrent oral ulcerations
Unexplained persistent parotid enlargement
Recurrent chronic URTI
Fungal nail Infections
Herpes zoster infections
Clinical Stage 3:-
Unexplained malnutrition not adequately responding to standard therapy
Unexplained persistent fever/diarrhea
Persistent oral candidiasis
Oral hairy leukoplakia
Lymph node TB
Pulmonary TB
Severe recurrent Bacterial Pneumonia
Unexplained Anemia , neutropenia or chronic thrombocytopenia
Clinical Stage 4:-
Unexplained Stunting ,wasting or severe malnutrition not responding to standard treatment
Extrapulmonary TB
Kaposi sarcoma
Esophageal Candidiasis
HIV encephalopathy
CMV infection
Fungal Infections
Disseminated non tuberculous mycobacterial infections
HIV associated cardiomyopathy or nephropathy
Progressive multifocal leukoencephalopathy
Diagnosis
FIRST TESTING WHILE CHILD IS ON AR
PROPHYLAXIS
AT 6 WEEKS
HIV DNA PCR
HIV DNA PCR+
START ART AND
ADD SYP
SEPTRAN TILL 5
YEARS
HIV DNA PCR-
FOLLOW UP AT 6
MONTHS WITH
PCR TESTING
IF POSITIVE IF NEGATIVE
DO ELISA
TESTING AT 18
MONTHS
POSITIVE
START ART
NEGATIVE
DO PREVENTIVE
MEASURES
BASELINE INVESTIGATIONS
• HEMOGRAM/CBC
• URINE FOR ROUTINE AND MICROSCOPIC EXAMINATION
• FASTING BLOOD SUGAR
• BLOOD UREA,SERUM CREATININE
• SERUM BILIRUBIN, ALT (SGPT)
• VDRL CD4 COUNT
• X-RAY CHEST PA VIEW
• SYMPTOMS AND SIGNS DIRECTED INVESTIGATIONS FOR RULING OUT OI’S.
• COMPLETE LFT
• LIPID PROFILE
• USG A+P
• RK-39 STRIP FOR LEISHMANIA IN CASE TRAVELLING TO ENDEMIC AREAS
• CBNAAT SPUTUM
• STOOL R/M AND CULTURE
Theme:-
Global,
Solidarity AND
Shared
Responsibility
Thank you

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HIV Clinical and Diagnosis 2.pptx

  • 1. Pediatric HIV Clinical Features and Investigations Dr Shivanjan Goyal Guide:- Dr Kanu Takam
  • 2. Introduction • As per WHO according to Global HIV Programme people living with HIV an estimated population is around 39 million at the end of 2022. • 1.5 million are children (0 to 14yrs ) . • Since 2010 , the number of people acquiring HIV has been reduced by 38% . • It has been seen 58% rapid decline in new HIV infections among children due to stepped up efforts to prevent mother to child transmission of HIV.
  • 3. Etiology It is caused by HIV 1 and HIV 2 virus belonging to Reterovirade family and lentivirus genus , which includes cytopathic viruses causing diverse disease in several animal species . Mode of transmission 1. Vertical Transmission 2. Postpartum/Breast feeding 3. Blood products 4. Sexual :- during child abuse / adolescence age group 5. Unsafe needles
  • 4. Pathophysiology:- 1. Selective tropism for CD4+ molecular receptors :- Uses gp120 envelope protein to bind CD4+ T cell 2. Internalisation :- For entering into cell membrane it uses CCR(Chemokine coreceptor) 3. Uncoating & Viral DNA formation :- After entering into T cell cytoplasm Viral RNA converted to DNA by reverse transcriptase enzyme ss DNA converted to form ds DNA by DNA polymerase enzyme This viral DNA then undergoes several mutations 4.Viral Integration :- Viral DNA in cytoplasm Enters into nucleus of host T cell using enzyme integrase At this stage it is called as Provirus
  • 5. 5.Viral Replication:- HIV provirus transcripts for Viral RNA , using tat gene Viral particle multiplies 6.Latent period and Immune attack:- May remain inactive in infected T-cell for long time period and immune system get activated and try to eliminate virus 7.CD4+ T cell destruction:- virus particle inside T cell forms buds it get detaches from host cell and causes cell damage. 8. Viral dissemination 9.Impact if HIV infection on other immune cells
  • 6. Case Definition: HIV Infection in Adults and children 18 months or older: Positive HIV antibody testing (rapid or laboratory-based enzyme immunoassay) confirmed by a second HIV antibody test (rapid or laboratory-based enzyme immunoassay) relying on different antigens or of different operating characteristics. and /or; Positive virological test for HIV or its components (HIV- RNA or HIV- DNA or ultrasensitive HIV p24 antigen) confirmed by a second virological test obtained from a separate determination. Case Definition:-Children younger than 18 months: Positive virological test for HIV or its components (HIV-RNA or HIV- DNA or ultrasensitive HIV p24 antigen) confirmed by a second virological test obtained from a separate determination taken more than four weeks after birth. Note: Positive antibody testing is not recommended for definitive or confirmatory diagnosis of HIV infection in children until 18 months of age.
  • 8. FOR CLINICALLY SYMPTOMATIC INDIVIDUALS 1) A patient who is clinically symptomatic and suspected to have hiv infection is referred to ICTC for confirmation of the diagnosis. 2)In this case the blood sample is tested twice using kits with either different antigens or principles. 3)The patient is declared hiv negative if the first test is negative 4)In case the first test is positive then a second assay is done. 5)In cases of indeterminate results testing is repeated at 14-28 days with new sample.
  • 9. ASSAY 2 INTERPRETATION A1 A1 + A2 A1+ A2+ REPORT POSITIVE A1+A2- A3 A1+ A2- A3+ INDETERMINATE A1+A2-A3- REPORT NEGATIVE A1-
  • 10. For clinically asymptomatic individuals 1) Confirmation of HIV diagnosis in asymptomatic patients is done at ICTC using three different rapid test of three different antigens. 2)The individual is considered hiv negative if first test is negative and positive when all three tests shows positive result 3)For intdeterminate results testing should be performed 14 -28 days later as shown. 4) All HIV testing should follow five essential C’S – Consent, Confidentiality , Counselling , Correct test results and immediate correction to services for hiv prevention.
  • 11. ASSAY 2 INTERPRETATION A1 A1+ A2 A1+A2+ A3 A3+ REPORT POSITIVE A3- INDETERMINATE A1+A2- A3 A3+ INDETERMINATE A3- HIGH RISK CONSIDER INDETERMINATE LOW RISK CONSIDER NEGATIVE A1- REPORT NEGATIVE
  • 12. WHO Clinical staging of HIV for infants and children with established HIV infection Clinical Stage 1:- Asymptomatic Persistent generalized lymphadenopathy Clinical Stage 2:- Unexplained persistent hepatosplenomegaly Papular pruritic eruptions Extensive wart virus infections Extensive molluscum contagiosum Recurrent oral ulcerations Unexplained persistent parotid enlargement Recurrent chronic URTI Fungal nail Infections Herpes zoster infections
  • 13. Clinical Stage 3:- Unexplained malnutrition not adequately responding to standard therapy Unexplained persistent fever/diarrhea Persistent oral candidiasis Oral hairy leukoplakia Lymph node TB Pulmonary TB Severe recurrent Bacterial Pneumonia Unexplained Anemia , neutropenia or chronic thrombocytopenia Clinical Stage 4:- Unexplained Stunting ,wasting or severe malnutrition not responding to standard treatment Extrapulmonary TB Kaposi sarcoma Esophageal Candidiasis HIV encephalopathy CMV infection Fungal Infections Disseminated non tuberculous mycobacterial infections HIV associated cardiomyopathy or nephropathy Progressive multifocal leukoencephalopathy
  • 15. FIRST TESTING WHILE CHILD IS ON AR PROPHYLAXIS AT 6 WEEKS HIV DNA PCR HIV DNA PCR+ START ART AND ADD SYP SEPTRAN TILL 5 YEARS HIV DNA PCR- FOLLOW UP AT 6 MONTHS WITH PCR TESTING IF POSITIVE IF NEGATIVE DO ELISA TESTING AT 18 MONTHS POSITIVE START ART NEGATIVE DO PREVENTIVE MEASURES
  • 16.
  • 17. BASELINE INVESTIGATIONS • HEMOGRAM/CBC • URINE FOR ROUTINE AND MICROSCOPIC EXAMINATION • FASTING BLOOD SUGAR • BLOOD UREA,SERUM CREATININE • SERUM BILIRUBIN, ALT (SGPT) • VDRL CD4 COUNT • X-RAY CHEST PA VIEW • SYMPTOMS AND SIGNS DIRECTED INVESTIGATIONS FOR RULING OUT OI’S. • COMPLETE LFT • LIPID PROFILE • USG A+P • RK-39 STRIP FOR LEISHMANIA IN CASE TRAVELLING TO ENDEMIC AREAS • CBNAAT SPUTUM • STOOL R/M AND CULTURE