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Page 30

allied

academies

August 16-17, 2018 | Paris, France

Primary Healthcare

12

th

International Conference on

International Conference and Medicare Expo on

&

Pediatrics Health Care

Joint Event

Journal of Current Pediatric Research | Volume: 22

Clinical profile of Paediatric HIV/AIDS

Meena Kumari Mili, Niru Prabha Saharia, Arati Deka

and

Swaroop Kumar Baruah

Gauhati Medical College & Hospital, India

INTRODUCTION:

Pediatric HIV/AIDS differs from adult HIV. With the availability

of antiretroviral therapy (ART), HIV infection, has now become

a chronic treatable condition in children. HIV means Human

Immunodeficiency Virus. HIV virus causes AIDS (Acquired

Immunodeficiency Syndrome) also known as SLIMdisease. AIDS

is the end stage of disease representing breakdown of immune

defense mechanism, leaving patient prey to progressive

opportunistic infections and malignancies. Infection occurs

when the virus integrates with the genetic material of a CD4

white blood cell in the immune system. Children of today are

the youth of tomorrow. HIV affects this very precious generation

and bears grave consequences to our future, our nation, the

continent and the world at large. Ever since the report of first

paediatric case in 1983, there has been an alarming increase

in the rate of disease. There is an increased frequency of

malnutrition and infections that may be more persistent,

severe and less responsive to treatment. In addition, these

growing children are left with inescapable challenges of facing

not only lifelong adherence with complex treatment regimens,

but also enormous psychosocial, mental and neuro-cognitive

issues. With the availability of antiretroviral therapy (ART),

HIV infection has now become a chronic treatable condition

in children. It is important to concentrate on paediatric HIV

as it differs from adult HIV regarding epidemiology, mode

of transmission, diagnosis, immunology, pathology clinical

spectrum, management and presentation.

AIMS & OBJECTIVES:

Study different clinical presentations of HIV/AIDS in paediatric

age group (18 months-15 years)

METHODS:

It was a hospital based observational study. The case records

of all children diagnosed with paediatric HIV infection between

1st July 2007 to 30th June 2017, who fulfill the inclusion and

exclusion criteria were reviewed and their clinical profile

prevalence were evaluated.

RESULTS:

In the study, 31 (25.84%) cases were between 18 months-3

years age, 49 (40.83%) were between >3 years – 5 years and

40 (33.33%) were of more than 5 years age. Majority of the

children were from rural area 68 (56.7%) and 52 (43.3%) were

from urban area. Perinatal (vertical) mode of transmission was

the most common mode of transmission. There were 10 (8.3%)

asymptomatic cases. Fever was the most common presenting

complaint. On clinical examination, undernutrition was the

most common finding.

In the present study, 45 cases who were on ART were followed

up at least once. Majority of the follow ups were for respiratory

problems and fever. The nutritional status and the rates of

common infection in these children on follow up were low.

CONCLUSIONS:

Intensified screening of HIV infection in

asymptomatic children by high suspicion will help in diagnosing

HIV at the earliest, and thus they can be subjected to early

management helping in improving the immunological status

and thereby increase the life span of the child.

Speaker Biography

Meena Kumari Mili has done her postgraduation in Paediatrics from Gauhati Medical

College, Assam, India. She has done her research on Paediatric HIV/AIDS while she

was post graduate trainee in Gauhati Medical College, India. She has presented her

research work on paediatric HIV/AIDS in various regional and national conferences

in India and has been awarded for the same. She has also published her works on

paediatric HIV/AIDS. She has been involved in building awareness on HIV/AIDS.

e:

kutcho.mili230@gmail.com

Notes:

Meena Kumari Mili et al.

, Pediatrics & Primary HealthCare 2018, Volume 22

DOI: 10.4066/0971-9032-C1-003