Clinical manifestations of adolescents with HIV/AIDS in Jamaica
To characterize the clinicopathological manifestations and outcomes of a cohort of HIV-infected Jamaican adolescents. This is a retrospective cohort study to determine demographic, clinical, immunological characteristics, antiretroviral uptake and mortality in 94 adolescents aged 10-19 years followe...
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Veröffentlicht in: | West Indian medical journal 2008-06, Vol.57 (3), p.257-264 |
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creator | Harrison, A Pierre, R B Palmer, P Moore, J Davis, D Dunkley-Thompson, J Figueroa, J P Christie, C D C |
description | To characterize the clinicopathological manifestations and outcomes of a cohort of HIV-infected Jamaican adolescents.
This is a retrospective cohort study to determine demographic, clinical, immunological characteristics, antiretroviral uptake and mortality in 94 adolescents aged 10-19 years followed in the Kingston Paediatric and Perinatal HIV/AIDS Programme (KPAIDS) between September 2002 and May 2007. Parametric and non-parametric tests are used to compare variables.
The median age at initial presentation was 10.0 years (interquartile range (IQR) 7.0-12.0 years), 54.3% (51) were female (p = 0.024), transmission was primarily mother-to-child (70, 73.4%), with 87% (61) of the latter presenting as slow progressors. Sexual transmission accounted for 19.1% and there was significant female predominance (n=15; p = 0.024). At most recent visit, perinatally infected adolescents were more likely (p < 0.0001) to reside with a non-parent (n=42) than a biological parent (n=19) and most had Centers for Disease Control and Prevention (CDC) category C (35/50%) disease, whereas the majority of non-perinatally infected children were classified CDC category A. Mean z scores for height-for-age was -1.47 +/- 1.21 (n=77), weight-for-age -1.06 +/- 1.44 (n=80) and BMI-for-age -0.34 +/- 1.21 (n=76) respectively; females (n=41) were taller than males (n=36) at their current height (p = 0.031). Lymphadenopathy (82%), dermatitis (72.0%), hepatomegaly (48%) and parotitis (48%) were the most common clinical manifestations, with significant predilection for lymphadenopathy (p < or = 0.0001), dermatitis (p = 0.010), splenomegaly (p = 0.008), hepatomegaly (p = 0.001) and parotitis (p = 0.007) among perinatally infected children. Median baseline CD4+ cell count was 256.0/microL (IQR 71.0 - 478.0 cells/microL); median most recent CD4+ cell count was 521/microL (IQR 271.0 - 911.0 cells/microL). Seventy-six per cent (n=71) were initiated with highly active antiretroviral therapy (HAART) and 62 (87.3%) were currently receiving first-line therapy. Six behaviourally infected females became pregnant, resulting in five live births. There were seven deaths (7.4%).
This study comprehensively characterizes HIV infection among perinatally infected teens with predominantly slow-progressor disease and an increasing population of sexually-infected adolescents. As the cohort transitions to adulthood, adolescent developmental, mental health and life planning issues must be urgently addressed. |
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This is a retrospective cohort study to determine demographic, clinical, immunological characteristics, antiretroviral uptake and mortality in 94 adolescents aged 10-19 years followed in the Kingston Paediatric and Perinatal HIV/AIDS Programme (KPAIDS) between September 2002 and May 2007. Parametric and non-parametric tests are used to compare variables.
The median age at initial presentation was 10.0 years (interquartile range (IQR) 7.0-12.0 years), 54.3% (51) were female (p = 0.024), transmission was primarily mother-to-child (70, 73.4%), with 87% (61) of the latter presenting as slow progressors. Sexual transmission accounted for 19.1% and there was significant female predominance (n=15; p = 0.024). At most recent visit, perinatally infected adolescents were more likely (p < 0.0001) to reside with a non-parent (n=42) than a biological parent (n=19) and most had Centers for Disease Control and Prevention (CDC) category C (35/50%) disease, whereas the majority of non-perinatally infected children were classified CDC category A. Mean z scores for height-for-age was -1.47 +/- 1.21 (n=77), weight-for-age -1.06 +/- 1.44 (n=80) and BMI-for-age -0.34 +/- 1.21 (n=76) respectively; females (n=41) were taller than males (n=36) at their current height (p = 0.031). Lymphadenopathy (82%), dermatitis (72.0%), hepatomegaly (48%) and parotitis (48%) were the most common clinical manifestations, with significant predilection for lymphadenopathy (p < or = 0.0001), dermatitis (p = 0.010), splenomegaly (p = 0.008), hepatomegaly (p = 0.001) and parotitis (p = 0.007) among perinatally infected children. Median baseline CD4+ cell count was 256.0/microL (IQR 71.0 - 478.0 cells/microL); median most recent CD4+ cell count was 521/microL (IQR 271.0 - 911.0 cells/microL). Seventy-six per cent (n=71) were initiated with highly active antiretroviral therapy (HAART) and 62 (87.3%) were currently receiving first-line therapy. Six behaviourally infected females became pregnant, resulting in five live births. There were seven deaths (7.4%).
This study comprehensively characterizes HIV infection among perinatally infected teens with predominantly slow-progressor disease and an increasing population of sexually-infected adolescents. As the cohort transitions to adulthood, adolescent developmental, mental health and life planning issues must be urgently addressed.</description><identifier>ISSN: 0043-3144</identifier><identifier>PMID: 19583125</identifier><language>eng</language><publisher>Jamaica</publisher><subject>Adaptation, Psychological ; Adolescent ; Anti-HIV Agents - therapeutic use ; CD4 Lymphocyte Count ; Child ; Cohort Studies ; Female ; HIV Infections - epidemiology ; HIV Infections - pathology ; HIV Infections - psychology ; HIV Infections - transmission ; Humans ; Jamaica - epidemiology ; Male ; Patient Education as Topic ; Pregnancy ; Pregnancy Complications, Infectious - epidemiology ; Pregnancy Complications, Infectious - pathology ; Pregnancy Complications, Infectious - psychology ; Retrospective Studies ; Risk Factors ; Sexually Transmitted Diseases, Viral - epidemiology ; Sexually Transmitted Diseases, Viral - pathology ; Sexually Transmitted Diseases, Viral - psychology ; Young Adult</subject><ispartof>West Indian medical journal, 2008-06, Vol.57 (3), p.257-264</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19583125$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harrison, A</creatorcontrib><creatorcontrib>Pierre, R B</creatorcontrib><creatorcontrib>Palmer, P</creatorcontrib><creatorcontrib>Moore, J</creatorcontrib><creatorcontrib>Davis, D</creatorcontrib><creatorcontrib>Dunkley-Thompson, J</creatorcontrib><creatorcontrib>Figueroa, J P</creatorcontrib><creatorcontrib>Christie, C D C</creatorcontrib><title>Clinical manifestations of adolescents with HIV/AIDS in Jamaica</title><title>West Indian medical journal</title><addtitle>West Indian Med J</addtitle><description>To characterize the clinicopathological manifestations and outcomes of a cohort of HIV-infected Jamaican adolescents.
This is a retrospective cohort study to determine demographic, clinical, immunological characteristics, antiretroviral uptake and mortality in 94 adolescents aged 10-19 years followed in the Kingston Paediatric and Perinatal HIV/AIDS Programme (KPAIDS) between September 2002 and May 2007. Parametric and non-parametric tests are used to compare variables.
The median age at initial presentation was 10.0 years (interquartile range (IQR) 7.0-12.0 years), 54.3% (51) were female (p = 0.024), transmission was primarily mother-to-child (70, 73.4%), with 87% (61) of the latter presenting as slow progressors. Sexual transmission accounted for 19.1% and there was significant female predominance (n=15; p = 0.024). At most recent visit, perinatally infected adolescents were more likely (p < 0.0001) to reside with a non-parent (n=42) than a biological parent (n=19) and most had Centers for Disease Control and Prevention (CDC) category C (35/50%) disease, whereas the majority of non-perinatally infected children were classified CDC category A. Mean z scores for height-for-age was -1.47 +/- 1.21 (n=77), weight-for-age -1.06 +/- 1.44 (n=80) and BMI-for-age -0.34 +/- 1.21 (n=76) respectively; females (n=41) were taller than males (n=36) at their current height (p = 0.031). Lymphadenopathy (82%), dermatitis (72.0%), hepatomegaly (48%) and parotitis (48%) were the most common clinical manifestations, with significant predilection for lymphadenopathy (p < or = 0.0001), dermatitis (p = 0.010), splenomegaly (p = 0.008), hepatomegaly (p = 0.001) and parotitis (p = 0.007) among perinatally infected children. Median baseline CD4+ cell count was 256.0/microL (IQR 71.0 - 478.0 cells/microL); median most recent CD4+ cell count was 521/microL (IQR 271.0 - 911.0 cells/microL). Seventy-six per cent (n=71) were initiated with highly active antiretroviral therapy (HAART) and 62 (87.3%) were currently receiving first-line therapy. Six behaviourally infected females became pregnant, resulting in five live births. There were seven deaths (7.4%).
This study comprehensively characterizes HIV infection among perinatally infected teens with predominantly slow-progressor disease and an increasing population of sexually-infected adolescents. As the cohort transitions to adulthood, adolescent developmental, mental health and life planning issues must be urgently addressed.</description><subject>Adaptation, Psychological</subject><subject>Adolescent</subject><subject>Anti-HIV Agents - therapeutic use</subject><subject>CD4 Lymphocyte Count</subject><subject>Child</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>HIV Infections - epidemiology</subject><subject>HIV Infections - pathology</subject><subject>HIV Infections - psychology</subject><subject>HIV Infections - transmission</subject><subject>Humans</subject><subject>Jamaica - epidemiology</subject><subject>Male</subject><subject>Patient Education as Topic</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Infectious - epidemiology</subject><subject>Pregnancy Complications, Infectious - pathology</subject><subject>Pregnancy Complications, Infectious - psychology</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Sexually Transmitted Diseases, Viral - epidemiology</subject><subject>Sexually Transmitted Diseases, Viral - pathology</subject><subject>Sexually Transmitted Diseases, Viral - psychology</subject><subject>Young Adult</subject><issn>0043-3144</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j7lOxDAURV2AmGHgF5A7qgjbz46TCo3CMoNGomBpoxcvwshZiBMh_p5IDNVtzr0694SsGZOQAZdyRc5T-mQsB56zM7LipSqAC7Umt1UMXTAYaYtd8C5NOIW-S7T3FG0fXTKumxL9DtMH3e3fb7b7uxcaOvqELS69C3LqMSZ3ecwNeXu4f6122eH5cV9tD9kgOJsyrhVHi6C4dWgNgHDM6UY0wmjuWa5A-xI1Ai-kKBdL01hvZK6ULHUhFWzI9d_uMPZf86JZt2FRixE718-p1gCQi7LgC3l1JOemdbYextDi-FP_f4ZfqKdP8g</recordid><startdate>200806</startdate><enddate>200806</enddate><creator>Harrison, A</creator><creator>Pierre, R B</creator><creator>Palmer, P</creator><creator>Moore, J</creator><creator>Davis, D</creator><creator>Dunkley-Thompson, J</creator><creator>Figueroa, J P</creator><creator>Christie, C D C</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200806</creationdate><title>Clinical manifestations of adolescents with HIV/AIDS in Jamaica</title><author>Harrison, A ; Pierre, R B ; Palmer, P ; Moore, J ; Davis, D ; Dunkley-Thompson, J ; Figueroa, J P ; Christie, C D C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p210t-1751ada351deadc332e0e7b2b2c71f06537f9a7a318429316cbdfc46554978453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adaptation, Psychological</topic><topic>Adolescent</topic><topic>Anti-HIV Agents - therapeutic use</topic><topic>CD4 Lymphocyte Count</topic><topic>Child</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>HIV Infections - epidemiology</topic><topic>HIV Infections - pathology</topic><topic>HIV Infections - psychology</topic><topic>HIV Infections - transmission</topic><topic>Humans</topic><topic>Jamaica - epidemiology</topic><topic>Male</topic><topic>Patient Education as Topic</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Infectious - epidemiology</topic><topic>Pregnancy Complications, Infectious - pathology</topic><topic>Pregnancy Complications, Infectious - psychology</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Sexually Transmitted Diseases, Viral - epidemiology</topic><topic>Sexually Transmitted Diseases, Viral - pathology</topic><topic>Sexually Transmitted Diseases, Viral - psychology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harrison, A</creatorcontrib><creatorcontrib>Pierre, R B</creatorcontrib><creatorcontrib>Palmer, P</creatorcontrib><creatorcontrib>Moore, J</creatorcontrib><creatorcontrib>Davis, D</creatorcontrib><creatorcontrib>Dunkley-Thompson, J</creatorcontrib><creatorcontrib>Figueroa, J P</creatorcontrib><creatorcontrib>Christie, C D C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>West Indian medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harrison, A</au><au>Pierre, R B</au><au>Palmer, P</au><au>Moore, J</au><au>Davis, D</au><au>Dunkley-Thompson, J</au><au>Figueroa, J P</au><au>Christie, C D C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical manifestations of adolescents with HIV/AIDS in Jamaica</atitle><jtitle>West Indian medical journal</jtitle><addtitle>West Indian Med J</addtitle><date>2008-06</date><risdate>2008</risdate><volume>57</volume><issue>3</issue><spage>257</spage><epage>264</epage><pages>257-264</pages><issn>0043-3144</issn><abstract>To characterize the clinicopathological manifestations and outcomes of a cohort of HIV-infected Jamaican adolescents.
This is a retrospective cohort study to determine demographic, clinical, immunological characteristics, antiretroviral uptake and mortality in 94 adolescents aged 10-19 years followed in the Kingston Paediatric and Perinatal HIV/AIDS Programme (KPAIDS) between September 2002 and May 2007. Parametric and non-parametric tests are used to compare variables.
The median age at initial presentation was 10.0 years (interquartile range (IQR) 7.0-12.0 years), 54.3% (51) were female (p = 0.024), transmission was primarily mother-to-child (70, 73.4%), with 87% (61) of the latter presenting as slow progressors. Sexual transmission accounted for 19.1% and there was significant female predominance (n=15; p = 0.024). At most recent visit, perinatally infected adolescents were more likely (p < 0.0001) to reside with a non-parent (n=42) than a biological parent (n=19) and most had Centers for Disease Control and Prevention (CDC) category C (35/50%) disease, whereas the majority of non-perinatally infected children were classified CDC category A. Mean z scores for height-for-age was -1.47 +/- 1.21 (n=77), weight-for-age -1.06 +/- 1.44 (n=80) and BMI-for-age -0.34 +/- 1.21 (n=76) respectively; females (n=41) were taller than males (n=36) at their current height (p = 0.031). Lymphadenopathy (82%), dermatitis (72.0%), hepatomegaly (48%) and parotitis (48%) were the most common clinical manifestations, with significant predilection for lymphadenopathy (p < or = 0.0001), dermatitis (p = 0.010), splenomegaly (p = 0.008), hepatomegaly (p = 0.001) and parotitis (p = 0.007) among perinatally infected children. Median baseline CD4+ cell count was 256.0/microL (IQR 71.0 - 478.0 cells/microL); median most recent CD4+ cell count was 521/microL (IQR 271.0 - 911.0 cells/microL). Seventy-six per cent (n=71) were initiated with highly active antiretroviral therapy (HAART) and 62 (87.3%) were currently receiving first-line therapy. Six behaviourally infected females became pregnant, resulting in five live births. There were seven deaths (7.4%).
This study comprehensively characterizes HIV infection among perinatally infected teens with predominantly slow-progressor disease and an increasing population of sexually-infected adolescents. As the cohort transitions to adulthood, adolescent developmental, mental health and life planning issues must be urgently addressed.</abstract><cop>Jamaica</cop><pmid>19583125</pmid><tpages>8</tpages></addata></record> |
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subjects | Adaptation, Psychological Adolescent Anti-HIV Agents - therapeutic use CD4 Lymphocyte Count Child Cohort Studies Female HIV Infections - epidemiology HIV Infections - pathology HIV Infections - psychology HIV Infections - transmission Humans Jamaica - epidemiology Male Patient Education as Topic Pregnancy Pregnancy Complications, Infectious - epidemiology Pregnancy Complications, Infectious - pathology Pregnancy Complications, Infectious - psychology Retrospective Studies Risk Factors Sexually Transmitted Diseases, Viral - epidemiology Sexually Transmitted Diseases, Viral - pathology Sexually Transmitted Diseases, Viral - psychology Young Adult |
title | Clinical manifestations of adolescents with HIV/AIDS in Jamaica |
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